A. Kong

发表

Large recurrent microdeletions associated with schizophrenia

Thomas W. Mühleisen, Bjarni V. Halldórsson, P. Matthews, 2008, Nature.

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

D. Postma, I. Hall, H. Stefánsson, 2009, Nature Genetics.

Finding the missing heritability of complex

Judy H. Cho, M. McCarthy, A. Kong, 2009 .

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24

D. Gudbjartsson, A. Sigurdsson, T. Blondal, 2007, Nature Genetics.

Large-scale whole-genome sequencing of the Icelandic population

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2015, Nature Genetics.

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

Kevin M. Bradley, D. Gudbjartsson, A. Sigurdsson, 2008, Nature Genetics.

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

H. Stefánsson, A. Gylfason, J. Gulcher, 2006, Nature Genetics.

Common variants conferring risk of schizophrenia

Pall I. Olason, P. Matthews, H. Stefánsson, 2009, Nature.

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

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2017, Nature.

The Y-chromosome point mutation rate in humans

Valdis B. Guðmundsdóttir, A. Kong, K. Stefánsson, 2015, Nature Genetics.

Genetics of gene expression and its effect on disease

H. Stefánsson, R. Fossdal, D. Gudbjartsson, 2008, Nature.

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Ayellet V. Segrè, 2012, Nature Genetics.

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

A. Hofman, H. Stefánsson, A. Ingason, 2015, Nature Neuroscience.

Finding the missing heritability of complex diseases

Judy H. Cho, A. Whittemore, M. McCarthy, 2009, Nature.

Mapping cis- and trans-regulatory effects across multiple tissues in twins

Simon C. Potter, T. Spector, J. Bell, 2012, Nature Genetics.

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Ayellet V. Segrè, C. Gieger, W. Rathmann, 2010, Nature Genetics.

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

H. Stefánsson, D. Rujescu, S. Cichon, 2011, Human molecular genetics.

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer

D. Gudbjartsson, L. Kiemeney, J. Gulcher, 2007, Nature Genetics.

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

A. Sigurdsson, L. Kiemeney, J. Gulcher, 2008, Nature Genetics.

A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

Ole A. Andreassen, Daniel F. Gudbjartsson, Erik G. Jönsson, 2012, Nature.

Neuregulin 1 and susceptibility to schizophrenia.

H. Stefánsson, A. Ingason, E. Sigurdsson, 2002, American journal of human genetics.

Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

Ellen Kampman, Kari Stefansson, Torben Hansen, 2009, Nature Genetics.

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

Gerard Tromp, Helena Kuivaniemi, Kari Stefansson, 2010, Nature Genetics.

The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland

Ole A. Andreassen, Alkes L. Price, Kari Stefansson, 2009, PLoS genetics.

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

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2010, Nature.

Two newly identified genetic determinants of pigmentation in Europeans

Snæbjörn Pálsson, Kari Stefansson, Gudmar Thorleifsson, 2008, Nature Genetics.

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

M. McCarthy, E. Zeggini, J. Marchini, 2008, Nature Genetics.

Many sequence variants affecting diversity of adult human height

Bjarni V. Halldórsson, H. Stefánsson, A. Ingason, 2008, Nature Genetics.

A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2007, Science.

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

Kari Stefansson, Johan Hansson, Rafael Botella-Estrada, 2008, Nature Genetics.

Single-Tissue and Cross-Tissue Heritability of Gene Expression Via Identity-by-Descent in Related or Unrelated Individuals

Alkes L. Price, Kari Stefansson, Gudmar Thorleifsson, 2011, PLoS genetics.

Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.

Paolo Vineis, Simonetta Guarrera, Giuseppe Matullo, 2014, Human molecular genetics.

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

Tanya M. Teslovich, Andrew D. Johnson, Kyle J. Gaulton, 2017, Diabetes.

Variants conferring risk of atrial fibrillation on chromosome 4q25

Eric E. Smith, D. Gudbjartsson, A. Sigurdsson, 2007, Nature.

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.

Kari Stefansson, Florian Zink, Gisli Masson, 2017, Blood.

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

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2006, Nature Genetics.

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

Pall I. Olason, H. Stefánsson, A. Ingason, 2008, Nature Genetics.

