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Listă de lucrări

Bănescu Claudia Violeta

a. Teza de doctorat

“Anomaliile cromozomiale - indicator independent de diagnostic şi de prognostic în

hemopatiile maligne”, conducător ştiinţific Prof. Dr. Marius Sabău, confirmat prin Ordinul

Ministerului Educaţiei, Cercetării şi Inovării. nr. 3492 /23.03.2010, calificativ Foarte bine.

b. Cărţi publicate

Cărți de specialitate apărute în edituri recunoscute CNCSIS/edituri internationale – prim-

autor sau editor/coordonator

Bănescu Claudia, Duicu Carmen, Todoran Butilă Anamaria, Moldovan G Valeriu,

Tripon Florin Noțiuni de genetică și implicaţii genetice în patologia cu interesare

cranio-maxilo-facială. Editura University Press, Tîrgu-Mureș, 2014, 156 pg. ISBN 978-

973-169-330-9. cod CNCSIS 210.

Bănescu Claudia. Noțiuni de genetică în asistența medicală. Editura University Press,

Tîrgu Mureș, 2013, 153 pg. ISBN 978-973-169-209-8, cod CNCSIS 210.

Bănescu Claudia. Citogenetica leucemiilor acute. Editura University Press, Tîrgu

Mureș, 2013, 125 pg. ISBN 978-973-169-224-1, cod CNCSIS 210.

Cărți de specialitate apărute în edituri recunoscute CNCSIS/edituri internationale – co-autor

sau co-editor

Ionela Paşcanu I, Katalin Csép, Claudia Mureşan. Aplicaţii practice în genetica

umană. Editura University Press, Tîrgu Mureș, 2005, 166 pg. ISBN: 973-7788-28-1,

cod CNCSIS: 210.

Katalin Csep, Claudia Bănescu, Anamaria Todoran Butilă. Genetica medicală axată pe

sfera oro-maxilo-facială. Editura University Press, Tîrgu Mureș, 2010, 112 pg, ISBN

978-973-169-117-6, cod CNCSIS: 210.

Katalin Csep, Claudia Bănescu, Anamaria Todoran Butilă. Genomica nutrițională –

aspecte practice. Editura University Press, Tîrgu Mureș, 2013, 169 pg. ISBN 978-973-

169-281-4, cod CNCSIS: 210.

c. Capitole in volume colective

Capitole în tratate/volume colective apărute în edituri recunoscute CNCSIS/edituri

internationale – prim-autor

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Bănescu Claudia. Mutațiile genice. Dobreanu Minodora. Biochimie clinică. Implicații

practice. Editia 3, Ed. University Press, 2015, cap. 24, pg. 303-320. ISBN 978-973-169-

357-6

Bănescu Claudia. Anomalii genetice în cancer. Analize genetice în cancer. Dobreanu

Minodora, Biochimie clinică. Implicații practice. Editia 3, Ed. University Press, 2015,

cap. 25, pg. 321-334, ISBN 978-973-169-357-6, cod CNCSIS: 210.

Bănescu Claudia. Tehnici de diagnostic molecular. Dobreanu Minodora. Biochimie

clinică. Implicații practice. Editia 3, Ed. University Press, 2015, cap. 26, pg:335-364

ISBN 978-973-169-357-6 , cod CNCSIS: 210.

Claudia Bănescu, Carmen Duicu and Minodora Dobreanu. The Association of the DNA

Repair Genes with Acute Myeloid Leukemia: The Susceptibility and the Outcome

After Therapy. Myeloid Leukemia - Basic Mechanisms of Leukemogenesis (Edited by:

Steffen Koschmieder and Utz Krug), Publisher: InTech, December 2011, pg 385-408,

ISBN 978-953-307-789-5.

Capitole in volume colective publicate la edituri recunoscute CNCSIS, cu ISBN- co-autor

Marginean Oana, Banescu Claudia, Chincesan Mihaela, Duicu Carmen, Man Lidia,

Marginean Claudiu. Polimorfismul genei enzimei de conversie a angiotensinei intr-o

populatie de copii cu malnutritie in Romania. In Arato A Kolacek S Burlea M Pleșca D

Mărginean C O Update în Patologia Pediatrică, Proceeding la al XI-lea Congres

Național de Pediatrie cu participare internațională, Tg. Mureș, 25-28 septembrie

2013, Editura University Press Tg. Mureș 2013, pg. 152-161, ISBN:978-973-169-244-9,

vol 2. 978-973-169-251-7.

Carmen Duicu, Oana Marginean, Eva Kiss, Iulia Dunca, Claudia Banescu, Virginia

Bodescu, Alina Grama. Usefulness of ambulatory blood pressure monitoring (ABPM)

in children with diabetes mellitus type 1. In Arato A Kolacek S Burlea M Pleșca D

Mărginean C O Update în Patologia Pediatrică, Proceeding la al XI-lea Congres

Național de Pediatrie cu participare internațională, Tg. Mureș, 25-28 septembrie

2013, Editura University Press Tg. Mureș 2013,, pg. 178-184, ISBN:978-973-169-244-

9, vol 2. 978-973-169-251-7

Adina Stoian, M Stoian, A. Ioniţă, C. Gârbovan, I. Kezdi, S. Petruţiu, C. Bănescu, C.

Feier, F. Gliga, B. Buda, Schiopu A. Pansinuzită acută complicată cu menigoencefalită

bacteriană – prezentare de caz. in "Managementul pacientului critic în patologia

infecţioasă", Adrian Streinu Cercel, Carmen Chiriac – Târgu Mureş, University Press

Tîrgu Mure; 2011, pg:84-90, ISBN: 978-973-169-154-1

d. Articole publicate in extenso în reviste de specialitate

1. Articole publicate in extenso în reviste cotate ISI, cu FI, autor principal

1. Bănescu C, Trifa AP, Demian S, Benedek Lazar E, Dima D, Duicu C, Dobreanu M.

Polymorphism of XRCC1, XRCC3, and XPD Genes and Risk of Chronic Myeloid

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Leukemia. Biomed Res Int. 2014; 2014:213790. doi: 10.1155/2014/213790. ISSN

1110-7243 , Epub 2014 May 15. (IF = 2.706)

2. Bănescu C, Trifa AP. The MTHFR (methylenetetrahydrofolate reductase) 677 C>T

polymorphism is associated with acute myeloid leukemia. Leuk Lymphoma. 2014 Aug

20:1-9. [Epub ahead of print]. (IF= 2.605)

3. Bănescu C, Iancu M, Trifa AP, Macarie I, Dima D, Dobreanu M. The MTHFR

(methylenetetrahydrofolate reductase) 677 C>T polymorphism increases the risk of

developing chronic myeloid leukemia - a case-control study. Tumour Biol. 2014 Dec

16. [Epub ahead of print] ,doi: 10.1007/s13277-014-2946-1 (IF=2.840)

4. Bănescu C, Trifa AP, Voidăzan S, Moldovan VG, Macarie I, Benedek-Lazar E, Dima D,

Duicu C, Dobreanu M. CAT, GPX1, MnSOD, GSTM1, GSTT1, and GSTP1 Genetic

Polymorphisms in Chronic Myeloid Leukemia: A Case-Control Study. Oxid Med Cell

Longev. 2014:875861; doi: 10.1155/2014/875861. Epub 2014 Nov 11. (IF=3.363)

5. Trifa AP, Popp RA, Cucuianu A, Bănescu C, Tevet M, Martin B, Murat M, Vesa SC,

Dima D, Cândea M, Militaru MS, Pop IV. CALR versus JAK2 mutated essential

thrombocythaemia - a report on 141 patients. Br J Haematol. 2014 Aug 8. doi:

10.1111/bjh.13076. (IF = 4.959)- contributie egala cu primul autor

6. Mărginean OC, Bănescu C, Duicu C, Pitea AM, Voidăzan S, Mărginean C. The role of

IL-6 572 C/G, 190 C/T, and 174 G/C gene polymorphisms in children's obesity. Eur J

Pediatr. 2014 Oct;173(10):1285-96. doi: 10.1007/s00431-014-2315-5. Epub 2014 Apr

17. (IF = 1.983), autor corespondent

7. Mărginean CO, Bănescu C, Voidăzan S, Duicu C. The IL-6 572 C/G, 190 C/T, and 174

G/C Gene Polymorphisms in Children's Malnutrition. J Pediatr Gastroenterol Nutr.

2014 Nov; 59(5):666-73. doi: 10.1097/MPG.0000000000000492. (IF=2.873) autor

corespondent

8. Mărginean CO, Bănescu C, Duicu C, Voidăzan S, Mărginean C. Angiotensin-converting

enzyme gene insertion/deletion polymorphism in nutritional disorders in children.

Eur J Nutr. 2014 Nov 22. [Epub ahead of print], PMID:25416682, doi 10.1007/s00394-

014-0802-0, (IF=3.84), autor corespondent

9. Stoian A, Bacârea A, Moţăţăianu A, Stoian M, Gliga F, Bacârea V, Duicu C, Bănescu C.

Vascular Endothelial Growth Factor Insertion/Deletion gene polymorphism in

patients with type 2 diabetes and diabetic peripheral polyneuropathy. Rev Romana

Med Lab. 2014; 22(2):165-72. DOI:10.2478/rrlm-2014-0023, (IF=0.171)

10. Bacârea A, Bănescu C, Macarie I, Köpeczi JB, Dorcioman B. Atypical case of B-cell

Chronic Lymphocytic Leukemia presenting with extreme hyperleukocytosis. Rev

Romana Med Lab. 2014;22(4):507-13. DOI:10.2478/rrlm-2014-0043 (IF=0.171) autor

corespondent

11. Negovan A, Voidazean S, Pantea M, Moldovan V, Bataga S, Cozlea L, Mocan S,

Banescu C. The AGT A-20 C gene polymorphism is associated with ulcer in Romanian

patients treated with low-dose aspirin", Rev Romana Med Lab. 2015, acceptat spre

publicare, in vol.23 , in press. (IF=0.171)

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12. Bănescu C, Tilinca M, Benedek EL, Demian S, Macarie I, Duicu C, Dobreanu M. XRCC3

Thr241Met polymorphism and risk of acute myeloid leukemia in a Romanian

population. Gene. 2013, 526(2):478-83. doi: 10.1016/j.gene.2013.05.054. IF= 2,196

13. Bănescu C, Duicu C, Trifa AP, Dobreanu M. XRCC1 Arg194Trp and Arg399Gln

polymorphisms are significantly associated with shorter survival in acute myeloid

leukemia. Leuk Lymphoma. 2014;55(2):365-70. doi: 10.3109/10428194.2013.802781.

IF=2,605

14. Rodica Togănel, Iolanda Muntean, Carmen Duicu, Amalia Făgărăşan, Liliana Gozar,

Claudia Bănescu. The role of eNOS and AGT gene polymorphisms in secondary

pulmonary arterial hypertension in Romanian children with congenital heart disease.

Rev Romana Med Lab. 2013; 21(3):267-274. DOI:10.2478/rrlm-2013-0031, (IF=0.171)

15. Carmen Duicu, Oana Marginean, Eva Kiss, Lilla Lőrinczi, Claudia Banescu.

Genitourinary tuberculosis in children - a diagnostic challenge. Rev Romana Med Lab.

