About: Bronya J. B. Keats

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Australian geneticist

Attributes	Values
rdf:type	Item
description	эрдэмтэн (mn) Australian geneticist (en) genetista australiana (es) عالمة وراثة أسترالية (ar) Avustralyalı genetikçi (d. 1951) (tr)
rdfs:label	Bronya J. B. Keats (en)
skos:prefLabel	Bronya J. B. Keats (en)
name	Bronya J. B. Keats (en)
instance of	wds:Q114430800-E18FF5CD-6A30-48E4-9321-3238F293B2D1
instance of	Homo sapiens
zbMATH author ID	wds:Q114430800-5E75CE77-C860-4342-95C3-DDBCBD951B41
Academic Tree ID	wds:Q114430800-74E529D4-E9EC-46C9-86C6-0E9E64539220
Google Knowledge Graph ID	wds:Q114430800-fa0a51ef-4094-65aa-2256-295f96b4ef77
Google Knowledge Graph ID	http://g.co/kg/g/113qjwlv4
zbMATH author ID	keats.bronya
Academic Tree ID	649388
Google Knowledge Graph ID	/g/113qjwlv4
skos:altLabel	Bronya B. Keats (en) Bronya J. Keats (en) Bronya Joy Beveridge Keats (en) Bronya Keats (en) Bronya Wierst (en) Bronya van Vierst (en)
Nationale Thesaurus voor Auteursnamen ID	wds:Q114430800-58f1a2c2-4532-d6b7-8673-d4eb7d3cdae4
occupation	wds:Q114430800-76C866BB-B9C7-4BE2-990B-2D54E018E60B
employer	wds:Q114430800-318f1d79-4d1a-6f60-1af6-cb09e3052a55 wds:Q114430800-d9a2ef60-48af-0ffe-6d45-a52fec199c81 wds:Q114430800-f6da1f16-42fc-5e01-38e3-f8a963b7875a
place of birth	wds:Q114430800-6a905d18-493e-7607-4ad4-177e996e8f1f
sex or gender	wds:Q114430800-9b37c4a3-45ad-2163-3007-59d3c0fe365a
ISNI	wds:Q114430800-821180cd-40ea-071c-02c8-822b20529b45
VIAF ID	wds:Q114430800-cc30f564-419e-fb80-ab07-4d7215576239
Bibliothèque nationale de France ID	wds:Q114430800-ef2864bb-4af4-e58d-8717-9b5723b7bee5
IdRef ID	wds:Q114430800-4167b8d4-470d-4cf9-1693-49d174623fea
country of citizenship	wds:Q114430800-c4cae908-4949-3656-13a0-387acba28bbc
date of birth	wds:Q114430800-d4d11524-4edd-a7df-551c-247b2e14250d
maintained by WikiProject	wds:Q114430800-DF6B650A-F85B-49EE-9880-C333AA0FDD5E
educated at	wds:Q114430800-afd0b694-4e4a-3803-5a1c-2d2b785e2388
family name	wds:Q114430800-12a4428f-4281-135b-5107-7d5cccc60e83
National Library of Israel J9U ID	wds:Q114430800-9785778A-5D81-4152-9C2A-40F1909DA1AE
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p071884769
VIAF ID	http://viaf.org/viaf/7637487
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb14601736x#about
IdRef ID	http://www.idref.fr/074733516/id
Nationale Thesaurus voor Auteursnamen ID	071884769
occupation	geneticist
employer	Australian National University LSU Health Sciences Center New Orleans University of Hawaiʻi
place of birth	Glenelg
sex or gender	female organism
ISNI	000000002024920X
VIAF ID	7637487
Bibliothèque nationale de France ID	14601736x
IdRef ID	074733516
country of citizenship	Australia
date of birth	1951-03-15 00:00:00Z (xsd:dateTime)
maintained by WikiProject	WikiProject Mathematics
educated at	Australian National University
family name	Keats
National Library of Israel J9U ID	987007366916205171
Dimensions author ID	wds:Q114430800-6E0E8C41-CE1A-4B18-8BB2-7F8BF392564B wds:Q114430800-C62FD478-ADF7-4E8B-A869-7AE0932A57B6 wds:Q114430800-CEE780DB-E00E-4E82-99A9-FD1C84EE51C7
Dimensions author ID	013101171607.41 016616341007.64
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q114430800
is author of	Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11. Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium Localization of two genes for Usher syndrome type I to chromosome 11. OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene Clinical variability and genetic heterogeneity within the Acadian Usher population A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis Chronic and recurrent otitis media: a genome scan for susceptibility loci Report of the committee on linkage and gene order Report of the committee on linkage and gene order A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26. A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10. Linkage map integration. Male sexual orientation and genetic evidence Genes and people in the Caspian Littoral: a population genetic study in Northern Iran Genomics and hearing impairment. Possible linkages (lod score over 1.5) and a tentative map of the Jk-Km linkage group A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells. A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14-21. Integration of gene maps: chromosome X Pathology and physiology of auditory neuropathy with a novel mutation in the MPZ gene (Tyr145->Ser). Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred. Ush1c216A knock-in mouse survives Katrina. Coagulation factor XIII: a useful polymorphic genetic marker Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness Bayesian analysis of haplotypes for linkage disequilibrium mapping A multivariate method for detecting genetic linkage, with application to a pedigree with an adverse lipoprotein phenotype Genetic heterogeneity in Usher syndrome Genetic variation of recent Alu insertions in human populations

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