A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV C Bruno, A Martinuzzi, Y Tang, AL Andreu, F Pallotti, E Bonilla, S Shanske, ... The American Journal of Human Genetics 65 (3), 611-620, 1999 | 175 | 1999 |
Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expression Y Tang, EA Schon, E Wilichowski, ME Vazquez-Memije, E Davidson, ... Molecular biology of the cell 11 (4), 1471-1485, 2000 | 157 | 2000 |
Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines Y Tang, G Manfredi, M Hirano, EA Schon Molecular biology of the cell 11 (7), 2349-2358, 2000 | 119 | 2000 |
Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with Pearson syndrome S Shanske, Y Tang, M Hirano, Y Nishigaki, K Tanji, E Bonilla, C Sue, ... The American Journal of Human Genetics 71 (3), 679-683, 2002 | 115 | 2002 |
Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths D Wang, KR Shah, SY Um, LS Eng, BO Zhou, Y Lin, AA Mitchell, L Nicaj, ... Forensic science international 237, 90-99, 2014 | 92 | 2014 |
Ethnic differences in out-of-hospital fatal pulmonary embolism Y Tang, B Sampson, S Pack, K Shah, S Yon Um, D Wang, T Wang, ... Circulation 123 (20), 2219-2225, 2011 | 75 | 2011 |
Mosaic mutations in early-onset genetic diseases M Halvorsen, S Petrovski, R Shellhaas, Y Tang, L Crandall, D Goldstein, ... Genetics in Medicine 18 (7), 746-749, 2016 | 64 | 2016 |
Applying high-resolution variant classification to cardiac arrhythmogenic gene testing in a demographically diverse cohort of sudden unexplained deaths Y Lin, N Williams, D Wang, W Coetzee, B Zhou, LS Eng, SY Um, R Bao, ... Circulation: Cardiovascular Genetics 10 (6), e001839, 2017 | 34 | 2017 |
Molecular diagnostics of cardiovascular diseases in sudden unexplained death Y Tang, J Stahl-Herz, BA Sampson Cardiovascular Pathology 23 (1), 1-4, 2014 | 34 | 2014 |
Primary adrenal insufficiency in a child with a mitochondrial DNA deletion C Bruno, C Minetti, Y Tang, PJ Magalhães, FM Santorelli, S Shanske, ... Journal of inherited metabolic disease 21 (2), 155-161, 1998 | 34 | 1998 |
Infant sudden death: Mutations responsible for impaired Nav1. 5 channel trafficking and function I Gando, J Morganstein, K Jana, TV McDonald, Y Tang, WA Coetzee Pacing and Clinical Electrophysiology 40 (6), 703-712, 2017 | 22 | 2017 |
Both heavy strand replication origins are active in partially duplicated human mitochondrial DNAs S Umeda, Y Tang, M Okamoto, N Hamasaki, EA Schon, D Kang Biochemical and biophysical research communications 286 (4), 681-687, 2001 | 21 | 2001 |
A Dual Mechanism for IKs Current Reduction by the Pathogenic Mutation KCNQ1‐S277L J Chen, M Weber, S Yon Um, CA Walsh, Y Tang, TV McDonald Pacing and clinical electrophysiology 34 (12), 1652-1664, 2011 | 18 | 2011 |
Holistic approach to determine cause of autopsy-negative sudden natural death BA Sampson, Y Tang Journal of the American College of Cardiology 69 (17), 2146-2148, 2017 | 16 | 2017 |
Whole exome sequencing reveals severe thrombophilia in acute unprovoked idiopathic fatal pulmonary embolism M Halvorsen, Y Lin, BA Sampson, D Wang, B Zhou, LS Eng, SY Um, ... EBioMedicine 17, 95-100, 2017 | 15 | 2017 |
Lessons learned from testing cardiac channelopathy and cardiomyopathy genes in individuals who died suddenly: A two‐year prospective study in a large medical examiner’s office … N Williams, E Manderski, S Stewart, R Bao, Y Tang Journal of genetic counseling 29 (2), 293-302, 2020 | 14 | 2020 |
Using postmortem formalin fixed paraffin-embedded tissues for molecular testing of sudden cardiac death: a cautionary tale of utility and limitations Y Lin, T Gryazeva, D Wang, B Zhou, SY Um, LS Eng, K Ruiter, L Rojas, ... Forensic science international 308, 110177, 2020 | 14 | 2020 |
Functional characterization of SCN10A variants in several cases of sudden unexplained death I Gando, N Williams, GI Fishman, BA Sampson, Y Tang, WA Coetzee Forensic science international 301, 289-298, 2019 | 12 | 2019 |
Functional characterization of TRPM4 variants identified in sudden unexpected natural death E Subbotina, N Williams, BA Sampson, Y Tang, WA Coetzee Forensic science international 293, 37-46, 2018 | 12 | 2018 |
Partially dominant mutant channel defect corresponding with intermediate LQT2 phenotype Y Krishnan, R Zheng, C Walsh, YY Tang, TV McDONALD Pacing and clinical electrophysiology 35 (1), 3-16, 2012 | 12 | 2012 |