T. Webb

3.3k total citations · 1 hit paper
60 papers, 2.4k citations indexed

About

T. Webb is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, T. Webb has authored 60 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 19 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in T. Webb's work include Genetics and Neurodevelopmental Disorders (32 papers), Genetic Syndromes and Imprinting (22 papers) and Genomic variations and chromosomal abnormalities (20 papers). T. Webb is often cited by papers focused on Genetics and Neurodevelopmental Disorders (32 papers), Genetic Syndromes and Imprinting (22 papers) and Genomic variations and chromosomal abnormalities (20 papers). T. Webb collaborates with scholars based in United Kingdom, Ireland and Australia. T. Webb's 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 and has published in prestigious journals such as British Journal of Cancer, Journal of Child Psychology and Psychiatry and Psychological Medicine.

In The Last Decade

T. Webb

60 papers receiving 2.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Prevalence of fragile X syndrome

1996 530 citations Gillian Turner, T. Webb et al. American Journal of Medical Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
T. Webb United Kingdom	24	2.1k	940	904	364	152	60	2.4k
Edmund C. Jenkins United States	31	1.7k 0.8×	822 0.9×	1.1k 1.3×	334 0.9×	81 0.5×	123	2.9k
W. Ted Brown United States	31	2.5k 1.2×	1.6k 1.7×	1.5k 1.7×	193 0.5×	130 0.9×	97	3.4k
Jeannie Visootsak United States	26	2.0k 0.9×	1.1k 1.2×	1.2k 1.4×	298 0.8×	212 1.4×	54	2.7k
M. W. Partington Canada	33	2.0k 0.9×	506 0.5×	1.8k 2.0×	314 0.9×	74 0.5×	110	3.5k
Sarika U. Peters United States	29	2.1k 1.0×	915 1.0×	1.3k 1.4×	374 1.0×	208 1.4×	63	2.7k
Richard J. Simensen United States	21	1.2k 0.6×	638 0.7×	912 1.0×	137 0.4×	103 0.7×	50	1.9k
Brenda Finucane United States	26	1.8k 0.9×	921 1.0×	1.2k 1.3×	163 0.4×	225 1.5×	65	2.6k
Ragnheiður Fossdal Iceland	15	1.5k 0.7×	580 0.6×	987 1.1×	211 0.6×	57 0.4×	21	2.2k
Nancy J. Carpenter United States	24	1.2k 0.6×	325 0.3×	1.0k 1.1×	292 0.8×	60 0.4×	72	2.2k
Jack Tarleton United States	19	1.5k 0.7×	749 0.8×	1.0k 1.1×	162 0.4×	115 0.8×	50	1.9k

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-authorship network of co-authors of T. Webb

This figure shows the co-authorship network connecting the top 25 collaborators of T. Webb. A scholar is included among the top collaborators of T. Webb based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with T. Webb. T. Webb is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Soni, Sarita, J. Whittington, Anthony Holland, et al.. (2008). The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome. Psychological Medicine. 38(10). 1505–1514. 115 indexed citations

Whittington, J., Anthony Holland, T. Webb, et al.. (2004). Cognitive abilities and genotype in a population‐based sample of people with Prader–Willi syndrome. Journal of Intellectual Disability Research. 48(2). 172–187. 121 indexed citations

Webb, T., J. Whittington, David Clarke, et al.. (2002). 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. 62(4). 273–281. 38 indexed citations

Webb, T., et al.. (2000). Familial Prader‐Willi syndrome: case report and a literature review. Clinical Genetics. 58(3). 216–223. 12 indexed citations

Bouras, Nick, David Clarke, Harm Boer, et al.. (1998). Prader–Willi syndrome and psychotic symptoms: I. Case descriptions and genetic studies*. Journal of Intellectual Disability Research. 42(6). 440–450. 31 indexed citations

Webb, T., et al.. (1998). A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes. Clinical Genetics. 53(1). 34–43. 40 indexed citations

Turner, Gillian, T. Webb, Shannon Wake, & Hazel M. Robinson. (1996). Prevalence of fragile X syndrome. American Journal of Medical Genetics. 64(1). 196–197. 530 indexed citations breakdown →

Webb, T., et al.. (1995). Alterations in replication timing of X‐chromosome bands in Rett syndrome. Journal of Intellectual Disability Research. 39(2). 91–96. 5 indexed citations

Webb, T., et al.. (1994). Family studies in Prader-Willi syndrome.. PubMed. 5(4). 329–36. 5 indexed citations

10.

Webb, T., et al.. (1993). Neither uniparental disomy nor skewed X‐inactivation explains Rett syndrome. Clinical Genetics. 44(5). 236–240. 20 indexed citations

11.

Clayton‐Smith, Jill, T. Webb, S. Robb, et al.. (1992). Further evidence for dominant inheritance at the chromosome 15q11‐13 locus in familial angelman syndrome. American Journal of Medical Genetics. 44(2). 256–260. 29 indexed citations

12.

Woods, C. Geoffrey, et al.. (1992). X‐inactivation in girls with Rett syndrome. Clinical Genetics. 42(6). 296–301. 11 indexed citations

13.

Webb, T.. (1991). Fragile Xq27 in somatic cells derived from different tissues. American Journal of Medical Genetics. 38(2-3). 425–428. 3 indexed citations

14.

Webb, T.. (1991). Molecular genetics of fragile X: a cytogenetics viewpoint. Report of the Fifth International Symposium on X Linked Mental Retardation, Strasbourg, France, 12 to 16 August 1991 (organiser Dr J-L Mandel).. Journal of Medical Genetics. 28(12). 814–817. 4 indexed citations

15.

Webb, T. & Karen E. Heath. (1991). Fragile 3p14 in patients with von Hippel-Lindau syndrome compared to controls. Cancer Genetics and Cytogenetics. 56(2). 157–162. 13 indexed citations

16.

Tuckerman, E. & T. Webb. (1989). The inactivation of the fragile X chromosome in female carriers of the Martin Bell syndrome as studied by two different methods. Clinical Genetics. 36(1). 25–30. 9 indexed citations

17.

Webb, T., et al.. (1989). Missed prenatal diagnosis of fragile‐X syndrome. Prenatal Diagnosis. 9(11). 777–781. 7 indexed citations

18.

Thake, A, J Todd, T. Webb, & Sarah Bundey. (1987). Children With The Fragile X Chromosome At Schools For The Mildly Mentally Retarded. Developmental Medicine & Child Neurology. 29(6). 711–719. 9 indexed citations

19.

Jones, Miren I, S.P. Spragg, & T. Webb. (1981). Detection of Proteins in Human Amniotic Fluid Using Two-Dimensional Gel Electrophoresis. Neonatology. 39(3-4). 171–177. 8 indexed citations

20.

Webb, T., et al.. (1981). The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.. Journal of Medical Genetics. 18(5). 366–373. 35 indexed citations

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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