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Author Details

Chimene Kesserwan
National Institutes of Health
2007
34
19
PMIDPaper TitleJournal TitlePublished Year
36373660CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.Nucleic Acids Res2023
36773602Genomic and transcriptomic analyses identify a prognostic gene signature and predict response to therapy in pleural and peritoneal mesothelioma.Cell Rep Med2023
36600593Optimising clinical care through <i>CDH1</i>-specific germline variant curation: improvement of clinical assertions and updated curation guidelines.J Med Genet2023
34643667Association Between Hereditary Lobular Breast Cancer Due to CDH1 Variants and Gastric Cancer Risk.JAMA Surg2022
35352025The TP53 Database: transition from the International Agency for Research on Cancer to the US National Cancer Institute.Cell Death Differ2022
34166225Germline RUNX1 variation and predisposition to childhood acute lymphoblastic leukemia.J Clin Invest2021
34885201Tumor Mutation Burden, Expressed Neoantigens and the Immune Microenvironment in Diffuse Gliomas.Cancers (Basel)2021
34301788Genomes for Kids: The Scope of Pathogenic Mutations in Pediatric Cancer Revealed by Comprehensive DNA and RNA Sequencing.Cancer Discov2021
30499906Anaplastic Astrocytoma in a Child With Coffin-Siris Syndrome and a Germline SMARCE1 Mutation: A Case Report.J Pediatr Hematol Oncol2020
31647544Molecular Mechanism of Telomere Length Dynamics and Its Prognostic Value in Pediatric Cancers.J Natl Cancer Inst2020
31736278Estimated number of adult survivors of childhood cancer in United States with cancer-predisposing germline variants.Pediatr Blood Cancer2020
32165484How I curate: applying American Society of Hematology-Clinical Genome Resource Myeloid Malignancy Variant Curation Expert Panel rules for <i>RUNX1</i> variant curation for germline predisposition to myeloid malignancies.Haematologica2020
32395682Factors Associated with Declining to Participate in a Pediatric Oncology Next Generation Sequencing Study.JCO Precis Oncol2020
31468188An update on the central nervous system manifestations of Li-Fraumeni syndrome.Acta Neuropathol2020
30886117From uncertainty to pathogenicity: clinical and functional interrogation of a rare <i>TP53</i> in-frame deletion.Cold Spring Harb Mol Case Stud2019
31648317ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.Blood Adv2019
31604778Enrichment of heterozygous germline <i>RECQL4</i> loss-of-function variants in pediatric osteosarcoma.Cold Spring Harb Mol Case Stud2019
30311369Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes.Hum Mutat2018
29847298Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer.J Clin Oncol2018
30366939Polygenic Determinants for Subsequent Breast Cancer Risk in Survivors of Childhood Cancer: The St Jude Lifetime Cohort Study (SJLIFE).Clin Cancer Res2018
30311375Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants.Hum Mutat2018
27984644Li-Fraumeni syndrome: a paradigm for the understanding of hereditary cancer predisposition.Br J Haematol2017
28487541Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndrome.Leukemia2017
28192596Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics.Cancer2017
29146900The genomic landscape of pediatric myelodysplastic syndromes.Nat Commun2017
27249705The Advantages and Challenges of Testing Children for Heritable Predisposition to Cancer.Am Soc Clin Oncol Educ Book2016
22153773Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase-deficient severe combined immune deficiency.J Allergy Clin Immunol2012
22968453Gene therapy for adenosine deaminase-deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans.Blood2012
21725047Myeloid dysplasia and bone marrow hypocellularity in adenosine deaminase-deficient severe combined immune deficiency.Blood2011
22053277Nonmyeloablative, HLA-haploidentical bone marrow transplantation with high dose, post-transplantation cyclophosphamide.Pediatr Rep2011
18237249Neoadjuvant therapy with celecoxib to women with early stage breast cancer.Neoplasma2008
18536577Recent advances in gene therapy for severe congenital immunodeficiency diseases.Curr Opin Hematol2008
17378689Isolated juvenile xanthogranuloma in the bone marrow: report of a case and review of the literature.Pediatr Dev Pathol2007
17638879The PAX3-FKHR fusion gene of rhabdomyosarcoma cooperates with loss of p16INK4A to promote bypass of cellular senescence.Cancer Res2007
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Co-authored papers 15
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Changhai Hospital, Second Military Medical University
Co-authored papers 7
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St. Jude Children's Research Hospital
Co-authored papers 6
Ti-Cheng Chang
Co-authored papers 5
Leslie L Robison
St. Jude Children's Research Hospital
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St Jude Children's Research Hospital
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St Jude Children's Research Hospital
Co-authored papers 5
Zhaoming Wang
St Jude Children's Research Hospital
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St Jude Children's Research Hospital
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Baylor College of Medicine
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St. Jude Children's Research Hospital
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Ching-Hon Pui
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Alan S Wayne
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Liying Zhang
The Fifth Affiliated Hospital, Sun Yat-sen University
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Michael F Walsh
Memorial Sloan Kettering Cancer Center
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Lucy A Godley
The University of Chicago
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Daniel E Pineda-Alvarez
Invitae Corporation
Co-authored papers 2
Deborah I Ritter
Baylor College of Medicine
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Tamara L Lamprecht
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Joy Nakitandwe
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Mary V Relling
Departments of Pharmaceutical Sciences.
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Amanda B Spurdle
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