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 | 451 | 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 | 339 | 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 | 310 | 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 | 305 | 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 | 252 | 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 | 188 | 2021 |
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 | 157 | 2018 |
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 | 152 | 2022 |
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 | 146 | 2009 |
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 | 145 | 2018 |
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 | 138 | 2010 |
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 | 135 | 2017 |
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 | 132 | 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 | 121 | 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, 2017 | 117 | 2017 |
The chromosome 9q subtelomere deletion syndrome DR Stewart, T Kleefstra American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2007 | 116 | 2007 |
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 | 116 | 2006 |
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 | 115 | 2011 |
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 | 109 | 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 | 104 | 2021 |