Carolyn Applegate

1.7k citations
24 papers · 821 · h-index 17

Impact in

  • Aging top 10%
  • Genetics top 10%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Congenital heart defects research 3
    • RNA Research and Splicing 2
    • Genomics and Rare Diseases 6
    • Genomic variations and chromosomal abnormalities 6
    • Genetics and Neurodevelopmental Disorders 5
    • BRCA gene mutations in cancer 2

Carolyn Applegate

23 papers receiving 804 citations

Peers

Carolyn Applegate
Comparison fields: 5 of 70
  • Aging 20
  • Genetics 270
  • Physiology 237
  • Genetics 56
  • Molecular Biology 328
Replace John Rendu with:
John Rendu France
Tanya M. McLaughlin United States
Virginie Carmignac France
Stavit A. Shalev Israel
P. Gallano Spain
Dashzeveg Bayarsaihan United States
Loydie A. Jerome‐Majewska Canada
John Broxholme United Kingdom
Katrin Koehler Germany
Thomas F. Manganaro United States
Carolyn Applegate relative to John Rendu France John Rendu's profile →
Citations per field
00.5×3.4×
John Rendu · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Carolyn Applegate, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Carolyn Applegate Line = papers co-authored together Carolyn Applegate links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2018144
2 2016129
3 201888
4 201456
5 201653
6 201639
7 201738
8 201330
9 202027
10 201727
11 201522
12 201522
13 201921
14 202221
15 201720
16 201417
17 201316
18 202314
19 201212
20 201411

About Carolyn Applegate

Carolyn Applegate is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Oncology and Epidemiology, having authored 24 papers that have together received 821 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital heart defects research (3 papers), Peptidase Inhibition and Analysis (3 papers), Prenatal Screening and Diagnostics (2 papers), RNA Research and Splicing (2 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Aging (20 citations), Genetics (270 citations), Physiology (237 citations), Genetics (56 citations) and Molecular Biology (328 citations). Carolyn Applegate has collaborated with scholars based in United States, Iceland and United Kingdom. Frequent co-authors include Mary Armanios, Jonathan K. Alder, Vidya Sagar Hanumanthu, Amy E. DeZern, Susan E. Stanley, Denise Batista, Christa L. Wagner, Dustin L. Gable, J. Brooks Jackson and Lindsay B. Henderson. Their work appears in journals such as Human Genetics, Annals of Neurology, European Journal of Human Genetics, Movement Disorders and Genetics in Medicine.

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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