Found: 29
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Genetic analysis and natural history of Parkinson's disease due to the LRRK2 G2019S variant.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 6, p. 1996, doi. 10.1093/brain/awae073
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- Article
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
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- Nature Genetics, 2013, v. 45, n. 8, p. 907, doi. 10.1038/ng.2686
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- Article
Novel Associations for Hypothyroidism Include Known Autoimmune Risk Loci.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0034442
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Efficient Replication of over 180 Genetic Associations with Self-Reported Medical Data.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023473
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- Article
Dazl Functions in Maintenance of Pluripotency and Genetic and Epigenetic Programs of Differentiation in Mouse Primordial Germ Cells In Vivo and In Vitro.
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- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005654
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- Article
Evolutionary comparison of the reproductive genes, DAZL and BOULE, in primates with and without DAZ.
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- Development Genes & Evolution, 2006, v. 216, n. 3, p. 158, doi. 10.1007/s00427-005-0039-2
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- Article
Variants in Deleted in AZoospermia-Like ( DAZL) are correlated with reproductive parameters in men and women.
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- Human Genetics, 2006, v. 118, n. 6, p. 730, doi. 10.1007/s00439-005-0098-5
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- Article
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08923-6
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- Article
Identifying Ashkenazi Jewish BRCA1/2 founder variants in individuals who do not self-report Jewish ancestry.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-63466-x
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- Article
Validity of the cold pressor test and pain sensitivity questionnaire via online self-administration.
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- PLoS ONE, 2020, v. 15, n. 4, p. 1, doi. 10.1371/journal.pone.0231697
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- Article
Novel missense mutations of the Deleted-in-AZoospermia-Like (DAZL) gene in infertile women and men.
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- Reproductive Biology & Endocrinology, 2006, v. 4, p. 1
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- Article
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person.
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- Nature Communications, 2016, v. 7, n. 2, p. 10448, doi. 10.1038/ncomms10448
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- Article
Corrigendum: Rare coding variants and X-linked loci associated with age at menarche.
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- Nature Communications, 2015, v. 6, n. 12, p. 10257, doi. 10.1038/ncomms10257
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- Article
Shared genetic aetiology of puberty timing between sexes and with health-related outcomes.
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- Nature Communications, 2015, v. 6, n. 11, p. 8842, doi. 10.1038/ncomms9842
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- Article
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.
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- Nature Communications, 2015, v. 6, n. 9, p. 8464, doi. 10.1038/ncomms9464
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- Article
Rare coding variants and X-linked loci associated with age at menarche.
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- Nature Communications, 2015, v. 6, n. 8, p. 7756, doi. 10.1038/ncomms8756
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- Article
Quantifying prion disease penetrance using large population control cohorts.
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- Science Translational Medicine, 2016, v. 8, n. 322, p. 1, doi. 10.1126/scitranslmed.aad5169
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- Article
Assessment of the Genetic Basis of Rosacea by Genome-Wide Association Study.
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- Journal of Investigative Dermatology, 2015, v. 135, n. 6, p. 1548, doi. 10.1038/jid.2015.53
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- Article
Genome-Wide Association Analysis Implicates Elastic Microfibrils in the Development of Nonsyndromic Striae Distensae.
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- Journal of Investigative Dermatology, 2013, v. 133, n. 11, p. 2628, doi. 10.1038/jid.2013.196
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- Article
Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology.
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- Journal of Investigative Dermatology, 2013, v. 133, n. 6, p. 1489, doi. 10.1038/jid.2013.43
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- Article
Modeling prior information of common genetic variants improves gene discovery for neuroticism.
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- Human Molecular Genetics, 2017, v. 26, n. 22, p. 4530, doi. 10.1093/hmg/ddx340
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Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
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- Human Molecular Genetics, 2016, v. 25, n. 9, p. 1867, doi. 10.1093/hmg/ddw037
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Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.
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- Human Molecular Genetics, 2015, v. 24, n. 9, p. 2700, doi. 10.1093/hmg/ddv028
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- Article
Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00257-5
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- Article
Genome-Wide Analysis Points to Roles for Extracellular Matrix Remodeling, the Visual Cycle, and Neuronal Development in Myopia.
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- PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003299
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- Article
Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases.
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- PLoS Genetics, 2012, v. 8, n. 5, p. 1, doi. 10.1371/journal.pgen.1002746
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- Article
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease.
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- PLoS Genetics, 2011, v. 7, n. 6, p. 1, doi. 10.1371/journal.pgen.1002141
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- Article
Web-Based, Participant-Driven Studies Yield Novel Genetic Associations for Common Traits.
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- PLoS Genetics, 2010, v. 6, n. 6, p. 1, doi. 10.1371/journal.pgen.1000993
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- Article
Genetic variants associated with breast size also influence breast cancer risk.
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- BMC Medical Genetics, 2012, v. 13, n. 1, p. 53, doi. 10.1186/1471-2350-13-53
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- Article