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Research | 7 January 2021
Differences between germline genomes of monozygotic twins
Nature Genetics 53 , 27–34

Rights & permissionsfor article Differences between germline genomes of monozygotic twins . Opens in a new window.
Amendments and Corrections | 24 May 2019 | Open
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
Nature Communications 10 , 1–2

Rights & permissionsfor article Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures . Opens in a new window.
Amendments and Corrections | 20 September 2018
Author Correction: The rate of meiotic gene conversion varies by sex and age
Nature Genetics 50 , 1616–1616

Rights & permissionsfor article Author Correction: The rate of meiotic gene conversion varies by sex and age . Opens in a new window.
Research | 21 September 2017 | Open
Whole genome characterization of sequence diversity of 15,220 Icelanders
Scientific Data 4 , 1–9

Rights & permissionsfor article Whole genome characterization of sequence diversity of 15,220 Icelanders . Opens in a new window.
Research | 25 March 2015 | Open
Sequence variants from whole genome sequencing a large group of Icelanders
Scientific Data 2 , 1–11

Rights & permissionsfor article Sequence variants from whole genome sequencing a large group of Icelanders . Opens in a new window.
Research | 9 October 2011
Identification of low-frequency variants associated with gout and serum uric acid levels
- Patrick Sulem
- , Daniel F Gudbjartsson
- , G Bragi Walters
- , Hafdis T Helgadottir
- , Agnar Helgason
- , Sigurjon A Gudjonsson
- , Carlo Zanon
- , Soren Besenbacher
- , Gyda Bjornsdottir
- , Olafur T Magnusson
- , Gisli Magnusson
- , Eirikur Hjartarson
- , Jona Saemundsdottir
- , Arnaldur Gylfason
- , Adalbjorg Jonasdottir
- , Hilma Holm
- , Ari Karason
- , Thorunn Rafnar
- , Hreinn Stefansson
- , Ole A Andreassen
- , Jesper H Pedersen
- , Allan I Pack
- , Marieke C H de Visser
- , Lambertus A Kiemeney
- , Arni J Geirsson
- , Gudmundur I Eyjolfsson
- , Isleifur Olafsson
- , Augustine Kong
- , Gisli Masson
- , Helgi Jonsson
- , Unnur Thorsteinsdottir
- , Ingileif Jonsdottir
- & Kari Stefansson
Nature Genetics 43 , 1127–1130

Rights & permissionsfor article Identification of low-frequency variants associated with gout and serum uric acid levels . Opens in a new window.
Research | 27 October 2010
Fine-scale recombination rate differences between sexes, populations and individuals
Nature 467 , 1099–1103

Rights & permissionsfor article Fine-scale recombination rate differences between sexes, populations and individuals . Opens in a new window.
Research | 15 January 2006
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
Nature Genetics 38 , 320–323

Rights & permissionsfor article Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes . Opens in a new window.
Research | 20 January 2020 | Open
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
Nature Communications 11 , 1–11

Rights & permissionsfor article Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis . Opens in a new window.
Research | 3 May 2019 | Open
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
Nature Communications 10 , 1–13

Rights & permissionsfor article GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures . Opens in a new window.
Research | 5 November 2018
Multiple transmissions of de novo mutations in families
Nature Genetics 50 , 1674–1680

Rights & permissionsfor article Multiple transmissions of de novo mutations in families . Opens in a new window.
Research | 19 June 2017
Identification of sequence variants influencing immunoglobulin levels
Nature Genetics 49 , 1182–1191

Rights & permissionsfor article Identification of sequence variants influencing immunoglobulin levels . Opens in a new window.
Research | 20 September 2017
Parental influence on human germline de novo mutations in 1,548 trios from Iceland
Nature 549 , 519–522

Rights & permissionsfor article Parental influence on human germline de novo mutations in 1,548 trios from Iceland . Opens in a new window.
Research | 1 February 2016
HLA class II sequence variants influence tuberculosis risk in populations of European ancestry
Nature Genetics 48 , 318–322

Rights & permissionsfor article HLA class II sequence variants influence tuberculosis risk in populations of European ancestry . Opens in a new window.
Research | 27 February 2017
Diversity in non-repetitive human sequences not found in the reference genome
Nature Genetics 49 , 588–593

Rights & permissionsfor article Diversity in non-repetitive human sequences not found in the reference genome . Opens in a new window.
Research | 19 September 2016
The rate of meiotic gene conversion varies by sex and age
Nature Genetics 48 , 1377–1384

Rights & permissionsfor article The rate of meiotic gene conversion varies by sex and age . Opens in a new window.
Research | 25 March 2015
Large-scale whole-genome sequencing of the Icelandic population
Nature Genetics 47 , 435–444