2013; 21(3):301-309. DOI:10.2478/rrlm-2013-0026, (IF=0.171)

16. Florina Gliga, Ionela Pascanu, Adina Stoian, Theodor Nicola, Claudia Bănescu. Insulin

resistance associated with polycystic ovary syndrome – is Pro12Ala polymorphism of

the PPAR-γ gene involved?. Rev Romana Med Lab. 2012; 20(4):345-352, IF=0,097

17. Claudia Bănescu, István Benedek, Carmen Duicu, Smaranda Demian, Septimiu

Voidăzan. Cytogenetic findings and their prognostic impact in myelodysplastic

syndrome patients. Rev Romana Med Lab. 2011;19(2):139-147, IF=0.091

18. Pașcanu I, Banescu C, Huțu S, Gozar H, Neagoe R. Two hypospadias cases in a family

with translocation involving chromosomes X and 21. Rev Romana Med Lab. 2015,

acceptat spre publicare, in vol.23 ,in press. (IF=0.171)

2. Articole publicate in extenso în reviste cotate ISI cu FI, co-autor

1. Costache RM, Bănescu C, Popp RA, Pop IV, Trifa AP. The GR (glucocorticoid receptor)

A3669G SNP is not associated with polycythemia vera, essential thrombocythemia or

primary myelofibrosis. Leuk Lymphoma. 2015 Apr 29:1-11. [Epub ahead of print] ,

IF=2.605, doi:10.3109/10428194.2015.1046065,

http://informahealthcare.com/doi/abs/10.3109/10428194.2015.1046065

2. Trifa AP, Popp RA, Cucuianu A, Coadă CA, Urian LG, Militaru MS, Bănescu C, Dima D,

Farcaş MF, Crişan TO, Petrov L, Gug C, Pop IV. Absence of BRAF V600E mutation in a

cohort of 402 patients with various chronic and acute myeloid neoplasms. Leuk

Lymphoma. 2012 Dec;53(12):2496-7. IF=2,301

3. Horváth A, Baghiu MD, Pap Z, Bănescu C, Mărginean CO, Pávai Z. Follow-up of

childhood chronic myelogenous leukemia with monitoring the BCR-ABL fusion gene

expression in peripheral blood. Rom J Morphol Embryol. 2011; 52(3):907-13. ISSN

(print) 1220-0522, A, IF=0,523

4. Pascanu I, Ruff R, Banescu C, Skrypnyk C. Prader-Willi syndrome with associated

triple X mosaicism. Acta Endo (Buc) 2010, 6: 521-532. ISSN 1841-0987, cod CNCSIS

676 A, IF=0,052

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5. Rodica Togănel, Claudia Bănescu, Carmen Duicu, Carmen Şuteu, Iolanda Muntean,

Amalia Făgărăşan, et al. Angiotensin-converting enzyme gene polymorphisms in

pulmonary arterial hypertension in children. Rev Romana Med Lab. 2010;18(4):31-36,

ISSN 1841-6624, cod CNCSIS 739 A, IF=0,113

6. Paşcanu I., Bănescu C., Benedek T., Duicu C., Csép K., Dema A. Thyroid Dysfunction In

Children With Down’s Syndrome. Acta Endo (Buc), 2009, 1(V), 85-92, doi:

10.4183/aeb.2009.85 ISSN 1841-0987, cod CNCSIS 676 A, IF=0.011

2.Articole publicate in extenso în reviste cotate ISI, fara factor de impact,

autor principal

1. Claudia Bănescu, Ionela Paşcanu, Katalin Csép, István Benedek, Erzsebét Benedek,

Carmen Duicu, et al. Cytogenetic analysis in acute myeloid leukemia in Tîrgu Mureş.

Rev Romana Med Lab. 2008;13(4):21-29, ISSN 1841-6624, cod CNCSIS 739 A, revistă

cotată ISI, fara factor de impact

2. Paşcanu I., Borda A., Bănescu C. Thyroid nodule with Hashimoto thyroiditis in

childhood – a challenging experience. Rom J Morphol Embryol. 2008; 49(4):541-5.

ISSN 1220-0522, cod CNCSIS 772 A, revistă cotată ISI, fara factor de impact

3. Claudia Bănescu, István Benedek, Erzsébet Benedek, Ionela Paşcanu, Katalin Csép,

Carmen Duicu, Demian Smaranda. Application of Cytogenetics for Chronic Myeloid

Leukemia in Tîrgu Mureş. Rev Romana Med Lab. 2009;14(1):31-39, ISSN 1841-6624,

cod CNCSIS 739 A, fara factor de impact

co-autor

1. Duicu C, Kiss E., Bănescu C., Bodescu V., Moreh Z., Horvath E. Congenital nephrotic

syndrome of Finnish type - cases report. Rev Romana Med Lab. 2009;17(4):43-49.

ISSN 1841-6624, cod CNCSIS 739 A, revistă cotată ISI, fara factor de impact

2. Paşcanu I., Todoran B. A. M., Csep K., Bănescu C., Togănel R. A case of 49,XXXXY

syndrome in endocrine practice. Acta Endo (Buc), 2008, 4(IV), 455-463. ISSN 1841-

0987, cod CNCSIS 676 A, revistă cotată ISI, fara factor de impact,

3. K.Csep, Gyongyi Dudutz, Marta Vitay, Ionela Paşcanu, Claudia Bănescu, L. Koranyi, L.

Rosivall. The relationship between the PRO12ALA polymorphism of the PPARγ2 gene

and the metabolic syndrome diagnosed in a population of central Romania according

to the IDF criteria. Acta Endo (Buc), 2008, 3(IV): 263-271, ISSN 1841-0987, doi:

10.4183/aeb.2008.263,cod CNCSIS 676 A, indexata ISI, fara factor de impact

Articole publicate in extenso în reviste BDI, autor principal / coautor

BDI autor principal

1. Togănel R, Muntean I, Făgărăşan A, Gozar L, Pașc S, Șuteu C, Bănescu C. Correlations

between three variants of MTHFR gene polymorphisms and congenital heart defects

risk: a Romanian case-control study. Exp Clin Cardiol 2014, 20(10):6336-6344.

2. Ionela Pașcanu, Oana Maria Capraru, Otilia Mărginean, Claudia Bănescu. Therapeutic

approach in Prader-Willi syndrome. Jurnalul Pediatrului, XVI(63):32-37. CNCSIS code:

6

213, B+ 2010,

http://journals.indexcopernicus.com/karta.php?action=masterlist&id=4260

3. Bănescu Claudia, Benedek I, Duicu Carmen, Demian Smaranda, Macarie I, Voidăzan

S, Dobreanu Minodora. The Prognostic Impact of the Karyotype in Patients with

Acute Lymphoblastic Leukemia. Acta Medica Marisiensis, 2012. 58(6):359-362, EBSCO

http://www.ebscohost.com/titleLists/tnh-coverage.htm

4. Claudia Bănescu, Minodora Dobreanu, Carmen Duicu, István Benedek, Ioan Macarie,

Judit Kopeczi. FLT3 internal tandem duplication and D835 mutations in acute myeloid

leukemia. Acta Medica Marisiensis, 2011. 57(6):571-574, EBSCO

http://www.ebscohost.com/titleLists/tnh-coverage.htm

5. Csep Katalin, Drugan Cristina, Bănescu Claudia. Possibilities and Challenges in the

Molecular Diagnosis of lysosomal Storage Disorders. Acta Medica Marisiensis, 2011.

57 (6): 780-783, EBSCO http://www.ebscohost.com/titleLists/tnh-coverage.htm

BDI co-autor

1. Carmen Duicu, Claudia Banescu, Iolanda Muntean, Oana Marginean, Horea Gozar.

Un caz de hidronefroza giganta asociata cu hipertensiune arteriala Revista Romana

de Pediatrie 2012, Vol. LXI, Nr. 2, 209-215, EBSCO

http://www.ebscohost.com/titleList

2. Mărginean Oana, Carmen Duicu, Claudia Bănescu, Ana Maria Pitea. Boala urinilor cu

miros de sirop de arțar – două prezentări de caz . Revista Română de Pediatrie, 2012,

Vol. LXI, Nr. 4 : 412-421. EBSCO http://www.ebscohost.com/titleList

3. Stoian Adina, Bănescu Claudia, M. Stoian, Buicu Gabriela, Chiotoroiu Andreea, Onişor

Danusia. A study of angiotensin converting enzyme gene polymorphism in the

patientswith diabetic neuropathy. Acta Medica Transilvanica 2012; 2(3):218-220,

EBSCO http://www.ebsco.com/

4. Duicu Carmen, Bănescu Claudia, Gall Zsuzsanna, Grama Alina, Gozar Horea

Association between angiotensin-converting enzyme gene insertion (I) / deletion (D)

polymorphism and secondary arterial hypertension in a romanian children

population. Acta Medica Marisiensis Acta Medica Marisiensis. 2011. 57(6):623-626,

EBSCO http://www.ebscohost.com/titleLists/tnh-coverage.htm

5. Tilinca Mariana, Benedek Lazar Erzsebet, Kopeczi Judith Beata, Bacarea Anca,

Banescu Claudia, Benedek I., Bataga Simona. Acute Myeloblastic Leukemia:

difficulties of treatment, complications and evolution. Acta Medica Marisiensis 2011.

57(6):776-779, EBSCO http://www.ebscohost.com/titleLists/tnh-coverage.htm

e) Articole publicate în rezumat în reviste și volumele unor manifestări științifice, cu ISBN

sau ISSN ( ISI)

1. Bănescu C, Duicu C, Trifa AP, Benedek Lazar E, Macarie I, Todoran Butila A, Dobreanu

M. XPD Lys751Gln and Arg156Arg polymorphisms and acute myeloid leukemia risk.

European Human Genetics Conference May 31-June 3, 2014, Milan, Italy, Eur J Hum

Genet 22(1):478. ISSN: 1018-4813

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2. Banescu C, Crauciuc A, Demian S, Macarie I, Todoran A, Duicu C, Dobreanu M. XRCC1

Arg194Trp and Arg399Gln polymorphisms and malignant lymphoma risk. European

Human Genetics Conference June 8-11, 2013, Paris, France, Eur J Hum Genet

21(2):532, ISSN: 1018-4813 , https://www.eshg.org/eshg2013.html

3. Banescu C, Duicu C, Benedek I, Pascanu I, Csep K, Todoran A, Dobreanu M. DNA

repair XRCC3 polymorphism and acute myeloid leukemia. European Human Genetics

Conference June 23 - 26, 2012, Nürnberg, Germany, Eur J Hum Genet, 2012, 20

(1):174, ISSN: 1018-4813 , https://www.eshg.org/eshg2012.html

4. Bănescu C, Dobreanu M, Duicu C, Benedek I, Paşcanu I, Csép K. Polymorphisms of the

DNA repair genes XRCC1 in acute leukemia 2011 Amsterdam , Eur J Hum Genet,

2011, 19(2): 204, ISSN 1018-4813. https://www.eshg.org/eshg2011.html

5. Bănescu C, Togănel R, Duicu C, Paşcanu I, Csép K, Suteu C. A study of angiotensin

converting enzyme gene polymorphism in children with pulmonary hypertension.

European Human Genetics Conference 2010, June 12 - 15, Gothenburg, Sweden, Eur

J Hum Genet, 2010, 14(1):291-292, ISSN 1018-4813,

https://www.eshg.org/eshg2010.html

6. Bănescu C, Toganel R, Pascanu I, Csep K, Duicu C. Investigation of cytogenetic causes

of congenital heart disease in Pediatric Cardiology Clinic Tg Mures, Romania.

