T. Webb

3.3k citations

60 papers · 2.4k indexed · 1 hit paper · h-index 24

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 32
- Genetic Syndromes and Imprinting 22
- Genomic variations and chromosomal abnormalities 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
Pediatrics, Perinatology and Child Health 11
- Prenatal Screening and Diagnostics 11

Co-authors: David Clarke (10 shared papers)Harm Boer (9 shared papers)Gillian Turner (1 shared paper)Shannon Wake (1 shared paper)Hazel M. Robinson (1 shared paper)Anthony Holland (7 shared papers)J. Whittington (7 shared papers)Sarah Bundey (11 shared papers)
Journals: Journal of Medical Genetics (15 papers)Journal of Intellectual Disability Research (10 papers)Clinical Genetics (10 papers)British Journal of Cancer (3 papers)Prenatal Diagnosis (3 papers)
Partner nations: United Kingdom Ireland Australia

In The Last Decade

T. Webb

60 papers receiving 2.3k citations

Hit Papers

align trajectories log scale

Prevalence of fragile X syndrome 1996 · 530 citations

Peers

Countries citing papers authored by T. Webb

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with T. Webb Line = papers co-authored together T. Webb links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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 American Journal of Medical Genetics ·Gillian Turner, T. Webb, Shannon Wake, Hazel M. Robinson Hit paper breakdown →	1996	530
2	Prevalence of, and risk factors for, physical ill‐health in people with Prader‐Willi syndrome: a population‐based study Developmental Medicine & Child Neurology ·Jill Butler, J. Whittington, Anthony Holland, Harm Boer, David Clarke, T. Webb	2002	209
3	The course and outcome of psychiatric illness in people with Prader–Willi syndrome: implications for management and treatment Journal of Intellectual Disability Research ·Sarita Soni, J. Whittington, Anthony Holland, T. Webb, Esther N. Maina, Harm Boer, David Clarke	2006	122
4	Cognitive abilities and genotype in a population‐based sample of people with Prader–Willi syndrome Journal of Intellectual Disability Research ·J. Whittington, Anthony Holland, T. Webb, Jill Butler, David Clarke, Harm Boer	2004	121
5	The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome Psychological Medicine ·Sarita Soni, J. Whittington, Anthony Holland, T. Webb, Esther N. Maina, Harm Boer, David Clarke	2008	115
6	The frequency of the fragile X chromosome among schoolchildren in Coventry. Journal of Medical Genetics ·T. Webb, Sarah Bundey, A Thake, J Todd	1986	105
7	Prevalence of the Fragile X Anomaly amongst Autistic Twins and Singletons Journal of Child Psychology and Psychiatry ·Anthony Bailey, Patrick Bolton, L. Butler, Ann Le Couteur, Michael P. Murphy, Stephen Scott, T. Webb, Michael Rutter	1993	91
8	Maladaptive behaviour in Prader‐Willi syndrome in adult life Journal of Intellectual Disability Research ·David Clarke, Harm Boer, Man Cheung Chung, Peter Sturmey, T. Webb	1996	80
9	Inv dup(15) supernumerary marker chromosomes. Journal of Medical Genetics ·T. Webb	1994	80
10	Fragile X syndrome is less common than previously estimated. Journal of Medical Genetics ·Jenny Morton, Sarah Bundey, T. Webb, Fiona MacDonald, P M Rindl, Sarah Bullock	1997	73
11	Maladaptive behaviour in Prader-Willi syndrome in adult life Journal of Intellectual Disability Research ·David Clarke, Harm Boer, Man Cheung Chung, Peter Sturmey, T. Webb	1996	58
12	A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology. Journal of Medical Genetics ·Sarah Bundey, T. Webb, A Thake, J Todd	1985	54
13	Cytogenetically marked clones in human fibroblasts cultured from normal subjects Somatic Cell and Molecular Genetics ·D.G. Harnden, Peter Benn, J. M. Oxford, A. Malcolm R. Taylor, T. Webb	1976	51
14	Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence. Journal of Medical Genetics ·E. Tuckerman, T. Webb, Sarah Bundey	1985	47
15	Academic underachievement by people with Prader–Willi syndrome Journal of Intellectual Disability Research ·J. Whittington, Anthony Holland, T. Webb, Jill Butler, David Clarke, Harm Boer	2004	46
16	A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes Clinical Genetics ·T. Webb, C Hardy, Marissa King, E Watkiss, Caroline Mitchell, Tim Cole	1998	40
17	A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS Clinical Genetics ·T. Webb, J. Whittington, David Clarke, Harm Boer, Jill Butler, Anthony Holland	2002	38
18	The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation. Journal of Medical Genetics ·R. Proops, T. Webb	1981	35
19	Prader–Willi syndrome and psychotic symptoms: I. Case descriptions and genetic studies* Journal of Intellectual Disability Research ·Nick Bouras, David Clarke, Harm Boer, T. Webb, Patrícia Scott, S. Frazer, Annick Vogels, Martine Borghgraef, Leopold Curfs	1998	31
20	Is it possible to make a clinical diagnosis of the fragile X syndrome in a boy? Archives of Disease in Childhood ·A Thake, J Todd, Sarah Bundey, T. Webb	1985	30

About T. Webb

T. Webb is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience, Speech and Hearing and Molecular Biology, having authored 60 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (32 papers), Genetic Syndromes and Imprinting (22 papers), Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (11 papers), Autism Spectrum Disorder Research (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), RNA modifications and cancer (4 papers) and Renal and related cancers (3 papers). The work is most often cited by research in Genetics (2.1k citations), Cognitive Neuroscience (940 citations), Pediatrics, Perinatology and Child Health (364 citations), Developmental Neuroscience (61 citations) and Molecular Biology (904 citations). T. Webb has collaborated with scholars based in United Kingdom, Ireland and Australia. Frequent co-authors include David Clarke, Harm Boer, Gillian Turner, Shannon Wake, Hazel M. Robinson, Anthony Holland, J. Whittington, Sarah Bundey, Jill Butler and A Thake. Their work appears in journals such as Journal of Medical Genetics, Journal of Intellectual Disability Research, Clinical Genetics, British Journal of Cancer 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.

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