1
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
2
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
7
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
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