Keith A. Choate

6.4k total citations · 2 hit papers
83 papers, 3.5k citations indexed

About

Keith A. Choate is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Keith A. Choate has authored 83 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 40 papers in Cell Biology and 25 papers in Genetics. Recurrent topics in Keith A. Choate's work include Skin and Cellular Biology Research (35 papers), Genetic and rare skin diseases. (20 papers) and Hedgehog Signaling Pathway Studies (11 papers). Keith A. Choate is often cited by papers focused on Skin and Cellular Biology Research (35 papers), Genetic and rare skin diseases. (20 papers) and Hedgehog Signaling Pathway Studies (11 papers). Keith A. Choate collaborates with scholars based in United States, Israel and Spain. Keith A. Choate's co-authors include Richard P. Lifton, David V. Milford, David B. Simon, Carol Nelson‐Williams, Frederick H. Wilson, Yin Lu, Graham Lipkin, David A. McCredie, Essam Al‐Sabban and Sami A. Sanjad and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Keith A. Choate

81 papers receiving 3.4k 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.

Human Hypertension Caused by Mutations in WNK Kinases

2001 1.1k citations Frederick H. Wilson, Sandra Disse-Nicodème et al. Science profile →
Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg ²⁺ Resorption

1999 819 citations David B. Simon, Yin Lu et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Keith A. Choate United States	24	2.3k	707	687	522	507	83	3.5k
Andreas Janecke Austria	37	2.2k 1.0×	1.3k 1.9×	694 1.0×	333 0.6×	271 0.5×	132	4.4k
Pamela R. Fain United States	37	1.9k 0.8×	1.4k 2.0×	1.4k 2.0×	503 1.0×	56 0.1×	106	5.3k
Atsushi Watanabe Japan	29	1.1k 0.5×	438 0.6×	414 0.6×	195 0.4×	320 0.6×	137	3.0k
Dani Bercovich Israel	28	1.2k 0.5×	696 1.0×	241 0.4×	85 0.2×	100 0.2×	74	2.9k
Marie Dziadek Australia	40	2.6k 1.1×	710 1.0×	900 1.3×	180 0.3×	52 0.1×	85	5.1k
Ruth Schmidt‐Ullrich Germany	26	2.0k 0.9×	318 0.4×	891 1.3×	76 0.1×	77 0.2×	39	4.1k
Lynn Sanford United States	20	2.0k 0.9×	460 0.7×	175 0.3×	160 0.3×	103 0.2×	37	2.8k
Vikram Prasad United States	29	2.6k 1.2×	365 0.5×	430 0.6×	166 0.3×	31 0.1×	66	4.0k
Craig L. Bennett United States	26	1.7k 0.7×	967 1.4×	210 0.3×	142 0.3×	506 1.0×	47	5.2k
Rosetta Pedotti Italy	27	1.5k 0.7×	374 0.5×	169 0.2×	90 0.2×	458 0.9×	40	4.9k

Countries citing papers authored by Keith A. Choate

Since Specialization

Citations

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

Fields of papers citing papers by Keith A. Choate

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Keith A. Choate. 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 Keith A. Choate. The network helps show where Keith A. Choate may publish in the future.

Co-authorship network of co-authors of Keith A. Choate

This figure shows the co-authorship network connecting the top 25 collaborators of Keith A. Choate. A scholar is included among the top collaborators of Keith A. Choate 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 Keith A. Choate. Keith A. Choate 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

Akiyama, Masashi, Keith A. Choate, Á. Hernández‐Martín, et al.. (2025). Nonsyndromic epidermal differentiation disorders: a new classification toward pathogenesis-based therapy. British Journal of Dermatology. 193(4). 619–641. 6 indexed citations

Paller, Amy S., Joyce Teng, J. Mazereeuw‐Hautier, et al.. (2025). Syndromic epidermal differentiation disorders: a new classification toward pathogenesis-based therapy. British Journal of Dermatology. 193(4). 592–618. 6 indexed citations

Hernández‐Martín, Á., Amy S. Paller, Eli Sprecher, et al.. (2025). A proposal for a new pathogenesis-guided classification for inherited epidermal differentiation disorders. British Journal of Dermatology. 193(3). 544–548. 5 indexed citations

Damsky, William, et al.. (2024). Intravenous immunoglobulin-induced eczematous dermatitis treated with dupilumab. JAAD Case Reports. 49. 102–105.

