Suchergebnisse - "Freimer, Nelson B"
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Variance component model to account for sample structure in genome-wide association studies
ISSN: 1061-4036, 1546-1718, 1546-1718Veröffentlicht: New York Nature Publishing Group US 01.04.2010Veröffentlicht in Nature genetics (01.04.2010)“… Eleazar Eskin and colleagues report a variance component model for correcting for sample structure in association studies. The EMMAX program is publicly …”
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Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
ISSN: 2041-1723, 2041-1723Veröffentlicht: London Nature Publishing Group UK 28.03.2022Veröffentlicht in Nature communications (28.03.2022)“… Few studies have explored the impact of rare variants (minor allele frequency < 1%) on highly heritable plasma metabolites identified in metabolomic screens …”
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
ISSN: 1097-4199, 1097-4199Veröffentlicht: United States 21.06.2017Veröffentlicht in Neuron (Cambridge, Mass.) (21.06.2017)“… Tourette syndrome (TS) is a model neuropsychiatric disorder thought to arise from abnormal development and/or maintenance of cortico-striato-thalamo-cortical …”
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Ancient hybridization and strong adaptation to viruses across African vervet monkey populations
ISSN: 1061-4036, 1546-1718, 1546-1718Veröffentlicht: New York Nature Publishing Group US 01.12.2017Veröffentlicht in Nature genetics (01.12.2017)“… Analysis of whole-genome sequencing data from 163 vervet monkeys from Africa and the Caribbean shows high diversity among taxa and identifies signatures of …”
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ForestQC: Quality control on genetic variants from next-generation sequencing data using random forest
ISSN: 1553-7358, 1553-734X, 1553-7358Veröffentlicht: United States Public Library of Science 01.12.2019Veröffentlicht in PLoS computational biology (01.12.2019)“… Next-generation sequencing technology (NGS) enables the discovery of nearly all genetic variants present in a genome. A subset of these variants, however, may …”
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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
ISSN: 1061-4036, 1546-1718, 1546-1718Veröffentlicht: New York Nature Publishing Group US 01.01.2009Veröffentlicht in Nature genetics (01.01.2009)“… Nelson Freimer and colleagues report the first genome-wide association study of a longitudinal birth cohort (the Northern Finland Birth Cohort 1966). The …”
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Evidence of selection in the uncoupling protein 1 gene region suggests local adaptation to solar irradiance in savannah monkeys ( Chlorocebus spp.)
ISSN: 1471-2954, 1471-2954Veröffentlicht: England 14.09.2022Veröffentlicht in Proceedings of the Royal Society. B, Biological sciences (14.09.2022)“… In the last 300 thousand years, the genus expanded from equatorial Africa into the southernmost latitudes of the continent, where colder climate was a probable …”
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Replicating genotype–phenotype associations
ISSN: 0028-0836, 1476-4687, 1476-4687Veröffentlicht: London Nature Publishing Group UK 07.06.2007Veröffentlicht in Nature (London) (07.06.2007)“… What constitutes replication of a genotype–phenotype association, and how best can it be achieved? Gene association pitfalls Reviews of the many genetic …”
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5-HTTLPR genotype and anxiety-related personality traits: A meta-analysis and new data
ISSN: 1552-4841, 1552-485X, 1552-485XVeröffentlicht: Hoboken Wiley Subscription Services, Inc., A Wiley Company 05.03.2009Veröffentlicht in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.03.2009)“… We investigated the strength of evidence for association of the 5‐HTTLPR polymorphism and the personality trait of Harm Avoidance. We used new primary data …”
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ACE2 and TMPRSS2 variation in savanna monkeys (Chlorocebus spp.): Potential risk for zoonotic/anthroponotic transmission of SARS-CoV-2 and a potential model for functional studies
ISSN: 1932-6203, 1932-6203Veröffentlicht: United States Public Library of Science 23.06.2020Veröffentlicht in PloS one (23.06.2020)“… The COVID-19 pandemic, caused by the coronavirus SARS-CoV-2, has devastated health infrastructure around the world. Both ACE2 (an entry receptor) and TMPRSS2 …”
