About: Minouk J Schoemaker

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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) forsker (nb) ikertzailea (eu) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) chercheuse (fr) investigadora (es) wetenschapper (nl) дослідниця (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) researcher (en-ca) researcher (en-gb) researcher (en-us) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast)
exact match	wds:Q37371896-D0CED9D5-CBED-4689-9E47-442DB6025593
exact match	https://scigraph.springernature.com/person.01331623740.48
rdfs:label	Minouk J Schoemaker (en) Minouk J Schoemaker (es) Minouk J Schoemaker (sl) Minouk J Schoemaker (ast) Minouk J. Schoemaker (nb) Minouk Schoemaker (nl)
skos:prefLabel	Minouk J Schoemaker (en) Minouk J Schoemaker (es) Minouk J Schoemaker (sl) Minouk J Schoemaker (ast) Minouk J. Schoemaker (nb) Minouk Schoemaker (nl)
name	Minouk J Schoemaker (en) Minouk J Schoemaker (es) Minouk J Schoemaker (sl) Minouk J Schoemaker (ast) Minouk J. Schoemaker (nb) Minouk Schoemaker (nl)
instance of	wds:Q37371896-7340E652-7D97-479B-AC50-CCAFCF5F5703
instance of	Homo sapiens
ResearchGate profile ID	wds:Q37371896-2ba91564-43e8-f968-3f24-454d77f6406d
ResearchGate profile ID	Minouk-Schoemaker
skos:altLabel	Minouk J Schoemaker (nl) Minouk Schoemaker (en) Minouk Schoemaker (nb)
occupation	wds:Q37371896-6640688B-007E-463A-A443-E500094A0C9B
X username	wds:Q37371896-b70471a4-488c-bb81-5214-0b28ce7de653
sex or gender	wds:Q37371896-6be9f22a-4540-51ec-7395-6e2ece7ce425
country of citizenship	wds:Q37371896-7e02537d-4a82-883d-293b-fc2a80007529
on focus list of Wikimedia project	wds:Q37371896-8E5CC5A1-9798-4B5F-85D0-2F65055E5A8B
date of birth	wds:Q37371896-CEDC1228-423C-4D81-9191-79DF06186E39
occupation	researcher
X username	minouk_schoe
sex or gender	female organism
country of citizenship	Kingdom of the Netherlands
on focus list of Wikimedia project	gender gap on Dutch Wikipedia
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
ORCID iD	wds:Q37371896-07F464BB-18BA-4D2B-AB1F-294E32D3DCCB
Dimensions author ID	wds:Q37371896-6E180348-9F84-4021-A26F-A4BA4E7179A7
ORCID iD	https://orcid.org/0000-0001-8403-2234
ORCID iD	0000-0001-8403-2234
Dimensions author ID	01331623740.48
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37371896
is author of	Mobile phone use and risk of acoustic neuroma: results of the Interphone case-control study in five North European countries Body mass index, exercise, and other lifestyle factors in relation to age at natural menopause: analyses from the breakthrough generations study Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors Prediction of breast cancer risk based on profiling with common genetic variants Allergic conditions and brain tumor risk Non-fatal work related injuries in a cohort of Brazilian steelworkers. Interaction between 5 genetic variants and allergy in glioma risk The INTERPHONE study: design, epidemiological methods, and description of the study population Chromosome 7p11.2 (EGFR) variation influences glioma risk Medical history, cigarette smoking and risk of acoustic neuroma: An international case-control study Mortality in patients with Klinefelter syndrome in Britain: a cohort study Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study The Breakthrough Generations Study: design of a long-term UK cohort study to investigate breast cancer aetiology CYP3A variation, premenopausal estrone levels, and breast cancer risk Mobile phone use and risk of glioma in adults: case-control study Mobile phone use and risk of glioma in 5 North European countries Meningioma and mobile phone use--a collaborative case-control study in five North European countries Risk of pituitary tumors in cellular phone users: a case-control study Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium Combined effects of endogenous sex hormone levels and mammographic density on postmenopausal breast cancer risk: results from the Breakthrough Generations Study Genome-wide association study identifies five susceptibility loci for glioma A genome-wide association study of early menopause and the combined impact of identified variants The relationship between obesity and exposure to light at night: cross-sectional analyses of over 100,000 women in the Breakthrough Generations Study Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression MNS16A minisatellite genotypes in relation to risk of glioma and meningioma and to glioblastoma outcome. Genetic predisposition to in situ and invasive lobular carcinoma of the breast Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry A novel approach to exploring potential interactions among single-nucleotide polymorphisms of inflammation genes in gliomagenesis: an exploratory case-only study Mortality in Women with Turner Syndrome in Great Britain: A National Cohort Study

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