Sarah B. Emery

5.7k total citations
23 papers, 954 citations indexed

About

Sarah B. Emery is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Sarah B. Emery has authored 23 papers receiving a total of 954 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Plant Science. Recurrent topics in Sarah B. Emery's work include Genomics and Phylogenetic Studies (6 papers), Chromosomal and Genetic Variations (5 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Sarah B. Emery is often cited by papers focused on Genomics and Phylogenetic Studies (6 papers), Chromosomal and Genetic Variations (5 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Sarah B. Emery collaborates with scholars based in United States, France and Ghana. Sarah B. Emery's co-authors include Jeffrey M. Kidd, Ryan E. Mills, Marci M. Lesperance, Gargi Dayama, Elżbieta Śliwerska, Adam R. Boyko, Amanda L. Pendleton, Krishna R. Veeramah, Angela M. Taravella Oill and Régis Nouvian and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Circulation.

In The Last Decade

Sarah B. Emery

23 papers receiving 946 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah B. Emery United States 15 546 307 243 108 104 23 954
Brandon J. Walters United States 18 729 1.3× 152 0.5× 212 0.9× 134 1.2× 72 0.7× 28 1.1k
Basile Tarchini United States 14 882 1.6× 250 0.8× 250 1.0× 32 0.3× 116 1.1× 36 1.1k
Edmund J. Koundakjian United States 8 739 1.4× 344 1.1× 313 1.3× 96 0.9× 77 0.7× 8 1.1k
Kwanghyuk Lee United States 16 566 1.0× 183 0.6× 310 1.3× 80 0.7× 56 0.5× 39 1.0k
Pedro León Costa Rica 15 471 0.9× 335 1.1× 326 1.3× 126 1.2× 221 2.1× 34 1.1k
Déborah Scheffer United States 13 532 1.0× 130 0.4× 548 2.3× 149 1.4× 36 0.3× 14 960
Luís Sánchez-Guardado Spain 12 749 1.4× 333 1.1× 170 0.7× 119 1.1× 28 0.3× 19 1.2k
Christopher M. Weber United States 12 1.1k 2.0× 84 0.3× 216 0.9× 143 1.3× 159 1.5× 16 1.4k
Carsten M. Pusch Germany 25 818 1.5× 374 1.2× 243 1.0× 66 0.6× 34 0.3× 76 1.7k
Tomoko Makishima United States 22 614 1.1× 100 0.3× 700 2.9× 168 1.6× 130 1.3× 37 1.3k

Countries citing papers authored by Sarah B. Emery

Since Specialization
Citations

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

Fields of papers citing papers by Sarah B. Emery

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah B. Emery. 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 Sarah B. Emery. The network helps show where Sarah B. Emery may publish in the future.

