List of works - Anders Albrechtsen

Genotype and SNP calling from next-generation sequencing data

scientific article

ANGSD: Analysis of Next Generation Sequencing Data.

scientific article

Ancient human genome sequence of an extinct Palaeo-Eskimo

scientific article

Low physical activity accentuates the effect of the FTO rs9939609 polymorphism on body fat accumulation

scientific article published on 17 October 2007

Recalibrating Equus evolution using the genome sequence of an early Middle Pleistocene horse

scientific article

An Aboriginal Australian genome reveals separate human dispersals into Asia

scientific article (publication date: 7 October 2011)

Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia

scientific article published on 6 September 2009

Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans

scientific article

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

The genome of a Late Pleistocene human from a Clovis burial site in western Montana

scientific article

Greenlandic Inuit show genetic signatures of diet and climate adaptation

scientific article

Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies

scientific article published on 7 September 2007

A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes

scientific article

SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing data

scientific article (publication date: 2012)

Ascertainment biases in SNP chips affect measures of population divergence

scientific article

Genomic evidence for the Pleistocene and recent population history of Native Americans

scientific article

Estimating individual admixture proportions from next generation sequencing data

scientific article

The genetic prehistory of the New World Arctic

scientific article

Prehistoric genomes reveal the genetic foundation and cost of horse domestication

scientific article

Darwinian and demographic forces affecting human protein coding genes

scientific article published on 11 March 2009

A genomic history of Aboriginal Australia

scientific article (publication date: 21 September 2016)

Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome.

scientific article

Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes

scientific article

Estimation of allele frequency and association mapping using next-generation sequencing data

scientific article

Quantifying population genetic differentiation from next-generation sequencing data

scientific article

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

scientific article published on 8 February 2016

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.

scientific article published on 19 November 2012

Association testing of novel type 2 diabetes risk alleles in the JAZF1, CDC123/CAMK1D, TSPAN8, THADA, ADAMTS9, and NOTCH2 loci with insulin release, insulin sensitivity, and obesity in a population-based sample of 4,516 glucose-tolerant middle-aged D

article by Niels Grarup et al published September 2008 in Diabetes

Speciation with gene flow in equids despite extensive chromosomal plasticity

scientific article

Natural selection and the distribution of identity-by-descent in the human genome

scientific article

Evolutionary Genomics and Conservation of the Endangered Przewalski's Horse

scientific article published on 22 September 2015

Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data

scientific article published on October 2, 2013

Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium

scientific article

Studies of the relationship between the ENPP1 K121Q polymorphism and type 2 diabetes, insulin resistance and obesity in 7,333 Danish white subjects

scientific article published on 25 July 2006

The origin and evolution of maize in the Southwestern United States

scientific article

The ancestry and affiliations of Kennewick Man

scientific article

Ancient genomic changes associated with domestication of the horse

scientific article

Ancient genomes show social and reproductive behavior of early Upper Paleolithic foragers

scientific article published on 5 October 2017

Ancient genomes revisit the ancestry of domestic and Przewalski's horses

scientific article published on 22 February 2018

Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets

scientific article

Terminal Pleistocene Alaskan genome reveals first founding population of Native Americans.

scientific article

Combined analysis of 19 common validated type 2 diabetes susceptibility gene variants shows moderate discriminative value and no evidence of gene–gene interaction

article

Combined analyses of 20 common obesity susceptibility variants

scientific article

Next-generation biology: Sequencing and data analysis approaches for non-model organisms

scientific article

Estimating inbreeding coefficients from NGS data: Impact on genotype calling and allele frequency estimation

scientific article

Uncovering the genetic history of the present-day Greenlandic population.

scientific article

Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History

A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics

scientific article

Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families

scientific article published on 12 June 2008

RelateAdmix: a software tool for estimating relatedness between admixed individuals

scientific article published on November 8, 2013

List of works by Anders Albrechtsen

Genotype and SNP calling from next-generation sequencing data

ANGSD: Analysis of Next Generation Sequencing Data.

Ancient human genome sequence of an extinct Palaeo-Eskimo

Low physical activity accentuates the effect of the FTO rs9939609 polymorphism on body fat accumulation

Recalibrating Equus evolution using the genome sequence of an early Middle Pleistocene horse

An Aboriginal Australian genome reveals separate human dispersals into Asia

Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia

Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

The genome of a Late Pleistocene human from a Clovis burial site in western Montana

Greenlandic Inuit show genetic signatures of diet and climate adaptation

Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies

A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes

SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing data

Ascertainment biases in SNP chips affect measures of population divergence

Genomic evidence for the Pleistocene and recent population history of Native Americans

Estimating individual admixture proportions from next generation sequencing data

The genetic prehistory of the New World Arctic

Prehistoric genomes reveal the genetic foundation and cost of horse domestication

Darwinian and demographic forces affecting human protein coding genes

A genomic history of Aboriginal Australia

Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome.

Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes

Estimation of allele frequency and association mapping using next-generation sequencing data

Quantifying population genetic differentiation from next-generation sequencing data

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

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.

Association testing of novel type 2 diabetes risk alleles in the JAZF1, CDC123/CAMK1D, TSPAN8, THADA, ADAMTS9, and NOTCH2 loci with insulin release, insulin sensitivity, and obesity in a population-based sample of 4,516 glucose-tolerant middle-aged D

Speciation with gene flow in equids despite extensive chromosomal plasticity

Natural selection and the distribution of identity-by-descent in the human genome

Evolutionary Genomics and Conservation of the Endangered Przewalski's Horse

Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data

Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium

Studies of the relationship between the ENPP1 K121Q polymorphism and type 2 diabetes, insulin resistance and obesity in 7,333 Danish white subjects

The origin and evolution of maize in the Southwestern United States

The ancestry and affiliations of Kennewick Man

Ancient genomic changes associated with domestication of the horse

Ancient genomes show social and reproductive behavior of early Upper Paleolithic foragers

Ancient genomes revisit the ancestry of domestic and Przewalski's horses

Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets

Terminal Pleistocene Alaskan genome reveals first founding population of Native Americans.

Combined analysis of 19 common validated type 2 diabetes susceptibility gene variants shows moderate discriminative value and no evidence of gene–gene interaction

Combined analyses of 20 common obesity susceptibility variants

Next-generation biology: Sequencing and data analysis approaches for non-model organisms

Estimating inbreeding coefficients from NGS data: Impact on genotype calling and allele frequency estimation

Uncovering the genetic history of the present-day Greenlandic population.

Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History

A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics

Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families

RelateAdmix: a software tool for estimating relatedness between admixed individuals