Skip to Main Content

Author Details

Jean Gekas
Laval University
1997
35
16
Vardit Ravitsky (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37293304Use of cell-free signals as biomarkers for early and easy prediction of preeclampsia.Front Med (Lausanne)2023
37152999Patient attitudes and preferences about expanded noninvasive prenatal testing.Front Genet2023
36105088Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes.Front Genet2022
34072979A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study.Cancers (Basel)2021
31231136Prospective head-to-head comparison of accuracy of two sequencing platforms for screening for fetal aneuploidy by cell-free DNA: the PEGASUS study.Eur J Hum Genet2019
28784564Cell-Free DNA-Based Non-invasive Prenatal Screening for Common Aneuploidies in a Canadian Province: A Cost-Effectiveness Analysis.J Obstet Gynaecol Can2018
29080223Comparison of first-tier cell-free DNA screening for common aneuploidies with conventional publically funded screening.Prenat Diagn2017
28098151Juvenile myelomonocytic leukemia-associated variants are associated with neo-natal lethal Noonan syndrome.Eur J Hum Genet2017
26893576Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues.Appl Clin Genet2016
26822682Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations.Am J Med Genet A2016
24238947Cost effectiveness of newborn screening for cystic fibrosis: a simulation study.J Cyst Fibros2014
25053891Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma.Appl Clin Genet2014
23301910Recurrent anencephaly: a case report and examination of the VANGL1 and FOXN1 genes.Fetal Pediatr Pathol2013
24007709Cost-effectiveness of the management of rh-negative pregnant women.J Obstet Gynaecol Can2013
22432933Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria.Fetal Pediatr Pathol2012
23181171Molecular prenatal diagnosis of a sporadic alobar holoprosencephalic fetus: genotype-phenotype correlations.J Prenat Med2012
22990676Myoblasts derived from normal hESCs and dystrophic hiPSCs efficiently fuse with existing muscle fibers following transplantation.Mol Ther2012
20842178Rapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities.Eur J Hum Genet2011
22094916Midtrimester intra-amniotic sludge and the risk of spontaneous preterm birth.Am J Perinatol2011
21779980A survey of APC mutations in Quebec.Fam Cancer2011
21965346Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation.J Med Genet2011
21074138Cost-effectiveness and accuracy of prenatal Down syndrome screening strategies: should the combined test continue to be widely used?Am J Obstet Gynecol2011
19730985In vitro and in vivo study of human amniotic fluid-derived stem cell differentiation into myogenic lineage.Clin Exp Med2010
20849990Current perspectives on the etiology of agnathia-otocephaly.Eur J Med Genet2010
20594144Prenatal diagnosis and molecular genetic studies on a new case of agnathia-otocephaly.Fetal Pediatr Pathol2010
19218323Comparison of different strategies in prenatal screening for Down's syndrome: cost effectiveness analysis of computer simulation.BMJ2009
19455667Amniotic stem cells for cellular cardiomyoplasty: promises and premises.Catheter Cardiovasc Interv2009
17486531[Outcome of pregnancy in patients with haemophilia B--two case reports].Z Geburtshilfe Neonatol2007
15063731The inhibition of cell spreading on a cellulose substrate (cuprophan) induces an apoptotic process via a mitochondria-dependent pathway.FEBS Lett2004
12659787[Value of karyotyping women patients of couples referred for sterility].Gynecol Obstet Fertil2003
11139542Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men.Hum Reprod2001
11232459[X-linked recessive chondrodysplasia punctata. Cytogenetic study and role of molecular biology].Arch Pediatr2001
11746136Cerebro-costo-mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission.Prenat Diagn2001
10073897Informed consent to serum screening for Down syndrome: are women given adequate information?Prenat Diagn1999
9581539Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation.Biochem J1997
  • 1 - 35 of 35

