Micheline Misrahi

Prof.

Université de Paris Faculté de Santé

France

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About

Prof. Micheline Misrahi is a faculty member at Université Paris-Saclay Faculté de Médecine in France. Her research areas focus on reproductive health, particularly diminished ovarian reserve and primary ovarian insufficiency. She has recently published articles exploring the genetic landscape of ovarian insufficiency and the implications of various mutations in ovarian function.

Articles (12)

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2024

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2024

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2020

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2020

Collaborators (4)

Sophie Catteau-Jonard

Head of department

Université de Lille

FRANCE

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Sandrine Caburet

Assistant Professor, Genomics

Université Paris-Saclay

FRANCE

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Julien Dang

Assistant Professor

Hôpital Ambroise-Paré

FRANCE

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Anne HELBLING-LECLERC

Assistant professor

Université Paris-Saclay

FRANCE

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Micheline Misrahi

Research Interests

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Articles (12)

Biallelic Germline <i>BRCA1</i> Frameshift Mutations Associated with Isolated Diminished Ovarian Reserve

Genetic Landscape of a Cohort of 120 Patients with Diminished Ovarian Reserve: Correlation with Infertility

Pathological spectrum of hereditary transthyretin renal amyloidosis and clinicopathologic correlation: a French observational study

Genetics of primary ovarian insufficiency: a careful step-by-step approach based on solid foundations to bring new knowledge

A SPIDR homozygous nonsense pathogenic variant in isolated primary ovarian insufficiency with chromosomal instability

Discussion suite à la communication : « L’ovaire, un miroir de longévité ? Ou nouveaux liens entre gènes d’Insuffisance Ovarienne Primitive et de tumeurs/cancers »

L’ovaire, un miroir de longévité ? Ou nouveaux liens entre gènes d’insuffisance ovarienne primitive et de tumeurs/cancers

The Roles of Luteinizing Hormone, Follicle-Stimulating Hormone and Testosterone in Spermatogenesis and Folliculogenesis Revisited

Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency

Homozygous hypomorphic BRCA2 variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait

Should FANCL heterozygous pathogenic variants be considered as potentially causative of primary ovarian insufficiency?

A Novel Phenotype Combining Primary Ovarian Insufficiency Growth Retardation and Pilomatricomas With MCM8 Mutation

Collaborators (4)

Sophie Catteau-Jonard

Sandrine Caburet

Julien Dang

Anne HELBLING-LECLERC

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