Elyse Mitchell

893 total citations
5 papers, 65 citations indexed

About

Elyse Mitchell is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Elyse Mitchell has authored 5 papers receiving a total of 65 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Pediatrics, Perinatology and Child Health and 1 paper in Surgery. Recurrent topics in Elyse Mitchell's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Prenatal Screening and Diagnostics (2 papers). Elyse Mitchell is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Prenatal Screening and Diagnostics (2 papers). Elyse Mitchell collaborates with scholars based in United States and China. Elyse Mitchell's co-authors include Jennelle C. Hodge, Carrie Hanscom, Jun Wang, Yiping Shen, Vamsee Pillalamarri, Lauren Margolin, Xiaoli Chen, James F. Gusella, Michael E. Talkowski and Jin Guo and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Medical Genetics Part A and BMC Medical Genetics.

In The Last Decade

Elyse Mitchell

4 papers receiving 53 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elyse Mitchell United States	4	45	20	17	11	10	5	65
Debra Rita United States	4	50 1.1×	32 1.6×	32 1.9×	6 0.5×	6 0.6×	5	78
Joanna Jarvis United Kingdom	5	55 1.2×	49 2.5×	13 0.8×	5 0.5×	12 1.2×	6	88
Stacy Gabriel United States	1	40 0.9×	27 1.4×	21 1.2×	8 0.7×	3 0.3×	2	60
Nobuhiko Okamoto Japan	4	34 0.8×	35 1.8×	8 0.5×	4 0.4×	7 0.7×	7	68
Florence Démurger France	5	50 1.1×	40 2.0×	33 1.9×	8 0.7×	5 0.5×	7	78
Una Maye United Kingdom	3	27 0.6×	16 0.8×	10 0.6×	7 0.6×	4 0.4×	4	38
Melissa A Dempsey United States	5	47 1.0×	63 3.1×	11 0.6×	7 0.6×	5 0.5×	8	86
Jin Fang Chai China	5	27 0.6×	32 1.6×	7 0.4×	10 0.9×	5 0.5×	13	72
Shelagh Joss United Kingdom	4	45 1.0×	30 1.5×	5 0.3×	8 0.7×	6 0.6×	6	59
Katherine Yates United Kingdom	3	43 1.0×	27 1.4×	13 0.8×	6 0.5×	10 1.0×	3	57

Countries citing papers authored by Elyse Mitchell

Since Specialization

Citations

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

Fields of papers citing papers by Elyse Mitchell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elyse Mitchell

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

All Works

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5 of 5 papers shown

1.

Cao, Yang, et al.. (2016). Two cases with de novo 3q26.31 microdeletion suggest a role for FNDC3B in human craniofacial development. American Journal of Medical Genetics Part A. 170(12). 3276–3281. 4 indexed citations

2.

Brand, Harrison, Ryan L. Collins, Carrie Hanscom, et al.. (2015). Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation. The American Journal of Human Genetics. 97(1). 170–176. 37 indexed citations

3.

Chen, Xiaoli, Jun Wang, Elyse Mitchell, et al.. (2014). Recurrent 8q13.2-13.3 microdeletions associated with Branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks. BMC Medical Genetics. 15(1). 90–90. 13 indexed citations

4.

Wain, Karen E., Erin Rooney Riggs, Karen Hanson, et al.. (2012). The Laboratory‐Clinician Team: A Professional Call to Action to Improve Communication and Collaboration for Optimal Patient Care in Chromosomal Microarray Testing. Journal of Genetic Counseling. 21(5). 631–637. 11 indexed citations

5.

Pollock, John C., et al.. (2006). Gay Rights: Nationwide Newspaper Coverage of Gay Adoption, Gay Marriage, and Gays in the Boy Scouts: A Community Structure Approach. 1–43.

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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