Missing heritability and strategies for finding the underlying causes of complex disease

Jason H. Moore, E. Eichler, A. Kong, 2010, Nature Reviews Genetics.

Genome-wide association study identifies 74 loci associated with educational attainment

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2016, Nature.

Mapping of a familial essential tremor gene, FET1, to chromosome 3q13

H. Stefánsson, J. Gulcher, A. Kong, 1997, Nature Genetics.

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

J. Gulcher, U. Thorsteinsdóttir, A. Kong, 2007, Nature Genetics.

A high-resolution recombination map of the human genome

D. Gudbjartsson, T. Thorgeirsson, J. Gulcher, 2002, Nature Genetics.

A common inversion under selection in Europeans

H. Stefánsson, A. Ingason, A. Gylfason, 2005, Nature Genetics.

Identification of a large set of rare complete human knockouts

H. Stefánsson, D. Gudbjartsson, A. Sigurdsson, 2015, Nature Genetics.

Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes

D. Gudbjartsson, A. Sigurdsson, T. Blondal, 2007, Nature Genetics.

Deconstructing the sources of genotype-phenotype associations in humans

A. Kong, M. Przeworski, A. I. Young, 2019, Science.

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Tanya M. Teslovich, Andrew D. Johnson, Kyle J. Gaulton, 2014, Nature Genetics.

Variant of TREM2 associated with the risk of Alzheimer's disease.

A. Hofman, H. Stefánsson, D. Rujescu, 2013, The New England journal of medicine.

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

N. Eriksson, M. Nalls, C. Gieger, 2016 .

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Tanya M. Teslovich, Ross M. Fraser, May E. Montasser, 2012, Nature Genetics.

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2019, Nature Genetics.

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

Thomas W. Mühleisen, Benjamin J. Wright, C. Gieger, 2011, Nature Genetics.

Selection against variants in the genome associated with educational attainment

H. Stefánsson, D. Gudbjartsson, U. Thorsteinsdóttir, 2017, Proceedings of the National Academy of Sciences.

Familial risk of lung carcinoma in the Icelandic population.

D. Gudbjartsson, J. Gulcher, U. Thorsteinsdóttir, 2004, JAMA.

Twenty bone mineral density loci identified by large-scale meta-analysis of genome-wide association studies

Yurii S. Aulchenko, Nicole Soranzo, Panagiotis Deloukas, 2009, Nature Genetics.

Recombination rate and reproductive success in humans

D. Gudbjartsson, T. Thorgeirsson, J. Gulcher, 2004, Nature Genetics.

Sequence variants from whole genome sequencing a large group of Icelanders

Kari Stefansson, Bjarni V Halldorsson, Florian Zink, 2015, Scientific Data.

Edinburgh Research Explorer Genome-wide association scan meta-analysis identifies three loci influencing adiposity and fat distribution

Laura J. Scott, Christian Gieger, Yurii S. Aulchenko, 2022 .

Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2013, PLoS genetics.

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

Tony Fletcher, Paolo Vineis, Simonetta Guarrera, 2008, Nature Genetics.

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

Kari Stefansson, Brian T Helfand, William J Catalona, 2009, Nature Genetics.

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

Dan M Roden, Kari Stefansson, Gudmar Thorleifsson, 2011, Nature Genetics.

CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD

Jian Ge, Paul S. Bernstein, Kari Stefansson, 2005, PLoS medicine.

Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans

Nancy J. Cox, Dan L. Nicolae, Graeme I. Bell, 1999, Nature Genetics.

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Thomas Meitinger, Pierre Fontanillas, Stefan Johansson, 2014, Nature Genetics.

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

Kari Stefansson, Brian T Helfand, Gudmar Thorleifsson, 2012, Nature Genetics.

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

Daniel F. Gudbjartsson, Kari Stefansson, Gudmar Thorleifsson, 2008, Nature.

A common variant on chromosome 9p21 affects the risk of myocardial infarction.

Kari Stefansson, Arshed A Quyyumi, Anna Helgadottir, 2007, Science.

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction

Vilmundur Gudnason, Kari Stefansson, Arshed A Quyyumi, 2006, Nature Genetics.

Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Christian Gieger, Jason Carey, Steven Wiltshire, 2016 .

