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Author Details
Full Name
Daniel Leongamornlert
Affiliation
Oncogenetics Team The Institute of Cancer Research London UK.
ORCID
Career Start Year
2003
Papers
66
H Index
41
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37025481
Serum testosterone and prostate cancer in men with germline <i>BRCA1/2</i> pathogenic variants.
BJUI Compass
2023
34657128
Prognostic impact of chromosomal abnormalities and copy number alterations in adult B-cell precursor acute lymphoblastic leukaemia: a UKALL14 study.
Leukemia
2022
35941135
Unified classification and risk-stratification in Acute Myeloid Leukemia.
Nat Commun
2022
35953478
Clonal diversification and histogenesis of malignant germ cell tumours.
Nat Commun
2022
35948631
Diverse mutational landscapes in human lymphocytes.
Nature
2022
34788984
Genetic and genomic analysis of acute lymphoblastic leukemia in older adults reveals a distinct profile of abnormalities: analysis of 210 patients from the UKALL14 and UKALL60+ clinical trials.
Haematologica
2022
33054126
<i>CDKN2A</i> deletion is a frequent event associated with poor outcome in patients with peripheral T-cell lymphoma not otherwise specified (PTCL-NOS).
Haematologica
2021
33767199
Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities.
Nat Commun
2021
34646017
Convergent somatic mutations in metabolism genes in chronic liver disease.
Nature
2021
34433962
The mutational landscape of human somatic and germline cells.
Nature
2021
34477813
IKZF1 alterations are not associated with outcome in 498 adults with B-precursor ALL enrolled in the UKALL14 trial.
Blood Adv
2021
32317634
Timing the initiation of multiple myeloma.
Nat Commun
2020
32087150
Type 1 Interferon Responses Underlie Tumor-Selective Replication of Oncolytic Measles Virus.
Mol Ther
2020
33392515
Revealing the impact of structural variants in multiple myeloma.
Blood Cancer Discov
2020
32350471
The mutational landscape of normal human endometrial epithelium.
Nature
2020
30622367
Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Nat Genet
2019
31346173
Author Correction: A practical guide for mutational signature analysis in hematological malignancies.
Nat Commun
2019
31278357
A practical guide for mutational signature analysis in hematological malignancies.
Nat Commun
2019
31444325
Genomic landscape and chronological reconstruction of driver events in multiple myeloma.
Nat Commun
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
30829413
Integration of transcriptional and mutational data simplifies the stratification of peripheral T-cell lymphoma.
Am J Hematol
2019
29301143
Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.
Br J Cancer
2018
29892050
Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.
Nat Commun
2018
29892016
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Nat Genet
2018
29915322
Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease.
Br J Cancer
2018
29662167
Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets.
Nat Genet
2018
29438362
Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.
Br J Cancer
2018
29509747
Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.
Br J Cancer
2018
26964030
Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array.
Br J Cancer
2016
26589274
LocusExplorer: a user-friendly tool for integrated visualization of human genetic association data and biological annotations.
Bioinformatics
2016
27262462
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Hum Genet
2016
25595936
Prevalence of the HOXB13 G84E germline mutation in British men and correlation with prostate cancer risk, tumour characteristics and clinical outcomes.
Ann Oncol
2015
26347108
High burden of copy number alterations and c-MYC amplification in prostate cancer from BRCA2 germline mutation carriers.
Ann Oncol
2015
25837820
Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci.
Cancer Epidemiol Biomarkers Prev
2015
26018901
Corrigendum: analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.
Nat Genet
2015
26025378
Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans.
Hum Mol Genet
2015
25730763
Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.
Nat Genet
2015
25454609
Effect of BRCA Mutations on Metastatic Relapse and Cause-specific Survival After Radical Treatment for Localised Prostate Cancer.
Eur Urol
2015
24489760
Telomere length shows no association with BRCA1 and BRCA2 mutation status.
PLoS One
2014
25217961
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.
Nat Genet
2014
25145435
Translating genetic risk factors for prostate cancer to the clinic: 2013 and beyond.
Future Oncol
2014
24556621
Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease.
Br J Cancer
2014
24550738
Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer.
PLoS Genet
2014
23065704
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.
Hum Mol Genet
2013
23535732
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
Nat Genet
2013
23569316
Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer.
J Clin Oncol
2013
23320731
Clinical implications of family history of prostate cancer and genetic risk single nucleotide polymorphism (SNP) profiles in an active surveillance cohort.
BJU Int
2013
22516946
Germline BRCA1 mutations increase prostate cancer risk.
Br J Cancer
2012
21465221
Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript.
Hum Genet
2011
1 - 50 of 66
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The Institute of Cancer Research
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The Institute of Cancer Research
Co-authored papers
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University of Cambridge
Co-authored papers
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Co-authored papers
29
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University of Oxford, John Radcliffe Hospital
Co-authored papers
26
Freddie C Hamdy
University of Oxford
Co-authored papers
22
Graham G Giles
Co-authored papers
19
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Wellcome Sanger Institute
Co-authored papers
16
Janet L Stanford
Fred Hutchinson Cancer Research Center
Co-authored papers
15
Stephen N Thibodeau
Mayo Clinic
Co-authored papers
15
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Institute of Biomedicine, University of Turku
Co-authored papers
15
Christopher A Haiman
University of Southern California
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15
Cezary Cybulski
International Hereditary Cancer Center, Pomeranian Medical University
Co-authored papers
15
Henrik Gr??nberg
Karolinska Institute
Co-authored papers
13
Judith A Clements
Co-authored papers
12
Daniel J Schaid
Mayo Clinic
Co-authored papers
12
Børge G Nordestgaard
Co-authored papers
12
Brian E Henderson
University of Southern California
Co-authored papers
11
Elaine A Ostrander
National Cancer Institute
Co-authored papers
11
Fredrik Wiklund
Co-authored papers
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Colin S Cooper
Norwich Medical School, University of East Anglia
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11
Ruth C Travis
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Sue A Ingles
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Alan Thompson
The Royal Marsden NHS Foundation Trust
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