Melissa A. Walker, Ph.D.
Affiliations: | 2010 | Columbia University, New York, NY |
Area:
Synapses and Circuits, Axon Pathfinding and Synaptogenesis, Biophysics/Ion Channels, Cellular/Molecular/Developmental NeuroscienceGoogle:
"Melissa Walker"Mean distance: 30533.1
Parents
Sign in to add mentor| Lawrence S. Shapiro | grad student | 2010 | Columbia | |
| (Structural studies of DN-cadherin, an invertebrate classical cadherin, and other, non-classical cadherins.) | ||||
| Vamsi Mootha | post-doc | Harvard (Cell Biology Tree) | ||
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Publications
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| Romo L, Gold NB, Walker MA. (2023) Endocrine features of primary mitochondrial diseases. Current Opinion in Endocrinology, Diabetes, and Obesity |
| McCormick EM, Keller K, Taylor JP, et al. (2023) Expert panel curation of 113 primary mitochondrial disease genes for the Leigh syndrome spectrum. Annals of Neurology |
| Ganapathi M, Friocourt G, Gueguen N, et al. (2022) A homozygous splice variant in ATP5PO, disrupts mitochondrial complex V function and causes Leigh syndrome in two unrelated families. Journal of Inherited Metabolic Disease |
| Walker MA, Miranda M, Allred A, et al. (2021) On the dynamic and even reversible nature of Leigh syndrome: Lessons from human imaging and mouse models. Current Opinion in Neurobiology. 72: 80-90 |
| Sharma R, Reinstadler B, Engelstad K, et al. (2021) Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity. The Journal of Clinical Investigation. 131 |
| Rath S, Sharma R, Gupta R, et al. (2020) MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations. Nucleic Acids Research |
| Walker MA, Lareau CA, Ludwig LS, et al. (2020) Purifying Selection against Pathogenic Mitochondrial DNA in Human T Cells. The New England Journal of Medicine |
| Dutta D, Briere LC, Kanca O, et al. (2020) De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment. Human Molecular Genetics |
| Walker MA, Lerman-Sagie T, Swoboda K, et al. (2019) Refining the phenotype of the THG1L (p.Val55Ala mutation)-related mitochondrial autosomal recessive congenital cerebellar ataxia. American Journal of Medical Genetics. Part A |
| Walker MA, Mohler KP, Hopkins KW, et al. (2016) Novel Compound Heterozygous Mutations Expand the Recognized Phenotypes of FARS2-Linked Disease. Journal of Child Neurology |