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Amendments and Corrections | 13 September 2016 | Open
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
- Manuel A. Rivas
- , Daniel Graham
- , Patrick Sulem
- , Christine Stevens
- , A. Nicole Desch
- , Philippe Goyette
- , Daniel Gudbjartsson
- , Ingileif Jonsdottir
- , Unnur Thorsteinsdottir
- , Frauke Degenhardt
- , Sören Mucha
- , Mitja I. Kurki
- , Dalin Li
- , Mauro D’Amato
- , Vito Annese
- , Severine Vermeire
- , Rinse K. Weersma
- , Jonas Halfvarson
- , Paulina Paavola-Sakki
- , Maarit Lappalainen
- , Monkol Lek
- , Beryl Cummings
- , Taru Tukiainen
- , Talin Haritunians
- , Leena Halme
- , Lotta L. E. Koskinen
- , Ashwin N. Ananthakrishnan
- , Yang Luo
- , Graham A. Heap
- , Marijn C. Visschedijk
- , J. Barrett
- , K. de Lange
- , C. Edwards
- , A. Hart
- , C. Hawkey
- , L. Jostins
- , N. Kennedy
- , C. Lamb
- , J. Lee
- , C. Lees
- , J. Mansfield
- , C. Mathew
- , C. Mowatt
- , W. Newman
- , E. Nimmo
- , M. Parkes
- , M. Pollard
- , N. Prescott
- , J. Randall
- , D. Rice
- , J. Satsangi
- , A. Simmons
- , M. Tremelling
- , H. Uhlig
- , D. Wilson
- , C. Abraham
- , J.P. Achkar
- , A. Bitton
- , G. Boucher
- , K. Croitoru
- , P. Fleshner
- , J. Glas
- , S. Kugathasan
- , J. V. Limbergen
- , R. Milgrom
- , D. Proctor
- , M. Regueiro
- , P. L. Schumm
- , Y. Sharma
- , J. M. Stempak
- , S. R. Targan
- , M. H. Wang
- , Daniel G. MacArthur
- , Benjamin M. Neale
- , Tariq Ahmad
- , Carl A. Anderson
- , Steven R. Brant
- , Richard H. Duerr
- , Mark S. Silverberg
- , Judy H. Cho
- , Aarno Palotie
- , Päivi Saavalainen
- , Kimmo Kontula
- , Martti Färkkilä
- , Dermot P. B. McGovern
- , Andre Franke
- , Kari Stefansson
- , John D. Rioux
- , Ramnik J. Xavier
- & Mark J. Daly
Nature Communications 7 , 1–1

