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Variants in 3p24.3 predicts the risk of early neurological deterioration in large artery atherosclerotic stroke

Brain research, 2024-06, Vol.1833, p.148867-148867, Article 148867

2024

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Effects of Ninjurin 2 polymorphisms on susceptibility to coronary heart disease

Cell cycle (Georgetown, Tex.), 2024-02, Vol.23 (3), p.328-337

2024

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The relationship between preeclampsia risk and SENCR rs555172 gene polymorphism and expression

Cellular and molecular biology (Noisy-le-Grand, France), 2024-03, Vol.70 (3), p.78

2024

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Association of adiponectin and its receptor gene polymorphisms with the risk of coronary heart disease in northern Guangxi

Cytokine (Philadelphia, Pa.), 2024-06, Vol.178, p.156567-156567, Article 156567

2024

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Gene Association Study of the Urokinase Plasminogen Activator and Its Receptor Gene in Alzheimer's Disease

Journal of Alzheimer's disease, 2024, Vol.99 (1), p.241

2024

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EGR3 Polymorphism Is a Potential Susceptibility Factor of Schizophrenia Risk in a Chinese Population

Genetic testing and molecular biomarkers, 2024-04, Vol.28 (4), p.144

2024

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Association between Interleukin-6 Gene Polymorphism (rs1800795 and rs1800796) and Type 2 Diabetes Mellitus in a Ghanaian Population: A Case-Control Study in the Ho Municipality

BioMed research international, 2024, Vol.2024, p.3610879-3610879

2024

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TBX5 genetic variants and SCD-CAD susceptibility: insights from Chinese Han cohorts

PeerJ (San Francisco, CA), 2024, Vol.12, p.e17139-e17139

2024

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Association between Polymorphisms of Heat Shock Protein HSPA5 and Risk of Type 2 Diabetes Mellitus

Bulletin of experimental biology and medicine, 2024-03, Vol.176 (5), p.599-602

2024

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Polymorphism of Transforming Growth Factor TGFB and Its Receptors TGFBRI, TGFBRII, TGFBRIIII Genes in Western Siberia Patients with Open-Angle Glaucoma

Bulletin of experimental biology and medicine, 2024-03, Vol.176 (5), p.603-606

2024

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Relationship between XPA , XPB/ERCC3 , XPF/ERCC4 , and XPG/ERCC5 Polymorphisms and the Susceptibility to Head and Neck Carcinoma: A Systematic Review, Meta-Analysis, and Trial Sequential Analysis

Medicina (Kaunas, Lithuania), 2024-03, Vol.60 (3), p.478

2024

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IGF2BP2 and IGFBP3 Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome

Journal of clinical laboratory analysis, 2024-03, Vol.38 (5), p.e25021-n/a

2024

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The Role of DNA Repair ( XPC , XPD , XPF , and XPG) Gene Polymorphisms in the Development of Myeloproliferative Neoplasms

Medicina (Kaunas, Lithuania), 2024-03, Vol.60 (3), p.506

2024

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Genetic variants of ANRIL and coronary artery disease: Insights from a Turkish study population

Gene, 2024-07, Vol.917, p.148475-148475, Article 148475

2024

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Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study

Investigative ophthalmology & visual science, 2024-05, Vol.65 (5), p.29-29

2024

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Investigation of HLA susceptibility alleles and genotypes with hematological disease among Chinese Han population

PloS one, 2024-04, Vol.19 (4), p.e0281698-e0281698

2024

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Epistasis Between HLA-DRB116:02:01 and SLC16A11 T-C-G-T-T Reduces Odds for Type 2 Diabetes in Southwest American Indians

Diabetes (New York, N.Y.), 2024-06, Vol.73 (6), p.1002

2024

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Effects of Glutathione S-Transferases (GSTM1, GSTT1 and GSTP1) gene variants in combination with smoking or drinking on cancers: A meta-analysis

