Daniel F. Gudbjartsson

发表

Allegro, a new computer program for multipoint linkage analysis

Daniel F. Gudbjartsson, Kristjan Jonasson, Michael L. Frigge, 2000, Nature genetics.

Graphtyper: Population-scale genotyping using pangenome graphs

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

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.

Parental origin of sequence variants associated with complex diseases

Daniel F. Gudbjartsson, Michael L. Frigge, Kari Stefansson, 2009, Nature.

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

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

Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene

Luigi Ferrucci, Sven Bergmann, Zoltán Kutalik, 2010, PLoS genetics.

Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

Daniel F. Gudbjartsson, Kari Stefansson, Runolfur Palsson, 2010, PLoS 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.

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

Daniel F. Gudbjartsson, Kari Stefansson, Gudmar Thorleifsson, 2008, Nature.

Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence

Michael C. Neale, Dorret I. Boomsma, Timothy B. Baker, 2017, Molecular Psychiatry.

A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

Ole A. Andreassen, Daniel F. Gudbjartsson, Erik G. Jönsson, 2012, Nature.