Microbiomics, Metabolomics, Predicted Metagenomics, and Hepatic Steatosis in a Population-Based Study of 1,355 Adults.
Hepatology.
2021 Mar;73(3):968-982. doi: 10.1002/hep.31417. PubMed PMID:
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Long-term effects of antimicrobial drugs on the composition of the human gut microbiota.
Gut Microbes.
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Reduced penetrance of pathogenic ACMG variants in a deeply phenotyped cohort study and evaluation of ClinVar classification over time.
Genet Med.
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Comparison of Illumina versus Nanopore 16S rRNA Gene Sequencing of the Human Nasal Microbiota.
Genes (Basel).
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Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length.
Front Genet.
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Exercise with food withdrawal at thermoneutrality impacts fuel use, the microbiome, AMPK phosphorylation, muscle fibers, and thyroid hormone levels in rats.
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Diversity, compositional and functional differences between gut microbiota of children and adults.
Sci Rep.
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Integration of epidemiologic, pharmacologic, genetic and gut microbiome data in a drug-metabolite atlas.
Nat Med.
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Relationship between gut microbiota and circulating metabolites in population-based cohorts.
Nat Commun.
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Intestinal microbiome composition and its relation to joint pain and inflammation.
Nat Commun.
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Novel taxonomy-independent deep learning microbiome approach allows for accurate classification of different forensically relevant human epithelial materials.
Forensic Sci Int Genet.
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Differences in Systemic IgA Reactivity and Circulating Th Subsets in Healthy Volunteers With Specific Microbiota Enterotypes.
Front Immunol.
2019;10:341. doi: 10.3389/fimmu.2019.00341. eCollection 2019. PubMed PMID:
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The effect of antimicrobial drug use on the composition of the genitourinary microbiota in an elderly population.
BMC Microbiol.
2019 Jan 9;19(1):9. doi: 10.1186/s12866-018-1379-1. PubMed PMID:
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Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels.
Nat Commun.
2018 Oct 12;9(1):4228. doi: 10.1038/s41467-018-06620-4. PubMed PMID:
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Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness.
Front Genet.
2018;9:420. doi: 10.3389/fgene.2018.00420. eCollection 2018. PubMed PMID:
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Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane.
Ophthalmology.
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Rare gene deletions in genetic generalized and Rolandic epilepsies.
PLoS One.
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Observational multi-centre, prospective study to characterize novel pathogen-and host-related factors in hospitalized patients with lower respiratory tract infections and/or sepsis - the "TAILORED-Treatment" study.
BMC Infect Dis.
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Rare coding variants in genes encoding GABA(A) receptors in genetic generalised epilepsies: an exome-based case-control study.
Lancet Neurol.
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Meta-analysis of human genome-microbiome association studies: the MiBioGen consortium initiative.
Microbiome.
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A rare missense variant in RCL1 segregates with depression in extended families.
Mol Psychiatry.
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Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease.
Brain.
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Microbiome measurement: Possibilities and pitfalls.
Best Pract Res Clin Gastroenterol.
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Establishing the role of rare coding variants in known Parkinson's disease risk loci.
Neurobiol Aging.
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Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea.
Front Genet.
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Population-specific genetic variation in large sequencing data sets: why more data is still better.
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Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations.
Biol Psychiatry.
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Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.
Mol Psychiatry.
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Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.
Mol Psychiatry.
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Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population.
Neurobiol Aging.
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Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis.
PLoS Genet.
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Uncompromised 10-year survival of oldest old carrying somatic mutations in DNMT3A and TET2.
Blood.
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Quantifying prion disease penetrance using large population control cohorts.
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Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
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Preclinical safety assessment of Ad[I/PPT-E1A], a novel oncolytic adenovirus for prostate cancer.
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Evaluating baculovirus as a vector for human prostate cancer gene therapy.
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