Found: 23
Select item for more details and to access through your institution.
Variable set enrichment analysis in genome-wide association studies.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 893, doi. 10.1038/ejhg.2011.46
- By:
- Publication type:
- Article
Evaluation of Lynch syndrome modifier genes in 748 MMR mutation carriers.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 887, doi. 10.1038/ejhg.2011.44
- By:
- Publication type:
- Article
Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 921, doi. 10.1038/ejhg.2011.41
- By:
- Publication type:
- Article
Clinical utility gene card for: Gorlin syndrome.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 1, doi. 10.1038/ejhg.2011.9
- By:
- Publication type:
- Article
Meta-analysis of genome-wide association for migraine in six population-based European cohorts.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 901, doi. 10.1038/ejhg.2011.48
- By:
- Publication type:
- Article
Clinical utility gene card for: Gitelman syndrome.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 1, doi. 10.1038/ejhg.2011.14
- By:
- Publication type:
- Article
Novel mutations affecting LRP5 splicing in patients with osteoporosis-pseudoglioma syndrome (OPPG).
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 875, doi. 10.1038/ejhg.2011.42
- By:
- Publication type:
- Article
The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 851, doi. 10.1038/ejhg.2011.52
- By:
- Publication type:
- Article
Clinical utility gene card for: Mowat-Wilson syndrome.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 1, doi. 10.1038/ejhg.2011.12
- By:
- Publication type:
- Article
Association of TH01 with human longevity revisited.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 924, doi. 10.1038/ejhg.2011.43
- By:
- Publication type:
- Article
Gene set analysis of SNP data: benefits, challenges, and future directions.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 837, doi. 10.1038/ejhg.2011.57
- By:
- Publication type:
- Article
Everything a health professional needs to know about genetics.
- Published in:
- 2011
- By:
- Publication type:
- Book Review
Strengthening the reporting of genetic risk prediction studies: the GRIPS statement.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 833, doi. 10.1038/ejhg.2011.25
- By:
- Publication type:
- Article
Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 857, doi. 10.1038/ejhg.2011.59
- By:
- Publication type:
- Article
Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14).
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 1, doi. 10.1038/ejhg.2010.243
- By:
- Publication type:
- Article
A novel approach for small sample size family-based association studies: sequential tests.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 915, doi. 10.1038/ejhg.2011.51
- By:
- Publication type:
- Article
Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 844, doi. 10.1038/ejhg.2011.47
- By:
- Publication type:
- Article
Clinical utility gene card for: Usher syndrome.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 1, doi. 10.1038/ejhg.2011.15
- By:
- Publication type:
- Article
Cancer GAMAdb: database of cancer genetic associations from meta-analyses and genome-wide association studies.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 928, doi. 10.1038/ejhg.2011.53
- By:
- Publication type:
- Article
New disease gene location and high genetic heterogeneity in idiopathic scoliosis.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 865, doi. 10.1038/ejhg.2011.31
- By:
- Publication type:
- Article
Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 870, doi. 10.1038/ejhg.2011.37
- By:
- Publication type:
- Article
Variants of gene for microsomal prostaglandin E2 synthase show association with disease and severe inflammation in rheumatoid arthritis.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 908, doi. 10.1038/ejhg.2011.50
- By:
- Publication type:
- Article
The genetic component of human longevity: analysis of the survival advantage of parents and siblings of Italian nonagenarians.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 882, doi. 10.1038/ejhg.2011.40
- By:
- Publication type:
- Article