Weighting sequence variants based on their annotation increases power of whole-genome association studies

Anders Albrechtsen, Kari Stefansson, Florian Zink, 2016, Nature Genetics.

Genome-wide association study yields variants at 20 p 12 . 2 that associate with urinary bladder cancer

Katja, Gerald, Anne, 2014 .

The genealogic approach to human genetics of disease.

A. Kong, K. Stefánsson, A Kong, 2001, Cancer journal.

A major susceptibility gene for asthma maps to chromosome 14q24.

J. Gulcher, A. Kong, K. Stefánsson, 2002, American journal of human genetics.

Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2

J. Gulcher, A. Kong, K. Stefánsson, 2003, PLoS biology.

Identification of an imprinted master trans-regulator at the KLF14 locus related to multiple metabolic phenotypes

Mark I. McCarthy, Kourosh R. Ahmadi, Nicole Soranzo, 2011, Nature Genetics.

Genomewide scan for hand osteoarthritis: a novel mutation in matrilin-3.

J. Gulcher, A. Kong, K. Stefánsson, 2003, American journal of human genetics.

The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland

J. Gulcher, U. Thorsteinsdóttir, A. Kong, 2006, PLoS medicine.

Cancer as a Complex Phenotype: Pattern of Cancer Distribution within and beyond the Nuclear Family

D. Gudbjartsson, J. Gulcher, U. Thorsteinsdóttir, 2004, PLoS medicine.

Familial predisposition and cosegregation analysis of adult obstructive sleep apnea and the sudden infant death syndrome.

J. Gulcher, A. Kong, K. Stefánsson, 2002, American journal of respiratory and critical care medicine.

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2017, Nature Communications.

Reconstructing an African haploid genome from the 18th century

Valdis B. Guðmundsdóttir, A. Kong, K. Stefánsson, 2018, Nature Genetics.

Anxiety with panic disorder linked to chromosome 9q in Iceland.

T. Thorgeirsson, J. Gulcher, A. Kong, 2003, American journal of human genetics.

Genetic factors contribute to the risk of developing endometriosis.

H. Stefánsson, A. Kong, K. Stefánsson, 2002, Human reproduction.

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2009, Nature Genetics.

Family Analysis with Mendelian Imputations

A. Kong, A. I. Young, S. Benonisdottir, 2020, bioRxiv.

Linkage of Essential Hypertension to Chromosome 18q

J. Gulcher, A. Kong, K. Stefánsson, 2002, Hypertension.

European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2010, PloS one.

Title European bone mineral density loci are also associated withBMD in East-Asian populations

Seung, B. Halldórsson, D. Gudbjartsson, 2010 .

Multiple genetic loci for bone mineral density and fractures.

Kari Stefansson, Claus Christiansen, Bjarni V Halldorsson, 2008, The New England journal of medicine.

A common variant at 8q24.21 is associated with renal cell cancer

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2013, Nature Communications.

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

J. Gulcher, U. Thorsteinsdóttir, A. Kong, 2007, Nature Genetics.

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

H. Stefánsson, S. Steinberg, J. Gulcher, 2009, Nature Genetics.

Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms

Bernhard Horsthemke, Bernward Klocke, Melina Claussnitzer, 2014, Cell.

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution

Laura J. Scott, Christian Gieger, Yurii S. Aulchenko, 2009, PLoS Genetics.

Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease

H. Stefánsson, D. Rujescu, A. Ingason, 2015, Nature Genetics.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Christian Gieger, Alex Doney, Inês Barroso, 2010, Nature Genetics.

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116))

Marc S. Orr, P. Elliott, L. Coin, 2010 .

Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2016, Human molecular genetics.

Rate of de novo mutations and the importance of father’s age to disease risk

S. Steinberg, D. Gudbjartsson, A. Sigurdsson, 2012, Nature.

Severe osteoarthritis of the hand associates with markers within the ALDH1A2 gene and with very rare variants at 1p31

T. Spector, A. Sigurdsson, Á. Jónasdóttir, 2017 .

Allegro, a new computer program for multipoint linkage analysis

Daniel F. Gudbjartsson, Kristjan Jonasson, Michael L. Frigge, 2000, Nature genetics.

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2018, Nature Genetics.

