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Modifiable factors affecting renal preservation in type I glycogen storage disease after liver transplantation: a single-center propensity-match cohort study.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Genome-Wide and Candidate Gene Association Analyses Identify a 14-SNP Combination for Hypertension in Patients With Type 2 Diabetes.
- Published in:
- American Journal of Hypertension, 2021, v. 34, n. 6, p. 651, doi. 10.1093/ajh/hpaa203
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- Publication type:
- Article
Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese.
- Published in:
- NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00178-9
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- Publication type:
- Article
Genetic risk score constructed from common genetic variants is associated with cardiovascular disease risk in type 2 diabetes mellitus.
- Published in:
- Journal of Gene Medicine, 2021, v. 23, n. 2, p. 1, doi. 10.1002/jgm.3305
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- Publication type:
- Article
Towards a reference genome that captures global genetic diversity.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-19311-w
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- Publication type:
- Article
Genetic Architecture Associated With Familial Short Stature.
- Published in:
- 2020
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- Publication type:
- journal article
Both IgM and IgG Antibodies against Polyethylene Glycol Can Alter the Biological Activity of Methoxy Polyethylene Glycol-Epoetin Beta in Mice.
- Published in:
- Pharmaceutics, 2020, v. 12, n. 1, p. 15, doi. 10.3390/pharmaceutics12010015
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- Publication type:
- Article
Genomic interrogation of familial short stature contributes to the discovery of the pathophysiological mechanisms and pharmaceutical drug repositioning.
- Published in:
- Journal of Biomedical Science, 2019, v. 26, n. 1, p. N.PAG, doi. 10.1186/s12929-019-0581-2
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- Publication type:
- Article
Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-36520-y
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- Publication type:
- Article
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07345-0
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- Publication type:
- Article
Immunoglobulin profiling identifies unique signatures in patients with Kawasaki disease during intravenous immunoglobulin treatment.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 15, p. 2671, doi. 10.1093/hmg/ddy176
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- Publication type:
- Article
Identification of functional single nucleotide polymorphisms in the branchpoint site.
- Published in:
- Human Genomics, 2017, v. 11, p. 1, doi. 10.1186/s40246-017-0122-6
- By:
- Publication type:
- Article
A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00622-4
- By:
- Publication type:
- Article
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 9, p. 1770, doi. 10.1093/hmg/ddx062
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- Publication type:
- Article
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
- Published in:
- Human Mutation, 2017, v. 38, n. 5, p. 540, doi. 10.1002/humu.23186
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- Publication type:
- Article
Identification of Susceptible Loci and Enriched Pathways for Bipolar II Disorder Using Genome-Wide Association Studies.
- Published in:
- International Journal of Neuropsychopharmacology, 2016, v. 19, n. 12, p. 1, doi. 10.1093/ijnp/pyw064
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- Publication type:
- Article
Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study.
- Published in:
- Human Genetics, 2016, v. 135, n. 11, p. 1287, doi. 10.1007/s00439-016-1716-0
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- Publication type:
- Article
Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.
- Published in:
- Molecular Autism, 2016, v. 7, p. 1, doi. 10.1186/s13229-016-0087-7
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- Publication type:
- Article
An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.
- Published in:
- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-2478-8
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- Publication type:
- Article
Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13-Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation.
- Published in:
- Journal of Investigative Dermatology, 2015, v. 135, n. 11, p. 2603, doi. 10.1038/jid.2015.240
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- Publication type:
- Article
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
- Published in:
- Nature Genetics, 2015, v. 47, n. 11, p. 1282, doi. 10.1038/ng.3405
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- Publication type:
- Article
Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan.
- Published in:
- Scientific Reports, 2015, p. 1, doi. 10.1038/srep14762
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- Publication type:
- Article
Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138695
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- Publication type:
- Article
Investigation of Associations between NR1D1, RORA and RORB Genes and Bipolar Disorder.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0121245
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- Publication type:
- Article
Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis.
- Published in:
- Clinical Endocrinology, 2014, v. 81, n. 5, p. 702, doi. 10.1111/cen.12428
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- Publication type:
- Article
Multiple Nonglycemic Genomic Loci Are Newly Associated With Blood Level of Glycated Hemoglobin in East Asians.
- Published in:
- Diabetes, 2014, v. 63, n. 7, p. 2551, doi. 10.2337/db13-1815
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- Publication type:
- Article
Genetic Polymorphisms of Metabolic Enzymes and the Pharmacokinetics of Indapamide in Taiwanese Subjects.
- Published in:
- AAPS Journal, 2014, v. 16, n. 2, p. 206, doi. 10.1208/s12248-013-9535-x
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- Publication type:
- Article
Palmitoyl Acyltransferase, <i>Zdhhc13,</i> Facilitates Bone Mass Acquisition by Regulating Postnatal Epiphyseal Development and Endochondral Ossification: A Mouse Model.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092194
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- Publication type:
- Article
Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population.
