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Amendments and Corrections |
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
- Mark K. Bakker
- , Rick A. A. van der Spek
- , Wouter van Rheenen
- , Sandrine Morel
- , Romain Bourcier
- , Isabel C. Hostettler
- , Varinder S. Alg
- , Kristel R. van Eijk
- , Masaru Koido
- , Masato Akiyama
- , Chikashi Terao
- , Koichi Matsuda
- , Robin G. Walters
- , Kuang Lin
- , Liming Li
- , Iona Y. Millwood
- , Zhengming Chen
- , Guy A. Rouleau
- , Sirui Zhou
- , Kristiina Rannikmäe
- , Cathie L. M. Sudlow
- , Henry Houlden
- , Leonard H. van den Berg
- , Christian Dina
- , Olivier Naggara
- , Jean-Christophe Gentric
- , Eimad Shotar
- , François Eugène
- , Hubert Desal
- , Bendik S. Winsvold
- , Sigrid Børte
- , Marianne Bakke Johnsen
- , Ben M. Brumpton
- , Marie Søfteland Sandvei
- , Cristen J. Willer
- , Kristian Hveem
- , John-Anker Zwart
- , W. M. Monique Verschuren
- , Christoph M. Friedrich
- , Sven Hirsch
- , Sabine Schilling
- , Jérôme Dauvillier
- , Olivier Martin
- , Zheng Bian
- , Junshi Chen
- , Yiping Chen
- , Robert Clarke
- , Rory Collins
- , Yu Guo
- , Xiao Han
- , Michael Hill
- , Depei Liu
- , Jun Lv
- , Iona Millwood
- , Richard Peto
- , Sam Sansome
- , Robin Walters
- , Xiaoming Yang
- , Canqing Yu
- , Stephen Bonner
- , Daniel Walsh
- , Diederik Bulters
- , Neil Kitchen
- , Martin Brown
- , Joan Grieve
- , Martin Dichgans
- , Gregory T. Jones
- , Matthew J. Bown
- , Nerissa U. Ko
- , Helen Kim
- , Jonathan R. I. Coleman
- , Gerome Breen
- , Jonathan G. Zaroff
- , Catharina J. M. Klijn
- , Rainer Malik
- , Martin Dichgans
- , Muralidharan Sargurupremraj
- , Turgut Tatlisumak
- , Philippe Amouyel
- , Stéphanie Debette
- , Gabriel J. E. Rinkel
- , Bradford B. Worrall
- , Joanna Pera
- , Agnieszka Slowik
- , Emília I. Gaál-Paavola
- , Mika Niemelä
- , Juha E. Jääskeläinen
- , Mikael von Und Zu Fraunberg
- , Antti Lindgren
- , Joseph P. Broderick
- , David J. Werring
- , Daniel Woo
- , Richard Redon
- , Philippe Bijlenga
- , Yoichiro Kamatani
- , Jan H. Veldink
- & Ynte M. Ruigrok
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Research |
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
- Mark K. Bakker
- , Rick A. A. van der Spek
- , Wouter van Rheenen
- , Sandrine Morel
- , Romain Bourcier
- , Isabel C. Hostettler
- , Varinder S. Alg
- , Kristel R. van Eijk
- , Masaru Koido
- , Masato Akiyama
- , Chikashi Terao
- , Koichi Matsuda
- , Robin G. Walters
- , Kuang Lin
- , Liming Li
- , Iona Y. Millwood
- , Zhengming Chen
- , Guy A. Rouleau
- , Sirui Zhou
- , Kristiina Rannikmäe
- , Cathie L. M. Sudlow
- , Henry Houlden
- , Leonard H. van den Berg
- , Christian Dina
- , Olivier Naggara
- , Jean-Christophe Gentric
- , Eimad Shotar
- , François Eugène
- , Hubert Desal
- , Bendik S. Winsvold
- , Sigrid Børte
- , Marianne Bakke Johnsen
- , Ben M. Brumpton
- , Marie Søfteland Sandvei
- , Cristen J. Willer
- , Kristian Hveem
- , John-Anker Zwart
- , W. M. Monique Verschuren
- , Christoph M. Friedrich
- , Sven Hirsch
- , Sabine Schilling
- , Jérôme Dauvillier
- , Olivier Martin
- , Zheng Bian
- , Junshi Chen
- , Yiping Chen
- , Robert Clarke
- , Rory Collins
- , Yu Guo
- , Xiao Han
- , Michael Hill
- , Depei Liu
- , Jun Lv
- , Iona Millwood
- , Richard Peto
- , Sam Sansome
- , Robin Walters