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

Daniel F. Gudbjartsson, Michael L. Frigge, Kari Stefansson, 2013, Nature.

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population.

H. Stefánsson, A. Ingason, C. Crombie, 2003, American journal of human genetics.

Multi-nucleotide de novo Mutations in Humans

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2016, PLoS genetics.

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

H. Stefánsson, J. Gulcher, U. Thorsteinsdóttir, 2008, Nature Genetics.

New sequence variants associated with bone mineral density

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2009, Nature Genetics.

Physical and neurobehavioral determinants of reproductive onset and success

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016, Nature Genetics.

The nature of nurture: Effects of parental genotypes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2017, Science.

Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease

Simon C. Potter, Thomas W. Mühleisen, Benjamin J. Wright, 2011, PLoS genetics.

A sequence variant on 17q21 is associated with age at onset and severity of asthma

D. Postma, I. Hall, D. Gudbjartsson, 2010, European Journal of Human Genetics.

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke

C. Gieger, D. Gudbjartsson, J. Gulcher, 2008, Annals of neurology.

Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor

H. Stefánsson, S. Steinberg, J. Gulcher, 2009, Nature Genetics.

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

D. Gudbjartsson, A. Sigurdsson, Á. Jónasdóttir, 2008, Nature Genetics.

Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

Daniel F. Gudbjartsson, Kari Stefansson, Runolfur Palsson, 2010, PLoS genetics.

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

Paolo Vineis, Simonetta Guarrera, Giuseppe Matullo, 2010, Nature Genetics.

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

Paolo Vineis, Giuseppe Matullo, Kari Stefansson, 2009, Nature Genetics.

A direct characterization of human mutation based on microsatellites

Swapan Mallick, Heng Li, Kari Stefansson, 2012, Nature Genetics.

Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma

Kari Stefansson, Gudmar Thorleifsson, Hreinn Stefansson, 2007, Science.

Male-pattern baldness susceptibility locus at 20p11

T. Spector, P. Deloukas, H. Stefánsson, 2008, Nature Genetics.

Rate of de novo mutations, father’s age, and disease risk

S. Steinberg, D. Gudbjartsson, A. Sigurdsson, 2012, Nature.

Rare mutations associating with serum creatinine and chronic kidney disease.

Kari Stefansson, Runolfur Palsson, Aslaug Jonasdottir, 2014, Human molecular genetics.

Edinburgh Research Explorer Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Tom R. Gaunt, Andrew D. Johnson, Nicholette D. Palmer, 2022 .

Mutations in BRIP1 confer high risk of ovarian cancer

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2011, Nature Genetics.

Rate of de novo mutations and the importance of father’s age to disease risk

S. Steinberg, D. Gudbjartsson, A. Sigurdsson, 2012, Nature.

Multiple transmissions of de novo mutations in families

Hannes P. Eggertsson, A. Gylfason, B. Halldórsson, 2018, Nature Genetics.

Recurrence of de novo mutations in families

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2017, bioRxiv.

Whole genome characterization of sequence diversity of 15,220 Icelanders

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2017, Scientific Data.

Reproductive fitness and genetic risk of psychiatric disorders in the general population

H. Stefánsson, A. Ingason, E. Sigurdsson, 2017, Nature Communications.

The rate of meiotic gene conversion varies by sex and age

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2016, Nature Genetics.

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

H. Stefánsson, A. Gylfason, D. Gudbjartsson, 2011, Nature Genetics.

Variants in MTNR1B influence fasting glucose levels

Inês Barroso, Paul Scheet, Nicole Soranzo, 2009, Nature Genetics.

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

C. Gieger, D. Gudbjartsson, J. Gulcher, 2009, Nature Genetics.

Corrigendum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

T. Spector, M. McCarthy, P. Deloukas, 2011, Nature Genetics.

Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate

Kari Stefansson, Gudmar Thorleifsson, Hreinn Stefansson, 2008, Science.

Truncating mutations in RBM12 are associated with psychosis

H. Stefánsson, S. Steinberg, E. Sigurdsson, 2017, Nature Genetics.

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

D. Gudbjartsson, Á. Jónasdóttir, L. Kiemeney, 2009, Nature Genetics.

Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31

Kari Stefansson, Evangelos Evangelou, Fernando Rivadeneira, 2014, Nature Genetics.

