Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

View all journals
Search
Log in

nature
search

Search

Advanced search

Filter By:

Journal Check one or more journals to show results from those journals only.

European Journal of Human Genetics (6)
Journal of Human Genetics (1)
Leukemia (1)
Oncogene (1)
British Journal of Cancer (1)

Choose more journals

Article type Check one or more article types to show results from those article types only.

Research (13)
Comments & Opinion (1)

Subject Check one or more subjects to show results from those subjects only.

Cancer
Cell biology
Diseases
Genetics
Health care
Medical research
Molecular biology
Molecular medicine
Oncology

Date Choose a date option to show results from those dates only.

Today
Last 7 days
Last 30 days
Last 12 months
Last 2 years
Last 5 years

Custom date range

Clear all filters

Sort by:

Relevance

Date published (new to old)

Date published (old to new)

Showing 1–14 of 14 results

Advanced filters: Author: Eric Pasmant Clear advanced filters

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

Laurence Pacot
Dominique Vidaud
Eric Pasmant
ResearchOpen Access08 Sept 2024
npj Genomic Medicine

Volume: 9, P: 1-7
SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

E Pasmant
B Gilbert-Dussardier
P Ballerini
Research27 Jan 2014
Oncogene

Volume: 34, P: 631-638
PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies

SUZ12, a component of the PRC2 complex, can also function as a tumour suppressor in certain tumours of the nervous system and melanomas.

Thomas De Raedt
Eline Beert
Karen Cichowski
Research13 Aug 2014
Nature

Volume: 514, P: 247-251
Predisposition to prostate cancer and clinical implications in a real-life cohort

Julie Chartier
Albain Chansavang
Camille Tlemsani
Research06 May 2025
European Journal of Human Genetics

P: 1-10
BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation

In Drosophila, the Calypso–ASX complex catalyzes H2A deubiquitination and aids Polycomb in transcriptional silencing. Here the authors show that the orthologous complex, BAP1.com, promotes gene activation by counteracting PRC1-mediated gene silencing.

Antoine Campagne
Ming-Kang Lee
Raphaël Margueron
ResearchOpen Access21 Jan 2019
Nature Communications

Volume: 10, P: 1-15
Characterization of a 7.6-Mb germline deletion encompassing the NF1 locus and about a hundred genes in an NF1 contiguous gene syndrome patient

Eric Pasmant
Aurélie de Saint-Trivier
Ivan Bièche
Research23 Jul 2008
European Journal of Human Genetics

Volume: 16, P: 1459-1466
First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis

Eric Pasmant
Philippe Goussard
Béatrice Parfait
Research12 Oct 2011
European Journal of Human Genetics

Volume: 20, P: 277-282
Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?

Eric Pasmant
Béatrice Parfait
Dominique Vidaud
Research30 Jul 2014
European Journal of Human Genetics

Volume: 23, P: 596-601
NF1 single and multi-exons copy number variations in neurofibromatosis type 1

Apolline Imbard
Eric Pasmant
Béatrice Parfait
Research29 Jan 2015
Journal of Human Genetics

Volume: 60, P: 221-224
NF1 mutations as biomarker of response to immune checkpoint blockades for lung adenocarcinoma patients

Jean-Stéphane Giraud
Anne Jouinot
Camille Tlemsani
ResearchOpen Access10 Feb 2024
npj Precision Oncology

Volume: 8, P: 1-6
RAS activation induces synthetic lethality of MEK inhibition with mitochondrial oxidative metabolism in acute myeloid leukemia

Justine Decroocq
Rudy Birsen
Jerome Tamburini
ResearchOpen Access30 Mar 2022
Leukemia

Volume: 36, P: 1237-1252
Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1

Laurence Pacot
Albain Chansavang
Eric Pasmant
Comments & Opinion03 Feb 2023
European Journal of Human Genetics

Volume: 31, P: 380-382
Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal study

Claire Forde
Emma Burkitt-Wright
Meena Upadhyaya
ResearchOpen Access13 Dec 2021
European Journal of Human Genetics

Volume: 30, P: 291-297
Prognostic value of a newly identified MALAT1 alternatively spliced transcript in breast cancer

Didier Meseure
Sophie Vacher
Ivan Bieche
ResearchOpen Access12 May 2016
British Journal of Cancer

Volume: 114, P: 1395-1404

Search

Search articles by subject, keyword or author

Show results from

Advanced search

Quick links

Explore articles by subject
Find a job
Guide to authors
Editorial policies

Nature.com

nature.com sitemap

About Nature Portfolio

About us
Press releases
Press office
Contact us

Discover content

Journals A-Z
Articles by subject
protocols.io
Nature Index

Publishing policies

Nature portfolio policies
Open access

Author & Researcher services

Reprints & permissions
Research data
Language editing
Scientific editing
Nature Masterclasses
Research Solutions

Libraries & institutions

Librarian service & tools
Librarian portal
Open research
Recommend to library

Advertising & partnerships

Advertising
Partnerships & Services
Media kits
Branded content

Professional development

Nature Careers
Nature Conferences

Regional websites

Nature Africa
Nature China
Nature India
Nature Italy
Nature Japan
Nature Middle East

Privacy Policy
Use of cookies
Legal notice
Accessibility statement
Terms & Conditions
Your US state privacy rights

Search

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

SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies

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

BAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation

Characterization of a 7.6-Mb germline deletion encompassing the NF1 locus and about a hundred genes in an NF1 contiguous gene syndrome patient

First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis

Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?

NF1 single and multi-exons copy number variations in neurofibromatosis type 1

NF1 mutations as biomarker of response to immune checkpoint blockades for lung adenocarcinoma patients

RAS activation induces synthetic lethality of MEK inhibition with mitochondrial oxidative metabolism in acute myeloid leukemia

Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1

Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal study

Prognostic value of a newly identified MALAT1 alternatively spliced transcript in breast cancer

Search

Quick links