Rights & permissionsfor article Erratum: A protein-truncating R179X variant in <i>RNF186</i> confers protection against ulcerative colitis . Opens in a new window.
Amendments and Corrections | 28 September 2016
Correction: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
- Padhraig Gormley
- , Verneri Anttila
- , Bendik S Winsvold
- , Priit Palta
- , Tonu Esko
- , Tune H Pers
- , Kai-How Farh
- , Ester Cuenca-Leon
- , Mikko Muona
- , Nicholas A Furlotte
- , Tobias Kurth
- , Andres Ingason
- , George McMahon
- , Lannie Ligthart
- , Gisela M Terwindt
- , Mikko Kallela
- , Tobias M Freilinger
- , Caroline Ran
- , Scott G Gordon
- , Anine H Stam
- , Stacy Steinberg
- , Guntram Borck
- , Markku Koiranen
- , Lydia Quaye
- , Hieab H H Adams
- , Terho Lehtimäki
- , Antti-Pekka Sarin
- , Juho Wedenoja
- , David A Hinds
- , Julie E Buring
- , Markus Schürks
- , Paul M Ridker
- , Maria Gudlaug Hrafnsdottir
- , Hreinn Stefansson
- , Susan M Ring
- , Jouke-Jan Hottenga
- , Brenda W J H Penninx
- , Markus Färkkilä
- , Ville Artto
- , Mari Kaunisto
- , Salli Vepsäläinen
- , Rainer Malik
- , Andrew C Heath
- , Pamela A F Madden
- , Nicholas G Martin
- , Grant W Montgomery
- , Mitja I Kurki
- , Mart Kals
- , Reedik Mägi
- , Kalle Pärn
- , Eija Hämäläinen
- , Hailiang Huang
- , Andrea E Byrnes
- , Lude Franke
- , Jie Huang
- , Evie Stergiakouli
- , Phil H Lee
- , Cynthia Sandor
- , Caleb Webber
- , Zameel Cader
- , Bertram Muller-Myhsok
- , Stefan Schreiber
- , Thomas Meitinger
- , Johan G Eriksson
- , Veikko Salomaa
- , Kauko Heikkilä
- , Elizabeth Loehrer
- , Andre G Uitterlinden
- , Albert Hofman
- , Cornelia M van Duijn
- , Lynn Cherkas
- , Linda M Pedersen
- , Audun Stubhaug
- , Christopher S Nielsen
- , Minna Männikkö
- , Evelin Mihailov
- , Lili Milani
- , Hartmut Göbel
- , Ann-Louise Esserlind
- , Anne Francke Christensen
- , Thomas Folkmann Hansen
- , Thomas Werge
- , Jaakko Kaprio
- , Arpo J Aromaa
- , Olli Raitakari
- , M Arfan Ikram
- , Tim Spector
- , Marjo-Riitta Järvelin
- , Andres Metspalu
- , Christian Kubisch
- , David P Strachan
- , Michel D Ferrari
- , Andrea C Belin
- , Martin Dichgans
- , Maija Wessman
- , Arn M J M van den Maagdenberg
- , John-Anker Zwart
- , Dorret I Boomsma
- , George Davey Smith
- , Kari Stefansson
- , Nicholas Eriksson
- , Mark J Daly
- , Benjamin M Neale
- , Jes Olesen
- , Daniel I Chasman
- , Dale R Nyholt
- & Aarno Palotie
Nature Genetics 48 , 1296–1296

Rights & permissionsfor article Correction: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine . Opens in a new window.
Amendments and Corrections | 21 October 2019 | 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
Molecular Psychiatry 25 , 1901–1903

Rights & permissionsfor article Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation . Opens in a new window.
Research | 3 April 2019 | Open
Biallelic loss-of-function P4HTM gene variants cause hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities (HIDEA syndrome)
- Elisa Rahikkala
- , Matti Myllykoski
- , Reetta Hinttala
- , Päivi Vieira
- , Naemeh Nayebzadeh
- , Simone Weiss
- , Astrid S. Plomp
- , Reginald E. Bittner
- , Mitja I. Kurki
- , Outi Kuismin
- , Andrea M. Lewis
- , Marja-Leena Väisänen
- , Hannaleena Kokkonen
- , Jonne Westermann
- , Günther Bernert
- , Hannu Tuominen
- , Aarno Palotie
- , Lauri Aaltonen
- , Yaping Yang
- , Lorraine Potocki
- , Jukka Moilanen
- , Silvana van Koningsbruggen
- , Xia Wang
- , Wolfgang M. Schmidt
- , Peppi Koivunen
- & Johanna Uusimaa
Genetics in Medicine 21 , 2355–2363

Rights & permissionsfor article Biallelic loss-of-function <i>P4HTM</i> gene variants cause hypotonia, hypoventilation, intellectual disability, dysautonomia, epilepsy, and eye abnormalities (HIDEA syndrome) . Opens in a new window.
Research | 3 October 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general population
- Andrea Ganna
- , Giulio Genovese
- , Daniel P Howrigan
- , Andrea Byrnes
- , Mitja I Kurki
- , Seyedeh M Zekavat
- , Christopher W Whelan
- , Mart Kals
- , Michel G Nivard
- , Alex Bloemendal
- , Jonathan M Bloom
- , Jacqueline I Goldstein
- , Timothy Poterba
- , Cotton Seed
- , Robert E Handsaker
- , Pradeep Natarajan
- , Reedik Mägi
- , Diane Gage
- , Elise B Robinson
- , Andres Metspalu
- , Veikko Salomaa
- , Jaana Suvisaari
- , Shaun M Purcell
- , Pamela Sklar
- , Sekar Kathiresan
- , Mark J Daly
- , Steven A McCarroll
- , Patrick F Sullivan
- , Aarno Palotie
- , Tõnu Esko
- , Christina M Hultman
- & Benjamin M Neale
Nature Neuroscience 19 , 1563–1565

