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The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males.
- Published in:
- Human Genetics, 2006, v. 120, n. 4, p. 447, doi. 10.1007/s00439-006-0198-x
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- Publication type:
- Article
On the applicability of a haplotype map to un-assayed populations.
- Published in:
- Human Genetics, 2004, v. 114, n. 2, p. 214, doi. 10.1007/s00439-003-1046-x
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- Publication type:
- Article
Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence.
- Published in:
- FASEB Journal, 2010, v. 24, n. 8, p. 3066, doi. 10.1096/fj.09-152611
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- Publication type:
- Article
Intracellular stress signaling pathways activated during human islet preparation and following acute cytokine exposure.
- Published in:
- 2004
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- Publication type:
- journal article
Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genes.
- Published in:
- 1994
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- Publication type:
- journal article
Linkage analysis and molecular scanning of glucokinase gene in NIDDM families.
- Published in:
- 1993
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- Publication type:
- journal article
Carriers of the fragile X mental retardation 1 (FMR1) premutation allele present with increased levels of cytokine IL-10.
- Published in:
- Journal of Neuroinflammation, 2012, v. 9, n. 1, p. 238, doi. 10.1186/1742-2094-9-238
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- Publication type:
- Article
Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.
- Published in:
- BMC Genomics, 2012, v. 13, n. 1, p. 241, doi. 10.1186/1471-2164-13-241
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- Publication type:
- Article
Calcium phosphate transfection generates mammalian recombinant cell lines with higher specific productivity than polyfection.
- Published in:
- Biotechnology & Bioengineering, 2008, v. 101, n. 5, p. 937, doi. 10.1002/bit.21972
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- Publication type:
- Article
Mapping Using Linkage Disequilibrium Estimates: A Comparative Study.
- Published in:
- Human Heredity, 1997, v. 47, n. 4, p. 237, doi. 10.1159/000154418
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- Publication type:
- Article
Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability.
- Published in:
- Nature Reviews Genetics, 2007, v. 8, n. 8, p. 639, doi. 10.1038/nrg2149
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- Publication type:
- Article
Mendelian disorders deserve more attention.
- Published in:
- 2006
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- Publication type:
- journal article
Influence of CRTC1 Polymorphisms on Body Mass Index and Fat Mass in Psychiatric Patients and the General Adult Population.
- Published in:
- JAMA Psychiatry, 2013, v. 70, n. 10, p. 1011, doi. 10.1001/jamapsychiatry.2013.187
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- Publication type:
- Article
GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 1, p. 259, doi. 10.1093/hmg/ddt404
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- Publication type:
- Article
Genome-wide meta-analysis of common variant differences between men and women.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 21, p. 4805, doi. 10.1093/hmg/dds304
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- Publication type:
- Article
Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 14, p. 3283, doi. 10.1093/hmg/dds137
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- Publication type:
- Article
Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 18, p. 3710, doi. 10.1093/hmg/ddr272
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- Publication type:
- Article
Two trans-acting eQTLs modulate the penetrance of PRPF31 mutations.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 20, p. 3154, doi. 10.1093/hmg/ddn212
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- Publication type:
- Article
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
- Published in:
- Nature, 2012, v. 485, n. 7398, p. 363, doi. 10.1038/nature11091
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- Publication type:
- Article
Methods for testing association between uncertain genotypes and quantitative traits.
- Published in:
- Biostatistics, 2011, v. 12, n. 1, p. 1, doi. 10.1093/biostatistics/kxq039
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- Publication type:
- Article
The phenotype of recurrent 10q22q23 deletions and duplications.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 4, p. 400, doi. 10.1038/ejhg.2010.211
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- Publication type:
- Article
Genetic male infertility and mutation of CATSPER ion channels.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1178, doi. 10.1038/ejhg.2010.108
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- Publication type:
- Article
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.
- Published in:
- 2007
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- Publication type:
- Correction notice
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1111, doi. 10.1038/sj.ejhg.5201675
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- Publication type:
- Article
Typing without calling the allele: a strategy for inferring SNP haplotypes.
- Published in:
- 2005
- By:
- Publication type:
- Letter
Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 6, p. 763, doi. 10.1038/sj.ejhg.5201406
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- Publication type:
- Article
USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses.
- Published in:
- European Journal of Human Genetics, 2002, v. 10, n. 6, p. 339, doi. 10.1038/sj.ejhg.5200831
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- Publication type:
- Article
Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families.
