The SLCO1B15 Genetic Variant Is Associated With Statin-Induced Side Effects
Voora, Deepak, MD, Shah, Svati H., MD, MHS, Spasojevic, Ivan, PhD, Ali, Shazia, PharmD, Reed, Carol R., MD, Salisbury, Benjamin A., PhD, Ginsburg, Geoffrey S., MD, PhD
Published in Journal of the American College of Cardiology (20.10.2009)
Published in Journal of the American College of Cardiology (20.10.2009)
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Journal Article
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test
Kapplinger, Jamie D, Tester, David J, Salisbury, Benjamin A, Carr, Janet L, Harris-Kerr, Carole, Pollevick, Guido D, Wilde, Arthur A M, Ackerman, Michael J
Published in Heart rhythm (01.09.2009)
Published in Heart rhythm (01.09.2009)
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Journal Article
Deconstructing the relationship between genetics and race
Bamshad, Michael, Wooding, Stephen, Salisbury, Benjamin A, Stephens, J. Claiborne
Published in Nature reviews. Genetics (01.08.2004)
Published in Nature reviews. Genetics (01.08.2004)
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Journal Article
Prevalence of early-onset atrial fibrillation in congenital long QT syndrome
Johnson, Jonathan N, Tester, David J, Perry, James, Salisbury, Benjamin A, Reed, Carol R, Ackerman, Michael J
Published in Heart rhythm (01.05.2008)
Published in Heart rhythm (01.05.2008)
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Journal Article
Computational pharmacogenotype extraction from clinical next-generation sequencing
Shugg, Tyler, Ly, Reynold C, Osei, Wilberforce, Rowe, Elizabeth J, Granfield, Caitlin A, Lynnes, Ty C, Medeiros, Elizabeth B, Hodge, Jennelle C, Breman, Amy M, Schneider, Bryan P, Sahinalp, S Cenk, Numanagić, Ibrahim, Salisbury, Benjamin A, Bray, Steven M, Ratcliff, Ryan, Skaar, Todd C
Published in Frontiers in oncology (04.07.2023)
Published in Frontiers in oncology (04.07.2023)
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Journal Article
Retention, Fasting Patterns, and Weight Loss With an Intermittent Fasting App: Large-Scale, 52-Week Observational Study
Torres, Luisa, Lee, Joy L, Park, Seho, Di Lorenzo, R Christian, Branam, Jonathan P, Fraser, Shelagh A, Salisbury, Benjamin A
Published in JMIR mHealth and uHealth (01.10.2022)
Published in JMIR mHealth and uHealth (01.10.2022)
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Journal Article
The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data
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
Published in PloS one (06.07.2015)
Published in PloS one (06.07.2015)
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Journal Article
A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM)
Romero, Roberto, MD, Friel, Lara A., MD, PhD, Velez Edwards, Digna R., PhD, Kusanovic, Juan Pedro, MD, Hassan, Sonia S., MD, Mazaki-Tovi, Shali, MD, Vaisbuch, Edi, MD, Kim, Chong Jai, MD, Erez, Offer, MD, Chaiworapongsa, Tinnakorn, MD, Pearce, Brad D., PhD, Bartlett, Jacquelaine, MS, Salisbury, Benjamin A., PhD, Anant, Madan Kumar, PhD, Vovis, Gerald F., PhD, Lee, Min Seob, PhD, Gomez, Ricardo, MD, Behnke, Ernesto, MD, Oyarzun, Enrique, MD, Tromp, Gerard, PhD, Williams, Scott M., PhD, Menon, Ramkumar, PhD
Published in American journal of obstetrics and gynecology (01.10.2010)
Published in American journal of obstetrics and gynecology (01.10.2010)
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Journal Article
Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes
Romero, Roberto, MD, Velez Edwards, Digna R., PhD, Kusanovic, Juan Pedro, MD, Hassan, Sonia S., MD, Mazaki-Tovi, Shali, MD, Vaisbuch, Edi, MD, Kim, Chong Jai, MD, Chaiworapongsa, Tinnakorn, MD, Pearce, Brad D., PhD, Friel, Lara A., MD, PhD, Bartlett, Jacquelaine, MS, Anant, Madan Kumar, PhD, Salisbury, Benjamin A., PhD, Vovis, Gerald F., PhD, Lee, Min Seob, PhD, Gomez, Ricardo, MD, Behnke, Ernesto, MD, Oyarzun, Enrique, MD, Tromp, Gerard, PhD, Williams, Scott M., PhD, Menon, Ramkumar, PhD
Published in American journal of obstetrics and gynecology (01.05.2010)
Published in American journal of obstetrics and gynecology (01.05.2010)
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Journal Article
Conference Proceeding
Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel
Kapplinger, Jamie D., Tseng, Andrew S., Salisbury, Benjamin A., Tester, David J., Callis, Thomas E., Alders, Marielle, Wilde, Arthur A. M., Ackerman, Michael J.
