Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Justin Rubio"'
1
The Role of Pharmacogenomics in Opioid Prescribing
Autor: Aaron K. Wong, Andrew A. Somogyi, Justin Rubio, Jennifer Philip
Publikováno v: Current Treatment Options in Oncology. 23:1353-1369
Opinion statementPharmacogenomics is increasingly important to guide objective, safe, and effective individualised prescribing. Personalised prescribing has revolutionised treatments in the past decade, allowing clinicians to maximise drug efficacy a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89da1c87eb8ea72934f40689fb8c45f1
https://doi.org/10.1007/s11864-022-01010-x
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3
A 'Candidate-Interactome' Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis
Autor: Federica Esposito, Arianna FORNASIERO, Helmut Butzkueven, Eleni Giannoulatou, Marcin Mycko, Trevor Kilpatrick, Françoise Clerget-Darpoux, Juliane Winkelmann, James Walters, Sandra D'Alfonso, Simon Foote, Richard Reynolds, Paola Cavalla, Laura Piccio, Vito A. G. Ricigliano, Silvia Romano, Matthew S. Gillman, Dianna Murray, Aiden Corvin, Joseph Glessner, Nicholas Wood, Jeannette Lechner-Scott, Izaura Lima Bomfim, Daniela Galimberti, Colin Palmer, Pablo Villoslada, Allan Kermode, Marie D'hooghe, JUSTIN RUBIO, Maurizio Leone, Robert Plomin, Christian Schulze, Matti Pirinen, Xavier Montalban, Rosella Mechelli, Sergio Baranzini, Fabio Macciardi, Jianjun Liu, Lars Alfredsson, Anna Rapa, Céline Bellenguez, Finn Sellebjerg, Loukas Moutsianas, Jenny Link, Erika Salvi, Anne Cross, Anna-Maija Sulonen, Ingrid Kockum, Krzysztof Selmaj, Jim Stankovich, Struan Grant, Per Soelberg Sorensen, Janusz Jankowski, Anne Spurkland, Frauke Zipp, Elvira Bramon, Giovanni RISTORI, Maria Chiara Buscarinu, Janna Saarela, Nikolaos Patsopoulos, Jacob McCauley, Refujia Gomez, Rodney Scott, An Goris, Filippo Martinelli boneschi, Manuel Comabella Lopez, James Wason, Tomas Olsson, Renato Umeton
Publikováno v: Mechelli, R, Umeton, R, Policano, C, Annibali, V, Coarelli, G, Ricigliano, V A G, Vittori, D, Fornasiero, A, Buscarinu, M C, Romano, S & Salvetti, M & Ristori, G 2013, ' A 'Candidate-Interactome' Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis ', PL o S One, vol. 8, no. 5, e63300 . https://doi.org/10.1371/journal.pone.0063300
PLoS ONE
PloS one, vol 8, iss 5
PLoS ONE 8 (5): e63300.
PLoS ONE, Vol 8, Iss 5, p e63300 (2013)
PLoS ONE 8:e63300 (2013)
This work was funded by Italian Multiple Sclerosis Foundation grants (2007/R/17 and 2011/R/31) to MS. Though difficult, the study of gene-environment interactions in multifactorial diseases is crucial for interpreting the relevance of non-heritable f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c19e9e30eb44a0c70360c6607981c809
https://kclpure.kcl.ac.uk/en/publications/6d7bd6b9-7b1b-40dd-92ce-37751a674f59
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4
Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips
Autor: James Wiley, Helmut Butzkueven, Trevor Kilpatrick, Simon Foote, Jeannette Lechner-Scott, Ruijie Liu, Allan Kermode, JUSTIN RUBIO, Matthew A Brown, Matthew Ritchie, Tony Merriman, Jim Stankovich, Ruth Topless, Pablo Moscato, Lyn Griffiths, Andrea Polanowski, Benilton Carvalho, Peter Csurhes, Michael Pender, Mark Slee, Rodney Scott, Judith Greer, Judith Field, Joanne Dickinson
Publikováno v: BMC Bioinformatics
BMC Bioinformatics, Vol 12, Iss 1, p 68 (2011)
Background Illumina's Infinium SNP BeadChips are extensively used in both small and large-scale genetic studies. A fundamental step in any analysis is the processing of raw allele A and allele B intensities from each SNP into genotype calls (AA, AB,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::967ec7c7622a17be6cb1d761b5625efa
https://doi.org/10.1186/1471-2105-12-68
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5
Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data
Autor: James Wiley, Helmut Butzkueven, Trevor Kilpatrick, Simon Foote, Jeannette Lechner-Scott, Allan Kermode, JUSTIN RUBIO, Sergio Baranzini, Jim Stankovich, Pablo Moscato, Lori Chibnik, Mark Slee, Rodney Scott, Paul M Matthews, Judith Greer, Judith Field
Publikováno v: Genome Medicine
Wang, J H, Pappas, D, de Jager, P L, Pelletier, D, Bakker, P I W, Kappos, L, Polman, C H, Chibnik, L B, Hafler, D A, Matthews, P M, Hauser, S L, Baranzini, S E & Oksenberg, J R 2011, ' Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data ', Genome Medicine, vol. 3, no. 1, pp. 3 . https://doi.org/10.1186/gm217
Genome Medicine, 3(1). BioMed Central
Background: Multiple sclerosis (MS) is the most common cause of chronic neurologic disability beginning in early to middle adult life. Results from recent genome-wide association studies (GWAS) have substantially lengthened the list of disease loci a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fefc84428fd5cd9e7e9373f15416edef
https://doi.org/10.1186/gm217
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6
Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studies
Autor: Allan Kermode, JUSTIN RUBIO, Matthew A Brown, Peter Hickey, Sharon Browning, Jim Stankovich, Melanie Bahlo, Judith Greer, Judith Field, Joanne Dickinson
Publikováno v: Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 19(3)
As of June 2009, 361 genome-wide association studies (GWAS) had been referenced by the HuGE database. GWAS require DNA from many thousands of individuals, relying on suitable DNA collections. We recently performed a multiple sclerosis (MS) GWAS where
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adeca639f345c91e820d812aff6a71f2
https://pubmed.ncbi.nlm.nih.gov/20200434
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