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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
- Published in:
- Nature, 2009, v. 460, n. 7256, p. 748, doi. 10.1038/nature08185
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- Article
Modifiers and Subtype-Specific Analyses in Whole-Genome Association Studies: A Likelihood Framework.
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- Human Heredity, 2011, v. 72, n. 1, p. 10, doi. 10.1159/000327158
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- Article
Statistical power and significance testing in large-scale genetic studies.
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- Nature Reviews Genetics, 2014, v. 15, n. 5, p. 335, doi. 10.1038/nrg3706
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- Article
Pleiotropy in complex traits: challenges and strategies.
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- Nature Reviews Genetics, 2013, v. 14, n. 7, p. 483, doi. 10.1038/nrg3461
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- Article
Exome Sequencing of Familial Bipolar Disorder.
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- 2016
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- Publication type:
- journal article
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.
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- Genome Medicine, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13073-021-00917-8
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- Article
No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia.
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- European Journal of Human Genetics, 2015, v. 23, n. 4, p. 555, doi. 10.1038/ejhg.2014.228
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- Article
Mosaic copy number variation in schizophrenia.
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- European Journal of Human Genetics, 2013, v. 21, n. 9, p. 1007, doi. 10.1038/ejhg.2012.287
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- Article
Rare chromosomal deletions and duplications increase risk of schizophrenia.
- Published in:
- Nature, 2008, v. 455, n. 7210, p. 237, doi. 10.1038/nature07239
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- Article
Sources of Variation in the Spectral Slope of the Sleep EEG.
- Published in:
- eNeuro, 2022, v. 9, n. 5, p. 1, doi. 10.1523/ENEURO.0094-22.2022
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- Article
A framework for the interpretation of de novo mutation in human disease.
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- Nature Genetics, 2014, v. 46, n. 9, p. 944, doi. 10.1038/ng.3050
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- Article
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
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- Nature Genetics, 2013, v. 45, n. 9, p. 984, doi. 10.1038/ng.2711
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- Publication type:
- Article
Exome sequencing and the genetic basis of complex traits.
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- Nature Genetics, 2012, v. 44, n. 6, p. 623, doi. 10.1038/ng.2303
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- Publication type:
- Article
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.
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- Nature Genetics, 2012, v. 44, n. 6, p. 631, doi. 10.1038/ng.2283
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- Publication type:
- Article
Testing for an Unusual Distribution of Rare Variants.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 3, p. 1, doi. 10.1371/journal.pgen.1001322
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- Article
Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions.
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- PLoS Genetics, 2009, v. 5, n. 6, p. 1, doi. 10.1371/journal.pgen.1000534
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- Publication type:
- Article
Genetic Association Analysis of 300 Genes Identifies a Risk Haplotype in SLC18A2 for Post-traumatic Stress Disorder in Two Independent Samples.
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- Neuropsychopharmacology, 2014, v. 39, n. 8, p. 1872, doi. 10.1038/npp.2014.34
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- Article
The Genomic Psychiatry Cohort: Partners in Discovery.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 4, p. 306, doi. 10.1002/ajmg.b.32160
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- Article
AI-Driven sleep staging from actigraphy and heart rate.
- Published in:
- PLoS ONE, 2023, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0285703
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- Article
The Genetic Structure of the Swedish Population.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0022547
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- Article
Protocol for investigating genetic determinants of posttraumatic stress disorder in women from the Nurses' Health Study II.
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- BMC Psychiatry, 2009, v. 9, p. 1, doi. 10.1186/1471-244X-9-29
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- Publication type:
- Article
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep.
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- PLoS Genetics, 2019, v. 15, n. 4, p. 1, doi. 10.1371/journal.pgen.1007739
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- Article
A polygenic burden of rare disruptive mutations in schizophrenia.
- Published in:
- Nature, 2014, v. 506, n. 7487, p. 185, doi. 10.1038/nature12975
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- Article
Second-generation PLINK: rising to the challenge of larger and richer datasets.
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- GigaScience, 2015, v. 4, n. 1, p. 1, doi. 10.1186/s13742-015-0047-8
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- Publication type:
- Article
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.
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- Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0497-y
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- Publication type:
- Article
Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese.
- Published in:
- 2014
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- 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
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- Publication type:
- Article
INRICH: interval-based enrichment analysis for genome-wide association studies.
- Published in:
- Bioinformatics, 2012, v. 28, n. 13, p. 1797, doi. 10.1093/bioinformatics/bts191
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- Article
A multivariate test of association.
- Published in:
- Bioinformatics, 2009, v. 25, n. 1, p. 132, doi. 10.1093/bioinformatics/btn563
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- Publication type:
- Article
Objectively regular sleep patterns and mortality in a prospective cohort: The Multi‐Ethnic Study of Atherosclerosis.
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- Journal of Sleep Research, 2024, v. 33, n. 1, p. 1, doi. 10.1111/jsr.14048
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- Publication type:
- Article
Statistical Power and the Classical Twin Design.
- Published in:
- 2020
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- Publication type:
- journal article
mTADA is a framework for identifying risk genes from de novo mutations in multiple traits.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16487-z
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- Article
Family-based genetic risk prediction of multifactorial disease.
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- Genome Medicine, 2010, v. 2, n. 1, p. 1, doi. 10.1186/gm123
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- Article
Statistics for X‐chromosome associations.
- Published in:
- Genetic Epidemiology, 2018, v. 42, n. 6, p. 539, doi. 10.1002/gepi.22132
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- Article
Causal Association Between Subtypes of Excessive Daytime Sleepiness and Risk of Cardiovascular Diseases.
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- Journal of the American Heart Association, 2023, v. 12, n. 24, p. 1, doi. 10.1161/JAHA.122.030568
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- Article
Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05415-4
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- Article
Synthetic Associations Created by Rare Variants Do Not Explain Most GWAS Results.
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- PLoS Biology, 2011, v. 9, n. 1, p. 1, doi. 10.1371/journal.pbio.1000579
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- Article
Sleep Architecture, Obstructive Sleep Apnea, and Cognitive Function in Adults.
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- JAMA Network Open, 2023, v. 6, n. 7, p. e2325152, doi. 10.1001/jamanetworkopen.2023.25152
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- Article