A. David B. Webster

2.4k total citations
20 papers, 1.0k citations indexed

About

A. David B. Webster is a scholar working on Immunology, Genetics and Epidemiology. According to data from OpenAlex, A. David B. Webster has authored 20 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Immunology, 6 papers in Genetics and 6 papers in Epidemiology. Recurrent topics in A. David B. Webster's work include Immunodeficiency and Autoimmune Disorders (16 papers), Immune Cell Function and Interaction (7 papers) and Chronic Lymphocytic Leukemia Research (5 papers). A. David B. Webster is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (16 papers), Immune Cell Function and Interaction (7 papers) and Chronic Lymphocytic Leukemia Research (5 papers). A. David B. Webster collaborates with scholars based in United Kingdom, Sweden and Italy. A. David B. Webster's co-authors include Lennart Hammarström, Igor Vořechovský, Alessandro Plebani, J. Farrant, Margaret North, Liping Luo, P L Amlot, Martin J.S. Dyer, Daniel Catovsky and Martin Yuille and has published in prestigious journals such as Nature Genetics, The Journal of Immunology and Journal of Allergy and Clinical Immunology.

In The Last Decade

A. David B. Webster

20 papers receiving 1.0k citations

Peers

A. David B. Webster

IMMUN

GENET

PRM

Pauline A. van Schouwenburg Netherlands

Kerry Dobbs United States

JM Crawford United States

Baerbel Keller Germany

Marie‐Claude Stolzenberg France

HE Heslop United States

Patricia Lugar United States

Catharina Schuetz Germany

Cathy Quilici Australia

Barbara H. Barendregt Netherlands

Pauline A. van Schouwenburg Netherlands

A. David B. Webster

990 ×1.4

IMMUN

246 ×0.8

GENET

248 ×1.0

247 ×1.2

GENET

82 ×0.5

PRM

Citations per year, relative to A. David B. Webster A. David B. Webster (= 1×) peers Pauline A. van Schouwenburg

Countries citing papers authored by A. David B. Webster

Since Specialization

Citations

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

Fields of papers citing papers by A. David B. Webster

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. David B. Webster. 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 A. David B. Webster. The network helps show where A. David B. Webster may publish in the future.

Co-authorship network of co-authors of A. David B. Webster

This figure shows the co-authorship network connecting the top 25 collaborators of A. David B. Webster. A scholar is included among the top collaborators of A. David B. Webster 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 A. David B. Webster. A. David B. Webster 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

Marashi, Sayed Mahdi, Sarita Workman, Afsar Rahbar, et al.. (2011). Inflammation in common variable immunodeficiency is associated with a distinct CD8+ response to cytomegalovirus. Journal of Allergy and Clinical Immunology. 127(6). 1385–1393.e4. 29 indexed citations

Yong, Patrick, Sarita Workman, Faisal Wahid, et al.. (2008). Selective deficits in blood dendritic cell subsets in common variable immunodeficiency and X-linked agammaglobulinaemia but not specific polysaccharide antibody deficiency. Clinical Immunology. 127(1). 34–42. 26 indexed citations

Meer, J.W.M. van der, Alejandro A. Schäffer, Claire Fieschi, et al.. (2006). Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q. European Journal of Human Genetics. 14(7). 867–875. 33 indexed citations

Schäffer, Alejandro A., et al.. (2005). Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q. Human Genetics. 118(6). 725–729. 28 indexed citations

Lachmann, Helen J., et al.. (2005). Hypercalcemia in a Patient With Common Variable Immunodeficiency and Renal Granulomas. American Journal of Kidney Diseases. 45(5). e90–e93. 18 indexed citations

Webster, A. David B.. (2004). Clinical and Immunological Spectrum of Common Variable Immunodeficiency (CVID).. PubMed. 3(3). 103–13. 19 indexed citations

