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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
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- Article
INSIDER: Interpretable sparse matrix decomposition for RNA expression data analysis.
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- PLoS Genetics, 2024, v. 20, n. 3, p. 1, doi. 10.1371/journal.pgen.1011189
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- Publication type:
- Article
SumVg: Total Heritability Explained by All Variants in Genome-Wide Association Studies Based on Summary Statistics with Standard Error Estimates.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 2, p. 1347, doi. 10.3390/ijms25021347
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- Article
Preliminary Evidence for Genetic Nurture in Depression and Neuroticism Through Polygenic Scores.
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- JAMA Psychiatry, 2023, v. 80, n. 8, p. 832, doi. 10.1001/jamapsychiatry.2023.1544
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- Article
Unveiling common psychological characteristics of proneness to aggression and general psychopathology in a large community youth cohort.
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- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02538-8
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- Article
The genetic basis of onset age in schizophrenia: evidence and models.
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- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1163361
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- Publication type:
- Article
Transcriptomics of Hirschsprung disease patient-derived enteric neural crest cells reveals a role for oxidative phosphorylation.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37928-5
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- Article
An autoimmune pleiotropic SNP modulates IRF5 alternative promoter usage through ZBTB3-mediated chromatin looping.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36897-z
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- Article
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36490-4
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- Article
Common and rare variant associations with latent traits underlying depression, bipolar disorder, and schizophrenia.
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- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02324-6
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- Article
Third-generation genome sequencing implicates medium-sized structural variants in chronic schizophrenia.
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- Frontiers in Neuroscience, 2023, v. 16, p. 1, doi. 10.3389/fnins.2022.1058359
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- Publication type:
- Article
First-Episode Psychosis Patients Who Deteriorated in the Premorbid Period Do Not Have Higher Polygenic Risk Scores Than Others: A Cluster Analysis of EU-GEI Data.
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- Schizophrenia Bulletin, 2023, v. 49, n. 1, p. 218, doi. 10.1093/schbul/sbac100
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- Article
Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-24077-w
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- 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
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- Publication type:
- Article
Polygenic power calculator: Statistical power and polygenic prediction accuracy of genome-wide association studies of complex traits.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.989639
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- Article
Clarifying the causes of consistent and inconsistent findings in genetics.
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- Genetic Epidemiology, 2022, v. 46, n. 7, p. 372, doi. 10.1002/gepi.22459
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- Article
Improved nonparametric penalized maximum likelihood estimation for arbitrarily censored survival data.
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- Statistics in Medicine, 2022, v. 41, n. 20, p. 4006, doi. 10.1002/sim.9489
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- Publication type:
- Article
Abnormal Brain Structure Morphology in Early-Onset Schizophrenia.
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- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.925204
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- Article
Associations between childhood maltreatment and psychiatric disorders: analysis from electronic health records in Hong Kong.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01986-y
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- Article
Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene.
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- 2022
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- Publication type:
- journal article
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases.
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- Nucleic Acids Research, 2022, v. 50, n. 6, p. e34, doi. 10.1093/nar/gkab1234
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- Publication type:
- Article
Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti‐seizure medications.
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- Epilepsia (Series 4), 2022, v. 63, n. 4, p. 936, doi. 10.1111/epi.17182
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- Publication type:
- Article
Integrative analysis of metabolomic, genomic, and imaging-based phenotypes identify very-low-density lipoprotein as a potential risk factor for lumbar Modic changes.
- Published in:
- European Spine Journal, 2022, v. 31, n. 3, p. 735, doi. 10.1007/s00586-021-06995-x
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- Publication type:
- Article
Mendelian randomization analysis of vitamin D in the secondary prevention of hypertensive-diabetic subjects: role of facilitating blood pressure control.
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- Genes & Nutrition, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s12263-022-00704-z
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- Article
VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. D1, p. D1408, doi. 10.1093/nar/gkab853
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- Publication type:
- Article
framework to decipher the genetic architecture of combinations of complex diseases: applications in cardiovascular medicine.
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- Bioinformatics, 2021, v. 37, n. 22, p. 4137, doi. 10.1093/bioinformatics/btab417
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- Article
Correction to: On the Transformation of Genetic Effect Size from Logit to Liability Scale.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Spatial Expression Pattern of ZNF391 Gene in the Brains of Patients With Schizophrenia, Bipolar Disorders or Major Depressive Disorder Identifies New Cross-Disorder Biotypes: A Trans-Diagnostic, Top-Down Approach.
