Andrew P Morris

发表

What Can Machine Learning Approaches in Genomics Tell Us about the Molecular Basis of Amyotrophic Lateral Sclerosis?

George Giannakopoulos, Christina Vasilopoulou, Andrew P Morris, 2020, Journal of personalized medicine.

Evaluation of methodology for the analysis of 'time-to-event' data in pharmacogenomic genome-wide association studies.

Andrew P Morris, Hamzah Syed, Andrea L Jorgensen, 2016, Pharmacogenomics.

Basic statistical analysis in genetic case-control studies

Andrew P Morris, Geraldine M Clarke, Carl A Anderson, 2011, Nature Protocols.

A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits

Inês Barroso, Andrew P Morris, Eleftheria Zeggini, 2015, Genetic epidemiology.

Trans-ethnic meta-analysis of white blood cell phenotypes.

Yusuke Nakamura, Ming-Huei Chen, Rehan Qayyum, 2014, Human molecular genetics.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2010, Nature Genetics.

Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany

Kerstin Dietrich, Joachim Thiery, Andrew P Morris, 2010, European Journal of Human Genetics.

Meta-analysis of sex-specific genome-wide association studies

Andrew P Morris, Reedik Magi, A. Morris, 2010, Genetic epidemiology.

Genome‐Wide Association Scan Allowing for Epistasis in Type 2 Diabetes

Nicholas J Timpson, Andrew P Morris, Mark I McCarthy, 2011, Annals of human genetics.

Association between endometriosis and the interleukin 1A (IL1A) locus.

Yadav Sapkota, Mark McEvoy, Rodney J Scott, 2015, Human reproduction.

A flexible Bayesian framework for modeling haplotype association with disease, allowing for dominance effects of the underlying causative variants.

Andrew P Morris, A. Morris, A. Morris, 2006, American journal of human genetics.

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

Jie Huang, Inês Barroso, Tom R. Gaunt, 2017, American journal of human genetics.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2011, Nature Genetics.

Linkage disequilibrium mapping via cladistic analysis of phase-unknown genotypes and inferred haplotypes in the Genetic Analysis Workshop 14 simulated data

Andrew P Morris, Caroline Durrant, 2005, BMC Genetics.

Edinburgh Research Explorer Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies

Jean-François Dartigues, Reinhold Schmidt, Sudha Seshadri, 2022 .

Optimizing the Power of Genome-Wide Association Studies by Using Publicly Available Reference Samples to Expand the Control Group

Fredrik Nyberg, Andrew P Morris, Ansar Jawaid, 2010, Genetic epidemiology.

Examining the statistical properties of fine‐scale mapping in large‐scale association studies

Steven Wiltshire, Andrew P Morris, Eleftheria Zeggini, 2008, Genetic epidemiology.

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

Andrew P Morris, Xiayi Ke, Panos Deloukas, 2004, Human molecular genetics.

Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Christian Gieger, Jason Carey, Steven Wiltshire, 2016 .

Rapid Testing of Gene-Gene Interactions in Genome-Wide Association Studies of Binary and Quantitative Phenotypes

Andrew P Morris, Mark I McCarthy, K. Bhattacharya, 2011, Genetic epidemiology.

Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis

Christian Gieger, Sanghoon Moon, Tien Yin Wong, 2017, PLoS Medicine.

Multi-ethnic genome-wide association study identifies novel locus for type 2 diabetes susceptibility

Andrew P Morris, J. Cook, A. Morris, 2016, European Journal of Human Genetics.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Christian Gieger, Alex Doney, Inês Barroso, 2010, Nature Genetics.

A rare-variant test for high-dimensional data

Andrew P Morris, Jani Heikkinen, Reedik Mägi, 2017, European Journal of Human Genetics.

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.

Tom M Palmer, Debbie A Lawlor, Marie-France Hivert, 2016, JAMA.

Genetic dissection of a behavioral quantitative trait locus shows that Rgs2 modulates anxiety in mice

Andrew P Morris, Janice M. Fullerton, Jonathan Flint, 2004, Nature Genetics.

Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci

Tien Yin Wong, Abdul Basit, Philippe Froguel, 2011, Nature Genetics.

Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes.

Andrew P Morris, Panos Deloukas, Sarah Hunt, 2004, American journal of human genetics.

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Christian Gieger, Gonçalo Abecasis, He Gao, 2018, Nature Genetics.

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Thomas Meitinger, Pierre Fontanillas, Stefan Johansson, 2014, Nature Genetics.

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

Jiannis Ragoussis, Andrew P Morris, Jean Golding, 2008, The American journal of psychiatry.

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.

Fernando Pires Hartwig, Claude Bouchard, Christian Gieger, 2018, American journal of human genetics.

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants.

Jiannis Ragoussis, Andrew P Morris, Xiayi Ke, 2005, Genome research.

Guidance for the utility of linear models in meta-analysis of genetic association studies of binary phenotypes

Andrew P Morris, Anubha Mahajan, J. Cook, 2016, European Journal of Human Genetics.

Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis

Vilmundur Gudnason, Hiroto Hatabu, Andrew P Morris, 2019, bioRxiv.

Discovery and fine mapping of serum protein loci through transethnic meta-analysis.

Christian Gieger, Yusuke Nakamura, Luigi Ferrucci, 2012, American journal of human genetics.

Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

Jie Huang, Uwe Völker, Ming-Huei Chen, 2017, The Journal of clinical investigation.

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.

Xiaofeng Zhu, Todd L Edwards, Dana C Crawford, 2016, American journal of human genetics.

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Christian Gieger, Gonçalo Abecasis, He Gao, 2017, bioRxiv.

Pooling DNA in the identification of parents

Andrew P Morris, Robert N Curnow, 1998, Heredity.

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

He Zhang, Andres Metspalu, Fotios Drenos, 2016, Nature Genetics.

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

Claude Bouchard, Christian Gieger, Joel Eriksson, 2016, Nature communications.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Taesung Park, Christian Gieger, Tien Yin Wong, 2017, Scientific Data.

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets

Christian Gieger, Ingo Ruczinski, H Lester Kirchner, 2017, Nature Genetics.