1.
Using published data in Mendelian randomization: a blueprint for efficient identification of causal risk factors
by Burgess, Stephen
European journal of epidemiology, 2015-01-01, Vol.30 (7), p.543-552
2.
Genome-wide Association Study of Three-Dimensional Facial Morphology Identifies a Variant in PAX3 Associated with Nasion Position
by Paternoster, Lavinia
American journal of human genetics, 2012-03-09, Vol.90 (3), p.478-485
3.
Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk
by Richardson, Tom G
American journal of human genetics, 2017-10-05, Vol.101 (4), p.590-602
4.
Genome-wide prediction of childhood asthma and related phenotypes in a longitudinal birth cohort
by Spycher, Ben D., PhD
Journal of allergy and clinical immunology, 2012, Vol.130 (2), p.503-509.e7
5.
C-reactive protein and its role in metabolic syndrome: mendelian randomisation study
by Timpson, Nicholas J
The Lancet (British edition), 2005-12-03, Vol.366 (9501), p.1954-1959
6.
Loss-of-function mutations in the melanocortin 4 receptor in a UK birth cohort
by Wade, Kaitlin H
Nature medicine, 2021-06, Vol.27 (6), p.1088-1096
7.
A Variant in LIN28B Is Associated with 2D:4D Finger-Length Ratio, a Putative Retrospective Biomarker of Prenatal Testosterone Exposure
by Medland, Sarah E
American journal of human genetics, 2010, Vol.86 (4), p.519-525
8.
Paradoxical Relationship Between Body Mass Index and Thyroid Hormone Levels: A Study Using Mendelian Randomization
by Taylor, Peter N
The journal of clinical endocrinology and metabolism, 2016-02, Vol.101 (2), p.730-738
9.
Does Greater Adiposity Increase Blood Pressure and Hypertension Risk?: Mendelian Randomization Using the FTO/MC4R Genotype
by Timpson, Nicholas J
Hypertension (Dallas, Tex. 1979), 2009-07, Vol.54 (1), p.84-90
10.
Association Between C-Reactive Protein Genotype, Circulating Levels, and Aortic Pulse Wave Velocity
by Schumacher, Wiebke
Hypertension (Dallas, Tex. 1979), 2009-02, Vol.53 (2), p.150-157
11.
Common Variation in the WNK1 Gene and Blood Pressure in Childhood: The Avon Longitudinal Study of Parents and Children
by Tobin, Martin D
Hypertension (Dallas, Tex. 1979), 2008-11, Vol.52 (5), p.974-979
12.
HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials
by Swerdlow, Daniel I, Dr
The Lancet (British edition), 2015-01-24, Vol.385 (9965), p.351-361
13.
The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis
by Holmes, Michael V
The Lancet (British edition), 2012, Vol.379 (9822), p.1214-1224
14.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
by Cardon, Lon R
Nature, 2007, Vol.447 (7145), p.661-678
15.
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits
by Kraja, Aldi T. Aldi T.
American journal of human genetics, 2018-12-27, Vol.104 (1), p.112-138
16.
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
by Manousaki, Despoina
American journal of human genetics, 2017-08-03, Vol.101 (2), p.227-238
17.
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
by Manousaki, Despoina
American journal of human genetics, 2017-08-03, Vol.101 (2), p.227-238
18.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
by Tachmazidou, Ioanna
American journal of human genetics, 2017-06-01, Vol.100 (6), p.865-884
19.
Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error
by Ikram, M. Kamran
American journal of human genetics, 2013-08-08, Vol.93 (2), p.264-277
20.
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height
by Guo, Yiran
American journal of human genetics, 2011-01-07, Vol.88 (1), p.6-18
