4 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
2021 McMeekin LJ, Fox SN, Boas SM, Cowell RM. Dysregulation of PGC-1α-Dependent Transcriptional Programs in Neurological and Developmental Disorders: Therapeutic Challenges and Opportunities. Cells. 10. PMID 33572179 DOI: 10.3390/cells10020352  0.493
2020 Schneeberger PE, Kortüm F, Korenke GC, Alawi M, Santer R, Woidy M, Buhas D, Fox S, Juusola J, Alfadhel M, Webb BD, Coci EG, Abou Jamra R, Siekmeyer M, Biskup S, et al. Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder. Brain : a Journal of Neurology. PMID 32761064 DOI: 10.1093/Brain/Awaa204  0.359
2019 Laszczyk AM, Nettles D, Pollock TA, Fox S, Garcia ML, Wang J, Quarles LD, King GD. FGF-23 Deficiency Impairs Hippocampal-Dependent Cognitive Function. Eneuro. 6. PMID 30911673 DOI: 10.1523/ENEURO.0469-18.2019  0.444
2018 McMeekin LJ, Li Y, Fox SN, Rowe GC, Crossman DK, Day JJ, Li Y, Detloff PJ, Cowell RM. Cell-specific deletion of PGC-1α from medium spiny neurons causes transcriptional alterations and age-related motor impairment. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29491012 DOI: 10.1523/Jneurosci.0848-17.2018  0.499
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