VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q57565500 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241221010722.0
008 241221nneanz||abbn n and d
035 ‎‡a (WKP)Q57565500‏
024 ‎‡a 0000-0002-3633-1659‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q57565500‏
100 0 ‎‡a Marta Cardoso‏ ‎‡c researcher ORCID ID = 0000-0002-3633-1659‏ ‎‡9 en‏
375 ‎‡a 2‏ ‎‡2 iso5218‏
400 0 ‎‡a Marta Cardoso‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci‏
670 ‎‡a Author's Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.‏
670 ‎‡a Author's Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients‏
670 ‎‡a Author's Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers‏
670 ‎‡a Author's Oncogenic mechanisms of HOXB13 missense mutations in prostate carcinogenesis.‏
670 ‎‡a Author's Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer.‏
670 ‎‡a Author's The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer‏
670 ‎‡a Author's Truncating and missense PPM1D mutations in early-onset and/or familial/hereditary prostate cancer patients.‏
909 ‎‡a (orcid) 0000000236331659‏ ‎‡9 1‏
912 ‎‡a associationanalysesofmorethan140000menidentify63newprostatecancersusceptibilityloci‏ ‎‡A Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci‏ ‎‡9 1‏
912 ‎‡a finemappingofprostatecancersusceptibilitylociinalargemetaanalysisidentifiescandidatecausalvariants‏ ‎‡A Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.‏ ‎‡9 1‏
912 ‎‡a interimresultsfromtheimpactstudyevidenceforprostatespecificantigenscreeninginbrca2mutationcarriers‏ ‎‡A Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers‏ ‎‡9 1‏
919 ‎‡a identificationof2novelhoxb13germlinemutationsinportugueseprostatecancerpatients‏ ‎‡A Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients‏ ‎‡9 1‏
919 ‎‡a oncogenicmechanismsofhoxb13missensemutationsinprostatecarcinogenesis‏ ‎‡A Oncogenic mechanisms of HOXB13 missense mutations in prostate carcinogenesis.‏ ‎‡9 1‏
919 ‎‡a targetednextgenerationsequencingidentifiesfunctionallydeleteriousgermlinemutationsinnovelgenesinearlyonsetfamilialprostatecancer‏ ‎‡A Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer.‏ ‎‡9 1‏
919 ‎‡a roleofgermlinemutationsinthebrca12andmismatchrepairgenesinmenascertainedforearlyonsetandorfamilialprostatecancer‏ ‎‡A The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer‏ ‎‡9 1‏
919 ‎‡a truncatingandmissenseppm1dmutationsinearlyonsetandorfamilialhereditaryprostatecancerpatients‏ ‎‡A Truncating and missense PPM1D mutations in early-onset and/or familial/hereditary prostate cancer patients.‏ ‎‡9 1‏
946 ‎‡a a‏ ‎‡9 1‏
996 ‎‡2 LC|n 2015034832‏
996 ‎‡2 SUDOC|159330947‏
996 ‎‡2 PTBNP|768600‏
996 ‎‡2 ISNI|000000044968735X‏
996 ‎‡2 ISNI|0000000395054951‏
996 ‎‡2 PTBNP|1504298‏
996 ‎‡2 PTBNP|28377‏
996 ‎‡2 ISNI|0000000072718274‏
996 ‎‡2 CAOONL|ncf11918420‏
996 ‎‡2 ISNI|0000000428324373‏
996 ‎‡2 SUDOC|194306135‏
996 ‎‡2 ISNI|0000000388614113‏
996 ‎‡2 LC|no2009160615‏
996 ‎‡2 BLBNB|000247220‏
996 ‎‡2 ISNI|0000000068915195‏
996 ‎‡2 LC|no2012143489‏
996 ‎‡2 PTBNP|948428‏
996 ‎‡2 CAOONL|ncf11018871‏
996 ‎‡2 ARBABN|000063356‏
996 ‎‡2 PTBNP|1504585‏
996 ‎‡2 SUDOC|174102968‏
996 ‎‡2 PTBNP|1393881‏
996 ‎‡2 DNB|1220365246‏
996 ‎‡2 ISNI|0000000068419538‏
996 ‎‡2 PTBNP|284385‏
996 ‎‡2 BNF|16626242‏
997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