Ty C. Lynnes

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 6 papers. Top paper: “Characterization of Reference Materials for Spinal Muscular Atrophy Genetic Testing”.

Characterization of Reference Materials for Spinal Muscular Atrophy Genetic Testing

Journal of Molecular Diagnostics(2020)10.1016/j.jmoldx.2020.10.011

N/A

0DataRank · unranked

9 citations

Pınar Bayrak‐Toydemir, Ty C. Lynnes, Rong Mao, James D. Metcalf, Kasinathan Muralidharan +9 more

Characterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.04.012

N/A

0DataRank · unranked

17 citations

Amy Turner, Ulrich Broeckel, D. Brian Dawson, Andrea Gaedigk, Ty C. Lynnes +6 more

Characterization of Reference Materials for TPMT and NUDT15

Journal of Molecular Diagnostics(2022)10.1016/j.jmoldx.2022.06.008

N/A

0DataRank · unranked

19 citations

Wendy Y. Wang, Erin C. Boone, Ulrich Broeckel, Neal Cody, Lisa Edelmann +10 more

Analytical Validation of a Computational Method for Pharmacogenetic Genotyping from Clinical Whole Exome Sequencing

Journal of Molecular Diagnostics(2022)10.1016/j.jmoldx.2022.03.008

N/A

0DataRank · unranked

17 citations

Tyler Shugg, Ryan Ratcliff, Wilberforce Osei, Ty C. Lynnes, Victoria M. Pratt +9 more

Characterization of Reference Materials for CYP3A4 and CYP3A5

Journal of Molecular Diagnostics(2023)10.1016/j.jmoldx.2023.06.005

N/A

0DataRank · unranked

15 citations

Erin C. Boone, Amy Turner, Ron H. N. van Schaik, Dilyara Chernova, Wendy Y. Wang +10 more

De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome

Brain(2025)10.1093/brain/awaf035

N/A

0DataRank · unranked

9 citations

Sharayu Jangam, Martin MC Chui, Kayla Treat, Lorenzo Graziani, Alessia Soldano +24 more