Sarah Nutland

发表

The Impact of NOD2 Variants on Fecal Microbiota in Crohn’s Disease and Controls Without Gastrointestinal Disease

Julian Parkhill, Alan W Walker, Miles Parkes, 2018, Inflammatory bowel diseases.

The serotonin transporter gene polymorphism and the effect of baseline on amygdala response to emotional faces

Luca Passamonti, Andrew J. Calder, S. Nutland, 2011, Neuropsychologia.

Haplotype tagging for the identification of common disease genes

Frank Dudbridge, John A. Todd, Heather J. Cordell, 2001, Nature Genetics.

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

Sarah Edkins, Cisca Wijmenga, Lude Franke, 2011, Nature Genetics.

Haplotype structure, LD blocks, and uneven recombination within the LRP5 gene.

Riitta Veijola, Heather J Cordell, John A Todd, 2003, Genome research.

Parameters for reliable results in genetic association studies in common disease

John A. Todd, Francesco Cucca, Heather J. Cordell, 2002, Nature Genetics.

Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus.

Adrian Vella, Cristian Guja, Susan M Ring, 2004, Diabetes.

Localization of a type 1 diabetes locus in the IL2RA/CD25 region by use of tag single-nucleotide polymorphisms.

Adrian Vella, Wendy McArdle, Susan M Ring, 2005, American journal of human genetics.

Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene.

Sergey Nejentsev, Constantin Ionescu-Tirgoviste, Jaakko Tuomilehto, 2004, Human molecular genetics.

The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes

John A. Todd, Francesco Cucca, Jaakko Tuomilehto, 2000, Nature Genetics.

Type 1 Diabetes-Associated IL2RA Variation Lowers IL-2 Signaling and Contributes to Diminished CD4+CD25+ Regulatory T Cell Function

Linda S. Wicker, John A. Todd, Garima Garg, 2012, The Journal of Immunology.

Development of an integrated genome informatics, data management and workflow infrastructure: A toolbox for the study of complex disease genetics

Helen Schuilenburg, Vincent H. Everett, Neil M Walker, 2004, Human Genomics.

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.

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

Luc J. Smink, Neil M. Walker, Linda S. Wicker, 2003, Nature.

Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource

Matthew Hardy, Nicholas J Wareham, Erik Fung, 2009, Nature Genetics.