Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Madhuchanda Bose"'
Autor:
Mykyta Matushyn, Madhuchanda Bose, Abdallah Amr Mahmoud, Lewis Cuthbertson, Carlos Tello, Karatuğ Ozan Bircan, Andrew Terpolovsky, Varuna Bamunusinghe, Umar Khan, Biljana Novković, Manfred G. Grabherr, Puya G. Yazdi
Publikováno v:
BMC Bioinformatics, Vol 23, Iss 1, Pp 1-12 (2022)
Abstract Background Generating polygenic risk scores for diseases and complex traits requires high quality GWAS summary statistic files. Often, these files can be difficult to acquire either as a result of unshared or incomplete data. To date, bioinf
Externí odkaz:
https://doaj.org/article/29bd617e2cfa42aba163bff8e64bb9dc
Autor:
Adriano De Marino, Abdallah Amr Mahmoud, Madhuchanda Bose, Karatuğ Ozan Bircan, Andrew Terpolovsky, Varuna Bamunusinghe, Sandra Bohn, Umar Khan, Biljana Novković, Puya G. Yazdi
Publikováno v:
PLoS ONE, Vol 17, Iss 10 (2022)
Whole-genome data has become significantly more accessible over the last two decades. This can largely be attributed to both reduced sequencing costs and imputation models which make it possible to obtain nearly whole-genome data from less expensive
Externí odkaz:
https://doaj.org/article/ed438db67878485ab4fdeaf92ffa20b2
Autor:
Matt Carland, Haley Pedersen, Madhuchanda Bose, Biljana Novković, Charles Manson, Shany Lahan, Alex Pavlenko, Puya G. Yazdi, Manfred G. Grabherr
Publikováno v:
PLoS ONE, Vol 17, Iss 5 (2022)
The vast majority of human traits, including many disease phenotypes, are affected by alleles at numerous genomic loci. With a continually increasing set of variants with published clinical disease or biomarker associations, an easy-to-use tool for n
Externí odkaz:
https://doaj.org/article/7943c473f4e34298b92171601b1de9e0
Autor:
Umar Khan, Varuna Bamunusinghe, Abdallah Amr Mahmoud, Puya G. Yazdi, Biljana Novković, Adriano De Marino, Madhuchanda Bose, Andrew Terpolovsky, Karatuğ Ozan Bircan
Whole-genome data has become significantly more accessible over the last two decades. This can largely be attributed to both reduced sequencing costs and imputation models which make it possible to obtain nearly whole-genome data from less expensive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e1763425f36d05840ca52f246dc1706
https://doi.org/10.1101/2021.11.04.467340
https://doi.org/10.1101/2021.11.04.467340
Autor:
Adriano De Marino, Abdallah Amr Mahmoud, Madhuchanda Bose, Karatuğ Ozan Bircan, Andrew Terpolovsky, Varuna Bamunusinghe, Sandra Bohn, Umar Khan, Biljana Novković, Puya G. Yazdi
Publikováno v:
PloS one. 17(10)
Whole-genome data has become significantly more accessible over the last two decades. This can largely be attributed to both reduced sequencing costs and imputation models which make it possible to obtain nearly whole-genome data from less expensive
Autor:
Alex Pavlenko, Manfred Grabherr, Haley Pedersen, Biljana Novković, Matt Carland, Charles Manson, Puya G. Yazdi, Shany Lahan, Madhuchanda Bose
The vast majority of human traits, including many disease phenotypes, are affected by alleles at numerous genomic loci. With a continually increasing set of variants with published clinical disease or biomarker associations, an easy-to-use tool for n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae1a8354a7dfe99358903d5fc680badd
https://doi.org/10.1101/2021.10.18.464896
https://doi.org/10.1101/2021.10.18.464896
Autor:
Elizabeth W Perry, Madhuchanda Bose, Brendan Marshall, Himangshu S. Bose, Zhi-Qing Zhao, Maheshinie Rajapaksha, Walter L. Miller, Randy M. Whittal, Ning Ping Wang
Publikováno v:
J Pharmacol Exp Ther
Aldosterone, which regulates renal salt retention, is synthesized in adrenocortical mitochondria in response to angiotensin II. Excess aldosterone causes myocardial injury and heart failure, but potential intracardiac aldosterone synthesis has been c