Influence of FCGRT gene polymorphisms on pharmacokinetics of therapeutic antibodies

Por Passot, Christophe, Azzopardi, Nicolas, Renault, Sylvaine, Baroukh, Nadine, Arnoult, Christophe, Ohresser, Marc, Boisdron-Celle, Michèle, Gamelin, Erick, Watier, Hervé, Paintaud, Gilles, Gouilleux-Gruart, Valérie
Publicado em 2013

Population-based biobank for analyzing the frequencies of clinically relevant DNA markers in the Russian population: bioinformatic aspects

Por I. O. Gorin, V. S. Petrushenko, Yu. S. Zapisetskaya, S. M. Koshel, O. P. Balanovsky
Publicado em 2020-12-01

Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines.

Por Edwin Choy, Roman Yelensky, Sasha Bonakdar, Robert M Plenge, Richa Saxena, Philip L De Jager, Stanley Y Shaw, Cara S Wolfish, Jacqueline M Slavik, Chris Cotsapas, Manuel Rivas, Emmanouil T Dermitzakis, Ellen Cahir-McFarland, Elliott Kieff, David Hafler, Mark J Daly, David Altshuler
Publicado em 2008-11-01

Genetic determinants of statin intolerance

Por Oh, Jisun, Ban, Matthew R, Miskie, Brooke A, Pollex, Rebecca L, Hegele, Robert A
Publicado em 2007

Genetic Analysis of Human Traits In Vitro: Drug Response and Gene Expression in Lymphoblastoid Cell Lines

Por Choy, Edwin, Yelensky, Roman, Bonakdar, Sasha, Plenge, Robert M., Saxena, Richa, De Jager, Philip L., Shaw, Stanley Y., Wolfish, Cara S., Slavik, Jacqueline M., Cotsapas, Chris, Rivas, Manuel, Dermitzakis, Emmanouil T., Cahir-McFarland, Ellen, Kieff, Elliott, Hafler, David, Daly, Mark J., Altshuler, David
Publicado em 2008

The International Consortium on Lithium Genetics (ConLiGen): An Initiative by the NIMH and IGSLI to Study the Genetic Basis of Response to Lithium Treatment

Por Schulze, Thomas G., Alda, Martin, Adli, Mazda, Akula, Nirmala, Ardau, Raffaella, Bui, Elise T., Chillotti, Caterina, Cichon, Sven, Czerski, Piotr, Del Zompo, Maria, Detera-Wadleigh, Sevilla D., Grof, Paul, Gruber, Oliver, Hashimoto, Ryota, Hauser, Joanna, Hoban, Rebecca, Iwata, Nakao, Kassem, Layla, Kato, Tadafumi, Kittel-Schneider, Sarah, Kliwicki, Sebastian, Kelsoe, John R., Kusumi, Ichiro, Laje, Gonzalo, Leckband, Susan G., Manchia, Mirko, MacQueen, Glenda, Masui, Takuya, Ozaki, Norio, Perlis, Roy H., Pfennig, Andrea, Piccardi, Paola, Richardson, Sara, Rouleau, Guy, Reif, Andreas, Rybakowski, Janusz K., Sasse, Johanna, Schumacher, Johannes, Severino, Giovanni, Smoller, Jordan W., Squassina, Alessio, Turecki, Gustavo, Young, L. Trevor, Yoshikawa, Takeo, Bauer, Michael, McMahon, Francis J.
Publicado em 2010

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson’s disease

Por Hamza, Taye H, Zabetian, Cyrus P, Tenesa, Albert, Laederach, Alain, Montimurro, Jennifer, Yearout, Dora, Kay, Denise M, Doheny, Kimberly F, Paschall, Justin, Pugh, Elizabeth, Kusel, Victoria I, Collura, Randall, Roberts, John, Griffith, Alida, Samii, Ali, Scott, William K, Nutt, John, Factor, Stewart A, Payami, Haydeh
Publicado em 2010

AutismKB: an evidence-based knowledgebase of autism genetics

Por Xu, Li-Ming, Li, Jia-Rui, Huang, Yue, Zhao, Min, Tang, Xing, Wei, Liping
Publicado em 2012

Inter and intra ethnic variation of vitamin K epoxide reductase complex and cytochrome P450 4F2 genetic polymorphisms and their prevalence in South Indian population

Por Kumar, Dhakchinamoorthi Krishna, Shewade, Deepak Gopal, Manjunath, Sajjanavar, Ushakiran, Prayaga, Reneega, Gangadharan, Adithan, Chandrasekaran
Publicado em 2013

