Brian T. Wilson

1.7k total citations
21 papers, 373 citations indexed

About

Brian T. Wilson is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Brian T. Wilson has authored 21 papers receiving a total of 373 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Oncology. Recurrent topics in Brian T. Wilson's work include DNA Repair Mechanisms (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Glycosylation and Glycoproteins Research (2 papers). Brian T. Wilson is often cited by papers focused on DNA Repair Mechanisms (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Glycosylation and Glycoproteins Research (2 papers). Brian T. Wilson collaborates with scholars based in United Kingdom, Australia and Norway. Brian T. Wilson's co-authors include Jennifer Munkley, Zornitza Stark, David J. Elliott, Malcolm Crundwell, Bridget Knight, Hing Y. Leung, Lorna W. Harries, Craig Robson, Paul McCullagh and Prabhakar Rajan and has published in prestigious journals such as The Journal of Experimental Medicine, Journal of Clinical Oncology and PEDIATRICS.

In The Last Decade

Brian T. Wilson

18 papers receiving 365 citations

Peers

Brian T. Wilson

GENET

IMMUN

ONCOL

PRM

Bert Eussen Netherlands

Donatella Montanaro Italy

Ephrem Chin United States

Tanya C. Burch United States

Mitsuo Fujimoto Japan

А. А. Вартанян Russia

Adam Lambert United Kingdom

Aimee Stablewski United States

Jörg Hartkamp Germany

Hannah Titheradge United Kingdom

Bert Eussen Netherlands

Brian T. Wilson

317 ×1.1

92 ×1.1

GENET

111 ×1.9

IMMUN

109 ×2.3

ONCOL

25 ×0.6

PRM

Citations per year, relative to Brian T. Wilson Brian T. Wilson (= 1×) peers Bert Eussen

Countries citing papers authored by Brian T. Wilson

Since Specialization

Citations

This map shows the geographic impact of Brian T. Wilson'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 Brian T. Wilson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brian T. Wilson more than expected).

Fields of papers citing papers by Brian T. Wilson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brian T. Wilson. 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 Brian T. Wilson. The network helps show where Brian T. Wilson may publish in the future.

Co-authorship network of co-authors of Brian T. Wilson

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Núñez, Enrique, Federico Gago, Jesús Vázquez, et al.. (2025). A New GlyT2 Variant Associated with Hyperekplexia. International Journal of Molecular Sciences. 26(14). 6753–6753.

Apelt, Katja, Susan M. White, Jung-Eun Yeo, et al.. (2020). ERCC1mutations impede DNA damage repair and cause liver and kidney dysfunction in patients. The Journal of Experimental Medicine. 218(3). 24 indexed citations

Wilson, Brian T., et al.. (2019). Joining the hidden revolution in rare diseases: working with family support groups. Archives of Disease in Childhood. 105(2). 107–108. 3 indexed citations

Cuthbert, Gavin, R O’Donnell, Brian T. Wilson, et al.. (2017). Functional characterisation of a novel ovarian cancer cell line, NUOC-1. Oncotarget. 8(16). 26832–26844. 3 indexed citations

Munkley, Jennifer, Daniel Vodák, Karen E. Livermore, et al.. (2016). Glycosylation is an Androgen-Regulated Process Essential for Prostate Cancer Cell Viability. EBioMedicine. 8. 103–116. 75 indexed citations

Wilson, Brian T., et al.. (2016). Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome. American Journal of Medical Genetics Part A. 170(3). 773–776. 5 indexed citations

Wilson, Brian T., Zornitza Stark, Sumita Danda, et al.. (2015). The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care. Genetics in Medicine. 18(5). 483–493. 108 indexed citations

Wilson, Brian T., et al.. (2015). Microdeletion 1p35.2: A recognizable facial phenotype with developmental delay. American Journal of Medical Genetics Part A. 167(8). 1916–1920. 2 indexed citations

Munkley, Jennifer, Sebastian Oltean, Daniel Vodák, et al.. (2015). The androgen receptor controls expression of the cancer-associated sTn antigen and cell adhesion through induction of ST6GalNAc1 in prostate cancer. Oncotarget. 6(33). 34358–34374. 62 indexed citations

10.

Wilson, Brian T., Andrew T. Strong, S W O'Kelly, Jennifer Munkley, & Zornitza Stark. (2015). Metronidazole Toxicity in Cockayne Syndrome: A Case Series. PEDIATRICS. 136(3). e706–e708. 15 indexed citations

11.

Patterson, Miranda, Robert Sharrock, Angelika Kaufmann, et al.. (2014). Assessing the function of homologous recombination DNA repair in malignant pleural effusion (MPE) samples. British Journal of Cancer. 111(1). 94–100. 19 indexed citations

12.

Wilson, Brian T., et al.. (2013). Juvenile idiopathic arthritis, mitral valve prolapse and a familial variant involving the integrin‐binding fragment of FBN1. American Journal of Medical Genetics Part A. 161(8). 2047–2051. 7 indexed citations

13.

Lederer, Damien, Brian T. Wilson, Pierre Lefesvre, et al.. (2012). Atypical findings in three patients with Pai syndrome and literature review. American Journal of Medical Genetics Part A. 158A(11). 2899–2904. 14 indexed citations

14.

Wilson, Brian T., et al.. (2012). Interstitial microduplication 12q13.2–q13.3 in a patient with dysmorphism, developmental delay, atypical seizures and hypospadias. Clinical Dysmorphology. 21(4). 196–199. 1 indexed citations

15.

Wilson, Brian T., et al.. (2011). A case of mosaic trisomy 19q12–q13.2 with high BMI, macrocephaly, and speech delay. Clinical Dysmorphology. 21(1). 33–36. 3 indexed citations

16.

Wilson, Brian T., et al.. (2010). Agenesis of the corpus callosum in mosaic tetrasomy 8p. Clinical Dysmorphology. 19(4). 215–217. 1 indexed citations

17.

Wilson, Brian T., et al.. (2010). Astrocytoma in a Breast Cancer Lineage: Part of the BRCA2 Phenotype?. Journal of Clinical Oncology. 28(30). e596–e598. 7 indexed citations

18.

Wilson, Brian T., et al.. (2009). Síndrome dismórfico con anomalías congénitas múltiples: Clasificación actual. 76(3). 132–135.

19.

Pinthus, Jehonathan H., et al.. (2006). 795: Androgens Induce Adaptation to Oxidative Stress-Implications for Prostate Cancer Radiation Therapy. The Journal of Urology. 175(4S). 257–257. 1 indexed citations

20.

Connolly, Bernard A., et al.. (2003). Uracil recognition by archaeal family B DNA polymerases. Biochemical Society Transactions. 31(3). 699–702. 19 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.

Explore authors with similar magnitude of impact