- , Xiaoming Yang
- , Canqing Yu
- , Stephen Bonner
- , Daniel Walsh
- , Diederik Bulters
- , Neil Kitchen
- , Martin Brown
- , Joan Grieve
- , Martin Dichgans
- , Gregory T. Jones
- , Matthew J. Bown
- , Nerissa U. Ko
- , Helen Kim
- , Jonathan R. I. Coleman
- , Gerome Breen
- , Jonathan G. Zaroff
- , Catharina J. M. Klijn
- , Rainer Malik
- , Martin Dichgans
- , Muralidharan Sargurupremraj
- , Turgut Tatlisumak
- , Philippe Amouyel
- , Stéphanie Debette
- , Gabriel J. E. Rinkel
- , Bradford B. Worrall
- , Joanna Pera
- , Agnieszka Slowik
- , Emília I. Gaál-Paavola
- , Mika Niemelä
- , Juha E. Jääskeläinen
- , Mikael von Und Zu Fraunberg
- , Antti Lindgren
- , Joseph P. Broderick
- , David J. Werring
- , Daniel Woo
- , Richard Redon
- , Philippe Bijlenga
- , Yoichiro Kamatani
- , Jan H. Veldink
- & Ynte M. Ruigrok
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Research | | Open
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
- Roddy Walsh
- , Najim Lahrouchi
- , Rafik Tadros
- , Florence Kyndt
- , Charlotte Glinge
- , Pieter G. Postema
- , Ahmad S. Amin
- , Eline A. Nannenberg
- , James S. Ware
- , Nicola Whiffin
- , Francesco Mazzarotto
- , Doris Škorić-Milosavljević
- , Christian Krijger
- , Elena Arbelo
- , Dominique Babuty
- , Hector Barajas-Martinez
- , Britt M. Beckmann
- , Stéphane Bézieau
- , J. Martijn Bos
- , Jeroen Breckpot
- , Oscar Campuzano
- , Silvia Castelletti
- , Candan Celen
- , Sebastian Clauss
- , Anniek Corveleyn
- , Lia Crotti
- , Federica Dagradi
- , Carlo de Asmundis
- , Isabelle Denjoy
- , Sven Dittmann
- , Patrick T. Ellinor
- , Cristina Gil Ortuño
- , Carla Giustetto
- , Jean-Baptiste Gourraud
- , Daisuke Hazeki
- , Minoru Horie
- , Taisuke Ishikawa
- , Hideki Itoh
- , Yoshiaki Kaneko
- , Jørgen K. Kanters
- , Hiroki Kimoto
- , Maria-Christina Kotta
- , Ingrid P. C. Krapels
- , Masahiko Kurabayashi
- , Julieta Lazarte
- , Antoine Leenhardt
- , Bart L. Loeys
- , Catarina Lundin
- , Takeru Makiyama
- , Jacques Mansourati
- , Raphaël P. Martins
- , Andrea Mazzanti
- , Stellan Mörner
- , Carlo Napolitano
- , Kimie Ohkubo
- , Michael Papadakis
- , Boris Rudic
- , Maria Sabater Molina
- , Frédéric Sacher
- , Hatice Sahin
- , Georgia Sarquella-Brugada
- , Regina Sebastiano
- , Sanjay Sharma
- , Mary N. Sheppard
- , Keiko Shimamoto
- , M. Benjamin Shoemaker
- , Birgit Stallmeyer
- , Johannes Steinfurt
- , Yuji Tanaka
- , David J. Tester
- , Keisuke Usuda
- , Paul A. van der Zwaag
- , Sonia Van Dooren
- , Lut Van Laer
- , Annika Winbo
- , Bo G. Winkel
- , Kenichiro Yamagata
- , Sven Zumhagen
- , Paul G. A. Volders
- , Steven A. Lubitz
- , Charles Antzelevitch
- , Pyotr G. Platonov
- , Katja E. Odening
- , Dan M. Roden
- , Jason D. Roberts
- , Jonathan R. Skinner
- , Jacob Tfelt-Hansen
- , Maarten P. van den Berg
- , Morten S. Olesen
- , Pier D. Lambiase
- , Martin Borggrefe
- , Kenshi Hayashi
- , Annika Rydberg
- , Tadashi Nakajima
- , Masao Yoshinaga
- , Johan B. Saenen
- , Stefan Kääb
- , Pedro Brugada
- , Tomas Robyns
- , Daniela F. Giachino
- , Michael J. Ackerman
- , Ramon Brugada
- , Josep Brugada
- , Juan R. Gimeno
- , Can Hasdemir
- , Pascale Guicheney
- , Silvia G. Priori
- , Eric Schulze-Bahr
- , Naomasa Makita
- , Peter J. Schwartz
- , Wataru Shimizu
- , Takeshi Aiba
- , Jean-Jacques Schott
- , Richard Redon
