Gabor T Marth
12PUBLICATIONS
130CO-AUTHORS
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Publications (12)
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|Feb 06, 2026
Phenotype-first patient matching with SimPheny identifies diagnostic candidates beyond curated gene associations.Isabelle B Cooperstein, Alistair Ward, Shilpa N Kobren
|Nov 24, 2025
Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data.Yoo-Jin Jiny Ha, Dominika Maziec, Julia Markowski
|Jul 03, 2025
The Somatic Mosaicism across Human Tissues Network.Tim H H Coorens, Ji Won Oh, Yujin Angelina Choi
|Mar 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit.Sabrina Malone Jenkins, Rachel N Palmquist, Barry Moore
|Feb 18, 2025
Long-read single-cell RNA sequencing enables the study of cancer subclone-specific genotypes and phenotypes in chronic lymphocytic leukemia.Gage S Black, Xiaomeng Huang, Yi Qiao
|Apr 01, 2024
Long-read single-cell RNA sequencing enables the study of cancer subclone-specific genotype and phenotype in chronic lymphocytic leukemia.Gage S Black, Xiaomeng Huang, Yi Qiao
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Frequent Collaborators
3 joint publications
Aaron R Quinlan
2 joint publications
Soren Germer
2 joint publications
Ryan L Collins
2 joint publications
Peter J Park
2 joint publications
Joon-Yong An
2 joint publications
Harsha V Doddapaneni
2 joint publications
Donna M Werling
2 joint publications
Andrew B Stergachis
2 joint publications
James T Bennett
2 joint publications
Tim H H Coorens
