About: Krzysztof Medrek

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

Polish gynecologist and geneticist

Attributes	Values
rdf:type	Item
description	дослідник (uk) 研究者 (zh) باحث (ar) Polish gynecologist and geneticist (en) polski lekarz, ginekolog i genetyk (pl)
rdfs:label	Krzysztof Medrek (en) Krzysztof Mędrek (ca) Krzysztof Mędrek (cs) Krzysztof Mędrek (gl) Krzysztof Mędrek (hr) Krzysztof Mędrek (it) Krzysztof Mędrek (pl) Krzysztof Mędrek (ro) Krzysztof Mędrek (sk) Krzysztof Mędrek (sl) Krzysztof Mędrek (hsb) Krzysztof Mędrek (ast)
skos:prefLabel	Krzysztof Medrek (en) Krzysztof Mędrek (ca) Krzysztof Mędrek (cs) Krzysztof Mędrek (gl) Krzysztof Mędrek (hr) Krzysztof Mędrek (it) Krzysztof Mędrek (pl) Krzysztof Mędrek (ro) Krzysztof Mędrek (sk) Krzysztof Mędrek (sl) Krzysztof Mędrek (hsb) Krzysztof Mędrek (ast)
name	Krzysztof Medrek (en) Krzysztof Mędrek (ca) Krzysztof Mędrek (cs) Krzysztof Mędrek (gl) Krzysztof Mędrek (hr) Krzysztof Mędrek (it) Krzysztof Mędrek (pl) Krzysztof Mędrek (ro) Krzysztof Mędrek (sk) Krzysztof Mędrek (sl) Krzysztof Mędrek (hsb) Krzysztof Mędrek (ast)
Polish scientist ID (deprecated)	wds:Q114374807-399e083b-4c93-4919-ad0f-b53551565fb2
Polish scientist ID (deprecated)	258195
given name	wds:q114374807-a9eaebb8-4d0a-9344-cae3-7581e40d4b4a
given name	Krzysztof
instance of	wds:Q114374807-E1C0E268-BBEA-4770-9AB5-96FA3D1BDEA9
instance of	Homo sapiens
skos:altLabel	Krzysztof Mędrek (en)
native language	wds:Q114374807-3870F62A-75C7-4C17-B534-19ECF4FD7465
occupation	wds:Q114374807-1B1FD7D9-969E-4897-A84A-0A2F61A14D2C wds:Q114374807-5961d50a-41cb-c5ae-cfde-569403cabf39 wds:Q114374807-d802698c-4b7b-97c5-5966-46cb4ab7b6b8
languages spoken, written or signed	wds:Q114374807-2A5812F5-2581-4771-ADAC-0B4CEC10D0FF
name in native language	wds:Q114374807-9423AA16-D552-4677-81B3-6D0744FD3C2D
sex or gender	wds:Q114374807-109fdc37-4d97-2e8d-4b2b-988fab43b9fa
VIAF ID	wds:Q114374807-E57B4D63-D0D9-4199-A7E6-111CABEFE686
country of citizenship	wds:Q114374807-9A5A245D-AF51-4BE3-AE3E-962F57DAA304
family name	wds:Q114374807-09806bcf-430a-e501-71b1-3eb2ab1bde97
VIAF ID	http://viaf.org/viaf/316011378
native language	Polish
occupation	researcher gynaecologist geneticist
languages spoken, written or signed	Polish
name in native language	Krzysztof Mędrek (pl)
sex or gender	male
VIAF ID	316011378
country of citizenship	Poland
family name	Mędrek
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q114374807
is author of	CHEK2 is a multiorgan cancer susceptibility gene A high proportion of founder BRCA1 mutations in Polish breast cancer families Common variants at 19p13 are associated with susceptibility to ovarian cancer MC1R common variants, CDKN2A and their association with melanoma and breast cancer risk Breast cancer predisposing alleles in Poland Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer. Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin. A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8 Association of common WRAP 53 variant with ovarian cancer risk in the Polish population CHEK2 variants predispose to benign, borderline and low-grade invasive ovarian tumors CDKN2A common variant and multi-organ cancer risk--a population-based study Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk Germline 657del5 mutation in the NBS1 gene in breast cancer patients Low-risk Genes and Multi-organ Cancer Risk in the Polish Population Lactase persistence and ovarian carcinoma risk in Finland, Poland and Sweden The 3020insC Allele of NOD2 Predisposes to Cancers of Multiple Organs Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology The results of prenatal screening in the group of 2285 pregnant women from Western Pomeranian Region of Poland diagnosed between 2005-2006. Erratum: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer Cancer risks in first degree relatives of BRCA1 mutation carriers: effects of mutation and proband disease status Breast cancer susceptibility genes ARLTS1 Trp149Stop Mutation and the Risk of Ovarian Cancer NOD2 variants and the risk of malignant melanoma The 3020insC NOD2 gene mutation in patients with ovarian cancer. Prenatal diagnosis of rare fetal anomalies--a case report Genotyping by induced Förster Resonance Energy Transfer(iFRET) mechanism and simultaneous mutation scanning

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