B. Halldórsson

发表

Large recurrent microdeletions associated with schizophrenia

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

An Interior-Point Method for a Class of Saddle-Point Problems

B. Halldórsson, R. Tütüncü, 2003 .

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.

Whole-genome shotgun assembly and comparison of human genome assemblies

Randall A. Bolanos, Xiangqun H. Zheng, Bjarni V. Halldórsson, 2004, Proceedings of the National Academy of Sciences of the United States of America.

DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Feinberg, 2018, Nature Communications.

GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2019, Nature Communications.

Many sequence variants affecting diversity of adult human height

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

Impact of Genetics on Low Bone Mass in Adults

Bjarni V. Halldórsson, B. Halldórsson, K. Stefánsson, 2008, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

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

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

Large-scale Meta-analysis of Genome-wide Association (GWA) Scans for Osteoporosis Traits: the GEFOS Consortium

Bjarni V. Halldórsson, D. Kiel, A. Uitterlinden, 2008 .

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.

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.

Graphtyper enables population-scale genotyping using pangenome graphs

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

PopDel identifies medium-size deletions jointly in tens of thousands of genomes

Doruk Beyter, Hannes P. Eggertsson, Kári Stefánsson, 2019, bioRxiv.

Sequence variants from whole genome sequencing a large group of Icelanders

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

Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.

Bjarni V. Halldórsson, D. Kiel, T. Spector, 2010, American journal of human genetics.

Islands of tractability for parsimony haplotyping

Roded Sharan, Sorin Istrail, Bjarni V. Halldorsson, 2005 .

Ratatosk: hybrid error correction of long reads enables accurate variant calling and assembly

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2021, Genome biology.

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

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

Max Point-Tolerance Graphs 1

Bjarni V. Halldórsson, B. Halldórsson, M. Halldórsson, 2015 .

Robustness of Inference of Haplotype Block Structure

Russell Schwartz, Andrew G. Clark, Sorin Istrail, 2003, J. Comput. Biol..

common underlying recombination pattern across four populations reflect their demographic history and a The linkage disequilibrium maps of three human chromosomes Material Supplemental

Hadar I. Isaac, Bjarni V. Halldórsson, B. Halldórsson, 2005 .

The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern.

Hadar I. Isaac, Bjarni V. Halldórsson, B. Halldórsson, 2005, Genome research.

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2020, Communications Biology.

Benchmarking small variant detection with ONT reveals high performance in challenging regions

Bjarni V. Halldórsson, B. Halldórsson, M. Nyegaard, 2020, bioRxiv.

PopAlu: population-scale discovery of Alu polymorphisms

Bjarni V. Halldórsson, B. Halldórsson, Birte Kehr, 2015 .

PopAlu: population-scale detection of Alu polymorphisms

Bjarni V. Halldórsson, B. Halldórsson, Birte Kehr, 2015, PeerJ.

Variable number tandem repeats mediate the expression of proximal genes

Bjarni V. Halldórsson, B. Halldórsson, K. Stefánsson, 2020, Nature Communications.

Sequence variants associating with urinary biomarkers

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

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

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

Estrogen Receptor Genotypes and Haplotypes Associated with Breast Cancer Risk

Bjarni V. Halldórsson, B. Halldórsson, A. Clark, 2004, Cancer Research.

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 .

read_haps: using read haplotypes to detect same species contamination in DNA sequences

Hannes P. Eggertsson, B. Halldórsson, 2020, Bioinform..

Multiple genetic loci for bone mineral density and fractures.

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

Identification of Lynch syndrome risk variants in the Romanian population

Hannes P. Eggertsson, B. Halldórsson, A. Sigurdsson, 2018, Journal of cellular and molecular medicine.

Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile

Christian Gieger, Inês Barroso, Meena Kumari, 2011, 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.

HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2

Hannes P. Eggertsson, B. Halldórsson, D. Gudbjartsson, 2022, Communications Biology.

New sequence variants associated with bone mineral density

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

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome

Bjarni V. Halldórsson, A. Uitterlinden, D. Lawlor, 2015, 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.

The nature of nurture: Effects of parental genotypes

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

A Branch & Price algorithm for the minimum cost clique cover problem in max-point tolerance graphs

Bjarni V. Halldórsson, B. Halldórsson, D. Catanzaro, 2018, 4OR.

