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Mendelian randomization with Egger pleiotropy correction and weakly informative Bayesian priors

International journal of epidemiology, 2018-08, Vol.47 (4), p.1217-1228

2018

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Genome‐wide analysis of adolescent psychotic‐like experiences shows genetic overlap with psychiatric disorders

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2018-06, Vol.177 (4), p.416-425

2018

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Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress

Molecular psychiatry, 2004-07, Vol.9 (7), p.684-697

2004

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Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress

Molecular psychiatry, 2004-07, Vol.9 (7), p.643-643

2004

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Self-reported walking pace, polygenic risk scores and risk of coronary artery disease in UK biobank

Nutrition, metabolism, and cardiovascular diseases, 2022-11, Vol.32 (11), p.2630-2637

2022

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Genes related to sex steroids, neural growth, and social–emotional behavior are associated with autistic traits, empathy, and Asperger syndrome

Autism research, 2009-06, Vol.2 (3), p.157-177

2009

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Pedigree disequilibrium tests for multilocus haplotypes

Genetic epidemiology, 2003-09, Vol.25 (2), p.115-121

Dudbridge, Frank

2003

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Comparison of variance estimators for meta-analysis of instrumental variable estimates

International journal of epidemiology, 2016-12, Vol.45 (6), p.1975-1986

2016

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Mapping the platelet profile for functional genomic studies and demonstration of the effect size of the GP6 locus

Journal of thrombosis and haemostasis, 2007-08, Vol.5 (8), p.1756-1765

2007

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Fibrinogen Aα Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension

The European respiratory journal, 2008-04, Vol.31 (4), p.736-741

2008

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Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs

Diabetologia, 2012-02, Vol.55 (2), p.349-357

2012

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Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD

Molecular psychiatry, 2005-10, Vol.10 (10), p.939-943

2005

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Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier

Journal of Obesity, 2011-01, Vol.2011, p.307542-7

2011

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Epigenome-based cancer risk prediction: rationale, opportunities and challenges

Nature reviews. Clinical oncology, 2018-05, Vol.15 (5), p.292-309

2018

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Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease

Genes and immunity, 2004-07, Vol.5 (5), p.381-388

2004

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Variants in the fetal genome near FLT1 are associated with risk of preeclampsia

Nature genetics, 2017-08, Vol.49 (8), p.1255-1260

2017

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A Note on Permutation Tests in Multistage Association Scans

American journal of human genetics, 2006-06, Vol.78 (6), p.1094-1095

Dudbridge, Frank

2006

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The use of edge-betweenness clustering to investigate biological function in protein interaction networks

BMC bioinformatics, 2005-03, Vol.6 (1), p.39-39, Article 39

2005

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Definition of novel GP6 polymorphisms and major difference in haplotype frequencies between populations by a combination of in‐depth exon resequencing and genotyping with tag single nucleotide polymorphisms

Journal of thrombosis and haemostasis, 2006-06, Vol.4 (6), p.1197-1205

2006

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Bone structural effects of variation in the TNFRSF1B gene encoding the tumor necrosis factor receptor 2

Osteoporosis international, 2008-07, Vol.19 (7), p.961-968

2008

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P2.06-11 MEDUSA: Phylogenetic Analysis of Mesothelioma Tumours by Multiregional Sampling, Whole Exome Sequencing, and Copy Number Analysis

Journal of thoracic oncology, 2019-10, Vol.14 (10), p.S759-S759

2019

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Accuracy of Gene Scores when Pruning Markers by Linkage Disequilibrium

Human heredity, 2015-01, Vol.80 (4), p.178-186

2015

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Functional genetic polymorphisms in cytokines and metabolic genes as additional genetic markers for susceptibility to develop type 1 diabetes

Genes and immunity, 2004-01, Vol.5 (1), p.36-40

2004

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Fibrinogen A{alpha} Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension

The European respiratory journal, 2008-04, Vol.31 (4), p.736-741

2008

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Adaptation of the extended transmission/disequilibrium test to distinguish disease associations of multiple loci: the Conditional Extended Transmission/Disequilibrium Test

Annals of human genetics, 2000-05, Vol.64, p.207-213

2000

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Mendelian randomization with Egger pleiotropy correction and weakly informative Bayesian priors

Genome‐wide analysis of adolescent psychotic‐like experiences shows genetic overlap with psychiatric disorders

Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress

Mitochondrial dysfunction in schizophrenia: evidence for compromised brain metabolism and oxidative stress

Self-reported walking pace, polygenic risk scores and risk of coronary artery disease in UK biobank

Genes related to sex steroids, neural growth, and social–emotional behavior are associated with autistic traits, empathy, and Asperger syndrome

Pedigree disequilibrium tests for multilocus haplotypes

Comparison of variance estimators for meta-analysis of instrumental variable estimates

Mapping the platelet profile for functional genomic studies and demonstration of the effect size of the GP6 locus

Fibrinogen Aα Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension

Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs

Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD

Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier

Epigenome-based cancer risk prediction: rationale, opportunities and challenges

Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease

Variants in the fetal genome near FLT1 are associated with risk of preeclampsia

A Note on Permutation Tests in Multistage Association Scans

The use of edge-betweenness clustering to investigate biological function in protein interaction networks

Definition of novel GP6 polymorphisms and major difference in haplotype frequencies between populations by a combination of in‐depth exon resequencing and genotyping with tag single nucleotide polymorphisms

Bone structural effects of variation in the TNFRSF1B gene encoding the tumor necrosis factor receptor 2

P2.06-11 MEDUSA: Phylogenetic Analysis of Mesothelioma Tumours by Multiregional Sampling, Whole Exome Sequencing, and Copy Number Analysis

Accuracy of Gene Scores when Pruning Markers by Linkage Disequilibrium

Functional genetic polymorphisms in cytokines and metabolic genes as additional genetic markers for susceptibility to develop type 1 diabetes

Fibrinogen A{alpha} Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension

Adaptation of the extended transmission/disequilibrium test to distinguish disease associations of multiple loci: the Conditional Extended Transmission/Disequilibrium Test

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