H. Helgason

发表

A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma

D. Gudbjartsson, A. Sigurdsson, A. Jonasdottir, 2017, PLoS genetics.

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.

Searching for a trail of evidence in a maze

E. Candès, O. Zeitouni, E. Arias-Castro, 2007, math/0701668.

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.

Multifractal analysis of fetal heart rate variability in fetuses with and without severe acidosis during labor.

Patrice Abry, Claude Gharib, Pascal Gaucherand, 2011, American journal of perinatology.

Nonparametric Detection and Estimation of Highly Oscillatory Signals

H. Helgason, Hannes Helgason, 2008 .

Methodology for multifractal analysis of heart rate variability: From LF/HF ratio to wavelet leaders

S. Jaffard, P. Abry, H. Helgason, 2010, 2010 Annual International Conference of the IEEE Engineering in Medicine and Biology.

Identification of a large set of rare complete human knockouts

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

Detecting highly oscillatory signals by chirplet path pursuit

Emmanuel J. Candes, E. Candès, H. Helgason, 2006, gr-qc/0604017.

Sequence variants from whole genome sequencing a large group of Icelanders

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

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

Katja, Gerald, Anne, 2014 .

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

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

Convex Optimization and Feasible Circulant Matrix Embeddings in Synthesis of Stationary Gaussian Fields

H. Helgason, V. Pipiras, Stefanos Kechagias, 2016 .

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

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

Detecting highly oscillatory signals by chirplet path pursuit

E. Candès, H. Helgason, P. Charlton, 2006, gr-qc/0604017.

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

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

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.

Multi-nucleotide de novo Mutations in Humans

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

Multiomics study of nonalcoholic fatty liver disease

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2022, Nature Genetics.

Physical and neurobehavioral determinants of reproductive onset and success

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

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

E. Demerath, Toshiko Tanaka, K. Lunetta, 2017, Nature Genetics.

Supplement to “Convex optimization and feasible circulant matrix embeddings in synthesis of stationary Gaussian ﬁelds”

H. Helgason, V. Pipiras, Stefanos Kechagias, 2015 .

A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2017, Human molecular genetics.

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

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2015, Nature Genetics.

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

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

Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

E. Demerath, Toshiko Tanaka, K. Lunetta, 2016, bioRxiv.

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

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

Whole genome characterization of sequence diversity of 15,220 Icelanders

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

Large-scale comparison of immunoassay- and aptamer-based plasma proteomics through genetics and disease

Pall I. Olason, Grimur Hjorleifsson Eldjarn, Bjarni V. Halldórsson, 2022, bioRxiv.

Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin

A. Uitterlinden, D. Gudbjartsson, A. Sigurdsson, 2018, Journal of the National Cancer Institute.

New basal cell carcinoma susceptibility loci

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

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

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

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

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

Epigenetic and genetic components of height regulation

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

Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2016, Nature Communications.

A genome-wide association study yields five novel thyroid cancer risk loci

Sandya Liyanarachchi, Kari Stefansson, Gudmar Thorleifsson, 2017, Nature Communications.

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

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

A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

D. Gudbjartsson, A. Sigurdsson, L. Kiemeney, 2015, PLoS genetics.

Adiposity-Dependent Regulatory Effects on Multi-tissue Transcriptomes

T. Spector, U. Thorsteinsdóttir, K. Stefánsson, 2016, American journal of human genetics.

A sequence variant associating with educational attainment also affects childhood cognition

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

Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.

D. Gudbjartsson, A. Sigurdsson, Á. Jónasdóttir, 2016, The New England journal of medicine.

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 8 q 24 . 21 is associated with renal cell cancer

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2017 .

Common and rare variants associated with kidney stones and biochemical traits

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2015, Nature Communications.

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.

Rare sequence variants that disrupt ASGR 1 function lower non-HDL cholesterol and protect against coronary artery disease

Nele, A. Sigurdsson, L. Kiemeney, 2016 .

Syddansk Universitet Variant ASGR1 associated with a reduced risk of coronary artery disease

A. Sigurdsson, Á. Jónasdóttir, L. Kiemeney, 2016 .

Demixing multivariate-operator self-similar processes

Patrice Abry, Hannes Helgason, Gustavo Didier, 2015, 2015 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP).

Fast and exact synthesis of stationary multivariate Gaussian time series using circulant embedding

Patrice Abry, Hannes Helgason, Vladas Pipiras, 2011, Signal Process..

Adaptive Multiscale Complexity Analysis of Fetal Heart Rate

Paulo Gonçalves, Patrice Abry, Hannes Helgason, 2011, IEEE Transactions on Biomedical Engineering.

Sequence variants affecting voice pitch in humans

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2023, Science advances.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

M. P. Concas, M. Jarvelin, E. Demerath, 2023, medRxiv.

Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

R. T. Lie, Bjarni V. Halldórsson, M. Daly, 2023, Nature communications.

Epigenetic and genetic components of height regulation

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

Synthesis of multivariate stationary series with prescribed marginal distributions and covariance using circulant matrix embedding

Patrice Abry, Hannes Helgason, Vladas Pipiras, 2011, Signal Process..

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

D Brandeis, M Brammer, H. Stefánsson, 2017, Translational Psychiatry.

Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2023, JAMA.

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

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

Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles - A Mendelian randomization analysis.

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2022, European journal of preventive cardiology.

Framework for adaptive multiscale analysis of nonhomogeneous point processes

Patrice Abry, Hannes Helgason, Jay Bartroff, 2011, 2011 Annual International Conference of the IEEE Engineering in Medicine and Biology Society.

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

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

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

Jens K. Boldsen, Pall I. Olason, Bjarni V. Halldórsson, 2023, Nature Genetics.

Large-scale plasma proteomics comparisons through genetics and disease associations

Pall I. Olason, Grimur Hjorleifsson Eldjarn, Bjarni V. Halldórsson, 2023, Nature.

Actionable Genotypes and Their Association with Life Span in Iceland.

Gudmundur A. Thorisson, Hannes P. Eggertsson, H. Stefánsson, 2023, The New England journal of medicine.

Physical and neurobehavioral determinants of reproductive onset and success

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

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

D. Gudbjartsson, A. Sigurdsson, A. Jonasdottir, 2015, Nature Genetics.

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

E. Demerath, K. Lunetta, J. Murabito, 2017, Nature Genetics.

Variants at the Interleukin 1 Gene Locus and Pericarditis.

Brynja D. Sigurpálsdóttir, B. Halldórsson, A. Sigurdsson, 2023, JAMA cardiology.