Sarah Hunt

发表

Transitioning Resolution Responsibility Between the Controller and Automation Team in Simulated NextGen Separation Assurance

Lynne Martin, Thomas Prevot, Joey Mercer, 2014 .

The value of primary transcripts to the clinical and non-clinical genomics community: survey results and roadmap for improvements.

Jane Loveland, Aoife McMahon, Joannella Morales, 2021 .

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

Matti Pirinen, Peter Donnelly, Robert Plomin, 2014, Nature Communications.

Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease

Alastair Forbes, Carlo Berzuini, Lon Cardon, 2008, Nature Genetics.

A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.

Stephan Beck, Xiayi Ke, Panos Deloukas, 2005, American journal of human genetics.

Population-Specific Risk of Type 2 Diabetes Conferred by HNF4A P2 Promoter Variants

Inês Barroso, Mark I. McCarthy, Mark Walker, 2008, Diabetes.

Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps

Andrew Collins, Panos Deloukas, William J Tapper, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21

Matti Pirinen, Peter Donnelly, Robert Plomin, 2010, Human molecular genetics.

Complete MHC haplotype sequencing for common disease gene mapping.

Sophie Palmer, Stephan Beck, Ian Dunham, 2004, Genome research.

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

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

The Influence of Recombination on Human Genetic Diversity

Peter Donnelly, Gil McVean, Simon Myers, 2006, PLoS genetics.

A re-examination of proximodistal patterning during vertebrate limb development

Lon R. Cardon, Andres Metspalu, Jaak Vilo, 2022 .

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Sarah Edkins, Cisca Wijmenga, Lude Franke, 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.

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

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

Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

Tariq Ahmad, Sarah Edkins, Christopher G Mathew, 2011, Nature Genetics.

Population-specific risk of type 2 diabetes ( T 2 D ) conferred by HNF 4 A P 2 promoter variants : a lesson for replication studies

Inês Barroso, Mark Walker, Panagiotis Deloukas, 2008 .

A comparison of tagging methods and their tagging space.

John Broxholme, Xiayi Ke, Panos Deloukas, 2005, Human molecular genetics.

Variants in MTNR1B influence fasting glucose levels

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

Edinburgh Research Explorer Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Peter Donnelly, Robert Plomin, Elvira Bramon, 2022 .