Valerie Chaudru

Valerie Chaudru

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Valerie Chaudru

Valerie Chaudru

Publications by authors named "Valerie Chaudru"

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17Publications

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A novel nonsense variant in SUPT20H gene associated with Rheumatoid Arthritis identified by Whole Exome Sequencing of multiplex families.

Authors:
Maëva Veyssiere Javier Perea Laetitia Michou Anne Boland Christophe Caloustian Robert Olaso Jean-François Deleuze François Cornelis Elisabeth Petit-Teixeira Valérie Chaudru

PLoS One 2019 7;14(3):e0213387. Epub 2019 Mar 7.

GenHotel-Univ Evry, University of Paris Saclay, Evry, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0213387PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405192PMC
March 2019

Investigation of candidate gene copy number identifies FCGR3B as a potential biomarker for rheumatoid arthritis.

Authors:
Mohamed Sahbi Ben Kilani François Cornélis Robert Olaso Valerie Chaudru Elisabeth Petit-Teixeira

Clin Exp Rheumatol 2019 Mar 7. Epub 2019 Mar 7.

GenHotel, Univ Evry, Université Paris-Saclay, Evry, France.

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March 2019

Characterization of copy number variants for CCL3L1 gene in rheumatoid arthritis for French trio families and Tunisian cases and controls.

Authors:
Mohamed Sahbi Ben Kilani Yosser Achour Javier Perea François Cornelis Thomas Bardin Valérie Chaudru Abdellatif Maalej Elisabeth Petit-Teixeira

Clin Rheumatol 2016 Aug 4;35(8):1917-1922. Epub 2016 Jan 4.

GenHotel-EA3886, Evry University, 2 rue Gaston Cremieux, 91057, Evry-cedex, France.

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http://dx.doi.org/10.1007/s10067-015-3156-yDOI Listing
August 2016

Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.

Authors:
Corine Bertolotto Fabienne Lesueur Sandy Giuliano Thomas Strub Mahaut de Lichy Karine Bille Philippe Dessen Benoit d'Hayer Hamida Mohamdi Audrey Remenieras Eve Maubec Arnaud de la Fouchardière Vincent Molinié Pierre Vabres Stéphane Dalle Nicolas Poulalhon Tanguy Martin-Denavit Luc Thomas Pascale Andry-Benzaquen Nicolas Dupin Françoise Boitier Annick Rossi Jean-Luc Perrot Bruno Labeille Caroline Robert Bernard Escudier Olivier Caron Laurence Brugières Simon Saule Betty Gardie Sophie Gad Stéphane Richard Jérôme Couturier Bin Tean Teh Paola Ghiorzo Lorenza Pastorino Susana Puig Celia Badenas Hakan Olsson Christian Ingvar Etienne Rouleau Rosette Lidereau Philippe Bahadoran Philippe Vielh Eve Corda Hélène Blanché Diana Zelenika Pilar Galan Valérie Chaudru Gilbert M Lenoir Mark Lathrop Irwin Davidson Marie-Françoise Avril Florence Demenais Robert Ballotti Brigitte Bressac-de Paillerets

Nature 2016 Mar 2;531(7592):126. Epub 2015 Dec 2.

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http://dx.doi.org/10.1038/nature16158DOI Listing
March 2016

Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families.

Authors:
Xueying Liang Ruth M Pfeiffer Wen-Qing Li Myriam Brossard Laura S Burke William Wheeler Donato Calista Maria Concetta Fargnoli Paola Ghiorzo Ketty Peris Giovanna Bianchi-Scarra Valerie Chaudru Diana Zelenika Dennis Maeder Laurie Burdette Meredith Yeager Stephen Chanock Maria Teresa Landi Florence Demenais Margaret A Tucker Alisa M Goldstein Xiaohong R Yang

J Invest Dermatol 2014 Feb 26;134(2):481-487. Epub 2013 Jul 26.

Division of Cancer Epidemiology and Genetics, NCI/NIH, Bethesda, Maryland, USA. Electronic address:

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http://dx.doi.org/10.1038/jid.2013.316DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873368PMC
February 2014

A variant in FTO shows association with melanoma risk not due to BMI.