European Human Genetics Conference 2009, May 23 – 26, Vienna, Austria, Eur J Hum

Genet, 2009, 17(2), 127. ISSN 1018-4813, https://www.eshg.org/eshg2009.html

Co-autor

1. Marginean O, Banescu C, Marginean M, Tripon F, Crauciuc G. The role of FTO

RS17817449 AND RS 9939609 SNP (SINGLE NUCLEOTIDE POLYMORPHISM) in

children’ obesity, The 5 th Congress of European Academy of Paediatric Society,

Barcelona 17-21 0ct 2014. Arch Dis Child 2014, 99 (suppl 2):A41, 2014, rev ISI, FI

2,905

2. Moldovan VG, Duicu C, Crauciuc A, Tripon F, Moldovan E, Bănescu C. „CAT C262T,

GSTM1, GSTT1 and CML risk”, European Human Genetics Conference May 31-June 3,

2014, Milan, Italy, Eur J Hum Genet 22(1): 461, ISSN: 1018-4813

3. Dobreanu M, Trifa A, Duicu C, Moldovan V, Dima D, Demian S, Bănescu C.

„Polymorphism of XRCC1, XRCC3 and XPD genes and risk of chronic myeloid leukemia

in a Romanian Population” European Human Genetics Conference May 31-June 3,

2014, Milan, Italy, Eur J Hum Genet 22(1):461-462, ISSN: 1018-4813

4. Mărginean O, Duicu C, Moldovan V, Craucuic A, Tripon F, Bănescu C. FTO

(rs17817449 and rs 9939609) mutations in a Romanian obese children population.

European Human Genetics Conference May 31-June 3, 2014, Milan, Italy, Eur J Hum

Genet 22(1):498, ISSN: 1018-4813

5. Duicu C, Moldovan V, Tripon F, Craucuic A, Bănescu C. NPHS2 and WT1 mutations in

a romanian children population with nephrotic syndrome. European Human Genetics

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Conference May 31-June 3, 2014, Milan, Italy, Eur J Hum Genet 22(1): 393, ISSN:

1018-4813

6. Marginean O, Banescu C, Pitea A. The Role of IL-6 190 C/T Gene Polymorphisms in

Children’s Malnutrition. Clinical Nutrition, Vol. 33 (suppl 1):S120–S121, Abstracts of

the 36th ESPEN Congress, Geneva, Switzerland, 6-9 September 2014, rev ISI , IF 3.94,

7. Marginean O, Banescu C, Duicu C, Marginean OM, Marginean C. The Role of

Interleukin-6 Gene 572 G/C Polymorphism in Child Obesity. Clinical Nutrition, Vol.

33(suppl 1):S117, Abstracts of the 36th ESPEN Congress, Geneva, Switzerland, 6-9

September 2014, rev ISI , IF 3.94,

8. Duicu C., Tripon F., Marginean O., Banescu C. NPHS2 R229Q polymorphism in

children with nephrotic syndrome. European Human Genetics Conference June 8-11,

2013, Paris, France, Eur J Hum Genet 21(2):499, ISSN: 1018-4813 ,

https://www.eshg.org/eshg2013.html

9. Marginean O., Banescu C., Duicu C. A rare case of Hunter syndrome. European

Human Genetics Conference June 8-11, 2013, Paris, France, Eur J Hum Genet

21(2):520, ISSN: 1018-4813 , https://www.eshg.org/eshg2013.html

10. Csep K., Banescu C., Todoran Butila A. The effect of Mediterranean diet and exercise

on insulin resistance in the presence of PPARG2 rs1801282 polymorphism in a central

Romanian population. European Human Genetics Conference June 8-11, 2013, Paris,

France, Eur J Hum Genet 21(2):260, ISSN: 1018-4813 ,

https://www.eshg.org/eshg2013.html

11. O. Mărginean, C Bănescu, C Duicu, AM Pitea, L Man, M Mărginean, M Chincesan, C

Marginean. IL-6-572 G/C gene polymorphism in a Romanian population of obese and

malnourished children. ESPGAN 2013 Berlin, United European Gastroenetrology

Journal, A283 ISSN 2050-6406

12. MargineanO.C, Duicu C, Banescu C. Correlation between polymorphism of ACE gene

and Insulin-like Growth Factor-l (IGF-1) in malnourished children. European Human

Genetics Conference June 23 - 26, 2012, Nürnberg, Germany Eur J Hum Genet, 2012,

20(1):218, ISSN: 1018-4813 , https://www.eshg.org/eshg2012.html

13. Oana Mărginean, Duicu Carmen, Bănescu Claudia. Angiotensin-Converting Enzyme

Insertion/ Deletion Gene Polymorphism in a Romanian Population of Obese and

Malnourished Children. ESPGHAN update 2012, Stockholm Sweden, 27-28 April 2012,

Abstract booklet p 103, PO-N-238; GUT, gut.bmj.com, vol 61, suppl 63, A 453. ISSN

0017-5749 (print), 1468-3288 (online). FI: 4,16 www.gut.bmj.com/

14. Duicu C., Banescu C., Macarie I, Dobreanu M. XPD Lys751Gln polymorphism in

Romanian patients with myelodisplastic syndrome. European Human Genetics

Conference June 23 - 26, 2012, Nürnberg, Germany Eur J Hum Genet,20 (1):174,

ISSN: 1018-4813 , https://www.eshg.org/eshg2012.html

15. Csep K, Banescu C, Argyo N, Todoran Butila A, Dudutz G. The relationship of the

COMT gene polymorphism rs4680 with the components of nicotine dependence in a

central Romanian population. European Human Genetics Conference June 23 - 26,

9

2012, Nürnberg, Germany Eur J Hum Genet,20 (1):238, ISSN: 1018-4813 ,

https://www.eshg.org/eshg2012.html

16. Ionela Pascanu; Rudolf Ruff; Claudia Banescu; Carmen Duicu, Raluca Petri.

Suprasellar germinoma with severe hypernatremia and hypopituitarysm in an adipsic

child. -51th Annual Meeting of the European Society for Paediatric Endocrinology

(ESPE), Leipzig, Germany, 20-23 September 2012. Hormone Research in paediatrics;

78(suppl 1): 271., ISBN: 978-3-318-02155-4

17. Carmen Duicu, Oana Marginean, Claudia Banescu. AGT M235T and ACE I/D gene

polymorphism associated with secondary high blood pressure in a Romanian

population. Free communication, 5th Europediatrics 23-26 june 2011, Vienna, A

Cochrane Review Journal. Evidence-Based Child Health, 6 (Suppl 1):54, ISSN: 2040-

4050

18. Carmen Duicu, Zsuzsanna Gall, Claudia Banescu. Endothelial nitric oxide synthase

gene intron 4a/b VNTR polymorphism in children with nephritic syndrome. Poster

presentation. 5th Europediatrics 23-26 june 2011, Vienna, A Cochrane Review

Journal. Evidence-Based Child Health, 6 (Suppl 1): 155 ISSN: 2040-4050

19. A. Stoian, C. Banescu, C. Duicu, M. Stoian, G. E. Buicu, C. Crisan, A. Cif, C. Feier, A.

Schiopu, V. G. Osan: "ACE gene polymorphism in Romanian patients with diabetic

neuropathy", Poster Presentation, Twenty-first Meeting of the European neurological

Society 28-31 May 2011, Lisbon, Portugal, Journal of Neurology, Abstracts. Volume

258, suppl 1: S109, ISSN: 0340-5354

20. Ionela Pascanu, Claudia Banescu, Carmen Duicu. An unusual case of mosaic triplo X

syndrome. Poster presentation, 50th Annual Meeting of European Society of

Pediatric Endocrinology, 25-28 September 2011, Glasgow, United Kindom; Hormone

Research in Paediatrics (Horm Res Paediatr) – From Developmental Endocrinology to

Clinical Research – Abstracts 2011; 76/Suppl 2. ISSN print: 978–3–8055–9546–9; e-

ISSN: 1663–2826.

21. Duicu C, Banescu C, Pascanu I. eNOS polymorphism and ACE polymorphism gene in

secondary arterial hypertension in a romanian children population. European Human

Genetics Conference May 28-31, 2011 Amsterdam, Eur J Hum Genet, 19(2): 326-327,

ISSN 1018-4813.

22. Gall Z, Duicu C, Banescu C, Kiss E. ACE gene polymorphism in children with nephrotic

syndrome in a Romanian population. European Human Genetics Conference May 28-

31, 2011 Amsterdam, Eur J Hum Genet, 19(2): 327, ISSN 1018-4813.

https://www.eshg.org/eshg2011

23. K. Csep, G. Dudutz, C. Banescu, N. Argyo, A. Todoran Butila; Bitter taste sensitivity

and nicotine dependence in a Romanian population. European Human Genetics

Conference May 28-31, 2011 Amsterdam, Eur J Hum Genet, 19(2): 326-327, ISSN

1018-4813.

24. Toganel R, Banescu C, Muntean I, Fagarasan A, Duicu C, Gozar L. Genetic

polymorphism of methylen tetrahydrofolate reductase as a risk factor for congenital

10

heart defect in Romanian children. 45th Annual Meeting of the Association for

European Paediatric Cardiology, Granada, Spain, May 18-21, 2011. Cardiology in

young, volume 21 supplement 1 may 2011. S 68. ISSN: 1047-9511

25. Ionela Pascanu, Claudia Banescu, Carmen Duicu, Rudolf Ruff. Ring chromosome 13

and hyperthyrotropinemia – just a coincidence?. Poster presentation, 49th Annual

Meeting of European Society of Pediatric Endocrinology, 22-25 September 2010,

Prague; Hormone Research in Paediatrics (Horm Res Paediatr) – From Developmental

Endocrinology to Clinical Research – Abstracts 2010; 74/Suppl 3: 254. ISSN print:

978–3–8055–9546–9; e-ISSN: 1663–2826.

26. Duicu C., Bănescu C., Kiss E., Bodescu V., Muntean I. Genetic analysis of ACE

polymorphisms in children with secondary high blood pressure. European Human

Genetics Conference 2010, June 12 - 15, 2010 Gothenburg, Sweden, Eur J Hum

Genet, 14(1), ISSN 1018-4813,

27. Kiss E., Duicu C., Bănescu C., Paşcanu I., Gozar H. Ambiguous external genitalia in

newborns. European Human Genetics Conference 2010, June 12 - 15, Gothenburg,

Sweden, 2010, Eur J Hum Genet, 14(1), ISSN 1018-4813.

https://www.eshg.org/eshg2010.

28. Paşcanu I., Bănescu C., Gozar H., Csep K., Laszlo A. Two hipospadias cases in a family

translocation involving chromosomes X and 21. LWPES/ESPE 8th Joint Meeting,

Global Care in Pediatric Endocrinology, September 9-12, 2009, New York, USA.

Hormone research, 72 (3), 364. ISSN 0301-0163.

29. Pávai Z., Pap Z., Bödör C., Benedek I., Köpeczi B., Horváth E., Mureşan C, Vasile K,

Dénes L. A comparative study between clinical behavior and real time quantitative

reverse transcriptase polymerase chain reaction results in chronic myelogenous

leukemia cases. The 22nd European Congress of Pathology, 4-9 septembrie 2009,

Florence, Italy, Virchows Archiv, 455(1), S254. ISSN 0945-6317.

30. Duicu C., Bănescu C., Kiss E., Popp R., Trifa A., Bodescu V. ACE polymorphisms in

children with arterial hypertension. European Human Genetics Conference 2009,

May 23 – 26, Vienna, Austria, Eur J Hum Genet, 2009, 17(2), 383. ISSN 1018-4813,

31. Kiss E., Duicu C., Bănescu C., Bodescu V., Csep K. Mucopolysaccharidosis TypeIH – A

case report. European Human Genetics Conference 2009, May 23 – 26, Vienna,

Austria, Eur J Hum Genet,2009, 17(2), 71. ISSN 1018-4813.

