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Author Details
Full Name
Mitchell J Machiela
Affiliation
National Cancer Institute
ORCID
Career Start Year
2008
Papers
113
H Index
36
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37919896
Genetic analyses identify evidence for a causal relationship between Ewing sarcoma and hernias.
HGG Adv
2024
37919896
Genetic analyses identify evidence for a causal relationship between Ewing sarcoma and hernias.
HGG Adv
2024
36082445
A pleiotropic variant in DNAJB4 is associated with multiple myeloma risk.
Int J Cancer
2023
36082445
A pleiotropic variant in DNAJB4 is associated with multiple myeloma risk.
Int J Cancer
2023
37945903
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.
Nat Genet
2023
38011490
JAK2 V617F mutation and associated chromosomal alterations in primary and secondary myelofibrosis and post-HCT outcomes.
Blood Adv
2023
37904051
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.
Nat Genet
2023
37723249
Identification of novel genetic loci for risk of multiple myeloma by functional annotation.
Leukemia
2023
37565819
Serum biomarkers are altered in UK Biobank participants with mosaic chromosomal alterations.
Hum Mol Genet
2023
38057307
Mosaic chromosomal alterations in peripheral blood leukocytes of children in sub-Saharan Africa.
Nat Commun
2023
38055050
Glyphosate Use and Mosaic Loss of Chromosome Y among Male Farmers in the Agricultural Health Study.
Environ Health Perspect
2023
37961155
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves cross-ancestry prediction.
medRxiv
2023
37205487
Transcriptome-Wide Association Analysis Identifies Novel Candidate Susceptibility Genes for Prostate-Specific Antigen Levels in Men Without Prostate Cancer.
medRxiv
2023
36706615
Clonal hematopoiesis due to mosaic chromosomal alterations: Impact on disease risk and mortality.
Leuk Res
2023
37264206
Genetically adjusted PSA levels for prostate cancer screening.
Nat Med
2023
36635305
GWAS Explorer: an open-source tool to explore, visualize, and access GWAS summary statistics in the PLCO Atlas.
Sci Data
2023
37386403
Increase in power by obtaining 10 or more controls per case when type-1 error is small in large-scale association studies.
BMC Med Res Methodol
2023
37239846
Polymorphisms within Autophagy-Related Genes as Susceptibility Biomarkers for Multiple Myeloma: A Meta-Analysis of Three Large Cohorts and Functional Characterization.
Int J Mol Sci
2023
37236969
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.
Nat Commun
2023
36927626
Mosaic chromosomal alterations detected in men living with HIV and the relationship to non-Hodgkin lymphoma.
AIDS
2023
36787739
Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding.
Am J Hum Genet
2023
37961155
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves cross-ancestry prediction.
medRxiv
2023
38011490
JAK2 V617F mutation and associated chromosomal alterations in primary and secondary myelofibrosis and post-HCT outcomes.
Blood Adv
2023
37904051
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.
Nat Genet
2023
38057307
Mosaic chromosomal alterations in peripheral blood leukocytes of children in sub-Saharan Africa.
Nat Commun
2023
38055050
Glyphosate Use and Mosaic Loss of Chromosome Y among Male Farmers in the Agricultural Health Study.
Environ Health Perspect
2023
37945903
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.
Nat Genet
2023
37565819
Serum biomarkers are altered in UK Biobank participants with mosaic chromosomal alterations.
Hum Mol Genet
2023
37723249
Identification of novel genetic loci for risk of multiple myeloma by functional annotation.
Leukemia
2023
37386403
Increase in power by obtaining 10 or more controls per case when type-1 error is small in large-scale association studies.
BMC Med Res Methodol
2023
37239846
Polymorphisms within Autophagy-Related Genes as Susceptibility Biomarkers for Multiple Myeloma: A Meta-Analysis of Three Large Cohorts and Functional Characterization.
Int J Mol Sci
2023
37236969
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population.
Nat Commun
2023
37205487
Transcriptome-Wide Association Analysis Identifies Novel Candidate Susceptibility Genes for Prostate-Specific Antigen Levels in Men Without Prostate Cancer.
medRxiv
2023
37264206
Genetically adjusted PSA levels for prostate cancer screening.
Nat Med
2023
36787739
Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding.
Am J Hum Genet
2023
36706615
Clonal hematopoiesis due to mosaic chromosomal alterations: Impact on disease risk and mortality.
Leuk Res
2023
36635305
GWAS Explorer: an open-source tool to explore, visualize, and access GWAS summary statistics in the PLCO Atlas.
Sci Data
2023
36927626
Mosaic chromosomal alterations detected in men living with HIV and the relationship to non-Hodgkin lymphoma.
AIDS
2023
34424336
Different Pigmentation Risk Loci for High-Risk Monosomy 3 and Low-Risk Disomy 3 Uveal Melanomas.
J Natl Cancer Inst
2022
35900159
PLCOjs, a FAIR GWAS web SDK for the NCI Prostate, Lung, Colorectal and Ovarian Cancer Genetic Atlas project.
Bioinformatics
2022
35764805
AuthorArranger automates formatting title pages and author affiliations for manuscript submissions.
Commun Biol
2022
35700034
Does a Multiple Myeloma Polygenic Risk Score Predict Overall Survival of Patients with Myeloma?
Cancer Epidemiol Biomarkers Prev
2022
36075929
Germline-somatic JAK2 interactions are associated with clonal expansion in myelofibrosis.
Nat Commun
2022
35676472
The renal lineage factor PAX8 controls oncogenic signalling in kidney cancer.
Nature
2022
36423637
Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity.
Am J Hum Genet
2022
34424336
Different Pigmentation Risk Loci for High-Risk Monosomy 3 and Low-Risk Disomy 3 Uveal Melanomas.
J Natl Cancer Inst
2022
35676472
The renal lineage factor PAX8 controls oncogenic signalling in kidney cancer.
Nature
2022
35764805
AuthorArranger automates formatting title pages and author affiliations for manuscript submissions.
Commun Biol
2022
35700034
Does a Multiple Myeloma Polygenic Risk Score Predict Overall Survival of Patients with Myeloma?
Cancer Epidemiol Biomarkers Prev
2022
36423637
Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity.
Am J Hum Genet
2022
1 - 50 of 226
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Edward L Giovannucci
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Cezary Cybulski
International Hereditary Cancer Center, Pomeranian Medical University
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Montserrat Garcia-Closas
National Cancer Institute
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Ruth C Travis
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