A. Dominiczak

发表

The UK10K project identifies rare variants in health and disease

Tom R. Gaunt, Hashem A. Shihab, Gail P. Clement, 2016 .

Implementation of proteomic biomarkers: making it work PERSPECTIVE

M. Manns, A. Vlahou, T. Attwood, 2012 .

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data

G. J. Swaminathan, N. Carter, M. Hurles, 2019, American journal of human genetics.

Copy number variation in the human Y chromosome in the UK population

Tomas W. Fitzgerald, C. Tyler-Smith, M. Hurles, 2015, Human Genetics.

Using ancestry-informative markers to identify fine structure across 15 populations of European origin

Graham M Lord, Günter P. Wagner, I. Ntalla, 2014, European Journal of Human Genetics.

Systems Medicine 2.0: Potential Benefits of Combining Electronic Health Care Records With Systems Science Models

T. Tillmann, O. Harrison, P. Hanlon, 2015, Journal of medical Internet research.

Dominance is common in mammals and is associated with trans-acting gene expression and alternative splicing

R. Mott, N. Hübner, M. McBride, 2023, bioRxiv.

The UK10K project identifies rare variants in health and disease

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2015, Nature.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

P. Donnelly, C. Spencer, A. Silman, 2007, Nature genetics.

Edinburgh Research Explorer Genome Sequencing Reveals Loci under Artificial Selection That Underlie Disease Phenotypes in the Laboratory Rat Genome Sequencing Reveals Loci under Artificial Selection That Underlie Disease Phenotypes in the Laboratory Rat

Thomas M. Keane, E. Petretto, D. Gauguier, 2022 .

Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression

D. Macintyre, P. Thomson, A. Simen, 2012, Front. Gene..

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

P. Donnelly, C. Spencer, A. Silman, 2007, Nature Genetics.

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Simon C. Potter, David M. Evans, P. Donnelly, 2007, Nature Genetics.

Copy number variation in the human Y chromosome in the UK population

Tomas W. Fitzgerald, C. Tyler-Smith, M. Hurles, 2015, Human Genetics.

Swab pooling enables rapid expansion of high-throughput capacity for SARS-CoV-2 community testing.

M. Futschik, P. Klapper, M. Sudhanva, 2023, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations

C. Gieger, M. Perola, M. Mangino, 2009, PLoS genetics.

Genome-wide association analysis identifies 20 loci that influence adult height

David M. Evans, M. McCarthy, J. Beckmann, 2008, Nature Genetics.

Genome-wide association analysis identifies 20 loci that influence adult height

P. Munroe, M. Caulfield, M. Farrall, 2008, Nature Genetics.