Authors:
Mark M Iles Matthew H Law Simon N Stacey Jiali Han Shenying Fang Ruth Pfeiffer Mark Harland Stuart Macgregor John C Taylor Katja K Aben Lars A Akslen Marie-Françoise Avril Esther Azizi Bert Bakker Kristrun R Benediktsdottir Wilma Bergman Giovanna Bianchi Scarrà Kevin M Brown Donato Calista Valérie Chaudru Maria Concetta Fargnoli Anne E Cust Florence Demenais Anne C de Waal Tadeusz Dębniak David E Elder Eitan Friedman Pilar Galan Paola Ghiorzo Elizabeth M Gillanders Alisa M Goldstein Nelleke A Gruis Johan Hansson Per Helsing Marko Hočevar Veronica Höiom John L Hopper Christian Ingvar Marjolein Janssen Mark A Jenkins Peter A Kanetsky Lambertus A Kiemeney Julie Lang G Mark Lathrop Sancy Leachman Jeffrey E Lee Jan Lubiński Rona M Mackie Graham J Mann Nicholas G Martin Jose I Mayordomo Anders Molven Suzanne Mulder Eduardo Nagore Srdjan Novaković Ichiro Okamoto Jon H Olafsson Håkan Olsson Hubert Pehamberger Ketty Peris Maria Pilar Grasa Dolores Planelles Susana Puig Joan Anton Puig-Butille Juliette Randerson-Moor Celia Requena Licia Rivoltini Monica Rodolfo Mario Santinami Bardur Sigurgeirsson Helen Snowden Fengju Song Patrick Sulem Kristin Thorisdottir Rainer Tuominen Patricia Van Belle Nienke van der Stoep Michelle M van Rossum Qingyi Wei Judith Wendt Diana Zelenika Mingfeng Zhang Maria Teresa Landi Gudmar Thorleifsson D Timothy Bishop Christopher I Amos Nicholas K Hayward Kari Stefansson Julia A Newton Bishop Jennifer H Barrett

Nat Genet 2013 Apr 3;45(4):428-32, 432e1. Epub 2013 Mar 3.

Section of Epidemiology and Biostatistics, Leeds Institute of Molecular Medicine, Leeds Cancer Research UK Centre, St. James's University Hospital, Leeds, UK.

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https://genepi.qimr.edu.au/contents/p/staff/Iles_etal_Nature
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http://www.nature.com/doifinder/10.1038/ng.2571
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http://dx.doi.org/10.1038/ng.2571DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640814PMC
April 2013

Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family.

Authors:
Eve Maubec Valérie Chaudru Hamida Mohamdi Christophe Blondel Patricia Margaritte-Jeannin Sébastien Forget Eve Corda Françoise Boitier Stéphane Dalle Pierre Vabres Jean-Luc Perrot Dominique Stoppa Lyonnet Hélène Zattara Sandrine Mansard Florent Grange Marie-Thérèse Leccia Lynda Vincent-Fetita Ludovic Martin Béatrice Crickx Pascal Joly Luc Thomas Brigitte Bressac-de Paillerets Marie-Françoise Avril Florence Demenais

J Am Acad Dermatol 2012 Dec 26;67(6):1257-64. Epub 2012 Jul 26.

INSERM (Institut National de Santé et de Recherche Médicale), Genetic Variation and Human Diseases Unit (U946), Paris, France.

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http://linkinghub.elsevier.com/retrieve/pii/S019096221200543
Publisher Site
http://dx.doi.org/10.1016/j.jaad.2012.05.014DOI Listing
December 2012

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.

