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Genetic Similarities Within and Between Human Populations

Genetics (Austin), 2007-05, Vol.176 (1), p.351-359

2007

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Linkage disequilibrium and the search for complex disease genes

Genome research, 2000-10, Vol.10 (10), p.1435

Jorde, L B

2000

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The Distribution of Human Genetic Diversity: A Comparison of Mitochondrial, Autosomal, and Y-Chromosome Data

American journal of human genetics, 2000-03, Vol.66 (3), p.979-988

2000

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Pharmacogenomics of 17‐alpha hydroxyprogesterone caproate for recurrent preterm birth: a case–control study

BJOG : an international journal of obstetrics and gynaecology, 2018-02, Vol.125 (3), p.343-350

2018

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Population genomics : a bridge from evolutionary history to genetic medicine

Human molecular genetics, 2001-10, Vol.10 (20), p.2199-2207

2001

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Patterns of Ancestral Human Diversity: An Analysis of Alu-Insertion and Restriction-Site Polymorphisms

American journal of human genetics, 2001-03, Vol.68 (3), p.738-752

2001

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Linkage disequilibrium as a gene-mapping tool

American journal of human genetics, 1995-01, Vol.56 (1), p.11-14

Jorde, L B

1995

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Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

Nature genetics, 1997-07, Vol.16 (3), p.311-315

1997

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DNA Sequence Variation in a 3.7-kb Noncoding Sequence 5′ of the CYP1A2 Gene: Implications for Human Population History and Natural Selection

American journal of human genetics, 2002-09, Vol.71 (3), p.528-542

2002

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The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome

American journal of human genetics, 1999-06, Vol.64 (6), p.1550-1562

1999

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Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1

Molecular biology and evolution, 2001-02, Vol.18 (2), p.214-222

2001

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Clinical and Biochemical Abnormalities in People Heterozygous for Hemochromatosis

The New England journal of medicine, 1996-12, Vol.335 (24), p.1799-1805

1996

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Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms

BMC genetics, 2008-12, Vol.9, p.86

2008

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Adaptive genetic changes related to haemoglobin concentration in native high‐altitude Tibetans

Experimental physiology, 2015-11, Vol.100 (11), p.1263-1268

2015

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Origins and affinities of modern humans : a comparison of mitochondrial and nuclear genetic data

American journal of human genetics, 1995-09, Vol.57 (3), p.523-538

1995

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Crohn's Disease and Genetic Hitchhiking at IBD5

Molecular biology and evolution, 2012-01, Vol.29 (1), p.101-111

2012

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Evidence for natural selection in the HAVCR1 gene: high degree of amino-acid variability in the mucin domain of human HAVCR1 protein

Genes and immunity, 2005-08, Vol.6 (5), p.398-406

2005

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Human Population Genetic Structure and Inference of Group Membership

American journal of human genetics, 2003-03, Vol.72 (3), p.578-589

2003

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Combined variants in factor VIII and prostaglandin synthase‐1 amplify hemorrhage severity across three generations of descendants

Journal of thrombosis and haemostasis, 2016-11, Vol.14 (11), p.2230-2240

2016

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Gene flow from the Indian subcontinent to Australia: evidence from the Y chromosome

Current biology, 2002-04, Vol.12 (8), p.673-677

2002

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Mitochondrial and Nuclear Genetic Relationships among Pacific Island and Asian Populations

American journal of human genetics, 1998-08, Vol.63 (2), p.613-624

1998

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Female gene flow stratifies Hindu castes

Nature (London), 1998-10, Vol.395 (6703), p.651-652

1998

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Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region

American journal of human genetics, 1994-05, Vol.54 (5), p.884-898

1994

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Ascertainment bias in estimates of average heterozygosity

American journal of human genetics, 1996-05, Vol.58 (5), p.1033-1041

1996

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Lack of association between beta 2-adrenergic receptor polymorphisms and juvenile idiopathic arthritis

Scandinavian journal of rheumatology, 2009-01, Vol.38 (2), p.91-95

2009

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Genetic Similarities Within and Between Human Populations

Linkage disequilibrium and the search for complex disease genes

The Distribution of Human Genetic Diversity: A Comparison of Mitochondrial, Autosomal, and Y-Chromosome Data

Pharmacogenomics of 17‐alpha hydroxyprogesterone caproate for recurrent preterm birth: a case–control study

Population genomics : a bridge from evolutionary history to genetic medicine

Patterns of Ancestral Human Diversity: An Analysis of Alu-Insertion and Restriction-Site Polymorphisms

Linkage disequilibrium as a gene-mapping tool

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

DNA Sequence Variation in a 3.7-kb Noncoding Sequence 5′ of the CYP1A2 Gene: Implications for Human Population History and Natural Selection

The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome

Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1

Clinical and Biochemical Abnormalities in People Heterozygous for Hemochromatosis

Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms

Adaptive genetic changes related to haemoglobin concentration in native high‐altitude Tibetans

Origins and affinities of modern humans : a comparison of mitochondrial and nuclear genetic data

Crohn's Disease and Genetic Hitchhiking at IBD5

Evidence for natural selection in the HAVCR1 gene: high degree of amino-acid variability in the mucin domain of human HAVCR1 protein

Human Population Genetic Structure and Inference of Group Membership

Combined variants in factor VIII and prostaglandin synthase‐1 amplify hemorrhage severity across three generations of descendants

Gene flow from the Indian subcontinent to Australia: evidence from the Y chromosome

Mitochondrial and Nuclear Genetic Relationships among Pacific Island and Asian Populations

Female gene flow stratifies Hindu castes

Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region

Ascertainment bias in estimates of average heterozygosity

Lack of association between beta 2-adrenergic receptor polymorphisms and juvenile idiopathic arthritis

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