Found: 43
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CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Ultraconserved Elements in the Human Genome: Association and Transmission Analyses of Highly Constrained Single-Nucleotide Polymorphisms.
- Published in:
- Genetics, 2012, v. 192, n. 1, p. 253, doi. 10.1534/genetics.112.141945
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- Publication type:
- Article
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR).
- Published in:
- BioData Mining, 2015, v. 8, p. 1, doi. 10.1186/s13040-015-0074-0
- By:
- Publication type:
- Article
Allele-specific repression of lymphotoxin-a by activated B cell factor-1.
- Published in:
- Nature Genetics, 2004, v. 36, n. 4, p. 394, doi. 10.1038/ng1331
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- Publication type:
- Article
In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading.
- Published in:
- Nature Genetics, 2003, v. 33, n. 4, p. 469, doi. 10.1038/ng1124
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- Publication type:
- Article
Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing.
- Published in:
- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0369-8
- By:
- Publication type:
- Article
IBC CARe Microarray Allelic Population Prevalences in an American Indian Population.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0075080
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- Publication type:
- Article
Two Variants of the C-Reactive Protein Gene Are Associated with Risk of Pre-Eclampsia in an American Indian Population.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0071231
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- Publication type:
- Article
Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies.
- Published in:
- PLoS ONE, 2008, v. 3, n. 10, p. 1, doi. 10.1371/journal.pone.0003583
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- Publication type:
- Article
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.
- Published in:
- Human Genetics, 2011, v. 129, n. 3, p. 307, doi. 10.1007/s00439-010-0925-1
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- Publication type:
- Article
Current and Future Approaches for Monitoring Responses to Anti-complement Therapeutics.
- Published in:
- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02539
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- Publication type:
- Article
Making the genomic leap in HCT: application of second-generation sequencing to clinical advances in hematopoietic cell transplantation.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 6, p. 715, doi. 10.1038/ejhg.2013.247
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- Publication type:
- Article
Early detection of SARS‐CoV‐2 and other infections in solid organ transplant recipients and household members using wearable devices.
- Published in:
- Transplant International, 2021, v. 34, n. 6, p. 1019, doi. 10.1111/tri.13860
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- Publication type:
- Article
Applying genomics in heart transplantation.
- Published in:
- Transplant International, 2018, v. 31, n. 3, p. 278, doi. 10.1111/tri.13119
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- Publication type:
- Article
Pharmacogenomics in kidney transplant recipients and potential for integration into practice.
- Published in:
- Journal of Clinical Pharmacy & Therapeutics, 2020, v. 45, n. 6, p. 1457, doi. 10.1111/jcpt.13223
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- Publication type:
- Article
Genome-Wide Study Updates in the International Genetics and Translational Research in Transplantation Network (iGeneTRAiN).
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01084
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- Publication type:
- Article
Machine learning derived risk prediction of anorexia nervosa.
- Published in:
- BMC Medical Genomics, 2016, p. 1, doi. 10.1186/s12920-016-0165-x
- By:
- Publication type:
- Article
Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls.
- Published in:
- Frontiers in Molecular Neuroscience, 2023, v. 16, p. 1, doi. 10.3389/fnmol.2023.1069375
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- Publication type:
- Article
Correcting the Standard Errors of 2-Stage Residual Inclusion Estimators for Mendelian Randomization Studies.
- Published in:
- American Journal of Epidemiology, 2017, v. 186, n. 9, p. 1104, doi. 10.1093/aje/kwx175
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- Publication type:
- Article
Gut microbiota analyses of Saudi populations for type 2 diabetes-related phenotypes reveals significant association.
- Published in:
- BMC Microbiology, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12866-022-02714-8
- By:
- Publication type:
- Article
LoFTK: a framework for fully automated calculation of predicted Loss-of-Function variants and genes.
- Published in:
- BioData Mining, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13040-023-00321-5
- By:
- Publication type:
- Article
Whole‐exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci.
- Published in:
- Human Genomics, 2022, v. 16, n. 1, p. 1, doi. 10.1186/s40246-022-00444-6
- By:
- Publication type:
- Article
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 8, p. 2297, doi. 10.1093/hmg/ddu747
- By:
- Publication type:
- Article
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 16, p. 3381, doi. 10.1093/hmg/ddt189
- By:
- Publication type:
- Article
Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 1, p. 184
- By:
- Publication type:
- Article
A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 17, p. 3525, doi. 10.1093/hmg/ddr264
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- Publication type:
- Article
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 11, p. 2273
- By:
- Publication type:
- Article
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 11, p. 2285, doi. 10.1093/hmg/ddr113
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- Publication type:
- Article
Elevated Fibroblast Growth Factor 23 Concentration: Prediction of Mortality among Chronic Kidney Disease Patients.
- Published in:
- CardioRenal Medicine, 2015, v. 6, n. 1, p. 73, doi. 10.1159/000440984
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- Publication type:
- Article
Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.
- Published in:
- American Journal of Hematology, 2015, v. 90, n. 6, p. 534, doi. 10.1002/ajh.24005
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- Publication type:
- Article
Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 6, p. 1, doi. 10.1371/journal.pgen.1002134
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- Publication type:
- Article
Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT).
- Published in:
- PLoS Genetics, 2011, v. 7, n. 6, p. 1, doi. 10.1371/journal.pgen.1002108
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- Publication type:
- Article
Polygenic risk score of non‐melanoma skin cancer predicts post‐transplant skin cancer across multiple organ types.
- Published in:
- Clinical Transplantation, 2020, v. 34, n. 8, p. 1, doi. 10.1111/ctr.13904
- By:
- Publication type:
- Article
Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Testing for non-linear causal effects using a binary genotype in a Mendelian randomization study: application to alcohol and cardiovascular traits.
- Published in:
- International Journal of Epidemiology, 2014, v. 43, n. 6, p. 1781, doi. 10.1093/ije/dyu187
- By:
- Publication type:
- Article
Genetic association studies in pre-eclampsia: systematic meta-analyses and field synopsis.
- Published in:
- International Journal of Epidemiology, 2012, v. 41, n. 6, p. 1764, doi. 10.1093/ije/dys162
- By:
- Publication type:
- Article
An integrated expression phenotype mapping approach defines common variants in LEP, ALOX15 and CAPNS1 associated with induction of IL-6.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 4, p. 720, doi. 10.1093/hmg/ddp530
- By:
- Publication type:
- Article
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1659, doi. 10.1093/hmg/ddl089
- By:
- Publication type:
- Article
Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-49105-1
- By:
- Publication type:
- Article
Advances in Risk Prediction of Type 2 Diabetes: Integrating Genetic Scores With Framingham Risk Models.
- Published in:
- 2015
- By:
- Publication type:
- Opinion
Donor genetic burden for cerebrovascular risk and kidney transplant outcome.
- Published in:
- Journal of Nephrology (JNonline), 2024, v. 37, n. 6, p. 1643, doi. 10.1007/s40620-024-01973-0
- By:
- Publication type:
- Article
The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 96, doi. 10.1186/1471-2350-11-96
- By:
- Publication type:
- Article
Gut microbiota analyses of inflammatory bowel diseases from a representative Saudi population.
- Published in:
- BMC Gastroenterology, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12876-023-02904-2
- By:
- Publication type:
- Article