A. Helgason

发表

Large-scale whole-genome sequencing of the Icelandic population

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

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.

mtDna and the islands of the North Atlantic: estimating the proportions of Norse and Gaelic ancestry.

K. Stefánsson, R. Ward, Agnar Helgason, 2001, American journal of human genetics.

The mutation rate in the human mtDNA control region.

P. Donnelly, J. Gulcher, K. Stefánsson, 2000, American journal of human 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.

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.

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

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

Schooling and Skipperhood: The Development of Dexterity

A. Helgason, G. Palsson, G. Pálsson, 1998 .

Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Suriname.

W. Rojas, G. Bedoya, M. Bortolini, 2017, American journal of human genetics.

Identification of a large set of rare complete human knockouts

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

Are We in the Same Boat or Not? The Opposite Effects of Absolute and Relative Income Shifts on Redistributive Preferences

A. Helgason, Vittorio Mérola, 2016, The Journal of Politics.

Selection against variants in the genome associated with educational attainment

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

Sequence variants from whole genome sequencing a large group of Icelanders

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

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

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

Essays in the comparative political economy oftaxation and redistribution

A. Helgason, 2015 .

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

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2017, Nature Genetics.

Introduction to Symposium on Time Series Error Correction Methods in Political Science

A. Helgason, J. Box-Steffensmeier, 2016, Political Analysis.

The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland

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

Ancient genomes from Iceland reveal the making of a human population

Valdis B. Guðmundsdóttir, T. Werge, K. Stefánsson, 2018, Science.

Title : Ancient genomes from Iceland reveal the making of a human population One

Valdis B. Guðmundsdóttir, Anuradha, T. Werge, 2017 .

Reconstructing an African haploid genome from the 18th century

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

The genetic structure of Norway

O. Andreassen, T. Werge, K. Stefánsson, 2020, European Journal of Human Genetics.

Y-chromosomal STR haplotypes in Pakistani populations.

C. Tyler-Smith, T. Zerjal, S. Q. Mehdi, 2001, Forensic science international.

The Anglo-Saxon migration and the formation of the early English gene pool

D. Reich, N. Patterson, N. Rohland, 2022, Nature.

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.

Electoral politics after the crisis: Change, fluctuations and stability in the 2021 Althingi Election

Eva H. Önnudóttir, A. Helgason, Ólafur Þ. Harðarson, 2022, Veftímaritið Stjórnmál og stjórnsýsla.

The Great Recession and new class voting in Iceland

A. Helgason, 2018, Veftímaritið Stjórnmál og stjórnsýsla.

Languages, geography and HLA haplotypes in Native American and Asian populations

D. Devine, A. Helgason, M. V. Monsalve, 1999, Proceedings of the Royal Society of London. Series B: Biological Sciences.

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.

Multi-nucleotide de novo Mutations in Humans

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

Unleashing the ‘money machine’: the domestic political foundations of VAT adoption

A. Helgason, 2017 .

A Reassessment of Genetic Diversity in Icelanders: Strong Evidence from Multiple Loci for Relative Homogeneity Caused by Genetic Drift

P. Donnelly, K. Stefánsson, Agnar Helgason, 2003, Annals of human genetics.

Employment Insecurity, Incumbent Partisanship, and Voting Behavior in Comparative Perspective

A. Helgason, Vittorio Mérola, 2017 .

Genetic evidence for a family-based Scandinavian settlement of Shetland and Orkney during the Viking periods

K. Stefánsson, R. Ward, Agnar Helgason, 2005, Heredity.

mtDNA and the origin of the Icelanders: deciphering signals of recent population history.

J. Gulcher, K. Stefánsson, R. Ward, 2000, American journal of human genetics.

A direct characterization of human mutation based on microsatellites

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

Humoral Immune Response to SARS-CoV-2 in Iceland

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2020, The New England journal of medicine.

Spread of SARS-CoV-2 in the Icelandic Population

Kari Stefansson, Thorolfur Gudnason, Aslaug Jonasdottir, 2020, The New England journal of medicine.

Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2021, Clinical Microbiology and Infection.

Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility

Kari Stefansson, Nicholas J Wareham, Claudia Langenberg, 2017, Nature Genetics.

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

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

mtDNA variation in Inuit populations of Greenland and Canada: migration history and population structure.

Kári Stefánsson, Gísli Pálsson, Agnar Helgason, 2006, American journal of physical anthropology.

Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus

Clement Adebamowo, Olufunmilayo I. Olopade, Robert Johansson, 2010, PLoS genetics.

Rare mutations associating with serum creatinine and chronic kidney disease.

