Common variants in the trichohyalin gene are associated with straight hair in Europeans - Test2 - elhamkhani - TriplyDB

Common variants in the trichohyalin gene are associated with straight hair in Europeans

Common variants in the trichohyalin gene are associated with straight hair in Europeans

http://www.wikidata.org/entity/Q24657996

about

Web-based, participant-driven studies yield novel genetic associations for common traits Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture Genome-wide association meta-analysis identifies new endometriosis risk loci Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking.A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality The Impact of Evolutionary Driving Forces on Human Complex Diseases: A Population Genetics Approach Epidermal transglutaminase (TGase 3) is required for proper hair development, but not the formation of the epidermal barrier Shared genetic control of expression and methylation in peripheral blood A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features Genome-wide association study reveals two new risk loci for bipolar disorder Genome-wide association study of blood lead shows multiple associations near ALAD The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics Trichohyalin-like proteins have evolutionarily conserved roles in the morphogenesis of skin appendages Efficient replication of over 180 genetic associations with self-reported medical data A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits Hair analysis as a biomonitor for toxicology, disease and health status Genetic basis of a cognitive complexity metric Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection.Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data.Gradient Boosting as a SNP Filter: an Evaluation Using Simulated and Hair Morphology Data.Transcriptome profile at different physiological stages reveals potential mode for curly fleece in Chinese tan sheep.Revealing phenotype-associated functional differences by genome-wide scan of ancient haplotype blocks.A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure.Contribution of genetic variation to transgenerational inheritance of DNA methylation A genome-wide association study of sleep habits and insomnia.Educational attainment: a genome wide association study in 9538 Australians A versatile gene-based test for genome-wide association studies.Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis.The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12 Improving human forensics through advances in genetics, genomics and molecular biology.GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis An integrated approach to reduce the impact of minor allele frequency and linkage disequilibrium on variable importance measures for genome-wide data.Genetic and environmental exposures constrain epigenetic drift over the human life course.Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study.

P2860

Q21092440-5292A477-8B7F-4D60-80E5-D2D6D89E0EAF Q21710707-F377CB92-C33B-4144-9195-1E99275B928E Q24273442-A1A8B003-13A5-4E64-ABFB-5E8C6FCA7BF5 Q24597781-08B36F76-4D12-483A-ADBD-624DF19EE9EC Q24601618-C2358277-3B12-4072-BD59-1DDEF308802A Q24612743-1BE8CDC3-8F12-4041-89A5-E67FC1C63955 Q24625579-9490C79C-8541-4CDA-8A4E-78B0BB3FCAC2 Q26744597-4819244D-D814-4A14-BB74-4088796AB832 Q27305334-5940A733-DA19-4B5E-87BE-AA6F4507C74F Q27316677-F09DC4BB-BC3C-478B-B43C-218090E53EB6 Q28005553-A3164DDB-2223-478B-97CC-251A46AA17CB Q28235753-BEB27F10-66DC-4D4B-935C-D1C23D21F6E1 Q28395960-F44393F2-CC08-4EBA-B43A-36759C80EBF1 Q28482577-B737B59B-71B2-4B97-BF38-08ECE06767B4 Q28650131-29F00BA4-5101-464F-8872-C93CD987D1FB Q28741344-C68C1444-A33E-4B21-9C1D-4EC57A692326 Q28943311-1DC5101C-EB41-4FD2-BF6D-E2710F466CD6 Q28943352-70A0CBBB-2CB4-44F6-B57A-8D274F04D99D Q29391798-004D2A0E-D133-48BD-AFFE-B47E16136502 Q30413889-6AB87331-3FC3-48CD-A8CD-5A3EB4CB62D1 Q30427895-83F97041-2595-4D67-8AAF-ED15651F15E9 Q30630709-2E8146E0-BC4A-4F37-98F2-66AC1ACC6297 Q30729547-7D35569E-6EE6-4329-939B-D318AFEF30C5 Q31131727-69CED311-53E0-4181-87D4-27A96D47A8D1 Q33606025-A370ACBB-8E73-4FDB-96A4-EC5E4BD94212 Q33772991-751B6954-F837-4D6A-8B90-9D9FCB30A540 Q33813301-DAF58142-26C7-4DF7-B40B-15E846CE3AF2 Q33851705-51DFFB40-6F13-4075-9C69-670E5C0C5F86 Q33939081-A233C38F-8A0A-4C52-8C98-6E1DD14E2A80 Q33960489-3ECB5093-91D8-4B43-836C-92725BE6B686 Q34115072-307D2215-4189-4743-B25C-4260B85414D8 Q34129017-CD9EFB93-EC27-4B81-A4C7-C4DE72B23083 Q34165424-FD5692A9-567C-47BB-8315-EBE2331953A7 Q34207484-6E82AC2A-997A-4421-BFE9-0AA537112D74 Q34243943-D8D7C8CE-BBA0-4DCC-A344-7ED3D44E39EE Q34289755-DDED1736-B6EE-4216-B69B-79C8D4FB8D94 Q34331816-1B088718-4C5D-47BF-AA1A-70C262194534 Q34357568-BD311EAA-259A-4B03-80A0-DD9E396592B8 Q34439314-752468FA-E8BE-4F69-A474-B88FF65847B3 Q34450263-37FB9C87-3DB6-461E-8815-79BC1A63E0C3

