About: Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology

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About: Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology Goto Sponge NotDistinct Permalink

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description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2013 (uk) im Juni 2013 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57264068-C565E64C-A2AD-4EF2-BC6F-3BD582AB7C3D
publication date	2013-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57264068-CE83D3C4-3414-4B52-BA37-22DCA54C2C48
language of work or name	English
exact match	wds:Q57264068-F9A6B4F9-20CF-45F3-8498-6601A58F649A
exact match	https://scigraph.springernature.com/pub.10.1038/jid.2013.43
cites work	wds:Q57264068-077E208A-005A-404A-8F0E-349F6A12DB97 wds:Q57264068-0CD4476C-E852-4BCC-A6EC-8815AD410DD7 wds:Q57264068-1443B3F3-8474-4E92-A453-FD21B8178E74 wds:Q57264068-18FF5721-93AE-4522-A05F-47156DA06F64 wds:Q57264068-1E055EEF-FDAE-4AD4-A278-C50C833B65E7 wds:Q57264068-1E338E01-56F8-43B9-AE45-5165FB9887EF wds:Q57264068-205A7E2C-DD4E-418D-B0E1-EAC61580E72B wds:Q57264068-2112AE63-BEFA-4B36-A880-5DDE555F9859 wds:Q57264068-2B8A94EC-0813-48E6-B26C-3806340DD0B1 wds:Q57264068-2F10BCE4-6010-4D34-9C0E-8E518B287BCB wds:Q57264068-310169E0-4FCA-4799-A411-13DECEA76614 wds:Q57264068-3E0141B0-7217-48EE-B0AB-18FF69C11C1B wds:Q57264068-3F8A0009-122B-445F-A03C-122B47C13329 wds:Q57264068-4233C42D-E6A4-4371-BED1-E7E8A3F10C7F wds:Q57264068-494FC70E-BD3A-46EE-81BA-B9928DE66105 wds:Q57264068-4B99AF06-DB9F-48A1-BFA9-64C516013E49 wds:Q57264068-62D466A5-C138-4913-B68F-746A60C921CF wds:Q57264068-6A301257-821F-488C-B033-30B28535EF85 wds:Q57264068-7C01E1ED-A2C9-42E9-B1A6-4FAFC49C2484 wds:Q57264068-8553DB0E-8685-49BE-A571-239B3D1CEFD1 wds:Q57264068-865C531B-2E43-4BF2-B1A9-59547AD61407 wds:Q57264068-9A5E2C28-E1E0-44FB-A78D-4710223DB9AA wds:Q57264068-9F143DB4-CD15-420C-93C7-9FA2F0AB666E wds:Q57264068-A1D862F8-DCA6-42FA-933D-5D46E2511767 wds:Q57264068-A64E4350-CAAD-4501-B17E-B758687B5E29 wds:Q57264068-A79A0187-E0F6-42B8-BFE1-322FE54B5B4C wds:Q57264068-AAE83980-D51B-4E97-B393-81018ADF99DE wds:Q57264068-AE2CE4F6-25A6-4A2F-8151-7688512E6E39 wds:Q57264068-B2D03D58-F1F2-4709-8B58-63929E31908A wds:Q57264068-B310131C-E26F-482C-81D8-0308432207A9 wds:Q57264068-B7EE6054-3CDE-4AAB-A528-9D27F5B98CD7 wds:Q57264068-B93877EF-A4DA-4AA5-9F31-732865D9DF6E wds:Q57264068-BB21BC69-6D77-4076-BE16-52DC9D289C7E wds:Q57264068-C05DB8CD-59C0-492A-B331-7C118055877D wds:Q57264068-C222FFD7-6B75-4C47-924F-FBBF823D7398 wds:Q57264068-CD3E0900-8534-4F65-842D-C512766D09BF wds:Q57264068-D001405D-E3BE-44D4-B576-CE2CB751D1E9 wds:Q57264068-D03A7136-DBE0-468C-8196-99DB3E39A48C wds:Q57264068-D25746B0-8C9B-4EFC-B828-0D0FD8E24AD9 wds:Q57264068-D388ACDE-4F2D-46F9-9867-6806179EAEB6 wds:Q57264068-DB8257FC-50F7-4561-9267-07E6AD7FD626
cites work	WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes Regulation of hair shedding by the type 3 IP3 receptor. Tests for Linear Trends in Proportions and Frequencies Practical aspects of imputation-driven meta-analysis of genome-wide association studies The Combination of Estimates from Different Experiments WNT signals are required for the initiation of hair follicle development Patterned loss of hair in man; types and incidence Androgenetic alopecia: pathogenesis and potential for therapy. Diagnostic and predictive value of horizontal sections of scalp biopsy specimens in male pattern androgenetic alopecia Wnt signaling through the beta-catenin pathway is sufficient to maintain, but not restore, anagen-phase characteristics of dermal papilla cells. A second generation human haplotype map of over 3.1 million SNPs Scratching the surface of skin development Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis Web-based, participant-driven studies yield novel genetic associations for common traits Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia EDA2R is associated with androgenetic alopecia. Wnt-frizzled signaling to G-protein-coupled effectors Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering Measuring inconsistency in meta-analyses A simple salting out procedure for extracting DNA from human nucleated cells The Wnt signaling pathway in development and disease Wnt/β-catenin signaling and disease Fast and accurate genotype imputation in genome-wide association studies through pre-phasing Genetic Basis of Male Pattern Baldness INTERSNP: genome-wide interaction analysis guided by a priori information WNT signaling in the control of hair growth and structure. Male hormone stimulation is prerequisite and an incitant in common baldness Common variants in the trichohyalin gene are associated with straight hair in Europeans Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26 Male-pattern baldness susceptibility locus at 20p11. Susceptibility variants for male-pattern baldness on chromosome 20p11. Hormonal regulation of hair follicles exhibits a biological paradox The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia Fine mapping of the human AR/EDA2R locus in androgenetic alopecia Androgens and alopecia Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases Hair loss among elderly men: etiology and impact on perceived age. Wnt10b promotes growth of hair follicles via a canonical Wnt signalling pathway. Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness. The genetics of androgenetic alopecia.
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