PROX1 GENE VARIANT IS ASSOCIATED WITH FASTING GLUCOSE CHANGE AFTER ANTIHYPERTENSIVE TREATMENT

Por Gong, Yan, McDonough, Caitrin W, Beitelshees, Amber L, Karnes, Jason H, O’Connell, Jeffrey R., Turner, Stephen T, Chapman, Arlene B, Gums, John G, Bailey, Kent R, Boerwinkle, Eric, Johnson, Julie A, Cooper-DeHoff, Rhonda M
Publicado em 2013

Future Trends in the Pharmacogenomics of Brain Disorders and Dementia: Influence of APOE and CYP2D6 Variants

Por Cacabelos, Ramón, Fernández-Novoa, Lucía, Martínez-Bouza, Rocío, McKay, Adam, Carril, Juan C., Lombardi, Valter, Corzo, Lola, Carrera, Iván, Tellado, Iván, Nebril, Laura, Alcaraz, Margarita, Rodríguez, Susana, Casas, Ángela, Couceiro, Verónica, Álvarez, Antón
Publicado em 2010

Comparison of pathogenicity prediction tools on missense variants in RYR1 and CACNA1S associated with malignant hyperthermia

Por Schiemann, A. H., Stowell, K. M.
Publicado no Br J Anaesth (2016)

Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium

Por Bis, Joshua C., Sitlani, Colleen, Irvin, Ryan, Avery, Christy L., Smith, Albert Vernon, Sun, Fangui, Evans, Daniel S., Musani, Solomon K., Li, Xiaohui, Trompet, Stella, Krijthe, Bouwe P., Harris, Tamara B., Quibrera, P. Miguel, Brody, Jennifer A., Demissie, Serkalem, Davis, Barry R., Wiggins, Kerri L., Tranah, Gregory J., Lange, Leslie A., Sotoodehnia, Nona, Stott, David J., Franco, Oscar H., Launer, Lenore J., Stürmer, Til, Taylor, Kent D., Cupples, L. Adrienne, Eckfeldt, John H., Smith, Nicholas L., Liu, Yongmei, Wilson, James G., Heckbert, Susan R., Buckley, Brendan M., Ikram, M. Arfan, Boerwinkle, Eric, Chen, Yii-Der Ida, de Craen, Anton J. M., Uitterlinden, Andre G., Rotter, Jerome I., Ford, Ian, Hofman, Albert, Sattar, Naveed, Slagboom, P. Eline, Westendorp, Rudi G. J., Gudnason, Vilmundur, Vasan, Ramachandran S., Lumley, Thomas, Cummings, Steven R., Taylor, Herman A., Post, Wendy, Jukema, J. Wouter, Stricker, Bruno H., Whitsel, Eric A., Psaty, Bruce M., Arnett, Donna
Publicado no PLoS One (2015)

ABC transporters and the proteasome complex are implicated in susceptibility to Stevens-Johnson syndrome and toxic epidermal necrolysis across multiple drugs.

Por Paola Nicoletti, Mukesh Bansal, Celine Lefebvre, Paolo Guarnieri, Yufeng Shen, Itsik Pe'er, Andrea Califano, Aris Floratos
Publicado em 2015-01-01

ABC Transporters and the Proteasome Complex Are Implicated in Susceptibility to Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis across Multiple Drugs

Por Nicoletti, Paola, Bansal, Mukesh, Lefebvre, Celine, Guarnieri, Paolo, Shen, Yufeng, Pe’er, Itsik, Califano, Andrea, Floratos, Aris
Publicado no PLoS One (2015)

High-Risk Childhood Acute Lymphoblastic Leukemia

Por Bhojwani, Deepa, Howard, Scott C., Pui, Ching-Hon
Publicado em 2009

Pharmacogenomics: a new paradigm to personalize treatments in nephrology patients

Por Zaza, G, Granata, S, Sallustio, F, Grandaliano, G, Schena, F P
Publicado em 2010

Pharmacogenomics and its importance in pediatric medicine

Por Shastry, Barkur S.
Publicado no J Pediatr Genet (2012)

Trend of medicine of the 21st century

Por Bakir Mehić
Publicado em 2013-02-01

Assessment of age-related changes in heritability and IGF-1 gene effect on circulating IGF-1 levels

Por Franco, Liran, Williams, Frances M. K., Trofimov, Svetlana, Malkin, Ida, Surdulescu, Gabriela, Spector, Timothy, Livshits, Gregory
Publicado em 2014