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Alexandre Reymond

17PUBLICATIONS

158CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Speciation and extinctionEpidemiology not elsewhere classified

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Publications (17)

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|Dec 12, 2024

Further delineation of the SCAF4-associated neurodevelopmental disorder.

Cosima M Schmid, Anne Gregor, Anna Ruiz

|Sep 10, 2024

Genetic modifiers and ascertainment drive variable expressivity of complex disorders.

Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina

|May 29, 2024

Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.

Sissy Bassani, Jacqueline Chrast, Giovanna Ambrosini

|Jan 31, 2024

Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.

Sissy Bassani, Jacqueline Chrast, Giovanna Ambrosini

|Jan 07, 2024

Rare copy-number variants as modulators of common disease susceptibility.

Chiara Auwerx, Maarja Jõeloo, Marie C Sadler

|May 24, 2023

Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.

Giuliana Giannuzzi, Nicolas Chatron, Katrin Mannik

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Frequent Collaborators

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Francesca Forzano

5 joint publications

Olga Antonova

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Angus Clarke

5 joint publications

Guido de Wert

5 joint publications

Yalda Jamshidi

5 joint publications

Vigdis Stefansdottir

5 joint publications

Carla van El

5 joint publications

Maurizio Genuardi

3 joint publications

Chiara Auwerx

2 joint publications

Francesca Mattioli

Frequent Collaborators

5 joint publications

Francesca Forzano

5 joint publications

Olga Antonova

5 joint publications

Angus Clarke

5 joint publications

Guido de Wert

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