New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing

Genomic Ancestry of North Africans Supports Back-to-Africa Migrations

(2012) Brenna M. Henn et al.   PLoS Genetics

mapDamage: testing for damage patterns in ancient DNA sequences

(2011) Aurelien Ginolhac et al.   BIOINFORMATICS

Parallel Evolution of Genes and Languages in the Caucasus Region

(2011) Oleg Balanovsky et al.   MOLECULAR BIOLOGY AND EVOLUTION

Ancient DNA reveals male diffusion through the Neolithic Mediterranean route

(2011) M. Lacan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

An Aboriginal Australian Genome Reveals Separate Human Dispersals into Asia

(2011) M. Rasmussen et al.   SCIENCE

Population Genetic Structure of the People of Qatar

(2010) Haley Hunter-Zinck et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Ancestry and Pathology in King Tutankhamun's Family

(2010) Zahi Hawass   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Heteroplasmic mitochondrial DNA mutations in normal and tumour cells

(2010) Yiping He et al.   NATURE

Ancient human genome sequence of an extinct Palaeo-Eskimo

(2010) Morten Rasmussen et al.   NATURE

Ancient DNA from European Early Neolithic Farmers Reveals Their Near Eastern Affinities

(2010) Wolfgang Haak et al.   PLOS BIOLOGY

Interactions BetweenHERC2,OCA2andMC1RMay Influence Human Pigmentation Phenotype

(2009) Wojciech Branicki et al.   ANNALS OF HUMAN GENETICS

The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis

(2009) Suet Nee Chen et al.   BMC Cardiovascular Disorders

Polymorphisms Associated with Both Noncardioembolic Stroke and Coronary Heart Disease: Vienna Stroke Registry

(2009) May M. Luke et al.   CEREBROVASCULAR DISEASES

A Common Variant at 9p21 Is Associated With Sudden and Arrhythmic Cardiac Death

(2009) Christopher Newton-Cheh et al.   CIRCULATION

Common Genetic Variants on Chromosome 9p21 Confers Risk of Ischemic Stroke

(2009) J. Gustav Smith et al.   Circulation-Cardiovascular Genetics

Improved Resolution Haplogroup G Phylogeny in the Y Chromosome, Revealed by a Set of Newly Characterized SNPs

(2009) Lynn M. Sims et al.   PLoS One

The Human Gene Mutation Database: 2008 update

(2009) Peter D Stenson et al.   Genome Medicine

The Population Reference Sample, POPRES: A Resource for Population, Disease, and Pharmacological Genetics Research

(2008) Matthew R. Nelson et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color

(2008) Richard A. Sturm et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Complete Mitochondrial Genome Sequence of the Tyrolean Iceman

(2008) Luca Ermini et al.   CURRENT BIOLOGY

New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree

(2008) T. M. Karafet et al.   GENOME RESEARCH

Interpreting principal component analyses of spatial population genetic variation

(2008) John Novembre et al.   NATURE GENETICS

Four SNPs on Chromosome 9p21 in a South Korean Population Implicate a Genetic Locus That Confers High Cross-Race Risk for Development of Coronary Artery Disease

(2007) Gong-Qing Shen et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY