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Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia.
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- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0107-9
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- Article
Online Self-Report Data for Duchenne Muscular Dystrophy Confirms Natural History and Can Be Used to Assess for Therapeutic Benefits.
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- PLoS Currents, 2014, p. 335, doi. 10.1371/currents.md.e1e8f2be7c949f9ffe81ec6fca1cce6a
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- Article
Adipose Co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes.
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- BMC Medical Genomics, 2012, v. 5, n. 1, p. 61, doi. 10.1186/1755-8794-5-61
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- Article
Identifying Heritable Brain Phenotypes in an Extended Pedigree of Vervet Monkeys.
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- Journal of Neuroscience, 2009, v. 29, n. 9, p. 2867, doi. 10.1523/JNEUROSCI.5153-08.2009
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- Article
Weighted variance FBAT: a powerful method for including covariates in FBAT analyses.
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- Genetic Epidemiology, 2007, v. 31, n. 4, p. 327, doi. 10.1002/gepi.20213
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- Article
Biostatistical Genetics and Genetic Epidemiology, Edited by Robert Elston, Jane Olson, and Lyle Palmer. Hoboken, NJ: John Wiley & Sons, Inc., 2002, 831 pages, U.S.$415.00.
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- Genetic Epidemiology, 2004, v. 27, n. 1, p. 84, doi. 10.1002/gepi.10324
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- Article
Quantitative Trait Loci Mapping of Serum IgE in an Isolated Hutterite Population.
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- Genetic Epidemiology, 2001, v. 21, p. S224, doi. 10.1002/gepi.2001.21.s1.s224
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- Article
Comparison of evidence supporting a chromosome 6 alcoholism gene.
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- Genetic Epidemiology, 1999, v. 17, p. S91, doi. 10.1002/gepi.1370170716
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- Article
Factors influencing the identification of major genes in a complex disease genome scan.
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- Genetic Epidemiology, 1997, v. 14, n. 6, p. 933, doi. 10.1002/(SICI)1098-2272(1997)14:6<933::AID-GEPI62>3.0.CO;2-M
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- Article
A genetic analysis of common disease data.
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- Genetic Epidemiology, 1995, v. 12, n. 6, p. 735, doi. 10.1002/gepi.1370120634
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- Article
Power and validity of methods to identify variability genes.
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- Genetic Epidemiology, 1991, v. 8, n. 6, p. 381, doi. 10.1002/gepi.1370080604
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- Article
A non-human primate system for large-scale genetic studies of complex traits.
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- Human Molecular Genetics, 2012, v. 21, n. 15, p. 3307, doi. 10.1093/hmg/dds160
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- Article
Association of common variants in the Joubert syndrome gene (AHI1) with autism.
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- Human Molecular Genetics, 2008, v. 17, n. 24, p. 3887, doi. 10.1093/hmg/ddn291
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- Article
High density SNP association study of a major autism linkage region on chromosome 17.
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- Human Molecular Genetics, 2007, v. 16, n. 6, p. 704, doi. 10.1093/hmg/ddm015
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- Article
Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism.
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- Human Molecular Genetics, 2006, v. 15, n. 3, p. 377, doi. 10.1093/hmg/ddi448
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- Article
Genome-wide burden of deleterious coding variants increased in schizophrenia.
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- Nature Communications, 2015, v. 6, n. 7, p. 7501, doi. 10.1038/ncomms8501
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- Article
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.
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- Nature Communications, 2014, v. 5, n. 6, p. 3983, doi. 10.1038/ncomms4983
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- Article
Detecting responses to treatment with fenofibrate in pedigrees.
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- BMC Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12863-018-0652-5
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- Article
Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
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- Nature, 2011, v. 474, n. 7351, p. 380, doi. 10.1038/nature10110
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- Article
Genetic influences contributing to LDL particle size in familial combined hyperlipidaemia.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 547, doi. 10.1038/sj.ejhg.5200844
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- Article
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).
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- Nature Genetics, 2004, v. 36, n. 4, p. 371, doi. 10.1038/ng1320
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- Article
Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression.
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-3484-1
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- Article
ANALYSIS OF THE COVARIANCE STRUCTURE OF DIGITAL RIDGE COUNTS IN THE OFFSPRING OF MONOZYGOTIC TWINS.
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- Genetics, 1983, v. 103, n. 3, p. 495
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- Article
Gut microbe-derived metabolites and the risk of cardiovascular disease in the METSIM cohort.
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- Frontiers in Microbiology, 2024, p. 1, doi. 10.3389/fmicb.2024.1411328
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- Article
Author Correction: Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS.
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- Nature Communications, 2018, v. 9, p. 1, doi. 10.1038/s41467-018-05849-3
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- Article
Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03554-9
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- Article
Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated german multi-generation families.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 855, doi. 10.1002/ajmg.b.32192
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- Article
Linkage Analysis in a Dutch Population Isolate Shows No Major Gene for Left-Handedness or Atypical Language Lateralization.
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- Journal of Neuroscience, 2015, v. 35, n. 23, p. 8730, doi. 10.1523/JNEUROSCI.3287-14.2015
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- Article
Anatomic Brain Asymmetry in Vervet Monkeys.
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- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0028243
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- Article
Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse.
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- Nature Genetics, 1998, v. 20, n. 2, p. 157, doi. 10.1038/2458
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- Article
Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan.
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- Human Mutation, 2007, v. 28, n. 5, p. 486, doi. 10.1002/humu.20473
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- Article
Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder.
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- Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-13
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- Article
Support for calcium channel gene defects in autism spectrum disorders.
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- Molecular Autism, 2012, v. 3, n. 1, p. 18, doi. 10.1186/2040-2392-3-18
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- Article
GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics.
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- BMC Proceedings, 2018, v. 12, n. 9, p. N.PAG, doi. 10.1186/s12919-018-0113-1
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- Article
Genetic complexity at expression quantitative trait loci.
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- BMC Proceedings, 2016, v. 10, p. 85, doi. 10.1186/s12919-016-0010-4
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- Article
Applications of Machine Learning and Data Mining Methods to Detect Associations of Rare and Common Variants with Complex Traits.
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- Genetic Epidemiology, 2014, v. 38, p. S81, doi. 10.1002/gepi.21830
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- Article
Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes.
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- Genetic Epidemiology, 2011, v. 35, p. S85, doi. 10.1002/gepi.20656
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- Article
Cover Image, Volume 39, Issue 9.
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- Human Mutation, 2018, v. 39, n. 9, p. i, doi. 10.1002/humu.23600
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- Article
DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype.
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- Human Mutation, 2018, v. 39, n. 9, p. 1193, doi. 10.1002/humu.23561
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- Article
Relationships and Mendelian Randomization of Gut Microbe-Derived Metabolites with Metabolic Syndrome Traits in the METSIM Cohort.
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- Metabolites (2218-1989), 2024, v. 14, n. 3, p. 174, doi. 10.3390/metabo14030174
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- Article
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish familiesMembers of the AGRE Consortium are listed in the Appendix on page 153.
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- Annals of Neurology, 2006, v. 59, n. 1, p. 145, doi. 10.1002/ana.20722
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- Article
Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder.
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- PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006046
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- Article
A Gene(s) for All-trans-Retinoic Acid-Induced Forelimb Defects Mapped and Confirmed to Murine Chromosome 11.
- Published in:
- Genetics, 2005, v. 170, n. 1, p. 345, doi. 10.1534/genetics.104.038620
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- Article
Gene expression in large pedigrees: analytic approaches.
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- BMC Genetics, 2016, v. 17, p. 13, doi. 10.1186/s12863-015-0311-z
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- Publication type:
- Article
Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors.
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- BMC Genetics, 2003, v. 4, p. S1, doi. 10.1186/1471-2156-4-S1-S1
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- Article
Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits.
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- BMC Biology, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s12915-015-0152-2
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- Article