Citation Impact
Citing Papers
The evolutionary history of human spindle genes includes back-and-forth gene flow with Neandertals
2022 StandoutNobel
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families
2009
Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis
2008
Probiotics and immunity
2009
Adrenal insufficiency
2014
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
2014 Standout
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
2009 Standout
Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline
2016 Standout
Inflammatory Bowel Disease
2009 Standout
Genetics of Type 1 Diabetes
2012
The X chromosome and immune associated genes
2011
Structural Basis for Recognizing Phosphoarginine and Evolving Residue-Specific Protein Phosphatases in Gram-Positive Bacteria
2013 StandoutNobel
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Type 2 diabetes
2017 Standout
Nasopharyngeal carcinoma
2015 Standout
Confirmation of HLA class II independent type 1 diabetes associations in the major histocompatibility complex including HLA‐B and HLA‐A
2009
Type 1 diabetes
2013 Standout
Targets of T Cell Responses to SARS-CoV-2 Coronavirus in Humans with COVID-19 Disease and Unexposed Individuals
2020 Standout
Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
2007 Nature
Variance component model to account for sample structure in genome-wide association studies
2010 Standout
Sex differences in immune responses
2016 Standout
Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21.3
2009
Regulatory T Cell-Specific Epigenomic Region Variants Are a Key Determinant of Susceptibility to Common Autoimmune Diseases
2020 StandoutNobel
Characterization of hNek6 Interactome Reveals an Important Role for Its Short N-Terminal Domain and Colocalization with Proteins at the Centrosome
2010
Tyrosine Phosphatase PTPN22: Multifunctional Regulator of Immune Signaling, Development, and Disease
2013
A Type 1 Diabetes Genetic Risk Score Can Aid Discrimination Between Type 1 and Type 2 Diabetes in Young Adults
2015
Effects of Probiotics, Prebiotics, and Synbiotics on Human Health
2017 Standout
The Effects of Animals on Human Health and Well‐Being
2009 Standout
Loss of the Protein Tyrosine Phosphatase PTPN22 Reduces Mannan-Induced Autoimmune Arthritis in SKG Mice
2016 StandoutNobel
Inflammatory Bowel Disease
2010 Standout
Sensitive detection of multiple islet autoantibodies in type 1 diabetes using small sample volumes by agglutination-PCR
2020 StandoutNobel
Mechanisms of Diabetic Complications
2013 Standout
Divergent Motifs but Overlapping Binding Repertoires of Six HLA-DQ Molecules Frequently Expressed in the Worldwide Human Population
2010
Management of adrenal incidentalomas: European Society of Endocrinology Clinical Practice Guideline in collaboration with the European Network for the Study of Adrenal Tumors
2016 Standout
Adrenal Steroidogenesis after B Lymphocyte Depletion Therapy in New-Onset Addison's Disease
2012
Human FoxP3+CD4+ regulatory T cells: their knowns and unknowns
2011 StandoutNobel
Impaired T cell receptor signaling and development of T cell–mediated autoimmune arthritis
2020 StandoutNobel
Works of Erin E. Baschal being referenced
The frequent and conserved DR3‐B8‐A1 extended haplotype confers less diabetes risk than other DR3 haplotypes
2009
The HLA-B*3906 allele imparts a high risk of diabetes only on specific HLA-DR/DQ haplotypes
2011
The fission yeast DNA structure checkpoint protein Rad26ATRIP/LCD1/UVSD accumulates in the cytoplasm following microtubule destabilization
2006
Extreme genetic risk for type 1A diabetes in the post-genome era
2008
Dominant Suppression of Addison's Disease Associated with HLA-B15
2011
rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype
2009
High Density SNP Analysis of the MHC Region Reveals Multiple Loci for Type 1A Diabetes
2007
Analysis of Single Nucleotide Polymorphisms Identifies Major Type 1A Diabetes Locus Telomeric of the Major Histocompatibility Complex
2007
Two Single Nucleotide Polymorphisms Identify the Highest-Risk Diabetes HLA Genotype
2008
Haplotype Analysis Discriminates Genetic Risk for DR3-Associated Endocrine Autoimmunity and Helps Define Extreme Risk for Addison’s Disease
2010
HLA-DPB1*0402 Protects Against Type 1A Diabetes Autoimmunity in the Highest Risk DR3-DQB1*0201/DR4-DQB1*0302 DAISY Population
2007