HapMap

Known as: Human Haplotype Map, Haplotype Maps, Human, Map, Human Haplotype 
The map of human HAPLOTYPES.
National Institutes of Health

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International HapMap Project

Papers overview

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2009
2009
OPRM1 Asn40Asp predicts response to naltrexone treatment: a haplotype-based approach.
BACKGROUND Individualized pharmacotherapy requires identification of genetic variants predictive of treatment response. In OPRM1… (More)
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Highly Cited
2006
Highly Cited
2006
Genetic association of the human corticotropin releasing hormone receptor 1 (CRHR1) with binge drinking and alcohol intake patterns in two independent samples
To investigate the role of the corticotropin releasing hormone receptor 1 (CRHR1) in patterns of human alcohol drinking and its… (More)
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Highly Cited
2006
Highly Cited
2006
Sirtuin 1 (SIRT1) sequence variation is not associated with exceptional human longevity.
The SIR2/Sirt1 gene has been demonstrated as regulating lifespan in many model organisms, including yeast, Caenorhabditis elegans… (More)
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2004
2004
Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population
The role of the serotonin transporter (5-HTT) in the development of neuropsychiatric disorders has been widely investigated. Two… (More)
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2004
2004
Association of estrogen receptor alpha polymorphisms with susceptibility to chronic hepatitis B virus infection.
Several studies have demonstrated that estrogen receptor alpha (ESR1) participates in the pathogenesis of persistent hepatitis B… (More)
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2003
2003
Interleukin-10 gene promoter region polymorphism is associated with eosinophil count and circulating immunoglobulin E in adult asthma.
BACKGROUND IL-10 has several functional effects relevant to asthma. It can modulate IgE production and induce apoptosis in… (More)
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Highly Cited
2002
Highly Cited
2002
HLA-DQ typing in the diagnosis of celiac disease
OBJECTIVE:More than 95% of celiac patients share the major histocompatibility complex II class human leukocyte antigen (HLA) DQ2… (More)
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Highly Cited
1998
Highly Cited
1998
An analysis of linkage disequilibrium in the interleukin-1 gene cluster, using a novel grouping method for multiallelic markers.
In population- and family-based association studies, it is useful to have some knowledge of the patterns of linkage… (More)
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Highly Cited
1997
Highly Cited
1997
Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda
BACKGROUND Sporadic porphyria cutanea tarda is a skin disease associated with hepatic siderosis. Depletion of iron stores by… (More)
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1991
1991
Two different forms of homozygous sickle cell disease occur in Saudi Arabia.
Haematological, clinical and some molecular genetic features of homozygous sickle cell (SS) disease in Saudi Arabia have been… (More)
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