Year |
Citation |
Score |
2023 |
Bodenstein DF, Powlowski P, Zachos KA, El Soufi El Sabbagh D, Jeong H, Attisano L, Edgar L, Wallace DC, Andreazza AC. Optimization of differential filtration-based mitochondrial isolation for mitochondrial transplant to cerebral organoids. Stem Cell Research & Therapy. 14: 202. PMID 37580812 DOI: 10.1186/s13287-023-03436-y |
0.312 |
|
2022 |
Schaefer PM, Scherer Alves L, Lvova M, Huang J, Rathi K, Janssen K, Butic A, Yardeni T, Morrow R, Lott M, Murdock D, Song A, Keller K, Garcia BA, Francomano CA, ... Wallace DC, et al. Combination of common mtDNA variants results in mitochondrial dysfunction and a connective tissue dysregulation. Proceedings of the National Academy of Sciences of the United States of America. 119: e2212417119. PMID 36322731 DOI: 10.1073/pnas.2212417119 |
0.327 |
|
2021 |
Singh LN, Ennis B, Loneragan B, Tsao NL, Lopez Sanchez MIG, Li J, Acheampong P, Tran O, Trounce IA, Zhu Y, Potluri P, Emanuel BS, Rader DJ, Arany Z, ... ... Wallace DC, et al. MitoScape: A big-data, machine-learning platform for obtaining mitochondrial DNA from next-generation sequencing data. Plos Computational Biology. 17: e1009594. PMID 34762648 DOI: 10.1371/journal.pcbi.1009594 |
0.312 |
|
2020 |
Aras S, Purandare N, Gladyck S, Somayajulu-Nitu M, Zhang K, Wallace DC, Grossman LI. Mitochondrial Nuclear Retrograde Regulator 1 (MNRR1) rescues the cellular phenotype of MELAS by inducing homeostatic mechanisms. Proceedings of the National Academy of Sciences of the United States of America. PMID 33257573 DOI: 10.1073/pnas.2005877117 |
0.323 |
|
2020 |
Bertholet AM, Chouchani ET, Kazak L, Angelin A, Fedorenko A, Long JZ, Vidoni S, Garrity R, Cho J, Terada N, Wallace D, Spiegelman BM, Kirichok YV. Molecular Identity and Regulatory Mechanisms of the Mitochondrial Uncoupling Protein of Non-Adipose Tissues Biophysical Journal. 118: 185a. DOI: 10.1016/J.Bpj.2019.11.1127 |
0.326 |
|
2019 |
Tian R, Colucci WS, Arany Z, Bachschmid MM, Ballinger SW, Boudina S, Bruce JE, Busija DW, Dikalov S, Dorn GW, Galis ZS, Gottlieb RA, Kelly DP, Kitsis RN, Kohr MJ, ... ... Wallace DC, et al. Unlocking the Secrets of Mitochondria in the Cardiovascular System: Path to a Cure in Heart Failure—A Report from the 2018 National Heart, Lung, and Blood Institute Workshop Circulation. 140: 1205-1216. PMID 31769940 DOI: 10.1161/Circulationaha.119.040551 |
0.517 |
|
2019 |
Kopinski PK, Janssen KA, Schaefer PM, Trefely S, Perry CE, Potluri P, Tintos-Hernandez JA, Singh LN, Karch KR, Campbell SL, Doan MT, Jiang H, Nissim I, Nakamaru-Ogiso E, Wellen KE, ... ... Wallace DC, et al. Regulation of nuclear epigenome by mitochondrial DNA heteroplasmy. Proceedings of the National Academy of Sciences of the United States of America. PMID 31253706 DOI: 10.1073/Pnas.1906896116 |
0.31 |
|
2019 |
Gudiseva HV, Pistilli M, Salowe R, Singh LN, Collins DW, Cole B, He J, Merriam S, Khachataryan N, Henderer J, Addis V, Cui Q, Sankar PS, Miller-Ellis E, Chavali VRM, ... ... Wallace D, et al. The association of mitochondrial DNA haplogroups with POAG in African Americans. Experimental Eye Research. PMID 30653964 DOI: 10.1016/J.Exer.2019.01.015 |