32. Csep K., Dudutz G., Vitay M., Pascanu I., Bănescu C., Koranyi L. Combined effect of

the FABP2, PPARG2 and PC1 gene polymorhisms on the metabolic syndrome risk in a

Romanian population. European Human Genetics Conference 2009, May 23 – 26,

Vienna, Austria, Eur J Hum Genet 2009, 17(2), 387. ISSN 1018-4813,

Articole publicate în rezumat în reviste și volumele unor manifestări științifice, cu ISBN sau

ISSN

- prim-autor

11

1. Banescu C, Moldovan GV, Tripon F, Crauciuc A, Benedek Lazar E, Macarie I, Dobreanu M.

GST gene polymorphism and the risk of AML in Romanian patients. Scientific Session of

University educational Staff, 12 december 2014, AMM, 60(4):75

2. Banescu C, Trifa PA, Voidazan S, Moldovan V, Macarie I, Benedek Lazar E, Dima D, Duicu

C, Crauciuc G, Tripon F, Dobreanu M. Polymorphisms in genes encoding antioxidant

enzymes (SOD2,CAT and GPX) and risk of Chronic Myeloid Leukemia in a Romanian

population, Congress of the Romanian Society of Medical Genetics, september 24 - 26,

2014, Bucharest. Medicine in Evolution, 2014, vol XX, nr 2:56, ISSN 1454-8224

3. Banescu C. Cytogenetic analysis in patients with hematological malignancies. Bulletin of

Romanian Society for cell biology, No 42- June 2014, 6th national Congress with

international participation and 32th annual scientific session of Romanian Society for Cell

Biology, june 4-7 , 2014, Tg Mures, 2014, 42:18, ISSN 1584-5532

4. Banescu C, Benedek I, Macarie I, Demian S,Moldovan V, Tripon F, Crauciuc A.

Investigation of point mutations of the Abl gene in patients with chronic myeloid

leukemia. Zilele Universităţii de Medicină şi Farmacie Tg. Mureş 9-13 decembrie 2013,

Acta Medica Marisiensis, 2013, 59(4):28. ISSN:2068-3324

5. Bănescu C, Benedek I, Benedek Lazar E, Macarie I, Demian S, Moldovan V, Dobreanu M.

Methylenetetrahydrofolate reductase (MTHFR 677 C>T and 1298 A>C) gene

polymorphisms in Romanian patients with acute myeloid leukemia. Zilele Universităţii de

Medicină şi Farmacie Tg. Mureş 9-13 decembrie 2013, Acta Medica Marisiensis, 2013,

59(4):27, ISSN:2068-3324

6. Bănescu C, Cucerea M, Marginean O, Duicu C. Fenotip particular la pacienții cu

iozcromozom 18q. Al XI -lea Congres Național de Pediatrie, 25 – 28 septembrie 2013,

Tîrgu Mureș Book of Abstracts, pg 191, ISSN 2344-3324. ISSN-L 2344-3324. Ed University

Press

7. Bănescu C, Bendek I, Demian S, Macarie I, Duicu C, Dobreanu M. The Arg194Trp

polymorphism in the XRCC1 gene and chronic myeloid leukemia. Zilele Universităţii de

Medicină şi Farmacie Tg. Mureş 13-15 decembrie 2012, Acta Medica Marisiensis 2012,

58(3):31, ISSN:2068-3324

8. Bănescu C, Benedek I, Duicu C, Demian S, Macarie I, Voidăzan S, Dobreanu M. The

prognostic impact of the karyotype in patients with acute lymphoblastic leukemia. A 5-a

Conferinţă a Doctoranzilor şi a 2-a Conferinţă a Postdoctoranzilor în Medicină şi

Farmacie, 4-6 iulie, 2012, Tîrgu Mureş, România, Acta Medica Marisiensis 2012, 58(2):13,

ISSN:2068-3324

9. Bănescu C, Dobreanu M, Duicu C, Benedek I, Macarie I, Kopeczi J. FLT3 internal tandem

duplication and D835 mutations in acute myeloid leukemia. The First Conference of

Postdoctoral Researchers in Medicine and Pharmacy. 6-8 iulie 2011, Tîrgu-Mureş,

România Acta Medica Marisiensis. 2011. Vol 57 (3):61, ISSN:2068-3324

10. Bănescu C, Dobreanu M, Benedek I, Benedek E, Duicu C, Demian S, Macarie I. Rare

cytogenetics findings in patients with leukemia. Cea de a 65-a aniversare a U.M.F. Târgu-

12

Mureş 15-18 decembrie 2010 Târgu-Mureş. Acta Medica Marisiensis. 2010. Vol 56 (3):92,

ISSN:2068-3324

11. Claudia Bănescu, Benedek I, Benedek E, Csép K, Duicu C, Paşcanu I, Butilă Todoran A,

Cândea M, Kopeczi J. Chromosomal abnormalities in patients with hematological

malignancies. Cea de a 65-a aniversare a U.M.F. Târgu-Mureş 15-18 decembrie 2010

Târgu-Mureş. Acta Medica Marisiensis. 2010. Vol 56 (3):90, ISSN:2068-3324

12. Bănescu C, Benedek I, Benedek E, Demian S, Duicu C, Csép K, Paşcanu I, Todoran AB.

Aspecte citogenetice în leucemia acută secundară. Zilele Universităţii de Medicină şi

Farmacie Tg. Mureş, 9-12 decembrie 2009. Revista de Medicină şi Farmacie UMF Tg.

Mureş, 2009, 55(6):10. ISSN 1221-2229,

13. Bănescu C, Benedek I, Benedek E, Kopeczi JB., Duicu C, Csép K, Paşcanu I, Todoran BA.

Anomalii cariotipice în leucemia acută bifenotipică. Zilele Universităţii de Medicină şi

Farmacie Tg. Mureş, Sesiune Anuală de Comunicări Ştiinţifice 9-12 decembrie 2009.

Revista de Medicină şi Farmacie UMF Tg. Mureş, 2009, 55(6):8. ISSN 1221-2229.

14. Bănescu C, Paşcanu I, Csép K, Benedek I, Benedek E, Duicu C, Todoran BA. Cytogenetic

analysis in malignant hematologic diseases in Tg.Mureş, Romania. Primul Congres al

Asociatiei Laboratoarelor Medicale din România, 24-27 iunie 2009, Tg Mureș, Revista

Română de Medicină de Laborator, 2(15), 14-15. ISSN 1841-6624, cod CNCSIS 739 A.

15. Bănescu C, Benedek I, Benedek E, Duicu C, Paşcanu I, Csép K, Todoran A. Modificări

citogenetice în leucemii acute şi cronice pre- şi posttransplant de celule stem. A IV-a

Conferinţă a Societăţii Române de Genetică Medicală, Craiova, 18-20 septembrie 2008.

Poster. Publicat în Volum de rezumate, 69, ISBN 978-973-746-982-3

Articole publicate în rezumat în reviste și volumele unor manifestări științifice, cu ISBN sau

ISSN

Co-autor)

1. Mărginean A, Bănescu C, Şular FL, Bălașa R, Maier S, Ispas M, Țăruși M, Dobreanu M. Resistance to antiplatelet therapy – is this a real problem in romanian population ? The 1st Congress of Romanian Association of Laboratory Medicine with international participationSighisoara, 20-23 May 2015, Revista Română de Medicină de Laborator, 2015, supliment la 23(1):S84-S85 ISSN 1841-6624.

2. Crauciuc G, Tripon F, Ștefan A, Radu C, Bănescu C. Is INFγ A874T gene a risk factor or a predictive factor in non-Hodgkin lymphoma? The 1st Congress of Romanian Association of Laboratory Medicine with international participationSighisoara, 20-23 May 2015, Revista Română de Medicină de Laborator, 2015, supliment la 23(1):S100-S101 ISSN 1841-6624.

3. Moldovan GV, Duicu C, Bogliș A, Crauciuc A, Tripon F, Bănescu C.Tumor necrosis factor-α, a risk factor for acute myeloid leukemia development. The 1st Congress of Romanian Association of Laboratory Medicine with international participationSighisoara, 20-23 May 2015, Revista Română de Medicină de Laborator, 2015, supliment la 23(1):S101-S102 ISSN 1841-6624.

4. Tripon F, Crauciuc G, Radu C, Ştefan A, Bӑnescu C. Effects of the TNF-α gene on the lymphoma development, prognosis and outcome: a case-control study. The 1st Congress

13

of Romanian Association of Laboratory Medicine with international participationSighisoara, 20-23 May 2015, Revista Română de Medicină de Laborator, 2015, 22(1):S48-S49, ISSN 1841-6624.

5. Bogliș A, Bănescu C, Kulcsar A, Moldovan V. Cytogenetic abnormalities in pediatric patients with multiple congenital anomalies. The 1st Congress of Romanian Association of Laboratory Medicine with international participationSighisoara, 20-23 May 2015, Revista Română de Medicină de Laborator, 2015, supliment la 23(1):S106-S107, ISSN 1841-6624.

6. Todoran-Butilă A, Sin A, Racoş Szabo E, Micheu C, Voidăzan S, Bănescu C. Possible ABCB1 gene polymorphisms associated with epileptic Romanian children. The 1st Congress of Romanian Association of Laboratory Medicine with international participationSighisoara, 20-23 May 2015, Revista Română de Medicină de Laborator, 2015, supliment la 23(1):S111-S112 ISSN 1841-6624.

7. Todoran-Butilă A, Sin A, Racoş Szabo E, Csep K, Moldovan V, Banescu C. ABCB1 C3435T polymorphism in epileptic and healthy children from central region of Romania. The 1st Congress of Romanian Association of Laboratory Medicine with international participationSighisoara, 20-23 May 2015, Revista Română de Medicină de Laborator, 2015, supliment la 23(1):S112-S113 ISSN 1841-6624.

8. Stefan AS, Radu CG, Crauciuc AG, Tripon F, Banescu C. CAT2 C262Tgene polymorphism and susceptibility ti malignant lymphoma. Asklepios, 8th International Medical Congress for Students and Young Doctors, 7-9 may, 2015, Sibiu, Romania. Vol rezumate pg.56, ISSN 1843-0406

9. Gheorghiu A, Tripon F, Banescu C. CRISPR-Cas9 new method for genome engineering: a meta-analysis of published studies. Asklepios, 8th International Medical Congress for Students and Young Doctors, 7-9 may, 2015, Sibiu, Romania. Vol rezumate pg.14, ISSN 1843-0406

10. Craucuic A, Tripon F, Banescu C. GPX1, GST T1/M1, GST P1 AND SOD2 genes polymorphisms versus acetaminophen susceptibility. Asklepios, 8th International Medical Congress for Students and Young Doctors, 7-9 may, 2015, Sibiu, Romania. Vol rezumate pg.28, ISSN 1843-0406

11. Tripon F, Craucuic A, Banescu C. GPX1, GST T1/M1, GST P1 AND SOD2 genes polymorphisms versus acetaminophen susceptibility. Asklepios, 8th International Medical Congress for Students and Young Doctors, 7-9 may, 2015, Sibiu, Romania. Vol rezumate pg.28, ISSN 1843-0406

12. Radu CG, Stefan AS, Tripon F, Crauciuc AG, Banescu C. Lymphoma prognosis and the polymorphism of glutathione peroxidase Pro198Leu. Asklepios, 8th International Medical Congress for Students and Young Doctors, 7-9 may, 2015, Sibiu, Romania. Vol rezumate pg.50, ISSN 1843-0406

13. Marginean M, Oprea C, Fanfaret I, Marginean C, Banescu C,Pitea A. The role of the IL 6 190 C/T and the IL/6 174 C/G polymorphisms in the development of gastritis in children. The 19th International Scientific Congress for students, Young physicians and Pharmacists, Marisiensis, 23-25 april 2015, Tg Mures. AMM, 2015, 61(suppl 1):39, ISSN-2068-3324

