نتائج البحث

Replication of the BANK1 genetic association with systemic lupus erythematosus in a European-derived population.

• Authors : Guo, L.^1,2; Deshmukh, H.¹; Lu, R.³

• Source: Genes & Immunity. Jul2009, Vol. 10 Issue 5, p531-538. 8p. 1 Diagram, 6 Charts.

تفاصيل العنوان

Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent.

• Authors : Lucas SEM; Menzies Institute for Medical Research, University of Tasmania, Hobart, Tasmania, Australia.; Zhou T

Subjects: Genetic Association Studies* ; Polymorphism, Single Nucleotide*; Keratoconus/Keratoconus/Keratoconus/*genetics

• Source: PloS one [PLoS One] 2018 Jun 20; Vol. 13 (6), pp. e0199178. Date of Electronic Publication: 2018 Jun 20 (Print Publication: 2018).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

تفاصيل العنوان

Novel quantitative pigmentation phenotyping enhances genetic association, epistasis, and prediction of human eye colour.

• Authors : Wollstein A; Department of Genetic Identification, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.

Subjects: Epistasis, Genetic*; Eye Color/Eye Color/Eye Color/*genetics ; Eye Proteins/Eye Proteins/Eye Proteins/*genetics Down Syndrome Critical Region

• Source: Scientific reports [Sci Rep] 2017 Feb 27; Vol. 7, pp. 43359. Date of Electronic Publication: 2017 Feb 27.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

Genotype-phenotype correlation identified a novel SARS-CoV-2 variant possibly linked to severe disease.

• Authors : Loney T; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.; Khansaheb H

Subjects: COVID-19*/COVID-19*/COVID-19*/epidemiology ; COVID-19*/COVID-19*/COVID-19*/veterinary ; SARS-CoV-2*/SARS-CoV-2*/SARS-CoV-2*/geneticsSARS-CoV-2 variants

• Source: Transboundary and emerging diseases [Transbound Emerg Dis] 2022 Mar; Vol. 69 (2), pp. 465-476. Date of Electronic Publication: 2021 Feb 21.Publisher: Blackwell Verlag Country of Publication: Germany NLM ID: 101319538 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the gene.

• Authors : Löfgren SE; Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.; Frostegård J

Subjects: Gene Expression Regulation* ; Genetic Predisposition to Disease*; Lupus Erythematosus, Systemic/Lupus Erythematosus, Systemic/Lupus Erythematosus, Systemic/*genetics

• Source: Genes and immunity [Genes Immun] 2012 Apr; Vol. 13 (3), pp. 268-74. Date of Electronic Publication: 2012 Jan 05.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 100953417 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

A screening methodology based on Random Forests to improve the detection of gene-gene interactions.

• Authors : De Lobel L; Department of Applied Mathematics and Computer Science, Ghent University, Ghent, Belgium. ; Geurts P

Subjects: Decision Trees* ; Epistasis, Genetic* ; Genetic Association Studies*

• Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2010 Oct; Vol. 18 (10), pp. 1127-32. Date of Electronic Publication: 2010 May 12.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان

Polymorphisms in fatty-acid-metabolism-related genes are associated with colorectal cancer risk.

• Authors : Hoeft B; German Cancer Research Center, Heidelberg, Germany.; Linseisen J

Subjects: Genetic Association Studies* ; Polymorphism, Single Nucleotide*; Adenocarcinoma/Adenocarcinoma/Adenocarcinoma/*genetics

• Source: Carcinogenesis [Carcinogenesis] 2010 Mar; Vol. 31 (3), pp. 466-72. Date of Electronic Publication: 2009 Dec 30.Publisher: Irl Press At Oxford University Press Country of Publication: England NLM ID: 8008055 Publication Model: Print-Electronic Cited Medium:

تفاصيل العنوان

Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study.

• Authors : Massat I; Department of Psychiatry, University Clinics of Brussels, Erasme Hospital, Free University of Brussels, Belgium. ; Souery D

Subjects: Bipolar Disorder/Bipolar Disorder/Bipolar Disorder/*genetics ; Catechol O-Methyltransferase/Catechol O-Methyltransferase/Catechol O-Methyltransferase/*genetics ; Depressive Disorder, Major/Depressive Disorder, Major/Depressive Disorder, Major/*genetics

• Source: Molecular psychiatry [Mol Psychiatry] 2005 Jun; Vol. 10 (6), pp. 598-605.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print

تفاصيل العنوان

APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups.

• Authors : Goyal S; Department of Pediatrics, College of Medicine, University of Oklahoma Health Sciences Center, 940 Stanton L. Young Blvd., Rm 317 BMSB, Oklahoma City, OK, 73104, USA.; Tanigawa Y

Subjects: Genetic Variation*; Apolipoprotein C-III/Apolipoprotein C-III/Apolipoprotein C-III/*genetics ; Coronary Artery Disease/Coronary Artery Disease/Coronary Artery Disease/*genetics

• Source: Lipids in health and disease [Lipids Health Dis] 2021 Sep 21; Vol. 20 (1), pp. 113. Date of Electronic Publication: 2021 Sep 21.Publisher: BioMed Central Country of Publication: England NLM ID: 101147696 Publication Model: Electronic Cited Medium: Internet ISSN: 1476-511X

تفاصيل العنوان

Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from Taiwan.

• Authors : Tsai MT; Department of Psychiatry, Tzu-Chi General Hospital, Hualien City, Taiwan.; Shaw CK

Subjects: Polymorphism, Genetic* ; Potassium Channels, Calcium-Activated* ; Trinucleotide Repeats*

• Source: Molecular psychiatry [Mol Psychiatry] 1999 May; Vol. 4 (3), pp. 271-3.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print

تفاصيل العنوان