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Fair allocation of scarce medical resources in the time of Covid-19 EJ Emanuel, G Persad, R Upshur, B Thome, M Parker, A Glickman, ... New England Journal of Medicine 382 (21), 2049-2055, 2020 | 3644 | 2020 |
Quantifying SARS-CoV-2 transmission suggests epidemic control with digital contact tracing L Ferretti, C Wymant, M Kendall, L Zhao, A Nurtay, L Abeler-Dörner, ... science 368 (6491), eabb6936, 2020 | 3143 | 2020 |
Prevalence and architecture of de novo mutations in developmental disorders Nature 542 (7642), 433-438, 2017 | 1011 | 2017 |
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data CF Wright, TW Fitzgerald, WD Jones, S Clayton, JF McRae, ... The Lancet 385 (9975), 1305-1314, 2015 | 885 | 2015 |
Large-scale discovery of novel genetic causes of developmental disorders Nature 519 (7542), 223-228, 2015 | 809 | 2015 |
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study J Lord, DJ McMullan, RY Eberhardt, G Rinck, SJ Hamilton, ... The Lancet 393 (10173), 747-757, 2019 | 591 | 2019 |
Genome-wide and fine-resolution association analysis of malaria in West Africa M Jallow, YY Teo, KS Small, KA Rockett, P Deloukas, TG Clark, K Kivinen, ... Nature genetics 41 (6), 657-665, 2009 | 473 | 2009 |
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel O Delaneau, J Marchini Nature communications 5 (1), 3934, 2014 | 468 | 2014 |
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing A Sifrim, MP Hitz, A Wilsdon, J Breckpot, SHA Turki, B Thienpont, ... Nature genetics 48 (9), 1060-1065, 2016 | 444 | 2016 |
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q C Toomes, HM Bottomley, RM Jackson, KV Towns, S Scott, DA Mackey, ... The American Journal of Human Genetics 74 (4), 721-730, 2004 | 429 | 2004 |
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders CF Wright, JF McRae, S Clayton, G Gallone, S Aitken, TW FitzGerald, ... Genetics in Medicine 20 (10), 1216-1223, 2018 | 349 | 2018 |
Australia's mothers and babies 2012 L Hilder, Z Zhichao, M Parker, S Jahan, G Chambers Australian Institute of Health and Welfare, 2014 | 271 | 2014 |
Prevention of pulmonary embolism and deep vein thrombosis with low dose aspirin: Pulmonary Embolism Prevention (PEP) trial J O'Brien, H Duncan, G Kirsh, V Allen, P King, R Hargraves, L Mendes, ... Lancet 355 (9212), 2000 | 259 | 2000 |
Ethics of instantaneous contact tracing using mobile phone apps in the control of the COVID-19 pandemic MJ Parker, C Fraser, L Abeler-Dörner, D Bonsall Journal of Medical Ethics 46 (7), 427-431, 2020 | 257 | 2020 |
Disclosure of individual genetic data to research participants: the debate reconsidered AL Bredenoord, HY Kroes, E Cuppen, M Parker, JJM van Delden Trends in Genetics 27 (2), 41-47, 2011 | 245 | 2011 |
Effective configurations of a digital contact tracing app: a report to NHSX R Hinch, W Probert, A Nurtay, M Kendall, C Wymant, M Hall, K Lythgoe, ... Retrieved July 23, 2020, 2020 | 243 | 2020 |
Histone lysine methylases and demethylases in the landscape of human developmental disorders V Faundes, WG Newman, L Bernardini, N Canham, J Clayton-Smith, ... The American Journal of Human Genetics 102 (1), 175-187, 2018 | 236 | 2018 |
Neuronal nicotinic receptor β2 and β4 subunits confer large differences in agonist binding affinity MJ Parker, A Beck, CW Luetje Molecular pharmacology 54 (6), 1132-1139, 1998 | 226 | 1998 |
Good and bad research collaborations: researchers’ views on science and ethics in global health research M Parker, P Kingori PloS one 11 (10), e0163579, 2016 | 221 | 2016 |