- , Seiko Ohno
- , Vincent Probst
- , Alain Al Arnaout
- , Mathieu Amelot
- , Frédéric Anselme
- , Olivier Billon
- , Pascal Defaye
- , Jean-Marc Dupuis
- , Laurence Jesel
- , Gabriel Laurent
- , Philippe Maury
- , Jean-Luc Pasquie
- , Francois Wiart
- , Elijah R. Behr
- , Julien Barc
- & Connie R. Bezzina
-
Amendments and Corrections |
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Research |
Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster
- Cédric Le Caignec
- , Olivier Pichon
- , Annaig Briand
- , Benoît de Courtivron
- , Christian Bonnard
- , Pierre Lindenbaum
- , Richard Redon
- , Caroline Schluth-Bolard
- , Flavie Diguet
- , Pierre-Antoine Rollat-Farnier
- , Marta Sanchez-Castro
- , Marie-Laure Vuillaume
- , Damien Sanlaville
- , Denis Duboule
- , André Mégarbané
- & Annick Toutain
-
Amendments and Corrections | | Open
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
- Joshua C. Bis
- , Xueqiu Jian
- , Brian W. Kunkle
- , Yuning Chen
- , Kara L. Hamilton-Nelson
- , William S. Bush
- , William J. Salerno
- , Daniel Lancour
- , Yiyi Ma
- , Alan E. Renton
- , Edoardo Marcora
- , John J. Farrell
- , Yi Zhao
- , Liming Qu
- , Shahzad Ahmad
- , Najaf Amin
- , Philippe Amouyel
- , Gary W. Beecham
- , Jennifer E. Below
- , Dominique Campion
- , Laura Cantwell
- , Camille Charbonnier
- , Jaeyoon Chung
- , Paul K. Crane
- , Carlos Cruchaga
- , L. Adrienne Cupples
- , Jean-François Dartigues
- , Stéphanie Debette
- , Jean-François Deleuze
- , Lucinda Fulton
- , Stacey B. Gabriel
- , Emmanuelle Genin
- , Richard A. Gibbs
- , Alison Goate
- , Benjamin Grenier-Boley
- , Namrata Gupta
- , Jonathan L. Haines
- , Aki S. Havulinna
- , Seppo Helisalmi
- , Mikko Hiltunen
- , Daniel P. Howrigan
- , M. Arfan Ikram
- , Jaakko Kaprio
- , Jan Konrad
- , Amanda Kuzma
- , Eric S. Lander
- , Mark Lathrop
- , Terho Lehtimäki
- , Honghuang Lin
- , Kari Mattila
- , Richard Mayeux
- , Donna M. Muzny
- , Waleed Nasser
- , Benjamin Neale
- , Kwangsik Nho
- , Gaël Nicolas
- , Devanshi Patel
- , Margaret A. Pericak-Vance
- , Markus Perola
- , Bruce M. Psaty
- , Olivier Quenez
- , Farid Rajabli
- , Richard Redon
- , Christiane Reitz
- , Anne M. Remes
- , Veikko Salomaa
- , Chloe Sarnowski
- , Helena Schmidt
- , Michael Schmidt
- , Reinhold Schmidt
- , Hilkka Soininen
- , Timothy A. Thornton
- , Giuseppe Tosto
- , Christophe Tzourio
- , Sven J. van der Lee
- , Cornelia M. van Duijn
- , Otto Valladares
- , Badri Vardarajan
- , Li-San Wang
- , Weixin Wang
- , Ellen Wijsman
- , Richard K. Wilson
- , Daniela Witten
- , Kim C. Worley
- , Xiaoling Zhang
- , Celine Bellenguez
- , Jean-Charles Lambert
- , Mitja I. Kurki
- , Aarno Palotie
- , Mark Daly
- , Eric Boerwinkle
- , Kathryn L. Lunetta
- , Anita L. Destefano
- , Josée Dupuis
- , Eden R. Martin
- , Gerard D. Schellenberg
- , Sudha Seshadri
- , Adam C. Naj
- , Myriam Fornage
- & Lindsay A. Farrer
-
Research |
Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluation
- Olivier Quenez
- , Kevin Cassinari
- , Sophie Coutant
- , François Lecoquierre
- , Kilan Le Guennec
- , Stéphane Rousseau
- , Anne-Claire Richard
- , Stéphanie Vasseur
- , Emilie Bouvignies
- , Jacqueline Bou
- , Gwendoline Lienard
- , Sandrine Manase
- , Steeve Fourneaux
- , Nathalie Drouot
- , Virginie Nguyen-Viet
- , Myriam Vezain
