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Isabelle Perthus

5PUBLICATIONS

45CO-AUTHORS

PharmacogenomicsEpigenetics (incl. genome methylation and epigenomics)Foetal development and medicineGene expression (incl. microarray and other genome-wide approaches)

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Publications (5)

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|Apr 30, 2026

The EUROmediCAT Network and Databases: A Resource for Pharmacovigilance in Pregnancy.

|Nov 24, 2025

Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network.

Jorieke E H Bergman, Annie Perraud, Ester Garne

|Feb 26, 2025

Antiretroviral drug exposure in pregnancy and risk of congenital anomalies: a European case/non-case malformed study.

Laura Saint-Lary, Anna-Belle Beau, Agnès Sommet

|Dec 09, 2023

Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination.

Carole Goumy, Zangbéwendé Guy Ouedraogo, Elodie Bellemonte

|Jan 21, 2022

Identification of the First Single <i>GSDME</i> Exon 8 Structural Variants Associated with Autosomal Dominant Hearing Loss.

Luke Mansard, Christel Vaché, Julie Bianchi

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Frequent Collaborators

3 joint publications

Anna Latos-Bielenska

3 joint publications

Anke Rissmann

3 joint publications

Ester Garne

3 joint publications

Florence Rouget

3 joint publications

Clara Cavero-Carbonell

2 joint publications

Christine Damase-Michel

2 joint publications

Joanna Sichitiu

2 joint publications

Helen Dolk

2 joint publications

David Tucker

2 joint publications

Maria Loane

Frequent Collaborators

3 joint publications

Anna Latos-Bielenska

3 joint publications

Anke Rissmann

3 joint publications

Ester Garne

3 joint publications

Florence Rouget

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