Brichta, Lars, et al.. (2024). Topical trametinib for epidermal and sebaceous nevi in a child with Schimmelpenning‐Feuerstein‐Mims syndrome. Pediatric Dermatology. 41(3). 523–525. 2 indexed citations

Hunt, Matthew, Nuoqi Wang, Mónica S. Torres, et al.. (2024). Dantrolene corrects cellular disease features of Darier disease and may be a novel treatment. EMBO Molecular Medicine. 16(9). 1986–2001. 1 indexed citations

Atzmony, Lihi, Lionel Bercovitch, Leslie Robinson‐Bostom, et al.. (2022). Segmental basaloid follicular hamartomas derive from a post‐zygotic SMO p.L412F pathogenic variant and express hair follicle development‐related proteins in a pattern that distinguish them from basal cell carcinomas. American Journal of Medical Genetics Part A. 188(12). 3525–3530. 3 indexed citations

Paller, Amy S., et al.. (2021). CARD14‐associated papulosquamous eruption (CAPE) in pediatric patients: Three additional cases and review of the literature. Pediatric Dermatology. 38(5). 1237–1242. 14 indexed citations

Vahidnezhad, Hassan, Leila Youssefian, Amir Hossein Saeidian, et al.. (2021). Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation. Matrix Biology. 99. 43–57. 5 indexed citations

10.

Vahidnezhad, Hassan, Leila Youssefian, Andrew Touati, et al.. (2021). 186 Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation. Journal of Investigative Dermatology. 141(5). S33–S33. 2 indexed citations

11.

Atzmony, Lihi, Gauri Panse, Dhanpat Jain, et al.. (2021). Cutaneous and hepatic vascular lesions due to a recurrent somatic GJA4 mutation reveal a pathway for vascular malformation. SHILAP Revista de lepidopterología. 2(2). 100028–100028. 10 indexed citations

12.

Lefferdink, Rachel, Margot Chima, Erin Ibler, et al.. (2021). 428 Randomized, double-blind, placebo-controlled study of efficacy and safety of secukinumab to treat adults with ichthyoses. Journal of Investigative Dermatology. 141(5). S74–S74. 2 indexed citations

13.

Boyden, Lynn M., Jing Zhou, Rong‐Hua Hu, et al.. (2020). Mutations in ASPRV1 Cause Dominantly Inherited Ichthyosis. The American Journal of Human Genetics. 107(1). 158–163. 13 indexed citations

14.

Boyden, Lynn M., Lihi Atzmony, Claire Hamilton, et al.. (2019). Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and Photophobia. The American Journal of Human Genetics. 105(5). 1023–1029. 18 indexed citations

15.

Duchatelet, Sabine, Lynn M. Boyden, Akemi Ishida‐Yamamoto, et al.. (2018). Mutations in PERP Cause Dominant and Recessive Keratoderma. Journal of Investigative Dermatology. 139(2). 380–390. 21 indexed citations

16.

Boyden, Lynn M. & Keith A. Choate. (2017). The Molecular Revolution in Cutaneous Biology: Identification of Skin Disease Genes. Journal of Investigative Dermatology. 137(5). e61–e65. 3 indexed citations

17.

Esmer, Carmen, et al.. (2016). Lethal Keratitis, Ichthyosis, and Deafness Syndrome Due to the A88V Connexin 26 Mutation. Revista de investigaci�n Cl�nica. 68(3). 143–146. 4 indexed citations

18.

Levinsohn, Jonathan, et al.. (2015). Somatic V600E BRAF Mutation in Linear and Sporadic Syringocystadenoma Papilliferum. Journal of Investigative Dermatology. 135(10). 2536–2538. 26 indexed citations

19.

Choate, Keith A., Yin Lu, Jing Zhou, et al.. (2010). Mitotic Recombination in Patients with Ichthyosis Causes Reversion of Dominant Mutations in KRT10. Science. 330(6000). 94–97. 116 indexed citations

20.

Wilson, Frederick H., Sandra Disse-Nicodème, Keith A. Choate, et al.. (2001). Human Hypertension Caused by Mutations in WNK Kinases. Science. 293(5532). 1107–1112. 1114 indexed citations breakdown →

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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