- , Pascal Chambon
- , Géraldine Joly-Helas
- , Nathalie Le Meur
- , Mathieu Castelain
- , Anne Boland
- , Jean-François Deleuze
- , Emmanuelle Génin
- , Dominique Campion
- , Jean-François Dartigues
- , Jean-François Deleuze
- , Jean-Charles Lambert
- , Richard Redon
- , Thomas Ludwig
- , Benjamin Grenier-Boley
- , Sébastien Letort
- , Pierre Lindenbaum
- , Vincent Meyer
- , Olivier Quenez
- , Christian Dina
- , Céline Bellenguez
- , Camille Charbonnier
- , Joanna Giemza
- , Stéphanie Chatel
- , Claude Férec
- , Hervé Le Marec
- , Luc Letenneur
- , Gaël Nicolas
- , Karen Rouault
- , Delphine Bacq
- , Anne Boland
- , Doris Lechner
- , Isabelle Tournier
- , Françoise Charbonnier
- , Edwige Kasper
- , Gaëlle Bougeard
- , Thierry Frebourg
- , Pascale Saugier-Veber
- , Stéphanie Baert-Desurmont
- , Dominique Campion
- , Anne Rovelet-Lecrux
- & Gaël Nicolas
-
Amendments and Corrections |
Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
- Connie R Bezzina
- , Julien Barc
- , Yuka Mizusawa
- , Carol Ann Remme
- , Jean-Baptiste Gourraud
- , Floriane Simonet
- , Arie O Verkerk
- , Peter J Schwartz
- , Lia Crotti
- , Federica Dagradi
- , Pascale Guicheney
- , Véronique Fressart
- , Antoine Leenhardt
- , Charles Antzelevitch
- , Susan Bartkowiak
- , Eric Schulze-Bahr
- , Sven Zumhagen
- , Elijah R Behr
- , Rachel Bastiaenen
- , Jacob Tfelt-Hansen
- , Morten Salling Olesen
- , Stefan Kääb
- , Britt M Beckmann
- , Peter Weeke
- , Hiroshi Watanabe
- , Naoto Endo
- , Tohru Minamino
- , Minoru Horie
- , Seiko Ohno
- , Kanae Hasegawa
- , Naomasa Makita
- , Akihiko Nogami
- , Wataru Shimizu
- , Takeshi Aiba
- , Philippe Froguel
- , Beverley Balkau
- , Olivier Lantieri
- , Margherita Torchio
- , Cornelia Wiese
- , David Weber
- , Rianne Wolswinkel
- , Ruben Coronel
- , Bas J Boukens
- , Stéphane Bézieau
- , Eric Charpentier
- , Stéphanie Chatel
- , Aurore Despres
- , Françoise Gros
- , Florence Kyndt
- , Simon Lecointe
- , Pierre Lindenbaum
- , Vincent Portero
- , Jade Violleau
- , Manfred Gessler
- , Hanno L Tan
- , Dan M Roden
- , Vincent M Christoffels
- , Hervé Le Marec
- , Arthur A Wilde
- , Vincent Probst
- , Jean-Jacques Schott
- , Christian Dina
- & Richard Redon
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Correspondence |
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Research |
Fine-scale human genetic structure in Western France
- Matilde Karakachoff
- , Nicolas Duforet-Frebourg
- , Floriane Simonet
- , Solena Le Scouarnec
- , Nadine Pellen
- , Simon Lecointe
- , Eric Charpentier
- , Françoise Gros
- , Stéphane Cauchi
- , Philippe Froguel
- , Nane Copin
- , B Balkau
- , P Ducimetière
- , E Eschwège;
- , F Alhenc-Gelas
- , A Girault
- , F Fumeron
- , M Marre
- , R Roussel
- , F Bonnet
- , S Cauchi
- , P Froguel
- , J Cogneau
- , C Born
- , E Caces
- , M Cailleau
- , O Lantieri
- , J G Moreau
- , F Rakotozafy
- , J Tichet
- , Thierry Le Tourneau
- , Vincent Probst
- , Hervé Le Marec
- , Sabrina Molinaro
- , Beverley Balkau
- , Richard Redon
- , Jean-Jacques Schott
- , Michael GB Blum
- & Christian Dina
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Research |
Genome assembly comparison identifies structural variants in the human genome
- Razi Khaja
- , Junjun Zhang
- , Jeffrey R MacDonald
- , Yongshu He
- , Ann M Joseph-George
- , John Wei