0.312 |
|
2018 |
Wallace DC. Mitochondrial genetic medicine. Nature Genetics. PMID 30374071 DOI: 10.1038/s41588-018-0264-z |
0.311 |
|
2018 |
McManus MJ, Picard M, Chen HW, De Haas HJ, Potluri P, Leipzig J, Towheed A, Angelin A, Sengupta P, Morrow RM, Kauffman BA, Vermulst M, Narula J, Wallace DC. Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing Cardiomyopathy. Cell Metabolism. PMID 30174309 DOI: 10.1016/J.Cmet.2018.08.002 |
0.334 |
|
2018 |
Barel O, Malicdan M, Ben-Zeev B, Kandel J, Pri-Chen H, Stephen J, Castro I, Metz J, Atawa O, Moshkovitz S, Ganelin E, Barshack I, Polak-Charcon S, Nass D, Marek-Yagel D, ... ... Wallace D, et al. Corrigendum: Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy Brain. PMID 29528374 DOI: 10.1093/Brain/Awy063 |
0.366 |
|
2017 |
Pei L, Wallace DC. Mitochondrial Etiology of Neuropsychiatric Disorders. Biological Psychiatry. PMID 29290371 DOI: 10.1016/J.Biopsych.2017.11.018 |
0.328 |
|
2017 |
Barel O, Christine V Malicdan M, Ben-Zeev B, Kandel J, Pri-Chen H, Stephen J, Castro IG, Metz J, Atawa O, Moshkovitz S, Ganelin E, Barshack I, Polak-Charcon S, Nass D, Marek-Yagel D, ... ... Wallace DC, et al. Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy. Brain : a Journal of Neurology. 140: 568-581. PMID 28364549 DOI: 10.1093/Brain/Awx002 |
0.301 |
|
2016 |
Weiss S, Zhang D, Graham K, Deutschman C, Kilbaugh T, Francis M, Becker L, Wallace D. 17: REDUCED MITOCHONDRIAL MASS UNDERLAYS DECREASED RESPIRATION IN SEPTIC IMMUNE CELLS. Critical Care Medicine. 44: 91. PMID 27849697 DOI: 10.1097/01.Ccm.0000508735.93826.6E |
0.342 |
|
2016 |
Kandel J, Angelin AA, Wallace DC, Eckmann DM. Mitochondrial respiration is sensitive to cytoarchitectural breakdown. Integrative Biology : Quantitative Biosciences From Nano to Macro. PMID 27734042 DOI: 10.1039/C6Ib00192K |
0.316 |
|
2016 |
Murphy E, Ardehali H, Balaban RS, DiLisa F, Dorn GW, Kitsis RN, Otsu K, Ping P, Rizzuto R, Sack MN, Wallace D, Youle RJ. Mitochondrial Function, Biology, and Role in Disease: A Scientific Statement From the American Heart Association. Circulation Research. 118: 1960-91. PMID 27126807 DOI: 10.1161/Res.0000000000000104 |
0.404 |
|
2015 |
Pham T, Zand K, Wallace D, Burke P. Fluorescence analysis of single mitochondria with nanofluidic channels. Methods in Molecular Biology (Clifton, N.J.). 1264: 35-46. PMID 25631001 DOI: 10.1007/978-1-4939-2257-4_4 |
0.313 |
|
2015 |
McManus M, Chen HW, Picard M, Potluri P, Angelin A, Narula J, Wallace D. Mitochondrial DNA: The heart of the matter Mitochondrion. 24. DOI: 10.1016/J.Mito.2015.07.113 |
0.38 |
|
2015 |
McManus M, Picard M, Angelin A, Potluri P, Narula J, Wallace D. Mitochondrial DNA: The Heart of the Matter Biophysical Journal. 108. DOI: 10.1016/J.Bpj.2014.11.3308 |
0.417 |
|
2013 |
Wallace DC. A mitochondrial bioenergetic etiology of disease. The Journal of Clinical Investigation. 123: 1405-12. PMID 23543062 DOI: 10.1172/JCI61398 |
0.301 |
|
2013 |
