Found: 77
Select item for more details and to access through your institution.
Genetically deprived vitamin D exposure predisposes to atrial fibrillation.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Transcriptomics of Hirschsprung disease patient-derived enteric neural crest cells reveals a role for oxidative phosphorylation.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37928-5
- By:
- Publication type:
- Article
An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36897-z
- By:
- Publication type:
- Article
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36490-4
- By:
- Publication type:
- Article
Unraveling NEK4 as a Potential Drug Target in Schizophrenia and Bipolar I Disorder: A Proteomic and Genomic Approach.
- Published in:
- Schizophrenia Bulletin, 2024, v. 50, n. 5, p. 1185, doi. 10.1093/schbul/sbae094
- By:
- Publication type:
- Article
Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese.
- Published in:
- Schizophrenia Bulletin, 2014, v. 40, n. 4, p. 777, doi. 10.1093/schbul/sbt104
- By:
- Publication type:
- Article
High-sensitivity troponin I and B-type natriuretic peptide biomarkers for prediction of cardiovascular events in patients with coronary artery disease with and without diabetes mellitus.
- Published in:
- Cardiovascular Diabetology, 2019, v. 18, n. 1, p. 1, doi. 10.1186/s12933-019-0974-2
- By:
- Publication type:
- Article
Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-24077-w
- By:
- Publication type:
- Article
Discovering the structure and organization of a free Cantonese emotion-label word association graph to understand mental lexicons of emotions.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-23995-z
- By:
- Publication type:
- Article
Prevalence, psychosocial correlates and service utilization of depressive and anxiety disorders in Hong Kong: the Hong Kong Mental Morbidity Survey (HKMMS).
- Published in:
- 2015
- By:
- Publication type:
- journal article
Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese.
- Published in:
- Journal of Human Genetics, 2013, v. 58, n. 11, p. 749, doi. 10.1038/jhg.2013.84
- By:
- Publication type:
- Article
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.
- Published in:
- Nucleic Acids Research, 2018, v. 46, n. W1, p. W114, doi. 10.1093/nar/gky407
- By:
- Publication type:
- Article
Linnorm: improved statistical analysis for single cell RNA-seq expression data.
- Published in:
- Nucleic Acids Research, 2017, v. 45, n. 22, p. 1, doi. 10.1093/nar/gkx828
- By:
- Publication type:
- Article
dbPSHP: a database of recent positive selection across human populations.
- Published in:
- Nucleic Acids Research, 2014, v. 42, n. D1, p. D910, doi. 10.1093/nar/gkt1052
- By:
- Publication type:
- Article
GWASdb: a database for human genetic variants identified by genome-wide association studies.
- Published in:
- Nucleic Acids Research, 2012, p. D1047, doi. 10.1093/nar/gkr1182
- By:
- Publication type:
- Article
Single-cell RNA sequencing shows the immunosuppressive landscape and tumor heterogeneity of HBV-associated hepatocellular carcinoma.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24010-1
- By:
- Publication type:
- Article
The support of human genetic evidence for approved drug indications.
- Published in:
- Nature Genetics, 2015, v. 47, n. 8, p. 856, doi. 10.1038/ng.3314
- By:
- Publication type:
- Article
Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.
- Published in:
- Nature Genetics, 2012, v. 44, n. 9, p. 1026, doi. 10.1038/ng.2367
- By:
- Publication type:
- Article
Genetic variants in GREM2 are associated with bone mineral density in a southern Chinese population.
- Published in:
- 2013
- By:
- Publication type:
- journal article
framework to decipher the genetic architecture of combinations of complex diseases: applications in cardiovascular medicine.
- Published in:
- Bioinformatics, 2021, v. 37, n. 22, p. 4137, doi. 10.1093/bioinformatics/btab417
- By:
- Publication type:
- Article
vSampler: fast and annotation-based matched variant sampling tool.
- Published in:
- Bioinformatics, 2021, v. 37, n. 13, p. 1915, doi. 10.1093/bioinformatics/btaa883
- By:
- Publication type:
- Article
PMCA4 ( ATP2B4) mutation in familial spastic paraplegia causes delay in intracellular calcium extrusion.
- Published in:
- Brain & Behavior, 2015, v. 5, n. 4, p. n/a, doi. 10.1002/brb3.321
- By:
- Publication type:
- Article
Unveiling common psychological characteristics of proneness to aggression and general psychopathology in a large community youth cohort.
- Published in:
- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02538-8
- By:
- Publication type:
- Article
Alterations in Gastric Microbiota After H. Pylori Eradication and in Different Histological Stages of Gastric Carcinogenesis.