Rights & permissionsfor article Large-scale whole-genome sequencing of the Icelandic population . Opens in a new window.
Research | 22 June 2015
Loss-of-function variants in ATM confer risk of gastric cancer
Nature Genetics 47 , 906–910

Rights & permissionsfor article Loss-of-function variants in ATM confer risk of gastric cancer . Opens in a new window.
Research | 6 March 2011
A rare variant in MYH6 is associated with high risk of sick sinus syndrome
Nature Genetics 43 , 316–320

Rights & permissionsfor article A rare variant in MYH6 is associated with high risk of sick sinus syndrome . Opens in a new window.
Research | 17 August 2008
Detection of sharing by descent, long-range phasing and haplotype imputation
- Augustine Kong
- , Gisli Masson
- , Michael L Frigge
- , Arnaldur Gylfason
- , Pasha Zusmanovich
- , Gudmar Thorleifsson
- , Pall I Olason
- , Andres Ingason
- , Stacy Steinberg
- , Thorunn Rafnar
- , Patrick Sulem
- , Magali Mouy
- , Frosti Jonsson
- , Unnur Thorsteinsdottir
- , Daniel F Gudbjartsson
- , Hreinn Stefansson
- & Kari Stefansson
Nature Genetics 40 , 1068–1075

Rights & permissionsfor article Detection of sharing by descent, long-range phasing and haplotype imputation . Opens in a new window.
Research | 7 May 2006
A common variant associated with prostate cancer in European and African populations
Nature Genetics 38 , 652–658

Rights & permissionsfor article A common variant associated with prostate cancer in European and African populations . Opens in a new window.
Research | 17 December 2009
Parental origin of sequence variants associated with complex diseases
- Augustine Kong
- , Valgerdur Steinthorsdottir
- , Gisli Masson
- , Gudmar Thorleifsson
- , Patrick Sulem
- , Soren Besenbacher
- , Aslaug Jonasdottir
- , Asgeir Sigurdsson
- , Kari Th. Kristinsson
- , Adalbjorg Jonasdottir
- , Michael L. Frigge
- , Arnaldur Gylfason
- , Pall I. Olason
- , Sigurjon A. Gudjonsson
- , Sverrir Sverrisson
- , Simon N. Stacey
- , Bardur Sigurgeirsson
- , Kristrun R. Benediktsdottir
- , Helgi Sigurdsson
- , Thorvaldur Jonsson
- , Rafn Benediktsson
- , Jon H. Olafsson
- , Oskar Th. Johannsson
- , Astradur B. Hreidarsson
- , Gunnar Sigurdsson
- , Benjamin F. Voight
- , Laura J. Scott
- , Valgerdur Steinthorsdottir
- , Christian Dina
- , Eleftheria Zeggini
- , Cornelia Huth
- , Yurii S. Aulchenko
- , Ryan P. Welch
- , Gudmar Thorleifsson
- , Laura J. McCulloch
- , Teresa Ferreira
- , Harald Grallert
- , Najaf Amin
- , Guanming Wu
- , Cristen J. Willer
- , Soumya Raychaudhuri
- , Shaun Purcell
- , Steve A. McCarroll
- , Claudia Langenberg
- , Oliver M. Hoffmann
- , Josée Dupuis
- , Lu Qi
- , Ayellet V. Segrè
- , Mandy van Hoek
- , Pau Navarro
- , Kristin Ardlie
- , Beverley Balkau
- , Rafn Benediktsson
- , Amanda J. Bennett
- , Roza Blagieva
- , Eric Boerwinkle
- , Lori L. Bonnycastle
- , Kristina Bengtsson Boström
- , Bert Bravenboer
- , Suzannah Bumpstead
- , Noël P. Burtt
- , Guillaume Charpentier
- , Peter S. Chines
- , Marilyn Cornelis
- , David J. Couper
- , Gabe Crawford
- , Alex S. F. Doney
- , Katherine S. Elliott
- , Amanda L. Elliott
- , Michael R. Erdos
- , Caroline S. Fox
- , Christopher S. Franklin
- , Martha Ganser
- , Christian Gieger
- , Niels Grarup
- , Todd Green
- , Simon Griffin
- , Christopher J. Groves
- , Candace Guiducci
- , Samy Hadjadj
- , Neelam Hassanali
- , Christian Herder
- , Bo Isomaa
- , Anne U. Jackson
- , Paul R. V. Johnson
- , Torben Jørgensen
- , Wen H. L. Kao
- , Norman Klopp
- , Augustine Kong
- , Peter Kraft
- , Johanna Kuusisto
- , Torsten Lauritzen
- , Man Li
- , Alouisius Lieverse
- , Cecilia M. Lindgren
- , Valeriya Lyssenko
- , Michel Marre
- , Thomas Meitinger
- , Kristian Midthjell
- , Mario A Morken
- , Narisu Narisu
- , Peter Nilsson
- , Katharine R. Owen
- , Felicity Payne
- , John R. B. Perry
- , Ann-Kristin Petersen
- , Carl Platou
- , Christine Proença
- , Inga Prokopenko
- , Wolfgang Rathmann
- , N. William Rayner
- , Neil R. Robertson
- , Ghislain Rocheleau
- , Michael Roden
- , Michael J. Sampson
- , Richa Saxena
- , Beverley M. Shields
- , Peter Shrader
- , Gunnar Sigurdsson
- , Nicholas Smith
- , Thomas Sparsø
- , Klaus Strassburger
- , Heather M. Stringham
- , Qi Sun
- , Amy J. Swift
- , Barbara Thorand
- , Jean Tichet
- , Tiinamaija Tuomi
- , Rob van Dam
- , Thijs van Herpt
- , G. Bragi Walters
- , Michael N. Weedon
- , Jacqueline Witteman
- , Richard N. Bergman
- , Stephane Cauchi
- , Francis S. Collins
- , Anna L. Gloyn
- , Ulf Gyllensten
- , Torben Hansen
- , Winston A. Hide
- , Graham A. Hitman
- , Albert Hofman
- , David Hunter
- , Kristian Hveem
- , Markku Laakso
- , Karen L. Mohlke
- , Andrew D. Morris
- , Colin N. A. Palmer
- , Peter P. Pramstaller
- , Igor Rudan
- , Eric Sijbrands
- , Lincoln D. Stein
- , Jaakko Tuomilehto
- , Andre Uitterlinden
- , Mark Walker
- , Nicholas J. Wareham
- , Richard M. Watanabe
- , Goncalo R. Abecasis
- , Inês Barroso
- , Bernhard O. Boehm
- , Harry Campbell
- , Mark J. Daly
- , Jose C. Florez
- , Timothy M. Frayling
- , Leif Groop
- , Andrew T. Hattersley
- , Frank B. Hu
- , James B. Meigs
- , Andrew P. Morris
- , James S. Pankow
- , Oluf Pedersen
- , Rob Sladek
- , Unnur Thorsteinsdottir
- , H.-Erich Wichmann
- , James F. Wilson
- , Thomas Illig
- , Philippe Froguel
- , Cornelia M. van Duijn
- , Kari Stefansson
- , David Altshuler
- , Michael Boehnke
- , Mark I. McCarthy.
- , Anne C. Ferguson-Smith
- , Daniel F. Gudbjartsson
- , Unnur Thorsteinsdottir
- & Kari Stefansson
Nature 462 , 868–874

