Publications - Pierson Lab Cedars-Sinai Skip to content Close Select your preferred language English عربى 简体中文 繁體中文 فارسي עִברִית 日本語 한국어 Русский Español Tagalog English English عربى 简体中文 繁體中文 فارسي עִברִית 日本語 한국어 Русский Español Tagalog Translation is unavailable for Internet Explorer Cedars-Sinai Home 1-800-CEDARS-1 1-800-CEDARS-1 Close Find a Doctor Locations Programs & Services Health Library Patient & Visitors Community My CS-Link RESEARCH clear Go Close Navigation Links Academics Faculty Development Community Engagement Calendar Research Research Areas Research Labs Departments & Institutes Find Clinical Trials Research Cores Research Administration Basic Science Research Clinical & Translational Research Center (CTRC) Technology & Innovations News & Breakthroughs Education Graduate Medical Education Continuing Medical Education Graduate School of Biomedical Sciences Professional Training Programs Medical Students Campus Life Office of the Dean Simulation Center Medical Library Program in the History of Medicine About Us All Education Programs Departments & Institutes Faculty Directory Pierson Lab Back to Pierson Lab Lab Members Personal Statement Publications Research Areas Publications See a complete PubMed list of publications by Tyler Mark Pierson, MD, PhD. Selected Key Publications Shieh C, Jones N, Vanle B, Au M, Huang AY, Silva APG, Lee H, Douine ED, Otero MG, Pierson TM et al. GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder. Genet Med. 2020 May;22(5):878-888. Pierson TM, Otero MG, Grand K, Choi A, Mackay J, Young JI, Graham Jr JM, Mackay J. The NuRD complex and macrocephaly associated neurodevelopmental disorders. Am J Med Genet. 2019 Dec;181(4):548-556. Johnson BV, Kumar R, Oishi S, Alexander S, Kasherman M, Vega MS, Ivancevic A, Gardner A, Domingo D, Corbett M, Pierson TM, et al. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling. Biol Psychiatry. 2020 Jan 15;87(2):100-112. Chen W, Shieh C, Graham JM, Tagliati M, Au M, Tankovic A, Wilcox W, Traynelis S, Yuan H, Pierson TM. GRIN1 mutation associated with developmental delay and movement disorder as a result of decreased NMDA receptor activity. J Hum Genet. 2017 Jun;62(6):589-597. Hjelm B, Grunseich C, Gowing G, Avalos P, Shelley B, Mooney MA, Narwani K, Shi Y, Svendsen CN, Wolfe JH, Fischbeck KH, Pierson TM. Mifepristone-inducible transgene expression in neural progenitor cells in vitro and in vivo. Gene Ther. 2016 May;23(5):424-437. Shieh C, Moser F, Graham JM, Watiker V, Pierson TM. Mutation in the sixth immunoglobulin domain of L1CAM is associated with migrational anomalies. Neurol Genet. 2015 Nov 16;1(4):e34. Pizzino A *, Pierson TM *, Guo Y, Helman G, Fortini S, Guerrero K, Saitta S, Murphy JLP, Padiath Q, Xie Y, et al. TUBB4A de novo mutations cause isolated hypomyelination. Neurology. 2014 Sep 2;83(10):898-902. Renvoisé B, Chang J, Singh R, Yonekawa S, FitzGibbon EJ, Schindler A, Toro C, Gahl WA, Mahuran D, Blackstone C, TM Pierson. Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11. Ann Clin Transl Neurol. 2014 Jun 1;1(6):379-389. Pierson TM, Yuan H, Marsh ED, Fuentes-Fajardo K, Markello TC, Adams DA, Golas G, Schreiber JM, Lehky TJ, Simeonov DR, et al. GRIN2A mutation and epileptic encephalopathy: therapy with memantine. Ann Clin Transl Neurol. 2014 Mar 1;1(3):190-198. Pierson TM, Adams D, Bonn F, Cherukuri PF, Teer JK, Hansen NF, Cruz P, Mullikin JC, Blakesley RW, Golas G, et al. Whole-exome sequencing identifies homozygous AFG3L2 mutations in a novel spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. PLoS Genet. 2011 Oct;7(10):e1002325. Contact the Pierson Lab Pavilion, Room 8418 8700 Beverly Blvd. Los Angeles, CA 90048 Lab 310-248-8551 Fax: 310-423-1244 Office 310-428-8558 Fax: 310-423-1244 Send a Message Please ensure Javascript is enabled for purposes of website accessibility