- Published in:
- 1998
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- Publication type:
- journal article
Pseudometabolic expression and phenotypic variability of calpain deficiency in two siblings.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Common variants associated with plasma triglycerides and risk for coronary artery disease.
- Published in:
- Nature Genetics, 2013, v. 45, n. 11, p. 1345, doi. 10.1038/ng.2795
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- Publication type:
- Article
Discovery and refinement of loci associated with lipid levels.
- Published in:
- Nature Genetics, 2013, v. 45, n. 11, p. 1274, doi. 10.1038/ng.2797
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- Publication type:
- Article
Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma.
- Published in:
- Nature Genetics, 2012, v. 44, n. 2, p. 133, doi. 10.1038/ng.1026
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- Publication type:
- Article
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.
- Published in:
- Nature Genetics, 2011, v. 43, n. 8, p. 753, doi. 10.1038/ng.866
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- Publication type:
- Article
Variants in MTNR1B influence fasting glucose levels.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 77, doi. 10.1038/ng.290
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- Publication type:
- Article
Common variants near MC4R are associated with fat mass, weight and risk of obesity.
- Published in:
- Nature Genetics, 2008, v. 40, n. 6, p. 768, doi. 10.1038/ng.140
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- Publication type:
- Article
Genome-wide association analysis identifies 20 loci that influence adult height.
- Published in:
- Nature Genetics, 2008, v. 40, n. 5, p. 575, doi. 10.1038/ng.121
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- Publication type:
- Article
RNAseq analysis of heart tissue from mice treated with atenolol and isoproterenol reveals a reciprocal transcriptional response.
- Published in:
- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-3059-6
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- Publication type:
- Article
Genome-Wide Association Study of Metabolic Traits Reveals Novel Gene-Metabolite-Disease Links.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 2, p. 1, doi. 10.1371/journal.pgen.1004132
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- Publication type:
- Article
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 6, p. 1, doi. 10.1371/journal.pgen.1000504
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- Publication type:
- Article
Myotilin is not the Causative Gene for Vocal Cord and Pharyngeal Weakness with Distal Myopathy (VCPDM).
- Published in:
- Annals of Human Genetics, 2006, v. 70, n. 3, p. 414, doi. 10.1111/j.1529-8817.2005.00252.x
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- Publication type:
- Article
Clarity and claims in variation/mutation databasing.
- Published in:
- 2011
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- Publication type:
- Letter
A modular approach for integrative analysis of large-scale gene-expression and drug-response data.
- Published in:
- Nature Biotechnology, 2008, v. 26, n. 5, p. 531, doi. 10.1038/nbt1397
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- Publication type:
- Article
Disease taxonomy – monogenic muscular dystrophy.
- Published in:
- British Medical Bulletin, 1999, v. 55, n. 2, p. 340, doi. 10.1258/0007142991902411
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- Publication type:
- Article
Mapping Genetic Variants Associated with Beta-Adrenergic Responses in Inbred Mice.
- Published in:
- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0041032
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- Publication type:
- Article
Network-Guided Analysis of Genes with Altered Somatic Copy Number and Gene Expression Reveals Pathways Commonly Perturbed in Metastatic Melanoma.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018369
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- Publication type:
- Article
Global Transcriptional Programs in Peripheral Nerve Endoneurium and DRG Are Resistant to the Onset of Type 1 Diabetic Neuropathy in Ins2<sup>Akita/+</sup> Mice.
- Published in:
- PLoS ONE, 2010, v. 5, n. 5, p. 1, doi. 10.1371/journal.pone.0010832
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- Publication type:
- Article
Cardiovascular Response to Beta-Adrenergic Blockade or Activation in 23 Inbred Mouse Strains.
- Published in:
- PLoS ONE, 2009, v. 4, n. 8, p. 1, doi. 10.1371/journal.pone.0006610
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- Publication type:
- Article
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
- Published in:
- Nature Genetics, 2001, v. 29, n. 1, p. 83, doi. 10.1038/ng718
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- Publication type:
- Article
Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome.
- Published in:
- Nature Genetics, 1999, v. 22, n. 2, p. 178, doi. 10.1038/9696
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- Publication type:
- Article
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B.
- Published in:
- Nature Genetics, 1998, v. 20, n. 1, p. 37, doi. 10.1038/1689
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- Publication type:
- Article