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Novel Association in Chromosome 4q27 Region with Rheumatoid Arthritis and Confirmation of Type 1 Diabetes Point to a General Risk Locus for Autoimmune Diseases

American journal of human genetics, 2007-12, Vol.81 (6), p.1284-1288

2007

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Possible Association Between Telomere Length and Renal Dysfunction in Patients With Chronic Heart Failure

The American journal of cardiology, 2008-07, Vol.102 (2), p.207-210

2008

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Level and course of FEV1 in relation to polymorphisms in NFE2L2 and KEAP1 in the general population

Respiratory research, 2009-08, Vol.10 (1), p.73-73, Article 73

2009

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Telomere Length of Circulating Leukocytes Is Decreased in Patients With Chronic Heart Failure

Journal of the American College of Cardiology, 2007-04, Vol.49 (13), p.1459-1464

2007

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Serum chemokine levels in Hodgkin lymphoma patients: highly increased levels of CCL17 and CCL22

British journal of haematology, 2008-03, Vol.140 (5), p.527-536

2008

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Influence of common variants near INSIG2, in FTO, and near MC4R genes on overweight and the metabolic profile in adolescence: the TRAILS (TRacking Adolescents' Individual Lives Survey) Study

The American journal of clinical nutrition, 2010-02, Vol.91 (2), p.321-328

2010

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Association between toll‐like receptor 4 and inflammatory bowel disease

Inflammatory bowel diseases, 2005-06, Vol.11 (6), p.567-575

2005

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Prothrombotic gene polymorphisms: possible contributors to hepatic artery thrombosis after orthotopic liver transplantation

Transplantation, 2011-09, Vol.92 (5), p.587-593

2011

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Variation in Bleomycin Hydrolase Gene Is Associated With Reduced Survival After Chemotherapy for Testicular Germ Cell Cancer

Journal of clinical oncology, 2008-04, Vol.26 (11), p.1817-1823

2008

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The Human Leukocyte Antigen Class I Region Is Associated with EBV-Positive Hodgkin's Lymphoma: HLA-A and HLA Complex Group 9 Are Putative Candidate Genes

Cancer epidemiology, biomarkers & prevention, 2006-11, Vol.15 (11), p.2280-2284

2006

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Haplotype Sharing Analysis Identifies a Retroviral dUTPase as Candidate Susceptibility Gene for Psoriasis

Journal of investigative dermatology, 2005-01, Vol.124 (1), p.99-102

2005

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Evaluation of the IRF-2 Gene as a Candidate for PSORS3

Journal of investigative dermatology, 2004-01, Vol.122 (1), p.61-64

2004

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No increased susceptibility to breast cancer from combined CHEK2 1100delC genotype and the HLA class III region risk factors

European journal of cancer (1990), 2005-08, Vol.41 (12), p.1819-1823

2005

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An Increased Coronary Risk Is Paradoxically Associated with Common Cholesteryl Ester Transfer Protein Gene Variations That Relate to Higher High-Density Lipoprotein Cholesterol: A Population-Based Study

The journal of clinical endocrinology and metabolism, 2006-09, Vol.91 (9), p.3382-3388

2006

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Deletion of a Cytoplasmic Domain of Integrin β4 Causes Epidermolysis Bullosa Simplex1

Journal of investigative dermatology, 2002-12, Vol.119 (6), p.1275-1281

2002

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Genetic susceptibility has a more important role in pediatric‐onset Crohn's disease than in adult‐onset Crohn's disease

Inflammatory bowel diseases, 2007-09, Vol.13 (9), p.1083-1092

2007

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The Effect of Cholesteryl Ester Transfer Protein −629C→A Promoter Polymorphism on High-Density Lipoprotein Cholesterol Is Dependent on Serum Triglycerides

The journal of clinical endocrinology and metabolism, 2005-07, Vol.90 (7), p.4198-4204

2005

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Association between donor MBL promoter haplotype and graft survival and the development of BOS after lung transplantation

Transplantation, 2008-12, Vol.86 (12), p.1857-1863

2008

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PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations

Human mutation, 2008-07, Vol.29 (7), p.939-947

2008

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Runt‐related transcription factor 3 is associated with ulcerative colitis and shows epistasis with solute carrier family 22, members 4 and 5

Inflammatory bowel diseases, 2008-12, Vol.14 (12), p.1615-1622

2008

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Deletion of a Cytoplasmic Domain of Integrin β4 Causes Epidermolysis Bullosa Simplex

