Thaddeus E. Kelly
- Immunology top 1%
- Genetics top 1%
- Genomic variations and chromosomal abnormalities 13
- Connective tissue disorders research 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
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- Prenatal Screening and Diagnostics 13
- Developmental Biology top 5%
- Congenital limb and hand anomalies 8
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 13
- Connective tissue disorders research 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
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- Lysosomal Storage Disorders Research 9
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- RNA regulation and disease 5
- Sexual Differentiation and Disorders 4
- Co-authors
- Frank T. SaulsburyPolly J. FergusonMary E. BrunkowCraig L. BennettPhillip F. ChanceFred RamsdellHans D. OchsLuke Whitesell
- Journals
- Clinical Genetics (7 papers)Journal of Medical Genetics (6 papers)American Journal of Medical Genetics (30 papers)
- Partner nations
- United StatesSpainPortugal
In The Last Decade
Thaddeus E. Kelly
88 papers receiving 4.5k citations
Hit Papers
Peers
Comparison fields: 5 of 116
- Immunology 2.3k
- Genetics 1.3k
- Pediatrics, Perinatology and Child Health 482
- Developmental Biology 44
- Genetics 194
Countries citing papers authored by Thaddeus E. Kelly
This map shows the geographic impact of Thaddeus E. Kelly'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 Thaddeus E. Kelly with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thaddeus E. Kelly more than expected).
Fields of papers citing papers by Thaddeus E. Kelly
This network shows the impact of papers produced by Thaddeus E. Kelly. 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 Thaddeus E. Kelly. The network helps show where Thaddeus E. Kelly may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Thaddeus E. Kelly, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 1 | |
| 2 | 2008 | 0 | |
| 3 | 2006 | 48 | |
| 4 | The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3breakdown → | 2001 | 2547 |
| 5 | 2000 | 12 | |
| 6 | 1999 | 19 | |
| 7 | 1998 | 9 | |
| 8 | 1996 | 6 | |
| 9 | 1996 | 7 | |
| 10 | 1995 | 61 | |
| 11 | 1993 | 20 | |
| 12 | 1993 | 6 | |
| 13 | 1993 | 31 | |
| 14 | 1992 | 20 | |
| 15 | 1992 | 6 | |
| 16 | 1991 | 43 | |
| 17 | 1989 | 5 | |
| 18 | 1985 | 23 | |
| 19 | 1984 | 18 | |
| 20 | 1977 | 8 |
About Thaddeus E. Kelly
Thaddeus E. Kelly is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 90 papers that have together received 4.7k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (13 papers), Lysosomal Storage Disorders Research (9 papers), Congenital limb and hand anomalies (8 papers), Connective tissue disorders research (6 papers), RNA regulation and disease (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Sexual Differentiation and Disorders (4 papers). The work is most often cited by research in Immunology (2.3k citations), Genetics (1.3k citations) and Pediatrics, Perinatology and Child Health (482 citations). Thaddeus E. Kelly has collaborated with scholars based in United States, Spain and Portugal. Frequent co-authors include Frank T. Saulsbury, Polly J. Ferguson, Mary E. Brunkow, Craig L. Bennett, Phillip F. Chance, Fred Ramsdell, Hans D. Ochs, Luke Whitesell, John M. Opitz and J.M. Rary. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, American Journal of Medical Genetics, Neurology 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.