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Kyle Metz - Publications

Affiliations: 
MMI Johns Hopkins Bloomberg School of Public Health 
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3 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Teng X, Aouacheria A, Lionnard L, Metz KA, Soane L, Kamiya A, Hardwick JM. KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders. Cns Neuroscience & Therapeutics. 25: 887-902. PMID 31197948 DOI: 10.1111/Cns.13156  0.689
2018 Metz KA, Teng X, Coppens I, Lamb HM, Wagner BE, Rosenfeld JA, Chen X, Zhang Y, Kim HJ, Meadow ME, Wang TS, Haberlandt ED, Anderson GW, Leshinsky-Silver E, Bi W, et al. KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect. Annals of Neurology. PMID 30295347 DOI: 10.1002/Ana.25351  0.643
2018 Chen X, Wang G, Zhang Y, Dayhoff-Brannigan M, Diny NL, Zhao M, He G, Sing CN, Metz KA, Stolp ZD, Aouacheria A, Cheng WC, Hardwick JM, Teng X. Whi2 is a conserved negative regulator of TORC1 in response to low amino acids. Plos Genetics. 14: e1007592. PMID 30142151 DOI: 10.1371/Journal.Pgen.1007592  0.341
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