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

J. Gulcher, U. Thorsteinsdóttir, A. Kong, 2004, Nature Genetics.

Reply to “A call for accurate phenotype definition in the study of complex disorders”

J. Gulcher, A. Kong, K. Stefánsson, 2004, Nature Genetics.

Localization of a gene for migraine without aura to chromosome 4q21.

J. Gulcher, A. Kong, K. Stefánsson, 2003, American journal of human genetics.

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke

Mark Gurney, Vilmundur Gudnason, Kari Stefansson, 2003, Nature Genetics.

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

J. Gulcher, A. Kong, K. Stefánsson, 2003, American journal of human genetics.

A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting.

D. Gudbjartsson, J. Gulcher, A. Kong, 2003, American journal of human genetics.

Localization of a gene for peripheral arterial occlusive disease to chromosome 1p31.

J. Gulcher, A. Kong, K. Stefánsson, 2002, American journal of human genetics.

Localization of a susceptibility gene for common forms of stroke to 5q12.

Vilmundur Gudnason, Kari Stefansson, Klaus Lindpaintner, 2002, American journal of human genetics.

Allelic frequencies and patterns of single-nucleotide polymorphisms in candidate genes for asthma and atopy in Iceland.

J. Gulcher, A. Kong, K. Stefánsson, 2001, American journal of respiratory and critical care medicine.

The role of linkage studies for common diseases.

A. Kong, K. Stefánsson, J. Gulcher, 2001, Current opinion in genetics & development.

Common and low-frequency variants associated with genome-wide recombination rate

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2013, Nature Genetics.

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

H. Stefánsson, A. Sigurdsson, A. Jonasdottir, 2010, Nature Genetics.

Several common variants modulate heart rate, PR interval and QRS duration

Kari Stefansson, Gudmar Thorleifsson, Aslaug Jonasdottir, 2010, Nature Genetics.

The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts

Xiaofeng Zhu, Thomas Meitinger, Christoph Lange, 2007, PLoS genetics.

The genetic spectrum of a population-based sample of familial hemiplegic migraine.

H. Stefánsson, A. Bjornsson, J. Olesen, 2007, Brain : a journal of neurology.

New basal cell carcinoma susceptibility loci

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2015, Nature Communications.

Sequence variant at 8 q 24 . 21 associates with sciatica caused by lumbar disc herniation

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2017 .

Common variant at 16p11.2 conferring risk of psychosis

M. Pirinen, H. Stefánsson, D. Rujescu, 2014, Molecular Psychiatry.

Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial.

D. Gudbjartsson, J. Gulcher, A. Kong, 2005, JAMA.

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

Kari Stefansson, Torben Hansen, Niels Grarup, 2014, Nature Genetics.

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

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2016, Nature Genetics.

Parental origin of sequence variants associated with complex diseases

Daniel F. Gudbjartsson, Michael L. Frigge, Kari Stefansson, 2009, Nature.

NPGRJ_NG_122 609..615

H. Stefánsson, A. Ingason, S. Steinberg, 2008 .

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.

D. Gudbjartsson, T. Thorgeirsson, L. Kiemeney, 2011, Cancer research.

Inheritance of human longevity in Iceland

Kári Stefánsson, Jeffrey R Gulcher, D. Gudbjartsson, 2000, European Journal of Human Genetics.

A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2017, European heart journal.

A genome-wide scan for preeclampsia in the Netherlands

H. Stefánsson, J. Gulcher, A. Kong, 2001, European Journal of Human Genetics.

A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13.

H. Stefánsson, J. Gulcher, A. Kong, 1999, Human molecular genetics.

Expanding the range of ZNF804A variants conferring risk of psychosis

R A Ophoff, T Sigmundsson, Pall I. Olason, 2011, Molecular Psychiatry.

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

Kari Stefansson, Wei Li, Jon Hrafnkelsson, 2009, Nature Genetics.

A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration).

H. Stefánsson, R. Fossdal, J. Gulcher, 2004, Human molecular genetics.

Epigenetic and genetic components of height regulation

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016, Nature Communications.

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

Kari Stefansson, Brian T Helfand, Torben Hansen, 2011, Nature Genetics.

