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Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants K Lee, K Krempely, ME Roberts, MJ Anderson, F Carneiro, E Chao, ... Human mutation 39 (11), 1553-1568, 2018 | 158 | 2018 |
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants X Luo, S Feurstein, S Mohan, CC Porter, SA Jackson, S Keel, M Chicka, ... Blood Advances 3 (20), 2962-2979, 2019 | 131 | 2019 |
Genetic risk for subsequent neoplasms among long-term survivors of childhood cancer Z Wang, CL Wilson, J Easton, A Thrasher, H Mulder, Q Liu, DJ Hedges, ... Journal of Clinical Oncology 36 (20), 2078, 2018 | 128 | 2018 |
Li‐Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition JM Valdez, KE Nichols, C Kesserwan British Journal of Haematology 176 (4), 539-552, 2017 | 122 | 2017 |
Genomes for kids: the scope of pathogenic mutations in pediatric cancer revealed by comprehensive DNA and RNA sequencing S Newman, J Nakitandwe, CA Kesserwan, EM Azzato, DA Wheeler, ... Cancer discovery 11 (12), 3008-3027, 2021 | 118 | 2021 |
Nonmyeloablative, HLA-haploidentical bone marrow transplantation with high dose, post-transplantation cyclophosphamide A Munchel, C Kesserwan, HJ Symons, L Luznik, YL Kasamon, RJ Jones, ... Pediatric Reports 3 (s2), e15, 2011 | 109 | 2011 |
Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome JR Schwartz, S Wang, J Ma, T Lamprecht, M Walsh, G Song, ... Leukemia 31 (8), 1827-1830, 2017 | 76 | 2017 |
Integrating next‐generation sequencing into pediatric oncology practice: an assessment of physician confidence and understanding of clinical genomics LM Johnson, JM Valdez, EA Quinn, AD Sykes, RB McGee, R Nuccio, ... Cancer 123 (12), 2352-2359, 2017 | 73 | 2017 |
The TP53 Database: transition from the International Agency for Research on Cancer to the US National Cancer Institute KC de Andrade, EE Lee, EM Tookmanian, CA Kesserwan, JJ Manfredi, ... Cell Death & Differentiation 29 (5), 1071-1073, 2022 | 71 | 2022 |
Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase–deficient severe combined immune deficiency C Kesserwan, R Sokolic, EW Cowen, E Garabedian, ... Journal of allergy and clinical immunology 129 (3), 762-769. e1, 2012 | 69 | 2012 |
An update on the central nervous system manifestations of Li–Fraumeni syndrome BA Orr, MR Clay, EM Pinto, C Kesserwan Acta neuropathologica 139 (4), 669-687, 2020 | 66 | 2020 |
Myeloid dysplasia and bone marrow hypocellularity in adenosine deaminase-deficient severe combined immune deficiency R Sokolic, I Maric, C Kesserwan, E Garabedian, IC Hanson, M Dodds, ... Blood, The Journal of the American Society of Hematology 118 (10), 2688-2694, 2011 | 56 | 2011 |
Recent advances in gene therapy for severe congenital immunodeficiency diseases R Sokolic, C Kesserwan, F Candotti Current opinion in hematology 15 (4), 375-380, 2008 | 52 | 2008 |
Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes MF Walsh, DI Ritter, C Kesserwan, D Sonkin, D Chakravarty, E Chao, ... Human mutation 39 (11), 1542-1552, 2018 | 50 | 2018 |
The advantages and challenges of testing children for heritable predisposition to cancer C Kesserwan, L Friedman Ross, AR Bradbury, KE Nichols American Society of Clinical Oncology Educational Book 36, 251-269, 2016 | 44 | 2016 |
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Germline RUNX1 variation and predisposition to childhood acute lymphoblastic leukemia Y Li, W Yang, M Devidas, SS Winter, C Kesserwan, W Yang, ... The Journal of Clinical Investigation 131 (17), 2021 | 24 | 2021 |
How I curate: applying American Society of Hematology-Clinical Genome Resource Myeloid Malignancy Variant Curation Expert Panel rules for RUNX1 variant curation for germline … D Wu, X Luo, S Feurstein, C Kesserwan, S Mohan, DE Pineda-Alvarez, ... Haematologica 105 (4), 870, 2020 | 24 | 2020 |