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Yingying Tang, MD, PhD, DABMGG
Yingying Tang, MD, PhD, DABMGG
New York City Office of Chief Medical Examiner
Verified email at ocme.nyc.gov - Homepage
Title
Cited by
Cited by
Year
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
1751999
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
1572000
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
1192000
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
1152002
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
922014
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
752011
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
642016
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
342017
Molecular diagnostics of cardiovascular diseases in sudden unexplained death
Y Tang, J Stahl-Herz, BA Sampson
Cardiovascular Pathology 23 (1), 1-4, 2014
342014
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
341998
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
222017
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
212001
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
182011
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
162017
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
152017
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
142020
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
142020
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
122019
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
122018
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
122012
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