SwePub - sökning: WFRF:(Levy SE)

Numrering	Referens	Omslagsbild	Hitta
1.	Ruderfer, DM, et al. (författare) Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes 2018 Ingår i: Cell. - : Elsevier BV. - 1097-4172 .- 0092-8674. ; 173:7, s. 1705- Tidskriftsartikel (refereegranskat)
2.	Musliner, KL, et al. (författare) Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population 2019 Ingår i: JAMA psychiatry. - Chicago : American Medical Association (AMA). - 2168-6238 .- 2168-622X. ; 76:5, s. 516-525 Tidskriftsartikel (refereegranskat)
3.	Stahl, EA, et al. (författare) Genome-wide association study identifies 30 loci associated with bipolar disorder 2019 Ingår i: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 51:5, s. 793- Tidskriftsartikel (refereegranskat)
4.	Stephens, SH, et al. (författare) Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking 2013 Ingår i: Genetic epidemiology. - : Wiley. - 1098-2272 .- 0741-0395. ; 37:8, s. 846-859 Tidskriftsartikel (refereegranskat)
5.	Chanez, P, et al. (författare) Severe asthma in adults: what are the important questions? 2007 Ingår i: The Journal of allergy and clinical immunology. - : Elsevier BV. - 0091-6749. ; 119:6, s. 1337-1348 Forskningsöversikt (övrigt vetenskapligt/konstnärligt)
6.	Lim, SS, et al. (författare) Measuring the health-related Sustainable Development Goals in 188 countries: a baseline analysis from the Global Burden of Disease Study 2015 2016 Ingår i: Lancet (London, England). - 1474-547X .- 0140-6736. ; 388:10053, s. 1813-1850 Tidskriftsartikel (refereegranskat)
7.	Marshall, CR, et al. (författare) Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects 2017 Ingår i: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 49:1, s. 27-35 Tidskriftsartikel (refereegranskat)
8.	Murray, CJL, et al. (författare) Global, regional, and national disability-adjusted life years (DALYs) for 306 diseases and injuries and healthy life expectancy (HALE) for 188 countries, 1990-2013: quantifying the epidemiological transition 2015 Ingår i: Lancet (London, England). - 1474-547X .- 0140-6736. ; 386, s. 2145-2191 Tidskriftsartikel (refereegranskat)
9.	Nievergelt, CM, et al. (författare) Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder 2024 Ingår i: Nature genetics. - 1546-1718. ; 56:5, s. 792-808 Tidskriftsartikel (refereegranskat)
10.	Rodriguez-Martinez, A, et al. (författare) Height and body-mass index trajectories of school-aged children and adolescents from 1985 to 2019 in 200 countries and territories: a pooled analysis of 2181 population-based studies with 65 million participants 2020 Ingår i: Lancet (London, England). - : Elsevier. - 1474-547X .- 0140-6736. ; 396:10261, s. 1511-1524 Tidskriftsartikel (refereegranskat)
11.	Schlosser, P, et al. (författare) Meta-analyses identify DNA methylation associated with kidney function and damage 2021 Ingår i: Nature communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 12:1, s. 7174- Tidskriftsartikel (refereegranskat)abstract Chronic kidney disease is a major public health burden. Elevated urinary albumin-to-creatinine ratio is a measure of kidney damage, and used to diagnose and stage chronic kidney disease. To extend the knowledge on regulatory mechanisms related to kidney function and disease, we conducted a blood-based epigenome-wide association study for estimated glomerular filtration rate (n = 33,605) and urinary albumin-to-creatinine ratio (n = 15,068) and detected 69 and seven CpG sites where DNA methylation was associated with the respective trait. The majority of these findings showed directionally consistent associations with the respective clinical outcomes chronic kidney disease and moderately increased albuminuria. Associations of DNA methylation with kidney function, such as CpGs at JAZF1, PELI1 and CHD2 were validated in kidney tissue. Methylation at PHRF1, LDB2, CSRNP1 and IRF5 indicated causal effects on kidney function. Enrichment analyses revealed pathways related to hemostasis and blood cell migration for estimated glomerular filtration rate, and immune cell activation and response for urinary albumin-to-creatinineratio-associated CpGs.