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

A Statistical Approach to Identify Ancient Template DNA

K. Stefánsson, C. Lalueza-Fox, A. Baker, 2007, Journal of Molecular Evolution.

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

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

The genetic origins of Saint Helena’s liberated Africans

G. Renaud, Agnar Helgason, A. Helgason, 2019, bioRxiv.

Characterizing mutagenic effects of recombination through a sequence-level genetic map

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2019, Science.

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.

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

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

Sequences From First Settlers Reveal Rapid Evolution in Icelandic mtDNA Pool

K. Stefánsson, C. Lalueza-Fox, A. Baker, 2009, PLoS genetics.

Tracking Five Millennia of Horse Management with Extensive Ancient Genome Time Series

Arne Ludwig, Vedat Onar, Wolf-Rüdiger Teegen, 2019, Cell.

A populationwide coalescent analysis of Icelandic matrilineal and patrilineal genealogies: evidence for a faster evolutionary rate of mtDNA lineages than Y chromosomes.

J. Gulcher, K. Stefánsson, R. Ward, 2003, American journal of human genetics.

Estimating Scandinavian and Gaelic ancestry in the male settlers of Iceland.

K. Stefánsson, R. Ward, Agnar Helgason, 2000, American journal of human genetics.

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

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

Y-chromosomal DNA variation in Pakistan.

Chris Tyler-Smith, Raheel Qamar, Qasim Ayub, 2002, American journal of human genetics.

Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2021, Nature Genetics.

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.

Associations of autozygosity with a broad range of human phenotypes

May E. Montasser, Annelot M. Dekker, Blair H. Smith, 2019, Nature Communications.

A Drastic Reduction in the Life Span of Cystatin C L68Q Carriers Due to Life-Style Changes during the Last Two Centuries

U. Thorsteinsdóttir, K. Stefánsson, A. Helgason, 2008, PLoS genetics.

Epigenetic and genetic components of height regulation

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

Figuring fish and measuring men : the individual transferable quota system in the Icelandic cod fishery

A. Helgason, G. Pálsson, 1995 .

Blondes, lost and found: representations of genes, identity, and history.

A. Helgason, G. Pálsson, 2003, Developing world bioethics.

Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2020, Current Biology.

COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

Gudmundur A. Thorisson, D. Gudbjartsson, A. Sigurdsson, 2017, BMC Medical 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.

CDKN2A mutations and melanoma risk in the Icelandic population

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

Icelandic population mutations and melanoma risk in the CDKN2A

J. Gulcher, U. Thorsteinsdóttir, P. Sulem, 2008 .

Differences between germline genomes of monozygotic twins

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2021, Nature Genetics.

The mother’s risk of premature death after child loss across two centuries

K. Stefánsson, A. Helgason, K. Fall, 2019, eLife.

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

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

Multiple transmissions of de novo mutations in families

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

The impact of real world information shocks on political attitudes: Evidence from the Panama Papers disclosures

A. Helgason, Vittorio Mérola, 2022, Research & Politics.

Fractional Integration Methods and Short Time Series: Evidence from a Simulation Study

A. Helgason, 2016, Political Analysis.

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

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

Molecular benchmarks of a SARS-CoV-2 epidemic

Hannes P. Eggertsson, A. Gylfason, D. Gudbjartsson, 2021, Nature Communications.

Income-based voting and polarization over redistribution under alternative electoral systems

A. Helgason, 2016 .

Contested commodities : The moral landscape of modernist regimes

A. Helgason, G. Pálsson, 1997 .

Early Spread of SARS-Cov-2 in the Icelandic Population

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2020, medRxiv.

Epigenetic and genetic components of height regulation

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

Associations of autozygosity with a broad range of human phenotypes

Peter K. Joshi, M. P. Concas, May E. Montasser, 2019, Nature Communications.

HaploGrouper: a generalized approach to haplogroup classification

Anuradha Jagadeesan, S. Sunna Ebenesersdóttir, Valdis B. Guðmundsdóttir, 2020, Bioinform..

Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Suriname.

W. Rojas, G. Bedoya, M. Bortolini, 2017, American journal of human genetics.

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

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2017, Nature Genetics.

Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2021, Nature Genetics.

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

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

The ancestry and geographical origins of St Helena’s liberated Africans

A. Helgason, Anuradha Jagadeesan, J. V. Moreno-Mayar, 2023, American journal of human genetics.

The nature of nurture: Effects of parental genotypes

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

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.

Electoral Politics in Crisis after the Great Recession

Eva H. Önnudóttir, A. Helgason, H. Thórisdóttir, 2021 .

Multiple transmissions of de novo mutations in families

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

Physical and neuro-behavioural determinants of reproductive onset and success

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

A new subclade of mtDNA haplogroup C1 found in Icelanders: evidence of pre-Columbian contact?

K. Stefánsson, Federico Sánchez-Quinto, C. Lalueza-Fox, 2011, American journal of physical anthropology.