H
Hélène Blanché
Researcher at Fondation Jean Dausset Centre d'Etude du Polymorphisme Humain
Publications - 18
Citations - 2537
Hélène Blanché is an academic researcher from Fondation Jean Dausset Centre d'Etude du Polymorphisme Humain. The author has contributed to research in topics: Longevity & Gene. The author has an hindex of 13, co-authored 18 publications receiving 2111 citations.
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Journal ArticleDOI
The complete genome sequence of a Neanderthal from the Altai Mountains
Kay Prüfer,Fernando Racimo,Nick Patterson,Flora Jay,Sriram Sankararaman,Susanna Sawyer,Anja Heinze,Gabriel Renaud,Peter H. Sudmant,Cesare de Filippo,Heng Li,Swapan Mallick,Michael Dannemann,Qiaomei Fu,Martin Kircher,Martin Kuhlwilm,Michael Lachmann,Matthias Meyer,Matthias Ongyerth,Michael Siebauer,Christoph Theunert,Arti Tandon,Priya Moorjani,Joseph K. Pickrell,James C. Mullikin,Samuel H. Vohr,Richard E. Green,Ines Hellmann,Philip L. F. Johnson,Hélène Blanché,Howard M. Cann,Jacob O. Kitzman,Jay Shendure,Evan E. Eichler,Ed S. Lein,Trygve E. Bakken,Liubov V. Golovanova,Vladimir B. Doronichev,Michael V. Shunkov,A.P. Derevianko,Bence Viola,Montgomery Slatkin,David Reich,Janet Kelso,Svante Pääbo +44 more
TL;DR: It is shown that interbreeding, albeit of low magnitude, occurred among many hominin groups in the Late Pleistocene and a definitive list of substitutions that became fixed in modern humans after their separation from the ancestors of Neanderthals and Denisovans is established.
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Variation in genomic landscape of clear cell renal cell carcinoma across Europe
Ghislaine Scelo,Yasser Riazalhosseini,Liliana Greger,Louis Letourneau,Mar Gonzàlez-Porta,Magdalena B. Wozniak,Mathieu Bourgey,Patricia Harnden,Lars Egevad,Sharon Jackson,Mehran Karimzadeh,Madeleine Arseneault,Pierre Lepage,Alexandre How-Kit,Antoine Daunay,Victor Renault,Hélène Blanché,Emmanuel Tubacher,Jeremy Sehmoun,Juris Viksna,Edgars Celms,Martins Opmanis,Andris Zarins,Naveen S. Vasudev,Morag Seywright,Behnoush Abedi-Ardekani,Christine Carreira,Peter Selby,Jon Cartledge,Graham Byrnes,Jiri Zavadil,Jing Su,Ivana Holcatova,Antonin Brisuda,David Zaridze,Anush Moukeria,Lenka Foretova,Marie Navratilova,Dana Mates,Viorel Jinga,Artem V. Artemov,Artem V. Nedoluzhko,Alexander Mazur,Sergey M. Rastorguev,Eugenia S. Boulygina,Simon Heath,Marta Gut,Marie-Therese Bihoreau,Doris Lechner,Mario Foglio,Ivo Gut,Konstantin G. Skryabin,Egor Prokhortchouk,Anne Cambon-Thomsen,Johan Rung,Guillaume Bourque,Paul Brennan,Jörg Tost,Rosamonde E. Banks,Alvis Brazma,G Mark Lathrop +60 more
TL;DR: The results show that the processes underlyingccRCC tumorigenesis may vary in different populations and suggest that AA may be an important ccRCC carcinogen in Romania, a finding with major public health implications.
Journal ArticleDOI
NF1 Molecular Characterization and Neurofibromatosis Type I Genotype–Phenotype Correlation: The French Experience
Audrey Sabbagh,Eric Pasmant,Apolline Imbard,Armelle Luscan,Magali Soares,Hélène Blanché,Ingrid Laurendeau,Salah Ferkal,Michel Vidaud,Stéphane Pinson,Christine Bellanné-Chantelot,Dominique Vidaud,Béatrice Parfait,Pierre Wolkenstein +13 more
TL;DR: An original NF1 investigation strategy is presented and a comprehensive mutation analysis of 565 unrelated patients from the NF‐France Network is reported, pointing out the need to perform an exhaustive NF1 screening in the case of molecular discordant‐related patients.
