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Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature.
- Published in:
- 2009
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- Publication type:
- journal article
Genetic Variation in Human 5-HT Receptors: Potential Pathogenetic and Pharmacological Role<sup>a</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 861, n. 1, p. 26, doi. 10.1111/j.1749-6632.1998.tb10169.x
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- Publication type:
- Article
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.
- Published in:
- Molecular Medicine, 2018, v. 24, n. 1, p. N.PAG, doi. 10.1186/s10020-018-0031-8
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- Publication type:
- Article
Association study of dopamine D2, D3, D4 receptor and serotonin transporter gene polymorphisms with sleep attacks in Parkinson's disease.
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- Movement Disorders, 2004, v. 19, n. 6, p. 705, doi. 10.1002/mds.20134
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- Publication type:
- Article
Molekulargenetische Erkenntnisse erweitern das Verständnis psychiatrischer Störungen.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Durchbrüche im Verständnis der molekularen Ursachen psychiatrischer Störungen.
- Published in:
- Der Nervenarzt, 2019, v. 90, n. 2, p. 99, doi. 10.1007/s00115-018-0670-6
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- Publication type:
- Article
Achalasia: will genetic studies provide insights?
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 353, doi. 10.1007/s00439-010-0874-8
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- Publication type:
- Article
Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness.
- Published in:
- Human Genetics, 2009, v. 126, n. 2, p. 255, doi. 10.1007/s00439-009-0668-z
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- Publication type:
- Article
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.
- Published in:
- Human Genetics, 2003, v. 114, n. 1, p. 115, doi. 10.1007/s00439-003-1022-5
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- Publication type:
- Article
Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.
- Published in:
- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2021, v. 76, n. 5, p. 786, doi. 10.1093/gerona/glab023
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- Publication type:
- Article
Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder.
- Published in:
- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0175-x
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- Publication type:
- Article
Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.
- Published in:
- Translational Psychiatry, 2017, v. 7, n. 1, p. e997, doi. 10.1038/tp.2016.272
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- Publication type:
- Article
Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide support.
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- Translational Psychiatry, 2013, v. 3, n. 7, p. 1, doi. 10.1038/tp.2013.57
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- Publication type:
- Article
Quantifying the heritability of glioma using genome-wide complex trait analysis.
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- Scientific Reports, 2015, v. 5, n. 1, p. 17267, doi. 10.1038/srep17267
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- Publication type:
- Article
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 7, p. 399, doi. 10.1038/jhg.2015.37
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- Publication type:
- Article
Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study.
- Published in:
- Molecular Autism, 2020, v. 11, n. 1, p. 1, doi. 10.1186/s13229-020-00345-2
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- Publication type:
- Article
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS).
- Published in:
- European Journal of Haematology, 2017, v. 99, n. 1, p. 70, doi. 10.1111/ejh.12892
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- Publication type:
- Article
Hippocampal Function in Healthy Carriers of the CLU Alzheimer's Disease Risk Variant.
- Published in:
- Journal of Neuroscience, 2011, v. 31, n. 49, p. 18180, doi. 10.1523/JNEUROSCI.4960-11.2011
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- Publication type:
- Article
Missing Heritability in the Tails of Quantitative Traits? A Simulation Study on the Impact of Slightly Altered True Genetic Models.
- Published in:
- Human Heredity, 2011, v. 72, n. 3, p. 173, doi. 10.1159/000332824
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- Publication type:
- Article
Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 10 Pair-Wise Interaction Tests.
- Published in:
- Human Heredity, 2010, v. 69, n. 4, p. 268, doi. 10.1159/000295896
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- Publication type:
- Article
Developmental Dyslexia – Recurrence Risk Estimates from a German Bi-Center Study Using the Single Proband Sib Pair Design.
- Published in:
- Human Heredity, 2005, v. 59, n. 3, p. 136, doi. 10.1159/000085572
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- Publication type:
- Article
Computer-Assisted Phenotype Characterization for Genetic Research in Psychiatry.
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- Human Heredity, 2004, v. 58, n. 3/4, p. 122, doi. 10.1159/000083538
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- Publication type:
- Article
A Novel Missense Mutation in the DNA Mismatch Repair Gene hMLH1 Present among East Asians but Not among Europeans.
