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Simon Verdez

5PUBLICATIONS

27CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Cancer geneticsGene expression (incl. microarray and other genome-wide approaches)Major global burdens of disease

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Publications (5)

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|Nov 30, 2022

A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort.

Philippine Garret, Martin Chevarin, Antonio Vitobello

|Aug 31, 2022

Detection of relevant pharmacogenetic information through exome sequencing in oncology.

Simon Verdez, Juliette Albuisson, Yannis Duffourd

|Aug 23, 2022

Detection of the novel allele, HLA-A*32:165, in a French individual by next-generation sequencing.

Simon Verdez, Martin Chevarin, Victor Couturier

|May 19, 2022

Exome sequencing allows detection of relevant pharmacogenetic variants in epileptic patients.

Simon Verdez, Quentin Thomas, Philippine Garret

|Feb 10, 2022

Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array-CGH.

Emilie Tisserant, Antonio Vitobello, Davide Callegarin

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Frequent Collaborators

3 joint publications

Antonio Vitobello

3 joint publications

Christophe Philippe

3 joint publications

Frédéric Tran-Mau-Them

2 joint publications

Ange-Line Bruel

2 joint publications

Christel Thauvin-Robinet

1 joint publications

Ludwig Serge Aho Glele

1 joint publications

Anne-Sophie Denommé-Pichon

1 joint publications

Eleonore Viora-Dupont

1 joint publications

Nathalie Marle

1 joint publications

Sébastien Moutton

Frequent Collaborators

3 joint publications

Antonio Vitobello

3 joint publications

Christophe Philippe

3 joint publications

Frédéric Tran-Mau-Them

2 joint publications

Ange-Line Bruel

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