Medicine (Baltimore), 2024-04, Vol.103 (14), p.e37707-e37707

2024

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Associations of the obesity gene FTO variant with complications and comorbidities in patients with type 1 diabetes

Diabetes research and clinical practice, 2024-05, Vol.211, p.111683-111683, Article 111683

2024

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Cerebral visual impairment: genetic diagnoses and phenotypic associations

Journal of medical genetics, 2024-05, Vol.61 (6), p.605

2024

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Genetic variant rs1205 is associated with COVID-19 outcomes: The Strong Heart Study and Strong Heart Family Study

PloS one, 2024-04, Vol.19 (4), p.e0302464-e0302464

2024

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Association of tuberculosis risk with genetic polymorphisms of the immune checkpoint genes PDCD1, CTLA-4, and TIM3

PloS one, 2024-05, Vol.19 (5), p.e0303431-e0303431

2024

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SNP-SNP positive interaction between MMP2 and MMP12 increases the risk of COPD

PloS one, 2024-05, Vol.19 (5), p.e0301807-e0301807

2024

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PNPLA3 fatty liver allele was fixed in Neanderthals and segregates neutrally in humans

Gut, 2024-05, Vol.73 (6), p.1008

2024

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RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses

Variants in 3p24.3 predicts the risk of early neurological deterioration in large artery atherosclerotic stroke

Effects of Ninjurin 2 polymorphisms on susceptibility to coronary heart disease

The relationship between preeclampsia risk and SENCR rs555172 gene polymorphism and expression

Association of adiponectin and its receptor gene polymorphisms with the risk of coronary heart disease in northern Guangxi

Gene Association Study of the Urokinase Plasminogen Activator and Its Receptor Gene in Alzheimer's Disease

EGR3 Polymorphism Is a Potential Susceptibility Factor of Schizophrenia Risk in a Chinese Population

Association between Interleukin-6 Gene Polymorphism (rs1800795 and rs1800796) and Type 2 Diabetes Mellitus in a Ghanaian Population: A Case-Control Study in the Ho Municipality

TBX5 genetic variants and SCD-CAD susceptibility: insights from Chinese Han cohorts

Association between Polymorphisms of Heat Shock Protein HSPA5 and Risk of Type 2 Diabetes Mellitus

Polymorphism of Transforming Growth Factor TGFB and Its Receptors TGFBRI, TGFBRII, TGFBRIIII Genes in Western Siberia Patients with Open-Angle Glaucoma

Relationship between XPA , XPB/ERCC3 , XPF/ERCC4 , and XPG/ERCC5 Polymorphisms and the Susceptibility to Head and Neck Carcinoma: A Systematic Review, Meta-Analysis, and Trial Sequential Analysis

IGF2BP2 and IGFBP3 Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome

The Role of DNA Repair ( XPC , XPD , XPF , and XPG) Gene Polymorphisms in the Development of Myeloproliferative Neoplasms

Genetic variants of ANRIL and coronary artery disease: Insights from a Turkish study population

Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study

Investigation of HLA susceptibility alleles and genotypes with hematological disease among Chinese Han population

Epistasis Between HLA-DRB116:02:01 and SLC16A11 T-C-G-T-T Reduces Odds for Type 2 Diabetes in Southwest American Indians

Effects of Glutathione S-Transferases (GSTM1, GSTT1 and GSTP1) gene variants in combination with smoking or drinking on cancers: A meta-analysis

Associations of the obesity gene FTO variant with complications and comorbidities in patients with type 1 diabetes

Cerebral visual impairment: genetic diagnoses and phenotypic associations

Genetic variant rs1205 is associated with COVID-19 outcomes: The Strong Heart Study and Strong Heart Family Study

Association of tuberculosis risk with genetic polymorphisms of the immune checkpoint genes PDCD1, CTLA-4, and TIM3

SNP-SNP positive interaction between MMP2 and MMP12 increases the risk of COPD

PNPLA3 fatty liver allele was fixed in Neanderthals and segregates neutrally in humans

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