Found: 40
Select item for more details and to access through your institution.
Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.
- Published in:
- Journal of Personalized Medicine, 2018, v. 8, n. 1, p. 2, doi. 10.3390/jpm8010002
- By:
- Publication type:
- Article
Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34456-6
- By:
- Publication type:
- Article
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization.
- Published in:
- World Journal of Surgery, 2020, v. 44, n. 1, p. 84, doi. 10.1007/s00268-019-05202-9
- By:
- Publication type:
- Article
A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies.
- Published in:
- 2020
- By:
- Publication type:
- journal article
A metadata framework for computational phenotypes.
- Published in:
- JAMIA Open, 2023, v. 6, n. 2, p. 1, doi. 10.1093/jamiaopen/ooad032
- By:
- Publication type:
- Article
Patients with Proliferative Lupus Nephritis Have Autoantibodies That React to Moesin and Demonstrate Increased Glomerular Moesin Expression.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 4, p. 793, doi. 10.3390/jcm10040793
- By:
- Publication type:
- Article
Lupus enhancer risk variant causes dysregulation of IRF8 through cooperative lncRNA and DNA methylation machinery.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29514-y
- By:
- Publication type:
- Article
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 204, doi. 10.1038/ng.81
- By:
- Publication type:
- Article
Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41057-4
- By:
- Publication type:
- Article
A GWAS Study on Liver Function Test Using eMERGE Network Participants.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138677
- By:
- Publication type:
- Article
The Effect of Inversion at 8p23 on BLK Association with Lupus in Caucasian Population.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0115614
- By:
- Publication type:
- Article
PTPN22 Association in Systemic Lupus Erythematosus (SLE) with Respect to Individual Ancestry and Clinical Sub-Phenotypes.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0069404
- By:
- Publication type:
- Article
Osteopontin and Systemic Lupus Erythematosus Association: A Probable Gene-Gender Interaction.
- Published in:
- PLoS ONE, 2008, v. 3, n. 3, p. 1, doi. 10.1371/journal.pone.0001757
- By:
- Publication type:
- Article
Identification of Four Novel Loci in Asthma in European American and African American Populations.
- Published in:
- 2017
- By:
- Publication type:
- journal article
SLEB3 in systemic lupus erythematosus (SLE) is strongly related to SLE families ascertained through neuropsychiatric manifestations.
- Published in:
- Human Genetics, 2002, v. 111, n. 1, p. 54, doi. 10.1007/s00439-002-0743-1
- By:
- Publication type:
- Article
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR.
- Published in:
- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0078-7
- By:
- Publication type:
- Article
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR.
- Published in:
- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0078-7
- By:
- Publication type:
- Article
47 Cross-ancestry GWAS meta-analysis of keloids discovers novel susceptibility loci in diverse populations.
- Published in:
- 2024
- By:
- Publication type:
- Abstract
Imputation and quality control steps for combining multiple genome-wide datasets.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00370
- By:
- Publication type:
- Article
Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00401
- By:
- Publication type:
- Article
Systemic lupus erythematosus (SLE) and chromosome 16: confirmation of linkage to 16q12-13 and evidence for genetic heterogeneity.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 8, p. 668, doi. 10.1038/sj.ejhg.5201209
- By:
- Publication type:
- Article
Systemic lupus erythematosus (SLE) and chromosome 16: confirmation of linkage to 16q12-13 and evidence for genetic heterogeneity.
- Published in:
- 2004
- By:
- Publication type:
- Correction Notice
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.
- Published in:
- 2019
- By:
- Publication type:
- journal article
The Lupus Family Registry and Repository.
- Published in:
- Rheumatology, 2011, v. 50, n. 1, p. 47, doi. 10.1093/rheumatology/keq302
- By:
- Publication type:
- Article
A plausibly causal functional lupus-associated risk variant in the STAT1-STAT4 locus.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 13, p. 2392, doi. 10.1093/hmg/ddy140
- By:
- Publication type:
- Article
The IRF5–TNPO3 association with systemic lupus erythematosus has two components that other autoimmune disorders variably share.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 2, p. 582, doi. 10.1093/hmg/ddu455
- By:
- Publication type:
- Article
Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder.
- Published in:
- PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0159621
- By:
- Publication type:
- Article
A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes.
- Published in:
- JAMA Network Open, 2021, v. 4, n. 6, p. e2112820, doi. 10.1001/jamanetworkopen.2021.12820
- By:
- Publication type:
- Article
Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome‐Wide Association Study and Inverse Variance–Weighted Meta‐Analysis.
- Published in:
- Arthritis & Rheumatology, 2020, v. 72, n. 9, p. 1483, doi. 10.1002/art.41291
- By:
- Publication type:
- Article
Haplotype-specific chromatin looping reveals genetic interactions of regulatory regions modulating gene expression in 8p23.1.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.1008582
- By:
- Publication type:
- Article
Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.
- Published in:
- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0268725
- By:
- Publication type:
- Article
Antiphospholipid syndrome: Genetic review.
- Published in:
- Current Rheumatology Reports, 2003, v. 5, n. 5, p. 391, doi. 10.1007/s11926-003-0030-8
- By:
- Publication type:
- Article
Validation of low‐coverage whole‐genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth.
- Published in:
- Human Mutation, 2021, v. 42, n. 12, p. 1602, doi. 10.1002/humu.24279
- By:
- Publication type:
- Article
Suboptimal Clinical Documentation in Young Children with Severe Obesity at Tertiary Care Centers.
- Published in:
- International Journal of Pediatrics, 2016, p. 1, doi. 10.1155/2016/4068582
- By:
- Publication type:
- Article
Horizons in Sjögren’s Syndrome Genetics.
- Published in:
- Clinical Reviews in Allergy & Immunology, 2007, v. 32, n. 3, p. 201, doi. 10.1007/s12016-007-8002-9
- By:
- Publication type:
- Article
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.
- Published in:
- Genetic Epidemiology, 2019, v. 43, n. 1, p. 63, doi. 10.1002/gepi.22167
- By:
- Publication type:
- Article
Quantifying the phenome‐wide disease burden of obesity using electronic health records and genomics.
- Published in:
- Obesity (19307381), 2022, v. 30, n. 12, p. 2477, doi. 10.1002/oby.23561
- By:
- Publication type:
- Article
SLE non-coding genetic risk variant determines the epigenetic dysfunction of an immune cell specific enhancer that controls disease-critical microRNA expression.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20460-1
- By:
- Publication type:
- Article
Changing the concepts of immune-mediated glomerular diseases through proteomics.
- Published in:
- Proteomics - Clinical Applications, 2015, v. 9, n. 11/12, p. 967, doi. 10.1002/prca.201400159
- By:
- Publication type:
- Article