Torthaí cuardaigh - Martin D. Tobin
- 1 - 20 toradh as 90 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Genotypes and haplotypes predisposing to myocardial infarction: a multilocus case-control study de réir Martin D. Tobin
Foilsithe / Cruthaithe 2004Artigo -
2
<i>P</i><sub>aO<sub>2</sub></sub>/<i>F</i><sub>IO<sub>2</sub></sub>ratio: the mismeasure of oxygenation in COVID-19 de réir Martin D. Tobin, Amal Jubran, Franco Laghi
Foilsithe / Cruthaithe 2021Carta -
3
Genomic copy number variation, human health, and disease de réir Louise V. Wain, John A.L. Armour, Martin D. Tobin
Foilsithe / Cruthaithe 2009Revisão -
4
Mendelian Randomisation and Causal Inference in Observational Epidemiology de réir Nuala A. Sheehan, Vanessa Didelez, Paul R. Burton, Martin D. Tobin
Foilsithe / Cruthaithe 2008Artigo -
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Molecular characterization of the acyl-coenzyme A:isopenicillin N acyltransferase gene (penDE) from Penicillium chrysogenum and Aspergillus nidulans and activity of recombinant enz... de réir Martin D. Tobin, Mark D. Fleming, Paul L. Skatrud, James R. Miller
Foilsithe / Cruthaithe 1990Artigo -
7
Adjusting for bias and unmeasured confounding in Mendelian randomization studies with binary responses de réir Tom Palmer, John R. Thompson, Martin D. Tobin, Nuala A. Sheehan, Paul R. Burton
Foilsithe / Cruthaithe 2008Artigo -
8
Common Variants in Genes Underlying Monogenic Hypertension and Hypotension and Blood Pressure in the General Population de réir Martin D. Tobin, Maciej Tomaszewski, Peter S. Braund, Cother Hajat, Stuart M. Raleigh, Tom Palmer, Mark J. Caulfield, Paul R. Burton, Nilesh J. Samani
Foilsithe / Cruthaithe 2008Artigo -
9
Haplotype estimation for biobank-scale data sets de réir Jared O’Connell, Kevin Sharp, Nick Shrine, Louise V. Wain, Ian P. Hall, Martin D. Tobin, Jean‐François Zagury, Olivier Delaneau, Jonathan Marchini
Foilsithe / Cruthaithe 2016Artigo -
10
Heritability of Early Repolarization de réir Wibke Reinhard, Bernhard M. Kaess, Radosław Dębiec, Christopher P. Nelson, Klaus Stark, Martin D. Tobin, Peter W. Macfarlane, Maciej Tomaszewski, Nilesh J. Samani, Christian Hengstenberg
Foilsithe / Cruthaithe 2011Artigo -
11
Pilot study of a multidisciplinary gout patient education and monitoring program de réir Theodore Fields, Adam Rifaat, Arthur M.F. Yee, Dalit Ashany, Katherine Kim, Martin D. Tobin, Nicole Oliva, Kara G. Fields, Monica Richey, S.Psi. Taufik Kasturi, Adena Batterman
Foilsithe / Cruthaithe 2016Artigo -
12
Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study de réir Shona M. Kerr, Archie Campbell, Lee Murphy, Caroline Hayward, Cathy Jackson, Louise V. Wain, Martin D. Tobin, Anna F. Dominiczak, Andrew D. Morris, Blair H. Smith, David J. Porteous
Foilsithe / Cruthaithe 2013Artigo -
13
A Comparison of Four Methods of Weaning Patients from Mechanical Ventilation de réir Martin Dres, Fernando Frutos–Vivar, Martin D. Tobin, Inmaculada Alía, José F. Solsona, Valverdú Valverdu, Rafael Fernández, Miguel A. de la Cal, S. Benito, Roser Boix Tomás, Demetrio Carriedo, Santiago Macías, Jesús Blanco
Foilsithe / Cruthaithe 1995Artigo -
14
