Author details

Full Name

Hannes Helgason

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
37606673	Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.	JAMA	2023
37937776	Actionable Genotypes and Their Association with Life Span in Iceland.	N Engl J Med	2023
37794188	Large-scale plasma proteomics comparisons through genetics and disease associations.	Nature	2023
37400429	Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.	Nat Commun	2023
37301908	Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.	Nat Commun	2023
37294764	Sequence variants affecting voice pitch in humans.	Sci Adv	2023
36125206	Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis.	Eur J Prev Cardiol	2022
36280732	Multiomics study of nonalcoholic fatty liver disease.	Nat Genet	2022
33035477	Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming.	Curr Biol	2020
29767749	Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin.	J Natl Cancer Inst	2018
28195142	A genome-wide association study yields five novel thyroid cancer risk loci.	Nat Commun	2017
28959963	Parental influence on human germline de novo mutations in 1,548 trios from Iceland.	Nature	2017
28933420	Whole genome characterization of sequence diversity of 15,220 Icelanders.	Sci Data	2017
28747754	Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.	Nat Genet	2017
28440815	15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.	Transl Psychiatry	2017
28398513	A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.	Hum Mol Genet	2017
28319091	Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.	Nat Genet	2017
28436984	Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.	Nat Genet	2017
28273074	A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma.	PLoS Genet	2017
28250455	Diversity in non-repetitive human sequences not found in the reference genome.	Nat Genet	2017
27742809	A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.	Eur Heart J	2017
27811963	A sequence variant associating with educational attainment also affects childhood cognition.	Sci Rep	2016
27192541	Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.	N Engl J Med	2016
26838040	Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.	Nat Commun	2016
26740556	Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer.	Hum Mol Genet	2016
27089180	Physical and neurobehavioral determinants of reproductive onset and success.	Nat Genet	2016
27848971	Epigenetic and genetic components of height regulation.	Nat Commun	2016
27846220	Multi-nucleotide de novo Mutations in Humans.	PLoS Genet	2016
27588447	Adiposity-Dependent Regulatory Effects on Multi-tissue Transcriptomes.	Am J Hum Genet	2016
26327206	A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.	PLoS Genet	2015
25855136	New basal cell carcinoma susceptibility loci.	Nat Commun	2015
25807286	Large-scale whole-genome sequencing of the Icelandic population.	Nat Genet	2015
25807283	Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease.	Nat Genet	2015
25807282	Identification of a large set of rare complete human knockouts.	Nat Genet	2015
26098866	Loss-of-function variants in ATM confer risk of gastric cancer.	Nat Genet	2015
26272126	Common and rare variants associated with kidney stones and biochemical traits.	Nat Commun	2015
25977816	Sequence variants from whole genome sequencing a large group of Icelanders.	Sci Data	2015
24861552	Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.	Hum Mol Genet	2014
24476768	The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms.	Leukemia	2014
24464100	Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.	Nat Genet	2014
24036950	A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.	Nat Genet	2013
24220699	A common variant at 8q24.21 is associated with renal cell cancer.	Nat Commun	2013
22914163	Rate of de novo mutations and the importance of father's age to disease risk.	Nature	2012
22256129	Framework for adaptive multiscale analysis of nonhomogeneous point processes.	Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference	2011
21382764	Adaptive multiscale complexity analysis of fetal heart rate.	IEEE Transactions on Biomedical Engineering	2011
21089007	Multifractal analysis of fetal heart rate variability in fetuses with and without severe acidosis during labor.	American Journal of Perinatology	2011
21095647	Methodology for multifractal analysis of heart rate variability: from LF/HF ratio to wavelet leaders.		2010