Emily Farrow

Also affiliated with Mercy Research, University of Missouri–Kansas City

Biochemistry, Genetics and Molecular BiologyMedicine

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 13 papers. Top paper: “Rapid and scalable personalized ASO screening in patient-derived organoids”.

Rapid and scalable personalized ASO screening in patient-derived organoids

Nature(2025)10.1038/s41586-024-08462-1

N/A

0.965DataRank · unranked

46 citations

Anabel Martinez‐Bengochea, Daniel Louiselle, Jacqelyn Nemechek, John M. Perry, Emily Farrow +3 more

Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency

Genetics in Medicine(2021)10.1016/j.gim.2021.10.014

N/A

0DataRank · unranked

4 citations

Siying Lin, Promita Ghosh, Francesca Clementina Radio, Emily Farrow, Isabelle Thiffault +35 more

CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis

Journal of Molecular Diagnostics(2022)10.1016/j.jmoldx.2021.12.011

N/A

0DataRank · unranked

47 citations

Erin C. Boone, Steven E. Scherer, Seung‐been Lee, Ibrahim Numanagić, S. Cenk Şahinalp +13 more

Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics

Brain(2023)10.1093/brain/awad427

N/A

0DataRank · unranked

23 citations

Reza Maroofian, Adeline Paimboeuf, Mina Zamani, Maha S. Zaki, Saeid Sadeghian +18 more

Characterization and visualization of tandem repeats at genome scale

Nature Biotechnology(2024)10.1038/s41587-023-02057-3

N/A

0DataRank · unranked

128 citations

Adam C. English, Harriet Dashnow, Guilherme De Sena Brandine, Tom Mokveld, William J. Rowell +18 more

Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans

The Journal of Experimental Medicine(2024)10.1084/jem.20232005

N/A

0DataRank · unranked

37 citations

Julian A. Yano, John Huizar, Leianna C. Slayden, Madeleine A. Weiss, Elizabeth A Turcotte +93 more

Genomic Answers for Kids: Toward more equitable access to genomic testing for rare diseases in rural populations

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.016

N/A

0DataRank · unranked

21 citations

Courtney Berrios, Tricia Zion, Cassandra Barrett, Riley Moore, Emelia Boillat +6 more

Complex trait associations in rare diseases and impacts on Mendelian variant interpretation

Nature Communications(2024)10.1038/s41467-024-52407-1

N/A

0DataRank · unranked

9 citations

Bing Ge, Marissa R. Keever-Keigher, Carl Schwendinger-Schreck, Warren Cheung, Jeffrey Johnston +8 more

Complex trait associations in rare diseases and impacts on Mendelian variant interpretation

medRxiv(2024)10.1101/2024.01.10.24301111

N/A

0DataRank · unranked

3 citations

Bing Ge, Marissa R. Keever-Keigher, Carl Schwendinger-Schreck, Warren Cheung, Jeffrey Johnston +8 more

More Than a Decade of Rapid Genomic Sequencing: Where Are We Now?

Clinical Chemistry(2024)10.1093/clinchem/hvae025

N/A

0DataRank · unranked

0 citations

Luca Brunelli, Michael J. Deem, Emily Farrow, Madhuri Hegde, Zornitza Stark +1 more

Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia Pigmenti

Research Square(2025)10.21203/rs.3.rs-5811417/v1

N/A

0DataRank · unranked

0 citations

Robin D. Clark, Abdallah F. Elias, Casie A. Genetti, Jill A. Madden, Dana Simpson +21 more

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.02.016

N/A

0DataRank · unranked

70 citations

Chloe Reuter, Maura Ruzhnikov, Anita E. Beck, Emily Farrow, Lisa Emrick +91 more

Long-read sequencing is required for precision diagnosis of incontinentia pigmenti

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100468

N/A

0DataRank · unranked

0 citations

Robin D. Clark, Abdallah F. Elias, Casie A. Genetti, Jill A. Madden, Dana Simpson +21 more