Jack C. Tarleton
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 48
- Genetics and Neurodevelopmental Disorders 35
- Genomic variations and chromosomal abnormalities 18
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- Autism Spectrum Disorder Research 19
- Co-authors
- Robert A. Saul (2 shared papers)Mary C. Phelan (7 shared papers)Ponmani Goonewardena (2 shared papers)Ave M. Lachiewicz (4 shared papers)Michelle M. Macias (2 shared papers)Gurpur Shashidhar Pai (2 shared papers)Charles E. Schwartz (6 shared papers)Gail A. Spiridigliozzi (3 shared papers)
- Journals
- Journal of Molecular Diagnostics (4 papers)Journal of Medical Genetics (4 papers)Journal of Bacteriology (3 papers)Nature Genetics (2 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- United StatesCanadaIndia
In The Last Decade
Jack C. Tarleton
52 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 83
- Genetics 1.7k
- Cognitive Neuroscience 758
- Molecular Biology 1.1k
- Developmental Neuroscience 60
- Cellular and Molecular Neuroscience 200
Countries citing papers authored by Jack C. Tarleton
This map shows the geographic impact of Jack C. Tarleton'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 Jack C. Tarleton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jack C. Tarleton more than expected).
Fields of papers citing papers by Jack C. Tarleton
This network shows the impact of papers produced by Jack C. Tarleton. 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 Jack C. Tarleton. The network helps show where Jack C. Tarleton may publish in the future.
Co-authors
The 25 scholars most cited alongside Jack C. Tarleton, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 312 | |
| 2 | A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases. | 1994 | 263 |
| 3 | 1992 | 169 | |
| 4 | 1997 | 164 | |
| 5 | Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. | 1993 | 148 |
| 6 | 1997 | 110 | |
| 7 | 1991 | 96 | |
| 8 | 1996 | 81 | |
| 9 | 1993 | 59 | |
| 10 | 1998 | 54 | |
| 11 | 1997 | 51 | |
| 12 | Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy. | 1992 | 51 |
| 13 | 1993 | 43 | |
| 14 | Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B. | 1998 | 41 |
| 15 | 2007 | 39 | |
| 16 | FMR1-Related Disorders | 2012 | 36 |
| 17 | 2000 | 36 | |
| 18 | 2009 | 30 | |
| 19 | 2010 | 27 | |
| 20 | 2011 | 21 |
About Jack C. Tarleton
Jack C. Tarleton is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Cellular and Molecular Neuroscience and Developmental Neuroscience, having authored 53 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (35 papers), Autism Spectrum Disorder Research (19 papers), Genomic variations and chromosomal abnormalities (18 papers), Congenital heart defects research (8 papers), Genetic Neurodegenerative Diseases (7 papers), Prenatal Screening and Diagnostics (5 papers), Epigenetics and DNA Methylation (5 papers) and RNA modifications and cancer (5 papers). The work is most often cited by research in Genetics (1.7k citations), Cognitive Neuroscience (758 citations), Molecular Biology (1.1k citations), Developmental Neuroscience (60 citations) and Cellular and Molecular Neuroscience (200 citations). Jack C. Tarleton has collaborated with scholars based in United States, Canada and India. Frequent co-authors include Robert A. Saul, Mary C. Phelan, Ponmani Goonewardena, Ave M. Lachiewicz, Michelle M. Macias, Gurpur Shashidhar Pai, Charles E. Schwartz, Gail A. Spiridigliozzi, Allyn McConkie‐Rosell and Gene S. Fisch. Their work appears in journals such as Journal of Molecular Diagnostics, Journal of Medical Genetics, Journal of Bacteriology, Nature Genetics and Prenatal Diagnosis.
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.