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Caitlin P. McHugh, Bjarni V. Halldórsson, M. Fornage, 2022, Nature communications.

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

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2021, Nature Genetics.

Optimal sequencing by hybridization in rounds

Alan M. Frieze, Bjarni V. Halldórsson, B. Halldórsson, 2001, RECOMB.

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

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

A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy

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

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, 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.

popSTR: population‐scale detection of STR variants

Bjarni V. Halldórsson, Birte Kehr, Snædís Kristmundsdóttir, 2016, Bioinform..

The rate of meiotic gene conversion varies by sex and age

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

Genome analysis popSTR : population-scale detection of STR variants

Brynja D. Sigurpálsdóttir, Bjarni V. Halldórsson, B. Halldórsson, 2016 .

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.

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2022, Nature Genetics.

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

Hannes P. Eggertsson, B. Halldórsson, D. Gudbjartsson, 2020, Communications Biology.

The sequences of 150,119 genomes in the UK Biobank

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

Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program

Andrew D. Johnson, Caitlin P. McHugh, Bjarni V. Halldórsson, 2021, medRxiv.

Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

B. Halldórsson, D. Gudbjartsson, U. Thorsteinsdóttir, 2018, Communications Biology.

DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism

Sorin Istrail, Bjarni V. Halldórsson, Derek Aguiar, 2012, Bioinform..

An Algorithm for Detecting High Frequency Copy Number Polymorphisms Using SNP Arrays

Bjarni V. Halldórsson, Daniel Gudbjartsson, B. Halldórsson, 2011, J. Comput. Biol..

New basal cell carcinoma susceptibility loci

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

Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2020, Nature Communications.

Profile of common prostate cancer risk variants in an unscreened Romanian population

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2017, Journal of cellular and molecular medicine.

Sleep–wake dynamics under extended light and extended dark conditions in adult zebrafish

Bjarni V. Halldórsson, B. Halldórsson, O. Sigurjonsson, 2013, Behavioural Brain Research.

PopDel identifies medium-size deletions simultaneously in tens of thousands of genomes

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

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.

Long read sequencing of 1,817 Icelanders provides insight into the role of structural variants in human disease

Guillaume Holley, Daniel F. Gudbjartsson, Kari Stefansson, 2019, bioRxiv.

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

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

Ratatosk: hybrid error correction of long reads enables accurate variant calling and assembly

Guillaume Holley, Helga Ingimundardottir, Snædis Kristmundsdottir, 2020, Genome Biology.

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

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

Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland

Bjarni V. Halldórsson, B. Halldórsson, A. Jonasdottir, 2021, Arteriosclerosis, thrombosis, and vascular biology.

NPGRJ_NG_122 609..615

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

Coding variants in RPL 3 L and MYZAP increase risk of atrial fi brillation

B. Halldórsson, D. Gudbjartsson, U. Thorsteinsdóttir, 2018 .

Mutations in RPL3L and MYZAP increase risk of atrial fibrillation

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

popSTR2 enables clinical and population-scale genotyping of microsatellites

Snædis Kristmundsdottir, Hannes P Eggertsson, Gudny A Arnadottir, 2019, Bioinform..

A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22.

Bjarni V. Halldórsson, A. Hofman, A. Uitterlinden, 2010, Arthritis and rheumatism.

A Genome-Wide Association Study Identifies an Osteoarthritis Susceptibility Locus on Chromosome 7 q 22

Bjarni V. Halldórsson, A. Hofman, A. Uitterlinden, 2010 .

Methylation of Bone SOST, Its mRNA, and Serum Sclerostin Levels Correlate Strongly With Fracture Risk in Postmenopausal Women

Bjarni V. Halldórsson, A. Hofman, A. Uitterlinden, 2015, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

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.

Graphtyper: Population-scale genotyping using pangenome graphs

Daniel F. Gudbjartsson, Kari Stefansson, Florian Zink, 2017, bioRxiv.

A hybrid micro-macroevolutionary approach to gene tree reconstruction.

Dannie Durand, Bjarni V. Halldórsson, Benjamin Vernot, 2006 .

A Hybrid Micro-Macroevolutionary Approach to Gene Tree Reconstruction

Dannie Durand, Bjarni V. Halldórsson, Benjamin Vernot, 2005, RECOMB.

