Carolyn Applegate

1.7k total citations
24 papers, 821 citations indexed

About

Carolyn Applegate is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Carolyn Applegate has authored 24 papers receiving a total of 821 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Carolyn Applegate's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Carolyn Applegate is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Carolyn Applegate collaborates with scholars based in United States, Iceland and United Kingdom. Carolyn Applegate's co-authors include Mary Armanios, Jonathan K. Alder, Vidya Sagar Hanumanthu, Amy E. DeZern, Susan E. Stanley, Denise Batista, J. Brooks Jackson, Dustin L. Gable, Christa L. Wagner and Lindsay B. Henderson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Carolyn Applegate

23 papers receiving 804 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carolyn Applegate United States 17 328 270 237 146 84 24 821
Shih‐hsin Kan United States 15 415 1.3× 337 1.2× 253 1.1× 40 0.3× 57 0.7× 47 873
Periklis Makrythanasis Switzerland 18 402 1.2× 278 1.0× 81 0.3× 111 0.8× 54 0.6× 58 798
Pagon Ra United States 6 450 1.4× 260 1.0× 96 0.4× 38 0.3× 86 1.0× 291 791
Masahito Yoshihara Japan 13 595 1.8× 122 0.5× 134 0.6× 34 0.2× 76 0.9× 36 991
Yutaka Negishi Japan 16 233 0.7× 199 0.7× 70 0.3× 38 0.3× 71 0.8× 37 576
Guy Helman United States 19 692 2.1× 108 0.4× 96 0.4× 58 0.4× 156 1.9× 41 1.0k
Lakshmi Mehta United States 16 403 1.2× 348 1.3× 83 0.4× 44 0.3× 35 0.4× 46 754
John Pappas United States 17 296 0.9× 309 1.1× 68 0.3× 47 0.3× 118 1.4× 54 885
Maria Garofalo Italy 16 285 0.9× 119 0.4× 73 0.3× 39 0.3× 89 1.1× 32 799

Countries citing papers authored by Carolyn Applegate

Since Specialization
Citations

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

Fields of papers citing papers by Carolyn Applegate

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carolyn Applegate

This figure shows the co-authorship network connecting the top 25 collaborators of Carolyn Applegate. A scholar is included among the top collaborators of Carolyn Applegate 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 Carolyn Applegate. Carolyn Applegate 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.
Applegate, Carolyn, et al.. (2025). Assessing genetic counseling efficiency with natural language processing. Journal of the American Medical Informatics Association. 33(2). 295–303.
2.
Harris, Jacqueline, et al.. (2023). Five years of experience in the Epigenetics and Chromatin Clinic: what have we learned and where do we go from here?. Human Genetics. 143(4). 607–624. 14 indexed citations
3.
Newton, Chad A., Justin M. Oldham, Carolyn Applegate, et al.. (2022). The Role of Genetic Testing in Pulmonary Fibrosis. CHEST Journal. 162(2). 394–405. 21 indexed citations
4.
Applegate, Carolyn, François Schiettecatte, Ada Hamosh, & Joanna Amberger. (2022). Exploring Genes and Phenotypes Within Chromosomal Regions Using OMIM's GeneScout. Current Protocols. 2(9). e530–e530. 2 indexed citations
5.
Schnappauf, Oskar, Qing Zhou, Natalia Sampaio Moura, et al.. (2020). Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance. Journal of Clinical Immunology. 40(6). 917–926. 27 indexed citations
6.
Applegate, Carolyn, et al.. (2019). Elements of genetic counseling for inborn errors of metabolism. 4(3-4). 197–208. 4 indexed citations
7.
Fichtman, Boris, Tamar Harel, Carolyn Applegate, et al.. (2019). Pathogenic Variants in NUP214 Cause “Plugged” Nuclear Pore Channels and Acute Febrile Encephalopathy. The American Journal of Human Genetics. 105(1). 48–64. 21 indexed citations
8.
Alder, Jonathan K., Vidya Sagar Hanumanthu, Margaret A. Strong, et al.. (2018). Diagnostic utility of telomere length testing in a hospital-based setting. Proceedings of the National Academy of Sciences. 115(10). E2358–E2365. 144 indexed citations
9.
Wagner, Christa L., Vidya Sagar Hanumanthu, C. Conover Talbot, et al.. (2018). Short telomere syndromes cause a primary T cell immunodeficiency. Journal of Clinical Investigation. 128(12). 5222–5234. 88 indexed citations
10.
Pilarowski, Genay, Hilary J. Vernon, Carolyn Applegate, et al.. (2017). Missense variants in the chromatin remodeler CHD1 are associated with neurodevelopmental disability. Journal of Medical Genetics. 55(8). 561–566. 38 indexed citations
11.
Applegate, Carolyn, et al.. (2017). Choices for return of primary and secondary genomic research results of 790 members of families with Mendelian disease. European Journal of Human Genetics. 25(5). 530–537. 27 indexed citations
12.
Berrios, Courtney, Cynthia A. James, Karen S. Raraigh, et al.. (2017). Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results. Journal of Genetic Counseling. 27(1). 263–273. 20 indexed citations
13.
Stanley, Susan E., Dustin L. Gable, Christa L. Wagner, et al.. (2016). Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis–emphysema. Science Translational Medicine. 8(351). 351ra107–351ra107. 129 indexed citations
14.
Okur, Volkan, Megan T. Cho, Lindsay B. Henderson, et al.. (2016). De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. Human Genetics. 135(7). 699–705. 53 indexed citations
15.
Wolfson, Yulia, Carolyn Applegate, Rupert W. Strauß, Ian C. Han, & Hendrik P. N. Scholl. (2015). CRB1-Related Maculopathy With Cystoid Macular Edema. JAMA Ophthalmology. 133(11). 1357–1357. 22 indexed citations
16.
Weiss, Karin, Carolyn Applegate, Tao Wang, & Denise Batista. (2015). Familial TAB2 microdeletion and congenital heart defects including unusual valve dysplasia and tetralogy of fallot. American Journal of Medical Genetics Part A. 167(11). 2702–2706. 22 indexed citations
17.
Henderson, Lindsay B., Carolyn Applegate, Elizabeth Wohler, et al.. (2014). The impact of chromosomal microarray on clinical management: a retrospective analysis. Genetics in Medicine. 16(9). 657–664. 56 indexed citations
18.
Burnside, Rachel D., John Pappas, Stephanie Sacharow, et al.. (2013). Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype. American Journal of Medical Genetics Part A. 161(4). 822–828. 30 indexed citations
19.
Lemmon, Monica E., Bennett Lavenstein, Carolyn Applegate, et al.. (2013). A novel presentation of DYT 16: Acute onset in infancy and association with MRI abnormalities. Movement Disorders. 28(14). 1937–1938. 16 indexed citations
20.
Fahrner, Jill A., Aisha H. Frazier, Michael F. Walsh, et al.. (2012). A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1. American Journal of Medical Genetics Part A. 158A(6). 1414–1421. 12 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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