About: Ketil R. Heimdal

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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) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) Noors onderzoeker (nl) chercheur norvégien (fr) ikertzaile norvegiarra (eu) investigador noruec (ca) investigador noruego (es) investigador noruegu (ast) investigador noruegués (gl) investigador norueguês (pt) ricercatore norvegese (it)
rdfs:label	Ketil R Heimdal (ca) Ketil R Heimdal (es) Ketil R. Heimdal (da) Ketil R. Heimdal (en) Ketil R. Heimdal (nb) Ketil R. Heimdal (nl) Ketil R. Heimdal (sl) ケティル・R・ヘイムダル (ja)
skos:prefLabel	Ketil R Heimdal (ca) Ketil R Heimdal (es) Ketil R. Heimdal (da) Ketil R. Heimdal (en) Ketil R. Heimdal (nb) Ketil R. Heimdal (nl) Ketil R. Heimdal (sl) ケティル・R・ヘイムダル (ja)
name	Ketil R Heimdal (ca) Ketil R Heimdal (es) Ketil R. Heimdal (da) Ketil R. Heimdal (en) Ketil R. Heimdal (nb) Ketil R. Heimdal (nl) Ketil R. Heimdal (sl) ケティル・R・ヘイムダル (ja)
Scopus author ID	wds:Q47117011-8080C885-48C6-484D-AA36-AF02EA128E37
Scopus author ID	7005437699
given name	wds:Q47117011-70F380CE-E95E-477D-8298-9A38B606BA45
given name	Ketil
instance of	wds:Q47117011-04CC6771-8E99-44C1-AFC0-9D4033BD5851
instance of	Homo sapiens
skos:altLabel	Ketil Heimdal (en) ケティル・ヘイムダル (ja)
occupation	wds:Q47117011-5336517C-0B70-4E09-8C62-CCE7DD5895B2
employer	wds:Q47117011-43BD0551-0FBA-4A7D-B997-0BCE3D87A7D7
sex or gender	wds:Q47117011-656B43C5-9C63-44F4-8C5F-185D206C4CBE
country of citizenship	wds:Q47117011-C98E3433-7A0D-422A-B209-19BE028B76B9
date of birth	wds:Q47117011-80952858-0DB0-4E05-B816-6796024A5F46
family name	wds:Q47117011-84AA6EF5-05D8-4C10-9C41-BAB364DD0325
occupation	researcher
employer	Oslo University Hospital
sex or gender	male
country of citizenship	Norway
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
family name	Heimdal
ORCID iD	wds:Q47117011-15D97BBE-4119-486B-BFCD-BC5E5C2A5B7E
ORCID iD	https://orcid.org/0000-0002-8911-3508
ORCID iD	0000-0002-8911-3508
Mendeley person ID	wds:Q47117011-C19431D9-02A8-4322-9968-EE46402F4632
Mendeley person ID	ketil-heimdal
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q47117011
is author of	Genome-wide linkage screen for testicular germ cell tumour susceptibility loci DNA ploidy in primary testicular cancer A segregation analysis of testicular cancer based on Norwegian and Swedish families Efficacy of early diagnosis and treatment in women with a family history of breast cancer. European Familial Breast Cancer Collaborative Group. Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history Oestrogen receptor (ESR) polymorphisms and breast cancer susceptibility Jervell and Lange-Nielsen syndrome in Norwegian children: aspects around cochlear implantation, hearing, and balance Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study. Hereditary Breast Cancer Clinical Study Group Prognostic significance of TP53 alterations in breast carcinoma Survival in prospectively ascertained familial breast cancer: Analysis of a series stratified by tumour characteristics,BRCAmutations and oophorectomy STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity The Y deletion gr/gr and susceptibility to testicular germ cell tumor Comprehensive clinical and molecular analysis of 12 families with type 1 recessive cutis laxa Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis Familial testicular cancer in Norway and southern Sweden Prospectively detected cancer in familial breast/ovarian cancer screening. BRCA1 testing with definitive results: a prospective study of psychological distress in a large clinic-based sample. Causes of hearing impairment in the Norwegian paediatric cochlear implant program. Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variability Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer 15q11.2 microdeletion - seven new patients with delayed development and/or behavioural problems. Risk of cancer in relatives of testicular cancer patients. Germline PTEN mutations are rare and highly penetrant Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers The cardiac phenotype in patients with a CHD7 mutation.

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