T. Webb

3.3k citations

65 papers · 2.7k · h-index 25

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Developmental Neuroscience top 10%

Papers in

Genetics 57
- Genetics and Neurodevelopmental Disorders 34
- Genetic Syndromes and Imprinting 16
- Genomic variations and chromosomal abnormalities 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
Pediatrics, Perinatology and Child Health 7
- Prenatal Screening and Diagnostics 7

Co-authors: Hazel M. Robinson (1 shared paper)GILLIAN M. TURNER (1 shared paper)Harm Boer (8 shared papers)J. E. Whittington (7 shared papers)Anthony John Holland (7 shared papers)Sarah Bundey (13 shared papers)Jill Butler (4 shared papers)A Thake (9 shared papers)
Journals: Journal of Medical Genetics (16 papers)Clinical Genetics (9 papers)Journal of Intellectual Disability Research (9 papers)The Lancet (3 papers)British Journal of Cancer (3 papers)
Partner nations: United Kingdom United States Australia

In The Last Decade

T. Webb

63 papers receiving 2.4k 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 65 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 M. TURNER, T. Webb, Hazel M. Robinson +1 other	1996	586
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. E. Whittington, Anthony John Holland, Harm Boer, T. Webb +1 other	2002	277
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. E. Whittington, Anthony John Holland, T. Webb, Esther N. Maina, Harm Boer +1 other	2006	138
4	Cognitive abilities and genotype in a population‐based sample of people with Prader–Willi syndrome Journal of Intellectual Disability Research ·J. E. Whittington, Anthony John Holland, T. Webb, Jill Butler, Harm Boer +1 other	2004	132
5	The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome Psychological Medicine ·Sarita Soni, J. E. Whittington, Anthony John Holland, T. Webb, Esther N. Maina, Harm Boer +1 other	2008	124
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	120
7	Prevalence of the Fragile X Anomaly amongst Autistic Twins and Singletons Journal of Child Psychology and Psychiatry ·Anthony J. Bailey, Patrick Bolton, Les Butler, Ann Le Couteur, Michael P. Murphy, Stephen Scott, T. Webb, Michael L. Rutter	1993	98
8	Maladaptive behaviour in Prader-Willi syndrome in adult life Journal of Intellectual Disability Research ·Harm Boer, Man Cheung Chung, T. Webb +2 others	1996	92
9	Inv dup(15) supernumerary marker chromosomes. Journal of Medical Genetics ·T. Webb	1994	88
10	Fragile X syndrome is less common than previously estimated. Journal of Medical Genetics ·Jenny E.V. Morton, Sarah Bundey, T. Webb, Fiona MacDonald, P. M. Rindl, Sarah L. Bullock	1997	76
11	A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes Clinical Genetics ·T. Webb, C Hardy, Marissa D. King, E Watkiss, Caroline Mitchell, Tim James Cole	1998	58
12	Cytogenetically marked clones in human fibroblasts cultured from normal subjects Somatic Cell and Molecular Genetics ·David G. Harnden, PETER A. BENN, J. M. Oxford, Alexander Malcolm R. Taylor, T. Webb	1976	55
13	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	53
14	Academic underachievement by people with Prader–Willi syndrome Journal of Intellectual Disability Research ·J. E. Whittington, Anthony John Holland, T. Webb, Jill Butler, Harm Boer +1 other	2004	50
15	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 ·Elizabeth M. Tuckerman, T. Webb, Sarah Bundey	1985	48
16	The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation. Journal of Medical Genetics ·Rosalyn Proops, T. Webb	1981	43
17	PRENATAL DIAGNOSIS OF MARTIN-BELL SYNDROME ASSOCIATED WITH FRAGILE SITE AT Xq27-28 The Lancet ·T. Webb, J Insley, Judith B. Weaver, S. Green, Charles H. Rodeck +1 other	1981	41
18	Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13. Journal of Medical Genetics ·T. Webb, Jill Clayton‐Smith, Xingbo Cheng, Joan H.M. Knoll, Marc Lalande, Marcus E Pembrey, Sue Malcolm	1992	41
19	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. E. Whittington, Harm Boer, Jill Butler, Anthony John Holland +1 other	2002	40
20	Prader–Willi syndrome and psychotic symptoms: I. Case descriptions and genetic studies* Journal of Intellectual Disability Research ·Nick Bouras, Harm Boer, T. Webb, S. Frazer, Annick Vogels, Martine Borghgraef, Leopold Curfs +2 others	1998	37

About T. Webb

T. Webb is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Oncology, Physiology and Cell Biology, having authored 65 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (34 papers), Genetic Syndromes and Imprinting (16 papers), Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Proteoglycans and glycosaminoglycans research (2 papers), Lysosomal Storage Disorders Research (2 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Genetics (2k citations), Developmental Neuroscience (37 citations), Pediatrics, Perinatology and Child Health (150 citations), Cognitive Neuroscience (201 citations) and Developmental Biology (14 citations). T. Webb has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Hazel M. Robinson, GILLIAN M. TURNER, Harm Boer, J. E. Whittington, Anthony John Holland, Sarah Bundey, Jill Butler, A Thake, J Todd and Sarita Soni. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Journal of Intellectual Disability Research, The Lancet 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.

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T. Webb

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T. Webb

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