Marie Bidart

Grenoble, France

Last Updated: 09/26/2026

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Found 38 publications

Biallelic Truncating Variant in LRGUK Is Associated With Severe Multiple Morphological Abnormalities of the Sperm Flagella and Sperm Nuclear Defects in Humans.

Biallelic Truncating Variant in LRGUK Is Associated With Severe Multiple Morphological Abnormalities of the Sperm Flagella and Sperm Nuclear Defects in Humans.

Journal: Clinical genetics

Published: May 15, 2026

Skin transient receptor potential channels expression and microvascular reactivity to cooling in primary and secondary Raynaud's phenomenon.

Skin transient receptor potential channels expression and microvascular reactivity to cooling in primary and secondary Raynaud's phenomenon.

Journal: Physiological reports

Published: February 25, 2025

BRCA1 promoter methylation predicts PARPi response in ovarian cancer: insights from the KOMET study.

BRCA1 promoter methylation predicts PARPi response in ovarian cancer: insights from the KOMET study.

Journal: Clinical epigenetics

Published: November 25, 2024

Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencing.

Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencing.

Journal: Familial cancer

Published: November 10, 2024

Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratories.

Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratories.

Journal: International journal of cancer

Published: September 26, 2024

BRCA1 Intragenic Duplication Combined with a Likely Pathogenic TP53 Variant in a Patient with Triple-Negative Breast Cancer: Clinical Risk and Management.

BRCA1 Intragenic Duplication Combined with a Likely Pathogenic TP53 Variant in a Patient with Triple-Negative Breast Cancer: Clinical Risk and Management.

Journal: International journal of molecular sciences

Published: April 17, 2024

Germline POT1 mutation and neuroblastoma: A mere coincidence or true association.

Germline POT1 mutation and neuroblastoma: A mere coincidence or true association.

Journal: Pediatric blood & cancer

Published: April 17, 2024

Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants.

Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants.

Journal: Andrology

Published: February 21, 2024

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function.

Novel axonemal protein ZMYND12 interacts with TTC29 and DNAH1, and is required for male fertility and flagellum function.

Journal: eLife

Published: November 07, 2023

New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella.

New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella.

Journal: International journal of molecular sciences

Published: December 23, 2022

Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry.

Sperm Meiotic Segregation Analysis of Reciprocal Translocations Carriers: We Have Bigger FISH to Fry.

Journal: International journal of molecular sciences

Published: December 20, 2022

OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum.

OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum.

Journal: Journal of medical genetics

Published: July 04, 2022

Showing 1-12 of 38

Last Updated: 09/26/2026