Wilfrid Carré

Agricultural and Biological Sciences · Life Sciences

31h-index4.8kcitations112works0.92yr avg
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Research Topics

Animal Nutrition and Physiology(23), Genetic and phenotypic traits in livestock(22), Animal Genetics and Reproduction(18), Genetic Mapping and Diversity in Plants and Animals(16), Hedgehog Signaling Pathway Studies(10)

Publications110 total

Genetic analyses using chromosomal microarray and exome sequencing in fetuses and women with Müllerian duct anomalies
Journal of Assisted Reproduction and Genetics·2025· 1 citedOpen Access
SWS1-complex in premature ovarian insufficiency: <i>SWSAP1</i> as a new POI gene
Human Reproduction·2025
The Clinical and Genetic Landscape of a French Multicenter Cohort of 2563 Epilepsy Patients Referred for Genetic Diagnosis
European Journal of Neurology·2025· 3 citedOpen Access
Mapping the temporal and functional landscape of Sonic Hedgehog signaling reveals new insights into early human forebrain development
2025· 1 citedOpen Access
Expanding the TUBB3‐Related Phenotypic Landscape: Fetal Diagnosis of Novel TUBB3 Variant Linked With Phenotypic Variability Within a Single Family
Prenatal Diagnosis·2024Open Access
Les voies de l’ovogenèse : quels groupes de gènes candidats dans l’insuffisance ovarienne prématurée ?
Morphologie·2024
DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations
Genetics in Medicine·2024· 2 citedOpen Access
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects
Genetics in Medicine·2022· 14 citedOpen Access
Oligogenic inheritance in neural tube defects: major involvment of primary cilia, planar cell polarity and extracellular matrix genes
SPIRE - Sciences Po Institutional REpository·2022
Pathogenicity assessment of DISP1 variants associated with midline anomalies spectrum
SPIRE - Sciences Po Institutional REpository·2022
Fetal Description of the Pancreatic Agenesis and Holoprosencephaly Syndrome Associated to a Specific <i>CNOT1</i> Variant
Pediatric and Developmental Pathology·2022· 8 citedOpen Access
Scarcity of available information resources for patients and clinicians after a diagnosis of ultra-rare diseases: retrospective on a cohort of 626 individuals with congenital abnormalities and/or intellectual disability
SPIRE - Sciences Po Institutional REpository·2022
Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes
European Journal of Human Genetics·2021· 42 citedOpen Access
<scp>Skraban‐Deardorff</scp> syndrome: Six new cases of <scp> <i>WDR</i> 26 </scp> ‐related disease and expansion of the clinical phenotype
Clinical Genetics·2021· 12 citedOpen Access
Author response for "Skraban-Deardorff syndrome: six new cases of WDR26-related disease and expansion of the clinical phenotype"
2021
Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency
The Journal of Clinical Endocrinology & Metabolism·2020· 16 citedOpen Access
Identification du premier cas autochtone de xeroderma pigmentosum de type A en France : mutation homozygote XPA H244R contrastant avec un phénotype modéré sans atteinte neurologique
Annales de Dermatologie et de Vénéréologie·2019
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
The American Journal of Human Genetics·2019· 97 citedOpen Access
Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy
2019· 1 citedOpen Access
Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders
Human Genetics·2019· 19 cited
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Frequent Co-authors

Christèle Dubourg(17), Larry A. Cogburn(14), Sylvie Odent(12), Laurent Pasquier(11), Xiaofei Wang(9), Samuel E. Aggrey(8), Valérie Dupé(8), Tom E. Porter(7), Jean Simon(7), Houda Hamdi‐Rozé(7), Linda Akloul(7), Alain Vignal(6), Marie de Tayrac(6), Marie Faoucher(6), Bertrand Isidor(5), Alinoë Lavillaureix(5), Sandrine Lagarrigue(5), Paul Rollier(5), Charlotte Mouden(5), Véronique David(5)