O. Mccann

发表

Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

M. Pirinen, P. Donnelly, C. Spencer, 2019, Nature Communications.

The DNA sequence and analysis of human chromosome 6

I. Dunham, J. L. Ashurst, D. R. Bentley, 2003, Nature.

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility

Simon C. Potter, Till F. M. Andlauer, M. Pirinen, 2019, Science.

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Matti Pirinen, Christian Gieger, Peter Donnelly, 2012 .

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Simon C. Potter, Joseph T. Glessner, M. Pirinen, 2011, Nature.

Corrigendum: Multiple common variants for celiac disease influencing immune gene expression

P. Deloukas, R. Ophoff, L. Peltonen, 2010, Nature Genetics.

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

P. Donnelly, C. Spencer, C. Freeman, 2010 .

A physical map of the human genome

D. Haussler, B. Trask, R. Wilson, 2001, Nature.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

Simon C. Potter, M. Pirinen, P. Donnelly, 2017, Translational Psychiatry.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Multiple common variants for celiac disease influencing immune gene expression

P. Deloukas, R. Ophoff, L. Peltonen, 2010, Nature Genetics.

Genome-wide Association Analysis Identifies 14 New Risk Loci for Schizophrenia

Simon C. Potter, M. Pirinen, P. Donnelly, 2013, Nature Genetics.

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Paul Weston, Robert Plomin, Elvira Bramon, 2011, Nature Genetics.

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes 1 2 Primary

John P. Rice, Melissa J. Green, Robert C. Thompson, 2018 .

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

The DNA sequence of human chromosome 22

Melanie E. Goward, Antony V. Cox, R. Durbin, 1999, Nature.

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X

P. Deloukas, R. Durbin, J. Sulston, 2001, Nature.

Variants in MTNR1B influence fasting glucose levels

Inês Barroso, Paul Scheet, Nicole Soranzo, 2009, Nature Genetics.

A polygenic resilience score moderates the genetic risk for schizophrenia

M. Pirinen, P. Donnelly, C. Spencer, 2019, Molecular Psychiatry.

Finishing the finished human chromosome 22 sequence

Fengtang Yang, D. Willey, C. Cole, 2008, Genome Biology.

Erratum: Replication timing of the human genome (Human Molecular Genetics) (2004) vol. 13 (191-202))

David Beare, Ian Dunham, Nigel P. Carter, 2004 .

Replication timing of the human genome.

Owen T McCann, Ian Dunham, Richard Mott, 2004, Human molecular genetics.

Complement genes contribute sex-biased vulnerability in diverse illnesses

Simon C. Potter, Christopher W. Whelan, M. Pirinen, 2020, Nature.

Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains.

Owen T McCann, Huriya Beyan, Siarhei Maslau, 2010, Genome research.

Using genome-wide complex trait analysis to quantify ‘ missing heritability ’ in Parkinson ’ s disease

Simon C. Potter, M. Pirinen, P. Deloukas, 2012 .

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

Matti Pirinen, David M. Herrington, Alex Doney, 2014, Nature Communications.

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

Adriana I. Iglesias, M. Pirinen, P. Donnelly, 2014, Nature Communications.

Complement genes contribute sex-biased vulnerability in diverse disorders

Christopher W. Whelan, M. Pirinen, C. Spencer, 2020, Nature.

Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease

Simon C. Potter, M. Pirinen, C. Spencer, 2016, npj Genomic Medicine.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.

John P. Rice, Simon C. Potter, Melissa J. Green, 2018, Cell.

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

Simon C. Potter, P. Donnelly, C. Spencer, 2009, Nature Genetics.

DNA sequence and analysis of human chromosome 9

I. Dunham, J. L. Ashurst, D. R. Bentley, 2003, Nature.

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Simon C. Potter, Adriana I. Iglesias, M. Pirinen, 2018, Nature Communications.

A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility

Simon C. Potter, M. Pirinen, P. Donnelly, 2014, Genes and Immunity.

Replication timing of the human genome.

N. Carter, H. Fiegler, R. Mott, 2004, Human molecular genetics.

Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains.

T. Spector, P. Whittaker, T. Down, 2010, Genome research.