Královičová, Jana, Lennart Hammarström, Alessandro Plebani, A. David B. Webster, & Igor Vořechovský. (2003). Fine-Scale Mapping at IGAD1 and Genome-Wide Genetic Linkage Analysis Implicate HLA-DQ/DR as a Major Susceptibility Locus in Selective IgA Deficiency and Common Variable Immunodeficiency. The Journal of Immunology. 170(5). 2765–2775. 78 indexed citations

Tormey, Vincent, et al.. (2002). Effect of anti‐CD20 (rituximab) on resistant thrombocytopenia in autoimmune lymphoproliferative syndrome. British Journal of Haematology. 118(4). 1078–1081. 30 indexed citations

Webster, A. David B.. (2001). COMMON VARIABLE IMMUNODEFICIENCY. Immunology and Allergy Clinics of North America. 21(1). 1–22. 31 indexed citations

10.

Vořechovský, Igor, Michael Cullen, Mary Carrington, Lennart Hammarström, & A. David B. Webster. (2000). Fine Mapping of IGAD1 in IgA Deficiency and Common Variable Immunodeficiency: Identification and Characterization of Haplotypes Shared by Affected Members of 101 Multiple-Case Families. The Journal of Immunology. 164(8). 4408–4416. 90 indexed citations

11.

Sewell, William A., et al.. (2000). Up-Regulation of IL-12 in Monocytes: A Fundamental Defect in Common Variable Immunodeficiency. The Journal of Immunology. 164(1). 488–494. 69 indexed citations

12.

Vořechovský, Igor, A. David B. Webster, Alessandro Plebani, & Lennart Hammarström. (1999). Genetic Linkage of IgA Deficiency to the Major Histocompatibility Complex: Evidence for Allele Segregation Distortion, Parent-of-Origin Penetrance Differences, and the Role of Anti-IgA Antibodies in Disease Predisposition. The American Journal of Human Genetics. 64(4). 1096–1109. 93 indexed citations

13.

Vořechovský, Igor, Elisabeth Blennow, Magnus Nordenskjöld, A. David B. Webster, & Lennart Hammarström. (1999). A Putative Susceptibility Locus on Chromosome 18 Is Not a Major Contributor to Human Selective IgA Deficiency: Evidence from Meiotic Mapping of 83 Multiple-Case Families. The Journal of Immunology. 163(4). 2236–2242. 12 indexed citations

14.

Sewell, William A. & A. David B. Webster. (1998). Infection in patients with congenital immune deficiencies. Current Opinion in Infectious Diseases. 11(4). 419–424. 4 indexed citations

15.

Spickett, Gavin P, et al.. (1997). Common variable immunodeficiency: how many diseases?. Immunology Today. 18(7). 325–328. 114 indexed citations

16.

Vořechovský, Igor, Liping Luo, Martin J.S. Dyer, et al.. (1997). Clustering of missense mutations in the ataxia-telanglectasia gene in a sporadic T-cell leukaemia. Nature Genetics. 17(1). 96–99. 223 indexed citations

17.

Luo, Liping, Jens Michael Hertz, Stig S. Frøland, et al.. (1997). Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X‐linked agammaglobulinemia. Human Mutation. 9(5). 418–425. 35 indexed citations

18.

Vořechovský, Igor, Sabrina Prudente, Luciana Chessa, et al.. (1996). Exon-Scanning Mutation Analysisof the ATM Gene in Patients withAtaxia-T elangiectasia. European Journal of Human Genetics. 4(6). 352–355. 31 indexed citations

19.

Vořechovský, Igor, Liping Luo, Geneviève de Saint Basile, et al.. (1995). Improved oligonucleotide primer set for molecular diagnosis of X-linked agammaglobulinaemia: predominance of amino acid substitutions in the catalytic domain of Bruton's tyrosine kinase. Human Molecular Genetics. 4(12). 2403–2405. 31 indexed citations

20.

Harkness, R. A., S. B. Coade, & A. David B. Webster. (1984). ATP, ADP and AMP in plasma from peripheral venous blood. Clinica Chimica Acta. 143(2). 91–98. 39 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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