About: Nelleke A Gruis

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

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) chercheuse (fr) investigadora (es) araştırmacı (tr) wetenschapper (nl) дослідниця (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast)
rdfs:label	Nelleke A Gruis (en) Nelleke A Gruis (es) Nelleke A Gruis (nl) Nelleke A Gruis (sl) Nelleke A Gruis (ast)
skos:prefLabel	Nelleke A Gruis (en) Nelleke A Gruis (es) Nelleke A Gruis (nl) Nelleke A Gruis (sl) Nelleke A Gruis (ast)
name	Nelleke A Gruis (en) Nelleke A Gruis (es) Nelleke A Gruis (nl) Nelleke A Gruis (sl) Nelleke A Gruis (ast)
LinkedIn personal profile ID	wds:Q42392971-45690A76-D6E3-4E26-97F8-CF65FFBE0819
LinkedIn personal profile ID	nellekegruis
given name	wds:Q42392971-463F0F53-09C9-4FF0-8F27-BFD042669BD9
given name	Nelleke
instance of	wds:Q42392971-A76B1276-C7BA-4B75-936C-0B340EC69AC1
instance of	Homo sapiens
skos:altLabel	Nelleke Gruis (en)
Nationale Thesaurus voor Auteursnamen ID	wds:Q42392971-11d4db59-a12f-439b-9df9-b01ce4b1ab47
occupation	wds:Q42392971-3B9AA848-02E4-4EFC-8E38-263F7B6DEEF6
sex or gender	wds:Q42392971-7B398FA4-8C1F-4740-B314-53FB610BFE15
ISNI	wds:Q42392971-7D168A74-1A01-45A4-A82C-A00A9596A427
VIAF ID	wds:Q42392971-3E313D18-97EC-49A9-97C4-FEE701BA93F1
educated at	wds:Q42392971-3D8DF6B3-7A21-42FB-BDCC-41B66958DFC3 wds:Q42392971-6F1602A7-D8FE-4B98-A16E-F026D233D56D
family name	wds:Q42392971-59D7C996-5447-4F02-9520-CF98E12C4085
WorldCat Identities ID (superseded)	wds:Q42392971-FC6BAACC-8BA0-4020-B297-800A730C986E
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p119516136
VIAF ID	http://viaf.org/viaf/281113380
Nationale Thesaurus voor Auteursnamen ID	119516136
occupation	researcher
sex or gender	female organism
ISNI	0000000388050688
VIAF ID	281113380
educated at	University of Applied Sciences Leiden Leiden University
family name	Gruis
WorldCat Identities ID (superseded)	viaf-281113380
ORCID iD	wds:Q42392971-B0399B2E-34CE-4757-B37D-6DF8FDFD8926
ORCID iD	https://orcid.org/0000-0002-5210-9150
ORCID iD	0000-0002-5210-9150
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42392971
is author of	Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus A pooled analysis of melanocytic nevus phenotype and the risk of cutaneous melanoma at different latitudes Sun exposure and melanoma risk at different latitudes: a pooled analysis of 5700 cases and 7216 controls The effect on melanoma risk of genes previously associated with telomere length Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma A variant in FTO shows association with melanoma risk not due to BMI Predictors of sun protection behaviors and severe sunburn in an international online study The Dutch FAMMM family material: Clinical and genetic data Genome-wide association study identifies three new melanoma susceptibility loci Promoter hypermethylation: a common cause of reduced p16(INK4a) expression in uveal melanoma. Class III β-tubulin, a novel biomarker in the human melanocyte lineage. Magnetic resonance imaging surveillance detects early-stage pancreatic cancer in carriers of a p16-Leiden mutation. Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion ofp16 (p16-Leiden) Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma. The melanocortin-1-receptor gene is the major freckle gene Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents Genome-wide association study identifies three loci associated with melanoma risk The Emergence of Networks in Human Genome Epidemiology MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: a pooled-analysis from the M-SKIP project Common sequence variants on 20q11.22 confer melanoma susceptibility A road map for efficient and reliable human genome epidemiology Familial melanoma: a complex disorder leading to controversy on DNA testing. Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 Geographical variation in the penetrance of CDKN2A mutations for melanoma Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study A mutation hotspot at the p14ARF splice site. CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. Increased Risk of Cancer Other Than Melanoma in CDKN2A Founder Mutation (p16-Leiden)-Positive Melanoma Families Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development.

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