Emily Farrow

6.6k total citations
73 papers, 2.5k citations indexed

About

Emily Farrow is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Emily Farrow has authored 73 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 25 papers in Molecular Biology and 17 papers in Nephrology. Recurrent topics in Emily Farrow's work include Genomics and Rare Diseases (17 papers), Parathyroid Disorders and Treatments (17 papers) and Genetic Syndromes and Imprinting (11 papers). Emily Farrow is often cited by papers focused on Genomics and Rare Diseases (17 papers), Parathyroid Disorders and Treatments (17 papers) and Genetic Syndromes and Imprinting (11 papers). Emily Farrow collaborates with scholars based in United States, United Kingdom and Italy. Emily Farrow's co-authors include Kenneth E. White, Lelia J. Summers, Siobhan I. Davis, Neil Miller, Carol Saunders, Stephen F. Kingsmore, Isabelle Thiffault, Sarah Soden, Darrell L. Dinwiddie and Matthew R. Allen and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Emily Farrow

69 papers receiving 2.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Emily Farrow United States 28 1.3k 1.1k 951 332 292 73 2.5k
Lorenz Sellin Germany 28 739 0.6× 1.0k 0.9× 1.5k 1.5× 488 1.5× 142 0.5× 59 2.8k
Peyman Björklund Sweden 30 797 0.6× 915 0.8× 917 1.0× 241 0.7× 534 1.8× 56 3.1k
Dongxing Zhu United Kingdom 22 337 0.3× 429 0.4× 676 0.7× 121 0.4× 146 0.5× 42 1.7k
Cynthia St. Hilaire United States 20 415 0.3× 388 0.3× 751 0.8× 154 0.5× 161 0.6× 42 2.1k
Sandra Merscher United States 26 314 0.3× 1.6k 1.4× 1.2k 1.2× 423 1.3× 116 0.4× 56 2.9k
Takamoto Ohse Japan 25 353 0.3× 1.1k 1.0× 914 1.0× 173 0.5× 70 0.2× 29 2.3k
Puneet Garg United States 18 261 0.2× 903 0.8× 538 0.6× 126 0.4× 51 0.2× 48 1.5k
Friedhelm Hildebrandt United States 22 618 0.5× 971 0.9× 958 1.0× 264 0.8× 31 0.1× 44 1.9k
Anne S. Olsen United States 12 462 0.4× 1.5k 1.3× 1.1k 1.2× 279 0.8× 54 0.2× 16 2.2k
László Hegyi United Kingdom 13 204 0.2× 319 0.3× 680 0.7× 96 0.3× 76 0.3× 23 1.6k

Countries citing papers authored by Emily Farrow

Since Specialization
Citations

This map shows the geographic impact of Emily Farrow's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Emily Farrow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emily Farrow more than expected).

Fields of papers citing papers by Emily Farrow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emily Farrow. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Emily Farrow. The network helps show where Emily Farrow may publish in the future.

Co-authorship network of co-authors of Emily Farrow

This figure shows the co-authorship network connecting the top 25 collaborators of Emily Farrow. A scholar is included among the top collaborators of Emily Farrow based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Emily Farrow. Emily Farrow is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Means, John C., Daniel Louiselle, John M. Perry, et al.. (2025). Rapid and scalable personalized ASO screening in patient-derived organoids. Nature. 638(8049). 237–243. 11 indexed citations
2.
Wang, Baihan, et al.. (2024). Early detection of anal squamous cell carcinoma with the use of high-resolution anoscopy. Clinical and Experimental Dermatology. 50(2). 395–398.
3.
Farrow, Emily, et al.. (2023). Clinical Course of A Patient With Agammaglobulinemia Caused By SLC39A7 Defect. Clinical Immunology. 250. 109392–109392.
4.
Harting, John, Emily Farrow, Isabelle Thiffault, et al.. (2023). Comprehensive SMN1 and SMN2 profiling for spinal muscular atrophy analysis using long-read PacBio HiFi sequencing. The American Journal of Human Genetics. 110(2). 240–250. 36 indexed citations
5.
Cadieux‐Dion, Maxime, Emily Farrow, Isabelle Thiffault, et al.. (2022). Phenotypic expansion and variable expressivity in individuals with JARID2 ‐related intellectual disability: A case series. Clinical Genetics. 102(2). 136–141. 2 indexed citations
6.
Gaedigk, Andrea, Erin C. Boone, Steven E. Scherer, et al.. (2022). CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis. Journal of Molecular Diagnostics. 24(4). 337–350. 28 indexed citations
7.
Farrow, Emily, et al.. (2022). Urinary tract obstruction. InnovAiT Education and inspiration for general practice. 15(5). 265–271. 5 indexed citations
8.
Cadieux‐Dion, Maxime, Byunggil Yoo, Neil Miller, et al.. (2021). Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing. Journal of Molecular Diagnostics. 23(5). 651–657. 12 indexed citations
9.
Berrios, Courtney, Emily A. Hurley, Laurel K. Willig, et al.. (2021). Challenges in genetic testing: clinician variant interpretation processes and the impact on clinical care. Genetics in Medicine. 23(12). 2289–2299. 13 indexed citations
10.
Jacobson, Jill D., Laurel K. Willig, Julie Strickland, et al.. (2020). High Molecular Diagnosis Rate in Undermasculinized Males with Differences in Sex Development Using a Stepwise Approach. Endocrinology. 161(5). 10 indexed citations
11.
Thiffault, Isabelle, Andrea M. Atherton, Bryce A. Heese, et al.. (2020). Pathogenic variants in KPTN gene identified by clinical whole-genome sequencing. Molecular Case Studies. 6(3). a003970–a003970. 4 indexed citations
12.
Thiffault, Isabelle, Emily Farrow, Lee Zellmer, et al.. (2018). Clinical genome sequencing in an unbiased pediatric cohort. Genetics in Medicine. 21(2). 303–310. 31 indexed citations
13.
Thiffault, Isabelle, Britton Zuccarelli, Xuan Yuan, et al.. (2017). Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease. BMC Medical Genetics. 18(1). 124–124. 11 indexed citations
14.
Conway, Robert L., Isabelle Thiffault, Carol Saunders, et al.. (2016). Neonatal progeriod syndrome associated with biallelic truncating variants in POLR3A. American Journal of Medical Genetics Part A. 170(12). 3343–3346. 27 indexed citations
15.
Saunders, Carol, Laurie D. Smith, Flemming Wibrand, et al.. (2015). CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria. The American Journal of Human Genetics. 96(2). 258–265. 44 indexed citations
16.
Farrow, Emily, Xijie Yu, Lelia J. Summers, et al.. (2011). Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice. Proceedings of the National Academy of Sciences. 108(46). E1146–55. 284 indexed citations
17.
Farrow, Emily, Lelia J. Summers, Susan C. Schiavi, et al.. (2010). Altered renal FGF23-mediated activity involving MAPK and Wnt: effects of the Hyp mutation. Journal of Endocrinology. 207(1). 67–75. 41 indexed citations
18.
Farrow, Emily & Kenneth E. White. (2009). Tumor-induced osteomalacia. Expert Review of Endocrinology & Metabolism. 4(5). 435–442. 27 indexed citations
19.
Garringer, Holly J., Mahdi Malekpour, Fatemehsadat Esteghamat, et al.. (2008). Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosis. American Journal of Physiology-Endocrinology and Metabolism. 295(4). E929–E937. 34 indexed citations
20.
Farrow, Emily, et al.. (2007). A case of de novo partial tetrasomy of distal 6p and review of the literature. American Journal of Medical Genetics Part A. 143A(17). 1978–1983. 13 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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