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1
The trans-ancestral genomic architecture of glycemic traits.
In: Nature genetics, vol. 53, no. 6, pp. 840-860 (2021)
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2
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
In: Molecular psychiatry, vol 25, iss 10 (2020)
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3
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
In: Molecular psychiatry, vol 25, iss 10 (2020)
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4
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene
In: Genes ; Volume 10 ; Issue 12 (2019)
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5
Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula
Pimenta, J; Lopes, AM; Carracedo, A. - : Nature Publishing Group, 2019
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6
Enrichment of genetic markers of recent human evolution in educational and cognitive traits.
In: Scientific reports, vol 8, iss 1 (2018)
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7
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
In: Nature genetics, vol 50, iss 7 (2018)
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8
Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018).
In: Twin research and human genetics : the official journal of the International Society for Twin Studies, vol 21, iss 5 (2018)
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9
Global genetic differentiation of complex traits shaped by natural selection in humans.
In: Nature communications, vol. 9, no. 1, pp. 1865 (2018)
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10
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
In: Molecular psychiatry, vol 22, iss 3 (2017)
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11
DISSECTING THE GENETICS OF HUMAN COMMUNICATION: INSIGHTS INTO SPEECH, LANGUAGE, AND READING
In: http://rave.ohiolink.edu/etdc/view?acc_num=case1473337776061224 (2017)
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12
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
In: American journal of human genetics, vol 99, iss 3 (2016)
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13
Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study
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14
Reconstructing Austronesian population history in Island Southeast Asia.
In: Nature communications, vol 5, iss 1 (2014)
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15
Functional annotation signatures of disease susceptibility loci improve SNP association analysis.
Iversen, ES; Lipton, G; Clyde, MA. - : BMC Genomics, 2014
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16
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.
In: Mol Psychiatry , 19 (2) 253 - 258. (2014) (2014)
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17
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014)
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18
Genome-wide association study of receptive language ability of 12-year-olds.
In: J Speech Lang Hear Res , 57 (1) 96 - 105. (2014) (2014)
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19
Neurophysiological and Genetic Bases of Developmental Language Disorder
In: Doctoral Dissertations (2014)
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20
Genome-wide association study of receptive language ability of 12-year-olds
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