Items where authors include "Markus, HS"

Article

Turro, E, Astle, WJ, Megy, K et al. (60 more authors) (2020) Whole-genome sequencing of patients with rare diseases in a national health system. Nature, 583. pp. 96-102. ISSN 0028-0836

Tay, J, Lisiecka-Ford, DM, Hollocks, MJ et al. (8 more authors) (2020) Network neuroscience of apathy in cerebrovascular disease. Progress in Neurobiology, 188. 101785. ISSN 0301-0082

Wei, W, Tuna, S, Keogh, MJ et al. (426 more authors) (2019) Germline selection shapes human mitochondrial DNA diversity. Science, 364 (6442). 749-+. ISSN 0036-8075

Whitworth, J, Smith, PS, Martin, J-E et al. (330 more authors) (2018) Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes. The American Journal of Human Genetics, 103 (1). pp. 3-18. ISSN 0002-9297

Horsburgh, K, Wardlaw, JM, van Agtmael, T et al. (43 more authors) (2018) Small vessels, dementia and chronic diseases – molecular mechanisms and pathophysiology. Clinical Science, 132 (8). pp. 851-868. ISSN 0143-5221

Telomeres Mendelian Randomization Collaboration, Haycock, PC, Burgess, S et al. (196 more authors) (2017) Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. JAMA Oncology, 3 (5). pp. 636-651. ISSN 2374-2437

Freitag, DF, Butterworth, AS, Willeit, P et al. (150 more authors) (2015) Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis. Lancet Diabetes and Endocrinology, 3 (4). pp. 243-253. ISSN 2213-8587