Claire Redin

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Distributed under Creative Commons Cc-by 4.0 Varank: a Simple and Powerful Tool for Ranking Genetic Variants

Véronique Geoffroy, Cécile Pizot, Claire Redin, 2022 .

[Precision medicine : at the crossroad of molecular biology, information sciences and humanities].

Jean Louis Raisaro, Claire Redin, Jacques Fellay, 2020, Revue medicale suisse.

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

Véronique Geoffroy, Claire Redin, Corinne Stoetzel, 2012, Journal of Medical Genetics.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Edwin Cuppen, Claire Redin, Ryan L. Collins, 2016, Nature Genetics.

A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

Jacques Fellay, Aurora Pujol, Claire Redin, 2020, Cell.

20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

Claire Redin, Jean Muller, Laurence Faivre, 2013, European Journal of Human Genetics.

A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila, and Humans

Claire Redin, Steven P. Gygi, Jared Rutter, 2012, Science.

Herzig Pyruvate Carrier Identification and Functional Expression of the Mitochondrial

Claire Redin, Steven P. Gygi, Noah Dephoure, 2012 .

Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing

Véronique Geoffroy, Claire Redin, Jean Muller, 2014, Journal of Medical Genetics.

XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.

Claire Redin, Jean-Louis Mandel, J. Mandel, 2013, American journal of human genetics.