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Author Details
Full Name
Jean Gekas
Affiliation
Laval University
ORCID
Career Start Year
1997
Papers
35
H Index
16
Expertise
CM4AI Collaborator
Vardit Ravitsky (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37293304
Use of cell-free signals as biomarkers for early and easy prediction of preeclampsia.
Front Med (Lausanne)
2023
37152999
Patient attitudes and preferences about expanded noninvasive prenatal testing.
Front Genet
2023
36105088
Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes.
Front Genet
2022
34072979
A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study.
Cancers (Basel)
2021
31231136
Prospective 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 Genet
2019
28784564
Cell-Free DNA-Based Non-invasive Prenatal Screening for Common Aneuploidies in a Canadian Province: A Cost-Effectiveness Analysis.
J Obstet Gynaecol Can
2018
29080223
Comparison of first-tier cell-free DNA screening for common aneuploidies with conventional publically funded screening.
Prenat Diagn
2017
28098151
Juvenile myelomonocytic leukemia-associated variants are associated with neo-natal lethal Noonan syndrome.
Eur J Hum Genet
2017
26893576
Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues.
Appl Clin Genet
2016
26822682
Three 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 A
2016
24238947
Cost effectiveness of newborn screening for cystic fibrosis: a simulation study.
J Cyst Fibros
2014
25053891
Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma.
Appl Clin Genet
2014
23301910
Recurrent anencephaly: a case report and examination of the VANGL1 and FOXN1 genes.
Fetal Pediatr Pathol
2013
24007709
Cost-effectiveness of the management of rh-negative pregnant women.
J Obstet Gynaecol Can
2013
22432933
Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria.
Fetal Pediatr Pathol
2012
23181171
Molecular prenatal diagnosis of a sporadic alobar holoprosencephalic fetus: genotype-phenotype correlations.
J Prenat Med
2012
22990676
Myoblasts derived from normal hESCs and dystrophic hiPSCs efficiently fuse with existing muscle fibers following transplantation.
Mol Ther
2012
20842178
Rapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities.
Eur J Hum Genet
2011
22094916
Midtrimester intra-amniotic sludge and the risk of spontaneous preterm birth.
Am J Perinatol
2011
21779980
A survey of APC mutations in Quebec.
Fam Cancer
2011
21965346
Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation.
J Med Genet
2011
21074138
Cost-effectiveness and accuracy of prenatal Down syndrome screening strategies: should the combined test continue to be widely used?
Am J Obstet Gynecol
2011
19730985
In vitro and in vivo study of human amniotic fluid-derived stem cell differentiation into myogenic lineage.
Clin Exp Med
2010
20849990
Current perspectives on the etiology of agnathia-otocephaly.
Eur J Med Genet
2010
20594144
Prenatal diagnosis and molecular genetic studies on a new case of agnathia-otocephaly.
Fetal Pediatr Pathol
2010
19218323
Comparison of different strategies in prenatal screening for Down's syndrome: cost effectiveness analysis of computer simulation.
BMJ
2009
19455667
Amniotic stem cells for cellular cardiomyoplasty: promises and premises.
Catheter Cardiovasc Interv
2009
17486531
[Outcome of pregnancy in patients with haemophilia B--two case reports].
Z Geburtshilfe Neonatol
2007
15063731
The inhibition of cell spreading on a cellulose substrate (cuprophan) induces an apoptotic process via a mitochondria-dependent pathway.
FEBS Lett
2004
12659787
[Value of karyotyping women patients of couples referred for sterility].
Gynecol Obstet Fertil
2003
11139542
Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men.
Hum Reprod
2001
11232459
[X-linked recessive chondrodysplasia punctata. Cytogenetic study and role of molecular biology].
Arch Pediatr
2001
11746136
Cerebro-costo-mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission.
Prenat Diagn
2001
10073897
Informed consent to serum screening for Down syndrome: are women given adequate information?
Prenat Diagn
1999
9581539
Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation.
Biochem J
1997
1 - 35 of 35
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Universite Laval
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University of Montreal
Co-authored papers
5
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Co-authored papers
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Co-authored papers
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University of Quebec at Rimouski.
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Guy A Rouleau
McGill University, Canada Montreal Neurological Institute and Hospital
Co-authored papers
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Julie Lapointe
CHU de Quebec-Universite Laval Research Center
Co-authored papers
1
Michel Dorval
CHU de Quebec-Universite Laval Research Center
Co-authored papers
1
Matthew S Lebo
Harvard Medical School, Brigham and Women's Hospital
Co-authored papers
1
Yann Joly
McGill University.
Co-authored papers
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Hermann Nabi
Universite Laval
Co-authored papers
1
Richard A Moore
Co-authored papers
1
William D Foulkes
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Co-authored papers
1
Anne-Marie Laberge
UNIVERSITY OF MONTREAL
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1
Sandrine Vuillaumier-Barrot
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1
Christopher McCabe
Queens University Belfast
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