Douglas R Stewart
Douglas R Stewart
Senior Investigator, National Cancer Institute
Verified email at
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Cited by
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)
DT Miller, K Lee, WK Chung, AS Gordon, GE Herman, TE Klein, ...
Genetics in medicine 23 (8), 1381-1390, 2021
Histopathologic evaluation of atypical neurofibromatous tumors and their transformation into malignant peripheral nerve sheath tumor in patients with neurofibromatosis 1—a …
MM Miettinen, CR Antonescu, CDM Fletcher, A Kim, AJ Lazar, ...
Human pathology 67, 1-10, 2017
DICER1 and Associated Conditions: Identification of At-risk Individuals and Recommended Surveillance Strategies
KAP Schultz, GM Williams, J Kamihara, DR Stewart, AK Harris, AJ Bauer, ...
Clinical Cancer Research 24 (10), 2251-2261, 2018
Pleuropulmonary blastoma: A report on 350 central pathology–confirmed pleuropulmonary blastoma cases by the I nternational P leuropulmonary B lastoma R egistry
YH Messinger, DR Stewart, JR Priest, GM Williams, AK Harris, ...
Cancer 121 (2), 276-285, 2015
Relationship between paediatric CT scans and subsequent risk of leukaemia and brain tumours: assessment of the impact of underlying conditions
AB De Gonzalez, JA Salotti, K McHugh, MP Little, RW Harbron, C Lee, ...
British journal of cancer 114 (4), 388-394, 2016
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 …
DT Miller, K Lee, AS Gordon, LM Amendola, K Adelman, SJ Bale, ...
Genetics in Medicine 23 (8), 1391-1398, 2021
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)
DT Miller, K Lee, NS Abul-Husn, LM Amendola, K Brothers, WK Chung, ...
Genetics in Medicine 24 (7), 1407-1414, 2022
Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
DR Stewart, BR Korf, KL Nathanson, DA Stevenson, K Yohay
Genetics in Medicine 20 (7), 671-682, 2018
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 …
M Brenneman, A Field, J Yang, G Williams, L Doros, C Rossi, KA Schultz, ...
F1000Research 4, 214, 2018
Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association
H Brems, C Park, O Maertens, A Pemov, L Messiaen, M Upadhyaya, ...
Cancer research 69 (18), 7393-7401, 2009
Quantification of Thyroid Cancer and Multinodular Goiter Risk in the DICER1 Syndrome: A Family-Based Cohort Study
NE Khan, AJ Bauer, KAP Schultz, L Doros, RM Decastro, A Ling, ...
The Journal of Clinical Endocrinology & Metabolism 102 (5), 1614-1622, 2017
Family-based analysis of candidate genes for polycystic ovary syndrome
KG Ewens, DR Stewart, W Ankener, M Urbanek, JM McAllister, C Chen, ...
The Journal of Clinical Endocrinology & Metabolism 95 (5), 2306-2315, 2010
Neoplasm risk among individuals with a pathogenic germline variant in DICER1
DR Stewart, AF Best, GM Williams, LA Harney, AG Carr, AK Harris, ...
Journal of Clinical Oncology 37 (8), 668, 2019
DICER1-pleuropulmonary blastoma familial tumor predisposition syndrome: a unique constellation of neoplastic conditions
KA Schultz, J Yang, L Doros, GM Williams, A Harris, DR Stewart, ...
AJSP: Reviews & Reports 19 (2), 90-100, 2014
Malignant peripheral nerve sheath tumors state of the science: leveraging clinical and biological insights into effective therapies
AR Kim, DR Stewart, KM Reilly, D Viskochil, MM Miettinen, BC Widemann
Sarcoma 2017 (1), 7429697, 2017
The chromosome 9q subtelomere deletion syndrome
DR Stewart, T Kleefstra
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2007
FTO and MC4R Gene Variants Are Associated with Obesity in Polycystic Ovary Syndrome
KG Ewens, MR Jones, W Ankener, DR Stewart, M Urbanek, A Dunaif, ...
PLoS One 6 (1), e16390, 2011
Fine mapping of genetic susceptibility to polycystic ovary syndrome on chromosome 19p13.2 and tests for regulatory activity
DR Stewart, B Dombroski, M Urbanek, W Ankener, KE Ewens, JR Wood, ...
Journal of Clinical Endocrinology and Metabolism 91, 4112-4117, 2006
DICER1-related Sertoli-Leydig cell tumor and gynandroblastoma: Clinical and genetic findings from the International Ovarian and Testicular Stromal Tumor Registry
KAP Schultz, AK Harris, M Finch, LP Dehner, JB Brown, DM Gershenson, ...
Gynecologic oncology 147 (3), 521-527, 2017
Genomic and evolutionary classification of lung cancer in never smokers
T Zhang, P Joubert, N Ansari-Pour, W Zhao, PH Hoang, R Lokanga, ...
Nature genetics 53 (9), 1348-1359, 2021
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