Works matching IS 03406717 AND DT 2012 AND VI 131 AND IP 7
Results: 28
Randall H. Morse (ed.): Chromatin remodelling: methods and protocols.
- Published in:
- 2012
- By:
- Publication type:
- Book Review
Erratum to: Association between gout and polymorphisms in GCKR in male Han Chinese.
- Published in:
- 2012
- By:
- Publication type:
- Correction Notice
Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1269, doi. 10.1007/s00439-012-1155-5
- By:
- Publication type:
- Article
Association between gout and polymorphisms in GCKR in male Han Chinese.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1261, doi. 10.1007/s00439-012-1151-9
- By:
- Publication type:
- Article
Genetic variants of the MRC1 gene and the IFNG gene are associated with leprosy in Han Chinese from Southwest China.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1251, doi. 10.1007/s00439-012-1153-7
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- Publication type:
- Article
The prevalence of CD33 and MS4A6A variant in Chinese Han population with Alzheimer's disease.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1245, doi. 10.1007/s00439-012-1154-6
- By:
- Publication type:
- Article
Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1235, doi. 10.1007/s00439-012-1152-8
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- Publication type:
- Article
Genome-wide two-locus epistasis scans in prostate cancer using two European populations.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1225, doi. 10.1007/s00439-012-1148-4
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- Publication type:
- Article
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1217, doi. 10.1007/s00439-012-1149-3
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- Publication type:
- Article
Evolutionary genetics of the human Rh blood group system.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1205, doi. 10.1007/s00439-012-1147-5
- By:
- Publication type:
- Article
Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1197, doi. 10.1007/s00439-012-1144-8
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- Publication type:
- Article
Cognitive and serum BDNF correlates of BDNF Val66Met gene polymorphism in patients with schizophrenia and normal controls.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1187, doi. 10.1007/s00439-012-1150-x
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- Publication type:
- Article
Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1173, doi. 10.1007/s00439-012-1139-5
- By:
- Publication type:
- Article
The human lactase persistence-associated SNP −13910*T enables in vivo functional persistence of lactase promoter-reporter transgene expression.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1153, doi. 10.1007/s00439-012-1140-z
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- Publication type:
- Article
Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1161, doi. 10.1007/s00439-012-1142-x
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- Publication type:
- Article
A multi-ethnic study of a PNPLA3 gene variant and its association with disease severity in non-alcoholic fatty liver disease.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1145, doi. 10.1007/s00439-012-1141-y
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- Publication type:
- Article
A functional variant of the collagen type III alpha1 gene modify risk of sporadic intracranial aneurysms.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1137, doi. 10.1007/s00439-012-1138-6
- By:
- Publication type:
- Article
Unraveling the genetic component of systemic sclerosis.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1023, doi. 10.1007/s00439-011-1137-z
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- Publication type:
- Article
LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z−) agrin.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1123, doi. 10.1007/s00439-011-1132-4
- By:
- Publication type:
- Article
Mutation risk associated with paternal and maternal age in a cohort of retinoblastoma survivors.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1115, doi. 10.1007/s00439-011-1126-2
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- Publication type:
- Article
Genetic association between human chitinases and lung function in COPD.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1105, doi. 10.1007/s00439-011-1127-1
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- Publication type:
- Article
Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1095, doi. 10.1007/s00439-011-1136-0
- By:
- Publication type:
- Article
GWAS-linked GAK locus in Parkinson's disease in Han Chinese and meta-analysis.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1089, doi. 10.1007/s00439-011-1133-3
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- Publication type:
- Article
Effects of MAOA promoter methylation on susceptibility to paranoid schizophrenia.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1081, doi. 10.1007/s00439-011-1131-5
- By:
- Publication type:
- Article
OPRM1 and EGFR contribute to skin pigmentation differences between Indigenous Americans and Europeans.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1073, doi. 10.1007/s00439-011-1135-1
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- Publication type:
- Article
Consistency of genome-wide associations across major ancestral groups.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1057, doi. 10.1007/s00439-011-1124-4
- By:
- Publication type:
- Article
Association of PDE4B polymorphisms and schizophrenia in Northwestern Han Chinese.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1047, doi. 10.1007/s00439-011-1120-8
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- Publication type:
- Article
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.
- Published in:
- Human Genetics, 2012, v. 131, n. 7, p. 1039, doi. 10.1007/s00439-011-1121-7
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- Publication type:
- Article