12.	Sikdar, S, et al. (författare) Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smoking 2019 Ingår i: Epigenomics. - : Future Medicine Ltd. - 1750-192X .- 1750-1911. ; 11:13, s. 1487-1500 Tidskriftsartikel (refereegranskat)abstract Aim: Cigarette smoking influences DNA methylation genome wide, in newborns from pregnancy exposure and in adults from personal smoking. Whether a unique methylation signature exists for in utero exposure in newborns is unknown. Materials & methods: We separately meta-analyzed newborn blood DNA methylation (assessed using Illumina450k Beadchip), in relation to sustained maternal smoking during pregnancy (9 cohorts, 5648 newborns, 897 exposed) and adult blood methylation and personal smoking (16 cohorts, 15907 participants, 2433 current smokers). Results & conclusion: Comparing meta-analyses, we identified numerous signatures specific to newborns along with many shared between newborns and adults. Unique smoking-associated genes in newborns were enriched in xenobiotic metabolism pathways. Our findings may provide insights into specific health impacts of prenatal exposure on offspring.
13.	Zhou, Bin, et al. (författare) Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants 2021 Ingår i: Lancet (London, England). - : Elsevier. - 1474-547X .- 0140-6736. ; 398:10304, s. 957-980 Tidskriftsartikel (refereegranskat)
14.	Niemi, MEK, et al. (författare) 2021 swepub:Mat__t
15.	Ehret, GB, et al. (författare) Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk 2011 Ingår i: Nature. - : Springer Science and Business Media LLC. - 1476-4687 .- 0028-0836. ; 478:7367, s. 103-109 Tidskriftsartikel (refereegranskat)
16.	Evangelou, E, et al. (författare) Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 2018 Ingår i: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 50:12, s. 1755-1755 Tidskriftsartikel (refereegranskat)
17.	Forouzanfar, MH, et al. (författare) Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015 2016 Ingår i: Lancet (London, England). - 1474-547X .- 0140-6736. ; 388:10053, s. 1659-1724 Tidskriftsartikel (refereegranskat)
18.	Gnatiuc, L, et al. (författare) Sex-specific relevance of diabetes to occlusive vascular and other mortality: a collaborative meta-analysis of individual data from 980 793 adults from 68 prospective studies 2018 Ingår i: The lancet. Diabetes & endocrinology. - 2213-8595. ; 6:7, s. 538-546 Tidskriftsartikel (refereegranskat)
19.	Hoogeveen, S, et al. (författare) A many-analysts approach to the relation between religiosity and well-being 2023 Ingår i: RELIGION BRAIN & BEHAVIOR. - : Taylor & Francis Group. - 2153-599X .- 2153-5981. ; 13:3, s. 237-283 Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
20.	Huffman, JE, et al. (författare) Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF 2015 Ingår i: Blood. - : American Society of Hematology. - 1528-0020 .- 0006-4971. ; 126:11, s. E19-E29 Tidskriftsartikel (refereegranskat)abstract Twelve independent, novel, low-frequency (n = 2) and rare (n = 10) genetic variants were associated with fibrinogen, FVII, FVIII, or vWF. Nine were within previously associated genes, and 3 novel candidate genes (KCNT1, HID1, and KATNB1) were confined to cohorts of African ancestry.
21.	Jakobsson, J., et al. (författare) Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 2021 Ingår i: Autophagy. - : Informa UK Limited. - 1554-8635 .- 1554-8627. ; 17:1, s. 1-382 Tidskriftsartikel (refereegranskat)
22.	Josefsson, SE, et al. (författare) TIGIT and PD-1 Mark Intratumoral T Cells with Reduced Effector Function in B-cell Non-Hodgkin Lymphoma 2019 Ingår i: Cancer immunology research. - 2326-6074. ; 7:3, s. 355-362 Tidskriftsartikel (refereegranskat)
23.	Keaton, JM, et al. (författare) Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits 2024 Ingår i: Nature genetics. - 1546-1718. ; 56:5, s. 778-791 Tidskriftsartikel (refereegranskat)
24.	Marioni, RE, et al. (författare) DNA methylation age of blood predicts all-cause mortality in later life 2015 Ingår i: Genome biology. - 1474-760X. ; 16, s. 25- Tidskriftsartikel (refereegranskat)
25.	Materna, M, et al. (författare) The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants 2024 Ingår i: Science (New York, N.Y.). - : American Association for the Advancement of Science (AAAS). - 1095-9203 .- 0036-8075. ; 383:6686, s. eadh4059- Tidskriftsartikel (refereegranskat)

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