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Author Details
Full Name
Jung Kim
Affiliation
Clinical Genetics Branch, National Cancer Institute
ORCID
Career Start Year
2017
Papers
31
H Index
9
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37246069
Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting Genes.
Eur Urol
2024
37688579
Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.
J Natl Cancer Inst
2024
37246069
Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting Genes.
Eur Urol
2024
37688579
Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.
J Natl Cancer Inst
2024
34331184
Unusual phenotypes in patients with a pathogenic germline variant in DICER1.
Fam Cancer
2023
37585199
Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1-Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome.
JAMA Dermatol
2023
38084291
Specifications of the ACMG/AMP Variant Classification Guidelines for Germline <i>DICER1</i> Variant Curation.
Hum Mutat
2023
37883719
Intronic Germline <i>DICER1</i> Variants in Patients With Sertoli-Leydig Cell Tumor.
JCO Precis Oncol
2023
38076939
AutoGVP: a dockerized workflow integrating ClinVar and InterVar germline sequence variant classification.
bioRxiv
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
36696392
Inflated expectations: Rare-variant association analysis using public controls.
PLoS One
2023
36747619
Germline pathogenic variants in 786 neuroblastoma patients.
medRxiv
2023
36692560
Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population.
JAMA
2023
36541551
Alternative lengthening of telomeres (ALT) in pediatric high-grade gliomas can occur without ATRX mutation and is enriched in patients with pathogenic germline mismatch repair (MMR) variants.
Neuro Oncol
2023
37492101
OpenPBTA: The Open Pediatric Brain Tumor Atlas.
Cell Genom
2023
34331184
Unusual phenotypes in patients with a pathogenic germline variant in DICER1.
Fam Cancer
2023
37492101
OpenPBTA: The Open Pediatric Brain Tumor Atlas.
Cell Genom
2023
38084291
Specifications of the ACMG/AMP Variant Classification Guidelines for Germline <i>DICER1</i> Variant Curation.
Hum Mutat
2023
38076939
AutoGVP: a dockerized workflow integrating ClinVar and InterVar germline sequence variant classification.
bioRxiv
2023
37585199
Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1-Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome.
JAMA Dermatol
2023
37883719
Intronic Germline <i>DICER1</i> Variants in Patients With Sertoli-Leydig Cell Tumor.
JCO Precis Oncol
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
36696392
Inflated expectations: Rare-variant association analysis using public controls.
PLoS One
2023
36747619
Germline pathogenic variants in 786 neuroblastoma patients.
medRxiv
2023
36692560
Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population.
JAMA
2023
36541551
Alternative lengthening of telomeres (ALT) in pediatric high-grade gliomas can occur without ATRX mutation and is enriched in patients with pathogenic germline mismatch repair (MMR) variants.
Neuro Oncol
2023
36409970
Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in <i>CDKN2A</i> and Pancreatic Cancer.
JCO Precis Oncol
2022
35805029
A Genome-First Approach to Estimate Prevalence of Germline Pathogenic Variants and Risk of Pancreatic Cancer in Select Cancer Susceptibility Genes.
Cancers (Basel)
2022
36409970
Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in <i>CDKN2A</i> and Pancreatic Cancer.
JCO Precis Oncol
2022
35776903
Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomes.
Blood
2022
35717579
Rare germline deleterious variants increase susceptibility for lung cancer.
Hum Mol Genet
2022
35805029
A Genome-First Approach to Estimate Prevalence of Germline Pathogenic Variants and Risk of Pancreatic Cancer in Select Cancer Susceptibility Genes.
Cancers (Basel)
2022
35717579
Rare germline deleterious variants increase susceptibility for lung cancer.
Hum Mol Genet
2022
35776903
Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomes.
Blood
2022
33051549
Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.
Leukemia
2021
33630087
A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype.
JAMA Netw Open
2021
33526862
Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.
Leukemia
2021
34308104
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study.
JNCI Cancer Spectr
2021
33402588
The efficacy and safety of onartuzumab in patients with solid cancers: A meta-analysis of randomized trials.
Indian J Cancer
2021
33051549
Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.
Leukemia
2021
34964002
Identification of Genetic Risk Factors for Familial Urinary Bladder Cancer: An Exome Sequencing Study.
JCO Precis Oncol
2021
34493867
Genomic and evolutionary classification of lung cancer in never smokers.
Nat Genet
2021
33630087
A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype.
JAMA Netw Open
2021
33526862
Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.
Leukemia
2021
34964002
Identification of Genetic Risk Factors for Familial Urinary Bladder Cancer: An Exome Sequencing Study.
JCO Precis Oncol
2021
34493867
Genomic and evolutionary classification of lung cancer in never smokers.
Nat Genet
2021
34308104
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study.
JNCI Cancer Spectr
2021
33402588
The efficacy and safety of onartuzumab in patients with solid cancers: A meta-analysis of randomized trials.
Indian J Cancer
2021
33158809
Lack of pathogenic germline DICER1 variants in males with testicular germ-cell tumors.
Cancer Genet
2020
31982544
Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic Anemia.
Biol Blood Marrow Transplant
2020
1 - 50 of 62
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row(s) 1 - 30 of 30
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National Cancer Institute, National Institutes of Health
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Mingyi Wang
National Cancer Institute
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Children's Hospital of Philadelphia
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National Cancer Institute
Co-authored papers
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4
Kristina A Cole
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Margaret A Tucker
National Cancer Institute
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4
David J Carey
Geisinger Medical Center
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Dana A Hill
Co-authored papers
4
Adam C Resnick
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Co-authored papers
3
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers
3
Gonzalo L??pez
Children's Hospital of Philadelphia
Co-authored papers
3
Meredith Yeager
Frederick National Laboratory for Cancer Research
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3
Michael Dean
National Cancer Institute
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Neil E Caporaso
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