14. Tripon F, Crauciuc A, Moldovan V , Duicu C, Banescu C. The TNF α G308A gene polymorphism in children with nephrotic syndrome. The 19th International Scientific Congress for students, Young physicians and Pharmacists, Marisiensis, 23-25 april 2015, Tg Mures. AMM, 2015, 61(suppl 1):21, ISSN-2068-3324

14

15. Humă MA, Crauciuc A, Curticăpian IM, Tripon F, Stoian A, Banescu C. Genetic Polymorphisms of Glutathione S-Transferase and Spontaneous Microalbuminuria in Patients with type 2 Diabetes Mellitus. The 19th International Scientific Congress for students, Young physicians and Pharmacists, Marisiensis, 23-25 april 2015, Tg Mures. AMM, 2015, 61(suppl 1):42, ISSN-2068-3324

16. Crauciuc A, Tripon F, Radu CG, Stefan AS, Moldovan V, Duicu C, Banescu C. GST T1 / M1 gene variations in non-Hodgkin lymphoma. The 19th International Scientific Congress for students, Young physicians and Pharmacists, Marisiensis, 23-25 april 2015, Tg Mures. AMM, 2015, 61(suppl 1):107, ISSN-2068-3324

17. Moldovan GV, Craucuic A, Tripon F, Demian S, Benedek Lazar E, Dobreanu M, Banescu C.

RS13181, RS238406 and the risk of acute myeloid leukemia. Scientific Session of

University educational Staff, 12 december 2014, AMM, 60(4):75

18. Moldovan GV, Tripon F, Craucuic A, Demian S, Macarie I, Candea M, Banescu C.

Polymorphisms of DNA repair gene XRCC1 in malignant lymphoma patients. Scientific

Session of University educational Staff, 12 december 2014, AMM, 60(4):76.

19. Marginean O, Pitea AM, Banescu C, Duicu C, Marginean MO. The association between

interleukin-6 gene – 190 T/C polymorphisms and antropometric parameters in obese

children. Scientific Session of University educational Staff, 12 december 2014, AMM,

60(4):113-114.

20. Duicu C, Mărginean O, Pitea A, Moldovan V, Crauciuc A, Banescu C. Analysis of the

contribution of RS17817449 SNP in FTO gene to obesity in Romanian children. Scientific

Session of University educational Staff, 12 december 2014, AMM, 60(4):114.

21. Duicu C, Mărginean O, Tripon F, Banescu C. Angiotensin-converting enzyme gene

polymorphism in children with idiopathic nephrotic syndrome. Scientific Session of

University educational Staff, 12 december 2014, AMM, 60(4):116.

22. Negovan A, Pantea M, Voidazan S, Bataga S, Cozlea L, Banescu C, Radoiu G. Gastro-

duodenal ulcer in low-dose aspirin consumers. Scientific Session of University

educational Staff, 12 december 2014, AMM, 60(4):152-153.

23. Todoran Butila A, Sin A , Micheu C, Csep K, Banescu C, Voidazan S, Racos Szabo E.

Predictive factors in the onset of epilepsy in children with cerebral palsy.Annual

Conference of the PhD and Post-Doc-Students, 10 December 2014, AMM, 60(4):23.

24. Marginean O, Bănescu C, Pitea AM; Grama A. The Role of Interleukin-6 Gene 572 G/C

Polymorphism in Child Obesity, Primul Congres Național de Diabet, Nutriție și

Endocrinologie Pediatrică – cu participare internațională, ENDOPED, Timișoara, 14-17

mai 2014, vol. rezumate, p. 39-40, ISSN 2065-4855

25. Crauciuc G, Tripon F, Moldovan V, Bănescu C. The molecular investigation of Human

Catalase gene (CAT C262T). Bulletin of Romanian Society for Cell Biology, 2014, 42:19,

ISSN: 1018-4813

26. Tripon F, Crauciuc G, Moldovan V, Bănescu C. It's possible that glutathione-s transferase

T1 and M1 genes polymorphisms to play a role in the susceptibility to chronic myeloid

leukemia? Bulletin of Romanian Society for Cell Biology, 2014, 42: 20, ISSN 1584-5532.

15

27. Moldovan GV, Craucuic A, Tripon F, Bănescu C. „Glutathione Peroxidase, Risk Factor for

Chronic Myeloid Leukemia”, a VIII-a Conferință a Asociației Laboratoarelor Medicale din

România cu participare Internațională, Revista Română de Medicină de Laborator, 2014,

22(1):S48-S49 ISSN 1841-6624.

28. Moldovan GV, Craucuic A, Tripon F, Bănescu C. „Glutathione Peroxidase and Catalase

Gene Polymorphisms in Romanian Population”, Revista Română de Medicină de

Laborator, Martie 2014, 22(suppl 1):S33-S34, ISSN 1841-6624.

29. Tripon F, Crauciuc G, Marginean MO, Marginean O, Banescu C. Molecular basis of

obesity. The 18th International Scientific Congrss for students, Young physicians and

Pharmacists, Marisiensis, 7-11 may 2014, Tg Mures, Acta Medica Marisiensis, 2014,

60(3):2, ISSN-2068-3324

30. Crauciuc G, Tripon F, Banescu C. Genetic polymorphisms of XPD Arg 156 Arg and

Lys751Lys DNA repair genes in patients whith acute myeloid leukemia. The 18th

International Scientific Congrss for students, Young physicians and Pharmacists,

Marisiensis, 7-11 may 2014, Tg Mures, Acta Medica Marisiensis, 2014, 60(3):3, ISSN-

2068-3324

31. Radu C, Stefan A, Tripon F, Crauciuc G, Demian S, Banescu C. The importance of

XRCC1Arg399Arg DNA repair gene in the determining of lymphoma response to

chemotherapy, radiotherapy and outcome. The 18th International Scientific Congrss for

students, Young physicians and Pharmacists, Marisiensis, 7-11 may 2014, Tg Mures, Acta

Medica Marisiensis, 2014, 60(3):25, ISSN-2068-3324

32. Stefan A, Radu CG, Crauciuc G, Macarie I, Banescu C. XRCC1 Arg194Trp gene

polymorphism and risk of lymphoma in a Romanian population. The 18th International

Scientific Congrss for students, Young physicians and Pharmacists, Marisiensis, 7-11 may

2014, Tg Mures, Acta Medica Marisiensis, 2014, 60(3):32, ISSN-2068-3324

33. Marginean OM, Tripon F, Banescu C, Pitea A. The relation of interleukin 6 gene-190 T/C

polymorphisms with anthropometric and biochemical characteristics in a group of obese

children. The 18th International Scientific Congrss for students, Young physicians and

Pharmacists, Marisiensis, 7-11 may 2014, Tg Mures, Acta Medica Marisiensis, AMM,

2014, 60(3):55, ISSN-2068-3324

34. Nechifor Oana, Banescu C. Genetic answering reproductive questions. The 18th

International Scientific Congrss for students, Young physicians and Pharmacists,

Marisiensis, 7-11 may 2014, Tg Mures, Acta Medica Marisiensis, AMM, 2014, 60(3):15-

16, ISSN-2068-3324

35. Beresteanu A, Tabacitu (Toma) A, Banescu C. The study of Arg399Gln polymorphism of

the X ray repair cross-complement group 1 (XRCC1) gene in chronic myeloiprolipherative

disorders. The 18th International Scientific Congrss for students, Young physicians and

Pharmacists, Marisiensis, 7-11 may 2014, Tg Mures. AMM, 2014, 60(3):59, ISSN-2068-

3324

16

36. Crauciuc G, Tripon F, Bianca I, Banescu C. Have some importance one of the DNA repair

pathways gene mutation in the predisposition to leukemia? Asklepios, 7th International

Medical Congress for Students and Young Doctors, Sibiu, 2014, pag. 1, ISSN-1843-0406.

37. Tripon F, Crauciuc G, Ilie B,Duicu C, Banescu C. The genetic polymorphism of VEGF I/D

and ACE I/D genes in children with nephrotic syndrome. Asklepios, 7th International

Medical Congress for Students and Young Doctors, Sibiu, 2014, pag. 7, ISSN-1843-0406.

38. Tripon F, Crauciuc G, Banescu C, Moldovan V, Duicu C. The VEGF I/D,ACE I/D, e NOS and

NPHS2 genes polymorphisms in children whit nephrotic syndrome, Congress of the

Romanian Society of Medical Genetics, september 24 - 26, 2014, Bucharest. Medicine in

Evolution, 2014, vol XX, nr 2:44, ISSN 1454-8224.

39. Crauciuc G, Tripon F, Moldovan V, Banescu C.Mutations of genes implicated in protection

of DNA and Chronic Myeloid Leukemia. Congress of the Romanian Society of Medical

Genetics, september 24 - 26, 2014, Bucharest. Medicine in Evolution, 2014, vol XX, nr

2:43, ISSN 1454-8224.

40. Trifa AP, Popp R, Cucuianu A, Bănescu C, Tevet M, Popov V, Martin B, Andrei C, Dima D,

Vasilache A, Petrov L, Urian L, Bojan A, Georgescu D, Popescu M, Vesa S, Militaru M,

Cândea M, Mocanu G, Truică C, Todincă A, Cătană A, Mihăilă R, Pop IV. JAK2 V617F, CALR

and C-MPL mutations in essential thrombocythemia and primary myelofibrosis –

biological and clinical correlates in 199 patients. Congress of the Romanian Society of

Medical Genetics, september 24 - 26, 2014, Bucharest. Medicine in Evolution, 2014, vol

XX, nr 2:11, ISSN 1454-8224.

41. Csep K, Ambrus A, Banescu C, Todoran Butila A. Animal testing as viewed by medical

medical students. Congress of the Romanian Society of Medical Genetics, september 24 -

26, 2014, Bucharest. Medicine in Evolution, 2014, vol XX, nr 2:56, ISSN 1454-8224.

42. Todoran Butilă A , Foişoreanu V, Bănescu C, CsepK, Racoş Szabo E.Epileptic

encephalopathy. A condition associated or no with neurophibromatosis type I. Case

report. Congress of the Romanian Society of Medical Genetics, september 24 - 26, 2014,

Bucharest. Medicine in Evolution, 2014, vol XX, nr 2:62, ISSN 1454-8224.

43. Kardos HL, Ivacson B, Banescu C. Study of chromosomal abnormalities in high risk

pregnancies (Studiul modificărilor cromozomiale la sarcinile cu risc). The21st Students

Scientific Conference, March 27-30, 2014, Tirgu Mures, Orvostudomanyi Ertesito, 2014,

87 (1):10, ISSN 1453-0953.