Authors:
Corine Bertolotto Fabienne Lesueur Sandy Giuliano Thomas Strub Mahaut de Lichy Karine Bille Philippe Dessen Benoit d'Hayer Hamida Mohamdi Audrey Remenieras Eve Maubec Arnaud de la Fouchardière Vincent Molinié Pierre Vabres Stéphane Dalle Nicolas Poulalhon Tanguy Martin-Denavit Luc Thomas Pascale Andry-Benzaquen Nicolas Dupin Françoise Boitier Annick Rossi Jean-Luc Perrot Bruno Labeille Caroline Robert Bernard Escudier Olivier Caron Laurence Brugières Simon Saule Betty Gardie Sophie Gad Stéphane Richard Jérôme Couturier Bin Tean Teh Paola Ghiorzo Lorenza Pastorino Susana Puig Celia Badenas Hakan Olsson Christian Ingvar Etienne Rouleau Rosette Lidereau Philippe Bahadoran Philippe Vielh Eve Corda Hélène Blanché Diana Zelenika Pilar Galan François Aubin Bertrand Bachollet Céline Becuwe Pascaline Berthet Yves Jean Bignon Valérie Bonadona Jean-Louis Bonafe Marie-Noëlle Bonnet-Dupeyron Fréderic Cambazard Jacqueline Chevrant-Breton Isabelle Coupier Sophie Dalac Liliane Demange Michel d'Incan Catherine Dugast Laurence Faivre Lynda Vincent-Fétita Marion Gauthier-Villars Brigitte Gilbert Florent Grange Jean-Jacques Grob Philippe Humbert Nicolas Janin Pascal Joly Delphine Kerob Christine Lasset Dominique Leroux Julien Levang Jean-Marc Limacher Cristina Livideanu Michel Longy Alain Lortholary Dominique Stoppa-Lyonnet Sandrine Mansard Ludovic Mansuy Karine Marrou Christine Matéus Christine Maugard Nicolas Meyer Catherine Nogues Pierre Souteyrand Laurence Venat-Bouvet Hélène Zattara Valérie Chaudru Gilbert M Lenoir Mark Lathrop Irwin Davidson Marie-Françoise Avril Florence Demenais Robert Ballotti Brigitte Bressac-de Paillerets

Nature 2011 Oct 19;480(7375):94-8. Epub 2011 Oct 19.

1] INSERM, U895 (équipe 1), Equipe labélisée Ligue Contre le Cancer, C3M, 06204 Nice, France [2] Université of Nice Sophia-Antipolis, UFR Médecine, 06204 Nice, France [3] Centre Hospitalier Universitaire de Nice, Service de Dermatologie, 06204 Nice, France [4].

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http://dx.doi.org/10.1038/nature10539DOI Listing
October 2011

Characteristics of the coexistence of melanoma and renal cell carcinoma.

Authors:
Eve Maubec Valérie Chaudru Hamida Mohamdi Florent Grange Jean-Jacques Patard Stéphane Dalle Béatrice Crickx Brigitte Bressac-de Paillerets Florence Demenais Marie-Françoise Avril

Cancer 2010 Dec;116(24):5716-24

National Institute of Health and Medical Research, Paris, France.

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http://dx.doi.org/10.1002/cncr.25562DOI Listing
December 2010

Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes.

Authors:
Valérie Chaudru M T Lo F Lesueur C Marian H Mohamdi K Laud M Barrois A Chompret M F Avril F Demenais B Bressac-de Paillerets

Fam Cancer 2009 31;8(4):371-7. Epub 2009 May 31.

INSERM, U946, Fondation Jean Dausset/CEPH, 75010 Paris, France.

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http://dx.doi.org/10.1007/s10689-009-9249-5DOI Listing
January 2010

MC1R variant alleles and malignant melanoma risk in Israel.

Authors:
Gilli Galore-Haskel Esther Azizi Hamida Mohamdi Alon Scope Valérie Chaudru Yael Laitman Frida Barak Felix Pavlotsky Florence Demenais Eitan Friedman

Eur J Cancer 2009 Jul 5;45(11):2015-22. Epub 2009 Mar 5.

The Susanne Levy Gertner Oncogenetic Unit, The Danek Gertner Institute of Human Genetics, Chaim Sheba Medical Center, Tel-Hashomer 52621, Israel.

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http://dx.doi.org/10.1016/j.ejca.2009.02.001DOI Listing
July 2009

Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries.