Rights & permissionsfor article Parental origin of sequence variants associated with complex diseases . Opens in a new window.
Research | 6 April 2008
Many sequence variants affecting diversity of adult human height
Nature Genetics 40 , 609–615

Rights & permissionsfor article Many sequence variants affecting diversity of adult human height . Opens in a new window.
Research | 20 September 2009
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
- Julius Gudmundsson
- , Patrick Sulem
- , Daniel F Gudbjartsson
- , Thorarinn Blondal
- , Arnaldur Gylfason
- , Bjarni A Agnarsson
- , Kristrun R Benediktsdottir
- , Droplaug N Magnusdottir
- , Gudbjorg Orlygsdottir
- , Margret Jakobsdottir
- , Simon N Stacey
- , Asgeir Sigurdsson
- , Tiina Wahlfors
- , Teuvo Tammela
- , Joan P Breyer
- , Kate M McReynolds
- , Kevin M Bradley
- , Berta Saez
- , Javier Godino
- , Sebastian Navarrete
- , Fernando Fuertes
- , Laura Murillo
- , Eduardo Polo
- , Katja K Aben
- , Inge M van Oort
- , Brian K Suarez
- , Brian T Helfand
- , Donghui Kan
- , Carlo Zanon
- , Michael L Frigge
- , Kristleifur Kristjansson
- , Jeffrey R Gulcher
- , Gudmundur V Einarsson
- , Eirikur Jonsson
- , William J Catalona
- , Jose I Mayordomo
- , Lambertus A Kiemeney
- , Jeffrey R Smith
- , Johanna Schleutker
- , Rosa B Barkardottir
- , Augustine Kong
- , Unnur Thorsteinsdottir
- , Thorunn Rafnar
- & Kari Stefansson
Nature Genetics 41 , 1122–1126

