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D. Stewart · SciRah

Researcher profile · Semantic Scholar

D. Stewart

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D. Stewart — researcher profile on SciRah

h-index: 44
Works: 141
Citations: 6,826

Most-cited papers

ACMG SF v3.0 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)
David T. Miller, Kristy Lee, W. Chung, A. Gordon +14 more
2021Genetics in Medicine461 citations Open access
Semantic Scholar
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)
David T. Miller, Kristy Lee, Noura S. Abul-Husn, L. Amendola +10 more
2023Genetics in Medicine399 citations Open access
Semantic Scholar
HISTOPATHOLOGIC EVALUATION OF ATYPICAL NEUROFIBROMATOUS TUMORS AND THEIR TRANSFORMATION INTO MALIGNANT PERIPHERAL NERVE SHEATH TUMOR IN NEUROFIBROMATOSIS 1 PATIENTS – A CONSENSUS OVERVIEW
M. Miettinen, C. Antonescu, C. Fletcher, AeRang Kim +8 more
2017Human Pathology373 citations Open access
Semantic Scholar
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
David T. Miller, Kristy Lee, A. Gordon, L. Amendola +14 more
2021Genetics in Medicine283 citations Open access
Semantic Scholar
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).
David T. Miller, Kristy Lee, Noura S. Abul-Husn, L. Amendola +10 more
2022Genetics in Medicine251 citations Open access
Semantic Scholar
Relationship between paediatric CT scans and subsequent risk of leukaemia and brain tumours: assessment of the impact of underlying conditions
A. D. de González, J. Salotti, K. McHugh, M. Little +10 more
2016British Journal of Cancer219 citations Open access
Semantic Scholar
Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population.
D. Beck, D. Bodian, Vandan Shah, U. Mirshahi +14 more
2023Journal of the American Medical Association (JAMA)216 citations Open access
Semantic Scholar
Genomic and evolutionary classification of lung cancer in never smokers
Tong-Wu Zhang, P. Joubert, N. Ansari-Pour, Wei Zhao +57 more
2021Nature Genetics212 citations Open access
Semantic Scholar
Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
D. Stewart, B. Korf, K. Nathanson, D. Stevenson +1 more
2018Genetics in Medicine179 citations Open access
Semantic Scholar
Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma / DICER1 syndrome: a unique variant of the two-hit tumor suppression model
Mark R. Brenneman, A. Field, Jiandong Yang, Gretchen M. Williams +15 more
2015F1000Research175 citations Open access
Semantic Scholar
DICER1 tumor predisposition syndrome: an evolving story initiated with the pleuropulmonary blastoma
Iván A. González, D. Stewart, K. Schultz, Amanda P. Field +2 more
2021Modern Pathology164 citations Open access
Semantic Scholar
DICER1-Related Sertoli-Leydig Cell Tumor and Gynandroblastoma: Clinical and Genetic Findings from the International Ovarian and Testicular Stromal Tumor Registry
K. Schultz, Anne K. Harris, M. Finch, L. Dehner +12 more
2017Gynecologic Oncology124 citations Open access
Semantic Scholar
Malignant Peripheral Nerve Sheath Tumors State of the Science: Leveraging Clinical and Biological Insights into Effective Therapies
AeRang Kim, D. Stewart, Karlyne M. Reilly, D. Viskochil +2 more
2017Sarcoma112 citations Open access
Semantic Scholar
Variable population prevalence estimates of germline TP53 variants: a gnomAD-based analysis
K. D. de Andrade, Megan N. Frone, T. Wegman-Ostrosky, Payal P. Khincha +11 more
2018Human Mutation101 citations Open access
Semantic Scholar
Neurofibromatosis Type 1–Associated MPNST State of the Science: Outlining a Research Agenda for the Future
Karlyne M. Reilly, AeRang Kim, Jaishri Blakely, R. Ferner +10 more
2017Journal of the National Cancer Institute100 citations Open access
Semantic Scholar
