Donald Basel

3.4k citations
98 papers · 2.2k · h-index 24

Impact in

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

Papers in

    • Connective tissue disorders research 21
    • Genomics and Rare Diseases 18
    • Genomic variations and chromosomal abnormalities 11
    • Genetics and Neurodevelopmental Disorders 7
    • Genetic factors in colorectal cancer 9

Donald Basel

95 papers receiving 2.1k citations

Peers

Donald Basel
Comparison fields: 5 of 107
  • Developmental Biology 127
  • Genetics 1.0k
  • Neurology 239
  • Rheumatology 209
  • Pediatrics, Perinatology and Child Health 222
Replace Julie C. Sapp with:
Julie C. Sapp United States
Ishwar C. Verma India
Giedré Grigelioniené Sweden
H. ‐R. Wiedemann Germany
Eva Sujansky United States
David Otto Walterhouse United States
R. Neil Schimke United States
Mahin Golabi United States
Piranit Nik Kantaputra Thailand
Ralph Lachman United States
Donald Basel relative to Julie C. Sapp United States Julie C. Sapp's profile →
Citations per field
00.5×2×2.6×
Julie C. Sapp · 1×
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 98 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2016278
2 2000249
3 2020140
4 2009119
5 2019100
6 201493
7 201581
8 201874
9 202173
10 201870
11 202165
12 201753
13 200642
14 202342
15
COL1A1/2-Related Osteogenesis Imperfecta
201336
16 202436
17 202336
18 201734
19 201634
20 202027

About Donald Basel

Donald Basel is a scholar working on Genetics, Pathology and Forensic Medicine, Neurology, Genetics and Molecular Biology, having authored 98 papers that have together received 2.2k indexed citations. Recurring topics across this work include Connective tissue disorders research (21 papers), Genomics and Rare Diseases (18 papers), Genomic variations and chromosomal abnormalities (11 papers), Genetic factors in colorectal cancer (9 papers), Neurofibromatosis and Schwannoma Cases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (6 papers) and Congenital limb and hand anomalies (4 papers). The work is most often cited by research in Developmental Biology (127 citations), Genetics (1.0k citations), Neurology (239 citations), Rheumatology (209 citations) and Pediatrics, Perinatology and Child Health (222 citations). Donald Basel has collaborated with scholars based in United States, Australia and Japan. Frequent co-authors include Robert D. Steiner, Kerry M. Dwan, Carrie Anne Phillipi, Petros Tsipouras, Michael W. Kilpatrick, Peter Beighton, Peter Ianakiev, Iva Toudjarska, Julie McCarrier and Dawn H. Siegel. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Clinical Genetics, Clinics in Perinatology and The Journal of Pediatrics.

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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