About: Paul D P Pharoah

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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) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) 研究者 (zh) հետազոտող (hy)
rdfs:label	Paul D P Pharoah (en) Paul D P Pharoah (es) Paul D P Pharoah (nl) Paul D P Pharoah (ast)
skos:prefLabel	Paul D P Pharoah (en) Paul D P Pharoah (es) Paul D P Pharoah (nl) Paul D P Pharoah (ast)
name	Paul D P Pharoah (en) Paul D P Pharoah (es) Paul D P Pharoah (nl) Paul D P Pharoah (ast)
Scopus author ID	wds:Q61822938-DA05A9A0-D7B6-45C7-88D9-E4BB4796F32A
Scopus author ID	7102929844
given name	wds:Q61822938-08376959-8172-4CF0-8779-EFF435A57AE6
given name	Paul
instance of	wds:Q61822938-3EC69A46-BF61-4B39-9588-40C45E3E4F6F
instance of	Homo sapiens
skos:altLabel	Paul Pharoah (en) Pharaoh PDP (en) Pharoah P (en) Pharoah PD (en) Pharoah PDP (en)
occupation	wds:Q61822938-4FA9517C-96C0-4AD8-A928-AC805A43DAB4
sex or gender	wds:Q61822938-5cb7bd69-4122-30fd-12e9-3988f5d13d1e
on focus list of Wikimedia project	wds:Q61822938-5680757D-97C0-427A-9890-03193C61966B
family name	wds:Q61822938-BE1335AA-0269-4BCF-9627-77FC584A76EB
occupation	researcher
sex or gender	male
on focus list of Wikimedia project	WikiProject COVID-19
family name	Pharoah
ORCID iD	wds:Q61822938-4912CF86-7521-4C21-9D62-37F38FE44BC7
ORCID iD	https://orcid.org/0000-0001-8494-732X
ORCID iD	0000-0001-8494-732X
Gateway to Research person ID	wds:Q61822938-4C054930-0DA7-481C-B576-F7658AFDD339
Gateway to Research person ID	8840EEA3-4086-4264-8D80-DB3FFF422E7D
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q61822938
is author of	Genome-wide association study identifies novel breast cancer susceptibility loci Combined effects of single nucleotide polymorphisms TP53 R72P and MDM2 SNP309, and p53 expression on survival of breast cancer patients Large-scale genotyping identifies 41 new loci associated with breast cancer risk A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. Public health genomics and personalized prevention: lessons from the COGS project Population-based screening in the era of genomics Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals Incorporating genomics into breast and prostate cancer screening: assessing the implications Public health implications from COGS and potential for risk stratification and screening Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer The inherited genetics of ovarian and endometrial cancer PREDICT: a new UK prognostic model that predicts survival following surgery for invasive breast cancer A randomized controlled study of post-injection rest following intra-articular steroid therapy for knee synovitis Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2 Frequent loss of BRCA1 mRNA and protein expression in sporadic ovarian cancers Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk Radiogenomics: radiobiology enters the era of big data and team science No association between SNPs regulating TGF-β1 secretion and late radiotherapy toxicity to the breast: results from the RAPPER study Association studies for finding cancer-susceptibility genetic variants Normal tissue reactions to radiotherapy: towards tailoring treatment dose by genotype A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus Telomere length in prospective and retrospective cancer case-control studies The effect on melanoma risk of genes previously associated with telomere length Most common 'sporadic' cancers have a significant germline genetic component Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma Gene-panel sequencing and the prediction of breast-cancer risk Prediction of breast cancer risk based on profiling with common genetic variants Evaluation of an algorithm of tagging SNPs selection by linkage disequilibrium. Issues of consent and feedback in a genetic epidemiological study of women with breast cancer Effects of common germline genetic variation in cell cycle control genes on breast cancer survival: results from a population-based cohort Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families Reducing salt intake in Iran: priorities and challenges Sipa1 is a candidate for underlying the metastasis efficiency modifier locus Mtes1. Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations Prediction of pathogenic mutations in patients with early-onset breast cancer by family history A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma Opium use and mortality in Golestan Cohort Study: prospective cohort study of 50,000 adults in Iran Multiple loci with different cancer specificities within the 8q24 gene desert Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing MicroRNA processing and binding site polymorphisms are not replicated in the Ovarian Cancer Association Consortium Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk Genome-wide association studies identify four ER negative-specific breast cancer risk loci Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls

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