Grant Lammi

Nationwide Children's Hospital — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

3h-index70citations16works0.82yr avg
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Research Topics

Genomics and Rare Diseases(7), Cancer Genomics and Diagnostics(6), Childhood Cancer Survivors' Quality of Life(4), RNA modifications and cancer(4), Genomics and Phylogenetic Studies(3)

Publications16 total

30. Enhancing data standardization and structure to improve clinical variant classification
Cancer Genetics·2025
PEDIA-BRAIN: A single nuclei multiomic encyclopedia of the human pons provides a resource for normal development and disease vulnerability
2025Open Access
O09: Prevalence of germline variants in cancer predisposition genes in patients with pediatric solid tumors using paired tumor-normal exome sequencing
Genetics in Medicine Open·2025Open Access
CAVaLRi: An Algorithm for Rapid Identification of Diagnostic Germline Variation
Human Mutation·2024· 3 citedOpen Access
58. Implementing the ClinGen/CGC/VICC oncogenicity guidelines in a pediatric variant classification workflow
Cancer Genetics·2023
O13: Clinical validation of copy number alteration using paired tumor-normal exome sequencing: Challenges and successes*
Genetics in Medicine Open·2023Open Access
P654: Evaluation of the ClinGen/CGC/VICC Oncogenicity Guidelines to support pediatric variant classification workflows
Genetics in Medicine Open·2023Open Access
Discovery of clinically relevant fusions in pediatric cancer
BMC Genomics·2021· 31 citedOpen Access
Outcomes of in-house rapid genome sequencing at a Children’s Hospital
Molecular Genetics and Metabolism·2021· 1 cited
Synonymous variants that disrupt messenger RNA structure are significantly constrained in the human population
GigaScience·2021· 30 citedOpen Access
Application of constitutional rapid genome sequencing to detect infectious disease in a critically ill neonate
Molecular Genetics and Metabolism·2021· 1 cited
Determinants of turnaround time in a rapid genome sequencing program
Molecular Genetics and Metabolism·2021
Discovery of Clinically Relevant Fusions in Pediatric Cancer
2021· 4 citedOpen Access
Additional file 2 of Discovery of clinically relevant fusions in pediatric cancer
Figshare·2021Open Access
Additional file 3 of Discovery of clinically relevant fusions in pediatric cancer
Figshare·2021Open Access
Global Analysis of Human mRNA Folding Disruptions in Synonymous Variants Demonstrates Significant Population Constraint
2019Open Access

Frequent Co-authors

Catherine E. Cottrell(11), Elaine R. Mardis(11), Benjamin Kelly(10), Peter White(10), Kathleen M. Schieffer(9), Kyle Voytovich(8), James Fitch(7), Vincent Magrini(7), Don Corsmeier(7), Adam Herman(6), Samuel J. Franklin(6), Natalie Bir(6), Kristy Lee(6), Alex H. Wagner(6), Richard K. Wilson(6), Harkness Kuck(6), Marco L. Leung(6), Jeffrey R. Leonard(5), Daniel C. Koboldt(5), Liana Hernandez(5)