Donald Basel

3.3k citations
69 papers · 1.3k · h-index 17

Impact in

    • Congenital limb and hand anomalies
  • Genetics top 2%
    • Connective tissue disorders research
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genomics and Rare Diseases 12
    • Connective tissue disorders research 11
    • Genomic variations and chromosomal abnormalities 9
    • Congenital heart defects research 3

Donald Basel

62 papers receiving 1.3k citations

Peers

Donald Basel
Comparison fields: 5 of 91
  • Developmental Biology 110
  • Genetics 669
  • Rheumatology 156
  • Oncology 243
  • Orthopedics and Sports Medicine 72
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Citations per field
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Citations per year

Countries citing papers authored by Donald Basel

Since Specialization
Citations

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

Fields of papers citing papers by Donald Basel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 69 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2016259
2 2000227
3 2014111
4 200998
5 201480
6 201568
7 201334
8 201731
9 201629
10 202329
11 200423
12 200123
13 200622
14 201919
15 201218
16 200316
17 201316
18 202016
19 201615
20 201614

About Donald Basel

Donald Basel is a scholar working on Genetics, Molecular Biology, Surgery, Pulmonary and Respiratory Medicine and Neurology, having authored 69 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Connective tissue disorders research (11 papers), Genomic variations and chromosomal abnormalities (9 papers), Neurofibromatosis and Schwannoma Cases (5 papers), Congenital limb and hand anomalies (4 papers), Congenital heart defects research (3 papers), Bone health and treatments (3 papers) and Tracheal and airway disorders (3 papers). The work is most often cited by research in Developmental Biology (110 citations), Genetics (669 citations), Rheumatology (156 citations), Oncology (243 citations) and Orthopedics and Sports Medicine (72 citations). Donald Basel has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Robert D. Steiner, Carrie A. Phillipi, Kerry Dwan, Petros Tsipouras, Peter Beighton, Michael W. Kilpatrick, Iva Toudjarska, Julie McCarrier, Dawn H. Siegel and M W Kilpatrick. Their work appears in journals such as Clinical Genetics, The American Journal of Human Genetics, Clinics in Perinatology, Genes and Journal of Pediatric 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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