- , Muhammad A Rafiq
- , Cheng Qian
- , Mary Shago
- , Lorena Pantano
- , Hiroyuki Aburatani
- , Keith Jones
- , Richard Redon
- , Matthew Hurles
- , Lluis Armengol
- , Xavier Estivill
- , Richard J Mural
- , Charles Lee
- , Stephen W Scherer
- & Lars Feuk
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Research |
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Research |
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Research |
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Research |
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Research |
Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome
- Thomas Besnard
- , Natacha Sloboda
- , Alice Goldenberg
- , Sébastien Küry
- , Benjamin Cogné
- , Flora Breheret
- , Eva Trochu
- , Solène Conrad
- , Marie Vincent
- , Wallid Deb
- , Xavier Balguerie
- , Sébastien Barbarot
- , Geneviève Baujat
- , Tawfeg Ben-Omran
- , Anne-Claire Bursztejn
- , Virginie Carmignac
- , Alexandre N. Datta
- , Aline Delignières
- , Laurence Faivre
- , Betty Gardie
- , Jean-Louis Guéant
- , Paul Kuentz
- , Marion Lenglet
- , Marie-Cécile Nassogne
- , Vincent Ramaekers
- , Rhonda E. Schnur
- , Yue Si
- , Erin Torti
- , Julien Thevenon
- , Pierre Vabres
- , Lionel Van Maldergem
- , Dorothea Wand
- , Arnaud Wiedemann
- , Bertrand Cariou
- , Richard Redon
- , Antonin Lamazière
- , Stéphane Bézieau
- , Francois Feillet
- & Bertrand Isidor
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Research | | Open
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
- Joshua C. Bis
- , Xueqiu Jian
- , Brian W. Kunkle
- , Yuning Chen
- , Kara L. Hamilton-Nelson
- , William S. Bush
- , William J. Salerno
- , Daniel Lancour
- , Yiyi Ma
- , Alan E. Renton
- , Edoardo Marcora
- , John J. Farrell
- , Yi Zhao
- , Liming Qu
- , Shahzad Ahmad
- , Najaf Amin
- , Philippe Amouyel
- , Gary W. Beecham
- , Jennifer E. Below
- , Dominique Campion
- , Laura Cantwell
- , Camille Charbonnier
- , Jaeyoon Chung
- , Paul K. Crane
- , Carlos Cruchaga
- , L. Adrienne Cupples
- , Jean-François Dartigues
- , Stéphanie Debette
- , Jean-François Deleuze
- , Lucinda Fulton
- , Stacey B. Gabriel
- , Emmanuelle Genin
- , Richard A. Gibbs
- , Alison Goate
- , Benjamin Grenier-Boley
- , Namrata Gupta
- , Jonathan L. Haines
- , Aki S. Havulinna
- , Seppo Helisalmi
- , Mikko Hiltunen
- , Daniel P. Howrigan
- , M. Arfan Ikram
- , Jaakko Kaprio
- , Jan Konrad
- , Amanda Kuzma
- , Eric S. Lander
- , Mark Lathrop
- , Terho Lehtimäki
- , Honghuang Lin
- , Kari Mattila
- , Richard Mayeux
- , Donna M. Muzny
- , Waleed Nasser
- , Benjamin Neale
- , Kwangsik Nho
- , Gaël Nicolas
- , Devanshi Patel
- , Margaret A. Pericak-Vance
- , Markus Perola
- , Bruce M. Psaty
- , Olivier Quenez
- , Farid Rajabli
- , Richard Redon
- , Christiane Reitz
- , Anne M. Remes
- , Veikko Salomaa
- , Chloe Sarnowski
- , Helena Schmidt
- , Michael Schmidt
- , Reinhold Schmidt
- , Hilkka Soininen
- , Timothy A. Thornton
- , Giuseppe Tosto
- , Christophe Tzourio
- , Sven J. van der Lee
- , Cornelia M. van Duijn
- , Otto Valladares
- , Badri Vardarajan
- , Li-San Wang
- , Weixin Wang
- , Ellen Wijsman
- , Richard K. Wilson
- , Daniela Witten
- , Kim C. Worley
- , Xiaoling Zhang
- , Celine Bellenguez
- , Jean-Charles Lambert
- , Mitja I. Kurki
- , Aarno Palotie
- , Mark Daly