Authors:
Alisa M Goldstein Valerie Chaudru Paola Ghiorzo Celia Badenas Josep Malvehy Lorenza Pastorino Karine Laud Benjamin Hulley Marie-Francoise Avril Joan A Puig-Butille Annie Miniere Rosa Marti Agnes Chompret Francisco Cuellar Isabel Kolm Montserrat Mila Margaret A Tucker Florence Demenais Giovanna Bianchi-Scarra Susana Puig Brigitte Bressac de-Paillerets

Int J Cancer 2007 Aug;121(4):825-31

Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1002/ijc.22712DOI Listing
August 2007

Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.

Authors:
Alisa M Goldstein May Chan Mark Harland Nicholas K Hayward Florence Demenais D Timothy Bishop Esther Azizi Wilma Bergman Giovanna Bianchi-Scarra William Bruno Donato Calista Lisa A Cannon Albright Valerie Chaudru Agnes Chompret Francisco Cuellar David E Elder Paola Ghiorzo Elizabeth M Gillanders Nelleke A Gruis Johan Hansson David Hogg Elizabeth A Holland Peter A Kanetsky Richard F Kefford Maria Teresa Landi Julie Lang Sancy A Leachman Rona M MacKie Veronica Magnusson Graham J Mann Julia Newton Bishop Jane M Palmer Susana Puig Joan A Puig-Butille Mitchell Stark Hensin Tsao Margaret A Tucker Linda Whitaker Emanuel Yakobson

J Med Genet 2007 Feb 11;44(2):99-106. Epub 2006 Aug 11.

Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Bethesda, Maryland 20892-7236, USA.

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http://dx.doi.org/10.1136/jmg.2006.043802DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2598064PMC
February 2007

Melanocortin-1 receptor (MC1R) gene variants and dysplastic nevi modify penetrance of CDKN2A mutations in French melanoma-prone pedigrees.

Authors:
Valérie Chaudru Karine Laud Marie-Françoise Avril Annie Minière Agnès Chompret Brigitte Bressac-de Paillerets Florence Demenais

Cancer Epidemiol Biomarkers Prev 2005 Oct;14(10):2384-90

Institut National de la Sante et de la Recherche Medicale, Université d'Evry, EMI 0006, Tour Evry 2, 523 Place des Terrasses de l'Agora, 91034 Evry, France.

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http://dx.doi.org/10.1158/1055-9965.EPI-04-0777DOI Listing
October 2005

Familial correlations and inter-relationships of four asthma-associated quantitative phenotypes in 320 French EGEA families ascertained through asthmatic probands.

Authors:
Emmanuelle Bouzigon Valérie Chaudru Anne-Sophie Carpentier Marie-Hélène Dizier Marie-Pierre Oryszczyn Jean Maccario Francine Kauffmann Florence Demenais

Eur J Hum Genet 2004 Nov;12(11):955-63

INSERM-Université d'Evry EMI0006, Evry, France.

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http://dx.doi.org/10.1038/sj.ejhg.5201241DOI Listing
November 2004

Influence of genes, nevi, and sun sensitivity on melanoma risk in a family sample unselected by family history and in melanoma-prone families.

Authors:
Valérie Chaudru Agnès Chompret Brigitte Bressac-de Paillerets Alain Spatz Marie-Françoise Avril Florence Demenais

J Natl Cancer Inst 2004 May;96(10):785-95

Institut National de la Santé et Recherche Médicale et Université d'Evry, Evry, France.

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http://dx.doi.org/10.1093/jnci/djh136DOI Listing
May 2004

Interactions between genetic and reproductive factors in breast cancer risk in a population-based sample of African-American families.

Authors:
Valérie Chaudru Amelia Laing Georgia M Dunston Lucile L Adams-Campbell Rosemary Williams John J Lynch LaSalle D Leffall Robert L DeWitty Barry L Gause George E Bonney Florence Demenais

Genet Epidemiol 2002 Apr;22(4):285-97

INSERM EMI 00-06, INSERM-Université d'Evry, Evry, France.

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http://dx.doi.org/10.1002/gepi.0171DOI Listing
April 2002