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

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

KmerStream: Streaming algorithms for k-mer abundance estimation

Páll Melsted, Bjarni V. Halldórsson, Bjarni V. Halldórsson, 2014, bioRxiv.

Combinatorial Problems Arising in SNP and Haplotype Analysis

Shibu Yooseph, Sorin Istrail, Vineet Bafna, 2003, DMTCS.

A Survey of Computational Methods for Determining Haplotypes

Shibu Yooseph, Sorin Istrail, Vineet Bafna, 2002, Computational Methods for SNPs and Haplotype Inference.

A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus

Bjarni V. Halldórsson, M. Peters, D. Kiel, 2013, Journal of Medical Genetics.

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

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

Large-scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand.

Bjarni V. Halldórsson, A. Hofman, A. Uitterlinden, 2009, Arthritis and rheumatism.

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2021, Communications biology.

A sequence variant associating with educational attainment also affects childhood cognition

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

The nature of Neanderthal introgression revealed by 27,566 Icelandic genomes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2020, Nature.

PopIns: population-scale detection of novel sequence insertions

Páll Melsted, Bjarni V. Halldórsson, Birte Kehr, 2015, Bioinform..

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.

Population-scale detection of non-reference sequence variants using colored de Bruijn graphs

Bjarni V. Halldórsson, B. Halldórsson, Birte Kehr, 2021, bioRxiv.

Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2019, Journal of the American College of Cardiology.

Identification of sequence variants influencing immunoglobulin levels

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

The Clark Phase-able Sample Size Problem: Long-Range Phasing and Loss of Heterozygosity in GWAS

Sorin Istrail, Bjarni V. Halldórsson, Derek Aguiar, 2010, RECOMB.

The Clark Phase-able Sample Size Problem: Long-Range Phasing and Loss of Heterozygosity in GWAS

Sorin Istrail, Bjarni V. Halldórsson, Derek Aguiar, 2010, RECOMB.

Epitope prediction algorithms for peptide-based vaccine design

Russell Schwartz, Sorin Istrail, Bjarni V. Halldórsson, 2003, Computational Systems Bioinformatics. CSB2003. Proceedings of the 2003 IEEE Bioinformatics Conference. CSB2003.

An Integer Programming Formulation of the Parsimonious Loss of Heterozygosity Problem

Martine Labbé, Bjarni V. Halldórsson, Daniele Catanzaro, 2013, IEEE/ACM Transactions on Computational Biology and Bioinformatics.

A Mixed Integer Programming Model for the Parsimonious Loss of Heterozygosity Problem

Martine Labbé, Bjarni V. Halldórsson, Daniele Catanzaro, 2012, ISBRA.

Lifelong Reduction in LDL Cholesterol Due to a Gain-of-Function Mutation in LDLR.

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2020, Circulation. Genomic and precision medicine.

Bioinformatics Research and Applications

Martine Labbé, Bjarni V. Halldórsson, Daniele Catanzaro, 2012, Lecture Notes in Computer Science.

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 .

PAIR: polymorphic Alu insertion recognition

Bjarni V. Halldórsson, Jón Sveinbjörnsson, B. Halldórsson, 2012, BMC Bioinformatics.

Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22

Bjarni V. Halldórsson, A. Hofman, A. Uitterlinden, 2010, Annals of the rheumatic diseases.

Max point-tolerance graphs pdf

Stefan Felsner, Steven Chaplick, Magnús M. Halldórsson, 2015, Discret. Appl. Math..

Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study

Simon C. Potter, Bjarni V. Halldórsson, A. Hofman, 2010, Annals of the rheumatic diseases.

Differences between germline genomes of monozygotic twins

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

Differences between germline genomes of monozygotic twins

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

Read_haps: using read haplotypes to detect same species contamination in DNA sequences.

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2020, Bioinformatics.

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

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

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

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

Comparative immunopeptidomics of humans and their pathogens.

Sorin Istrail, Oliver Kohlbacher, Liliana Florea, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Clinical decision support system for the management of osteoporosis compared to NOGG guidelines and an osteology specialist: a validation pilot study

Haukur T. Gudmundsson, Karen E. Hansen, Bjarni V. Halldorsson, 2019, BMC Medical Informatics and Decision Making.

