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Mahajan, Anubha, Go, Min Jin, Zhang, Weihua, Below, Jennifer E, Gaulton, Kyle J, Ferreira, Teresa, Horikoshi, Momoko, Johnson, Andrew D, Ng, Maggie CY, Prokopenko, Inga
et al (show 322 more authors) (2014) Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics, 46 (3). pp. 234-244.


Ruderfer, Douglas M, Ripke, Stephan, McQuillin, Andrew, Boocock, James, Stahl, Eli A, Pavlides, Jennifer M Whitehead, Mullins, Niamh, Charney, Alexander W, Ori, Anil PS, Loohuis, Loes M Olde
et al (show 534 more authors) (2018) Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. CELL, 173 (7). pp. 1705-1715.


Hamilton, William L ORCID: 0000-0002-3330-353X, Tonkin-Hill, Gerry ORCID: 0000-0003-4397-2224, Smith, Emily R ORCID: 0000-0003-4925-467X, Aggarwal, Dinesh ORCID: 0000-0002-5938-8172, Houldcroft, Charlotte J ORCID: 0000-0002-1833-5285, Warne, Ben ORCID: 0000-0003-1326-0373, Meredith, Luke W, Hosmillo, Myra ORCID: 0000-0002-3514-7681, Jahun, Aminu S ORCID: 0000-0002-4585-1701, Curran, Martin D
et al (show 28 more authors) (2021) Genomic epidemiology of COVID-19 in care homes in the east of England. eLife, 10. e64618-.


Vöhringer, Harald S, Sanderson, Theo, Sinnott, Matthew, De Maio, Nicola, Nguyen, Thuy, Goater, Richard, Schwach, Frank, Harrison, Ian, Hellewell, Joel, Ariani, Cristina V
et al (show 923 more authors) (2021) Genomic reconstruction of the SARS-CoV-2 epidemic in England. Nature, 600 (7889). pp. 506-511.


Tonkin-Hill, Gerry, Martincorena, Inigo, Amato, Roberto, Lawson, Andrew RJ, Gerstung, Moritz, Johnston, Ian, Jackson, David K, Park, Naomi, Lensing, Stefanie V, Quail, Michael A
et al (show 29 more authors) (2021) Patterns of within-host genetic diversity in SARS-CoV-2. eLife, 10.


Harold, Denise, Connolly, Siobhan, Riley, Brien P, Kendler, Kenneth S, McCarthy, Shane E, McCombie, William R, Richards, Alex, Owen, Michael J, O'Donovan, Michael C, Walters, James
et al (show 350 more authors) (2019) Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180 (3). pp. 223-231.

This list was generated on Sun Oct 8 04:15:29 2023 BST.