- Published in:
- Schizophrenia Bulletin, 2021, v. 47, n. 5, p. 1351, doi. 10.1093/schbul/sbaa167
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- Publication type:
- Article
Neurological Soft Signs Are Associated With Altered Cerebellar-Cerebral Functional Connectivity in Schizophrenia.
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- Schizophrenia Bulletin, 2021, v. 47, n. 5, p. 1452, doi. 10.1093/schbul/sbaa200
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- Publication type:
- Article
vSampler: fast and annotation-based matched variant sampling tool.
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- Bioinformatics, 2021, v. 37, n. 13, p. 1915, doi. 10.1093/bioinformatics/btaa883
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- Publication type:
- Article
Single-cell RNA sequencing shows the immunosuppressive landscape and tumor heterogeneity of HBV-associated hepatocellular carcinoma.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24010-1
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- Publication type:
- Article
Coagulation factors and the incidence of COVID-19 severity: Mendelian randomization analyses and supporting evidence.
- Published in:
- 2021
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- Publication type:
- Letter
On the Transformation of Genetic Effect Size from Logit to Liability Scale.
- Published in:
- Behavior Genetics, 2021, v. 51, n. 3, p. 215, doi. 10.1007/s10519-021-10042-2
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- Article
Modeling Parent-Specific Genetic Nurture in Families with Missing Parental Genotypes: Application to Birthweight and BMI.
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- Behavior Genetics, 2021, v. 51, n. 3, p. 289, doi. 10.1007/s10519-020-10040-w
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- Publication type:
- Article
An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population.
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- Human Molecular Genetics, 2021, v. 30, n. 9, p. 836, doi. 10.1093/hmg/ddab062
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- Article
Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene.
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- Frontiers in Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fnins.2021.649588
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- Article
MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes.
- Published in:
- Cardiovascular Research, 2021, v. 117, n. 3, p. 767, doi. 10.1093/cvr/cvaa019
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- Publication type:
- Article
DIPPER, a spatiotemporal proteomics atlas of human intervertebral discs for exploring ageing and degeneration dynamics.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.64940
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- Publication type:
- Article
Valproate Reverses Mania-Like Behavior of Clock<sup>delta19</sup> Mouse and Alters Monoamine Neurotransmitters Metabolism in the Hippocampus.
- Published in:
- Neuropsychiatric Disease & Treatment, 2021, v. 17, p. 471, doi. 10.2147/NDT.S293482
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- 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
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- Article
Estimating indirect parental genetic effects on offspring phenotypes using virtual parental genotypes derived from sibling and half sibling pairs.
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- PLoS Genetics, 2020, v. 16, n. 10, p. 1, doi. 10.1371/journal.pgen.1009154
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- Publication type:
- Article
The Genes We Inherit and Those We Don't: Maternal Genetic Nurture and Child BMI Trajectories.
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- Behavior Genetics, 2020, v. 50, n. 5, p. 310, doi. 10.1007/s10519-020-10008-w
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- Publication type:
- Article
Positive effects of low LDL-C and statins on bone mineral density: an integrated epidemiological observation analysis and Mendelian randomization study.
- Published in:
- 2020
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- Publication type:
- journal article
Intermediate confounding in trio relationships: The importance of complete data in effect size estimation.
- Published in:
- Genetic Epidemiology, 2020, v. 44, n. 4, p. 395, doi. 10.1002/gepi.22294
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- Publication type:
- Article
Knowledge-based analyses reveal new candidate genes associated with risk of hepatitis B virus related hepatocellular carcinoma.
- Published in:
- 2020
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- Publication type:
- journal article
Premorbid Adjustment and IQ in Patients With First-Episode Psychosis: A Multisite Case-Control Study of Their Relationship With Cannabis Use.
- Published in:
- Schizophrenia Bulletin, 2020, v. 46, n. 3, p. 517, doi. 10.1093/schbul/sbz077
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- Publication type:
- Article
COGNITION, METACOGNITION AND SOCIAL COGNITION AFTER A FIRST EPISODE PSYCHOSIS. PRELIMINARY RESULTS FROM A 5-YEAR-FOLLOW-UP STUDY.
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- Schizophrenia Bulletin, 2020, v. 46, p. S251, doi. 10.1093/schbul/sbaa029.612
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- Article
Statistical Power and the Classical Twin Design.
- Published in:
- 2020
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- Publication type:
- journal article
CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies.
- Published in:
- Nucleic Acids Research, 2020, v. 48, n. D1, p. D807, doi. 10.1093/nar/gkz1026
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- Publication type:
- Article
QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes.
- Published in:
- Nucleic Acids Research, 2020, v. 48, n. D1, p. D983, doi. 10.1093/nar/gkz888
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- Publication type:
- Article