P2860

Common variants in the trichohyalin gene are associated with straight hair in Europeans

http://www.wikidata.org/entity/Q24657996

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@ast

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@en

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@nl

type

label

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@ast

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@en

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@nl

prefLabel

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@ast

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@en

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@nl

P1433

Q24657996-E982F84C-9DF1-488E-A69F-4C05337C02CF

P1476

Q24657996-2D41D33D-61C9-4E9D-9FA6-F31CE8BF1002

P2093

Q24657996-47168D1D-1206-418D-ADB1-E2B116505C78

Q24657996-48DF90EE-6A54-4E5E-BD5A-E97BBABE04A0

Q24657996-61A3CF8B-E1A7-4E95-9130-ED75681E6796

Q24657996-8BDEB803-ACCE-4A44-BC37-DAFF0DB3D657

Q24657996-98E277FF-5E3F-4F98-9574-9603C9836EC2

P2860

Q24657996-01B1F77A-2D07-4C85-A2D5-8F7D7117C9A3

Q24657996-0324C46A-7CCA-4AD1-9F4F-5996862003DD

Q24657996-071A8AF1-3AC1-4D39-8D08-15B58D080DC4

Q24657996-0B85096D-A292-46B0-A1EC-CC7140C5825D

Q24657996-227FF2C5-A7CC-4720-9CB0-50A851A33FDA

Q24657996-31DE304A-7B63-42D2-8354-C549C7280F61

Q24657996-328398B1-8F39-4CE3-B009-69AFE316D80F

Q24657996-41210288-BC54-45F8-819A-D1172D64AE0C

Q24657996-46AF8C2D-41D3-4286-925F-DED50D114623

Q24657996-60924077-520D-4EAE-838A-E36F854B9C2A

P304

Q24657996-6FE80257-EF9C-4092-B170-7268C1C9252E

P31

Q24657996-DFD25369-D8A9-4708-A3AC-610F5FA0EE6B

P3181

Q24657996-EE3C7E83-BEA3-4E50-B634-FF70BA2E83F1

P356

Q24657996-BBCA54A9-B6AF-4F9B-8D33-0FC093FEC8D1

P407

Q24657996-4D9F5E1D-AB62-4A1A-B819-3D3FB89655CD

P433

Q24657996-5DB6A738-1265-432F-AC81-9FE3283CA49B

P478

Q24657996-6840279B-AD7D-42E9-830D-DE9D91417BDA

P50

Q24657996-24DF235D-83AB-4E5F-A415-53C6CB1FA490

Q24657996-2AD71638-F7E7-4ED5-B654-06584CBDD7CC

Q24657996-2B69BB03-B577-4EA5-BBFD-37A1348F1FFC

Q24657996-3D4226D9-8019-4A64-A3E4-419D9EA11A28

Q24657996-49915D69-12D4-479D-AE36-2128A3702333

Q24657996-5975A58E-8A9D-4619-B832-2EF6A876BF4E

Q24657996-770C88E3-ECAA-4FE8-87CE-5C09A95C1885

Q24657996-C234824C-9F86-41B5-88B5-F0D3B17E7FE4

Q24657996-CEF75DD8-3369-4598-B3BC-B652D6576FB4

Q24657996-EA79BE1A-6D5F-49F6-879B-0C2E4598B4F7

P577

Q24657996-B192C716-707A-4535-BFCC-C41E27B4DB6A

P5875

Q24657996-C29F0A99-721B-4A6A-BDC7-898E0289CC2F

P698

Q24657996-97DF8BAC-4905-406E-9097-7BB62A2DCD3E

P932

Q24657996-87EA50C8-139A-483D-938F-AF273A716FB4

P3181

P356

J.AJHG.2009.10.009

P1433

American Journal of Human Genetics

P1476

Common variants in the trichohyalin gene are associated with straight hair in Europeans

@en

P2093

Brian P McEvoy

http://www.w3.org/2001/XMLSchema#string

Jodie N Painter

http://www.w3.org/2001/XMLSchema#string

Manuel A R Ferreira

http://www.w3.org/2001/XMLSchema#string

Megan J Campbell

http://www.w3.org/2001/XMLSchema#string

Scott D Gordon

http://www.w3.org/2001/XMLSchema#string

P2860

A map of recent positive selection in the human genome

Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia

The structure of human trichohyalin. Potential multiple roles as a functional EF-hand-like calcium-binding protein, a cornified cell envelope precursor, and an intermediate filament-associated (cross-linking) protein

Signals of recent positive selection in a worldwide sample of human populations

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color

A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation

The International HapMap Project

SIFT: Predicting amino acid changes that affect protein function

Worldwide human relationships inferred from genome-wide patterns of variation

Human non-synonymous SNPs: server and survey

P304

750-5

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

1199846

http://www.w3.org/2001/XMLSchema#string

P356

10.1016/J.AJHG.2009.10.009

http://www.w3.org/2001/XMLSchema#string

P407

P433

5

http://www.w3.org/2001/XMLSchema#string

P478

85

http://www.w3.org/2001/XMLSchema#string

P50

Narelle Hansell

Sarah E. Medland

Anjali K. Henders

Margaret J. Wright

Stuart Macgregor

Grant W. Montgomery

P577

2009-11-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

38073360

http://www.w3.org/2001/XMLSchema#string

P698

19896111

http://www.w3.org/2001/XMLSchema#string

P932

2775823

http://www.w3.org/2001/XMLSchema#string