Valerie Malan

12PUBLICATIONS
45CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Child language acquisitionGene mappingEpigenetics (incl. genome methylation and epigenomics)Non-Newtonian fluid flows (incl. rheology)
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Journal

Publications (12)

|Oct 08, 2025
ACTB deletions or single-nucleotide loss-of-function variants: expansion and further delineation of the phenotype and review of the literature.

Marion Lesieur-Sebellin, Kristen Wigby, Elise Schaefer

|Feb 13, 2025
Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech.

Clothilde Ormieres, Marion Lesieur-Sebellin, Karine Siquier-Pernet

|Mar 21, 2024
Clinical and molecular cytogenetic studies of five new patients with 20q11q12 deletion and review of the literature: Proposition of two critical regions.

Souad Bensaid, Malika Bendahmane, Sara Loddo

|Mar 14, 2023
Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome).

Cécile Courdier, John Boudjarane, Valérie Malan

|Dec 20, 2022
Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1.

Yosra Lajmi, Laurence Loeuillet, Giulia Petrilli

|Apr 07, 2022
16p13.11p11.2 triplication syndrome: a new recognizable genomic disorder characterized by optical genome mapping and whole genome sequencing.

Romain Nicolle, Karine Siquier-Pernet, Marlène Rio

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Frequent Collaborators

2 joint publications

François Vialard

2 joint publications

Vincent Cantagrel

2 joint publications

Marlène Rio

2 joint publications

Sarah Guterman