Torthaí cuardaigh - Vincenzo Forgetta
- 1 - 20 toradh as 39 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Mendelian randomisation applied to drug development in cardiovascular disease: a review de réir Lauren E. Mokry, Omar Ahmad, Vincenzo Forgetta, George Thanassoulis, J. Brent Richards
Foilsithe / Cruthaithe 2014Revisão -
2
Circulating Proteins Influencing Psychiatric Disease: A Mendelian Randomization Study de réir Tianyuan Lu, Vincenzo Forgetta, Celia M.T. Greenwood, Sirui Zhou, J. Brent Richards
Foilsithe / Cruthaithe 2022Artigo -
3
Genetically decreased vitamin D and risk of Alzheimer disease de réir Lauren E. Mokry, Stephanie Ross, John Morris, Despoina Manousaki, Vincenzo Forgetta, J. Brent Richards
Foilsithe / Cruthaithe 2016Artigo -
4
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study de réir Guillaume Butler‐Laporte, Devin Kreuzer, Tomoko Nakanishi, Adil Harroud, Vincenzo Forgetta, J. Brent Richards
Foilsithe / Cruthaithe 2020Artigo -
5
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6
Pathogenic and multidrug-resistant Escherichia fergusonii from broiler chicken de réir Vincenzo Forgetta, Heidi Rempel, François Malouin, René E. Vaillancourt, Edward Topp, Ken Dewar, Moussa S. Diarra
Foilsithe / Cruthaithe 2012Artigo -
7
A Mendelian Randomization Study of the Effect of Type-2 Diabetes and Glycemic Traits on Bone Mineral Density de réir Omar Ahmad, Aaron Leong, Julie Ann Miller, John Morris, Vincenzo Forgetta, Muhammad Mujammami, J. Brent Richards
Foilsithe / Cruthaithe 2016Artigo -
8
Clinically Relevant Circulating Protein Biomarkers for Type 1 Diabetes: Evidence From a Two-Sample Mendelian Randomization Study de réir Nahid Yazdanpanah, Mojgan Yazdanpanah, Ye Wang, Vincenzo Forgetta, Michaël Pollak, Constantin Polychronakos, J. Brent Richards, Despoina Manousaki
Foilsithe / Cruthaithe 2021Artigo -
9
The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypes de réir Tomoko Nakanishi, Vincenzo Forgetta, Tomohiro Handa, Toyohiro Hirai, Vincent Mooser, G.M. Lathrop, William Cookson, J. Brent Richards
Foilsithe / Cruthaithe 2020Artigo -
10
Genetic predisposition to increased serum calcium, bone mineral density, and fracture risk in individuals with normal calcium levels: mendelian randomisation study de réir Agustin Cerani, Sirui Zhou, Vincenzo Forgetta, John A. Morris, Katerina Trajanoska, Fernando Rivadeneira, Susanna C. Larsson, Karl Michaëlsson, J. Brent Richards
Foilsithe / Cruthaithe 2019Revisão -
11
Childhood obesity and multiple sclerosis: A Mendelian randomization study de réir Adil Harroud, Ruth E. Mitchell, Tom G. Richardson, John Morris, Vincenzo Forgetta, George Davey Smith, Sergio E. Baranzini, J. Brent Richards
Foilsithe / Cruthaithe 2021Artigo -
12
Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study de réir Lauren E. Mokry, Stephanie Ross, Omar Ahmad, Vincenzo Forgetta, George Davey Smith, Aaron Leong, Celia M.T. Greenwood, George Thanassoulis, J. Brent Richards
Foilsithe / Cruthaithe 2015Artigo -
13
Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study de réir Despoina Manousaki, Adil Harroud, Ruth E. Mitchell, Stephanie Ross, Vincenzo Forgetta, Nicholas J. Timpson, George Davey Smith, Constantin Polychronakos, J. Brent Richards
