Eric Pasmant

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Head

Institut Curie

France

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About

Eric Pasmant is the Head at Institut Curie in France. His research areas include neurofibromatosis type 1, genetic predispositions to various cancers, and advancements in genomic medicine integration into national healthcare. Recent publications highlight his work on genotype-phenotype correlations, germline epimutation detection, and genetic alterations in adrenal hyperplasia.

Recent Grants

Grant: Close

European Network for improved molecular diagnostics of the Neurofibromatoses-schwannomatoses and related disorders – EURONET- NF

Open Date: 2023-05-20

Close Date: 2026-05-19

Articles (10)

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2025

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2024

Collaborators (12)

Peter Kamenický

Université Paris-Saclay

FRANCE

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Anne Jouinot

Institut Cochin

FRANCE

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Paul Kuentz

Professeur des Universités-Praticien Hospitalier

Centre Hospitalier Universitaire Vaudois

FRANCE

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Richard Redon

INSERM

FRANCE

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Louise-Marie CHEVALIER

Institut de Cancérologie de l'Ouest

FRANCE

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Caroline Rooryck

University of Bordeaux

FRANCE

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Djihad Hadjadj

Assistant professeur

Institut Cochin

FRANCE

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Pierre Wolkenstein

Université Paris-Est Créteil Val de Marne

FRANCE

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Sarah Baer

Chief of resident

Hôpitaux universitaires de Strasbourg

FRANCE

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Pierre Vande Perre

Institut Claudius Regaud

FRANCE

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Hélène Cavé

PUPH, Head of the molecular Genetics unit

Hôpital Robert-Debré

FRANCE

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Mathilde Sibony

Université Paris Descartes

FRANCE

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Eric Pasmant

Research Interests

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About

Recent Grants

Articles (10)

Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with <i>NF1</i> point variants.

Methylation-sensitive high-resolution melting technology is a simple and sensitive method to detect germline epimutation of the MLH1 gene promoter.

High prevalence of constitutional BRCA1 epimutation in patients with early-onset triple-negative breast cancer.

Lower Prevalence of Overweight and Obesity in Adults with Neurofibromatosis

Predisposition to prostate cancer and clinical implications in a real-life cohort.

KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlation.

The mutational landscape of ARMC5 in Primary Bilateral Macronodular Adrenal Hyperplasia: an update.

<i>PFMG2025</i>-integrating genomic medicine into the national healthcare system in France.

PDE11A is a phenotype modulator of Primary Bilateral Macronodular Adrenal Hyperplasia: results of a 334 patients' series.

Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaics.

Collaborators (12)

Peter Kamenický

Anne Jouinot

Paul Kuentz

Richard Redon

Louise-Marie CHEVALIER

Caroline Rooryck

Djihad Hadjadj

Pierre Wolkenstein

Sarah Baer

Pierre Vande Perre

Hélène Cavé

Mathilde Sibony

Make your next move.

Eric Pasmant

Research Interests

Explore related searches

Contact this professor

About

Recent Grants

Articles (10)

Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with &lt;i&gt;NF1&lt;/i&gt; point variants.

Methylation-sensitive high-resolution melting technology is a simple and sensitive method to detect germline epimutation of the MLH1 gene promoter.

High prevalence of constitutional BRCA1 epimutation in patients with early-onset triple-negative breast cancer.

Lower Prevalence of Overweight and Obesity in Adults with Neurofibromatosis

Predisposition to prostate cancer and clinical implications in a real-life cohort.

KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlation.

The mutational landscape of ARMC5 in Primary Bilateral Macronodular Adrenal Hyperplasia: an update.

&lt;i&gt;PFMG2025&lt;/i&gt;-integrating genomic medicine into the national healthcare system in France.

PDE11A is a phenotype modulator of Primary Bilateral Macronodular Adrenal Hyperplasia: results of a 334 patients' series.

Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaics.

Collaborators (12)

Peter Kamenický

Anne Jouinot

Paul Kuentz

Richard Redon

Louise-Marie CHEVALIER

Caroline Rooryck

Djihad Hadjadj

Pierre Wolkenstein

Sarah Baer

Pierre Vande Perre

Hélène Cavé

Mathilde Sibony

Make your next move.

Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with <i>NF1</i> point variants.

<i>PFMG2025</i>-integrating genomic medicine into the national healthcare system in France.