44. Duicu C, Bănescu C, Kiss E, Bodescu V, Moldovam GV. ACE I/D and NPHS2 R229Q gene

polymorphisms in children with nephrotic syndrome. Zilele Universității de Medicină și

Farmacie Tîrgu Mureș, 9-13 decembrie TgMureș, Acta Medica Marisiensis, 2013,

59(4):53, ISSN:2068-3324

45. Mărginean O, Bănescu C, Duicu C, Pitea A, Moldovan V, Marginean M, Marginean C. The

polymorphism of IL-6-572 G/C gene in obese children. Zilele Universității de Medicină și

Farmacie Tîrgu Mureș, 9-13 decembrie TgMureș, Acta Medica Marisiensis, 2013,

59(4):53, ISSN:2068-3324

17

46. Moldovan GV, Bănescu C. Investigation of catalase gene polymorphisms in Romanian

population. Zilele Universității de Medicină și Farmacie Tîrgu Mureș, 9-13 decembrie

TgMureș, Acta Medica Marisiensis, 2013, 59(4):24, ISSN:2068-3324

47. Todoran A, Racos-Szabo E, Micheu C, Csep K, Bănescu C. Possible association of GABRG2

receptor gene polymorphisms with idiopathic generalized epilepsy. Zilele Universității de

Medicină și Farmacie Tîrgu Mureș, 9-13 decembrie 2013, TgMureș, Acta Medica

Marisiensis, 2013, 59(4):63, ISSN:2068-3324

48. Tripon F, Crauciuc GA, Merlan I, Bănescu C, Duicu C. The polymorphism of NPHS2

R229Q gene in young nephrotic syndrome patients from Tirgu Mures-Romania. A XVII-a

editie a Congresului Ştiinţific Internaţional pentru Studenţi, Tineri Medici şi Farmacişti

Marisiensis 2013, 17-21 Aprilie 2013, Tîrgu Mureş. Acta Medica Marisiensis, 2013,

59(1):4, ISSN:2068-3324

49. Crauciuc GA, Tripon F, Merlan I, Bănescu C. The relationship between the resistance to

treatment and T315, T351 mutations on patients with chronic myeloid leukemia from

Tirgu Mures, Romania. A XVII-a editie a Congresului Ştiinţific Internaţional pentru

Studenţi, Tineri Medici şi Farmacişti Marisiensis 2013, 17-21 Aprilie 2013 , Tîrgu Mureş.

Acta Medica Marisiensis, 2013, 59(1):4, ISSN:2068-3324

50. Merlan I, Crauciuc GA, Tripon F, Bănescu C. Detection of DNMT3 mutation in acute

myeloid leukemia and myelodysplastic syndrome. A XVII-a editie a Congresului

Ştiinţific Internaţional pentru Studenţi, Tineri Medici şi Farmacişti Marisiensis 2013, 17-

21 Aprilie 2013, Tîrgu Mureş. Acta Medica Marisiensis, 2013, 59(1):5, ISSN:2068-3324

51. Tripon F, Crauciuc GA, Bănescu C. Genetic investigation of patients with chronic

myeloid leukemia from Tirgu Mures Romania. The 15th Craiova International Medical

Students Conference, Craiova 7-10 November 2013-Abstract Journal, pag.25, ISSN 2285-

6420

52. Crauciuc GA, Tripon F, Bănescu C. MTHFR gene polymorphism in chronic myeloid

leukemia. The 15th Craiova International Medical Students Conference, Craiova 7-10

November 2013-Abstract Journal, pag.28, ISSN 2285-6420

53. Duicu C, Kiss E, Bănescu C, Tripon F. Angiotensin-converting enzyme insertion/deletion

and NPSH2 R229Q gene polymorphisms in children with nephrotic syndrome in a

romanian population. Al XI-lea Congres national de Pediatrie cu participare

internationala. Tg Mures 25-28 septembrie 2013. Book of Abstracts:p156.ISSN 2344-

3324. ISSN-L 2344-3324. Ed University Press Tg Mureș

54. Marginean O, Banescu C, Chincesan M, Duicu C, Man L. Polimorfismul genei enzimei de

conversie a angiotensinei intr-o populatie de copii cu malnutritie din Romania. Al XI -lea

Congres Național de Pediatrie, 25 – 28 septembrie 2013, Tîrgu Mureș, Book of Abstracts,

pg 191,ISSN 2344-3324. ISSN-L 2344-3324. Ed University Press Tg Mureș,

55. Boglis A, Rac DC, Marginean O, Bănescu C. A rare chromosomal disorder-14q interstitial

deletion syndrome. Al XI -lea Congres Național de Pediatrie, 25 – 28 septembrie 2013,

Tîrgu Mureș, Book of Abstracts, pg 191,ISSN 2344-3324. ISSN-L 2344-3324. Ed University

Press Tg Mureș,

18

56. Todoran A, Racos Szabo E, Micheu C, Csep K, Duicu C, Bănescu C. Possible association of

the VEGF gene polymorphism with epileptic syndromes in pediatric patients. Zilele

Universităţii de Medicină şi Farmacie Tg. Mureş 13-15 decembrie 2012, Acta Medica

Marisiensis 2012, 58(3):11, ISSN:2068-3324

57. A Stoian, Stoian M, Banescu C, Duicu C, Alecusan A, Buicu G, Motataianu A, Crisan C, Cif

A, SchiopuA. "Clinical and demographic correlations in patients with diabetic peripheral

neuropathy addressed to the neurology Ambulatory of County Hospital Tirgu Mures",

Yhe 9th Congress of The Romanian Society of neurology, 18-21 may, 2011, Bucuresti.

Romanian Joural of Neurology, 2011, X(1):85-86, ISSN 1843-8148

58. Stoian A, Bănescu C, Duicu C, Stoian M, Oşan VG., Alecuşan A, Şchiopu A. A study of

angiotensin converting enzyme gene polymorphism in patients with diabetic neuropathy.

The First Conference of Postdoctoral Researchers in Medicine and Pharmacy. 6-8 iulie

2011, Tîrgu-Mureş, RomâniaActa Medica Marisiensis. 2011. 57(3):34, ISSN:2068-3324

59. Duicu C, Kiss E, Bănescu C. Angiotensin converting enzyme insertion/deletion gene

polymorphism in children with nephrotic syndrome in a romanian population. Congresul

national de Pediatrie. 28 septembrie-1 octombrie 2011, Bucuresti. Vol de rezumate -

P103, ISSN 2247-9015

60. Duicu C, Bănescu C, Gall Z, Grama A, Gozar H. Association between angiotensin-

converting enzyme gene insertion (I) / deletion (D) polymorphism and secondary arterial

hypertension in a romanian children population. The First Conference of Postdoctoral

Researchers in Medicine and Pharmacy. 6-8 iulie 2011, Tîrgu-Mureş, România. Acta

Medica Marisiensis. 2011. 57(3):36, ISSN:2068-3324.

61. Tilinca M, Benedek Lazar E, Kopeczi JB, Bacarea A, Banescu C, Benedek I, Bataga S. Acute

Myeloblastic Leukemia: difficulties of treatment, complications and evolution. The First

Conference of Postdoctoral Researchers in Medicine and Pharmacy. 6-8 iulie 2011, Tîrgu-

Mureş, România, Acta Medica Marisiensis. 2011. 57(3):62, ISSN:2068-3324.

62. Borosteanu A. Banescu C. Cytogenetics of plurimalformative syndromes. Marisiensis

2011, 7-10 aprilie, Tg Mures Acta Medica Marisiensis. 2011. 57(suppl1):10, ISSN:2068-

3324.

63. Raluca M, Cucerea M, Simon M, Sin A, Bănescu C. A rare chromosomal disorder:

chromosome 4 ring syndrome. Cea de a 65-a aniversare a U.M.F. Târgu-Mureş 15-18

decembrie 2010, Târgu-Mureş. Acta Medica Marisiensis. 2010. 56(3):70, ISSN:2068-3324

64. Todoran Butila A, Foisoreanu V, Csep K, Banescu C. Genotype-phenotype correlation in

mucopolysaccharidosis. Diagnostical characteristics. Treatment. The 33rd national

Conference of Child and Adolescente Neurology and Psychiatry and allied Professions.

TgMures, 22-26 september, 2010, Supplement to the Journal of Romanian Child and

adolescent neurology and Psychiatry. 2010, 13(3):77, ISSN: 2068-8040

65. Csep K, Dudutz G, Banescu C, Todoran Butila A, Koranyi L. Combined effect of diet and

the rs1799883 polymorhism of the intestinal fatty acid binding protein 2 gene on the risk

of developing the metabolic syndrome. Al III lea Congres Național de Genetică Medicală

19

22-25 septembrie 2010, Timișoara, Romanian Journal of Rare Diseases 2010 |

Supplement 1/2010, p.83, ISSN 2068-5882.

66. Duicu C, Kiss E, Dunca I, Banescu C, Grama A, Voicu S. Evaluation of blood pressure

changes by 24-hours ambulatory blood pressure monitoring (ABPM) in children with

diabetes mellitus type I. Cea de a 65-a aniversare a U.M.F. Târgu-Mureş 15-18 decembrie

2010 Târgu-Mureş. Acta Medica Marisiensis. 2010. 56(3):96, ISSN:2068-3324.

67. Paşcanu I, Bănescu C, Csep K, Todoran Butilă A, Lazslo A, Balasz J. Unusual sex

chromosomes abnormalities in endocrine practice Cea de a 65-a aniversare a U.M.F.

Târgu-Mureş 15-18 decembrie 2010 Târgu-Mureş. Acta Medica Marisiensis. 2010.

56(3):5, ISSN:2068-3324

68. Duicu C, Kiss E, Banescu C, Muntean I, Bodescu V. AGT gene polymorphism and high

blood pressure in children. linkage study. Cea de a 65-a aniversare a UMF Tîrgu-Mureş

15-18 decembrie 2010 Târgu-Mureş. Acta Medica Marisiensis. 2010. 56(3):97, ISSN:2068-

3324

69. Csep K, Banescu C, Todoran Butila A.Possibilities of prevention and therapy in monogenic

metabolic disorders. The 33rd national Conference of Child and Adolescente Neurology

and Psychiatry and allied Professions. TgMures, 22-26 september, 2010, Supplement to

the Journal of Romanian Child and adolescent neurology and Psychiatry. 2010, 13(3):98

ISSN: 2068-8040.

70. Bercea A,Pascanu I, Banescu C. Sindromul de rezistenta completa la androgeni.

Congresul National de Comunicari Stiintifice pentru Studenti, Tineri Medici. 15-18 aprilie

2010. Revista de Medicină şi Farmacie UMF Tg. Mureş, 2010. 56(2), 92. ISSN 1221-2229,

71. Duicu C, Kiss E, Bănescu C, Muntean I, Bodescu V, Moreh Z, Grama A. Giant

hydronephrosis cause of arterial hypertension- case report. Zilele Universităţii de

Medicină şi Farmacie Tg. Mureş, Sesiune Anuală de Comunicări Ştiinţifice 9-12

Decembrie 2009. Revista de Medicină şi Farmacie UMF Tg. Mureş, 55(6), 187. ISSN 1221-

2229, cod CNCSIS 103 B.

72. Csep K, Drugan C, Paşcanu I, Bănescu C, Anamaria Todoran BAM (2009). Possibilities and

challenges in the molecular diagnosis of monogenic diseases: lysosomal storage

disorders. Primul Congres al Asociatiei Laboratoarelor Medicale din România, 24-27 iunie

2009, Tg Mureș, Revista Română de Medicină de Laborator, 2009, Supliment la 2(15), 27-

28, ISSN 1841-6624, cod CNCSIS 739 A.

73. Todoran BA, Paşcanu I, Bănescu C, Csep K. Molecular Mechanism of Spinal Muscular

Atrophy. Primul Congres al Asociatiei Laboratoarelor Medicale din România, 24-27 iunie

2009, Tg Mureș, Revista Română de Medicină de Laborator, Supliment la 2(15), 31-32,

ISSN 1841-6624, cod CNCSIS 739 A.

74. Paşcanu I, Bănescu C, Csep K., Todoran B A, Gliga C. Sex Chromosome abnormalities the

experience of Cytogenetic Laboratory in Tîrgu Mureş. Primul Congres al Asociatiei

Laboratoarelor Medicale din România, 24-27 iunie 2009, Tg Mureș, Revista Română de

Medicină de Laborator, 2009 Supliment la 2(15):30-31. ISSN 1841-6624, CNCSIS 739 A.

