Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Rachel Marceau West"'
Autor:
John Timmerman, David Lavie, Nathalie Johnson, Abraham Avigdor, Peter Borchmann, Charalambos Andreadis, Ali Bazargan, Gareth Gregory, Colm Keane, Inna Tzoran, Vladan Vucinic, Pier Luigi Zinzani, Rachel Marceau West, Pallavi Pillai, Patricia Marinello, Alex F. Herrera
Publikováno v:
HemaSphere, Vol 7, p e5990067 (2023)
Externí odkaz:
https://doaj.org/article/22031be9c69f424280efb74b4ea89e20
Autor:
Nathalie Johnson, David Lavie, Peter Borchmann, Gareth Gregory, Alex F. Herrera, Leonard Minuk, Vladan Vucinic, Philippe Armand, Abraham Avigdor, Robin Gasiorowski, Yair Herishanu, Colm Keane, John Kuruvilla, Rachel Marceau West, Pallavi Pillai, Patricia Marinello, John Timmerman
Publikováno v:
HemaSphere, Vol 7, p e0274602 (2023)
Externí odkaz:
https://doaj.org/article/a8737852cae34698a0c1cb539063a54a
Autor:
Amanda Brucker, Wenbin Lu, Rachel Marceau West, Qi-You Yu, Chuhsing Kate Hsiao, Tzu-Hung Hsiao, Ching-Heng Lin, Patrik K E Magnusson, Patrick F Sullivan, Jin P Szatkiewicz, Tzu-Pin Lu, Jung-Ying Tzeng
Publikováno v:
PLoS Computational Biology, Vol 16, Iss 5, p e1007797 (2020)
Copy number variants (CNVs) are the gain or loss of DNA segments in the genome that can vary in dosage and length. CNVs comprise a large proportion of variation in human genomes and impact health conditions. To detect rare CNV associations, kernel-ba
Externí odkaz:
https://doaj.org/article/88a8bc6a56c04085b78960c936494bce
Autor:
Rachel Marceau West, Wenbin Lu, Daniel M Rotroff, Melaine A Kuenemann, Sheng-Mao Chang, Michael C Wu, Michael J Wagner, John B Buse, Alison A Motsinger-Reif, Denis Fourches, Jung-Ying Tzeng
Publikováno v:
PLoS Computational Biology, Vol 15, Iss 2, p e1006722 (2019)
Rare variants are of increasing interest to genetic association studies because of their etiological contributions to human complex diseases. Due to the rarity of the mutant events, rare variants are routinely analyzed on an aggregate level. While ag
Externí odkaz:
https://doaj.org/article/cfa869d9762a4af085de4661762e40ed
Autor:
John Timmerman, David Lavie, Nathalie A. Johnson, Abraham Avigdor, Peter Borchmann, Charalambos Andreadis, Ali Bazargan, Gareth P. Gregory, Colm Keane, Inna Tsoran-Rosenthal, Vladan Vucinic, Pier Luigi Zinzani, Rachel Marceau West, Pallavi Pillai, Akash Nahar, Alex F. Herrera
Publikováno v:
Blood. 140:768-770
Publikováno v:
Statistics in medicine. 41(21)
Personalized medicine, a paradigm of medicine tailored to a patient's characteristics, is an increasingly attractive field in health care. An important goal of personalized medicine is to identify a subgroup of patients, based on baseline covariates,
Autor:
Rachel Marceau West, Devan V. Mehrotra
Publikováno v:
Statistics in Medicine. 39:4724-4744
Randomized clinical trials are often designed to assess whether a test treatment prolongs survival relative to a control treatment. Increased patient heterogeneity, while desirable for generalizability of results, can weaken the ability of common sta
Autor:
Jonathan A. Robbins, Karsten Menzel, Michael Lassman, Tian Zhao, Craig Fancourt, Xiaoyan Chu, Kate Mostoller, Rose Witter, Rachel Marceau West, S. Aubrey Stoch, Jacqueline B. McCrea, Marian Iwamoto
Publikováno v:
Clinical pharmacology and therapeutics. 111(3)
Rifampin has acute inhibitory and chronic inductive effects that can cause complex drug-drug interactions. Rifampin inhibits transporters including organic-anion-transporting polypeptide (OATP)1B and P-glycoprotein (P-gp), and induces enzymes and tra
Publikováno v:
The Lancet. 398:578-579
Autor:
Chuhsing Kate Hsiao, Jung-Ying Tzeng, Patrick Sullivan, Jin P. Szatkiewicz, Amanda Brucker, Wenbin Lu, Tzu-Pin Lu, Qi You Yu, Patrik K. E. Magnusson, Ching-Heng Lin, Rachel Marceau West, Tzu Hung Hsiao
Publikováno v:
PLoS Computational Biology, Vol 16, Iss 5, p e1007797 (2020)
PLoS Computational Biology
PLoS Computational Biology
Copy number variants (CNVs) are the gain or loss of DNA segments in the genome that can vary in dosage and length. CNVs comprise a large proportion of variation in human genomes and impact health conditions. To detect rare CNV associations, kernel-ba