Kerry K. Brown

3.2k total citations · 2 hit papers
8 papers, 1.4k citations indexed

About

Kerry K. Brown is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Kerry K. Brown has authored 8 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Kerry K. Brown's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Kerry K. Brown is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Kerry K. Brown collaborates with scholars based in United States, United Kingdom and Canada. Kerry K. Brown's co-authors include Fabiola Quintero‐Rivera, Sarah T. South, Erik C. Thorland, Hutton M. Kearney, Heidi L. Rehm, Madhuri Hegde, Birgit Funke, Joshua L. Deignan, Michael J. Friez and Pınar Bayrak‐Toydemir and has published in prestigious journals such as Human Mutation, Human Genetics and Genetics in Medicine.

In The Last Decade

Kerry K. Brown

7 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

2011 643 citations Hutton M. Kearney, Erik C. Thorland et al. Genetics in Medicine profile →
ACMG clinical laboratory standards for next-generation sequencing

2013 631 citations Heidi L. Rehm, Sherri J. Bale et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kerry K. Brown United States	7	914	532	322	258	132	8	1.4k
Erin Rooney Riggs United States	14	950 1.0×	462 0.9×	377 1.2×	153 0.6×	89 0.7×	21	1.3k
Deborah Ritter United States	14	904 1.0×	538 1.0×	333 1.0×	216 0.8×	132 1.0×	29	1.5k
Jayne Y. Hehir‐Kwa Netherlands	24	1.1k 1.2×	854 1.6×	378 1.2×	217 0.8×	108 0.8×	53	1.9k
Sibel Kantarci United States	15	1.0k 1.1×	821 1.5×	385 1.2×	126 0.5×	126 1.0×	23	1.8k
Fabiola Quintero‐Rivera United States	16	907 1.0×	634 1.2×	357 1.1×	68 0.3×	61 0.5×	54	1.4k
Beata Nowakowska Poland	21	741 0.8×	563 1.1×	218 0.7×	85 0.3×	87 0.7×	87	1.5k
Cuiping Hou United States	20	791 0.9×	740 1.4×	97 0.3×	292 1.1×	58 0.4×	39	1.6k
Carol Saunders United States	22	635 0.7×	744 1.4×	110 0.3×	89 0.3×	87 0.7×	59	1.3k
Karen Duran Netherlands	21	575 0.6×	755 1.4×	136 0.4×	150 0.6×	113 0.9×	28	1.4k
Andreas Dufke Germany	22	865 0.9×	695 1.3×	351 1.1×	50 0.2×	109 0.8×	60	1.4k

Countries citing papers authored by Kerry K. Brown

Since Specialization

Citations

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

Fields of papers citing papers by Kerry K. Brown

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kerry K. Brown. 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 Kerry K. Brown. The network helps show where Kerry K. Brown may publish in the future.

Co-authorship network of co-authors of Kerry K. Brown

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

All Works

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8 of 8 papers shown

1.

Muthukumarasamy, Premala, et al.. (2020). 64 Walker Warburg syndrome (WWS) with ISPD genetic mutation- a case report. A22.2–A22.

2.

Anger, G, Susan Crocker, Kerry K. Brown, et al.. (2014). X-Linked Deafness-2 (DFNX2) Phenotype Associated With a Paracentric Inversion Upstream of POU3F4. American Journal of Audiology. 23(1). 1–6. 18 indexed citations

3.

Rehm, Heidi L., Sherri J. Bale, Pınar Bayrak‐Toydemir, et al.. (2013). ACMG clinical laboratory standards for next-generation sequencing. Genetics in Medicine. 15(9). 733–747. 631 indexed citations breakdown →

4.

Brown, Kerry K., Lucas Moura Viana, Maria A. Artunduaga, et al.. (2013). HOXA2Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss. Human Mutation. 34(10). 1347–1351. 38 indexed citations

5.

Brown, Kerry K. & Heidi L. Rehm. (2012). Molecular Diagnosis of Hearing Loss. Current Protocols in Human Genetics. 72(1). Unit 9.16–Unit 9.16. 18 indexed citations

6.

Kearney, Hutton M., Erik C. Thorland, Kerry K. Brown, Fabiola Quintero‐Rivera, & Sarah T. South. (2011). American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genetics in Medicine. 13(7). 680–685. 643 indexed citations breakdown →

7.

Brown, Kerry K., et al.. (2009). Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35). Human Genetics. 127(1). 19–31. 37 indexed citations

8.

Brown, Kerry K., et al.. (2009). NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness. American Journal of Medical Genetics Part A. 149A(5). 931–938. 30 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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