20

75. Duicu C, Bănescu C, Popp R, Kiss E. Actualităţi în evaluarea copiilor cu hipertensiunie

arterială. Revista de Medicină şi Farmacie UMF Tg. Mureş, 2008, 54:148. ISSN 1221-2229,

cod CNCSIS 103 C.

76. Csép K, Dudutz G, Vitay M, Paşcanu I, Bănescu C, Koranyi L. Joint effect of the FABP2 –

A54T and PPARG2 – P12A polymorhisms on the development if the metabolic syndrome.

A IV-a Coneferinţă a Societăţii Române de Genetică Medicală, Craiova, 18-20 septembrie

2008. Poster. Publicat în Volum de rezumate, 49-50. ISBN 978-973-746-982-3

77. Todoran B. A, Paşcanu I, Csep K, Bănescu C. Importanţa sfatului genetic în cazul

distrofinopatiilor cu transmitere recesivă X-linkată. Caz ilustrativ. Zilele Universității de

Medicină și Farmacie Tîrgu Mureș, decembrie TgMureș, Revista de Medicină şi Farmacie

UMF Tg. Mureş, 2008, 54:149. ISSN 1221-2229, cod CNCSIS 103 C.

78. Paşcanu I, Bănescu C, Gliga C. Thyroid dysfunction in children with Down Syndrome. Al

XVI-lea Congres Naţional Român de Endocrinologie cu Participare Internaţionala,

Timişoara, 23 – 25 Octombrie 2008, prezentare orală. Revista Română de Endocrinologie

si Metabolism, 2008, 7(4):47-48. ISSN 1582-8115, cod CNCSIS 684 C .

79. Mureşan Claudia, Ionela Paşcanu, Katalin Csép, Erzsébet Benedek, I. Benedek, Carmen

Duicu. Modificări citogenetice în fazele evolutive ale leucemiei mieloide cronice.

Sesiunea de Comunicări Ştiinţifice a Cadrelor Didactice, Tg. Mureş, 14-16 decembrie

2006. Prezentare orală. Publicat în Revista de Medicină şi Framacie 2006, vol. 52, pag. 38,

ISSN 1221-2229, cod CNCSIS 103 C.

80. Benedek I., Benedek Erzebet, Mureşan Claudia, Kopeczi Judith, Eniko Kakucs, Benedek I.

Jr. Importanţa examenului citogenetic în diagnosticul şi urmărirea evoluţiei bolnavilor cu

leucemie granulocitară cronică. Sesiunea de Comunicări Ştiinţifice a Cadrelor Didactice,

Tg. Mureş, 14-16 decembrie 2006. Prezentare orală. Publicat în Revista de Medicină şi

Farmacie 2006, vol. 52, pag. 14, ISSN 1221-2229, cod CNCSIS 103 C.

81. Carmen Duicu, Virginia Bodescu, Zsuzsanna Moreh, Claudia Mureşan. Uropatii

obstructive - serie de cazuri. Sesiunea de Comunicări Ştiinţifice a Cadrelor Didactice, Tg.

Mureş, 14-16 decembrie 2006. Prezentare orală. Publicat în Revista de Medicină şi

Farmacie 2006, vol. 52, pag. 144, ISSN 1221-2229, cod CNCSIS 103 C.

82. Carmen Duicu, Eva Kiss, Csilla Todea, I. Egyed, Eniko Varo, Claudia Mureşan, Virginia

Bodescu, Anamaria Barabas. Artrita reumatoidă juvenilă asociaă cu afecţiuni

dermatologice rare. Sesiunea ştiinţifică anuală a cadrelor didactice, Tg. Mureş, 2005,.

Prezentare orală. Publicat în Revista de Medicină şi Farmacie UMF Tg. Mureş 2005; vol

51, supl 5, p. 316. ISSN 1221-2229, cod CNCSIS 103 C.

83. Ionela Paşcanu, A. Borda, H. Emoke, Claudia Mureşan, C. Gliga. HLA DR expression in

thyroid malignant tumor-imunohistochimic study. The XIIIth Balkan Congress of

Endocrinology. Acta Endocrinologica. The International Journal of the Romanian Society

of Endocrinology, Vol.I, Supl. 3, July-September, 2005. Prezentare orala. Endocrine

abstract. pg 55. ISSN 1841-0987.

84. Csép Katalin, Paşcanu Ionela, Claudia Mureşan. Influenţa antecedentelor heredo-

colaterale asupra riscului de dezvoltare a sindromului metabolic. Sesiunea ştiinţifică

21

anuală a cadrelor didactice Tg. Mureş, 2005,. Prezentare orală. Publicat în Revista de

Medicină şi Farmacie UMF Tg. Mureş, 2005; vol 51, supl 5, p. 345. ISSN 1221-2229, cod

CNCSIS 103 C.

85. Claudia Mureşan, Ionela Pascanu, Katalin Csep, Eva Kiss, Carmen Duicu. Sindromul

Christ-Siemens-Touraine. Prezentare de caz. Sesiunea ştiinţifică anuală a cadrelor

didactice, Tg. Mureş 19-20 noiembrie 2004. Poster. Publicat în Revista de Medicină şi

Farmacie UMF Tg. Mureş 2004; vol 50, supl 3, p. 102. ISSN 1221-2229, cod CNCSIS 103 C.

86. Carmen Duicu, Eva Kiss, Claudia Mureşan, Moreh Zsuzsanna, Anamaria Barabas.

Sindromul Bardet-Biedl - dificultăţi de diagnostic. Sesiunea ştiinţifică anuală a cadrelor

didactice, Tg. Mureş, 19-20 noiembrie 2004. Prezentare orală. Publicat în Revista de

Medicină şi Farmacie UMF Tg. Mureş 2004; vol 50, supl 3, p. 37. ISSN 1221-2229, cod

CNCSIS 103 C.

87. Ionela Paşcanu, Claudia Mureşan, Csép Katalin. Osteogeneza imperfectă – dificultăţi de

clasificare a cazurilor aflate în evidenţa cabinetului de genetică Tg. Mureş. Al III-lea

Simpozion Naţional de Boli genetice, endocrine şi de metabolism la copil, Cluj, 10-12

iunie, 2004. Poster. Publicat în Volum de rezumate. p.129. ISBN 973-686-578-9.

88. Csép Katalin, Paşcanu Ionela, Claudia Mureşan. Arborele genealogic al unei familii

afectate de sindromul Bardet-Biedl. Al III-lea Simpozion Naţional de Boli genetice,

endocrine şi de metabolism la copil. Cluj. 10-12 iunie, 2004. Poster. Publicat în Volum de

rezumate. p.159. ISBN 973-686-578-9

89. Claudia Mureşan, Paşcanu Ionela, Csép Katalin. Malformaţia Dandy-Walker – prezentare

de caz. Al III-lea Simpozion Naţional de Boli genetice, endocrine şi de metabolism la copil.

Cluj. 10-12 iunie, 2004. Poster. Publicat în Volum de rezumate. p.160. ISBN 973-686-578-

9

90. Carmen Muntean, Eva Kiss, Claudia Mureşan. Factorii favorizanţi locali ai infecţiei

tractului urinar la copil. Sesiunea de comunicări ştiinţifice a studenţilor şi tinerilor medici

UMF Tg.Mureş. Poster. Publicat în Revista de Medicină şi Farmacie Tg.Mureş 2000,

vol.46, supl 1:151, ISSN 1221-2229

91. Claudia Mureşan, Oana Marginean, Carmen Muntean. Bolile renale şi renovasculare la

copil. Sesiunea de comunicări ştiinţifice a studenţilor şi tinerilor medici UMF Tg.Mureş.

Poster. Publicat în Revista de Medicină şi Farmacie Tg.Mureş 2000, vol.46, supl 1:151,

ISSN 1221-2229

f) Alte lucrări și contribuții științifice

1. Reviste cotate B, C, D

1. Bănescu C, Paşcanu I, Csép K, Duicu C, Candea M. Cytogenetic Aberrations in Chronic

Lymphocytic Leukemia. Revista de Medicină şi Farmacie UMF Targu Mures, 2009,

55:393-397. ISSN 1221-2229, cod CNCSIS 103 B,

2. Bănescu C, Benedek I, Benedek E, Duicu C, Paşcanu I, Csep K. Analiza citogenetică la

pacienţii cu hemopatii maligne pre şi posttransplant de celule stem. Revista de

22

Medicină şi Farmacie Tg. Mureş, 2008, 54(3): 28-29, ISSN 1221-2229, cod CNCSIS 103

C.

3. Cândea M, Oltean G, Demian S, Macarie I, Bănescu C. Prognosticul pacienţilor cu

modificări citogenetice în leucemia limfatică cronică. Revista de Medicină şi Farmacie

Tg. Mureş, 2008, 54(3), 107-109. ISSN 1221-2229, cod CNCSIS 103 C.

4. Paşcanu I, Bănescu C, Csép K, Todoran AMB. 48,XXYY syndrome - a case presentation

and review of the literature. Revista de Medicină şi Farmacie Tg. Mureş, 2008, 54(4):

221-225. ISSN 1221-2229, cod CNCSIS 103 C.

5. Duicu C, Bănescu C, Togănel R, Muntean I, Kiss E. Atrial Septal defects as an

uncommon cardiovascular malformation in Turners syndrome, Revista de Medicină

şi Farmacie UMF Tg. Mureş, 2008, 54(5):80-85. ISSN 1221-2229, cod CNCSIS 103 C

6. Todoran Butilă Anamaria, Foişoreanu Voica, Szabo-Racos Elisabeta, Bănescu Claudia,

Paşcanu Ionela. Retardul mental în bolile neurologice cu determinism genetic. Caz

ilustrativ. Revista Societăţii de neurologie şi Psihiatrie a Copilului şi Adolescentului

din România 2008, 11(4): 45-49. ISSN 145-4237 cod CNCSIS 627 D .

7. Csép K, Dudutz G, Paşcanu I, Bănescu C. A PPARG2 – P12A és PC1 – K121Q

génpolimorfizmusok kölcsönhatása a metabolikus szindróma kialakításában.

Orvostudományi Értesítő, 2008, 81(3):195-198. ISSN 1453-0953 cod CNCSIS 274 B.

8. Carmen Duicu, Eva Kiss, Claudia Muresan, Virginia Bodescu, Zsuzsanna Moreh,

Ilonka Orban. Boala Weber Christian- prezentare de caz. Revista Satu Mare -

Studii si comunicari. Seria Ştiintele Naturii 2006, nr. VII: 100 -103, ISSN 1582-201X

Master Journal List no. 12223, revistă indexată ISI.

9. I.Benedek, Claudia Mureşan, Erzsebet Benedek, Kopeczi Judit Beata, Kakus

Eniko, Benedek I. jr. Utilizarea examenului citogenetic în diagnosticul pozitiv şi

urmărirea evoluţiei pacienţilor cu leucemie granulocitară cronică. Revista Satu

Mare - Studii şi comunicări. Seria Ştiintele Naturii 2006, nr. V II: 177-181, ISSN

1582-201X. Master Journal List no. 12223, revistă indexată ISI

10. I. Paşcanu, S. Băţagă, C. Mureşan, K. Csép, A. Laszló. Cancerul gastric – mecanisme

genetice şi moleculare. Revista de Medicină şi Farmacie Tg. Mureş 2006; vol. 52,

supl. 4: 50-53. ISSN 1221-2229, cod CNCSIS 103 C.

Articole, studii publicate în rezumat în volumele unor manifestări ştiinţifice internaţionale

(fără ISSN sau ISBN)

1. Bănescu C, Benedek I, Benedek E, Paşcanu I, Csép K, Duicu C. The importance of

cytogenetic analysis before and after stem cell transplantation in malignant

haemopathies. FISH-ESC. First International Symposium on Human Embryonic Stem

Cell Research. Evry-Paris, Jan 31-Febr 2, 2008. Poster. Final Program. Pg.43.