Co-authorship network of co-authors of Sarah B. Emery

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah B. Emery. A scholar is included among the top collaborators of Sarah B. Emery 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 Sarah B. Emery. Sarah B. Emery 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.
Jagannathan, Vidhya, Christophe Hitte, Jeffrey M. Kidd, et al.. (2021). Dog10K_Boxer_Tasha_1.0: A Long-Read Assembly of the Dog Reference Genome. Genes. 12(6). 847–847. 29 indexed citations
2.
Pendleton, Amanda L., Aurélien J. Doucet, Thomas Derrien, et al.. (2021). Long-read assembly of a Great Dane genome highlights the contribution of GC-rich sequence and mobile elements to canine genomes. Proceedings of the National Academy of Sciences. 118(11). 31 indexed citations
3.
Read, David F., Kalyani Pyaram, Feng Yang, et al.. (2019). Stable integrant-specific differences in bimodal HIV-1 expression patterns revealed by high-throughput analysis. PLoS Pathogens. 15(10). e1007903–e1007903. 3 indexed citations
4.
Song, Shiya, Elżbieta Śliwerska, Sarah B. Emery, & Jeffrey M. Kidd. (2016). Modeling Human Population Separation History Using Physically Phased Genomes. Genetics. 205(1). 385–395. 33 indexed citations
5.
Oetjens, Matthew T., et al.. (2016). Y-Chromosome Structural Diversity in the Bonobo and Chimpanzee Lineages. Genome Biology and Evolution. 8(7). 2231–2240. 17 indexed citations
6.
Zhao, Xuefang, Sarah B. Emery, Bridget Myers, Jeffrey M. Kidd, & Ryan E. Mills. (2016). Resolving complex structural genomic rearrangements using a randomized approach. Genome biology. 17(1). 126–126. 25 indexed citations
7.
Dayama, Gargi, Sarah B. Emery, Jeffrey M. Kidd, & Ryan E. Mills. (2014). The genomic landscape of polymorphic human nuclear mitochondrial insertions. Nucleic Acids Research. 42(20). 12640–12649. 127 indexed citations
8.
Green, Glenn E., et al.. (2014). CHD7 Mutations and CHARGE Syndrome in Semicircular Canal Dysplasia. Otology & Neurotology. 35(8). 1466–1470. 15 indexed citations
9.
Goonewardena, Sascha N., Jeremy D. Kratz, Hong Zong, et al.. (2013). Design considerations for PAMAM dendrimer therapeutics. Bioorganic & Medicinal Chemistry Letters. 23(10). 2872–2875. 15 indexed citations
10.
Goonewardena, Sascha N., et al.. (2013). Fluorogenic ‘click-on’ dendrimer reporter for rapid profiling of cell proliferation. Bioorganic & Medicinal Chemistry Letters. 23(7). 2230–2233. 5 indexed citations
11.
12.
Rieder, Mark J., Glenn E. Green, Sarah S. Park, et al.. (2012). A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome. The American Journal of Human Genetics. 91(2). 397–397. 6 indexed citations
13.
Rieder, Mark J., Glenn E. Green, Sarah S. Park, et al.. (2012). A Human Homeotic Transformation Resulting from Mutations in PLCB4 and GNAI3 Causes Auriculocondylar Syndrome. The American Journal of Human Genetics. 90(5). 907–914. 67 indexed citations
14.
Emery, Sarah B., et al.. (2011). Autosomal Dominant Progressive Sensorineural Hearing Loss Due to a Novel Mutation in the KCNQ4 Gene. Archives of Otolaryngology - Head and Neck Surgery. 137(1). 54–54. 24 indexed citations
15.
Rendtorff, Nanna Dahl, Marianne Lodahl, Houda Boulahbel, et al.. (2011). Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment. American Journal of Medical Genetics Part A. 155(6). 1298–1313. 89 indexed citations
16.
Emery, Sarah B., Marc C. Thorne, Elżbieta Śliwerska, et al.. (2010). Increased activity of Diaphanous homolog 3 ( DIAPH3 )/ diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila. Proceedings of the National Academy of Sciences. 107(30). 13396–13401. 82 indexed citations
17.
Emery, Sarah B., et al.. (2010). Congenital cataracts in two siblings with Wolfram Syndrome. Ophthalmic Genetics. 31(4). 227–229. 11 indexed citations
18.
Emery, Sarah B., et al.. (2009). Otosclerosis or Congenital Stapes Ankylosis? The Diagnostic Role of Genetic Analysis. Otology & Neurotology. 30(8). 1204–1208. 6 indexed citations
19.
Grati, Francesca Romana, Marci M. Lesperance, Simona De Toffol, et al.. (2009). Pure monosomy and pure trisomy of 13q21.2–31.1 consequent to a familial insertional translocation: Exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1). American Journal of Medical Genetics Part A. 149A(5). 906–913. 10 indexed citations
20.
Ruel, Jérôme, Sarah B. Emery, Régis Nouvian, et al.. (2008). Impairment of SLC17A8 Encoding Vesicular Glutamate Transporter-3, VGLUT3, Underlies Nonsyndromic Deafness DFNA25 and Inner Hair Cell Dysfunction in Null Mice. The American Journal of Human Genetics. 83(2). 278–292. 195 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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