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Chimene A. Kesserwan

Observed names: C Kesserwan, C. Kesserwan, Chimene A Kesserwan, Chimene Kesserwan, Chimène Kesserwan, Kesserwan, Chimene, Kesserwan, Chimene A.
Observed institutions: Dalhousie University, National Institutes of Health, Albert Einstein College of Medicine, St. Jude Children's Research Hospital, Memorial Sloan Kettering Cancer Center, Johns Hopkins University, University of Chicago, Alpine Immune Sciences (United States), National Human Genome Research Institute, National Cancer Institute, National Cancer Institute, Center for Cancer Research, Sidney Kimmel Comprehensive Cancer Center, New York University, University of Nebraska Medical Center, University of Pennsylvania, Incyte (United States)
ORCID: 0000-0001-6043-2065
Observed ORCID: 0000-0001-6043-2065
OpenAlex ID: A5074600159
Gene therapy for adenosine deaminase–deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans
2012 · Fabio Candotti, Kit L. Shaw, et al. · Blood · 234
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The genomic landscape of pediatric myelodysplastic syndromes
2017 · Jason R. Schwartz, Jing Ma, et al. · Nature Communications · 211
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The TP53 Database: transition from the International Agency for Research on Cancer to the US National Cancer Institute
2022 · Kelvin César de Andrade, Elaine E. Lee, et al. · Cell Death and Differentiation · 161
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Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants
2018 · Kristy Lee, Kate Krempely, et al. · Human Mutation · 157
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ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants
2019 · Xi Luo, Simone Feurstein, et al. · Blood Advances · 155
Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer
2018 · Zhaoming Wang, Carmen L. Wilson, et al. · Journal of Clinical Oncology · 139
Li‐Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition
2016 · Jessica M. Valdez, Kim E. Nichols, et al. · British Journal of Haematology · 122
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Integrating next‐generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics
2017 · Liza‐Marie Johnson, Jessica M. Valdez, et al. · Cancer · 84
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Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase–deficient severe combined immune deficiency
2011 · Chimene Kesserwan, Robert Sokolic, et al. · Journal of Allergy and Clinical Immunology · 78
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An update on the central nervous system manifestations of Li–Fraumeni syndrome
2019 · Brent A. Orr, Michael R. Clay, et al. · Acta Neuropathologica · 74
Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome
2017 · J R Schwartz, S Wang, et al. · Leukemia · 74
Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes
2018 · Michael F. Walsh, Deborah I. Ritter, et al. · Human Mutation · 65
Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants
2019 · Michael N. Edmonson, Aman N. Patel, et al. · Genome Research · 49
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Myeloid dysplasia and bone marrow hypocellularity in adenosine deaminase-deficient severe combined immune deficiency
2011 · Robert Sokolic, Irina Maric, et al. · Blood · 47
Germline RUNX1 variation and predisposition to childhood acute lymphoblastic leukemia
2021 · Yizhen Li, Wentao Yang, et al. · Journal of Clinical Investigation · 44
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CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase
2022 · Kilannin Krysiak, Arpad M Danos, et al. · Nucleic Acids Research · 42
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The Advantages and Challenges of Testing Children for Heritable Predisposition to Cancer
2016 · Chimene Kesserwan, Lainie Friedman Ross, et al. · American Society of Clinical Oncology Educational Book · 42
Recent advances in gene therapy for severe congenital immunodeficiency diseases
2008 · Robert Sokolic, Chimene Kesserwan, et al. · Current Opinion in Hematology · 40
Tumor Mutation Burden, Expressed Neoantigens and the Immune Microenvironment in Diffuse Gliomas
2021 · Guangyang Yu, Ying Pang, et al. · Cancers · 35
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Association Between Hereditary Lobular Breast Cancer Due to CDH1 Variants and Gastric Cancer Risk
2021 · Lauren A. Gamble, Alexander Rossi, et al. · JAMA Surgery · 34
How I curate: applying American Society of Hematology-Clinical Genome Resource Myeloid Malignancy Variant Curation Expert Panel rules for RUNX1 variant curation for germline predisposition to myeloid malignancies
2020 · David Wu, Xi Luo, et al. · Haematologica · 33
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Factors Associated With Declining to Participate in a Pediatric Oncology Next-Generation Sequencing Study
2020 · Katianne M. Howard Sharp, Niki Jurbergs, et al. · JCO Precision Oncology · 28
Genomic and transcriptomic analyses identify a prognostic gene signature and predict response to therapy in pleural and peritoneal mesothelioma
2023 · Nishanth Ulhas Nair, Qun Jiang, et al. · Cell Reports Medicine · 27
Estimated number of adult survivors of childhood cancer in United States with cancer‐predisposing germline variants
2019 · Carmen L. Wilson, Zhaoming Wang, et al. · Pediatric Blood & Cancer · 26
Enrichment of heterozygous germline RECQL4 loss-of-function variants in pediatric osteosarcoma
2019 · Jamie L. Maciaszek, Ninad Oak, et al. · Molecular Case Studies · 26
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Works count: 108
Citation count: 2,159
H-index: 26
I10-index: 31
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