Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pritesh R Jain"'
Autor:
Pritesh R Jain, Madison Yates, Carlos Rubin de Celis, Petros Drineas, Neda Jahanshad, Paul Thompson, Peristera Paschou
Publikováno v:
NeuroImage, Vol 284, Iss , Pp 120466- (2023)
Alterations in subcortical brain structure volumes have been found to be associated with several neurodegenerative and psychiatric disorders. At the same time, genome-wide association studies (GWAS) have identified numerous common variants associated
Externí odkaz:
https://doaj.org/article/2dd552bc8201481fa0f9cd9fb54d6167
Tourette Syndrome (TS) is a complex neurodevelopmental disorder characterized by vocal and motor tics lasting more than a year. It is highly polygenic in nature with both rare and common previously associated variants. Epidemiological studies have sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0202424438a2cd5dddb6beee1bf1ec76
https://doi.org/10.1101/2022.09.01.22279340
https://doi.org/10.1101/2022.09.01.22279340
Autor:
J. Dakshinamoorthy, Usha Balasundaram, Thilagavathi Ramamoorthy, Rajapriya Ayyappan, Pritesh R. Jain
Publikováno v:
International Journal of Biological Macromolecules. 144:663-670
Polycystic ovary syndrome (PCOS), a gynaecological endocrine disorder affects 9% of Indian women and is linked to type II diabetes. The association of INSR (INSulin Receptor gene) variants (rs2059807 and rs1799817) with PCOS was established through g
Autor:
Susanne Walitza, Chaim Huyser, Astrid Morer, Pritesh R Jain, Jeffrey Glennon, Odile Van den Heuvel
Tourette Syndrome (TS) is a childhood-onset neurodevelopmental disorder of complex genetic architecture, characterized by multiple motor tics and at least one vocal tic persisting for more than one year. We performed a genome-wide meta-analysis integ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13c2edd8e6bdbba3038c377e9f429d16
https://doi.org/10.1101/2021.12.11.21267560
https://doi.org/10.1101/2021.12.11.21267560
Autor:
Jakub Piotr Fichna, Myson C. Burch, Cezary Zekanowski, Petros Drineas, Renata Rizzo, Zeynep Tümer, Csaba Barta, Peristera R Paschou, Melanie B. Martinez, John A. Stamatoyannopoulos, Pablo Mir, Evangelia Yannaki, Pritesh R Jain
BackgroundComplex disorders are caused by a combination of genetic, environmental and lifestyle factors, and their prevalence can vary greatly across different populations. Genome wide association studies (GWAS) can help identify common variants that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::781f2e4708cf072b5caca4e6ea00d235
https://doi.org/10.1101/2021.11.13.21265898
https://doi.org/10.1101/2021.11.13.21265898
Autor:
Pritesh R. Jain, Myson Burch, Melanie Martinez, Pablo Mir, Jakub P. Fichna, Cezary Zekanowski, Renata Rizzo, Zeynep Tümer, Csaba Barta, Evangelia Yannaki, John Stamatoyannopoulos, Petros Drineas, Peristera Paschou
Publikováno v:
BMC Genomic Data, Vol 24, Iss 1, Pp 1-12 (2023)
Abstract Complex disorders are caused by a combination of genetic, environmental and lifestyle factors, and their prevalence can vary greatly across different populations. The extent to which genetic risk, as identified by Genome Wide Association Stu
Externí odkaz:
https://doaj.org/article/8998ed9cbc534c00a98e747b63320443