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Author Details
Full Name
Zsofia Kote-Jarai
Affiliation
The Institute of Cancer Research
ORCID
Career Start Year
1988
Papers
200
H Index
60
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36018819
Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men.
Hum Mol Genet
2023
37945903
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.
Nat Genet
2023
37612283
Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects.
Nat Commun
2023
37733366
Germline Sequencing Analysis to Inform Clinical Gene Panel Testing for Aggressive Prostate Cancer.
JAMA Oncol
2023
37932350
Impact of germline DNA repair gene variants on prognosis and treatment of men with advanced prostate cancer.
Sci Rep
2023
37025481
Serum testosterone and prostate cancer in men with germline <i>BRCA1/2</i> pathogenic variants.
BJUI Compass
2023
37311464
Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.
Am J Hum Genet
2023
37292833
Evaluating Approaches for Constructing Polygenic Risk Scores for Prostate Cancer in Men of African and European Ancestry.
medRxiv
2023
36872133
Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry.
Eur Urol
2023
36528478
Family History of Prostate Cancer and Survival Outcomes in the UK Genetic Prostate Cancer Study.
Eur Urol
2023
36493335
CanRisk-Prostate: A Comprehensive, Externally Validated Risk Model for the Prediction of Future Prostate Cancer.
J Clin Oncol
2023
36629487
RE: Polygenic risk of any, metastatic, and fatal prostate cancer in the Million Veteran Program.
J Natl Cancer Inst
2023
34214236
The BARCODE1 Pilot: a feasibility study of using germline single nucleotide polymorphisms to target prostate cancer screening.
BJU Int
2022
35659150
Rare Germline Variants Are Associated with Rapid Biochemical Recurrence After Radical Prostate Cancer Treatment: A Pan Prostate Cancer Group Study.
Eur Urol
2022
35152271
Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score.
Prostate Cancer Prostatic Dis
2022
35031163
A Rare Germline HOXB13 Variant Contributes to Risk of Prostate Cancer in Men of African Ancestry.
Eur Urol
2022
34903604
Functional Analysis Identifies Damaging CHEK2 Missense Variants Associated with Increased Cancer Risk.
Cancer Res
2022
34923574
Prostate cancer risk in men of differing genetic ancestry and approaches to disease screening and management in these groups.
Br J Cancer
2022
34127801
Performance of African-ancestry-specific polygenic hazard score varies according to local ancestry in 8q24.
Prostate Cancer Prostatic Dis
2022
32930425
African-specific improvement of a polygenic hazard score for age at diagnosis of prostate cancer.
Int J Cancer
2021
33623038
Polygenic hazard score is associated with prostate cancer in multi-ethnic populations.
Nat Commun
2021
33673083
Identification of Germline Genetic Variants that Increase Prostate Cancer Risk and Influence Development of Aggressive Disease.
Cancers (Basel)
2021
34678156
A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study.
Lancet Oncol
2021
33941403
Combined Effect of a Polygenic Risk Score and Rare Genetic Variants on Prostate Cancer Risk.
Eur Urol
2021
34275018
Marital status and prostate cancer incidence: a pooled analysis of 12 case-control studies from the PRACTICAL consortium.
Eur J Epidemiol
2021
34355204
Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signals.
HGG Adv
2021
33436325
Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study.
Eur Urol Oncol
2021
33249427
FRMD6 has tumor suppressor functions in prostate cancer.
Oncogene
2021
33398198
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Nat Genet
2021
33473200
Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Nat Genet
2021
33420416
Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer.
Prostate Cancer Prostatic Dis
2021
32800727
Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer.
Eur Urol
2021
32853339
Germline Sequencing DNA Repair Genes in 5545 Men With Aggressive and Nonaggressive Prostate Cancer.
J Natl Cancer Inst
2021
32514134
The effect of sample size on polygenic hazard models for prostate cancer.
Eur J Hum Genet
2020
35050761
Genomic Profiles of De Novo High- and Low-Volume Metastatic Prostate Cancer: Results From a 2-Stage Feasibility and Prevalence Study in the STAMPEDE Trial.
JCO Precis Oncol
2020
31776447
Germline genetic variation in prostate susceptibility does not predict outcomes in the chemoprevention trials PCPT and SELECT.
Prostate Cancer Prostatic Dis
2020
33158149
The <i>CHEK2</i> Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor.
Cancers (Basel)
2020
32941451
Relationship of self-reported body size and shape with risk for prostate cancer: A UK case-control study.
PLoS One
2020
32620889
Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers.
Nat Commun
2020
32409115
A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry.
Eur Urol
2020
30527799
Homeobox B13 G84E Mutation and Prostate Cancer Risk.
Eur Urol
2019
31860675
Polygenic risk-tailored screening for prostate cancer: A benefit-harm and cost-effectiveness modelling study.
PLoS Med
2019
31548585
Publisher Correction: Shared heritability and functional enrichment across six solid cancers.
Nat Commun
2019
31337649
Analysis of Over 140,000 European Descendants Identifies Genetically Predicted Blood Protein Biomarkers Associated with Prostate Cancer Risk.
Cancer Res
2019
31537406
Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers.
Eur Urol
2019
31101764
Identification of Novel Susceptibility Loci and Genes for Prostate Cancer Risk: A Transcriptome-Wide Association Study in Over 140,000 European Descendants.
Cancer Res
2019
30777372
Germline DNA Repair Gene Mutations in Young-onset Prostate Cancer Cases in the UK: Evidence for a More Extensive Genetic Panel.
Eur Urol
2019
30837682
Correction: Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease.
Br J Cancer
2019
30683880
Shared heritability and functional enrichment across six solid cancers.
Nat Commun
2019
30622367
Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Nat Genet
2019
1 - 50 of 200
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Collaborators
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University of Cambridge
Co-authored papers
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University of Oxford, John Radcliffe Hospital
Co-authored papers
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Christopher A Haiman
University of Southern California
Co-authored papers
66
Fredrik Wiklund
Co-authored papers
61
Janet L Stanford
Fred Hutchinson Cancer Research Center
Co-authored papers
59
Graham G Giles
Co-authored papers
58
Freddie C Hamdy
University of Oxford
Co-authored papers
58
Henrik Gr??nberg
Karolinska Institute
Co-authored papers
58
Johanna Schleutker
Institute of Biomedicine, University of Turku
Co-authored papers
53
Stephen N Thibodeau
Mayo Clinic
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Cezary Cybulski
International Hereditary Cancer Center, Pomeranian Medical University
Co-authored papers
46
Tokhir Dadaev
The Institute of Cancer Research
Co-authored papers
45
Ruth C Travis
Co-authored papers
43
Børge G Nordestgaard
Co-authored papers
42
Daniel Leongamornlert
Oncogenetics Team The Institute of Cancer Research London UK.
Co-authored papers
42
Sonja I Berndt
Co-authored papers
37
Stephen J Chanock
National Cancer Institute, National Institutes of Health
Co-authored papers
36
Kay-Tee Khaw
Co-authored papers
35
Paul D P Pharoah
Center for Cancer Genetic Epidemiology, University of Cambridge
Co-authored papers
34
David V Conti
Co-authored papers
31
Daniel J Schaid
Mayo Clinic
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Fredrick R Schumacher
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