T. Webb
Impact in
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 52
- Genetics and Neurodevelopmental Disorders 30
- Genetic Syndromes and Imprinting 22
- Genomic variations and chromosomal abnormalities 16
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
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- RNA modifications and cancer 4
- Co-authors
- David Clarke (10 shared papers)Harm Boer (9 shared papers)Shannon Wake (1 shared paper)Gillian Turner (1 shared paper)Hazel M. Robinson (1 shared paper)J. Whittington (7 shared papers)Anthony Holland (7 shared papers)Sarah Bundey (11 shared papers)
- Journals
- Journal of Medical Genetics (15 papers)Clinical Genetics (10 papers)Journal of Intellectual Disability Research (10 papers)Prenatal Diagnosis (3 papers)British Journal of Cancer (3 papers)
- Partner nations
- United KingdomUnited StatesIreland
In The Last Decade
T. Webb
58 papers receiving 2.3k citations
T. Webb's Hit Papers
Peers
Comparison fields: 5 of 80
- Genetics 2.1k
- Cognitive Neuroscience 795
- Pediatrics, Perinatology and Child Health 301
- Developmental Neuroscience 59
- Molecular Biology 790
Countries citing papers authored by T. Webb
This map shows the geographic impact of T. Webb'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 T. Webb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Webb more than expected).
Fields of papers citing papers by T. Webb
This network shows the impact of papers produced by T. Webb. 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 T. Webb. The network helps show where T. Webb may publish in the future.
Co-authors
The 25 scholars most cited alongside T. Webb, 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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Prevalence of fragile X syndrome Hit paper breakdown → | 1996 | 530 |
| 2 | 2002 | 210 | |
| 3 | 2006 | 121 | |
| 4 | 2004 | 121 | |
| 5 | 2008 | 115 | |
| 6 | 1986 | 105 | |
| 7 | 1993 | 91 | |
| 8 | 1996 | 80 | |
| 9 | 1994 | 79 | |
| 10 | 1997 | 73 | |
| 11 | 1996 | 58 | |
| 12 | 1985 | 54 | |
| 13 | 1976 | 51 | |
| 14 | 1985 | 47 | |
| 15 | 2004 | 46 | |
| 16 | 1998 | 40 | |
| 17 | 2002 | 38 | |
| 18 | 1981 | 35 | |
| 19 | 1998 | 31 | |
| 20 | 1985 | 30 |
About T. Webb
T. Webb is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Pediatrics, Perinatology and Child Health and Speech and Hearing, having authored 60 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (30 papers), Genetic Syndromes and Imprinting (22 papers), Genomic variations and chromosomal abnormalities (16 papers), Autism Spectrum Disorder Research (10 papers), Prenatal Screening and Diagnostics (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), RNA modifications and cancer (4 papers) and Adolescent and Pediatric Healthcare (3 papers). The work is most often cited by research in Genetics (2.1k citations), Cognitive Neuroscience (795 citations), Pediatrics, Perinatology and Child Health (301 citations), Developmental Neuroscience (59 citations) and Molecular Biology (790 citations). T. Webb has collaborated with scholars based in United Kingdom, United States and Ireland. Frequent co-authors include David Clarke, Harm Boer, Shannon Wake, Gillian Turner, Hazel M. Robinson, J. Whittington, Anthony Holland, Sarah Bundey, Jill Butler and A Thake. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Journal of Intellectual Disability Research, Prenatal Diagnosis and British Journal of Cancer.
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.