The Structure of Common Genetic Variation in United States Populations

Por Guthery, Stephen L. , Salisbury, Benjamin A. , Pungliya, Manish S. , Stephens, J. Claiborne , Bamshad, Michael 
Publicado em 2007

The SLCO1B1*5 Genetic Variant is Associated with Statin-Induced Side Effects

Por Voora, Deepak, Shah, Svati H., Spasojevic, Ivan, Ali, Shazia, Reed, Carol R., Salisbury, Benjamin A., Ginsburg, Geoffrey S.
Publicado em 2009

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome

Por Johnson, Jonathan N., Tester, David J., Perry, James, Salisbury, Benjamin A., Reed, Carol R., Ackerman, Michael J.
Publicado em 2008

Distinguishing Hypertrophic Cardiomyopathy-Associated Mutations from Background Genetic Noise

Por Kapplinger, Jamie D., Landstrom, Andrew P., Bos, J. Martijn, Salisbury, Benjamin A., Callis, Thomas E., Ackerman, Michael J.
Publicado no J Cardiovasc Transl Res (2014)

Pharmacogenetic Predictors of Statin-Mediated Low-Density Lipoprotein Cholesterol Reduction and Dose Response

Por Voora, Deepak, Shah, Svati H., Reed, Carol R., Zhai, Jun, Crosslin, David R., Messer, Chad, Salisbury, Benjamin A., Ginsburg, Geoffrey S.
Publicado em 2008

Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Non-Synonymous Single Nucleotide Variants in Type 1 and 2 Long QT Syndrome

Por Giudicessi, John R., Kapplinger, Jamie D., Tester, David J., Alders, Marielle, Salisbury, Benjamin A., Wilde, Arthur A.M., Ackerman, Michael J.
Publicado em 2012

Genetic Testing for Long QT Syndrome - Distinguishing Pathogenic Mutations from Benign Variants

Por Kapa, Suraj, Tester, David J., Salisbury, Benjamin A., Harris-Kerr, Carole, Pungliya, Manish S., Alders, Marielle, Wilde, Arthur A. M., Ackerman, Michael J.
Publicado em 2009

Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation

Por Tester, David J., Valdivia, Carmen, Harris-Kerr, Carole, Alders, Marielle, Salisbury, Benjamin A., Wilde, Arthur A. M., Makielski, Jonathan C., Ackerman, Michael J.
Publicado em 2010

Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel

Por Kapplinger, Jamie D., Tseng, Andrew S., Salisbury, Benjamin A., Tester, David J., Callis, Thomas E., Alders, Marielle, Wilde, Arthur A.M., Ackerman, Michael J.
Publicado no J Cardiovasc Transl Res (2015)

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION(®) long QT syndrome genetic test

Por Kapplinger, Jamie D., Tester, David J., Salisbury, Benjamin A., Carr, Janet L., Harris-Kerr, Carole, Pollevick, PhD, Guido D., Wilde, Arthur A. M., Ackerman, Michael J.
Publicado em 2009

The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data

Por Ferrarini, Alberto, Xumerle, Luciano, Griggio, Francesca, Garonzi, Marianna, Cantaloni, Chiara, Centomo, Cesare, Vargas, Sergio Marin, Descombes, Patrick, Marquis, Julien, Collino, Sebastiano, Franceschi, Claudio, Garagnani, Paolo, Salisbury, Benjamin A., Harvey, John Max, Delledonne, Massimo
Publicado no PLoS One (2015)

Identification of Fetal and Maternal Single Nucleotide Polymorphisms in Candidate Genes That Predispose to Spontaneous Preterm Labor with Intact Membranes

Por Romero, Roberto, Velez, Digna R., Kusanovic, Juan Pedro, Hassan, Sonia S., Mazaki-Tovi, Shali, Vaisbuch, Edi, Kim, Chong Jai, Chaiworapongsa, Tinnakorn, Pearce, Brad, Friel, Lara A., Bartlett, Jacquelaine, Anant, Madan Kumar, Salisbury, Benjamin A., Vovis, Gerald F., Lee, Min Seob, Gomez, Ricardo, Behnke, Ernesto, Oyarzun, Enrique, Tromp, Gerard, Williams, Scott M., Menon, Ramkumar
Publicado em 2010

A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM)

Por ROMERO, Roberto, FRIEL, Lara A., EDWARDS, Digna R. VELEZ, KUSANOVIC, Juan Pedro, HASSAN, Sonia S., MAZAKI-TOVI, Shali, VAISBUCH, Edi, KIM, Chong Jai, EREZ, Offer, CHAIWORAPONGSA, Tinnakorn, PEARCE, Brad D., BARTLETT, Jacquelaine, SALISBURY, Benjamin A., ANANT, Madan Kumar, VOVIS, Gerald F., LEE, Min Seob, GOMEZ, Ricardo, BEHNKE, Ernesto, OYARZUN, Enrique, TROMP, Gerard, WILLIAMS, Scott M., MENON, Ramkumar
Publicado em 2010

Polymorphisms in Maternal and Fetal Genes Encoding for Proteins Involved in Extracellular Matrix Metabolism Alter the Risk for Small-for-Gestational-Age

Por Edwards, Digna R. Velez, Romero, Roberto, Kusanovic, Juan Pedro, Hassan, Sonia S., Mazaki-Tovi, Shali, Vaisbuch, Edi, Kim, Chong Jai, Erez, Offer, Chaiworapongsa, Tinnakorn, Pearce, Brad D., Bartlett, Jacquelaine, Friel, Lara A., Salisbury, Benjamin A., Anant, Madan Kumar, Vovis, Gerald F., Lee, Min Seob, Gomez, Ricardo, Behnke, Ernesto, Oyarzun, Enrique, Tromp, Gerard, Menon, Ramkumar, Williams, Scott M.
Publicado em 2010

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Por Kapplinger, Jamie D., Tester, David J., Alders, Marielle, Benito, Begoña, Berthet, Myriam, Brugada, Josep, Brugada, Pedro, Fressart, Véronique, Guerchicoff, Alejandra, Harris-Kerr, Carole, Kamakura, Shiro, Kyndt, Florence, Koopmann, Tamara T., Miyamoto, Yoshihiro, Pfeiffer, Ryan, Pollevick, Guido D., Probst, Vincent, Zumhagen, Sven, Vatta, Matteo, Towbin, Jeffrey A., Shimizu, Wataru, Schulze-Bahr, Eric, Antzelevitch, Charles, Salisbury, Benjamin A., Guicheney, Pascale, Wilde, Arthur A. M., Brugada, Ramon, Schott, Jean-Jacques, Ackerman, Michael J.
Publicado em 2009