Carol Booth

1.0k citations
9 papers · 437 · h-index 9

Impact in

    • Connective tissue disorders research
    • Genomic variations and chromosomal abnormalities
    • Pediatric Hepatobiliary Diseases and Treatments
    • Congenital Anomalies and Fetal Surgery

Papers in

    • Genomic variations and chromosomal abnormalities 2
    • Connective tissue disorders research 2
    • Neurogenetic and Muscular Disorders Research 1
    • Genetic Syndromes and Imprinting 1
    • Pediatric Hepatobiliary Diseases and Treatments 2

Carol Booth

9 papers receiving 417 citations

Peers

Carol Booth
Comparison fields: 5 of 63
  • Genetics 141
  • Surgery 146
  • Rheumatology 43
  • Pulmonary and Respiratory Medicine 90
  • Developmental Biology 6
Replace Lawrence G. Leichtman with:
Lawrence G. Leichtman United States
Inge B. Mathijssen Netherlands
Van den Berghe H Belgium
J S Fitzsimmons United Kingdom
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Mamoru Ozaki Japan
Ken Hashimoto United States
Hana Abouzeid Switzerland
Patrizia Bertolini Italy
Mitzi L. Murray United States
Carol Booth relative to Lawrence G. Leichtman United States Lawrence G. Leichtman's profile →
Citations per field
00.5×
Lawrence G. Leichtman · 1×
Citations per year

Countries citing papers authored by Carol Booth

Since Specialization
Citations

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

Fields of papers citing papers by Carol Booth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Carol Booth, 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 Carol Booth Line = papers co-authored together Carol Booth links everyone, so they are left out of the graph.

All Works

9 of 9 papers shown
#Work
1 2004219
2 201167
3 199536
4 199027
5
Acute myeloid leukemia and myelodysplasia following intensive chemotherapy for breast cancer.
199526
6 198817
7
Ethnic heterogeneity and cystic fibrosis transmembrane regulator (CFTR) mutation frequencies in Chicago-area CF families.
199216
8 198115
9 198514

About Carol Booth

Carol Booth is a scholar working on Genetics, Surgery, Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 9 papers that have together received 437 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Pediatric Hepatobiliary Diseases and Treatments (2 papers), Connective tissue disorders research (2 papers), Acute Myeloid Leukemia Research (1 paper), Epigenetics and DNA Methylation (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (141 citations), Surgery (146 citations), Rheumatology (43 citations), Pulmonary and Respiratory Medicine (90 citations) and Developmental Biology (6 citations). Carol Booth has collaborated with scholars based in United States and Canada. Frequent co-authors include Binita M. Kamath, Nancy B. Spinner, Karan M. Emerick, David A. Piccoli, Albert E. Chudley, Ian D. Krantz, Leena Ala‐Kokko, Stuart G. Baker, Michael P. Blair and James Hyland. Their work appears in journals such as Circulation, The Journal of Pediatrics, Prenatal Diagnosis, Biochemistry and American Journal of Medical Genetics.

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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