Jack 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 46
- Genetics and Neurodevelopmental Disorders 34
- Genomic variations and chromosomal abnormalities 16
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- Autism Spectrum Disorder Research 18
- Co-authors
- Robert A. Saul (2 shared papers)Charles E. Schwartz (6 shared papers)Ave M. Lachiewicz (4 shared papers)P. Goonewardena (2 shared papers)Gail A. Spiridigliozzi (3 shared papers)Allyn McConkie‐Rosell (3 shared papers)Mary C. Phelan (7 shared papers)Dominique Heitz (2 shared papers)
- Journals
- Journal of Molecular Diagnostics (4 papers)Journal of Bacteriology (3 papers)Journal of Medical Genetics (3 papers)Nature Genetics (2 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- United StatesCanadaIndia
In The Last Decade
Jack Tarleton
49 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 85
- Genetics 1.5k
- Cognitive Neuroscience 749
- Molecular Biology 1.0k
- Developmental Neuroscience 50
- Cellular and Molecular Neuroscience 188
Countries citing papers authored by Jack Tarleton
This map shows the geographic impact of Jack 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 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 Tarleton more than expected).
Fields of papers citing papers by Jack Tarleton
This network shows the impact of papers produced by Jack 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 Tarleton. The network helps show where Jack Tarleton may publish in the future.
Co-authors
The 25 scholars most cited alongside Jack 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 266 | |
| 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 | 238 |
| 3 | 1997 | 154 | |
| 4 | 1992 | 152 | |
| 5 | Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. | 1993 | 138 |
| 6 | 1991 | 93 | |
| 7 | 1997 | 72 | |
| 8 | 1996 | 67 | |
| 9 | 1993 | 58 | |
| 10 | Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy. | 1992 | 53 |
| 11 | 1997 | 48 | |
| 12 | 2007 | 39 | |
| 13 | 1993 | 38 | |
| 14 | Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B. | 1998 | 37 |
| 15 | 1998 | 34 | |
| 16 | FMR1-Related Disorders | 2012 | 31 |
| 17 | 2009 | 27 | |
| 18 | 2010 | 24 | |
| 19 | 2012 | 20 | |
| 20 | 2011 | 18 |
About Jack Tarleton
Jack Tarleton is a scholar working on Genetics, Cognitive Neuroscience, Developmental Neuroscience, Molecular Biology and Cellular and Molecular Neuroscience, having authored 50 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (34 papers), Autism Spectrum Disorder Research (18 papers), Genomic variations and chromosomal abnormalities (16 papers), Congenital heart defects research (8 papers), Genetic Neurodegenerative Diseases (6 papers), Epigenetics and DNA Methylation (5 papers), RNA modifications and cancer (5 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (1.5k citations), Cognitive Neuroscience (749 citations), Molecular Biology (1.0k citations), Developmental Neuroscience (50 citations) and Cellular and Molecular Neuroscience (188 citations). Jack Tarleton has collaborated with scholars based in United States, Canada and India. Frequent co-authors include Robert A. Saul, Charles E. Schwartz, Ave M. Lachiewicz, P. Goonewardena, Gail A. Spiridigliozzi, Allyn McConkie‐Rosell, Mary C. Phelan, Dominique Heitz, Christopher G. Mathew and Angela Barnicoat. Their work appears in journals such as Journal of Molecular Diagnostics, Journal of Bacteriology, Journal of Medical Genetics, 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.