Zobrazeno 1 - 10
of 38
pro vyhledávání: '"genome-wide linkage scan"'
Autor:
Lihua Wang, Siyu Wang, Jason A. Anema, Vaha A. Moghaddam, Yanli Lu, Shiow Lin, E. Warwick Daw, Allison L. Kuipers, Iva Miljkovic, Michael Brent, Gary J. Patti, Bharat Thygarajan, Joseph M. Zmuda, Michael A. Province, Ping An
Publikováno v:
Journal of Lipid Research, Vol 66, Iss 1, Pp 100702- (2025)
Triglyceride (TG)/HDL-C ratio (THR) is a surrogate predictor of hyperinsulinemia. To identify novel genetic loci for THR change over time (ΔTHR), we conducted genome-wide association study (GWAS) and genome-wide linkage scan (GWLS) among nondiabetic
Externí odkaz:
https://doaj.org/article/1ff1f421f24742b3ae61246fa204dca1
Autor:
J. Michael Bailey, Alan R. Sanders, Gerulf Rieger, Gary W. Beecham, Shengru Guo, Khytam Dawood, Alana B. Kolundzija, Eden R. Martin, Ritesha S Krishnappa
Publikováno v:
Archives of Sexual Behavior
Male sexual orientation is influenced by environmental and complex genetic factors. Childhood gender nonconformity (CGN) is one of the strongest correlates of homosexuality with substantial familiality. We studied brothers in families with two or mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7f8d3dc72e34b07b132cfa45642345e
https://doi.org/10.1007/s10508-021-02146-x
https://doi.org/10.1007/s10508-021-02146-x
Autor:
Brian Mustanski, Shengru Guo, Dean H. Hamer, Eden R. Martin, Judith A. Badner, Sven Bocklandt, Gary W. Beecham, Alan R. Sanders
Publikováno v:
Archives of Sexual Behavior
Male sexual orientation is a scientifically and socially important trait shown by family and twin studies to be influenced by environmental and complex genetic factors. Individual genome-wide linkage studies (GWLS) have been conducted, but not jointl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c7f61d01bf108d65e960557a9a3e550
http://europepmc.org/articles/PMC8604844
http://europepmc.org/articles/PMC8604844
Akademický článek
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Akademický článek
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Autor:
Elisa T. Lee, Yun Zhu, Jue Lin, Lyle G. Best, Jean W. MacCluer, Tet Matsuguchi, Shelley A. Cole, Elizabeth H. Blackburn, V. Saroja Voruganti, Jinying Zhao
Publikováno v:
Blackburn, Elizabeth; Zhu, Y; Voruganti, VS; Lin, J; Matsuguchi, T; Best, LG; et al.(2013). QTL mapping of leukocyte telomere length in American Indians: The strong heart family study. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/2nq5z80v
Scopus-Elsevier
Aging (Albany NY)
Scopus-Elsevier
Aging (Albany NY)
Telomeres play a central role in cellular senescence and are associated with a variety of age-related disorders such as dementia, Alzheimer's disease and atherosclerosis. Telomere length varies greatly among individuals of the same age, and is herita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fabeef634560103c751ba748c7894b1
https://doi.org/10.18632/aging.100600
https://doi.org/10.18632/aging.100600
Autor:
Gonneke Willemsen, Marijn A. Distel, Eco J. C. de Geus, Viatcheslav Saviouk, Jouke-Jan Hottenga, Dorret I. Boomsma, Eline Slagboom
Publikováno v:
Savyuk, V, Hottenga, J J, Slagboom, P E, Distel, M A, de Geus, E J C, Willemsen, G & Boomsma, D I 2011, ' ADHD in Dutch adults: heritability and linkage study ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 156, no. 3, pp. 352-362 . https://doi.org/10.1002/ajmg.b.31170
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 156(3), 352-362. Wiley-Liss Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 156B(3), 352-362
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 156(3), 352-362. Wiley-Liss Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 156B(3), 352-362
Attention deficit/hyperactivity disorder (ADHD) is a neurodevelopmental phenotype that persists into adulthood. This study investigated the heritability of inattentive and hyperactive symptoms and of total ADHD symptomatology load (ADHD index) in adu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3767d3ed641d2da218566bfe761771ad
https://pubmed.ncbi.nlm.nih.gov/21294247
https://pubmed.ncbi.nlm.nih.gov/21294247
Autor:
Minkelen, R. van
Publikováno v:
None
Venous thrombosis (VT) is a multicausal disease that is caused by the interaction of both genetic and acquired risk factors. The aim of the studies described in this thesis was to identify novel genes or genomic regions that contribute to the suscept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c07e231c49dc4494a91deae94fac2fc3
https://hdl.handle.net/1887/13501
https://hdl.handle.net/1887/13501
Akademický článek
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