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)

|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 GSDME Exon 8 Structural Variants Associated with Autosomal Dominant Hearing Loss.

Luke Mansard, Christel Vaché, Julie Bianchi

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