| Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ... autophagy 17 (1), 1-382, 2021 | 12298* | 2021 |
| Genetic basis and molecular mechanism for idiopathic ventricular fibrillation Q Chen, GE Kirsch, D Zhang, R Brugada, J Brugada, P Brugada, ... Nature 392 (6673), 293-296, 1998 | 2472 | 1998 |
| Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias Q Wang, ME Curran, I Splawski, TC Burn, JM Millholland, TJ VanRaay, ... Nature genetics 12 (1), 17-23, 1996 | 2252 | 1996 |
| SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome Q Wang, J Shen, I Splawski, D Atkinson, Z Li, JL Robinson, AJ Moss, ... Cell 80 (5), 805-811, 1995 | 2161 | 1995 |
| Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder W Du, JF Bautista, H Yang, A Diez-Sampedro, SA You, L Wang, P Kotagal, ... Nature genetics 37 (7), 733-738, 2005 | 655 | 2005 |
| Spectrum of ST-T–wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes L Zhang, KW Timothy, GM Vincent, MH Lehmann, J Fox, LC Giuli, J Shen, ... Circulation 102 (23), 2849-2855, 2000 | 650 | 2000 |
| KCNE1 mutations cause Jervell and Lange-Nielsen syndrome E Schulze-Bahr, Q Wang, H Wedekind, W Haverkamp, Q Chen, Y Sun, ... Nature genetics 17 (3), 267-268, 1997 | 597 | 1997 |
| Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation X Zhang, D Bogunovic, B Payelle-Brogard, V Francois-Newton, SD Speer, ... Nature 517 (7532), 89-93, 2015 | 565 | 2015 |
| Mutation of MEF2A in an inherited disorder with features of coronary artery disease L Wang, C Fan, SE Topol, EJ Topol, Q Wang Science 302 (5650), 1578-1581, 2003 | 543 | 2003 |
| Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia Q Wang, J Shen, Z Li, K Timothy, GM Vincent, SG Priori, PJ Schwartz, ... Human molecular genetics 4 (9), 1603-1607, 1995 | 450 | 1995 |
| Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis JC Jen, WM Chan, TM Bosley, J Wan, JR Carr, U Rüb, D Shattuck, ... Science 304 (5676), 1509-1513, 2004 | 441 | 2004 |
| Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis C Wang, Y Li, L Shi, J Ren, M Patti, T Wang, JRM de Oliveira, MJ Sobrido, ... Nature genetics 44 (3), 254-256, 2012 | 432 | 2012 |
| Multiple Mechanisms of Na+ Channel– Linked Long-QT Syndrome R Dumaine, Q Wang, MT Keating, HA Hartmann, PJ Schwartz, AM Brown, ... Circulation research 78 (5), 916-924, 1996 | 432 | 1996 |
| Genomic Organization of the HumanSCN5AGene Encoding the Cardiac Sodium Channel Q Wang, Z Li, J Shen, MT Keating Genomics 34 (1), 9-16, 1996 | 407 | 1996 |
| Identification of an angiogenic factor that when mutated causes susceptibility to Klippel–Trenaunay syndrome XL Tian, R Kadaba, SA You, M Liu, AA Timur, L Yang, Q Chen, ... Nature 427 (6975), 640-645, 2004 | 381 | 2004 |
| Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death X Zhang, S Chen, S Yoo, S Chakrabarti, T Zhang, T Ke, C Oberti, SL Yong, ... Cell 135 (6), 1017-1027, 2008 | 319 | 2008 |
| Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population F Wang, CQ Xu, Q He, JP Cai, XC Li, D Wang, X Xiong, YH Liao, QT Zeng, ... Nature genetics 43 (4), 345-349, 2011 | 282 | 2011 |
| Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis Q Wang, S Rao, GQ Shen, L Li, DJ Moliterno, LK Newby, WJ Rogers, ... The American Journal of Human Genetics 74 (2), 262-271, 2004 | 277 | 2004 |
| Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p S Chen, WG Ondo, S Rao, L Li, Q Chen, Q Wang The American Journal of Human Genetics 74 (5), 876-885, 2004 | 260 | 2004 |
| Molecular genetics of coronary artery disease Q Wang Current opinion in cardiology 20 (3), 182-188, 2005 | 251 | 2005 |