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Minita Shah

New York Genome Center · US
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Area of research
Cancer Research · Oncology
Research interest
Research interests include Cancer Genomics and Diagnostics, Pancreatic and Hepatic Oncology Research, Genomics and Phylogenetic Studies, and Genomics and Rare Diseases.
h-index
19
citations
3,263
works
76
NIH funding
primary concept
Biology
email

Recent publications

Ultrasensitive plasma-based monitoring of tumor burden using machine-learning-guided signal enrichment
Nature Medicine 2024cited by 91position: middledoi
The interplay of mutagenesis and ecDNA shapes urothelial cancer evolution
Nature 2024cited by 50position: middledoi
Childhood cancer mutagenesis caused by transposase-derived PGBD5
Science Advances 2024cited by 8position: middledoi
Somatic whole genome dynamics of precancer in Barrett’s esophagus reveals features associated with disease progression
Nature Communications 2022cited by 43position: middledoi
Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway
Cell Reports 2021cited by 32position: middledoi
Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring
Nature Medicine 2020cited by 429position: middledoi
Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs
Cell 2020cited by 277position: middledoi
Genetic mechanisms of primary chemotherapy resistance in pediatric acute myeloid leukemia
Leukemia 2019cited by 131position: middledoi
Sequencing and curation strategies for identifying candidate glioblastoma treatments
BMC Medical Genomics 2019cited by 10position: middledoi
Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer
Cancer Discovery 2018cited by 1,083position: middledoi
Whole Genome Sequencing-Based Discovery of Structural Variants in Glioblastoma
Methods in molecular biology 2018cited by 15position: middledoi
PGBD5 promotes site-specific oncogenic mutations in human tumors
Nature Genetics 2017cited by 92position: middledoi
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing
Nature Communications 2012cited by 460position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Nicolas Robine · Weill Cornell Medicine3 papers (2019–2024)Anne‐Katrin Emde · Varian Medical Systems (Switzerland)3 papers (2018–2022)Kanika Arora · Graphic Era University2 papers (2019–2022)Alex Kentsis · St. Jude Children's Research Hospital2 papers (2019–2024)Daniela S. Gerhard · National Institutes of Health1 papers (2019–2019) · 1 papers (2022–2022)E. Anders Kolb · Fred Hutch Cancer Center1 papers (2019–2019) · 1 papers (2024–2024)William F. Hooper · Rensselaer Polytechnic Institute1 papers (2024–2024)Nicole McNeer · Synta Pharmaceuticals (United States)1 papers (2019–2019)Marcin Imieliński · European Bioinformatics Institute1 papers (2022–2022) · 1 papers (2019–2019)Rhonda E. Ries · Seattle Children's Hospital1 papers (2019–2019)Vanessa Felice · New York Genome Center1 papers (2018–2018) · 1 papers (2024–2024) · 1 papers (2024–2024)Brian J. Reid · University of East Anglia1 papers (2022–2022)Mayu O. Frank · Rockefeller University1 papers (2018–2018) · 1 papers (2019–2019) · 1 papers (2024–2024)
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