The primacy of NF1 loss as the driver of tumorigenesis in neurofibromatosis type 1-associated plexiform neurofibromas
A. Pemov, Hua Li, R. Patidar, N. Hansen +12 more
2017Oncogene100 citations Open access
Semantic Scholar
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define pre-malignant neurofibromatosis type 1-associated atypical neurofibromas.
A. Pemov, N. Hansen, Sivasish Sindiri, R. Patidar +15 more
2019Neuro-Oncology94 citations Open access
Semantic Scholar
Germline Cancer-Predisposition Variants in Pediatric Rhabdomyosarcoma: A Report from the Children's Oncology Group.
He Li, S. Sisoudiya, Bailey A. Martin-Giacalone, M. Khayat +17 more
2020Journal of the National Cancer Institute88 citations Open access
Semantic Scholar
Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG)
Marilyn M. Li, Elizabeth C. Chao, E. Esplin, David T. Miller +5 more
2020Genetics in Medicine85 citations Open access
Semantic Scholar
Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
M. Tischkowitz, J. Balmaña, W. Foulkes, P. James +6 more
2021Genetics in Medicine80 citations Open access
Semantic Scholar
Association of Inherited Pathogenic Variants in Checkpoint Kinase2(CHEK2)With Susceptibility to Testicular Germ Cell Tumors
S. AlDubayan, L. Pyle, M. Gamulin, T. Kuliš +24 more
2019JAMA Oncology70 citations Open access
Semantic Scholar
ACMG PRACTICE RESOURCE: 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)
H. Hanson, Esteban Astiazaran-Symonds, L. Amendola, J. Balmaña +10 more
2023Genetics in Medicine68 citations Open access
Semantic Scholar
OpenPBTA: The Open Pediatric Brain Tumor Atlas
Joshua A. Shapiro, Krutika S. Gaonkar, S. Spielman, Candace Savonen +62 more
2023Cell Genomics62 citations Open access
Semantic Scholar
Germline Mutations in Protection of Telomeres 1 in Two Families with Hodgkin Lymphoma
M. McMaster, Chong-Kui Sun, M. Landi, S. Savage +17 more
2018British Journal of Haematology59 citations Open access
Semantic Scholar
Higher-than-expected population prevalence of potentially pathogenic germline TP53 variants in individuals unselected for cancer history.
K. D. de Andrade, L. Mirabello, D. Stewart, E. Karlins +10 more
2017Human Mutation59 citations Open access
Semantic Scholar
Advancing RAS/RASopathy Therapies (ART): An NCI-sponsored Intramural and Extramural Collaboration for the study of RASopathies
A. Gross, Megan N. Frone, K. Gripp, B. Gelb +18 more
2020American Journal of Medical Genetics. Part A51 citations Open access
Semantic Scholar
Macrocephaly associated with the DICER1 syndrome
Nicholas E. Khan, A. Bauer, L. Doros, K. Schultz +9 more
2016Genetics in Medicine50 citations Open access
Semantic Scholar
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study.
Jung Kim, Matthew Gianferante, D. Karyadi, S. Hartley +40 more
2021JNCI Cancer Spectrum44 citations Open access
Semantic Scholar
Mosaic chromosome Y loss and testicular germ cell tumor risk
M. Machiela, C. Dagnall, A. Pathak, J. Loud +4 more
2017Journal of Human Genetics44 citations Open access
Semantic Scholar
DICER1 RNase IIIb domain mutations trigger widespread miRNA dysregulation and MAPK activation in pediatric thyroid cancer
J. Ricarte-Filho, Victoria Casado-Medrano, Erin R. Reichenberger, Zach H Spangler +11 more
2023Frontiers in Endocrinology43 citations Open access
Semantic Scholar
A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype
U. Mirshahi, Jung Kim, Ana F. Best, Z. Chen +16 more
2021JAMA Network Open41 citations Open access
Semantic Scholar
Pathogenic Germline Variants in Cancer Susceptibility Genes in Children and Young Adults With Rhabdomyosarcoma
Jung Kim, Nicholas Light, V. Subasri, E. Young +23 more
2021JCO Precision Oncology40 citations Open access
Semantic Scholar
Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family
A. Pathak, K. Seipel, A. Pemov, Ramita Dewan +13 more