Journal of investigative dermatology, 2002-12, Vol.119 (6), p.1275-1281

2002

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Influence of common variants near INSIG2, in FTO, and near MC4R genes on overweight and the metabolic profile in adolescence: the TRAILS (TRacking Adolescents’ Individual Lives Survey) Study123

The American journal of clinical nutrition, 2010-02, Vol.91 (2), p.321-328

2010

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The VEGF +405 CC Promoter Polymorphism is Associated With an Impaired Prognosis in Patients With Chronic Heart Failure: A MERIT-HF Substudy

Journal of cardiac failure, 2005-05, Vol.11 (4), p.279-284

2005

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Lack of association of C-C chemokine receptor 5 Δ32 deletion status with rheumatoid arthritis, systemic lupus erythematosus, lupus nephritis, and disease severity

Journal of rheumatology, 2010-11, Vol.37 (11), p.2226-2231

2010

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Methylenetetrahydrofolate reductase (MTHFR) and susceptibility for (pre)neoplastic cervical disease

Human genetics, 2005-03, Vol.116 (4), p.247-254

2005

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Novel Association in Chromosome 4q27 Region with Rheumatoid Arthritis and Confirmation of Type 1 Diabetes Point to a General Risk Locus for Autoimmune Diseases

Possible Association Between Telomere Length and Renal Dysfunction in Patients With Chronic Heart Failure

Level and course of FEV1 in relation to polymorphisms in NFE2L2 and KEAP1 in the general population

Telomere Length of Circulating Leukocytes Is Decreased in Patients With Chronic Heart Failure

Serum chemokine levels in Hodgkin lymphoma patients: highly increased levels of CCL17 and CCL22

Influence of common variants near INSIG2, in FTO, and near MC4R genes on overweight and the metabolic profile in adolescence: the TRAILS (TRacking Adolescents' Individual Lives Survey) Study

Association between toll‐like receptor 4 and inflammatory bowel disease

Prothrombotic gene polymorphisms: possible contributors to hepatic artery thrombosis after orthotopic liver transplantation

Variation in Bleomycin Hydrolase Gene Is Associated With Reduced Survival After Chemotherapy for Testicular Germ Cell Cancer

The Human Leukocyte Antigen Class I Region Is Associated with EBV-Positive Hodgkin's Lymphoma: HLA-A and HLA Complex Group 9 Are Putative Candidate Genes

Haplotype Sharing Analysis Identifies a Retroviral dUTPase as Candidate Susceptibility Gene for Psoriasis

Evaluation of the IRF-2 Gene as a Candidate for PSORS3

No increased susceptibility to breast cancer from combined CHEK2 1100delC genotype and the HLA class III region risk factors

An Increased Coronary Risk Is Paradoxically Associated with Common Cholesteryl Ester Transfer Protein Gene Variations That Relate to Higher High-Density Lipoprotein Cholesterol: A Population-Based Study

Deletion of a Cytoplasmic Domain of Integrin β4 Causes Epidermolysis Bullosa Simplex1

Genetic susceptibility has a more important role in pediatric‐onset Crohn's disease than in adult‐onset Crohn's disease

The Effect of Cholesteryl Ester Transfer Protein −629C→A Promoter Polymorphism on High-Density Lipoprotein Cholesterol Is Dependent on Serum Triglycerides

Association between donor MBL promoter haplotype and graft survival and the development of BOS after lung transplantation

PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations

Runt‐related transcription factor 3 is associated with ulcerative colitis and shows epistasis with solute carrier family 22, members 4 and 5

Deletion of a Cytoplasmic Domain of Integrin β4 Causes Epidermolysis Bullosa Simplex

Influence of common variants near INSIG2, in FTO, and near MC4R genes on overweight and the metabolic profile in adolescence: the TRAILS (TRacking Adolescents’ Individual Lives Survey) Study123

The VEGF +405 CC Promoter Polymorphism is Associated With an Impaired Prognosis in Patients With Chronic Heart Failure: A MERIT-HF Substudy

Lack of association of C-C chemokine receptor 5 Δ32 deletion status with rheumatoid arthritis, systemic lupus erythematosus, lupus nephritis, and disease severity

Methylenetetrahydrofolate reductase (MTHFR) and susceptibility for (pre)neoplastic cervical disease

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