Rights & permissionsfor article Ultra-rare disruptive and damaging mutations influence educational attainment in the general population . Opens in a new window.
Research | 26 June 2019 | Open
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum
- Enrico D. H. Konrad
- , Niels Nardini
- , Almuth Caliebe
- , Inga Nagel
- , Dana Young
- , Gabriella Horvath
- , Stephanie L. Santoro
- , Christine Shuss
- , Alban Ziegler
- , Dominique Bonneau
- , Marlies Kempers
- , Rolph Pfundt
- , Eric Legius
- , Arjan Bouman
- , Kyra E. Stuurman
- , Katrin Õunap
- , Sander Pajusalu
- , Monica H. Wojcik
- , Georgia Vasileiou
- , Gwenaël Le Guyader
- , Hege M. Schnelle
- , Siren Berland
- , Evelien Zonneveld-Huijssoon
- , Simone Kersten
- , Aditi Gupta
- , Patrick R. Blackburn
- , Marissa S. Ellingson
- , Matthew J. Ferber
- , Radhika Dhamija
- , Eric W. Klee
- , Meriel McEntagart
- , Klaske D. Lichtenbelt
- , Amy Kenney
- , Samantha A. Vergano
- , Rami Abou Jamra
- , Konrad Platzer
- , Mary Ella Pierpont
- , Divya Khattar
- , Robert J. Hopkin
- , Richard J. Martin
- , Marjolijn C. J. Jongmans
- , Vivian Y. Chang
- , Julian A. Martinez-Agosto
- , Outi Kuismin
- , Mitja I. Kurki
- , Olli Pietiläinen
- , Aarno Palotie
- , Timothy J. Maarup
- , Diana S. Johnson
- , Katja Venborg Pedersen
- , Lone W. Laulund
- , Sally A. Lynch
- , Moira Blyth
- , Katrina Prescott
- , Natalie Canham
- , Rita Ibitoye
- , Eva H. Brilstra
- , Marwan Shinawi
- , Emily Fassi
- , Heinrich Sticht
- , Anne Gregor
- , Hilde Van Esch
- & Christiane Zweier
Genetics in Medicine 21 , 2723–2733

Rights & permissionsfor article <i>CTCF</i> variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum . Opens in a new window.
Research | 24 January 2019 | Open
Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
- Mitja I. Kurki
- , Elmo Saarentaus
- , Olli Pietiläinen
- , Padhraig Gormley
- , Dennis Lal
- , Sini Kerminen
- , Minna Torniainen-Holm
- , Eija Hämäläinen
- , Elisa Rahikkala
- , Riikka Keski-Filppula
- , Merja Rauhala
- , Satu Korpi-Heikkilä
- , Jonna Komulainen–Ebrahim
- , Heli Helander
- , Päivi Vieira
- , Minna Männikkö
- , Markku Peltonen
- , Aki S. Havulinna
- , Veikko Salomaa
- , Matti Pirinen
- , Jaana Suvisaari
- , Jukka S. Moilanen
- , Jarmo Körkkö
- , Outi Kuismin
- , Mark J. Daly
- & Aarno Palotie
Nature Communications 10 , 1–15