Journal ArticleDOI
Genome-wide association study identifies multiple risk loci for renal cell carcinoma.
Ghislaine Scelo,Mark P. Purdue,Kevin M. Brown,Mattias Johansson,Zhaoming Wang,Jeanette E. Eckel-Passow,Yuanqing Ye,Jonathan N. Hofmann,Jiyeon Choi,Matthieu Foll,Valerie Gaborieau,Mitchell J. Machiela,Leandro M. Colli,Peng Li,Joshua N. Sampson,Behnoush Abedi-Ardekani,Céline Besse,Hélène Blanché,Anne Boland,Laurie Burdette,Amelie Chabrier,Geoffroy Durand,Florence Le Calvez-Kelm,Egor Prokhortchouk,Nivonirina Robinot,Konstantin G. Skryabin,Magdalena B. Wozniak,Meredith Yeager,Gordana Basta-Jovanovic,Zoran Dzamic,Lenka Foretova,Ivana Holcatova,Vladimir Janout,Dana Mates,Anush Mukeriya,Stefan Rascu,David Zaridze,Vladimir Bencko,Cezary Cybulski,Eleonora Fabianova,Viorel Jinga,Jolanta Lissowska,Jan Lubinski,Marie Navratilova,Peter Rudnai,Neonila Szeszenia-Dabrowska,Simone Benhamou,Geraldine Cancel-Tassin,Olivier Cussenot,Laura Baglietto,Heiner Boeing,Kay-Tee Khaw,Elisabete Weiderpass,Börje Ljungberg,Raviprakash T. Sitaram,Fiona Bruinsma,Susan J. Jordan,Susan J. Jordan,Gianluca Severi,Ingrid Winship,Ingrid Winship,Kristian Hveem,Lars J. Vatten,Tony Fletcher,Kvetoslava Koppova,Susanna C. Larsson,Alicja Wolk,Rosamonde E. Banks,Peter Selby,Douglas F. Easton,Paul D.P. Pharoah,Gabriella Andreotti,Laura E. Beane Freeman,Stella Koutros,Demetrius Albanes,Satu Männistö,Stephanie J. Weinstein,Peter E. Clark,Todd L. Edwards,Loren Lipworth,Susan M. Gapstur,Victoria L. Stevens,Hallie Carol,Matthew L. Freedman,Mark Pomerantz,Eunyoung Cho,Peter Kraft,Mark A. Preston,Kathryn M. Wilson,J. Michael Gaziano,Howard D. Sesso,Howard D. Sesso,Amanda Black,Neal D. Freedman,Wen-Yi Huang,John Anema,Richard J. Kahnoski,Brian R. Lane,Brian R. Lane,Sabrina L. Noyes,David Petillo,Bin Tean Teh,Ulrike Peters,Emily White,Garnet L. Anderson,Lisa Johnson,Juhua Luo,Julie E. Buring,Julie E. Buring,I-Min Lee,I-Min Lee,Wong-Ho Chow,Lee E. Moore,Christopher G. Wood,Timothy Eisen,Marc Henrion,James Larkin,Poulami Barman,Bradley C. Leibovich,Toni K. Choueiri,G. Mark Lathrop,Nathaniel Rothman,Jean-François Deleuze,Jean-François Deleuze,James D. McKay,Alexander S. Parker,Xifeng Wu,Richard S. Houlston,Paul Brennan,Stephen J. Chanock +129 more
TL;DR: This paper conducted a meta-analysis of two new scans of 5,198 cases and 7,331 controls together with four existing scans, totalling 10,784 cases and 20,406 controls of European ancestry.
Journal ArticleDOI
New polymorphisms in the human poly(ADP-ribose) polymerase-1 coding sequence: lack of association with longevity or with increased cellular poly(ADP-ribosyl)ation capacity.
Florence Cottet,Hélène Blanché,Patrick Verasdonck,Isabelle Le Gall,Francois Schächter,Alexander Bürkle,Marie-Laure Muiras +6 more
TL;DR: The results strongly suggest that the longevity-related differences in the poly(ADP-ribosyl)ation capacity of human lymphoblastoid cell lines cannot be explained by genetic polymorphisms in the PARP-1 coding sequence and that other mechanisms have to be considered as potential regulators of specific poly( ADP- ribosyl]ation capacity.