Didier Lacombe

12PUBLICATIONS
83CO-AUTHORS
Gene mappingNeurology and neuromuscular diseasesCardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)
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Publications (12)

|Feb 24, 2026
Phenotypic description of a large French series of individuals with Potocki-Lupski syndrome.

Alicia Coudert, Pauline Le Tanno, William Dufour

|Apr 27, 2025
Neurofibromatosis-Noonan syndrome: a prospective monocentric study of 26 patients and literature review.

Didier Bessis, Dominique Vidaud, Pierre Meyer

|Oct 02, 2024
Classification of PTEN germline non-truncating variants: a new approach to interpretation.

Henri Margot, Natalie Jones, Thibaut Matis

|Aug 24, 2024
Splice site variants in the canonical donor site of MED13L exon 7 lead to intron retention in patients with MED13L syndrome.

Jade Fauqueux, Simon Boussion, Caroline Thuillier

|Apr 09, 2024
Investigations of an individual with a Marfanoid habitus, mild intellectual disability, and severe social anxiety identifies PCDHGA5 as a candidate neurodevelopmental disorder gene.

Henri Margot, Adrien Pizano, Anouck Amestoy

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