Support for involvement of the AHI1 locus in schizophrenia

H. Stefánsson, A. Ingason, S. Steinberg, 2007, European Journal of Human Genetics.

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

A Sigurdsson, G Masson, D. Gudbjartsson, 2014, Leukemia.

Estimating heritability without environmental bias

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2017, bioRxiv.

Mendelian imputation of parental genotypes for genome-wide estimation of direct and indirect genetic effects

A. Kong, D. Benjamin, D. Cesarini, 2020, bioRxiv.

Allegro version 2

Anna Ingolfsdottir, D. Gudbjartsson, A. Kong, 2005, Nature Genetics.

A sequence variant associating with educational attainment also affects childhood cognition

Bjarni V. Halldórsson, H. Stefánsson, D. Rujescu, 2016, Scientific Reports.

Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture

D. Kiel, A. Hofman, T. Spector, 2009, Annals of Internal Medicine.

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma

D. Gudbjartsson, Á. Jónasdóttir, U. Thorsteinsdóttir, 2014, Human molecular genetics.

New common variants affecting susceptibility to basal cell carcinoma

D. Gudbjartsson, A. Sigurdsson, T. Blondal, 2009, Nature Genetics.

Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

H. Stefánsson, D. Gudbjartsson, A. Sigurdsson, 2017, Nature genetics.

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

H. Stefánsson, D. Gudbjartsson, A. Sigurdsson, 2017, Nature Genetics.

A common variant at 8q24.21 is associated with renal cell cancer

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2013, Nature Communications.

Mutations in BRIP 1 / FANCJ confer high risk of ovarian cancer

Kari, Gisli, A. Gylfason, 2015 .

A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

Kari Stefansson, Kang Zhang, Gudmar Thorleifsson, 2013, Nature Genetics.

Discovery of common variants associated with low TSH levels and thyroid cancer risk

Kari Stefansson, Gudmar Thorleifsson, Jon Hrafnkelsson, 2012, Nature Genetics.

Familial aggregation of Parkinson's disease in Iceland.

A A Hicks, J. Gulcher, A. Kong, 2000, The New England journal of medicine.

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

Paolo Vineis, Abbas Ghaderi, Simonetta Guarrera, 2011, Human molecular genetics.

A susceptibility gene for late‐onset idiopathic Parkinson's disease

Hreinn Stefánsson, Kári Stefánsson, Jeffrey R Gulcher, 2002, Annals of neurology.

Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2010, Science Translational Medicine.

CDKN2A mutations and melanoma risk in the Icelandic population

J. Gulcher, U. Thorsteinsdóttir, A. Kong, 2008, Journal of Medical Genetics.

A genetic risk factor for periodic limb movements in sleep.

Kari Stefansson, Alex Iranzo, Hreinn Stefansson, 2007, The New England journal of medicine.

Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

S. Steinberg, D. Gudbjartsson, L. Kiemeney, 2008, Nature Genetics.

Erratum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (Nature Genetics (2011) 43 (561-564))

Mark I. McCarthy, Kourosh R. Ahmadi, Nicole Soranzo, 2011 .

Correction: Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2010, PLoS Genetics.

Twenty loci associated with bone mineral density identified by large-scale meta-analysis of genome-wide association datasets

John P. A. Ioannidis, Nicole Soranzo, Panagiotis Deloukas, 2009 .

Diabetes, dependence, asymptotics, selection and significance

M. Daly, E. Lander, A. Kong, 1997, Nature Genetics.

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

A. Gylfason, B. Halldórsson, D. Gudbjartsson, 2018, Nature Genetics.

Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population.

U. Thorsteinsdóttir, A. Kong, K. Stefánsson, 2005, American journal of human genetics.

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1

A. Kong, J. Seidman, M. Fishman, 1994, Nature Genetics.

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.

R. Mägi, D. Gudbjartsson, T. Thorgeirsson, 2011, Human molecular genetics.

Multiple transmissions of de novo mutations in families

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2018, Nature Genetics.

Sequence variants at CYP 1 A 1 – CYP 1 A 2 and AHR associate with coffee consumption

R. Mägi, D. Gudbjartsson, T. Thorgeirsson, 2011 .

A systematic evaluation of 151 candidate genes for their association with osteoporosis and osteoporotic fracture in a meta-analysis of genome-wide association data

Bjarni V. Halldórsson, D. Kiel, A. Hofman, 2009 .

