Tianna Zhao

Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease

Marialuisa Quadri, Antonio Federico, Tianna Zhao et al. · The American Journal of Human Genetics · 2012 · 411 citations · Full text

Mendelian Disorder, Genetic Disorder, Parkinson Disease +8

<i>FBXO7</i> mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome

Alessio Di Fonzo, Marieke C. J. Dekker, P. Montagna et al. · Neurology · 2008 · 353 citations

LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

Marialuisa Quadri, Wim Mandemakers, Martyna M. Grochowska et al. · The Lancet Neurology · 2018 · 159 citations

Neurodegenerative Diseases, Genetic Disorder, Genetics +9

ACT001 reduces the expression of PD-L1 by inhibiting the phosphorylation of STAT3 in glioblastoma

Luqing Tong, Jiabo Li, Qiuying Li et al. · Theranostics · 2020 · 148 citations · Full text

Loss of Nuclear Activity of the FBXO7 Protein in Patients with Parkinsonian-Pyramidal Syndrome (PARK15)

Tianna Zhao, Esther de Graaff, Guido J. Breedveld et al. · PLoS ONE · 2011 · 53 citations · Full text

Neurodegenerative Diseases, Nuclear Activity, Parkinsonian-pyramidal Syndrome +15