B. Richards

发表

Large-scale Meta-analysis of Genome-wide Association (GWA) Scans for Osteoporosis Traits: the GEFOS Consortium

Bjarni V. Halldórsson, D. Kiel, A. Uitterlinden, 2008 .

Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experience

P. Waters, M. Lambert, R. Laframboise, 1998, European Journal of Human Genetics.

A reference panel of 64,976 haplotypes for genotype imputation

Laura J. Scott, He Zhang, Gonçalo Abecasis, 2015, bioRxiv.

Circulating Proteins Influencing COVID-19 Susceptibility and Severity: a Mendelian Randomization Study

V. Mooser, J. Afilalo, D. Kaufmann, 2020, medRxiv.

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

Gail Clement, Jie Huang, Antonio Ciampi, 2014, Nature Communications.

Tuberculosis surveillance among new immigrants in Montreal.

K. Schwartzman, D. Menzies, R. Kozak, 2005, The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

Laboratory Assessment of Disease Activity in Childhood Crohn's Disease and Ulcerative Colitis

B. Richards, P. Macfarlane, V. Miller, 1986, Journal of pediatric gastroenterology and nutrition.

Genetic Regulation of Vitamin D Levels

Z. Dastani, Rui Li, B. Richards, 2013, Calcified Tissue International.

Making Sense of Intratumor Genetic Heterogeneity: Altered Frequency of Androgen Receptor CAG Repeat Length Variants in Breast Cancer Tissues

G. Batist, M. Basik, Chunlin Wang, 2013, Human mutation.

Genetic polymorphisms of innate immunity-related inflammatory pathways and their association with factors related to type 2 diabetes

T. Spector, A. El-Sohemy, A. Badawi, 2011, BMC Medical Genetics.

P2-16 High burden of rheumatic diseases in a population based study from Lebanon

T. Spector, A. El-Sohemy, A. Badawi, 2011, Journal of Epidemiology & Community Health.

Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity

J. Baillie, S. Furini, F. Colombo, 2021, medRxiv.

Functional characterization of GWAS loci associated with fracture risk

Guo Li, John P. A. Ioannidis, Peter M. Visscher, 2013 .

Bone Research Society, Annual Meeting 2017 Proceedings

P. Tsai, T. Spector, J. Bell, 2018, Journal of musculoskeletal & neuronal interactions.

Genetic Regulation of Vitamin D Levels

Z. Dastani, B. Richards, Rui Li, 2012, Calcified Tissue International.

consortiumwith hand osteoarthritis: the Treat-OA locus within the ataxin 2 binding protein 1 gene is A genome-wide association study suggests that a

A. Uitterlinden, T. Spector, P. Deloukas, 2009 .

Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activity

Daniel L. Koller, D. Kiel, A. Uitterlinden, 2011 .

Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study

D. Kiel, R. Mägi, F. Rivadeneira, 2018, British Medical Journal.

Sequencing of SCN5A Identifies Rare and Common Variants Associated With Cardiac Conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

Tom R. Gaunt, Gail P. Clement, Shane A. McCarthy, 2014, Circulation. Cardiovascular genetics.

An effector index to predict target genes at GWAS loci

M. McCarthy, C. Greenwood, J. Flannick, 2021, Human Genetics.

Exome Sequencing Studies Identify Mutations in STAB2 As a Genetic Risk for Venous Thromboembolic Disease

D. Goldstein, Jun Z. Li, P. Reitsma, 2017 .