michael parker
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An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
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
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
International network of cancer genome projects
Data coordination centre Kasprzyk (Leader) Arek 1 Stein (Leader) Lincoln D ...
Nature 464 (7291), 993-998, 2010
Prevalence and architecture of de novo mutations in developmental disorders
Nature 542 (7642), 433-438, 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
Large-scale discovery of novel genetic causes of developmental disorders
Nature 519 (7542), 223-228, 2015
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
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
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
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
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
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
Australia's mothers and babies 2012
L Hilder, Z Zhichao, M Parker, S Jahan, G Chambers
Australian Institute of Health and Welfare, 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
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
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
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
Deciding for imperilled newborns: medical authority or parental autonomy?
HE McHaffie, IA Laing, M Parker, J McMillan
Journal of Medical Ethics 27 (2), 104-109, 2001
T lymphocyte T cell-B cell-activating molecule/CD40-L molecules induce normal B cells or chronic lymphocytic leukemia B cells to express CD80 (B7/BB-1) and enhance their …
MJ Yellin, J Sinning, LR Covey, W Sherman, JJ Lee, E Glickman-Nir, ...
Journal of immunology (Baltimore, Md.: 1950) 153 (2), 666-674, 1994
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