Publications by authors named "Reyna Favis"

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SCN9A Variants May be Implicated in Neuropathic Pain Associated With Diabetic Peripheral Neuropathy and Pain Severity.
Qingqin S Li, Peter Cheng, Reyna Favis, Alan Wickenden, Gary Romano

Clin J Pain· November 2015

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In vitro metabolism of canagliflozin in human liver, kidney, intestine microsomes, and recombinant uridine diphosphate glucuronosyltransferases (UGT) and the effect of genetic variability of UGT enzymes on the pharmacokinetics of canagliflozin in humans.
Stephan Francke, Rao N V S Mamidi, Bhavna Solanki, Ellen Scheers, Andrew Jadwin, Reyna Favis

J Clin Pharmacol· September 2015

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SULT4A1 haplotype: conflicting results on its role as a biomarker of antipsychotic response.
Dai Wang, Qingqin Li, Reyna Favis, Andrew Jadwin, Hedy Chung

Pharmacogenomics· June 2015

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Large-scale candidate gene study to identify genetic risk factors predictive of paliperidone treatment response in patients with schizophrenia.
Dai Wang, Dong-Jing Fu, Xiaodong Wu, Alice Shapiro, Reyna Favis

Pharmacogenet Genomics· April 2015

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Prespecified candidate biomarkers identify follicular lymphoma patients who achieved longer progression-free survival with bortezomib-rituximab versus rituximab.
Bertrand Coiffier, Weimin Li, Erin D Henitz, Jayaprakash D Karkera, Reyna Favis

Clin Cancer Res· May 2013

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Allosteric alpha-7 nicotinic receptor modulation and P50 sensory gating in schizophrenia: a proof-of-mechanism study.
Georg Winterer, Jürgen Gallinat, Jürgen Brinkmeyer, Francesco Musso, Johannes Kornhuber, Reyna Favis

Neuropharmacology· January 2013

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MAGI1 copy number variation in bipolar affective disorder and schizophrenia.
Robert Karlsson, Lisette Graae, Magnus Lekman, Dai Wang, Reyna Favis

Biol Psychiatry· May 2012

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Genetic variation associated with bortezomib-induced peripheral neuropathy.
Reyna Favis, Yu Sun, Helgi van de Velde, Erin Broderick, Laura Levey

Pharmacogenet Genomics· March 2011

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Polymorphisms in the multiple drug resistance protein 1 and in P-glycoprotein 1 are associated with time to event outcomes in patients with advanced multiple myeloma treated with bortezomib and pegylated liposomal doxorubicin.
Gabriele Buda, Deborah Ricci, C Chris Huang, Reyna Favis, Nadine Cohen

Ann Hematol· November 2010

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A randomized phase 2 study of erlotinib alone and in combination with bortezomib in previously treated advanced non-small cell lung cancer.
Thomas J Lynch, David Fenton, Vera Hirsh, David Bodkin, Edward L Middleman, Reyna Favis

J Thorac Oncol· August 2009

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Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta.
Peter Brooks, Charles Marcaillou, Maud Vanpeene, Jean-Paul Saraiva, Daniel Stockholm, Reyna Favis

BMC Genet· March 2009

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Applications of the universal DNA microarray in molecular medicine.
Reyna Favis, Norman P Gerry, Yu-Wei Cheng, Francis Barany

Methods Mol Med· October 2005

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Harmonized microarray/mutation scanning analysis of TP53 mutations in undissected colorectal tumors.
Reyna Favis, Jianmin Huang, Norman P Gerry, Alfred Culliford, Philip Paty

Hum Mutat· July 2004

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Rapid and sensitive p53 alteration analysis in biopsies from lung cancer patients using a functional assay and a universal oligonucleotide array: a prospective study.
Coralie Fouquet, Martine Antoine, Pascaline Tisserand, Reyna Favis, Marie Wislez

Clin Cancer Res· May 2004

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The presence of p53 mutations in human osteosarcomas correlates with high levels of genomic instability.
Michael Overholtzer, Pulivarthi H Rao, Reyna Favis, Xin-Yan Lu, Michael B Elowitz

Proc Natl Acad Sci U S A· September 2003

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Single nucleotide polymorphism seeking long term association with complex disease.
Brian W Kirk, Matthew Feinsod, Reyna Favis, Richard M Kliman, Francis Barany

Nucleic Acids Res· August 2002

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An endonuclease/ligase based mutation scanning method especially suited for analysis of neoplastic tissue.
Jianmin Huang, Brian Kirk, Reyna Favis, Thierry Soussi, Philip Paty

Oncogene· March 2002

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