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The MHC2TA –168A/G polymorphism and risk for rheumatoid arthritis: a meta-analysis of 6861 patients and 9270 controls reveals no evidence for association

Annals of the rheumatic diseases, 2008-07, Vol.67 (7), p.933-936

2008

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Analysis of maternal-offspring HLA compatibility, parent-of-origin and non-inherited maternal effects for the classical HLA loci in type 1 diabetes

Diabetes, obesity & metabolism, 2009-02, Vol.11 (s1), p.74-83

2009

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Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer’s disease

Journal of medical genetics, 2005-10, Vol.42 (10), p.787-792

2005

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Linkage and Association Study of Late‐Onset Alzheimer Disease Families Linked to 9p21.3

Annals of human genetics, 2008-11, Vol.72 (6), p.725-731

2008

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Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease

Neurology, 2006-07, Vol.67 (1), p.64

2006

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Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

Nature genetics, 2016-11, Vol.48 (11), p.1425-1429

2016

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Lack of association between UBQLN1 and Alzheimer disease

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2006-04, Vol.141B (3), p.208-213

2006

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A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis

Genes and immunity, 2010-09, Vol.11 (6), p.504-508

2010

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The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus

Genes and immunity, 2011-12, Vol.12 (8), p.667-671

2011

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CIITA is not associated with risk of developing rheumatoid arthritis

Genes and immunity, 2011-04, Vol.12 (3), p.235-238

2011

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A sequence-based approach demonstrates that balancing selection in classical human leukocyte antigen (HLA) loci is asymmetric

Human molecular genetics, 2013-01, Vol.22 (2), p.252-261

2013

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STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency

Frontiers in genetics, 2021-12, Vol.12, p.736235-736235

2021

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Interaction between the -T catenin gene (VR22) and APOE in Alzheimer's disease

Journal of medical genetics, 2005-10, Vol.42 (10), p.787-792

Martin, E R

2005

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SELECTIVE IMMUNOGLOBULIN A DEFICIENCY IS ASSOCIATED WITH IFIH1, PVT1, FAS, CDH13 AND KIF3 IN A GENOMEWIDE ASSOCIATION STUDY AND META-ANALYSIS

TISSUE ANTIGENS, 2012, Vol.79 (6), p.413

2012

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Full Study Report of Andexanet Alfa for Bleeding Associated with Factor Xa Inhibitors

The New England journal of medicine, 2019-04, Vol.380 (14), p.1326-1335

2019

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The Global Burden of Esophageal Cancer: A Disability-Adjusted Life-Year Approach

World journal of surgery, 2016-02, Vol.40 (2), p.395-401

2016

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Phosphorylation of ETS1 by Src Family Kinases Prevents Its Recognition by the COP1 Tumor Suppressor

Cancer cell, 2014-08, Vol.26 (2), p.222-234

2014

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Mice mutant for Egfr and Shp2 have defective cardiac semilunar valvulogenesis

Nature genetics, 2000-03, Vol.24 (3), p.296-299

2000

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A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica

Nature communications, 2018-05, Vol.9 (1), p.1929-10, Article 1929

2018

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Loss of the retinoblastoma binding protein 2 (RBP2) histone demethylase suppresses tumorigenesis in mice lacking Rb1 or Men1

Proceedings of the National Academy of Sciences - PNAS, 2011-08, Vol.108 (33), p.13379-13386

2011

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Neurology-related protein biomarkers are associated with cognitive ability and brain volume in older age

Nature communications, 2020-02, Vol.11 (1), p.800-800, Article 800

2020

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A spatially and temporally restricted mouse model of soft tissue sarcoma

Nature medicine, 2007-08, Vol.13 (7), p.992-997

2007

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BRG1 Loss Predisposes Lung Cancers to Replicative Stress and ATR Dependency

Cancer research (Chicago, Ill.), 2020-09, Vol.80 (18), p.3841-3854

2020

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Mutational landscape of EGFR-, MYC-, and Kras-driven genetically engineered mouse models of lung adenocarcinoma

Proceedings of the National Academy of Sciences - PNAS, 2016-10, Vol.113 (42), p.E6409-E6417

2016

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Pyruvate Kinase M1 Suppresses Development and Progression of Prostate Adenocarcinoma

Cancer research (Chicago, Ill.), 2022-07, Vol.82 (13), p.2403-2416

2022

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The MHC2TA –168A/G polymorphism and risk for rheumatoid arthritis: a meta-analysis of 6861 patients and 9270 controls reveals no evidence for association

Analysis of maternal-offspring HLA compatibility, parent-of-origin and non-inherited maternal effects for the classical HLA loci in type 1 diabetes

Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer’s disease

Linkage and Association Study of Late‐Onset Alzheimer Disease Families Linked to 9p21.3

Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease

Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

Lack of association between UBQLN1 and Alzheimer disease

A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis

The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus

CIITA is not associated with risk of developing rheumatoid arthritis

A sequence-based approach demonstrates that balancing selection in classical human leukocyte antigen (HLA) loci is asymmetric

STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency

Interaction between the -T catenin gene (VR22) and APOE in Alzheimer's disease

SELECTIVE IMMUNOGLOBULIN A DEFICIENCY IS ASSOCIATED WITH IFIH1, PVT1, FAS, CDH13 AND KIF3 IN A GENOMEWIDE ASSOCIATION STUDY AND META-ANALYSIS

Full Study Report of Andexanet Alfa for Bleeding Associated with Factor Xa Inhibitors

The Global Burden of Esophageal Cancer: A Disability-Adjusted Life-Year Approach

Phosphorylation of ETS1 by Src Family Kinases Prevents Its Recognition by the COP1 Tumor Suppressor

Mice mutant for Egfr and Shp2 have defective cardiac semilunar valvulogenesis

A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica

Loss of the retinoblastoma binding protein 2 (RBP2) histone demethylase suppresses tumorigenesis in mice lacking Rb1 or Men1

Neurology-related protein biomarkers are associated with cognitive ability and brain volume in older age

A spatially and temporally restricted mouse model of soft tissue sarcoma

BRG1 Loss Predisposes Lung Cancers to Replicative Stress and ATR Dependency

Mutational landscape of EGFR-, MYC-, and Kras-driven genetically engineered mouse models of lung adenocarcinoma

Pyruvate Kinase M1 Suppresses Development and Progression of Prostate Adenocarcinoma

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