| Biparental inheritance of mitochondrial DNA in humans S Luo, CA Valencia, J Zhang, NC Lee, J Slone, B Gui, X Wang, Z Li, ... Proceedings of the National Academy of Sciences 115 (51), 13039-13044, 2018 | 538 | 2018 |
| Different TBX5 interactions in heart and limb defined by Holt–Oram syndrome mutations CT Basson, T Huang, RC Lin, DR Bachinsky, S Weremowicz, A Vaglio, ... Proceedings of the National Academy of Sciences 96 (6), 2919-2924, 1999 | 470 | 1999 |
| Live birth derived from oocyte spindle transfer to prevent mitochondrial disease J Zhang, H Liu, S Luo, Z Lu, A Chávez-Badiola, Z Liu, M Yang, Z Merhi, ... Reproductive biomedicine online 34 (4), 361-368, 2017 | 370 | 2017 |
| Determination of influenza virus proteins required for genome replication TS Huang, P Palese, M Krystal Journal of virology 64 (11), 5669-5673, 1990 | 332 | 1990 |
| Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations E Kang, J Wu, NM Gutierrez, A Koski, R Tippner-Hedges, K Agaronyan, ... Nature 540 (7632), 270-275, 2016 | 318 | 2016 |
| Species identification through mitochondrial rRNA genetic analysis L Yang, Z Tan, D Wang, L Xue, M Guan, T Huang, R Li Scientific reports 4 (1), 4089, 2014 | 272 | 2014 |
| Age-related accumulation of somatic mitochondrial DNA mutations in adult-derived human iPSCs E Kang, X Wang, R Tippner-Hedges, H Ma, CDL Folmes, NM Gutierrez, ... Cell stem cell 18 (5), 625-636, 2016 | 239 | 2016 |
| Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder AJ Abrams, RB Hufnagel, A Rebelo, C Zanna, N Patel, MA Gonzalez, ... Nature genetics 47 (8), 926-932, 2015 | 221 | 2015 |
| Metabolic rescue in pluripotent cells from patients with mtDNA disease H Ma, CDL Folmes, J Wu, R Morey, S Mora-Castilla, A Ocampo, L Ma, ... Nature 524 (7564), 234-238, 2015 | 203 | 2015 |
| Rescue of a foreign gene by Sendai virus. KH Park, T Huang, FF Correia, M Krystal Proceedings of the National Academy of Sciences 88 (13), 5537-5541, 1991 | 167 | 1991 |
| Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans F Ji, MS Sharpley, O Derbeneva, LS Alves, P Qian, Y Wang, D Chalkia, ... Proceedings of the National academy of Sciences 109 (19), 7391-7396, 2012 | 156 | 2012 |
| TBX3 and its isoform TBX3+ 2a are functionally distinctive in inhibition of senescence and are overexpressed in a subset of breast cancer cell lines W Fan, X Huang, C Chen, J Gray, T Huang Cancer research 64 (15), 5132-5139, 2004 | 153 | 2004 |
| Mitochondrial genome analysis of Ochotona curzoniae and implication of cytochrome c oxidase in hypoxic adaptation Y Luo, W Gao, Y Gao, S Tang, Q Huang, X Tan, J Chen, T Huang Mitochondrion 8 (5-6), 352-357, 2008 | 152 | 2008 |
| Characterization of mitochondrial DNA heteroplasmy using a parallel sequencing system S Tang, T Huang Biotechniques 48 (4), 287-296, 2010 | 144 | 2010 |
| TBX3 is overexpressed in breast cancer and represses p14ARF by interacting with histone deacetylases W Yarosh, T Barrientos, T Esmailpour, L Lin, PM Carpenter, K Osann, ... Cancer research 68 (3), 693-699, 2008 | 140 | 2008 |
| Current status of thalassemia in minority populations in Guangxi, China HF Pan, GF Long, Q Li, YN Feng, ZY Lei, HW Wei, YY Huang, JH Huang, ... Clinical genetics 71 (5), 419-426, 2007 | 139 | 2007 |
| The Molecular Mechanisms of OPA1-Mediated Optic Atrophy in Drosophila Model and Prospects for Antioxidant Treatment W Yarosh, J Monserrate, JJ Tong, S Tse, PK Le, K Nguyen, ... PLoS genetics 4 (1), e6, 2008 | 132 | 2008 |
| Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes RB Hufnagel, G Arno, ND Hein, J Hersheson, M Prasad, Y Anderson, ... Journal of medical genetics 52 (2), 85-94, 2015 | 131 | 2015 |
| Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome M Simon, EM Richard, X Wang, M Shahzad, VH Huang, TA Qaiser, ... PLoS genetics 11 (3), e1005097, 2015 | 130 | 2015 |
| Left ventricular noncompaction is associated with mutations in the mitochondrial genome S Tang, A Batra, Y Zhang, ES Ebenroth, T Huang Mitochondrion 10 (4), 350-357, 2010 | 128 | 2010 |
Jesse SloneResearch Assistant Professor, University at Buffalo確認したメール アドレス: buffalo.edu