| An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing JD Kapplinger, DJ Tester, M Alders, B Benito, M Berthet, J Brugada, ... Heart rhythm 7 (1), 33-46, 2010 | 792 | 2010 |
| The SLCO1B1*5Genetic Variant Is Associated With Statin-Induced Side Effects D Voora, SH Shah, I Spasojevic, S Ali, CR Reed, BA Salisbury, ... Journal of the American college of cardiology 54 (17), 1609-1616, 2009 | 533 | 2009 |
| Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test JD Kapplinger, DJ Tester, BA Salisbury, JL Carr, C Harris-Kerr, ... Heart rhythm 6 (9), 1297-1303, 2009 | 483 | 2009 |
| Deconstructing the relationship between genetics and race M Bamshad, S Wooding, BA Salisbury, JC Stephens Nature reviews genetics 5 (8), 598-609, 2004 | 450 | 2004 |
| Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants S Kapa, DJ Tester, BA Salisbury, C Harris-Kerr, MS Pungliya, M Alders, ... Circulation 120 (18), 1752-1760, 2009 | 377 | 2009 |
| Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia–associated mutations from background genetic noise JD Kapplinger, AP Landstrom, BA Salisbury, TE Callis, GD Pollevick, ... Journal of the American College of Cardiology 57 (23), 2317-2327, 2011 | 336 | 2011 |
| SNP and haplotype variation in the human genome BA Salisbury, M Pungliya, JY Choi, R Jiang, XJ Sun, JC Stephens Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 526 (1 …, 2003 | 229 | 2003 |
| Prevalence of early-onset atrial fibrillation in congenital long QT syndrome JN Johnson, DJ Tester, J Perry, BA Salisbury, CR Reed, MJ Ackerman Heart Rhythm 5 (5), 704-709, 2008 | 208 | 2008 |
| Candidate-gene association study of mothers with pre-eclampsia, and their infants, analyzing 775 SNPs in 190 genes KAB Goddard, G Tromp, R Romero, JM Olson, Q Lu, Z Xu, N Parimi, ... Human heredity 63 (1), 1-16, 2007 | 160 | 2007 |
| Candidate Gene Analysis Identifies a Polymorphism in HLA-DQB1 Associated With Clozapine-Induced Agranulocytosis MC Athanasiou, M Dettling, I Cascorbi, I Mosyagin, BA Salisbury, KA Pierz, ... The Journal of clinical psychiatry 71 (4), 2240, 2010 | 147 | 2010 |
| A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM) R Romero, LA Friel, DRV Edwards, JP Kusanovic, SS Hassan, ... American journal of obstetrics and gynecology 203 (4), 361. e1-361. e30, 2010 | 138 | 2010 |
| How many SNPs does a genome-wide haplotype map require? R Judson, B Salisbury, J Schneider, A Windemuth, JC Stephens Pharmacogenomics 3 (3), 379-391, 2002 | 136 | 2002 |
| Ancestral state estimation and taxon sampling density BA Salisbury, J Kim Systematic Biology 50 (4), 557-564, 2001 | 123 | 2001 |
| Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes R Romero, DRV Edwards, JP Kusanovic, SS Hassan, S Mazaki-Tovi, ... American journal of obstetrics and gynecology 202 (5), 431. e1-431. e34, 2010 | 119 | 2010 |
| Pharmacogenetic predictors of statin-mediated low-density lipoprotein cholesterol reduction and dose response D Voora, SH Shah, CR Reed, J Zhai, DR Crosslin, C Messer, ... Circulation: Cardiovascular Genetics 1 (2), 100-106, 2008 | 107 | 2008 |
| DNA variability of human genes JA Schneider, MS Pungliya, JY Choi, R Jiang, XJ Sun, BA Salisbury, ... Mechanisms of ageing and development 124 (1), 17-25, 2003 | 74 | 2003 |
| The structure of common genetic variation in United States populations SL Guthery, BA Salisbury, MS Pungliya, JC Stephens, M Bamshad The American Journal of Human Genetics 81 (6), 1221-1231, 2007 | 68 | 2007 |
| Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndrome JR Giudicessi, JD Kapplinger, DJ Tester, M Alders, BA Salisbury, ... Circulation: Cardiovascular Genetics 5 (5), 519-528, 2012 | 65 | 2012 |
| Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise JD Kapplinger, AP Landstrom, JM Bos, BA Salisbury, TE Callis, ... Journal of cardiovascular translational research 7, 347-361, 2014 | 63 | 2014 |
| Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results DJ Tester, LB Cronk, JL Carr, V Schulz, BA Salisbury, RS Judson, ... Heart Rhythm 3 (7), 815-821, 2006 | 55 | 2006 |
