Tessa Webb

946 total citations
19 papers, 403 citations indexed

About

Tessa Webb is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Tessa Webb has authored 19 papers receiving a total of 403 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in Tessa Webb's work include Genetics and Neurodevelopmental Disorders (10 papers), Genetic Syndromes and Imprinting (6 papers) and Prenatal Screening and Diagnostics (6 papers). Tessa Webb is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Genetic Syndromes and Imprinting (6 papers) and Prenatal Screening and Diagnostics (6 papers). Tessa Webb collaborates with scholars based in United Kingdom, Nigeria and Switzerland. Tessa Webb's co-authors include James F. Reynolds, J Todd, A Thake, Sarah Bundey, John M. Opitz, C. N. D. Cruickshank, S. A. Barker, David Clarke, Harm Boer and Esther N. Maina and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Experimental Cell Research and Cancer Letters.

In The Last Decade

Tessa Webb

19 papers receiving 386 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tessa Webb United Kingdom 12 304 186 143 62 28 19 403
Shashidhar Pai United States 8 237 0.8× 278 1.5× 61 0.4× 49 0.8× 25 0.9× 13 391
Wout H. Deelen Netherlands 11 256 0.8× 232 1.2× 87 0.6× 69 1.1× 15 0.5× 16 413
G. Glóver Spain 12 364 1.2× 257 1.4× 126 0.9× 86 1.4× 17 0.6× 26 484
Michael S. Krawczun United States 11 299 1.0× 193 1.0× 148 1.0× 34 0.5× 5 0.2× 28 372
W. Ted Brown United States 9 244 0.8× 202 1.1× 129 0.9× 18 0.3× 17 0.6× 11 326
Ellen Taub Israel 8 263 0.9× 207 1.1× 121 0.8× 88 1.4× 19 0.7× 12 446
Louise Christie Australia 10 294 1.0× 197 1.1× 68 0.5× 73 1.2× 30 1.1× 14 409
Babett Heye Germany 7 206 0.7× 147 0.8× 48 0.3× 21 0.3× 17 0.6× 7 365
P Ostertag Germany 3 292 1.0× 142 0.8× 45 0.3× 49 0.8× 16 0.6× 4 396
Marja‐Leena Väisänen Finland 8 336 1.1× 200 1.1× 203 1.4× 26 0.4× 13 0.5× 11 447

Countries citing papers authored by Tessa Webb

Since Specialization
Citations

This map shows the geographic impact of Tessa 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 Tessa Webb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tessa Webb more than expected).

Fields of papers citing papers by Tessa Webb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tessa 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 Tessa Webb. The network helps show where Tessa Webb may publish in the future.

Co-authorship network of co-authors of Tessa Webb

This figure shows the co-authorship network connecting the top 25 collaborators of Tessa Webb. A scholar is included among the top collaborators of Tessa 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 Tessa Webb. Tessa Webb is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Webb, Tessa, Esther N. Maina, Sarita Soni, et al.. (2008). In search of the psychosis gene in people with Prader‐Willi syndrome. American Journal of Medical Genetics Part A. 146A(7). 843–853. 24 indexed citations
2.
Maina, Esther N., Tessa Webb, Sarita Soni, et al.. (2007). Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter. Journal of Human Genetics. 52(4). 297–307. 15 indexed citations
3.
Clarke, David, Harm Boer, & Tessa Webb. (1995). GENETIC AND BEHAVIOURAL ASPECTS OF PRADER‐WILLI SYNDROME: A REVIEW WITH A TRANSLATION OF THE ORIGINAL PAPER. 8(1). 38–53. 12 indexed citations
4.
Clarke, David J., et al.. (1995). Prader-Willi syndrome and psychotic symptoms: report of a further case. Irish Journal of Psychological Medicine. 12(1). 27–29. 11 indexed citations
5.
Webb, Tessa. (1994). Sister chromatid exchange in families with Angelman or Prader‐Willi syndrome. Clinical Genetics. 46(2). 181–186. 1 indexed citations
6.
Clayton‐Smith, Jill, Daniel J. Driscoll, Michael F. Waters, et al.. (1993). Difference in methylation patterns within the D15S9 region of chromosome 15qll–13 in first cousins with Angelman syndrome and Prader–Willi syndrome. American Journal of Medical Genetics. 47(5). 683–686. 27 indexed citations
7.
Webb, Tessa. (1992). Delayed replication of Xq27 in individuals with the fragile X syndrome. American Journal of Medical Genetics. 43(6). 1057–1062. 28 indexed citations
8.
Macpherson, James, John F. Harvey, Tessa Webb, et al.. (1992). A reinvestigation of thirty three fragile(X) families using probe StB12.3. American Journal of Medical Genetics. 43(5). 905–912. 15 indexed citations
9.
Webb, Tessa. (1991). Expression of fragile‐x in a female fetus diagnosed after chorionic villus sampling. Prenatal Diagnosis. 11(5). 333–338. 2 indexed citations
10.
11.
Nicolaides, K. H., et al.. (1988). Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture. American Journal of Medical Genetics. 30(1-2). 355–368. 14 indexed citations
12.
Webb, Tessa, Sarah Bundey, A Thake, et al.. (1986). Population incidence and segregation ratios in the Martin‐Bell syndrome. American Journal of Medical Genetics. 23(1-2). 573–580. 157 indexed citations
13.
Jacobs, Patricia A., Stephanie L. Sherman, Gillian Turner, et al.. (1986). The fragile(X) syndrome: The mutation problem. American Journal of Medical Genetics. 23(1-2). 611–617. 18 indexed citations
14.
Webb, Tessa, et al.. (1986). A randomized study of three cannulas for transcervical chorionic villus sampling. American Journal of Obstetrics and Gynecology. 154(1). 34–39. 9 indexed citations
15.
Bird, G. W. G., et al.. (1982). ANOTHER EXAMPLE OF HAEMOPOIETIC (TWIN) CHIMAERISM IN A SUBJECT UNAWARE OF BEING A TWIN. International Journal of Immunogenetics. 9(5). 317–322. 8 indexed citations
16.
17.
Barker, S. A., C. N. D. Cruickshank, & Tessa Webb. (1965). Mucopolysaccharides in rat skin. Carbohydrate Research. 1(1). 62–70. 7 indexed citations
18.
Barker, S. A., C. N. D. Cruickshank, & Tessa Webb. (1965). Mucopolysaccharides in rat skin. Carbohydrate Research. 1(1). 52–61. 22 indexed citations
19.
Barker, S. A., C. N. D. Cruickshank, & Tessa Webb. (1964). The effect of vitamin A, hydrocortisone and citral upon sulphate metabolism in skin. Experimental Cell Research. 35(2). 255–261. 30 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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