Zobrazeno 1 - 10
of 193
pro vyhledávání: '"Genetic association analysis"'
Publikováno v:
Ecosphere, Vol 15, Iss 10, Pp n/a-n/a (2024)
Abstract Climate change is motivating a reassessment of how seeds are selected for reforestation, as rapid environmental change can lead to local maladaptation in trees. Genetic association studies and past seed source climate both have the potential
Externí odkaz:
https://doaj.org/article/b54cf69f6c5346ce85ebe2886d7ac9fd
Autor:
Joe Kossowsky, Megan S. Schuler, Franco Giulianini, Charles B. Berde, Ben Reis, Paul M Ridker, Julie E. Buring, Tobias Kurth, Daniel I. Chasman
Publikováno v:
Frontiers in Neurology, Vol 11 (2021)
Migraine is heritable and formally diagnosed by structured criteria that require presence of some but not all possible migraine symptoms which include aura, several distinct manifestations of pain, nausea/vomiting, and sensitivity to light or sound.
Externí odkaz:
https://doaj.org/article/c158d34e5e63486ebb75e8ce673561a3
Autor:
Xixi Liu, Pengfei Wu, Lu Shen, Bin Jiao, Xinxin Liao, Haochen Wang, Jiangnan Peng, Zhangyuan Lin
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Vitamin D insufficiency has been considered a risk factor for Alzheimer's disease (AD) in several studies. Recently, four single-nucleotide polymorphisms (SNPs) to be genome-wide significant for 25-hydroxyvitamin D [25(OH)D] were identifi
Externí odkaz:
https://doaj.org/article/af0fc9409f684ac7966d78a032ca8d0e
Autor:
Amadou Gaye, Sharon K. Davis
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
Abstract Objective The underlying model of the genetic determinant of a trait is generally not known with certainty a priori. Hence, in genetic association studies, a dominant model might be erroneously modelled as additive, an error investigated pre
Externí odkaz:
https://doaj.org/article/db71a111105145ec8f6922976b93ee6b
Autor:
Tianyou Yang, Jiahao Li, Yang Wen, Tianbao Tan, Jiliang Yang, Jing Pan, Chao Hu, Yuxiao Yao, Jiao Zhang, Yijuan Xin, Suhong Li, Huimin Xia, Jing He, Yan Zou
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
BackgroundHepatoblastoma (HB) is the most common hepatic malignancy in children, accounting for approximately 80% of all childhood liver tumors. Previous genome-wide association studies (GWASs) have found that the LINC00673 rs11655237 C>T polymorphis
Externí odkaz:
https://doaj.org/article/51833dc73b274bcbba33c1d7d559ab13
Akademický článek
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Autor:
Susana David
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Submitted by Susana David (suzana.david@insa.min-saude.pt) on 2021-09-30T13:15:18Z No. of bitstreams: 1 2021_Trends_in_Genetics.pdf: 283135 bytes, checksum: e2a78a5cabf84900746c742b067f6d34 (MD5) Approved for entry into archive by Paula Faustino (pau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c3808ea7621e166e0520eaa305a9d36
https://hdl.handle.net/10400.18/7805
https://hdl.handle.net/10400.18/7805
Publikováno v:
Genetic Epidemiology
An important aspect of disease gene mapping is replication, that is, a putative finding in one group of individuals is confirmed in another set of individuals. As it can happen by chance that individuals share an estimated disease position, we develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fa9a6347428807ca6506c56c37b9f7c
http://europepmc.org/articles/PMC7540579
http://europepmc.org/articles/PMC7540579
Autor:
Andrea Vereczkei, Csaba Barta, Anna Magi, Judit Farkas, Andrea Eisinger, Orsolya Király, Andrea Belik, Mark D. Griffiths, Anna Szekely, Mária Sasvári-Székely, Róbert Urbán, Marc N. Potenza, Rajendra D. Badgaiyan, Kenneth Blum, Zsolt Demetrovics, Eszter Kotyuk
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 5; Pages: 690
Epidemiological and phenomenological studies suggest shared underpinnings between multiple addictive behaviors. The present genetic association study was conducted as part of the Psychological and Genetic Factors of Addictions study (n = 3003) and ai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1213238e731ce860fc8f07276ee3abdd
https://irep.ntu.ac.uk/id/eprint/46201/1/1540048_Griffiths.pdf
https://irep.ntu.ac.uk/id/eprint/46201/1/1540048_Griffiths.pdf
Autor:
Adebowale eAdeyemo, Fasil eTekola-Ayele, Ayo Priscille Doumatey, Amy R Bentley, Guanjie eChen, Hanxia eHuang, Jie eZhou, Daniel eShriner, Olufemi eFasanmade, Godfrey eOkafor, Benjamin eEghan, Kofi eAgyenim-Boateng, Jokotade eAdeleye, Williams eBalogun, Abdel eElkahloun, Settara eChandrasekharappa, Samuel eOwusu, Albert eAmoah, Joseph eAcheampong, Thomas eJohnson, Johnnie eOli, Clement eAdebamowo, Francis eCollins, Georgia eDunston, Charles eRotimi
Publikováno v:
Frontiers in Genetics, Vol 6 (2015)
Genome wide association studies (GWAS) for type 2 diabetes (T2D) undertaken in European and Asian ancestry populations have yielded dozens of robustly associated loci. However, the genomics of T2D remains largely understudied in sub-Saharan Africa (S
Externí odkaz:
https://doaj.org/article/fe4c16a7d7dc489a86c04e2fb408e7d5