Florian Zink

发表

New basal cell carcinoma susceptibility loci

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

The sequences of 150,119 genomes in the UK Biobank

Hannes P. Eggertsson, Brynja D. Sigurpálsdóttir, Pall I. Olason, 2021, Nature.

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

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

Multiple transmissions of de novo mutations in families

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

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 rate of meiotic gene conversion varies by sex and age

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

Graphtyper enables population-scale genotyping using pangenome graphs

Kari Stefansson, Hannes P Eggertsson, Bjarni V Halldorsson, 2017, Nature Genetics.

Genetic predisposition to mosaic Y chromosome loss in blood

Jacob C. Ulirsch, A. Auton, D. Gudbjartsson, 2019, bioRxiv.

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

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

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.

Genetics of gene expression and its effect on disease

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

Large-scale whole-genome sequencing of the Icelandic population

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

Differences between germline genomes of monozygotic twins

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

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

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

Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2018, Nature Genetics.

A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2019, Nature Genetics.

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

A. Uitterlinden, J. V. van Meurs, E. Zeggini, 2019, Nature Communications.

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

Bjarni V. Halldórsson, A. Ingason, B. Halldórsson, 2018, Nature Communications.

Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases

H. Stefánsson, A. Gylfason, D. Gudbjartsson, 2021, BMJ Open.

Selection against variants in the genome associated with educational attainment

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

Large-scale integration of the plasma proteome with genetics and disease

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2021, 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, JAMA.

Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2020, Communications Biology.

Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence

S. Steinberg, D. Gudbjartsson, T. Thorgeirsson, 2015, Translational Psychiatry.

Genome-wide association meta-analysis yields 20 loci associated with gallstone disease

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Nature Communications.

Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk

Hannes P. Eggertsson, Pall I. Olason, Bjarni V. Halldórsson, 2021, Cancer Research.

Differences between germline genomes of monozygotic twins

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

Profiling of genes expressed in peripheral blood mononuclear cells predicts glucocorticoid sensitivity in asthma patients.

J. Gulcher, K. Stefánsson, H. Hakonarson, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Identification of a large set of rare complete human knockouts

H. Stefánsson, D. Gudbjartsson, A. Sigurdsson, 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.

Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis

D. Gudbjartsson, A. Sigurdsson, U. Thorsteinsdóttir, 2018, 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.

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

Bjarni V. Halldórsson, A. Ingason, B. Halldórsson, 2018, Nature Communications.

Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis

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

Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

Laurent F. Thomas, J. V. van Meurs, R. Mägi, 2022, Nature communications.

Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

Laurent F. Thomas, J. V. van Meurs, R. Mägi, 2022, Nature Communications.

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.

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.

Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis

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

Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2018, 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.

Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis

D. Gudbjartsson, T. Thorgeirsson, U. Thorsteinsdóttir, 2023, Nature Genetics.

Large-scale plasma proteomics comparisons through genetics and disease associations

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

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.

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.

Sequence variants from whole genome sequencing a large group of Icelanders

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

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).

Multiple transmissions of de novo mutations in families

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

The correlation between CpG methylation and gene expression is driven by sequence variants

Brynja D. Sigurpálsdóttir, H. Stefánsson, B. Halldórsson, 2024, Nature genetics.

Recurrence of de novo mutations in families

B. Halldórsson, D. Gudbjartsson, Á. Jónasdóttir, 2017 .