Willow Coyote-Maetas

16PUBLICATIONS
61CO-AUTHORS
Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Medical ethicsMolecular targetsGene and molecular therapy
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Publications (16)

|Feb 10, 2026
Disruption of Polycystin Ciliary Localization and Channel Function by Autosomal Dominant Polycystic Kidney Disease-Causing Polycystin-1 Variants.

Kotdaji Ha, Gabriel B Loeb, Meyeon Park

|Aug 13, 2025
Cosmos: A Position-Resolution Causal Model for Direct and Indirect Effects in Protein Functions.

Jingyou Rao, Mingsen Wang, Matthew Howard

|Jul 16, 2025
Accurate variant effect estimation in FACS-based deep mutational scanning data with Lilace.

Jerome Freudenberg, Jingyou Rao, Matthew K Howard

|Mar 06, 2025
SLCO1B1 Functional Variants, Bilirubin, Statin-Induced Myotoxicity, and Recent Sub-Saharan African Ancestry: A Precision Medicine Health Equity Study.

Tanushree Haldar, Mark Kvale, Jia Yang

|Feb 17, 2025
Mapping kinase domain resistance mechanisms for the MET receptor tyrosine kinase via deep mutational scanning.

Gabriella O Estevam, Edmond Linossi, Jingyou Rao

|Sep 13, 2024
Conserved regulatory motifs in the juxtamembrane domain and kinase N-lobe revealed through deep mutational scanning of the MET receptor tyrosine kinase domain.

Gabriella O Estevam, Edmond M Linossi, Christian B Macdonald

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Frequent Collaborators

6 joint publications

James S Fraser

6 joint publications

Christian Macdonald

4 joint publications

Gabriella O Estevam

4 joint publications

Edmond M Linossi