Strauss KA, DuBiner L, Simon M, Zaragoza M, Sengupta PP, Li P, Narula N, Dreike S, Platt J, Procaccio V, Ortiz-González XR, Puffenberger EG, Kelley RI, Morton DH, Narula J, ... Wallace DC, et al. Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup. Proceedings of the National Academy of Sciences of the United States of America. 110: 3453-8. PMID 23401503 DOI: 10.1073/Pnas.1300690110 |
0.313 |
|
2013 |
Chalkia D, Lowery R, Derbeneva O, Lvova M, Sing C, Shimmin L, Hixson J, Simham H, Wadhwa P, Wallace D. Preterm birth is associated with mitochondrial DNA variation Mitochondrion. 13: 929-930. DOI: 10.1016/J.Mito.2013.07.082 |
0.354 |
|
2011 |
Chang I, Heiske M, Letellier T, Wallace D, Baldi P. Modeling of mitochondria bioenergetics using a composable chemiosmotic energy transduction rate law: theory and experimental validation. Plos One. 6: e14820. PMID 21931590 DOI: 10.1371/Journal.Pone.0014820 |
0.312 |
|
2011 |
Zaragoza MV, Brandon MC, Diegoli M, Arbustini E, Wallace DC. Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny. European Journal of Human Genetics : Ejhg. 19: 200-7. PMID 20978534 DOI: 10.1038/ejhg.2010.169 |
0.302 |
|
2010 |
Arnold R, Osunkoya A, O'Hearn S, Marshall F, Wallace D, Yi H, Wright E, Sun C, Costello L, Petros J. 221 FUNCTIONAL ANALYSIS OF A RARE MUTATION OF MITOCHONDRIAL DNA FOUND IN A PROSTATE CANCER Journal of Urology. 183. DOI: 10.1016/J.Juro.2010.02.279 |
0.33 |
|
2009 |
Wallace DC, Fan W. The pathophysiology of mitochondrial disease as modeled in the mouse. Genes & Development. 23: 1714-36. PMID 19651984 DOI: 10.1101/gad.1784909 |
0.356 |
|
2008 |
Khidr L, Wu G, Davila A, Procaccio V, Wallace D, Lee WH. Role of SUV3 helicase in maintaining mitochondrial homeostasis in human cells. The Journal of Biological Chemistry. 283: 27064-73. PMID 18678873 DOI: 10.1074/Jbc.M802991200 |
0.341 |
|
2006 |
Naïmi M, Bannwarth S, Procaccio V, Pouget J, Desnuelle C, Pellissier JF, Rötig A, Munnich A, Calvas P, Richelme C, Jonveaux P, Castelnovo G, Simon M, Simon M, Clanet M, ... Wallace D, et al. Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay. European Journal of Human Genetics : Ejhg. 14: 917-22. PMID 16639411 DOI: 10.1038/Sj.Ejhg.5201627 |
0.318 |
|
2005 |
Loeb LA, Wallace DC, Martin GM. The mitochondrial theory of aging and its relationship to reactive oxygen species damage and somatic mtDNA mutations Proceedings of the National Academy of Sciences of the United States of America. 102: 18769-18770. PMID 16365283 DOI: 10.1073/Pnas.0509776102 |
0.31 |
|
2005 |
Wallace DC. The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement. Gene. 354: 169-80. PMID 16024186 DOI: 10.1016/j.gene.2005.05.001 |
0.35 |
|
2002 |
Wallace DC. Animal models for mitochondrial disease. Methods in Molecular Biology (Clifton, N.J.). 197: 3-54. PMID 12013805 DOI: 10.1385/1-59259-284-8:003 |
0.316 |
|
2002 |
Sukernik R, Derbeneva O, Starikovskaya E, Volodko N, Mikhailovskaya I, Bychkov I, Lott M, Brown M, Wallace D. The Mitochondrial Genome And Human Mitochondrial Diseases Journal of the Peripheral Nervous System. 7: 211-212. DOI: 10.1046/J.1529-8027.2002.02026_25.X |
0.418 |
|
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