- Published in:
- BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-81
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- Publication type:
- Article
Genome-wide expression profiles of subchondral bone in osteoarthritis.
- Published in:
- Arthritis Research & Therapy, 2013, v. 15, n. 6, p. 1, doi. 10.1186/ar4380
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- Publication type:
- Article
Association between <i>GRIN3A</i> Gene Polymorphism in Kawasaki Disease and Coronary Artery Aneurysms in Taiwanese Children.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0081384
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- Publication type:
- Article
Runs of Homozygosity Associated with Speech Delay in Autism in a Taiwanese Han Population: Evidence for the Recessive Model.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072056
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- Publication type:
- Article
Association of Genes on Chromosome 6, GRIK2, TMEM217 and TMEM63B (Linked to MRPL14) with Diabetic Retinopathy.
- Published in:
- Ophthalmologica, 2012, v. 229, n. 1, p. 54, doi. 10.1159/000342616
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- Publication type:
- Article
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
- Published in:
- Nature Genetics, 2012, v. 44, n. 8, p. 904, doi. 10.1038/ng.2352
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- Publication type:
- Article
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.
- Published in:
- Nature Genetics, 2012, v. 44, n. 3, p. 302, doi. 10.1038/ng.1086
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- Publication type:
- Article
A Mutation in Cartilage Oligomeric Matrix Protein (COMP) Causes Early-Onset Osteoarthritis in a Large Kindred Study.
- Published in:
- Annals of Human Genetics, 2011, v. 75, n. 5, p. 575, doi. 10.1111/j.1469-1809.2011.00667.x
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- Publication type:
- Article
A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease.
- Published in:
- Human Genetics, 2011, v. 129, n. 5, p. 487, doi. 10.1007/s00439-010-0937-x
- By:
- Publication type:
- Article
Identification of Novel Susceptibility Loci for Kawasaki Disease in a Han Chinese Population by a Genome-Wide Association Study.
- Published in:
- PLoS ONE, 2011, v. 6, n. 2, p. 1, doi. 10.1371/journal.pone.0016853
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- Publication type:
- Article
SAQC: SNP Array Quality Control.
- Published in:
- BMC Bioinformatics, 2011, v. 12, n. 1, p. 100, doi. 10.1186/1471-2105-12-100
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- Publication type:
- Article
Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder.
- Published in:
- Journal of Inherited Metabolic Disease, 2010, v. 33, p. 83, doi. 10.1007/s10545-009-9026-5
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- Publication type:
- Article
Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 6, p. 1, doi. 10.1371/journal.pgen.1000985
- By:
- Publication type:
- Article
A Genome-Wide Association Study Identifies Susceptibility Variants for Type 2 Diabetes in Han Chinese.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 2, p. 1, doi. 10.1371/journal.pgen.1000847
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- Publication type:
- Article
A new analysis tool for individual-level allele frequency for genomic studies.
- Published in:
- BMC Genomics, 2010, v. 11, p. 415, doi. 10.1186/1471-2164-11-415
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- Publication type:
- Article
Three novel beta-galactosidase gene mutations in Han Chinese patients with GM1 gangliosidosis are correlated with disease severity.
- Published in:
- Journal of Biomedical Science, 2010, v. 17, p. 79, doi. 10.1186/1423-0127-17-79
- By:
- Publication type:
- Article
Genome-Wide Association Study of Young-Onset Hypertension in the Han Chinese Population of Taiwan.
- Published in:
- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005459
- By:
- Publication type:
- Article
A large kindred of early-onset osteoarthritis of the knee and hip: excluding the link to COL2A1 gene.
- Published in:
- Rheumatology, 2009, v. 48, n. 4, p. 371
- By:
- Publication type:
- Article
Granulysin is a key mediator for disseminated keratinocyte death in Stevens-Johnson syndrome and toxic epidermal necrolysis.
- Published in:
- Nature Medicine, 2008, v. 14, n. 12, p. 1343, doi. 10.1038/nm.1884
- By:
- Publication type:
- Article
Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.
- Published in:
- Human Mutation, 2008, v. 29, n. 8, p. 1055, doi. 10.1002/humu.20760
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- Publication type:
- Article
MPDA: Microarray pooled DNA analyzer.
- Published in:
- BMC Bioinformatics, 2008, v. 9, p. 1, doi. 10.1186/1471-2105-9-196
- By:
- Publication type:
- Article
Dysregulation of C/EBPα by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 5, p. 483, doi. 10.1093/hmg/ddl481
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- Publication type:
- Article