- , Eric Boerwinkle
- , Kathryn L. Lunetta
- , Anita L. Destefano
- , Josée Dupuis
- , Eden R. Martin
- , Gerard D. Schellenberg
- , Sudha Seshadri
- , Adam C. Naj
- , Myriam Fornage
- & Lindsay A. Farrer
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Research | | Open
Parallel derivation of isogenic human primed and naive induced pluripotent stem cells
- Stéphanie Kilens
- , Dimitri Meistermann
- , Diego Moreno
- , Caroline Chariau
- , Anne Gaignerie
- , Arnaud Reignier
- , Yohann Lelièvre
- , Miguel Casanova
- , Céline Vallot
- , Steven Nedellec
- , Léa Flippe
- , Julie Firmin
- , Juan Song
- , Eric Charpentier
- , Jenna Lammers
- , Audrey Donnart
- , Nadège Marec
- , Wallid Deb
- , Audrey Bihouée
- , Cédric Le Caignec
- , Claire Pecqueur
- , Richard Redon
- , Paul Barrière
- , Jérémie Bourdon
- , Vincent Pasque
- , Magali Soumillon
- , Tarjei S. Mikkelsen
- , Claire Rougeulle
- , Thomas Fréour
- , Laurent David
- , Laurent Abel
- , Andres Alcover
- , Kalla Astrom
- , Philippe Bousso
- , Pierre Bruhns
- , Ana Cumano
- , Darragh Duffy
- , Caroline Demangel
- , Ludovic Deriano
- , James Di Santo
- , Françoise Dromer
- , Gérard Eberl
- , Jost Enninga
- , Jacques Fellay
- , Antonio Freitas
- , Odile Gelpi
- , Ivo Gomperts-Boneca
- , Serge Hercberg
- , Olivier Lantz
- , Claude Leclerc
- , Hugo Mouquet
- , Etienne Patin
- , Sandra Pellegrini
- , Stanislas Pol
- , Lars Rogge
- , Anavaj Sakuntabhai
- , Olivier Schwartz
- , Benno Schwikowski
- , Spencer Shorte
- , Vassili Soumelis
- , Frédéric Tangy
- , Eric Tartour
- , Antoine Toubert
- , Marie-Noëlle Ungeheuer
- , Lluis Quintana-Murci
- & Matthew L. Albert
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Research |
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
- Connie Bezzina, Richard Redon and colleagues show that common...
- Connie R Bezzina
- , Julien Barc
- , Yuka Mizusawa
- , Carol Ann Remme
- , Jean-Baptiste Gourraud
- , Floriane Simonet
- , Arie O Verkerk
- , Peter J Schwartz
- , Lia Crotti
- , Federica Dagradi
- , Pascale Guicheney
- , Véronique Fressart
- , Antoine Leenhardt
- , Charles Antzelevitch
- , Susan Bartkowiak
- , Martin Borggrefe
- , Rainer Schimpf
- , Eric Schulze-Bahr
- , Sven Zumhagen
- , Elijah R Behr
- , Rachel Bastiaenen
- , Jacob Tfelt-Hansen
- , Morten Salling Olesen
- , Stefan Kääb
- , Britt M Beckmann
- , Peter Weeke
- , Hiroshi Watanabe
- , Naoto Endo
- , Tohru Minamino
- , Minoru Horie
- , Seiko Ohno
- , Kanae Hasegawa
- , Naomasa Makita
- , Akihiko Nogami
- , Wataru Shimizu
- , Takeshi Aiba
- , Philippe Froguel
- , Beverley Balkau
- , Olivier Lantieri
- , Margherita Torchio
- , Cornelia Wiese
- , David Weber
- , Rianne Wolswinkel
- , Ruben Coronel
- , Bas J Boukens
- , Stéphane Bézieau
- , Eric Charpentier
- , Stéphanie Chatel
- , Aurore Despres
- , Françoise Gros
- , Florence Kyndt
- , Simon Lecointe
- , Pierre Lindenbaum
- , Vincent Portero
- , Jade Violleau
- , Manfred Gessler
- , Hanno L Tan
- , Dan M Roden
- , Vincent M Christoffels
- , Hervé Le Marec
- , Arthur A Wilde
- , Vincent Probst
- , Jean-Jacques Schott
- , Christian Dina
- & Richard Redon
-
Research |
Genetic association analyses highlight biological pathways underlying mitral valve prolapse
- Christian Dina
- , Nabila Bouatia-Naji
- , Nathan Tucker
- , Francesca N Delling
- , Katelynn Toomer
