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Author Details
Full Name
Douglas R Stewart
Affiliation
Clinical Genetics Branch, National Cancer Institute
ORCID
Career Start Year
2003
Papers
116
H Index
36
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
36137255
Outcomes for Children With Type II and Type III Pleuropulmonary Blastoma Following Chemotherapy: A Report From the International PPB/<i>DICER1</i> Registry.
J Clin Oncol
2023
36424733
Health-related quality of life in children and adolescents with pleuropulmonary blastoma: A report from the International PPB/DICER1 Registry.
Pediatr Blood 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
37347242
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
2023
36966234
Cancer in Costello syndrome: a systematic review and meta-analysis.
Br J Cancer
2023
36896180
<i>DICER1</i> RNase IIIb domain mutations trigger widespread miRNA dysregulation and MAPK activation in pediatric thyroid cancer.
Front Endocrinol (Lausanne)
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
36547466
The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
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
36541021
Type I and Ir pleuropulmonary blastoma (PPB): A report from the International PPB/DICER1 Registry.
Cancer
2023
37492101
OpenPBTA: The Open Pediatric Brain Tumor Atlas.
Cell Genom
2023
37490054
Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
2023
34331184
Unusual phenotypes in patients with a pathogenic germline variant in DICER1.
Fam Cancer
2023
38084291
Specifications of the ACMG/AMP Variant Classification Guidelines for Germline <i>DICER1</i> Variant Curation.
Hum Mutat
2023
37490054
Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
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
37492101
OpenPBTA: The Open Pediatric Brain Tumor Atlas.
Cell Genom
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
37347242
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
2023
36966234
Cancer in Costello syndrome: a systematic review and meta-analysis.
Br J Cancer
2023
36696392
Inflated expectations: Rare-variant association analysis using public controls.
PLoS One
2023
36547466
The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
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
36541021
Type I and Ir pleuropulmonary blastoma (PPB): A report from the International PPB/DICER1 Registry.
Cancer
2023
36424733
Health-related quality of life in children and adolescents with pleuropulmonary blastoma: A report from the International PPB/DICER1 Registry.
Pediatr Blood Cancer
2023
36896180
<i>DICER1</i> RNase IIIb domain mutations trigger widespread miRNA dysregulation and MAPK activation in pediatric thyroid cancer.
Front Endocrinol (Lausanne)
2023
36137255
Outcomes for Children With Type II and Type III Pleuropulmonary Blastoma Following Chemotherapy: A Report From the International PPB/<i>DICER1</i> Registry.
J Clin Oncol
2023
34415349
Another Weak Link in the Electron Transport Chain: Variants in SUCLG2 and Risk for Pheochromocytoma and Paraganglioma.
J Natl Cancer Inst
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
35802134
ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
2022
35405740
Examination of Genetic Susceptibility in Radiation-Associated Meningioma.
Radiat Res
2022
36409970
Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in <i>CDKN2A</i> and Pancreatic Cancer.
JCO Precis Oncol
2022
36533693
Cancer incidence and surveillance strategies in individuals with RASopathies.
Am J Med Genet C Semin Med Genet
2022
33782093
Testicular Sertoli cell tumour and potentially testicular Leydig cell tumour are features of <i>DICER1</i> syndrome.
J Med Genet
2022
34854873
Insights Into Immune-Mediated Disease and Cancer Risk-Delivering on the Promise of UK Biobank Big Data.
JAMA Oncol
2022
34599283
DICER1 tumor predisposition syndrome: an evolving story initiated with the pleuropulmonary blastoma.
Mod Pathol
2022
34415349
Another Weak Link in the Electron Transport Chain: Variants in SUCLG2 and Risk for Pheochromocytoma and Paraganglioma.
J Natl Cancer Inst
2022
1 - 50 of 232
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Co-authored papers
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Illumina Inc.
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National Cancer Institute, National Institutes of Health
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6
Maria Teresa Landi
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National Cancer Institute
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6
Karlyne M Reilly
Center for Cancer Research, National Cancer Institute
Co-authored papers
5
Carolyn Sue Richards
Oregon Health & Science University (OHSU)
Co-authored papers
5
Settara C Chandrasekharappa
National Institutes of Health
Co-authored papers
5
Kristy Lee
The University of North Carolina at Chapel Hill
Co-authored papers
5
James C Mullikin
National Human Genome Research Institute, National Institutes of Health
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Andrew J Bauer
Children's Hospital of Philadelphia
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David T Miller
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Adam S Gordon
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