Rights & permissionsfor article Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland . Opens in a new window.
Research | 19 March 2019 | Open
Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans
- Eevi Kaasinen
- , Outi Kuismin
- , Kristiina Rajamäki
- , Heikki Ristolainen
- , Mervi Aavikko
- , Johanna Kondelin
- , Silva Saarinen
- , Davide G. Berta
- , Riku Katainen
- , Elina A. M. Hirvonen
- , Auli Karhu
- , Aurora Taira
- , Tomas Tanskanen
- , Amjad Alkodsi
- , Minna Taipale
- , Ekaterina Morgunova
- , Kaarle Franssila
- , Rainer Lehtonen
- , Markus Mäkinen
- , Kristiina Aittomäki
- , Aarno Palotie
- , Mitja I. Kurki
- , Olli Pietiläinen
- , Morgane Hilpert
- , Elmo Saarentaus
- , Jaakko Niinimäki
- , Juhani Junttila
- , Kari Kaikkonen
- , Pia Vahteristo
- , Radek C. Skoda
- , Mikko R. J. Seppänen
- , Kari K. Eklund
- , Jussi Taipale
- , Outi Kilpivaara
- & Lauri A. Aaltonen
Nature Communications 10 , 1–17

Rights & permissionsfor article Impact of constitutional <i>TET2</i> haploinsufficiency on molecular and clinical phenotype in humans . Opens in a new window.
Research | 14 August 2018 | 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
Molecular Psychiatry 25 , 1859–1875

Rights & permissionsfor article Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation . Opens in a new window.
Research | 11 July 2018
Molecular genetic overlap between migraine and major depressive disorder
- Yuanhao Yang
- , Huiying Zhao
- , Dorret I Boomsma
- , Lannie Ligthart
- , Andrea C. Belin
- , George Davey Smith
- , Tonu Esko
- , Tobias M. Freilinger
- , Thomas Folkmann Hansen
- , M. Arfan Ikram
- , Mikko Kallela
- , Christian Kubisch
- , Christofidou Paraskevi
- , David P. Strachan
- , Maija Wessman
- , Padhraig Gormley
- , Verneri Anttila
- , Bendik S. Winsvold
- , Priit Palta
- , Tonu Esko
- , Tune H. Pers
- , Kai-How Farh
- , Ester Cuenca-Leon
- , Mikko Muona
- , Nicholas A. Furlotte
- , Tobias Kurth
- , Andres Ingason
- , George McMahon
- , Lannie Ligthart
- , Gisela M. Terwindt
- , Mikko Kallela
- , Tobias M. Freilinger
- , Caroline Ran
- , Scott G. Gordon
- , Anine H. Stam
- , Stacy Steinberg
- , Guntram Borck
- , Markku Koiranen
- , Lydia Quaye
- , Hieab H. H. Adams
- , Terho Lehtimäki
- , Antti-Pekka Sarin
- , Juho Wedenoja
- , David A. Hinds
- , Julie E. Buring
- , Markus Schürks
- , Paul M. Ridker
- , Maria Gudlaug Hrafnsdottir
- , Hreinn Stefansson
- , Susan M. Ring
- , Jouke-Jan Hottenga
- , Brenda W. J. H. Penninx
- , Markus Färkkilä
- , Ville Artto
- , Mari Kaunisto
- , Salli Vepsäläinen
- , Rainer Malik
- , Andrew C. Heath
- , Pamela A. F. Madden
- , Nicholas G. Martin
- , Grant W Montgomery
- , Mitja I Kurki
- , Mart Kals
- , Reedik Mägi
- , Kalle Pärn
- , Eija Hämäläinen
- , Hailiang Huang
- , Andrea E. Byrnes
- , Lude Franke
- , Jie Huang
- , Evie Stergiakouli
- , Phil H. Lee
- , Cynthia Sandor
- , Caleb Webber
- , Zameel Cader
- , Bertram Muller-Myhsok
- , Stefan Schreiber
- , Thomas Meitinger
- , Johan G. Eriksson
- , Veikko Salomaa
- , Kauko Heikkilä
- , Elizabeth Loehrer
- , Andre G. Uitterlinden
- , Albert Hofman
- , Cornelia M. van Duijn
- , Lynn Cherkas
- , Linda M. Pedersen
- , Audun Stubhaug
- , Christopher S. Nielsen
- , Minna Männikkö
- , Evelin Mihailov
- , Lili Milani
- , Hartmut Göbel
- , Ann-Louise Esserlind
- , Anne Francke Christensen
- , Thomas Folkmann Hansen
- , Thomas Werge
- , Jaakko Kaprio
- , Arpo J. Aromaa
- , Olli Raitakari
- , M. Arfan Ikram
- , Tim Spector
- , Marjo-Riitta Järvelin
- , Andres Metspalu
- , Christian Kubisch
- , David P. Strachan
- , Michel D. Ferrari
- , Andrea C. Belin
- , Martin Dichgans
- , Maija Wessman
- , Arn M. J. M. van den Maagdenberg
- , John-Anker Zwart
- , Dorret I. Boomsma
- , George Davey Smith
- , Kari Stefansson
- , Nicholas Eriksson
- , Mark J. Daly
- , Benjamin M. Neale
- , Jes Olesen
- , Daniel I. Chasman
- , Dale R. Nyholt
- , Aarno Palotie
- , Arn M. J. M. van den Maagdenberg
- , Gisela M. Terwindt
- & Dale R. Nyholt
European Journal of Human Genetics 26 , 1202–1216