Articole, studii publicate în rezumat în volumele unor manifestări ştiinţifice naţionale (fără

ISSN sau ISBN)

1. Claudia Bănescu, Carmen Duicu, Adrian P. Trifa, Istvan Benedek, Erzsebet Lazar

Benedek, Smaranda Demian, Ioan Macarie, Minodora Dobreanu. Incidence and

23

prognostic influence of FLT3 mutations in acute myeloid leukemia. A VII-a Conferinta

Nationala de Genetica Medicala cu Participare Internationala, 26-28 septembrie

2013, Păltiniș, Romania

2. Katalin Csép, Claudia Bănescu, Anamaria Butilă Todoran, Nóra Árgyó. Components of

nicotine dependence, Phenylthiocarbamide bitterness perception and COMT

polymorphism. A VII-a Conferinta Nationala de Genetica Medicala cu Participare

Internationala, 26-28 septembrie 2013, Sibiu-Păltiniș, Romania

3. Banescu C, Duicu C, Demian S, Macarie I, Dobreanu M. Polimorfismul XRCC1 Arg 399

Gln la pacienţii romani cu leucemie mieloida cronica. A VI-a Conferinta Nationala de

Genetica Medicala cu Participare Internationala, 5-8 octombrie 2012, Iasi, Romania

4. Bănescu C., Paşcanu I., Csép K., Duicu C. Analiza citogenetică în diagnosticul, evoluţia

şi stabilirea conduitei terapeutice în leucemia acută mieloblastică secundară.

Conferinţa anuală a Societăţii Române de Genetică Medicală, Cheile Grădiştei,

Braşov, 25-27 mai 2007. Poster. Publicat în Culegere rezumate ştiinţifice. p. 43.

5. Bănescu C., Cîndea M., Duicu C., Paşcanu I., Csep K. Aspecte citogenetice în leucemia

limfocitară cronică. Conferinţa Anuală a Societăţii Române de Genetică Medicală,

Cheile Grădiştei, Braşov, 25-27 mai 2007. Poster. Publicat în Culegere rezumate

ştiinţifice. p. 43.

6. Ionela Paşcanu, Katalin Csép, Mureşan Claudia şi colab. Densitatea minerală osoasă

în sindromul Turner. Al 2-lea Congres Naţional de Genetică Medicală, Cluj-Napoca,

20-23 septembrie 2006. Poster. Publicat în Culegere rezumate ştiinţifice. p. 27.

7. Mureşan Claudia, Ionela Paşcanu, Katalin Csép, Erzsébet Benedek, István Benedek,

Carmen Duicu. Modificări citogenetice în leucemia mileoidă cronică. Al II-lea Congres

Naţional de Genetică Medicală, Cluj-Napoca, 20-23 septembrie 2006. Poster. Publicat

în Culegere rezumate ştiinţifice. p. 80.

8. Katalin Csep, I. Koranyi, M. Vitay, Gy. Dudutz, L. Rosivall, I. Pascanu, Claudia

Mureşan. Relaţia polimorfismului K 121q al genei PC1 cu sindromul metabolic

diagnosticat conform criteriilor recomandate de IDF. Al II-lea Congres Naţional de

Genetică Medicală, Cluj-Napoca, 20-23 septembrie 2006. Poster. Publicat în Culegere

rezumate ştiinţifice. p. 52.

6. Comunicări ştiinţifice făcute în cadrul unor manifestări ştiinţifice naţionale, fără volum

de rezumate

1. Claudia Bănescu , Carmen Duicu, I. Benedek, Smaranda Demian, I. Macarie,

Minodora Dobreanu. DNA repair XRCC1 Arg399Gln gene polymorphism in acute

myeloid leukemia. Zilele Universității de Medicină și Farmacie din Tîrgu Mureș, 15-17

decembrie 2011

2. Claudia Bănescu, Ionela Paşcanu, Anamaria Butilă Todoran, Katalin Csep, Carmen

Duicu. Methylenetetrahydrofolate reductase polymorphism 677C>T and risk of

mental retardation in children with down syndrome. Zilele Universității de Medicină

și Farmacie din Tîrgu Mureș, 15-17 decembrie 2011.

24

1. Carmen Duicu, Claudia Bănescu, R. Popp, EvaKiss. Actualităţi în evaluarea copiilor cu

hipertensiunie arterială. Zilele Universităţii de Medicină şi Farmacie din Tg. Mureş,

11-13 decembrie 2008. Prezentare orală.

2. Anamaria Todoran Butilă, Ionela Paşcanu, Katalin Csep, Claudia Bănescu. Importanţa

sfatului genetic în cazul distrofinopatiilor cu transmitere recesivă X-linkată. Caz

ilustrativ. Zilele Universităţii de Medicină şi Farmacie din Tg. Mureş, 11-12 decembrie

2008. Prezentare orală.

3. Carmen Duicu, Claudia Bănescu, R. Popp, Eva Kiss. Aspecte actuale în etiopatogenia

hipertensiunii arteriale la copil. Prima Conferinţă a Doctoranzilor în Medicină şi

Farmacie, Tg. Mureş, 9-11 iulie 2008. Prezentare orală.

4. Ionela Paşcanu, Claudia Bănescu, Camelia Gliga, Annamaria Laszló, Anisia Năsălean,

Katalin Csép. Treatment of hypophosphatemic rickets-evolution in a case with

puberty onset. Al XV-lea Congres Naţional Al Societăţii Române De Endocrinologie,

Poiana Braşov, 25-28 octombrie, 2007. Poster.

5. Carmen Duicu, Eva Kiss, Anamaria Barabas, Zsuzsa Moreh, Claudia Mureşan.

Complicaţiile sindromului nefrotic la copil. Meeting de nefrologie pediatrică cu

participare internaţională, Iaşi, 14-16 aprilie 2005. Poster.

6. Eva Kiss, Carmen Duicu, sanda Voicu, Zsuzsa Moreh, Claudia Mureşan. Sindrom

nefrotic congenital Finish type - caz particular. Meeting de nefrologie pediatrică cu

participare internaţională, Iaşi, 14-16 aprilie 2005. Prezentare orală.

Grant/proiect câștigat prin competiție -director – 2 granturi

1. Director de proiect. Proiectului de cercetarea depus în cadrul Competitiei interne

pentru granturi de cercetare stiintifică- Colective de cercetare (CIGCS-CC) organizată

de UMF TgMureş, competiția 2013 „Identificarea profilului molecular complex în

diagnosticul și prognosticul leucemiei acute mieloide”, contract nr. 19/11.12.2013.,

perioada 11.12.2013-31.12.2015, valoare 88984,3 lei.

2. Director de proiect. Proiectului de cercetarea depus în cadrul Competitiei interne

pentru granturi de cercetare stiintifică (CIGCS) organizată de UMF TgMureş,

competiția 2012. “Impactul mutaţiei în gena pentru nucleofosmină NPM1 în

diagnosticul şi monitorizarea bolii reziduale minime în leucemia acută mieloidă”,

contract nr. 2/30.01.2013, perioada ianuarie 2013-decembrie 2013, valoare 22495

lei.

Grant/proiect câștigat prin competiție – membru în proiect – 2 granturi

1. Membru al echipei tehnice, în proiectul “Centru Avansat de Cercetări Medicale şi

Farmaceutice, prin programul operaţional POS CCE O2.2.1” valoare 10.4 milioane Euro

(nerambursabili 8.4 milioane Euro), 2014-2015, ID proiect 1837, nr contract

659/7.08.2014, director proiect Prof.dr Minodora Dobreanu.

http://www.umftgm.ro/universitate/media/noutati/stiri-detalii/articol/centrul-

avansat-de-cercetari-medicale-si-farmaceutice-proiect-castigat-de-umf.html

25

2. Translarea cercetarilor genomice referitoare la etiologia malformatiilor cardiace

congenitale in metode inovative de screening, preventie prenatala, diagnostic genetic

si imagistica tridimensionala - MAMI, contract nr. 41-042/, 2007, CNMP – PNCD II -

Parteneriate în domeniile prioritare, UMF.Tg.Mureş - Director de proiect: Prof. Dr.

Rodica Togănel; funcţia în cadrul proiectului - asistent de cercetare, valoare contract:

2000000 lei, 2007-2010, www.upm.ro/medicina/mami/contact.html

Studii multicentrice internaţionale - membru în echipa de cercetare

1. Membru în COST 8M0902 "Network of experts in the diagnosis of myleproliferative

disorders (MPD)", grup de lucru WG1, 2010-2013

2. Membru in acțiunea COST BM1208, “European Network for Human Congenital Imprinting

Disorders”, 2014

Studii multicentrice naţionale - membru în echipa de cercetare

1. A multi-center, randomized, double-blind, placebo-controlled, clinical trial of

deferasirox in patients with myelodysplastic syndromes (Low/Intermediate-1Risk)

and transfusional iron overload, sub-investigator, November 2011- December 2012

Proiecte de formare continuă și de dezvoltare instituțională – membru în echipa de

management

1. Expert dezvoltare curriculă in proiectul "Calitate si competenta profesionala

europeana in educatia medicala si in managementul activitatilor educationale" -

POSDRU /86/ 1.2/ S/ 63815, 1 ianuarie 2011 - 31 decembrie 2013), Partener lider de

proiect: Universitatea de Medicina si Farmacie "Victor Babes" din Timisoara.

Parteneri:P1: Universitatea de Medicina si Farmacie "Iuliu Hatieganu" Cluj-Napoca;

P2: Universitatea de Medicina si Farmacie "Gr.T Popa" Iasi; P3: Universitatea de

Medicina si Farmacie Craiova; P4: Universitatea de Medicina si Farmacie Tirgu-Mures;

P5: Universitatea de Medicina Viena; P6: Universitatea de Stiinte din Szeged,

Facultatea de Medicina

Depunere de proiect la o competitie de proiecte națională, în calitate de director de

proiect

1. “Contribuția polimorfismelor CLPTMIL rs31490, TERT rs10069690 și

rs2511714 la apariția leucemiei limfocitare cronice și a mutațiilor somatice asociate”

în cadrul competiției 2014 “Tinere echipe de cercetare” PN-II-RU-TE-2014-4-1368,

2. Anomaliile cromozomiale - indicator independent de diagnostic si de prognostic in

hemopatiile maligne – director de proiect Claudia Banescu, Institutia conducatoare:

Universitatea de Medicina si Farmacie Tîrgu Mureș PN2 - Proiecte de cercetare

pentru tineri doctoranzi tip TD 2008 (cod CNCSIS PN-II-RU-TD-2008-3, numarul 350).

3. “Unravelling the complex molecular profile in diagnosing and monitoring minimal

residual disease in acute myeloid leukemia - Identificarea profilului molecular

complex în diagnosticul și monitorizarea bolii reziduale minime în leucemia acută

mieloidă”, director de proiect Claudia Banescu, Proiecte de cercetare postdoctorale,

cu numărul de înregistrare PN-II-RU-PD-2012-3-0556.

Bursa postdoctorală

26

1. „Studiul unor mutaţii genice în scopul stabilirii prognosticului şi monitorizării bolii

reziduale minime în hemopatiile maligne” în cadrul "Cercetare avansata prin

programe post-doctorale in stiinte fundamentale si clinice medicale"-

POSDRU/89/1.5/S/60782, Iulie 2010-Decembrie 2012

Tîrgu Mureş

27.05.2015

Claudia Violeta Bănescu