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Kim Erika Nichols

Has grant

Full Member

St. Jude Children's Research Hospital

United States

Research Interests

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Recent Grants

Grant: Open

Towards a Unified Platform for Li-Fraumeni Syndrome Cancer Risk Protection and Cell-free DNA Surveillance

Open Date: 2026-03-01

Close Date: 2028-02-01

Grant: Open

In vitro validation of variants of uncertain significance in the genes associated with HLH

Open Date: 2025-01-01

Close Date: 2026-12-01

Grant: Close

Validation of a novel tool for predicting pathogenicity of VUS in familial HLH genes

Open Date: 2024-07-01

Close Date: 2026-06-01

Grant: Close

Targeting the immunoproteasome as a novel therapeutic strategy for hemophagocytic lymphohistiocytosis

Open Date: 2023-07-05

Close Date: 2026-06-30

Grant: Open

Barriers and facilitators of parent-child communication in children with cancer predisposition

Open Date: 2023-05-01

Close Date: 2026-12-01

Articles (20)

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Collaborators (11)

Sharon E. Plon

Professor and Assistant Dean

Baylor College of Medicine

UNITED STATES

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Sharon Savage

Clinical Director

National Cancer Institute

UNITED STATES

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Garrett Brodeur

Professor

Children's Hospital of Philadelphia

UNITED STATES

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Sinisa Savic

Professor of Clinical immunology

University of Leeds

UNITED KINGDOM

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Motomi Mori

Member and Chair

St. Jude Children's Research Hospital

UNITED STATES

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Anna Jones

Assistant Member

St. Jude Children's Research Hospital

UNITED STATES

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Belinda Mandrell

Director, Division of Nursing Research

St. Jude Children's Research Hospital

UNITED STATES

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Nickhill Bhakta

St. Jude Children's Research Hospital

UNITED STATES

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Katianne Howard Sharp

Assistant Member

St. Jude Children's Research Hospital

UNITED STATES

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Haitao Pan

Associate Professor

St. Jude Children's Research Hospital

UNITED STATES

View details

Rachel Tillery Webster

Assistant Member

St. Jude Children's Research Hospital

UNITED STATES

View details

ApplyKite TwinLearns as you apply

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Kim Erika Nichols

Research Interests

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Recent Grants

Articles (20)

Fear of Cancer Recurrence Among Parents of Children with Cancer Who Underwent Germline Genetic Testing

From a Restrictive to Relational Approach: the Concept of Parental Utility in Germline Genomic Testing

Reply to: Beyond Parametric Assumptions: Unsupervised Methods Enhance DNA Repair Gene Discovery in SMARCAL1 Identification

Inferring germline pharmacogenomics from tumor transcriptome

Telomere length of both parents contributes to heritable POT1 cancer-predisposition syndrome

Somatic UBA1 mutations in pediatric MDS/AML: first cases suggest distinct pathogenesis from adult VEXAS syndrome

HLHRUXO: A prospective trial of a ruxolitinib-containing regimen for children with hemophagocytic lymphohistiocytosis.

Multimodal Cytogenetic and Molecular Approach for the Detection of a Constitutional Balanced Paracentric Inversion Disrupting RB1 in an Infant With Bilateral Retinoblastoma.

Precision-Based Care: A Multidisciplinary Approach.

Imaging Approaches to Surveillance in Children With Cancer Predisposition Syndromes, From the <i>AJR</i> Special Series on Screening.

The moderating role of parental cognitive perceptions in the link between children's cancer predisposition genetic testing results and parent psychological adjustment.

Deletion 9p drives B-ALL through the heterozygous inactivation of Pax5 and Cd72 in pre-leukemic cells.

Pediatric Cancer Predisposition and Surveillance Update: Summary Perspective and Future Directions

Insights into germline predisposition to pediatric lymphoid malignancies

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

Clinical Characteristics and Treatment of Familial Hemophagocytic Lymphohistiocytosis

Clinical experience of using integrated whole genome and transcriptome sequencing as a framework for pediatric and adolescent acute myeloid leukemia diagnosis and risk assessment

Contribution of Germline Predisposition to Pediatric Thyroid Cancer

Genetics of Familial Hemophagocytic Lymphohistiocytosis (HLH)

Histiocyte Society blueprint for hemophagocytic lymphohistiocytosis research: deciphering underlying disease mechanisms to optimize diagnosis and therapy

Collaborators (11)

Sharon E. Plon

Sharon Savage

Garrett Brodeur

Sinisa Savic

Motomi Mori

Anna Jones

Belinda Mandrell

Nickhill Bhakta

Katianne Howard Sharp

Haitao Pan

Rachel Tillery Webster

Make your next move.

Kim Erika Nichols

Research Interests

Make your next move.

Explore related searches

Recent Grants

Articles (20)

Fear of Cancer Recurrence Among Parents of Children with Cancer Who Underwent Germline Genetic Testing

From a Restrictive to Relational Approach: the Concept of Parental Utility in Germline Genomic Testing

Reply to: Beyond Parametric Assumptions: Unsupervised Methods Enhance DNA Repair Gene Discovery in SMARCAL1 Identification

Inferring germline pharmacogenomics from tumor transcriptome

Telomere length of both parents contributes to heritable POT1 cancer-predisposition syndrome

Somatic UBA1 mutations in pediatric MDS/AML: first cases suggest distinct pathogenesis from adult VEXAS syndrome

HLHRUXO: A prospective trial of a ruxolitinib-containing regimen for children with hemophagocytic lymphohistiocytosis.

Multimodal Cytogenetic and Molecular Approach for the Detection of a Constitutional Balanced Paracentric Inversion Disrupting RB1 in an Infant With Bilateral Retinoblastoma.

Precision-Based Care: A Multidisciplinary Approach.

Imaging Approaches to Surveillance in Children With Cancer Predisposition Syndromes, From the &lt;i&gt;AJR&lt;/i&gt; Special Series on Screening.

The moderating role of parental cognitive perceptions in the link between children's cancer predisposition genetic testing results and parent psychological adjustment.

Deletion 9p drives B-ALL through the heterozygous inactivation of Pax5 and Cd72 in pre-leukemic cells.

Pediatric Cancer Predisposition and Surveillance Update: Summary Perspective and Future Directions

Insights into germline predisposition to pediatric lymphoid malignancies

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

Clinical Characteristics and Treatment of Familial Hemophagocytic Lymphohistiocytosis

Clinical experience of using integrated whole genome and transcriptome sequencing as a framework for pediatric and adolescent acute myeloid leukemia diagnosis and risk assessment

Contribution of Germline Predisposition to Pediatric Thyroid Cancer

Genetics of Familial Hemophagocytic Lymphohistiocytosis (HLH)

Histiocyte Society blueprint for hemophagocytic lymphohistiocytosis research: deciphering underlying disease mechanisms to optimize diagnosis and therapy

Collaborators (11)

Sharon E. Plon

Sharon Savage

Garrett Brodeur

Sinisa Savic

Motomi Mori

Anna Jones

Belinda Mandrell

Nickhill Bhakta

Katianne Howard Sharp

Haitao Pan

Rachel Tillery Webster

Make your next move.

Imaging Approaches to Surveillance in Children With Cancer Predisposition Syndromes, From the <i>AJR</i> Special Series on Screening.