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- Human Heredity, 1998, v. 48, n. 2, p. 87, doi. 10.1159/000022786
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- Publication type:
- Article
Investigation of Complement C4B Deficiency in Schizophrenia.
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- Human Heredity, 1997, v. 47, n. 5, p. 279, doi. 10.1159/000154424
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- Publication type:
- Article
A Common Ser/Thr Polymorphism in the Perforin-Homologous Region of Human Complement Component C7.
- Published in:
- Human Heredity, 1994, v. 44, n. 6, p. 301, doi. 10.1159/000154235
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- Publication type:
- Article
Addressing Global Environmental Challenges to Mental Health Using Population Neuroscience: A Review.
- Published in:
- JAMA Psychiatry, 2023, v. 80, n. 10, p. 1066, doi. 10.1001/jamapsychiatry.2023.2996
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- Publication type:
- Article
Association of a Reproducible Epigenetic Risk Profile for Schizophrenia With Brain Methylation and Function.
- Published in:
- 2020
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- Publication type:
- journal article
Implication of a rare deletion at distal 16p11.2 in schizophrenia.
- Published in:
- 2013
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- Publication type:
- journal article
Implication of a Rare Deletion at Distal 16pll.2 in Schizophrenia.
- Published in:
- JAMA Psychiatry, 2013, v. 70, n. 3, p. 253, doi. 10.1001/2013.jamapsychiatry.71
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- Publication type:
- Article
Observations that suggest a contribution of altered dermal papilla mitochondrial function to androgenetic alopecia.
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- Experimental Dermatology, 2022, v. 31, n. 6, p. 906, doi. 10.1111/exd.14536
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- Publication type:
- Article
Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies.
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- Experimental Dermatology, 2020, v. 29, n. 9, p. 814, doi. 10.1111/exd.14130
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- Publication type:
- Article
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.
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- Experimental Dermatology, 2017, v. 26, n. 6, p. 536, doi. 10.1111/exd.13123
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- Publication type:
- Article
Hunting the genes in male-pattern alopecia: how important are they, how close are we and what will they tell us?
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- Experimental Dermatology, 2016, v. 25, n. 4, p. 251, doi. 10.1111/exd.12965
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- Publication type:
- Article
Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified.
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- Experimental Dermatology, 2012, v. 21, n. 5, p. 390, doi. 10.1111/j.1600-0625.2012.01469.x
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- Publication type:
- Article
Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01959-1
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- Publication type:
- Article
Identification of pleiotropy at the gene level between psychiatric disorders and related traits.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01530-4
- By:
- Publication type:
- Article
Transcriptome-wide analysis of filarial extract-primed human monocytes reveal changes in LPS-induced PTX3 expression levels.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-38985-x
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- Publication type:
- Article
Mendelian randomization provides support for obesity as a risk factor for meningioma.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-36186-6
- By:
- Publication type:
- Article
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 14, p. 2719, doi. 10.1093/hmg/ddp204
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- Publication type:
- Article
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 6, p. 667, doi. 10.1093/hmg/ddm009
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- Publication type:
- Article
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01818-4
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- Publication type:
- Article
Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01220-0
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- Publication type:
- Article
Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00366-1
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- Publication type:
- Article
Genome-wide association study identifies multiple susceptibility loci for glioma.
- Published in:
- Nature Communications, 2015, v. 6, n. 10, p. 8559, doi. 10.1038/ncomms9559
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- Publication type:
- Article
Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes.
- Published in:
- Nature Communications, 2014, v. 5, n. 10, p. 5236, doi. 10.1038/ncomms6236
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- Publication type:
- Article
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.
- Published in:
- Nature Communications, 2013, v. 4, n. 11, p. 2739, doi. 10.1038/ncomms3739
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- Publication type:
- Article
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
- Published in:
- Nature Communications, 2013, v. 4, n. 10, p. 2549, doi. 10.1038/ncomms3549
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- Publication type:
- Article
DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations.
- Published in:
- Clinical Epigenetics, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13148-015-0112-2
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- Publication type:
- Article
Brief Report: No Association Between Premorbid Adjustment in Adult-Onset Schizophrenia and Genetic Variation in Dysbindin.
- Published in:
- Journal of Autism & Developmental Disorders, 2008, v. 38, n. 10, p. 1977, doi. 10.1007/s10803-008-0582-6
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- Publication type:
- Article