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Advanced Search Results For "Estonia"

1 - 10 of 13,265 results for
 "Estonia"
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Teatr zawieszony nad codziennością. (Polish)

Publication Type: Periodical

Source(s): Glass & Ceramics / Szklo i Ceramika; 2022, Issue 3, p8-11, 4p

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Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection

Publication Type: Academic Journal

Source(s): Nature Communications, Vol 13, Iss 1, Pp 1-13 (2022)

Abstract: Immune genes under selection can shed light on phenotypes contributing to survival and modern inflammatory conditions. Here, the authors prioritize adaptive disease variants in 535 risk loci for 21 inflammatory conditions and report promising SNPs for ...

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Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes

Publication Type: Academic Journal

Source(s): Translational Psychiatry, Vol 12, Iss 1, Pp 1-10 (2022)

Abstract: Abstract Despite advances in identifying the genetic basis of psychiatric and neurological disorders, fundamental questions about their evolutionary origins remain elusive. Here, introgressed variants from archaic humans such as Neandertals can serve a...

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ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma

Publication Type: Academic Journal

Source(s): Communications Biology, Vol 5, Iss 1, Pp 1-15 (2022)

Abstract: Rare variant association data from human genetics combined with in vitro and in vivo functional validation highlight ANGPTL7 as a promising therapeutic target for intraocular pressure reduction, and protection from glaucoma.

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Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

Publication Type: Academic Journal

Source(s): Communications Biology, Vol 5, Iss 1, Pp 1-16 (2022)

Abstract: A genome-wide association study identifies MFGE8 as protective against coronary atherosclerosis in European and East Asian populations.

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Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse

Publication Type: Academic Journal

Source(s): Nature Communications, Vol 13, Iss 1, Pp 1-12 (2022)

Abstract: Although pelvic organ prolapse is a common gynecological condition, the genetic component of disease risk is not well known. Here the authors find common genetic variants associated with the disease and present a polygenic risk score to enhance individ...

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A Principal Component Informed Approach to Address Polygenic Risk Score Transferability Across European Cohorts

Publication Type: Academic Journal

Source(s): Frontiers in Genetics, Vol 13 (2022)

Abstract: One important confounder in genome-wide association studies (GWASs) is population genetic structure, which may generate spurious associations if not properly accounted for. This may ultimately result in a biased polygenic risk score (PRS) prediction, e...

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Meta-analyses identify DNA methylation associated with kidney function and damage

Publication Type: Academic Journal

Source(s): Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)

Abstract: Many genetic loci have been identified to be associated with kidney disease, but the molecular mechanisms are not well understood. Here, the authors perform epigenome-wide association studies on kidney function measures to identify epigenetic marks and...

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Genome-wide association study identifies five risk loci for pernicious anemia

Publication Type: Academic Journal

Source(s): Nature Communications, Vol 12, Iss 1, Pp 1-9 (2021)

Abstract: Pernicious anemia shows co-incidence with autoimmune disorders, yet the genetic basis for this condition is understudied. Here, the authors perform a genome-wide association study meta-analysis on pernicious anemia, identifying five susceptibility loci...

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