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Missingness adapted group informed clustered (MAGIC)-LASSO: a novel paradigm for phenotype prediction to improve power for genetic loci discovery.
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- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1162690
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- Article
Case-only exome variation analysis of severe alcohol dependence using a multivariate hierarchical gene clustering approach.
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- PLoS ONE, 2023, v. 17, n. 4, p. 1, doi. 10.1371/journal.pone.0283985
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- Article
Examining the source of increased bipolar disorder and major depressive disorder common risk variation burden in multiplex schizophrenia families.
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- Schizophrenia (2754-6993), 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41537-022-00317-w
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- Article
Determining the stability of genome-wide factors in BMI between ages 40 to 69 years.
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- PLoS Genetics, 2022, v. 18, n. 8, p. 1, doi. 10.1371/journal.pgen.1010303
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- Article
DECO: a framework for jointly analyzing de novo and rare case/control variants, and biological pathways.
- Published in:
- Briefings in Bioinformatics, 2021, v. 22, n. 5, p. 1, doi. 10.1093/bib/bbab067
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- Article
Increasing the resolution and precision of psychiatric genome‐wide association studies by re‐imputing summary statistics using a large, diverse reference panel.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2021, v. 186, n. 1, p. 16, doi. 10.1002/ajmg.b.32834
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- Article
TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2020, v. 183, n. 8, p. 454, doi. 10.1002/ajmg.b.32823
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- Article
An epigenome-wide association study of early-onset major depression in monozygotic twins.
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- Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-00984-2
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- Article
DNA methylation associated with postpartum depressive symptoms overlaps findings from a genome-wide association meta-analysis of depression.
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- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0769-z
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- Article
Expanding the phenotype for the recurrent p.Ala391Glu variant in FGFR3: Beyond crouzon syndrome and acanthosis nigricans.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 6, p. N.PAG, doi. 10.1002/mgg3.656
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- Article
Replication of the Interaction of PRKG1 and Trauma Exposure on Alcohol Misuse in an Independent African American Sample.
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- 2018
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- Publication type:
- journal article
JEPEGMIX2: improved gene-level joint analysis of eQTLs in cosmopolitan cohorts.
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- Bioinformatics, 2018, v. 34, n. 2, p. 286, doi. 10.1093/bioinformatics/btx509
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- Article
The utility of empirically assigning ancestry groups in cross-population genetic studies of addiction.
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- 2017
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- journal article
Age of onset and family history as indicators of polygenic risk for major depression.
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- 2017
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- Publication type:
- journal article
Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students.
- Published in:
- Frontiers in Genetics, 2017, v. 8, p. 1, doi. 10.3389/fgene.2017.00030
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- Article
Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students.
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- Frontiers in Immunology, 2017, v. 8, p. 1, doi. 10.3389/fgene.2017.00030
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- Article
The Genetic Architecture of Major Depressive Disorder in Han Chinese Women.
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- 2017
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- journal article
CHRONICITY OF DEPRESSION AND MOLECULAR MARKERS IN A LARGE SAMPLE OF HAN CHINESE WOMEN.
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- 2016
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- Publication type:
- journal article
JEPEGMIX: gene-level joint analysis of functional SNPs in cosmopolitan cohorts.
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- Bioinformatics, 2016, v. 32, n. 2, p. 295, doi. 10.1093/bioinformatics/btv567
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- Publication type:
- Article
Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence.
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- Addiction Biology, 2014, v. 19, n. 4, p. 708, doi. 10.1111/adb.12035
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- Article
On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis.
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- BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-368
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- Article
Molecular Validation of the Schizophrenia Spectrum.
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- Schizophrenia Bulletin, 2014, v. 40, n. 1, p. 60, doi. 10.1093/schbul/sbt122
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- Article
Molecular Validation of the Schizophrenia Spectrum.
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- 2014
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- Journal Article
Association Study of 167 Candidate Genes for Schizophrenia Selected by a Multi-Domain Evidence-Based Prioritization Algorithm and Neurodevelopmental Hypothesis.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0067776
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- Article
Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes.
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- European Journal of Human Genetics, 2012, v. 20, n. 10, p. 1078, doi. 10.1038/ejhg.2012.47
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- Publication type:
- Article
Multi-species data integration and gene ranking enrich significant results in an alcoholism genome-wide association study.
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- BMC Genomics, 2012, v. 13, n. Suppl 8, p. 1, doi. 10.1186/1471-2164-13-S8-S16
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- Publication type:
- Article
Comprehensive Gene-Based Association Study of a Chromosome 20 Linked Region Implicates Novel Risk Loci for Depressive Symptoms in Psychotic Illness.
- Published in:
- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0021440
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- Article
ACSL6 Is Associated with the Number of Cigarettes Smoked and Its Expression Is Altered by Chronic Nicotine Exposure.
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- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0028790
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- Publication type:
- Article
Copy Number Variation Accuracy in Genome-Wide Association Studies.
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- Human Heredity, 2011, v. 71, n. 3, p. 141, doi. 10.1159/000324683
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- Article
Genetic risk sum score comprised of common polygenic variation is associated with body mass index.
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- Human Genetics, 2011, v. 129, n. 2, p. 221, doi. 10.1007/s00439-010-0917-1
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- Article
Proteomic biomarkers in plasma that differentiate rapid and slow decline in lung function in adult cigarette smokers with chronic obstructive pulmonary disease (COPD).
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- Analytical & Bioanalytical Chemistry, 2010, v. 397, n. 5, p. 1809, doi. 10.1007/s00216-010-3742-4
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- Publication type:
- Article
A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases–schizophrenia as a case.
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- Bioinformatics, 2009, v. 25, n. 19, p. 2595, doi. 10.1093/bioinformatics/btp428
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- Publication type:
- Article
Efficient Calculation of Empirical P-values for Genome-Wide Linkage Analysis Through Weighted Permutation.
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- Behavior Genetics, 2009, v. 39, n. 1, p. 91, doi. 10.1007/s10519-008-9229-9
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- Article
ERGR: An ethanol-related gene resource.
- Published in:
- Nucleic Acids Research, 2009, v. 37, n. suppl_1, p. D840, doi. 10.1093/nar/gkn816
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- Publication type:
- Article
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.
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- Human Molecular Genetics, 2003, v. 12, n. 10, p. 1155, doi. 10.1093/hmg/ddg127
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- Article