Shawn Fayer

Also affiliated with Brotman Baty Institute

Biochemistry, Genetics and Molecular Biology

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 14 papers. Top paper: “Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing”.

Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing

Value in Health(2020)10.1016/j.jval.2020.01.017

N/A

0.416DataRank · unranked

15 citations

Dmitry Dukhovny, Kathryn A. Phillips, Alan H. Beggs, Robert C. Green, Richard B. Parad +27 more

Defining and Reducing Variant Classification Disparities

medRxiv(2024)10.1101/2024.04.11.24305690

N/A

0.165DataRank · unranked

2 citations

Shawn Fayer, Sriram Pendyala, Mason Post, Divya Kalra, Karynne Patterson +13 more

Assigning credit where it’s due: An information content score to capture the clinical value of Multiplexed Assays of Variant Effect

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.20.562794

N/A

0.104DataRank · unranked

1 citations

Carolyn Horton, Tina Pesaran, Shawn Fayer, Lea M. Starita, Brian H. Shirts +1 more

CRaTER enrichment for on-target gene-editing enables generation of variant libraries in hiPSCs

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.25.525582

N/A

0DataRank · unranked

2 citations

Shawn Fayer, Sriram Pendyala, Wei‐Ming Chien, Linda Tran, Leslie S. Chao +9 more

Workshop report: the clinical application of data from multiplex assays of variant effect (MAVEs), 12 July 2023

European Journal of Human Genetics(2024)10.1038/s41431-024-01566-2

N/A

0DataRank · unranked

22 citations

Alice Garrett, Lara A. Muffley, Shawn Fayer, Julia Foreman, David J. Adams +7 more

Multiplexed functional assessments of MYH7 variants in human cardiomyocytes at scale

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.28.551073

N/A

0DataRank · unranked

0 citations

Shawn Fayer, Sriram Pendyala, Wei‐Ming Chien, Linda Tran, Leslie S. Chao +11 more

Calibration of variant effect predictors on genome-wide data masks heterogeneous performance across genes

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.018

N/A

0DataRank · unranked

34 citations

Shawn Fayer, Abbye E. McEwen, Jake Flynn, Lea M. Starita, Douglas M. Fowler +1 more

Multiplexed Functional Assessments of MYH7 Variants in Human Cardiomyocytes

Circulation Genomic and Precision Medicine(2024)10.1161/circgen.123.004377

N/A

0DataRank · unranked

13 citations

Shawn Fayer, Sriram Pendyala, Wei‐Ming Chien, Alexander Loiben, Linda Tran +11 more

Family genetic risk communication and reverse cascade testing in the BabySeq project

Genetics in Medicine(2024)10.1016/j.gim.2024.101350

N/A

0DataRank · unranked

3 citations

Hadley Stevens Smith, Stacey Pereira, Casie A. Genetti, Amy L. McGuire, Alan H. Beggs +38 more

Assigning credit where it is due: an information content score to capture the clinical value of multiplexed assays of variant effect

BMC Bioinformatics(2024)10.1186/s12859-024-05920-5

N/A

0DataRank · unranked

1 citations

Carolyn Horton, Tina Pesaran, Shawn Fayer, Lea M. Starita, Brian H. Shirts +1 more

Gene-based calibration of high-throughput functional assays for clinical variant classification

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.04.29.651326

N/A

0DataRank · unranked

6 citations

Ross Stewart, Shantanu Jain, Malvika Tejura, Abbye E. McEwen, Shawn Fayer +9 more

Evidence for G6PD variant classification from multiplexed functional assays

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.08.11.669723

N/A

0DataRank · unranked

1 citations

Melinda Wheelock, Rachel L. Powell, Ziyu R. Wang, Daniel L. Holmes, Shawn Fayer +9 more

Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTEN

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.001

N/A

0DataRank · unranked

128 citations

Carolyn Horton, Jennifer N. Dines, Alan F. Rubin, Marcy E. Richardson, Kelly McGoldrick +7 more

CRaTER enrichment for on-target gene editing enables generation of variant libraries in hiPSCs

Journal of Molecular and Cellular Cardiology(2023)10.1016/j.yjmcc.2023.03.017

N/A

0DataRank · unranked

11 citations

Shawn Fayer, Sriram Pendyala, Wei‐Ming Chien, Alexander Loiben, Linda Tran +10 more