A Branch & Price algorithm for the minimum cost clique cover problem in max-point tolerance graphs

Bjarni V. Halldórsson, Daniele Catanzaro, Bernard Fortz, 2018, 4OR.

Multiple transmissions of de novo mutations in families

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

A Clinical Decision Support System for the Diagnosis, Fracture Risks and Treatment of Osteoporosis

Bjarni V. Halldórsson, Aron Hjalti Bjornsson, Haukur Tyr Gudmundsson, 2015, Comput. Math. Methods Medicine.

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.

Approximation algorithms for the test cover problem

R. Ravi, Jan Karel Lenstra, Leen Stougie, 2003, Math. Program..

DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis

Hannes P. Eggertsson, Till F. M. Andlauer, Bjarni V. Halldórsson, 2018, Nature Communications.

Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis

A. Gylfason, B. Halldórsson, D. Gudbjartsson, 2020, Nature Communications.

Estimating population size via line graph reconstruction

B. Halldórsson, R. Sharan, Dima Blokh, 2012, Algorithms for Molecular Biology.

Sequence variants affecting voice pitch in humans

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

Optimal Haplotype Block-free Selection of Tagging Snps for Genome-wide Association Studies

Russell Schwartz, Sorin Istrail, Vineet Bafna, 2022 .

Network-based interpretation of genomic variation data.

Roded Sharan, Bjarni V. Halldórsson, B. Halldórsson, 2013, Journal of molecular biology.

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 .

Optimal Selection of SNP Markers for Disease Association Studies

Sorin Istrail, Francisco M. De La Vega, Bjarni V. Halldórsson, 2005, Human Heredity.

Lessons from the past: Familial aggregation analysis of fatal pandemic influenza (Spanish flu) in Iceland in 1918

Cécile Viboud, Kári Stefánsson, Jeffrey R Gulcher, 2008, Proceedings of the National Academy of Sciences.

Islands of Tractability for Parsimony Haplotyping

Roded Sharan, Sorin Istrail, Bjarni V. Halldórsson, 2005, IEEE/ACM Transactions on Computational Biology and Bioinformatics.

Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria

Grimur Hjorleifsson Eldjarn, Bjarni V. Halldórsson, B. Halldórsson, 2023, Communications biology.

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.

PAIR: polymorphic Alu insertion recognition

Bjarni V. Halldórsson, B. Halldórsson, Jón Sveinbjörnsson, 2012, BMC Bioinformatics.

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2018, Nature Genetics.

The nature of nurture: Effects of parental genotypes

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

Whole-genome sequencing of half-a-million UK Biobank participants

B. Halldórsson, K. Carss, The UK Biobank Whole-Genome Sequencing Consortium, 2023, medRxiv.

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.

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

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

A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus

M. Peters, J. V. van Meurs, D. Pinto, 2013, Journal of Medical 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.

Streaming Algorithms for Independent Sets

Magnús M. Halldórsson, Mario Szegedy, Bjarni V. Halldórsson, 2010, ICALP.

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Gerardus A. Meddens, Joseph K. Pickrell, Steven F. Lehrer, 2018, Nature Genetics.

Sequence variants affecting the genome-wide rate of germline microsatellite mutations

Hannes P. Eggertsson, Pall I. Olason, Bjarni V. Halldórsson, 2023, Nature communications.

Variable number tandem repeats mediate the expression of proximal genes

B. Halldórsson, K. Stefánsson, V. Bafna, 2020, Nature Communications.

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.

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

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

Variants at the Interleukin 1 Gene Locus and Pericarditis.

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

Large-scale plasma proteomics comparisons through genetics and disease associations

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

Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination

B. Halldórsson, D. Gudbjartsson, P. Sulem, 2024, Nature structural & molecular biology.

Complex effects of sequence variants on lipid levels and coronary artery disease

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2023, Cell.

Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

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

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

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

Estimating population size via line graph reconstruction

Roded Sharan, Bjarni V. Halldórsson, Dima Blokh, 2012, Algorithms for Molecular Biology.

Sequence variants influencing the regulation of serum IgG subclass levels

B. Halldórsson, D. Gudbjartsson, A. Sigurdsson, 2024, Nature communications.

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

H. Stefánsson, B. Halldórsson, D. Gudbjartsson, 2024, Nature genetics.

Recurrence of de novo mutations in families

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