Published in Journal of cardiovascular translational research (01.04.2015)
Published in Journal of cardiovascular translational research (01.04.2015)
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Journal Article
Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation
Tester, David J, Valdivia, Carmen, Harris-Kerr, Carole, Alders, Marielle, Salisbury, Benjamin A, Wilde, Arthur A M, Makielski, Jonathan C, Ackerman, Michael J
Published in Heart rhythm (01.07.2010)
Published in Heart rhythm (01.07.2010)
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Journal Article
Genetic Testing for Long-QT Syndrome: Distinguishing Pathogenic Mutations From Benign Variants
KAPA, Suraj, TESTER, David J, SALISBURY, Benjamin A, HARRIS-KERR, Carole, PUNGLIYA, Manish S, ALDERS, Marielle, WILDE, Arthur A. M, ACKERMAN, Michael J
Published in Circulation (New York, N.Y.) (03.11.2009)
Published in Circulation (New York, N.Y.) (03.11.2009)
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Journal Article
Analytical Validation of a Computational Method for Pharmacogenetic Genotyping from Clinical Whole Exome Sequencing
Ly, Reynold C., Shugg, Tyler, Ratcliff, Ryan, Osei, Wilberforce, Lynnes, Ty C., Pratt, Victoria M., Schneider, Bryan P., Radovich, Milan, Bray, Steven M., Salisbury, Benjamin A., Parikh, Baiju, Sahinalp, S. Cenk, Numanagić, Ibrahim, Skaar, Todd C.
Published in The Journal of molecular diagnostics : JMD (01.06.2022)
Published in The Journal of molecular diagnostics : JMD (01.06.2022)
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Journal Article
Candidate gene analysis identifies a polymorphism in HLA-DQB1 associated with clozapine-induced agranulocytosis
Athanasiou, Maria C, Dettling, Michael, Cascorbi, Ingolf, Mosyagin, Igor, Salisbury, Benjamin A, Pierz, Kerri A, Zou, Wei, Whalen, Heidi, Malhotra, Anil K, Lencz, Todd, Gerson, Stanton L, Kane, John M, Reed, Carol R
Published in The journal of clinical psychiatry (01.04.2011)
Published in The journal of clinical psychiatry (01.04.2011)
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Journal Article
Expression of a Common LQT1 Mutation in Five Apparently Unrelated Families in a Regional Inherited Arrhythmia Clinic
GRAY, CHRISTOPHER, GULA, LORNE J., KLEIN, GEORGE J., SKANES, ALLAN C., YEE, RAYMOND, SY, RAYMOND, SALISBURY, BENJAMIN A., WONG, JORGE, CHATTHA, ISHVINDER, SUBBIAH, RAJESH N., KRAHN, ANDREW D.
Published in Journal of cardiovascular electrophysiology (01.03.2010)
Published in Journal of cardiovascular electrophysiology (01.03.2010)
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Journal Article
Pharmacogenetic Predictors of Statin-Mediated Low-Density Lipoprotein Cholesterol Reduction and Dose Response
Voora, Deepak, Shah, Svati H, Reed, Carol R, Zhai, Jun, Crosslin, David R, Messer, Chad, Salisbury, Benjamin A, Ginsburg, Geoffrey S
Published in Circulation. Cardiovascular genetics (01.12.2008)
Published in Circulation. Cardiovascular genetics (01.12.2008)
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Journal Article
Distinguishing Hypertrophic Cardiomyopathy-Associated Mutations from Background Genetic Noise
Kapplinger, Jamie D., Landstrom, Andrew P., Bos, J. Martijn, Salisbury, Benjamin A., Callis, Thomas E., Ackerman, Michael J.
Published in Journal of cardiovascular translational research (01.04.2014)
Published in Journal of cardiovascular translational research (01.04.2014)
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Journal Article
Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-QT Syndrome
Giudicessi, John R, Kapplinger, Jamie D, Tester, David J, Alders, Marielle, Salisbury, Benjamin A, Wilde, Arthur A.M, Ackerman, Michael J
Published in Circulation. Cardiovascular genetics (01.10.2012)
Published in Circulation. Cardiovascular genetics (01.10.2012)
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Journal Article
Candidate-Gene Association Study of Mothers with Pre-Eclampsia, and Their Infants, Analyzing 775 SNPs in 190 Genes
Goddard, Katrina A. B., Tromp, Gerard, Romero, Roberto, Olson, Jane M., Lu, Qing, Xu, Zhiying, Parimi, Neeta, Nien, Jyh Kae, Gomez, Ricardo, Behnke, Ernesto, Solari, Margarita, Espinoza, Jimmy, Santolaya, Joaquin, Chaiworapongsa, Tinnakorn, Lenk, Guy M., Volkenant, Kimberly, Anant, Madan Kumar, Salisbury, Benjamin A., Carr, Janet, Lee, Min Soeb, Vovis, Gerald F., Kuivaniemi, Helena
Published in Human heredity (01.01.2007)
Published in Human heredity (01.01.2007)
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