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Yuen, Michaela, Sarah Sandaradura, James Dowling, Alla Kostyukova, Natalia Moroz, Kate Quinlan, Vilma-Lotta Lehtokari, et al. 2014. “Leiomodin-3 Dysfunction Results in Thin Filament Disorganization and Nemaline Myopathy.”. J Clin Invest 124 (11): 4693-708.

Ludwig, Leif, Hanna Gazda, Jennifer Eng, Stephen Eichhorn, Prathapan Thiru, Roxanne Ghazvinian, Tracy George, et al. 2014. “Altered Translation of GATA1 in Diamond-Blackfan Anemia.”. Nat Med 20 (7): 748-53.

Lawlor, Michael, Marissa Viola, Hui Meng, Rachel Edelstein, Fujun Liu, Ke Yan, Elizabeth Luna, et al. 2014. “Differential Muscle Hypertrophy Is Associated With Satellite Cell Numbers and Akt Pathway Activation Following Activin Type IIB Receptor Inhibition in Mtm1 P.R69C Mice.”. Am J Pathol 184 (6): 1831-42.

Zhang, Zhou, Ogmundsdottir, Möller, Siddaway, Larue, Hsing, et al. 2015. “Mitf Is a Master Regulator of the V-ATPase Forming an Mitf/V-ATPase/TORC1 Control Module for Cellular Homeostasis.”. J Cell Sci.

Sheth, Kevin, Timothy Yu, Keith Vossel, and Tracey Cho. 2008. “Education Research: A Program Perspective on Learning How to Teach.”. Neurology 70 (19): e75-7.

Sanders, Stephan, Xin He, Jeremy Willsey, Gulhan Ercan-Sencicek, Kaitlin Samocha, Ercument Cicek, Michael Murtha, et al. 2015. “Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.”. Neuron 87 (6): 1215-33.

Yu, Timothy, Ganeshwaran Mochida, David Tischfield, Sema Sgaier, Laura Flores-Sarnat, Consolato Sergi, Meral Topçu, et al. 2010. “Mutations in WDR62, Encoding a Centrosome-Associated Protein, Cause Microcephaly With Simplified Gyri and Abnormal Cortical Architecture.”. Nat Genet 42 (11): 1015-20.

Clapham, Yu, Ganesh, Barry, Chan, Mei, Parrini, et al. 2012. “FLNA Genomic Rearrangements Cause Periventricular Nodular Heterotopia.”. Neurology 78 (4): 269-78.

Zhang, Xiaochang, Jiqiang Ling, Giulia Barcia, Lili Jing, Jiang Wu, Brenda Barry, Ganeshwaran Mochida, et al. 2014. “Mutations in QARS, Encoding Glutaminyl-TRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures.”. Am J Hum Genet 94 (4): 547-58.

Di Costanzo, Stefania, Anuradha Balasubramanian, Heather Pond, Anete Rozkalne, Chiara Pantaleoni, Simona Saredi, Vandana Gupta, et al. 2014. “POMK Mutations Disrupt Muscle Development Leading to a Spectrum of Neuromuscular Presentations.”. Hum Mol Genet 23 (21): 5781-92.