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Centre de recherche

BOTTIN

Jean Gekas

Formation
Md

PhD

Médecin Généticien

Aucune offre active

Autres opportunités de carrière
Axe principal
Reproduction, santé de la mère et de l'enfant
Adresse(s)
Hôpital Saint-François-d'Assise
10, rue de l'Espinay
D0-738
Québec (Québec)
CANADA G1L 3L5

Téléphone(s)
+1 418-525-4444, poste 53251
Télécopieur(s)
+1 418-525-4195
Courriel(s)
Jean.Gekas@mail.chuq.qc.ca

Publications récentes (voir toutes les publications de ce chercheur)

Nshimyumukiza L, Beaumont JA, Duplantie J, Langlois S, Little J, Audibert F, McCabe C, Gekas J, Giguere Y, Gagne C, Reinharz D, Rousseau F. Cell-Free DNA-Based Non-invasive Prenatal Screening for Common Aneuploidies in a Canadian Province: A Cost-Effectiveness Analysis. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC,  2017. Epub
Mason-Suares H, Toledo D, Gekas J, Lafferty KA, Meeks N, Pacheco MC, Sharpe D, Mullen TE, Lebo MS. Juvenile myelomonocytic leukemia-associated variants are associated with neo-natal lethal Noonan syndrome. European journal of human genetics : EJHG,  2017. Epub
Gekas J, Langlois S, Ravitsky V, Audibert F, van den Berg DG, Haidar H, Rousseau F. Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues. The application of clinical genetics,  2016. 9: 15-26
Ayub S, Gadji M, Krabchi K, Cote S, Gekas J, Maranda B, Drouin R. Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations. American journal of medical genetics. Part A,  2016. 170A: 896-907
Gekas J, Langlois S, Ravitsky V, Audibert F, van den Berg DG, Haidar H, Rousseau F. Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma. The application of clinical genetics,  2014. 7: 127-31
Nshimyumukiza L, Bois A, Daigneault P, Lands L, Laberge AM, Fournier D, Duplantie J, Giguere Y, Gekas J, Gagne C, Rousseau F, Reinharz D. Cost effectiveness of newborn screening for cystic fibrosis: a simulation study. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society,  2014. 13: 267-74
Sergi C, Gekas J, Kamnasaran D. Recurrent anencephaly: a case report and examination of the VANGL1 and FOXN1 genes. Fetal and pediatric pathology,  2013. 32: 293-7
Duplantie J, Martinez Gonzales O, Bois A, Nshimyumukiza L, Gekas J, Bujold E, Morin V, Vallee M, Giguere Y, Gagne C, Rousseau F, Reinharz D. Cost-effectiveness of the management of rh-negative pregnant women. Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC,  2013. 35: 730-40
Sergi C, Gekas J, Kamnasaran D. Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria. Fetal and pediatric pathology,  2012. 31: 315-8
Goudenege S, Lebel C, Huot NB, Dufour C, Fujii I, Gekas J, Rousseau J, Tremblay JP. Myoblasts derived from normal hESCs and dystrophic hiPSCs efficiently fuse with existing muscle fibers following transplantation. Molecular therapy : the journal of the American Society of Gene Therapy,  2012. 20: 2153-67
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