- , Ronen Durst
- , Maelle Perrocheau
- , Leticia Fernandez-Friera
- , Jorge Solis
- , Thierry Le Tourneau
- , Ming-Huei Chen
- , Vincent Probst
- , Yohan Bosse
- , Philippe Pibarot
- , Diana Zelenika
- , Mark Lathrop
- , Serge Hercberg
- , Ronan Roussel
- , Emelia J Benjamin
- , Fabrice Bonnet
- , Su Hao Lo
- , Elena Dolmatova
- , Floriane Simonet
- , Simon Lecointe
- , Florence Kyndt
- , Richard Redon
- , Hervé Le Marec
- , Philippe Froguel
- , Patrick T Ellinor
- , Ramachandran S Vasan
- , Patrick Bruneval
- , Roger R Markwald
- , Russell A Norris
- , David J Milan
- , Susan A Slaugenhaupt
- , Robert A Levine
- , Jean-Jacques Schott
- , Albert A Hagege
- & Xavier Jeunemaitre
-
Research |
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
- Nick Craddock
- , Matthew E. Hurles
- , Niall Cardin
- , Richard D. Pearson
- , Vincent Plagnol
- , Samuel Robson
- , Damjan Vukcevic
- , Chris Barnes
- , Donald F. Conrad
- , Eleni Giannoulatou
- , Chris Holmes
- , Jonathan L. Marchini
- , Kathy Stirrups
- , Martin D. Tobin
- , Louise V. Wain
- , Chris Yau
- , Jan Aerts
- , Tariq Ahmad
- , T. Daniel Andrews
- , Hazel Arbury
- , Anthony Attwood
- , Adam Auton
- , Stephen G. Ball
- , Anthony J. Balmforth
- , Jeffrey C. Barrett
- , Inês Barroso
- , Anne Barton
- , Amanda J. Bennett
- , Sanjeev Bhaskar
- , Katarzyna Blaszczyk
- , John Bowes
- , Oliver J. Brand
- , Peter S. Braund
- , Francesca Bredin
- , Gerome Breen
- , Morris J. Brown
- , Ian N. Bruce
- , Jaswinder Bull
- , Oliver S. Burren
- , John Burton
- , Jake Byrnes
- , Sian Caesar
- , Chris M. Clee
- , Alison J. Coffey
- , John M. C. Connell
- , Jason D. Cooper
- , Anna F. Dominiczak
- , Kate Downes
- , Hazel E. Drummond
- , Darshna Dudakia
- , Andrew Dunham
- , Bernadette Ebbs
- , Diana Eccles
- , Sarah Edkins
- , Cathryn Edwards
- , Anna Elliot
- , Paul Emery
- , David M. Evans
- , Gareth Evans
- , Steve Eyre
- , Anne Farmer
- , I. Nicol Ferrier
- , Lars Feuk
- , Tomas Fitzgerald
- , Edward Flynn
- , Alistair Forbes
- , Liz Forty
- , Jayne A. Franklyn
- , Rachel M. Freathy
- , Polly Gibbs
- , Paul Gilbert
- , Omer Gokumen
- , Katherine Gordon-Smith
- , Emma Gray
- , Elaine Green
- , Chris J. Groves
- , Detelina Grozeva
- , Rhian Gwilliam
- , Anita Hall
- , Naomi Hammond
- , Matt Hardy
- , Pile Harrison
- , Neelam Hassanali
- , Husam Hebaishi
- , Sarah Hines
- , Anne Hinks
- , Graham A Hitman
- , Lynne Hocking
- , Eleanor Howard
- , Philip Howard
- , Joanna M. M. Howson
- , Debbie Hughes
- , Sarah Hunt
- , John D. Isaacs
- , Mahim Jain
- , Derek P. Jewell
- , Toby Johnson
- , Jennifer D. Jolley
- , Ian R. Jones
- , Lisa A. Jones
- , George Kirov
- , Cordelia F. Langford
- , Hana Lango-Allen
- , G. Mark Lathrop
- , James Lee
- , Kate L. Lee
- , Charlie Lees
- , Kevin Lewis
- , Cecilia M. Lindgren
- , Meeta Maisuria-Armer
- , Julian Maller
- , John Mansfield
- , Paul Martin
- , Dunecan C. O. Massey
- , Wendy L. McArdle
- , Peter McGuffin
- , Kirsten E. McLay
- , Alex Mentzer
- , Michael L. Mimmack
- , Ann E. Morgan
- , Andrew P. Morris
- , Craig Mowat
- , Simon Myers
- , William Newman
- , Elaine R. Nimmo
- , Michael C. O’Donovan
- , Abiodun Onipinla
- , Ifejinelo Onyiah
- , Nigel R. Ovington
- , Michael J. Owen
- , Kimmo Palin
- , Kirstie Parnell
- , David Pernet
- , John R. B. Perry
- , Anne Phillips