Recommended Authors

Baylor College of Medicine
Career Start Year 2011
Number of shared co-authors 0
Riga Stradins University
Career Start Year 2011
Number of shared co-authors 0
Zeynep Kamil Maternity and Children's Training and Research Hospital
Career Start Year 2010
Number of shared co-authors 0
University of California San Francisco
Career Start Year 2009
Number of shared co-authors 0
Cambridge University Hospitals NHS Foundation Trust
Career Start Year 2008
Number of shared co-authors 0
Hopital Universitaire de Nantes
Career Start Year 2005
Number of shared co-authors 0
University Hospital Basel and University of Basel
Career Start Year 2002
Number of shared co-authors 0
Murdoch Children's Research Institute
Career Start Year 2001
Number of shared co-authors 2
Pathology and Laboratory Medicine Institute, Cleveland Clinic
Career Start Year 2001
Number of shared co-authors 0
Institute of Medical Genetics and Applied Genomics, University of Tuebingen
Career Start Year 2000
Number of shared co-authors 0
University of British Columbia
Career Start Year 1997
Number of shared co-authors 3
Baylor College of Medicine
Career Start Year 1997
Number of shared co-authors 0
Radboud University Medical Center
Career Start Year 1996
Number of shared co-authors 0
Birmingham Women's and Children's NHS Foundation Trust
Career Start Year 1995
Number of shared co-authors 0
Institute of Medical and Molecular Genetics
Career Start Year 1993
Number of shared co-authors 0
Institute of Medical and Molecular Genetics
Career Start Year 1993
Number of shared co-authors 1
Guy's and St Thomas' NHS Foundation Trust
Career Start Year 1992
Number of shared co-authors 0
Royal Adelaide Hospital
Career Start Year 1990
Number of shared co-authors 2
Clinical Genetics, Addenbrooke's Hospital, Cambridge University Hospitals
Career Start Year 1990
Number of shared co-authors 2
University College Dublin
Career Start Year 1989
Number of shared co-authors 0
UCL Institute of Child Health and Great Ormond Street NHS Foundation Trust
Career Start Year 1989
Number of shared co-authors 1
Genomics England Ltd.
Career Start Year 1987
Number of shared co-authors 1
Kaiser Permanente Washington
Career Start Year 1987
Number of shared co-authors 2
Institute of Genetics and Cancer, The University of Edinburgh MRC Human Genetics Unit
Career Start Year 1984
Number of shared co-authors 1
Columbia University
Career Start Year 1980
Number of shared co-authors 0
University of Newcastle upon Tyne.
Career Start Year 1978
Number of shared co-authors 0
University of Adelaide
Career Start Year 1977
Number of shared co-authors 3
Paris Brain Institute-ICM, Inserm U 7, CNRS UMR 7225, Sorbonne Universite
Career Start Year 1974
Number of shared co-authors 0
University of Oklahoma
Career Start Year 1968
Number of shared co-authors 2
The Children's Hospital of Philadelphia
Career Start Year 1961
Number of shared co-authors 0

Collaborators

Universite Laval
Co-authored papers 11
University of Montreal
Co-authored papers 5
Research Center, Centre Hospitalier Universitaire Sainte-Justine
Co-authored papers 5
Research Center of the CHU de Quebec-Universite Laval, Universite Laval
Co-authored papers 5
Universite Laval
Co-authored papers 3
The Hastings Center
Co-authored papers 2
University of Quebec at Rimouski.
Co-authored papers 2
McGill University, Canada Montreal Neurological Institute and Hospital
Co-authored papers 1
CHU de Quebec-Universite Laval Research Center
Co-authored papers 1
CHU de Quebec-Universite Laval Research Center
Co-authored papers 1
Harvard Medical School, Brigham and Women's Hospital
Co-authored papers 1
McGill University.
Co-authored papers 1
Universite Laval
Co-authored papers 1
Co-authored papers 1
Segal Cancer Centre, Jewish General Hospital
Co-authored papers 1
UNIVERSITY OF MONTREAL
Co-authored papers 1
Co-authored papers 1
Queens University Belfast
Co-authored papers 1
University of California san francisco
Co-authored papers 1
Canada British Columbia Cancer Research Centre, University of British Columbia
Co-authored papers 1
Lady David Institute for Medical Research, Jewish General Hospital
Co-authored papers 1