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Maria Lvova

Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming
2014 · Martin Picard, Jiangwen Zhang, et al. · Proceedings of the National Academy of Sciences · 311
Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans
2012 · Fuyun Ji, Mark S. Sharpley, et al. · Proceedings of the National Academy of Sciences · 143
Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort
2010 · Anita Lakatos, Olga Derbeneva, et al. · Neurobiology of Aging · 97
Mitochondrial Disease Sequence Data Resource (MSeqDR): A global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities
2014 · Marni J. Falk, Lishuang Shen, et al. · Molecular Genetics and Metabolism · 87
Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders
2017 · Dimitra Chalkia, Larry N. Singh, et al. · JAMA Psychiatry · 78
Dual MAPK Inhibition Is an Effective Therapeutic Strategy for a Subset of Class II BRAF Mutant Melanomas
2018 · Matthew Dankner, Mathieu Lajoie, et al. · Clinical Cancer Research · 75
Peripheral Blood Mitochondrial DNA as a Biomarker of Cerebral Mitochondrial Dysfunction following Traumatic Brain Injury in a Porcine Model
2015 · Todd J. Kilbaugh, Maria Lvova, et al. · PLoS ONE · 48
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Mitochondrial DNA associations with East Asian metabolic syndrome
2018 · Dimitra Chalkia, Yi-Cheng Chang, et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 33
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Clinical Application of a Cancer Genomic Profiling Assay to Guide Precision Medicine Decisions
2017 · Cheryl Eifert, Angeliki Pantazi, et al. · Personalized Medicine · 30
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Combination of common mtDNA variants results in mitochondrial dysfunction and a connective tissue dysregulation
2022 · Patrick M. Schaefer, Leonardo Scherer Alves, et al. · Proceedings of the National Academy of Sciences · 22
Spectrum of pathogenic mtDNA mutations in Leber’s hereditary optic neuropathy families from Siberia
2006 · N. V. Volodko, M. A. L’vova, et al. · Russian Journal of Genetics · 13
Characterization of tumor mutation burden (TMB) and microsatellite instability (MSI) interplay for gastroesophageal adenocarcinoma (GA) and colorectal carcinoma (CRC).
2018 · Xiu Huang, Julie Y Tse, et al. · Journal of Clinical Oncology · 4
Characterization of biomarkers to immune checkpoint blockade therapy across solid tumors.
2018 · Meaghan Russell, Xiu Huang, et al. · Journal of Clinical Oncology · 2
Identification of very rare clinically actionable KRAS variants in colorectal cancer patients using a comprehensive large gene panel.
2018 · Shyamal Dilhan Weeraratne, Julie Y Tse, et al. · Journal of Clinical Oncology · 1
119 Mitochondrial DNA mutations found in native Central and South American samples provide evidence for mitochondrial adaptation to new environments
2010 · O. Derbeneva, D. Chalkia, et al. · Mitochondrion · 1
Utility of comprehensive genomic profiling (CGP) for personal cancer vaccine development via neoantigen analysis.
2018 · Dana Vuzman, Shermin Pei, et al. · Journal of Clinical Oncology
Semi-automated platform for efficient and accurate annotation and interpretation of somatic variants in cancer.
2018 · Meaghan Russell, Julie Y Tse, et al. · Journal of Clinical Oncology
Multi-platform characterization of cutaneous melanoma from patients treated with immune checkpoint inhibitors.
2018 · Dan Moldoveanu, Mathieu Lajoie, et al. · Journal of Clinical Oncology
Dual MAPK inhibition (dMAPKi) as an effective therapeutic strategy for class II BRAF mutant (mt) metastatic melanoma (MM).
2018 · Matthew Dankner, Mathieu Lajoie, et al. · Journal of Clinical Oncology
Cytoskeletal mitochondrial interactions in collagen VI related disorders
2016 · Alessia Angelin, Prasanth Potluri, et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics
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A mitochondrial bioenergetic hypothesis for autism spectrum disorder (570.3)
2014 · Dimitra Chalkia, Olga Derbeneva, et al. · The FASEB Journal
Preterm birth is associated with mitochondrial DNA variation
2013 · Dimitra Chalkia, Ray Lowery, et al. · Mitochondrion
Leber Hereditary Optic Neuropathy (LHON) associated mutation 3394 is also a high-altitude adaptive polymorphism
2012 · Leonardo S. Alves, Fuyun Ji, et al. · Mitochondrion
117 Asian mitochondrial DNA (mtDNA) lineage F4 is associated with increased risk of developing metabolic syndrome
2010 · Maria A. Lvova, Olga A. Derbeneva, et al. · Mitochondrion
Works count: 24
Citation count: 945
H-index: 11
I10-index: 11
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