Rights & permissionsfor article Molecular genetic overlap between migraine and major depressive disorder . Opens in a new window.
Research | 9 August 2016 | Open
A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
- Manuel A. Rivas
- , Daniel Graham
- , Patrick Sulem
- , Christine Stevens
- , A. Nicole Desch
- , Philippe Goyette
- , Daniel Gudbjartsson
- , Ingileif Jonsdottir
- , Unnur Thorsteinsdottir
- , Frauke Degenhardt
- , Sören Mucha
- , Mitja I. Kurki
- , Dalin Li
- , Mauro D’Amato
- , Vito Annese
- , Severine Vermeire
- , Rinse K. Weersma
- , Jonas Halfvarson
- , Paulina Paavola-Sakki
- , Maarit Lappalainen
- , Monkol Lek
- , Beryl Cummings
- , Taru Tukiainen
- , Talin Haritunians
- , Leena Halme
- , Lotta L. E. Koskinen
- , Ashwin N. Ananthakrishnan
- , Yang Luo
- , Graham A. Heap
- , Marijn C. Visschedijk
- , J. Barrett
- , K. de Lange
- , C. Edwards
- , A. Hart
- , C. Hawkey
- , L. Jostins
- , N. Kennedy
- , C. Lamb
- , J. Lee
- , C. Lees
- , J. Mansfield
- , C. Mathew
- , C. Mowatt
- , W. Newman
- , E. Nimmo
- , M. Parkes
- , M. Pollard
- , N. Prescott
- , J. Randall
- , D. Rice
- , J. Satsangi
- , A. Simmons
- , M. Tremelling
- , H. Uhlig
- , D. Wilson
- , C. Abraham
- , J.P. Achkar
- , A. Bitton
- , G. Boucher
- , K. Croitoru
- , P. Fleshner
- , J. Glas
- , S. Kugathasan
- , J. V. Limbergen
- , R. Milgrom
- , D. Proctor
- , M. Regueiro
- , P. L. Schumm
- , Y. Sharma
- , J. M. Stempak
- , S. R. Targan
- , M. H. Wang
- , Daniel G. MacArthur
- , Benjamin M. Neale
- , Tariq Ahmad
- , Carl A. Anderson
- , Steven R. Brant
- , Richard H. Duerr
- , Mark S. Silverberg
- , Judy H Cho
- , Aarno Palotie
- , Päivi Saavalainen
- , Kimmo Kontula
- , Martti Färkkilä
- , Dermot P. B. McGovern
- , Andre Franke
- , Kari Stefansson
- , John D. Rioux
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Research | 20 June 2016
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