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Chimene Kesserwan
Chimene Kesserwan
Verified email at stjude.org
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Cited by
Year
Gene therapy for adenosine deaminase–deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans
F Candotti, KL Shaw, L Muul, D Carbonaro, R Sokolic, C Choi, ...
Blood, The Journal of the American Society of Hematology 120 (18), 3635-3646, 2012
2792012
The genomic landscape of pediatric myelodysplastic syndromes
JR Schwartz, J Ma, T Lamprecht, M Walsh, S Wang, V Bryant, G Song, ...
Nature communications 8 (1), 1557, 2017
1832017
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
1582018
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
1312019
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
1272018
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
1222017
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
1162021
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
1092011
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
762017
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
732017
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
702022
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
692012
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
662020
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
562011
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
522008
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
492018
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
442016
Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants
MN Edmonson, AN Patel, DJ Hedges, Z Wang, E Rampersaud, ...
Genome research 29 (9), 1555-1565, 2019
362019
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
242020
Polygenic determinants for subsequent breast cancer risk in survivors of childhood cancer: The St Jude Lifetime Cohort Study (SJLIFE)
Z Wang, Q Liu, CL Wilson, J Easton, H Mulder, TC Chang, MC Rusch, ...
Clinical Cancer Research 24 (24), 6230-6235, 2018
242018
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