Augustine Kong Recombination Rate Gene Associate with Genome-Wide RNF 212 Sequence Variants in the

H. Stefánsson, D. Gudbjartsson, Á. Jónasdóttir, 2022 .

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Tanya M. Teslovich, Andrew D. Johnson, Kyle J. Gaulton, 2014 .

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Simon C. Potter, 2012, Nature Genetics.

A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans

Simon C. Potter, Nicholette D. Palmer, Joshua P. Lewis, 2012, PLoS ONE.

Epigenetic and genetic components of height regulation

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016, Nature Communications.

Allele-sharing models: LOD scores and accurate linkage tests.

N J Cox, A. Kong, A. Kong, 1997, American journal of human genetics.

Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals

Karen L. Mohlke, Luigi Ferrucci, Florian Kronenberg, 2012, PLoS genetics.

Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution

George Davey Smith, P. Elliott, L. Coin, 2009 .

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Simon C. Potter, P. Elliott, M. Jarvelin, 2010, Nature Genetics.

Contributors and Participants

D. Cox, A. Kong, N. Mendell, 1982 .

Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Tanya M. Teslovich, Kyle J. Gaulton, Sara M. Willems, 2015, Nature Genetics.

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

Thomas W. Mühleisen, A. Hofman, A. Uitterlinden, 2012, Molecular Psychiatry.

Nutrition, sirtuins and renin-angiotensin system: Cross talk in metabolic regulation

C. Gieger, W. Rathmann, J. Pankow, 2015 .

Edinburgh Explorer Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture

Bjarni V. Halldórsson, D. Kiel, B. Halldórsson, 2017 .

Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))

Benjamin J. Wright, C. Gieger, J. Pankow, 2011 .

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Tom R. Gaunt, Nicholette D. Palmer, Y. J. Kim, 2016, Nature Communications.

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (vol 42, pg 579, 2010)

C. Gieger, W. Rathmann, J. Pankow, 2011 .

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

H. Stefánsson, D. Rujescu, S. Cichon, 2011, Human molecular genetics.

Common variant at 16p11.2 conferring risk of psychosis

Janice M. Fullerton, M. Pirinen, H. Stefánsson, 2014, Molecular Psychiatry.

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2019, Nature Genetics.

Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms

C. Gieger, J. Pankow, E. Zeggini, 2014, Cell.

The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland

H. Stefánsson, A. Kong, O. Andreassen, 2009, PLoS genetics.

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Tanya M. Teslovich, Ross M. Fraser, May E. Montasser, 2012, Nature Genetics.

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Tanya M. Teslovich, Andrew D. Johnson, Ross M. Fraser, 2012, Nature Genetics.

Erratum to “MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans”

D. Gudbjartsson, A. Kong, M. Frigge, 2000, Nature Genetics.

The nature of nurture: Effects of parental genotypes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2017, Science.

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Tom R. Gaunt, Nicholette D. Palmer, Y. J. Kim, 2016, Nature Communications.

Physical and neurobehavioral determinants of reproductive onset and success

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016, Nature Genetics.

The Y-chromosome point mutation rate in humans

Valdis B. Guðmundsdóttir, A. Kong, K. Stefánsson, 2015, Nature Genetics.

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

H. Stefánsson, S. Steinberg, J. Gulcher, 2009, Nature Genetics.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

P. Elliott, M. Jarvelin, L. Coin, 2010, Nature Genetics.

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Tanya M. Teslovich, Ross M. Fraser, May E. Montasser, 2012, Nature Genetics.

Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial.

D. Gudbjartsson, J. Gulcher, A. Kong, 2005, Journal of the American Medical Association (JAMA).

Reply to “Many hypotheses but no replication for the association between PDE4D and stroke”

J. Gulcher, A. Kong, K. Stefánsson, 2006, Nature Genetics.

Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution

Waterworth, Steinthorsdottir, L. Coin, 2009 .

Physical and neuro-behavioural determinants of reproductive onset and success

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016 .

Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))

Benjamin J. Wright, C. Gieger, J. Pankow, 2011 .