Emily Place

2.7k total citations
41 papers, 879 citations indexed

About

Emily Place is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Emily Place has authored 41 papers receiving a total of 879 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 14 papers in Genetics and 12 papers in Ophthalmology. Recurrent topics in Emily Place's work include Retinal Development and Disorders (21 papers), Genomics and Rare Diseases (9 papers) and Mitochondrial Function and Pathology (9 papers). Emily Place is often cited by papers focused on Retinal Development and Disorders (21 papers), Genomics and Rare Diseases (9 papers) and Mitochondrial Function and Pathology (9 papers). Emily Place collaborates with scholars based in United States, Canada and France. Emily Place's co-authors include Eric A. Pierce, Marni J. Falk, Kinga M. Bujakowska, Daniel Navarro-Gomez, Jason Comander, Elizabeth M. McCormick, Mark Consugar, Xiaowu Gai, Xiang Q. Werdich and Anne B. Fulton and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Emily Place

35 papers receiving 868 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emily Place United States	17	677	229	209	106	66	41	879
Cody R. Fisher United States	10	402 0.6×	349 1.5×	37 0.2×	42 0.4×	35 0.5×	14	588
Pabalu P. Karunadharma United States	13	742 1.1×	328 1.4×	35 0.2×	62 0.6×	87 1.3×	18	1.1k
Carlo Gesualdo Italy	16	307 0.5×	316 1.4×	26 0.1×	56 0.5×	22 0.3×	35	655
Ankita Umapathy New Zealand	8	337 0.5×	214 0.9×	17 0.1×	39 0.4×	53 0.8×	12	470
Diego Carrella Italy	13	397 0.6×	38 0.2×	44 0.2×	47 0.4×	36 0.5×	18	639
Nawajes Mandal United States	19	535 0.8×	292 1.3×	27 0.1×	23 0.2×	28 0.4×	61	909
Yuriko Minegishi Japan	16	320 0.5×	126 0.6×	38 0.2×	17 0.2×	20 0.3×	32	704
Takuji Nabetani Japan	12	312 0.5×	74 0.3×	34 0.2×	17 0.2×	68 1.0×	19	523
Patricia Lenhart United States	11	267 0.4×	50 0.2×	41 0.2×	21 0.2×	113 1.7×	17	500
Yoshiyuki Tamada Japan	14	417 0.6×	85 0.4×	70 0.3×	32 0.3×	66 1.0×	27	621

Countries citing papers authored by Emily Place

Since Specialization

Citations

This map shows the geographic impact of Emily Place'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 Place with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emily Place more than expected).

Fields of papers citing papers by Emily Place

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emily Place. 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 Place. The network helps show where Emily Place may publish in the future.

Co-authorship network of co-authors of Emily Place

This figure shows the co-authorship network connecting the top 25 collaborators of Emily Place. A scholar is included among the top collaborators of Emily Place 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 Place. Emily Place is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Sangermano, Riccardo, Emily Place, Eric A. Pierce, & Kinga M. Bujakowska. (2025). Novel Potentially Pathogenic Variants in TBC1D32 Cause Non-syndromic Rod-Cone Degeneration. Advances in experimental medicine and biology. 1468. 41–44. 1 indexed citations

Zaslavsky, Kirill, et al.. (2025). Low population penetrance of variants associated with inherited retinal degenerations. The American Journal of Human Genetics. 113(1). 71–82.

Nakamichi, Kazuo, Riccardo Sangermano, Emily Place, et al.. (2024). Targeted long-read sequencing enriches disease-relevant genomic regions of interest to provide complete Mendelian disease diagnostics. JCI Insight. 9(20). 3 indexed citations

Hauser, Blake M., Yuyang Luo, Anusha Nathan, et al.. (2024). Structure-based network analysis predicts pathogenic variants in human proteins associated with inherited retinal disease. npj Genomic Medicine. 9(1). 31–31.

Borchert, John R., et al.. (2023). P259: The impact of no-cost testing programs for inherited retinal degeneration on post-testing follow-up genetic services. SHILAP Revista de lepidopterología. 1(1). 100287–100287.

Dahéron, Laurence, et al.. (2023). Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donor. Stem Cell Research. 74. 103280–103280. 1 indexed citations

Berrocal, Audina M., Emily Place, Heather Mason‐Suares, et al.. (2022). Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome. Ophthalmic Genetics. 44(2). 198–203. 2 indexed citations

Sangermano, Riccardo, Pooja Biswas, Lori S. Sullivan, et al.. (2022). Identification of a novel large multigene deletion and a frameshift indel inPDE6Bas the underlying cause of early-onset recessive rod–cone degeneration. Molecular Case Studies. 8(7). a006247–a006247.

Bronstein, Revital, Elizabeth E. Capowski, Sudeep Mehrotra, et al.. (2020). A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families. Human Molecular Genetics. 29(6). 967–979. 18 indexed citations

10.

Kinde, Benyam, Emily Place, Daniel Navarro-Gomez, et al.. (2020). Copy-number variation contributes 9% of pathogenicity in the inherited retinal degenerations. Genetics in Medicine. 22(6). 1079–1087. 66 indexed citations

11.

Place, Emily, Katherine R. Chao, Stephanie DiTroia, et al.. (2020). Expanding the phenotypic spectrum in RDH12-associated retinal disease. Molecular Case Studies. 6(1). a004754–a004754. 20 indexed citations

12.

Place, Emily, et al.. (2019). Predictive value of genetic testing for inherited retinal diseases in patients with suspected atypical autoimmune retinopathy. American Journal of Ophthalmology Case Reports. 15. 100461–100461. 9 indexed citations

13.

Jamshidi, Farzad, Emily Place, Sudeep Mehrotra, et al.. (2018). Contribution of noncoding pathogenic variants to RPGRIP1-mediated inherited retinal degeneration. Genetics in Medicine. 21(3). 694–704. 17 indexed citations

14.

Pierce, Eric A., et al.. (2017). The Effect Of Vitamin A On Progression Of Retinitis Pigmentosa Is Not Determined By The Underlying Genetic Cause Of Disease. Investigative Ophthalmology & Visual Science. 58(8). 2011–2011. 2 indexed citations

15.

Falk, Marni J., Xiaowu Gai, Megumi Shigematsu, et al.. (2016). A novelHSD17B10mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression. RNA Biology. 13(5). 477–485. 41 indexed citations

16.

Bujakowska, Kinga M., Rosario Fernández‐Godino, Emily Place, et al.. (2016). Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations. Genetics in Medicine. 19(6). 643–651. 40 indexed citations

17.

Bujakowska, Kinga M., Joseph White, Emily Place, Mark Consugar, & Jason Comander. (2015). Efficient In Silico Identification of a Common Insertion in the MAK Gene which Causes Retinitis Pigmentosa. PLoS ONE. 10(11). e0142614–e0142614. 11 indexed citations

18.

Consugar, Mark, Daniel Navarro-Gomez, Emily Place, et al.. (2014). Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing. Genetics in Medicine. 17(4). 253–261. 179 indexed citations

19.

Clarke, Colleen, Rui Xiao, Emily Place, et al.. (2013). Mitochondrial respiratory chain disease discrimination by retrospective cohort analysis of blood metabolites. Molecular Genetics and Metabolism. 110(1-2). 145–152. 42 indexed citations

20.

McCormick, Elizabeth M., Emily Place, & Marni J. Falk. (2012). Molecular Genetic Testing for Mitochondrial Disease: From One Generation to the Next. Neurotherapeutics. 10(2). 251–261. 57 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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