(Q34105177)

31 July 2017

1 reference

title

The pursuit of genome-wide association studies: where are we now? (English)

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genome-wide association study

31 July 2017

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3

Yudi Pawitan

1 reference

31 July 2017

Chee Seng Ku

1

1 reference

31 July 2017

En Yun Loy

series ordinal

2

1 reference

31 July 2017

Kee Seng Chia

series ordinal

4

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31 July 2017

language of work or name

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19 March 2010

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Journal of Human Genetics

31 July 2017

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31 July 2017

55

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31 July 2017

195-206

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31 July 2017

4

1 reference

https://scigraph.springernature.com/pub.10.1038/jhg.2010.19

31 July 2017

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Genetic mapping in human disease

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

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Genotyping technologies for genetic research

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7 January 2021

Common vs. rare allele hypotheses for complex diseases

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7 January 2021

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

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7 January 2021

Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients

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7 January 2021

Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genetic variations in the gene encoding ELMO1 are associated with susceptibility to diabetic nephropathy

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A high-throughput SNP typing system for genome-wide association studies

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

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7 January 2021

JSNP: a database of common gene variations in the Japanese population

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7 January 2021

A haplotype map of the human genome

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A second generation human haplotype map of over 3.1 million SNPs

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Evaluating coverage of genome-wide association studies

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Power to detect risk alleles using genome-wide tag SNP panels

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Evaluation of coverage variation of SNP chips for genome-wide association studies.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

HTRA1 promoter polymorphism in wet age-related macular degeneration

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Systematic review and meta-analysis of the association between complement factor H Y402H polymorphisms and age-related macular degeneration

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Meta-analysis of the association of the HTRA1 polymorphisms with the risk of age-related macular degeneration

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

New links to the pathogenesis of Crohn disease provided by genome-wide association scans

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A common genetic variant is associated with adult and childhood obesity

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

High-resolution whole-genome association study of Parkinson disease.

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design?

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

New models of collaboration in genome-wide association studies: the Genetic Association Information Network

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

https://api.crossref.org/works/10.1038%2FJHG.2010.19

1 reference

7 January 2021

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

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https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common variants at ten loci influence QT interval duration in the QTGEN Study

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A common variant on chromosome 9p21 affects the risk of myocardial infarction

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Breakthrough of the year. Human genetic variation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies novel breast cancer susceptibility loci

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association study identifies novel risk loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Type 2 diabetes: new genes, new understanding

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association studies in cancer.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Replicating genotype-phenotype associations

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Clinical review: the genetics of type 2 diabetes: a realistic appraisal in 2008.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Practical aspects of imputation-driven meta-analysis of genome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Validating, augmenting and refining genome-wide association signals

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Meta-analysis in genome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common variants at CD40 and other loci confer risk of rheumatoid arthritis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common 5p15.33 and 6p21.33 variants influence lung cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Multiple loci identified in a genome-wide association study of prostate cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Multiple newly identified loci associated with prostate cancer susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies five susceptibility loci for glioma

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies three loci associated with melanoma risk

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

New common variants affecting susceptibility to basal cell carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Lung cancer susceptibility locus at 5p15.33

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

When the smoke clears ..

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genetic variation in LIN28B is associated with the timing of puberty

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Meta-analysis of genome-wide association data identifies two loci influencing age at menarche

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Loci at chromosomes 13, 19 and 20 influence age at natural menopause

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association studies identify loci associated with age at menarche and age at natural menopause

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association study of testicular germ cell tumor

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The genetics of multiple sclerosis: SNPs to pathways to pathogenesis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Recent progress in rheumatoid arthritis genetics: one step towards improved patient care

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Review of recent genome-wide association scans in lupus

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

GWA studies: rewriting the story of IBD.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The genetics of chronic inflammatory diseases

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Autoimmune diseases: insights from genome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common variants at five new loci associated with early-onset inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study reveals genetic risk underlying Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Sorl1 as an Alzheimer's disease predisposition gene?

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common variants on chromosome 6p22.1 are associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common variants conferring risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Schizophrenia genetics: advancing on two fronts

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The genetics and immunopathogenesis of inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Mapping complex disease traits with global gene expression

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Personal genomes: The case of the missing heritability

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Finding the missing heritability of complex diseases

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Polygenes, risk prediction, and targeted prevention of breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Cumulative association of five genetic variants with prostate cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common genetic variation and human traits

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genomewide association studies--illuminating biologic pathways

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genetic risk prediction--are we there yet?

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Detecting shared pathogenesis from the shared genetics of immune-related diseases

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genetic variants associated with complex human diseases show wide variation across multiple populations

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The diploid genome sequence of an individual human

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The complete genome of an individual by massively parallel DNA sequencing

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Accurate whole human genome sequencing using reversible terminator chemistry

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The diploid genome sequence of an Asian individual

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

A highly annotated whole-genome sequence of a Korean individual

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Single-molecule sequencing of an individual human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

1000 Genomes Project promises closer look at variation in human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Human genetic variation and its contribution to complex traits

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Relative impact of nucleotide and copy number variation on gene expression phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Segmental copy number variation shapes tissue transcriptomes.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The impact of copy number variation on local gene expression in mouse hematopoietic stem and progenitor cells

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Common deletion polymorphisms in the human genome.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Integrated detection and population-genetic analysis of SNPs and copy number variation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Origins and functional impact of copy number variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Psoriasis is associated with increased beta-defensin genomic copy number

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Genomic copy number variation, human health, and disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Tandem repeat polymorphisms: modulators of disease susceptibility and candidates for 'missing heritability'.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Targeted capture and massively parallel sequencing of 12 human exomes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.19

7 January 2021

Identifiers

DOI

10.1038/JHG.2010.19

1 reference

Dimensions Publication ID

31 July 2017

0 references

1 reference