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Diversity matters: opportunities in the study of the genetics of psychotic disorders in low- and middle-income countries in Latin America
ISSN: 1516-4446, 1809-452X, 1809-452XVeröffentlicht: Brazil Associação Brasileira de Psiquiatria 01.11.2021Veröffentlicht in Revista brasileira de psiquiatria (01.11.2021)“… Lack of diversity regarding genetic and environmental backgrounds weakens the generalization and clinical applicability of research findings on psychotic …”
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Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder
ISSN: 1091-6490, 1091-6490Veröffentlicht: United States 09.02.2016Veröffentlicht in Proceedings of the National Academy of Sciences - PNAS (09.02.2016)“… Abnormalities in sleep and circadian rhythms are central features of bipolar disorder (BP), often persisting between episodes. We report here, to our …”
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Decomposing decision components in the stop-signal task: a model-based approach to individual differences in inhibitory control
ISSN: 1530-8898, 1530-8898Veröffentlicht: United States 01.08.2014Veröffentlicht in Journal of cognitive neuroscience (01.08.2014)“… The stop-signal task, in which participants must inhibit prepotent responses, has been used to identify neural systems that vary with individual differences in …”
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Geographic Patterns of Genome Admixture in Latin American Mestizos
ISSN: 1553-7404, 1553-7390, 1553-7404Veröffentlicht: United States Public Library of Science 01.03.2008Veröffentlicht in PLoS genetics (01.03.2008)“… The large and diverse population of Latin America is potentially a powerful resource for elucidating the genetic basis of complex traits through admixture …”
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Polygenic Hyperlipidemias and Coronary Artery Disease Risk
ISSN: 2574-8300, 2574-8300Veröffentlicht: United States 01.04.2020Veröffentlicht in Circulation. Genomic and precision medicine (01.04.2020)“… Hyperlipidemia is a highly heritable risk factor for coronary artery disease (CAD). While monogenic familial hypercholesterolemia associates with severely …”
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Differences in presentation and progression between severe FIC1 and BSEP deficiencies
ISSN: 0168-8278, 1600-0641, 1600-0641Veröffentlicht: Kidlington Elsevier B.V 01.07.2010Veröffentlicht in Journal of hepatology (01.07.2010)“… Progressive familial intrahepatic cholestasis (PFIC) with normal serum levels of gamma-glutamyltranspeptidase can result from mutations in ATP8B1 (encoding …”
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The Contribution of GWAS Loci in Familial Dyslipidemias
ISSN: 1553-7404, 1553-7390, 1553-7404Veröffentlicht: United States Public Library of Science 26.05.2016Veröffentlicht in PLoS genetics (26.05.2016)“… Familial combined hyperlipidemia (FCH) is a complex and common familial dyslipidemia characterized by elevated total cholesterol and/or triglyceride levels …”
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The enduring gap in educational attainment in schizophrenia according to the past 50 years of published research: a systematic review and meta-analysis
ISSN: 2215-0374, 2215-0374Veröffentlicht: England 01.07.2022Veröffentlicht in The Lancet. Psychiatry (01.07.2022)“… Educational attainment is associated with wellbeing and health, but patients with schizophrenia achieve lower levels of education than people without. Several …”
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Advancing digital sensing in mental health research
ISSN: 2398-6352, 2398-6352Veröffentlicht: London Nature Publishing Group UK 18.12.2024Veröffentlicht in NPJ digital medicine (18.12.2024)“… Digital sensing tools, like smartphones and wearables, offer transformative potential for mental health research by enabling scalable, longitudinal data …”
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Recombination rates in admixed individuals identified by ancestry-based inference
ISSN: 1061-4036, 1546-1718, 1546-1718Veröffentlicht: New York Nature Publishing Group US 01.09.2011Veröffentlicht in Nature genetics (01.09.2011)“… John Novembre and colleagues present a new approach for constructing recombination maps based on ancestry switch points among individuals. They construct a …”
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