KN
Kim E. Nichols
Also known as: Nichols KE
St. Jude Children's Research Hospital, University of Pennsylvania Perelman School of Medicine, Massachusetts General Hospital, Dana-Farber Cancer Institute, Harvard University School of Medicine
Research areas: Biochemistry, Genetics and Molecular Biology · Genetics · BRCA gene mutations in cancer · Immunodeficiency and Autoimmune Disorders · Cancer Genomics and Diagnostics
Employment
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St. Jude Children's Research Hospital Full Member2014 - Present
- 2014 - Present
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University of Pennsylvania Perelman School of Medicine Associate Professor2007 - 2014
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University of Pennsylvania Perelman School of Medicine Assistant Professor1999 - 2007
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Harvard University School of Medicine Attending Physician1995 - 1999
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University of Pennsylvania Perelman School of Medicine Director1995 - 1999
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Boston Children's Hospital Instructor in Medicine1995 - 1999
Education
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Massachusetts General Hospital Post-Doc1993 - 1995
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Dana-Farber Cancer Institute Fellowship1992 - 1995
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Boston Children's Hospital Residency1989 - 1992
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Duke University School of Medicine M.D.1985 - 1989
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Dartmouth College B.A.1980 - 1984
Projects & Funding
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Towards a Unified Platform for Li-Fraumeni Syndrome Cancer Risk Protection and Cell-free DNA Surveillance The Mark Foundation for Cancer Research2026 - 2028
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In vitro validation of variants of uncertain significance in the genes associated with HLH Histiocytosis Association2025 - 2026
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Validation of a novel tool for predicting pathogenicity of VUS in familial HLH genes Jeffrey Modell Foundation2024 - 2026
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Immunoproteasome inhibition in HLH Histiocytosis Association2023 - 2024
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Barriers and facilitators of parent-child communication in children with cancer predisposition American Cancer Society2023 - 2026
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Targeting the immunoproteasome as a novel therapeutic strategy for hemophagocytic lymphohistiocytosis National Institute of Allergy and Infectious Diseases2023 - 2026
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Pathogenesis of ETV6-Related Acute Lymphoblastic Leukemia National Cancer Institute2020 - 2026
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Pathogenesis of ETV6-related acute lymphoblastic leukemia Division of Cancer Epidemiology and Genetics, National Cancer Institute2020 - 2026
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Consortium for Childhood Cancer Predisposition St. Baldrick's Foundation2020 - 2026
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Consortium for Childhood Cancer Predisposition St. Baldrick's Foundation2019 - 2020
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Pathogenesis of ETV6-Related Acute Lymphoblastic Leukemia American Society of Hematology2019 - 2021
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Therapy with ruxolitinib and dexamethasone in HLH Cures Within Reach2019 - 2025
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iPSC-based systems to study predisposition to B-ALL St. Jude Children's Research Hospital2018 - 2020
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Community-based STEM professional learning for teachers of middle years Australian Research Council2018 - 2021
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Genomic analysis of familial leukemia National Institutes of Health2016 - 2017
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The St. Jude Lifetime Cohort St. Jude Children's Research Hospital2015 - 2020
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JAK inhibition as a novel treatment for hemophagocytic lymphohistiocytosis National Institute of Allergy and Infectious Diseases2014 - 2016
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Janus kinase inhibition in HLH Histiocytosis Association2014 - 2016
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JAK inhibition in HLH University of Pennsylvania2014 - 2015
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Genetic studies in cancer predisposition CHOP2014 - 2015
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Consortium for Clinical and Translational Research in LCH St. Baldrick's Foundation2014 - 2016
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Tumor targeting of iNKT cells using a novel CD1d-CD19 fusion protein SAS Foundation2013 - 2014
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Immunogenomics to create new therapies for high-risk childhood cancers St. Baldrick's Foundation2013 - 2017
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Cytokine directed therapies in HLH CHOP2013 - 2014
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JAK inhibition in the treatment of HLH CHOP2013 - 2014
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NKT cell anti-leukemia therapies University of Pennsylvania2013 - 2013
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iNKT cell-based cancer therapies CHOP2012 - 2014
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Adolescent perspectives regarding genetic testing for Li-Fraumeni Syndrome CHOP2012 - 2014
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Early Identification & Linkage to Care for Persons w/Chronic HBV & HCV Infections Centers for Disease Control and Prevention2012 - 2014
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2012 Summer Fellowship Award St. Baldrick's Foundation2012 - 2012
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Transforming primary teachers' representational practices: effects on students' scientific reasoning and discourse within contemporary sciences Australian Research Council2011 - 2014
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Parent communication about TP53 genetic testing University of Pennsylvania2011 - 2014
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NKT cells and control of EBV CHOP2011 - 2012
