Ashley Driver - Publications

2012- Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States 

5 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
2017 Driver AM, Shumrick C, Stottmann RW. Ttc21b Is Required in Bergmann Glia for Proper Granule Cell Radial Migration. Journal of Developmental Biology. 5. PMID 29615573 DOI: 10.3390/jdb5040018  0.72
2017 DiStasio A, Driver A, Sund K, Donlin M, Muraleedharan RM, Pooya S, Kline-Fath B, Kaufman KM, Prows CA, Schorry E, DasGupta B, Stottmann RW. Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly. Human Molecular Genetics. PMID 29036432 DOI: 10.1093/Hmg/Ddx362  0.72
2017 Li Z, Peng Y, Hufnagel RB, Hu YC, Zhao C, Queme LF, Khuchua Z, Driver AM, Dong F, Lu QR, Lindquist DM, Jankowski MP, Stottmann RW, Kao WWY, Huang T. Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice. Human Molecular Genetics. 26: 3776-3791. PMID 28934388 DOI: 10.1093/Hmg/Ddx262  0.72
2016 Stottmann RW, Driver A, Gutierrez A, Skelton MR, Muntifering M, Stepien C, Knudson L, Kofron M, Vorhees CV, Williams MT. A HETEROZYGOUS MUTATION IN TUBULIN, BETA 2B (TUBB2B) CAUSES COGNITIVE DEFICITS AND HIPPOCAMPAL DISORGANIZATION. Genes, Brain, and Behavior. PMID 27594048 DOI: 10.1111/Gbb.12327  0.72
2016 Driver AM, Kratz LE, Kelley RI, Stottmann RW. Altered cholesterol biosynthesis causes precocious neurogenesis in the developing mouse forebrain. Neurobiology of Disease. PMID 26921468 DOI: 10.1016/J.Nbd.2016.02.017  0.4
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