Rights & permissionsfor article Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility . Opens in a new window.
Research | 11 September 2008
Large recurrent microdeletions associated with schizophrenia
- Hreinn Stefansson
- , Dan Rujescu
- , Sven Cichon
- , Olli P. H. Pietiläinen
- , Andres Ingason
- , Stacy Steinberg
- , Ragnheidur Fossdal
- , Engilbert Sigurdsson
- , Thordur Sigmundsson
- , Jacobine E. Buizer-Voskamp
- , Thomas Hansen
- , Klaus D. Jakobsen
- , Pierandrea Muglia
- , Clyde Francks
- , Paul M. Matthews
- , Arnaldur Gylfason
- , Bjarni V. Halldorsson
- , Daniel Gudbjartsson
- , Thorgeir E. Thorgeirsson
- , Asgeir Sigurdsson
- , Adalbjorg Jonasdottir
- , Aslaug Jonasdottir
- , Asgeir Bjornsson
- , Sigurborg Mattiasdottir
- , Thorarinn Blondal
- , Magnus Haraldsson
- , Brynja B. Magnusdottir
- , Ina Giegling
- , Hans-Jürgen Möller
- , Annette Hartmann
- , Kevin V. Shianna
- , Dongliang Ge
- , Anna C. Need
- , Caroline Crombie
- , Gillian Fraser
- , Nicholas Walker
- , Jouko Lonnqvist
- , Jaana Suvisaari
- , Annamarie Tuulio-Henriksson
- , Tiina Paunio
- , Timi Toulopoulou
- , Elvira Bramon
- , Marta Di Forti
- , Robin Murray
- , Mirella Ruggeri
- , Evangelos Vassos
- , Sarah Tosato
- , Muriel Walshe
- , Tao Li
- , Catalina Vasilescu
- , Thomas W. Mühleisen
- , August G. Wang
- , Henrik Ullum
- , Srdjan Djurovic
- , Ingrid Melle
- , Jes Olesen
- , Lambertus A. Kiemeney
- , Barbara Franke
- , René S. Kahn
- , Don H. Linszen
- , Jim van Os
- , Durk Wiersma
- , Richard Bruggeman
- , Wiepke Cahn
- , Lieuwe de Haan
- , Lydia Krabbendam
- , Inez Myin-Germeys
- , Chiara Sabatti
- , Nelson B. Freimer
- , Jeffrey R. Gulcher
- , Unnur Thorsteinsdottir
- , Augustine Kong
- , Ole A. Andreassen
- , Roel A. Ophoff
- , Alexander Georgi
- , Marcella Rietschel
- , Thomas Werge
- , Hannes Petursson
- , David B. Goldstein
- , Markus M. Nöthen
- , Leena Peltonen
- , David A. Collier
- , David St Clair
- & Kari Stefansson
Nature 455 , 232–236

Rights & permissionsfor article Large recurrent microdeletions associated with schizophrenia . Opens in a new window.
Research | 2 October 2011
Mutations in BRIP1 confer high risk of ovarian cancer
Nature Genetics 43 , 1104–1107

Rights & permissionsfor article Mutations in BRIP1 confer high risk of ovarian cancer . Opens in a new window.
Research | 16 January 2005
A common inversion under selection in Europeans
Nature Genetics 37 , 129–137

Rights & permissionsfor article A common inversion under selection in Europeans . Opens in a new window.

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Differences between germline genomes of monozygotic twins

Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

Author Correction: The rate of meiotic gene conversion varies by sex and age

Whole genome characterization of sequence diversity of 15,220 Icelanders

Sequence variants from whole genome sequencing a large group of Icelanders

Identification of low-frequency variants associated with gout and serum uric acid levels

Fine-scale recombination rate differences between sexes, populations and individuals

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis

GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

Multiple transmissions of de novo mutations in families

Identification of sequence variants influencing immunoglobulin levels

Parental influence on human germline de novo mutations in 1,548 trios from Iceland

HLA class II sequence variants influence tuberculosis risk in populations of European ancestry

Diversity in non-repetitive human sequences not found in the reference genome

The rate of meiotic gene conversion varies by sex and age

Large-scale whole-genome sequencing of the Icelandic population

Loss-of-function variants in ATM confer risk of gastric cancer

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

Detection of sharing by descent, long-range phasing and haplotype imputation

A common variant associated with prostate cancer in European and African populations

Parental origin of sequence variants associated with complex diseases

Many sequence variants affecting diversity of adult human height

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility

Large recurrent microdeletions associated with schizophrenia

Mutations in BRIP1 confer high risk of ovarian cancer

A common inversion under selection in Europeans

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