- Published in:
- Scientific Reports, 2017, p. 44935, doi. 10.1038/srep44935
- By:
- Publication type:
- Article
CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens.
- Published in:
- Scientific Reports, 2016, p. 25954, doi. 10.1038/srep25954
- By:
- Publication type:
- Article
Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy.
- Published in:
- Scientific Reports, 2016, p. 26362, doi. 10.1038/srep26362
- By:
- Publication type:
- Article
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease.
- Published in:
- Scientific Reports, 2015, p. 16473, doi. 10.1038/srep16473
- By:
- Publication type:
- Article
PMCA4 (ATP2B4) Mutation in Familial Spastic Paraplegia.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104790
- By:
- Publication type:
- Article
Gene Network Analysis of Candidate Loci for Human Anorectal Malformations.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0069142
- By:
- Publication type:
- Article
Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066631
- By:
- Publication type:
- Article
Mutations in the NRG1 gene are associated with Hirschsprung disease.
- Published in:
- Human Genetics, 2012, v. 131, n. 1, p. 67, doi. 10.1007/s00439-011-1035-4
- By:
- Publication type:
- Article
Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene.
- Published in:
- Frontiers in Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fnins.2021.649588
- By:
- Publication type:
- Article
Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Relationship of Plasma Interleukin-6 and Its Genetic Variants With Hypertension in Hong Kong Chinese.
- Published in:
- American Journal of Hypertension, 2011, v. 24, n. 12, p. 1331, doi. 10.1038/ajh.2011.141
- By:
- Publication type:
- Article
Commonality in dysregulated expression of gene sets in cortical brains of individuals with autism, schizophrenia, and bipolar disorder.
- Published in:
- Translational Psychiatry, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41398-019-0488-4
- By:
- Publication type:
- Article
Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet.
- Published in:
- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0167-x
- By:
- Publication type:
- Article
Targeted Next-Generation Sequencing on Hirschsprung Disease: A Pilot Study Exploits DNA Pooling.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 5, p. 381, doi. 10.1111/ahg.12076
- By:
- Publication type:
- Article
Genetic variant representation, annotation and prioritization in the post-GWAS era.
- Published in:
- Cell Research, 2012, v. 22, n. 10, p. 1505, doi. 10.1038/cr.2012.106
- By:
- Publication type:
- Article
INSIDER: Interpretable sparse matrix decomposition for RNA expression data analysis.
- Published in:
- PLoS Genetics, 2024, v. 20, n. 3, p. 1, doi. 10.1371/journal.pgen.1011189
- By:
- Publication type:
- Article
Methods and resources to access mutation-dependent effects on cancer drug treatment.
- Published in:
- Briefings in Bioinformatics, 2020, v. 21, n. 6, p. 1886, doi. 10.1093/bib/bbz109
- By:
- Publication type:
- Article
Evaluation of tools for highly variable gene discovery from single-cell RNA-seq data.
- Published in:
- Briefings in Bioinformatics, 2019, p. 1583, doi. 10.1093/bib/bby011
- By:
- Publication type:
- Article
Attention‐deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2‐repeat allele.
- Published in:
- Annals of Human Genetics, 2024, v. 88, n. 5, p. 382, doi. 10.1111/ahg.12560
- By:
- Publication type:
- Article
Mendelian randomization analysis of vitamin D in the secondary prevention of hypertensive-diabetic subjects: role of facilitating blood pressure control.
- Published in:
- Genes & Nutrition, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s12263-022-00704-z
- By:
- Publication type:
- Article
An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 9, p. 836, doi. 10.1093/hmg/ddab062
- By:
- Publication type:
- Article
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 5, p. 1184, doi. 10.1093/hmg/ddr550
- By:
- Publication type:
- Article
The Effect of Oxytocin on Social and Non-Social Behaviour and Striatal Protein Expression in C57BL/6N Mice.
- Published in:
- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0145638
- By:
- Publication type:
- Article
GENECOUNTING: haplotype analysis with missing genotypes.
- Published in:
- Bioinformatics, 2002, v. 18, n. 12, p. 1694, doi. 10.1093/bioinformatics/18.12.1694
- By:
- Publication type:
- Article
Computational Retinal Microvascular Biomarkers from an OCTA Image in Clinical Investigation.
- Published in:
- Biomedicines, 2024, v. 12, n. 4, p. 868, doi. 10.3390/biomedicines12040868
- By:
- Publication type:
- Article