DNA variations in human and medical genetics: 25 years of my experience (Q37374228)

20 August 2017

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title

DNA variations in human and medical genetics: 25 years of my experience (English)

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20 August 2017

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Yusuke Nakamura

1

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20 August 2017

9 January 2009

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Journal of Human Genetics

20 August 2017

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20 August 2017

54

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20 August 2017

1

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20 August 2017

1-8

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https://scigraph.springernature.com/pub.10.1038/jhg.2008.6

20 August 2017

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cites work

Variable number of tandem repeat (VNTR) markers for human gene mapping

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Hypervariable 'minisatellite' regions in human DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Characterization of eight VNTR loci by agarose gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Allelotype of colorectal carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genetic alterations during colorectal-tumor development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

An extended genetic linkage map of markers for human chromosome 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A polymorphic DNA marker genetically linked to Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

The International HapMap Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A SNP in the ABCC11 gene is the determinant of human earwax type

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Coding SNP in tenascin-C Fn-III-D domain associates with adult asthma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Functional promoter polymorphism in the TBX21 gene associated with aspirin-induced asthma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A functional SNP in EDG2 increases susceptibility to knee osteoarthritis in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Common variants in DVWA on chromosome 3p24.3 are associated with susceptibility to knee osteoarthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Association of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Single nucleotide polymorphisms in the gene encoding Krüppel-like factor 7 are associated with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A genetic risk factor for periodic limb movements in sleep

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Variants conferring risk of atrial fibrillation on chromosome 4q25.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genome-wide association study identifies novel breast cancer susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A common allele on chromosome 9 associated with coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Risk alleles for multiple sclerosis identified by a genomewide study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Male-pattern baldness susceptibility locus at 20p11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Identification of loci associated with schizophrenia by genome-wide association and follow-up

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Molecular mechanisms for genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genomic rearrangements and sporadic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Lamin B1 duplications cause autosomal dominant leukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Segmental duplications and copy-number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Fine-scale structural variation of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A worldwide survey of haplotype variation and linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Studies in 3,523 Norwegians and Meta-Analysis in 11,571 Subjects Indicate That Variants in the Hepatocyte Nuclear Factor 4 (HNF4A) P2 Region Are Associated With Type 2 Diabetes in Scandinavians

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Common variants in maturity-onset diabetes of the young genes and future risk of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Common variants in WFS1 confer risk of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Telomerase mutations in families with idiopathic pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Adult-onset pulmonary fibrosis caused by mutations in telomerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Randomized trial of genotype-guided versus standard warfarin dosing in patients initiating oral anticoagulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

The role of genetic variation in thiopurine methyltransferase activity and the efficacy and/or side effects of azathioprine therapy in dermatologic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Medical genetics: a marker for Stevens-Johnson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-transcriptase inhibitor abacavir

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Pharmacogenomics-based tailored versus standard therapeutic regimen for eradication of H. pylori

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Disposition and metabolic fate of atomoxetine hydrochloride: the role of CYP2D6 in human disposition and metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Codeine intoxication associated with ultrarapid CYP2D6 metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

The impact of cytochrome P450 2D6 metabolism in women receiving adjuvant tamoxifen

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Impact of CYP2D6*10 on recurrence-free survival in breast cancer patients receiving adjuvant tamoxifen therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Successful efavirenz dose reduction in HIV type 1-infected individuals with cytochrome P450 2B6 *6 and *26.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

The effect of CYP3A5 and MDR1 (ABCB1) polymorphisms on cyclosporine and tacrolimus dose requirements and trough blood levels in stable renal transplant patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

ABCB1 (MDR1) gene polymorphisms are associated with the clinical response to paroxetine in patients with major depressive disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

SLCO1B1 variants and statin-induced myopathy--a genomewide study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

Effect of genetic variation in the organic cation transporter 1 (OCT1) on metformin action

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

Functional haplotypes of IL-12B are associated with childhood atopic asthma

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

Association of the RIP2 gene with childhood atopic asthma

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

HLA-B*3505 allele is a strong predictor for nevirapine-induced skin adverse drug reactions in HIV-infected Thai patients

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

Hereditary pancreatitis caused by triplication of the trypsinogen locus

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

A high-resolution survey of deletion polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

Validation of the associations between single nucleotide polymorphisms or haplotypes and responses to disease-modifying antirheumatic drugs in patients with rheumatoid arthritis: a proposal for prospective pharmacogenomic study in clinical practice

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.6

7 January 2021

Identifiers

DOI

10.1038/JHG.2008.6

1 reference

20 August 2017

1 reference

PubMed ID

19158818