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个人简介
Matt Brown is a clinician-scientist who trained initially as a rheumatologist before heading into a career in immunogenetics research. He has made major contributions to the development of gene-mapping approaches in human diseases. He has played a significant role in the development of genomewide association study methodology, leading to the discovery of thousands of genetic variants associated with a wide range of human diseases. His particular interest is in the disease ankylosing spondylitis, where he has helped to develop new treatments by dissecting the genetic causes of the disease. He is deeply interested in the translation of genomics into clinical applications, including in common and rare heritable diseases, and cancers. More recently, he contributed to the development of sequencing approaches to mutation mapping in unrelated cases, enabling early life or prenatal genetic diagnoses for monogenic diseases. He has led international efforts in mapping genes in rheumatic diseases (ankylosing spondylitis, rheumatoid arthritis, scleroderma), osteoporosis, neurological diseases (motor neurone disease, epilepsy), and TB, as well as contributing to efforts in many other diseases. These findings have led to major translational benefits such as the development of IL-23 pathway inhibitors for psoriasis, IBD and AS, as well as many drug development initiatives. He is expert in genomic technologies and has played a leading role in the development and introduction of next-generation sequencing for medical genomics including cancers and heritable diseases.
研究兴趣
论文共 698 篇作者统计合作学者相似作者
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Annals of the rheumatic diseases (2024)
Seminars in arthritis and rheumatism (2023): 152330-152330
Matthew Brown, Alicia Leon,Katarzyna Kedzierska, Charlotte Moore,Hayley L Belnoue-Davis,Susanne Flach,John P Lydon,Francesco J DeMayo,Annabelle Lewis,Tjalling Bosse,Ian Tomlinson,David N Church
crossref(2023)
Future Rare Diseasesno. 1 (2023)
crossref(2023)
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