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Communication about childhood cancer risk CHOP2011 - 2012
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Pediatric Developmental Funds CHOP2010 - 2011
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Comparative effectiveness of two strategic and meta-cognitive questioning approaches on children's explanatory behaviour, problem-solving, and learning during cooperative, inquiry-based learning Australian Research Council2008 - 2011
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Regulation of NKT cell development by SAP XLP Research Trust Award2008 - 2010
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Application of genomic approaches to classify Retinoblastoma National Institutes of Health2007 - 2010
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Transforming the technologies and modalities of learning: The case of the New Life Sciences in secondary schooling Australian Research Council2007 - 2012
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Roles of SAP, SLAM and Fyn in NKT cell ontogeny and activation National Institutes of Health2007 - 2013
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Parental genotypes and exposures in sporadic Retinoblastoma National Institutes of Health2007 - 2013
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Role of SAP,SLAM and Fyn in NKT Cell Ontogeny and Activation National Heart, Lung, and Blood Institute2007 - 2014
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Role of SAP,SLAM and Fyn in NKT Cell Ontogeny and Activation National Heart Lung and Blood Institute2007 - 2014
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SH2D1A/SAP in NKT development and activation National Institutes of Health2004 - 2009
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Regulation of PMN activation by SLP-76, PRAM-1 and ADAP National Institutes of Health2004 - 2010
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SH2D1A genotype and T/B phenotype in XLP United States Immunodeficiency Network2004 - 2007
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ROLE OF SH2D1A/SAP IN NKT CELL DEVELOPMENT AND FUNCTION National Heart, Lung, and Blood Institute2004 - 2009
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Regulation of T lymphocyte function by SH2D1A American Society of Hematology2002 - 2004
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Institutional Research Grant American Cancer Society2001 - 2003
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Evaluation of retinoblastomas for mutations in RB1 American Cancer Society2000 - 2001
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Detection of germline mutations in hereditary retinoblastoma W. W. Smith Charitable Trust2000 - 2001
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Characterization of the 2B4 pathway in XLP Histiocytosis Association2000 - 2001
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Characterisation of the distribution and role of voltage-gated calcium channels in autonomic neurons National Health and Medical Research Council1999 - 2003
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Genetic predisposition to second malignancies Dana-Farber Cancer Institute1997 - 1999
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Establishing a histiocytosis research program Dana-Farber Cancer Institute1997 - 1999
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Isolation of the XLP gene National Institutes of Health1995 - 2001
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Neuronal basis for the triggering of intestinal peristalsis International Human Frontier Science Program Organization1995 - 1998
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IDENTIFICATION OF THE XLP GENE National Institute of Allergy and Infectious Diseases1995 - 2001
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Genome Remodeling in Developmental Cancers National Cancer Institute
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Mechanisms of Immune Dysregulation Disorders Underlying Inborn errors of the Cytolytic Pathway National Institute of Allergy and Infectious Diseases
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Targeting thProtein Arginine Methyltransferase 5 Enzyme in Hemophagocytic Lymphohistiocytosis National Institutes of Health
Publications (310)
- Telomere length of both parents contributes to heritable POT1 cancer-predisposition syndrome Save
- Somatic UBA1 mutations in pediatric MDS/AML: first cases suggest distinct pathogenesis from adult VEXAS syndrome Save
- HLHRUXO: A prospective trial of a ruxolitinib-containing regimen for children with hemophagocytic lymphohistiocytosis. Save
- Reply to: Beyond Parametric Assumptions: Unsupervised Methods Enhance DNA Repair Gene Discovery in SMARCAL1 Identification Save
- From a Restrictive to Relational Approach: the Concept of Parental Utility in Germline Genomic Testing Save
- Multimodal Cytogenetic and Molecular Approach for the Detection of a Constitutional Balanced Paracentric Inversion Disrupting RB1 in an Infant With Bilateral Retinoblastoma. Save
- Precision-Based Care: A Multidisciplinary Approach. Save
- Imaging Approaches to Surveillance in Children With Cancer Predisposition Syndromes, From the AJR Special Series on Screening. Save
- The moderating role of parental cognitive perceptions in the link between children's cancer predisposition genetic testing results and parent psychological adjustment. Save
- Deletion 9p drives B-ALL through the heterozygous inactivation of Pax5 and Cd72 in pre-leukemic cells. Save
- Telomere length of both parents contribute to heritable POT1 cancer-predisposition syndrome Save
- Telomere length of both parents contributes to heritable POT1 cancer-predisposition syndrome Save
- Fear of Cancer Recurrence Among Parents of Children with Cancer Who Underwent Germline Genetic Testing Save
- Inferring germline pharmacogenomics from tumor transcriptome Save
- Insights into germline predisposition to pediatric lymphoid malignancies Save
- Pediatric Cancer Predisposition and Surveillance Update: Summary Perspective and Future Directions Save
- Li-Fraumeni Syndrome Save
- Case Report: A rare pediatric case of B-cell lymphoblastic lymphoma presenting as an isolated renal mass with EWSR1::FLI1 translocation and germline CHEK2 variant Save
- Clinical Characteristics and Treatment of Familial Hemophagocytic Lymphohistiocytosis Save
- Clinical experience of using integrated whole genome and transcriptome sequencing as a framework for pediatric and adolescent acute myeloid leukemia diagnosis and risk assessment Save