Genetic and clinical characteristics of treatment-resistant depression using primary care records in two UK cohorts de réir Chiara Fabbri, Saskia P. Hagenaars, Catherine John, Alexander T. Williams, Nick Shrine, Louise Moles, Ken B. Hanscombe, Alessandro Serretti, David Shepherd, Robert C. Free, Louise V. Wain, Martin D. Tobin, Cathryn M. Lewis
Foilsithe / Cruthaithe 2021Artigo -
15
DataSHIELD: resolving a conflict in contemporary bioscience--performing a pooled analysis of individual-level data without sharing the data de réir Michael Wolfson, Susan Wallace, Nicholas G. D. Masca, Geoffrey M. Rowe, Nuala A. Sheehan, Vincent Ferretti, Philippe Laflamme, Martin D. Tobin, John Macleod, Julian Little, Isabel Fortier, Bartha Maria Knoppers, Paul R. Burton
Foilsithe / Cruthaithe 2010Artigo -
16
Identifying potential causal effects of age at menarche: a Mendelian randomization phenome-wide association study de réir Maria C. Magnus, Anna L. Guyatt, Rebecca B. Lawn, Annah B. Wyss, Katerina Trajanoska, Leanne K. Küpers, Fernando Rivadeneira, Martin D. Tobin, Stephanie J. London, Debbie A. Lawlor, Louise A C Millard, Abigail Fraser
Foilsithe / Cruthaithe 2020Artigo -
17
Genome-Wide Gene-by-Smoking Interaction Study of Chronic Obstructive Pulmonary Disease de réir Woori Kim, Dmitry Prokopenko, Phuwanat Sakornsakolpat, Brian D. Hobbs, Sharon M. Lutz, John E. Hokanson, Louise V. Wain, Carl Melbourne, Nick Shrine, Martin D. Tobin, Edwin K. Silverman, Michael H. Cho, Terri H. Beaty
Foilsithe / Cruthaithe 2020Artigo -
18
Detection of mutations in <i>KLHL3</i> and <i>CUL3</i> in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome) de réir Mark Glover, James S. Ware, Amanda P. Henry, Martin Wolley, Roddy Walsh, Louise V. Wain, Shengxin Xu, William G. van’t Hoff, Martin D. Tobin, Ian P. Hall, Stuart A. Cook, Richard D. Gordon, Michael Stowasser, Kevin M. O’Shaughnessy
Foilsithe / Cruthaithe 2013Artigo -
19
Smoking, DNA Methylation, and Lung Function: a Mendelian Randomization Analysis to Investigate Causal Pathways de réir Emily Jamieson, Roxanna Korologou‐Linden, Robyn E. Wootton, Anna L. Guyatt, Thomas Battram, Kimberley Burrows, Tom R. Gaunt, Martin D. Tobin, Marcus R. Munafò, George Davey Smith, Kate Tilling, Caroline L. Relton, Tom G. Richardson, Rebecca C. Richmond
Foilsithe / Cruthaithe 2020Artigo -
20
Association of <i>WNK1</i> Gene Polymorphisms and Haplotypes With Ambulatory Blood Pressure in the General Population de réir Martin D. Tobin, Stuart M. Raleigh, Stephen Newhouse, Peter S. Braund, Clare L. Bodycote, Jenny Ogleby, Deborah F Cross, Jay Gracey, Saija Hayes, Terry Smith, Cathy Ridge, Mark J. Caulfield, Nuala A. Sheehan, Patricia B. Munroe, Paul R. Burton, Nilesh J. Samani
Foilsithe / Cruthaithe 2005Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Medicine
Genotype
Internal medicine
Single-nucleotide polymorphism
Genome-wide association study
Genetic association
Environmental health
Population
Computational biology
Disease
Lung
COPD
Allele
Blood pressure
Locus (genetics)
SNP
Lung function
Computer science
Endocrinology
Genome
Pathology
Bioinformatics
Cardiology
Genetic variants
Mendelian randomization
Asthma
Pulmonary function testing