2016Haematologica40 citations Open access
Semantic Scholar
The prevalence of germline DICER1 pathogenic variation in cancer populations
Jung Kim, K. Schultz, D. Hill, D. Stewart
2019Molecular Genetics & Genomic Medicine36 citations Open access
Semantic Scholar
A Genotype-First Approach to Exploring Mendelian Cardiovascular Traits with Clear External Manifestations
Brittany M. Wenger, N. Patel, M. Lui, A. Moscati +7 more
2020Genetics in Medicine30 citations Open access
Semantic Scholar
PLEUROPULMONARY BLASTOMA-LIKE PERITONEAL SARCOMA
K. Schultz, A. Nelson, Anne K. Harris, M. Finch +18 more
2020Modern Pathology30 citations Open access
Semantic Scholar
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls
Jung Kim, W. Luo, Mingyi Wang, T. Wegman-Ostrosky +46 more
2018Genome Medicine28 citations Open access
Semantic Scholar
Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.
Jung Kim, Z. Vaksman, Laura E. Egolf, Rebecca S. Kaufman +24 more
2023Journal of the National Cancer Institute27 citations Open access
Semantic Scholar
Correction to: ACMG SF v3.0 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)
David T. Miller, Kristy Lee, W. Chung, A. Gordon +14 more
2021Genetics in Medicine27 citations Open access
Semantic Scholar
Incidence of Benign Meningiomas in the United States: Current and Future Trends.
Sonia Bhala, D. Stewart, Victoria Kennerley, V. Petkov +2 more
2021JNCI Cancer Spectrum27 citations Open access
Semantic Scholar
Research participant interest in primary, secondary and incidental genomic findings
J. Loud, R. Bremer, Phuong L. Mai, J. Peters +5 more
2016Genetics in Medicine27 citations Open access
Semantic Scholar
Increase in power by obtaining 10 or more controls per case when type-1 error is small in large-scale association studies
H. Katki, S. Berndt, M. Machiela, D. Stewart +5 more
2023BMC Medical Research Methodology26 citations Open access
Semantic Scholar
Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas
A. Pemov, Ramita Dewan, N. Hansen, S. Chandrasekharappa +8 more
2020Scientific Reports24 citations Open access
Semantic Scholar
Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants
K. D. de Andrade, N. T. Strande, Jung Kim, J. Haley +16 more
2023HGG advances22 citations Open access
Semantic Scholar
Cancer incidence and surveillance strategies in individuals with RASopathies
Gina M. Ney, A. Gross, Alicia A Livinski, C. Kratz +1 more
2022American Journal of Medical Genetics. Part C, Seminars in Medical Genetics21 citations Open access
Semantic Scholar
Outcomes for Children With Type II and Type III Pleuropulmonary Blastoma Following Chemotherapy: A Report From the International PPB/DICER1 Registry
K. Schultz, Anne K. Harris, A. Nelson, Dave Watson +16 more
2022Journal of Clinical Oncology21 citations Open access
Semantic Scholar
Identification of Genetic Risk Factors for Familial Urinary Bladder Cancer: An Exome Sequencing Study
A. Pemov, T. Wegman-Ostrosky, Jung Kim, S. Koutros +18 more
2021JCO Precision Oncology20 citations Open access
Semantic Scholar
Structural renal abnormalities in the DICER1 syndrome: a family-based cohort study
Nicholas E. Khan, A. Ling, M. Raske, Laura A Harney +9 more
2018Pediatric nephrology (Berlin, West)20 citations Open access
Semantic Scholar
No Association between Radiation Dose from Pediatric CT Scans and Risk of Subsequent Hodgkin Lymphoma
Amy Berrington de González, N. Journy, Choonsik Lee, L. Morton +7 more
2017Cancer Epidemiology, Biomarkers and Prevention20 citations Open access
Semantic Scholar
Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting Genes
Louise C. Pyle, Jung Kim, J. Bradfield, S. Damrauer +17 more
2023European Urology19 citations Open access
Semantic Scholar

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