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Carré, Wilfrid
153  results:
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1

DISP1 deficiency: Monoallelic and biallelic variants cause ..:

Lavillaureix, Alinoë ; Rollier, Paul ; Kim, Artem...
Genetics in Medicine.  26 (2024)  7 - p. 101126 , 2024
Link: https://doi.org/10.1016/..
 
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2

FOSL2 truncating variants in the last exon cause a neurodev..:

Cospain, Auriane ; Rivera-Barahona, Ana ; Dumontet, Erwan...
Genetics in Medicine.  24 (2022)  12 - p. 2475-2486 , 2022
Link: https://doi.org/10.1016/..
 
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3

Fetal Description of the Pancreatic Agenesis and Holoprosen..:

Cospain, Auriane ; Faoucher, Marie ; Cauchois, Aurélie...
Pediatric and Developmental Pathology.  25 (2022)  5 - p. 548-552 , 2022
Link: https://doi.org/10.1177/..
 
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4

Skraban‐Deardorff syndrome: Six new cases of WDR26‐related ..:

Cospain, Auriane ; Schaefer, Elise ; Faoucher, Marie...
Clinical Genetics.  99 (2021)  5 - p. 732-739 , 2021
Link: https://doi.org/10.1111/..
 
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5

Meiotic genes in premature ovarian insufficiency: variants ..:

Tucker, Elena J. ; Bell, Katrina M. ; Robevska, Gorjana...
European Journal of Human Genetics.  30 (2021)  2 - p. 219-228 , 2021
Link: https://doi.org/10.1038/..
 
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6

Disrupted Hypothalamo-Pituitary Axis in Association With Re..:

Hamdi-Rozé, Houda ; Ware, Michelle ; Guyodo, Hélène...
The Journal of Clinical Endocrinology & Metabolism.  105 (2020)  9 - p. e3183-e3196 , 2020
Link: https://doi.org/10.1210/..
 
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7

Targeted panel sequencing establishes the implication of pl..:

Beaumont, Marie ; Akloul, Linda ; Carré, Wilfrid...
Human Genetics.  138 (2019)  4 - p. 363-374 , 2019
Link: https://doi.org/10.1007/..
 
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8

Transcriptional profiling of liver during the critical embr..:

Cogburn, Larry A. ; Trakooljul, Nares ; Chen, Chuming...
BMC Genomics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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9

Transcriptional profiling of liver in riboflavin-deficient ..:

Cogburn, Larry A. ; Smarsh, Danielle N. ; Wang, Xiaofei...
BMC Genomics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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10

Integrated clinical and omics approach to rare diseases: no..:

Kim, Artem ; Savary, Clara ; Dubourg, Christèle...
Brain.  142 (2018)  1 - p. 35-49 , 2018
Link: https://doi.org/10.1093/..
 
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11

HCN1mutation spectrum: from neonatal epileptic encephalopat..:

Marini, Carla ; Porro, Alessandro ; Rastetter, Agnès...
Brain.  141 (2018)  11 - p. 3160-3178 , 2018
Link: https://doi.org/10.1093/..
 
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12

Mutational Spectrum in Holoprosencephaly Shows That FGF is ..:

Dubourg, Christèle ; Carré, Wilfrid ; Hamdi-Rozé, Houda...
Human Mutation.  37 (2016)  12 - p. 1329-1339 , 2016
Link: https://doi.org/10.1002/..
 
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13

Matching the Diversity of Sulfated Biomolecules: Creation o..:

Barbeyron, Tristan ; Brillet-Guéguen, Loraine ; Carré, Wilfrid...
PLOS ONE.  11 (2016)  10 - p. e0164846 , 2016
Link: https://doi.org/10.1371/..
 
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14

microRNAs and the evolution of complex multicellularity: id..:

Tarver, James E. ; Cormier, Alexandre ; Pinzón, Natalia...
Nucleic Acids Research.  43 (2015)  13 - p. 6384-6398 , 2015
Link: https://doi.org/10.1093/..
 
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15

Homozygous STIL Mutation Causes Holoprosencephaly and Micro..:

Mouden, Charlotte ; de Tayrac, Marie ; Dubourg, Christèle...
PLOS ONE.  10 (2015)  2 - p. e0117418 , 2015
Link: https://doi.org/10.1371/..
 
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