About: Deborah A Nickerson

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

genome scientist

Attributes	Values
rdf:type	Item
description	wetenschapper (nl) дослідниця (uk) 研究者 (zh) genome scientist (en)
rdfs:label	Deborah A Nickerson (en) Deborah A Nickerson (nl)
skos:prefLabel	Deborah A Nickerson (en) Deborah A Nickerson (nl)
name	Deborah A Nickerson (en) Deborah A Nickerson (nl)
given name	wds:Q92804625-A08745B2-92FE-48E2-8041-91C7BD494689
given name	Deborah
image	wds:Q92804625-35f6aa61-4065-d97e-6b16-085738b0e803
instance of	wds:Q92804625-EC7F2A38-4A22-4C19-A0FF-11C59FE06BB5
image
instance of	Homo sapiens
Academic Tree ID	wds:Q92804625-dcbc4cba-4007-0d0c-34dd-d2bf92db0c78
Google Knowledge Graph ID	wds:Q92804625-76414B5E-D8C2-4430-91FB-32B631E2C8B0
Google Knowledge Graph ID	http://g.co/kg/g/11ghv7c_bf
Academic Tree ID	510488
Google Knowledge Graph ID	/g/11ghv7c_bf
Google Scholar author ID	wds:Q92804625-8ecd96db-48d8-67ae-2921-db80803cd32b
Google Scholar author ID	zDdAnqwAAAAJ
skos:altLabel	Debbie Nickerson (en) Deborah A. Nickerson (en) Deborah Ann Nickerson (en) Deborah Nickerson (en)
occupation	wds:Q92804625-CF36A098-B261-4B67-A647-D3AAEC23D3FC wds:Q92804625-e8cb7db8-4c2c-dc91-a8cf-eec1773c4556
employer	wds:Q92804625-31e36118-4a9a-b1a4-1704-9559086963a3 wds:Q92804625-34622712-48db-4688-a312-a7c503920425 wds:Q92804625-7dd39ea7-497c-3047-1bc9-760df3d53a1f
nickname	wds:Q92804625-231f3d3d-4fb7-d123-f04f-c94609fd1b50
place of birth	wds:Q92804625-de450c97-42c3-afb3-7f1b-cbe9231c7c93
sex or gender	wds:Q92804625-77b90ede-4720-13db-1e4d-96baca2f5c34
ISNI	wds:q92804625-aff8e36f-4af7-d260-610d-aa8b83253bbc
VIAF ID	wds:Q92804625-a4e1b98c-4a64-a558-b416-d52d49e4b2ff
Library of Congress authority ID	wds:q92804625-865d72c2-4286-e945-978f-79dd412943d1
on focus list of Wikimedia project	wds:Q92804625-F4808781-DC79-400A-882B-7514EE27B230
date of birth	wds:Q92804625-5eba14d9-4e86-9102-db10-bed0af941ec8
date of death	wds:Q92804625-3f8175c7-46f1-6a2f-5620-07fc4bf2965f
educated at	wds:Q92804625-80832c18-4b84-fc29-bda1-3a0a19ede8e5 wds:Q92804625-f83dd35f-4adb-e824-c2c9-a7810f53ee97
family name	wds:Q92804625-55D9DCEB-0B50-4B05-BD85-DD4412FF917E
WorldCat Identities ID (superseded)	wds:q92804625-6c20059c-4ae7-5cfe-05a2-049584e1848c
VIAF ID	http://viaf.org/viaf/102146331987118692936
Library of Congress authority ID	http://id.loc.gov/authorities/names/no2016061312
occupation	researcher genomicist
employer	University of Washington California Institute of Technology University of South Florida
nickname	Debbie (en)
place of birth	Mineola
sex or gender	female organism
ISNI	0000000497264984
VIAF ID	102146331987118692936
Library of Congress authority ID	no2016061312
on focus list of Wikimedia project	WikiProject COVID-19
date of birth	1954-01-01 00:00:00Z (xsd:dateTime)
date of death	2021-12-24 00:00:00Z (xsd:dateTime)
educated at	University of Tennessee, Knoxville Adelphi University
family name	Nickerson
WorldCat Identities ID (superseded)	lccn-no2016061312
ORCID iD	wds:Q92804625-120693D8-5F1B-4E6D-AC66-AEC9476A1180
ORCID iD	https://orcid.org/0000-0002-9954-4897
ORCID iD	0000-0002-9954-4897
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q92804625 Deborah Nickerson
is author of	Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome Mutation of ATF6 causes autosomal recessive achromatopsia USF1 gene variants, cardiovascular risk, and mortality in European Americans: analysis of two US cohort studies. Exome sequencing identifies the cause of a mendelian disorder Targeted capture and massively parallel sequencing of 12 human exomes Mapping complex disease loci in whole-genome association studies Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals The environmental genome project: reference polymorphisms for drug metabolism genes and genome-wide association studies Single-nucleotide evolutionary constraint scores highlight disease-causing mutations The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions. Novel paraoxonase (PON1) nonsense and missense mutations predicted by functional genomic assay of PON1 status Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89 The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster High-throughput genotyping of intermediate-size structural variation Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes Mapping and sequencing of structural variation from eight human genomes Genome-wide association of lipid-lowering response to statins in combined study populations Combined influence of LDLR and HMGCR sequence variation on lipid-lowering response to simvastatin Evidence for involvement of GNB1L in autism Definition and clinical importance of haplotypes Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease Toll-like receptor 1 polymorphisms affect innate immune responses and outcomes in sepsis Efficient selection of tagging single-nucleotide polymorphisms in multiple populations. "Mandibulofacial dysostosis with microcephaly" caused by EFTUD2 mutations: expanding the phenotype. Population analysis of large copy number variants and hotspots of human genetic disease

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