- , Dalila Pinto
- , Natalie J. Prescott
- , Inga Prokopenko
- , Michael A. Quail
- , Suzanne Rafelt
- , Nigel W. Rayner
- , Richard Redon
- , David M. Reid
- , Anthony Renwick
- , Susan M. Ring
- , Neil Robertson
- , Ellie Russell
- , David St Clair
- , Jennifer G. Sambrook
- , Jeremy D. Sanderson
- , Helen Schuilenburg
- , Carol E. Scott
- , Richard Scott
- , Sheila Seal
- , Sue Shaw-Hawkins
- , Beverley M. Shields
- , Matthew J. Simmonds
- , Debbie J. Smyth
- , Elilan Somaskantharajah
- , Katarina Spanova
- , Sophia Steer
- , Jonathan Stephens
- , Helen E. Stevens
- , Millicent A. Stone
- , Zhan Su
- , Deborah P. M. Symmons
- , John R. Thompson
- , Wendy Thomson
- , Mary E. Travers
- , Clare Turnbull
- , Armand Valsesia
- , Mark Walker
- , Neil M. Walker
- , Chris Wallace
- , Margaret Warren-Perry
- , Nicholas A. Watkins
- , John Webster
- , Michael N. Weedon
- , Anthony G. Wilson
- , Matthew Woodburn
- , B. Paul Wordsworth
- , Allan H. Young
- , Eleftheria Zeggini
- , Nigel P. Carter
- , Timothy M. Frayling
- , Charles Lee
- , Gil McVean
- , Patricia B. Munroe
- , Aarno Palotie
- , Stephen J. Sawcer
- , Stephen W. Scherer
- , David P. Strachan
- , Chris Tyler-Smith
- , Matthew A. Brown
- , Paul R. Burton
- , Mark J. Caulfield
- , Alastair Compston
- , Martin Farrall
- , Stephen C. L. Gough
- , Alistair S. Hall
- , Andrew T. Hattersley
- , Adrian V. S. Hill
- , Christopher G. Mathew
- , Marcus Pembrey
- , Jack Satsangi
- , Michael R. Stratton
- , Jane Worthington
- , Panos Deloukas
- , Audrey Duncanson
- , Dominic P. Kwiatkowski
- , Mark I. McCarthy
- , Willem H. Ouwehand
- , Miles Parkes
- , Nazneen Rahman
- , John A. Todd
- , Nilesh J. Samani
- & Peter Donnelly
-
Research |
Origins and functional impact of copy number variation in the human genome
- Donald F. Conrad
- , Dalila Pinto
- , Richard Redon
- , Lars Feuk
- , Omer Gokcumen
- , Yujun Zhang
- , Jan Aerts
- , T. Daniel Andrews
- , Chris Barnes
- , Peter Campbell
- , Tomas Fitzgerald
- , Min Hu
- , Chun Hwa Ihm
- , Kati Kristiansson
- , Daniel G. MacArthur
- , Jeffrey R. MacDonald
- , Ifejinelo Onyiah
- , Andy Wing Chun Pang
- , Sam Robson
- , Kathy Stirrups
- , Armand Valsesia
- , Klaudia Walter
- , John Wei
- , Chris Tyler-Smith
- , Nigel P. Carter
- , Charles Lee
- , Stephen W. Scherer
- & Matthew E. Hurles
-
Research |
Global variation in copy number in the human genome
- Richard Redon
- , Shumpei Ishikawa
- , Karen R. Fitch
- , Lars Feuk
- , George H. Perry
- , T. Daniel Andrews
- , Heike Fiegler
- , Michael H. Shapero
- , Andrew R. Carson
- , Wenwei Chen
- , Eun Kyung Cho
- , Stephanie Dallaire
- , Jennifer L. Freeman
- , Juan R. González
- , Mònica Gratacòs
- , Jing Huang
- , Dimitrios Kalaitzopoulos
- , Daisuke Komura
- , Jeffrey R. MacDonald
- , Christian R. Marshall
- , Rui Mei
- , Lyndal Montgomery
- , Kunihiro Nishimura
- , Kohji Okamura
- , Fan Shen
- , Martin J. Somerville
- , Joelle Tchinda
- , Armand Valsesia
- , Cara Woodwark
- , Fengtang Yang
- , Junjun Zhang
- , Tatiana Zerjal
- , Jane Zhang
- , Lluis Armengol
- , Donald F. Conrad
- , Xavier Estivill
- , Chris Tyler-Smith
- , Nigel P. Carter
- , Hiroyuki Aburatani
- , Charles Lee
- , Keith W. Jones
- , Stephen W. Scherer
- & Matthew E. Hurles
-
Research |
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Protocols |