Foilsithe / Cruthaithe 2021Artigo -
14
Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci de réir Despoina Manousaki, Ruth E. Mitchell, Tom Dudding, Simon Haworth, Adil Harroud, Vincenzo Forgetta, Rupal Shah, Jian’an Luan, Claudia Langenberg, Nicholas J. Timpson, J. Brent Richards
Foilsithe / Cruthaithe 2020Artigo -
15
A Mendelian randomization study of the effect of type-2 diabetes on coronary heart disease de réir Omar Ahmad, John Morris, Muhammad Mujammami, Vincenzo Forgetta, Aaron Leong, Rui Li, Maxime Turgeon, Celia M.T. Greenwood, George Thanassoulis, James B. Meigs, Robert Sladek, J. Brent Richards
Foilsithe / Cruthaithe 2015Artigo -
16
Vitamin D and COVID-19 susceptibility and severity in the COVID-19 Host Genetics Initiative: A Mendelian randomization study de réir Guillaume Butler‐Laporte, Tomoko Nakanishi, Vincent Mooser, David Morrison, Tala Abdullah, Olumide Adeleye, Noor Mamlouk, Nofar Kimchi, Zaman Afrasiabi, Nardin Rezk, Annarita Giliberti, Alessandra Renieri, Yiheng Chen, Sirui Zhou, Vincenzo Forgetta, J. Brent Richards
Foilsithe / Cruthaithe 2021Artigo -
17
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes de réir Vincenzo Forgetta, Despoina Manousaki, Roman Istomine, Stephanie Ross, Marie-Catherine Tessier, Luc Marchand, Min Li, Hui‐Qi Qu, Jonathan P. Bradfield, Struan F.A. Grant, Hákon Hákonarson, Andrew D. Paterson, Ciriaco A. Piccirillo, Constantin Polychronakos, J. Brent Richards
Foilsithe / Cruthaithe 2020Artigo -
18
Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA) de réir Vincenzo Forgetta, Rui Li, Corinne Darmond-Zwaig, Alexandre Bélisle, Cynthia Balion, Delnaz Roshandel, Christina Wolfson, Guillaume Lettre, Guillaume Paré, Andrew D. Paterson, Lauren E. Griffith, Chris P. Verschoor, Mark Lathrop, Susan Kirkland, Parminder Raina, J. Brent Richards, Jiannis Ragoussis
Foilsithe / Cruthaithe 2022Artigo -
19
An effector index to predict target genes at GWAS loci de réir Vincenzo Forgetta, Lai Jiang, Nicholas A. Vulpescu, Megan S. Hogan, Siyuan Chen, John Morris, Stepan Grinek, Christian Benner, Dongkeun Jang, Quy Hoang, Noël P. Burtt, Jason Flannick, Mark I. McCarthy, Eric B. Fauman, Celia M.T. Greenwood, Matthew T. Maurano, J. Brent Richards
Foilsithe / Cruthaithe 2022Artigo -
20
Epigenome-wide Association of DNA Methylation in Whole Blood With Bone Mineral Density de réir John Morris, Pei-Chien Tsai, Roby Joehanes, Jie Zheng, Katerina Trajanoska, Mette Soerensen, Vincenzo Forgetta, Juan Castillo‐Fernandez, Morten Frost, Tim D. Spector, Kaare Christensen, Lene Christiansen, Fernando Rivadeneira, Jonathan H. Tobias, David M. Evans, Douglas P. Kiel, Yi‐Hsiang Hsu, J. Brent Richards, Jordana T. Bell
Foilsithe / Cruthaithe 2017Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Gene
Genetics
Genotype
Medicine
Internal medicine
Single-nucleotide polymorphism
Genome-wide association study
Odds ratio
Genetic variants
Mendelian randomization
Endocrinology
Genetic association
Bioinformatics
Disease
Bone mineral
Computational biology
Osteoporosis
Computer science
Diabetes mellitus
Phenotype
Population
Type 2 diabetes
Confidence interval
Environmental health
Genome
Quantitative trait locus
Vitamin D and neurology
Allele
Confounding