Google Scholars Citations
BIBLIOGRAPHY
Pre-print
Tidball AM, Luo J, Walker JC, Takla TN, Carvill G, & Parent JM. (2023).
Genome-wide CRISPRi Screen in Human iNeurons to Identify Novel Focal Cortical Dysplasia Genes.
bioRxiv, 2023-12.
Peer-reviewed
Tidball AM, Niu W, Ma Q, Takla TN, Walker JC, Margolis JL, Mojica-Perez SP, Sudyk R, Moore SJ, Chopra R, Shakkottai VG, Yuan Y, Murphy GG, Li JZ, Parent JM. Deriving early single-rosette brain organoids from human pluripotent stem cells,
Stem Cell Reports 18.12 (2023): 2498-2514.
Takla TN, Luo J, Sudyk R, Huang J, Walker JC, Vora NL, Sexton J., Parent JM, and Tidball AM. 2023. A shared pathogenic mechanism for valproic acid and SHROOM3 knockout in a brain organoid model of neural tube defects. Cells, 12(13), p.1697.
Tidball AM, Lopez-Santiago LF, Yuan Y, Glenn TW, Margolis JL, Clayton Walker J, Kilbane EG, Miller CA, Martina Bebin E, Scott Perry M, Isom LL, Parent JM: Variant-specific changes in persistent or resurgent sodium current in SCN8A-related epilepsy patient-derived neurons., Brain.143(10): 3025-3040, 09/2020. PM32968789
Tidball AM, Swaminathan P, Dang LT, Parent JM: Generating Loss-of-function iPSC Lines with Combined CRISPR Indel Formation and Reprogramming from Human Fibroblasts., Bio Protoc. 8(7)04/2018. United States, PM30320153
Tidball AM, Dang LT, Glenn TW, Kilbane EG, Klarr DJ, Margolis JL, Uhler MD, Parent JM: Rapid Generation of Human Genetic Loss-of-Function iPSC Lines by Simultaneous Reprogramming and Gene Editing, Stem Cell Reports.9(3): 725-731, 09/2017. PM28781079
Tidball AM, Neely MD, Chamberlin R, Aboud AA, Kumar KK, Han B, Bryan MR, Aschner M, Ess KC, Bowman AB: Genomic instability associated with p53 knockdown in the generation of Huntington’s disease human induced pluripotent stem cells, PLoS ONE.11(3)03/2016. PM26982737
Tidball AM, Parent JM: Concise Review: Exciting Cells: Modeling Genetic Epilepsies with Patient- Derived Induced Pluripotent Stem Cells, Stem Cells.34(1): 27-33, 01/2016. PM26373465
Tidball AM, Aboud AA, Kumar KK, Neely MD, Han B, Ess KC, Hong CC, Erikson KM, Hedera P, Bowman AB: PARK2 patient neuroprogenitors show increased mitochondrial sensitivity to copper, Neurobiology of Disease.73: 204-212, 01/2015. PM25315681
Tidball AM, Bryan MR, Uhouse MA, Kumar KK, Aboud AA, Feist JE, Ess KC, Diana Neely M, Aschner M, Bowman AB: A novel manganese dependent ATM-p53 signaling pathway is selectively impaired in patient-based neuroprogenitor and murine striatal models of Huntington's disease, Human Molecular Genetics.24(7): 1929-1944, 10/2014. PM25489053
Aboud AA, Tidball AM, Kumar KK, Neely MD, Ess KC, Erikson KM, Bowman AB: Genetic risk for Parkinson's disease correlates with alterations in neuronal manganese sensitivity between two human subjects, NeuroToxicology.33(6): 1443-1449, 12/2012. PM23099318
Book Chapter
Tidball AM: Disease in a dish: Cellular models to understand human conditions. In Walz K; Young J Ed. 1st, Elsevier Science Publishing Co, (2019) Andrew Tidball 5 09/26/2022
BIBLIOGRAPHY
Pre-print
Tidball AM, Luo J, Walker JC, Takla TN, Carvill G, & Parent JM. (2023).
Genome-wide CRISPRi Screen in Human iNeurons to Identify Novel Focal Cortical Dysplasia Genes.
bioRxiv, 2023-12.
Peer-reviewed
Tidball AM, Niu W, Ma Q, Takla TN, Walker JC, Margolis JL, Mojica-Perez SP, Sudyk R, Moore SJ, Chopra R, Shakkottai VG, Yuan Y, Murphy GG, Li JZ, Parent JM. Deriving early single-rosette brain organoids from human pluripotent stem cells,
Stem Cell Reports 18.12 (2023): 2498-2514.
Takla TN, Luo J, Sudyk R, Huang J, Walker JC, Vora NL, Sexton J., Parent JM, and Tidball AM. 2023. A shared pathogenic mechanism for valproic acid and SHROOM3 knockout in a brain organoid model of neural tube defects. Cells, 12(13), p.1697.
Tidball AM, Lopez-Santiago LF, Yuan Y, Glenn TW, Margolis JL, Clayton Walker J, Kilbane EG, Miller CA, Martina Bebin E, Scott Perry M, Isom LL, Parent JM: Variant-specific changes in persistent or resurgent sodium current in SCN8A-related epilepsy patient-derived neurons., Brain.143(10): 3025-3040, 09/2020. PM32968789
Tidball AM, Swaminathan P, Dang LT, Parent JM: Generating Loss-of-function iPSC Lines with Combined CRISPR Indel Formation and Reprogramming from Human Fibroblasts., Bio Protoc. 8(7)04/2018. United States, PM30320153
Tidball AM, Dang LT, Glenn TW, Kilbane EG, Klarr DJ, Margolis JL, Uhler MD, Parent JM: Rapid Generation of Human Genetic Loss-of-Function iPSC Lines by Simultaneous Reprogramming and Gene Editing, Stem Cell Reports.9(3): 725-731, 09/2017. PM28781079
Tidball AM, Neely MD, Chamberlin R, Aboud AA, Kumar KK, Han B, Bryan MR, Aschner M, Ess KC, Bowman AB: Genomic instability associated with p53 knockdown in the generation of Huntington’s disease human induced pluripotent stem cells, PLoS ONE.11(3)03/2016. PM26982737
Tidball AM, Parent JM: Concise Review: Exciting Cells: Modeling Genetic Epilepsies with Patient- Derived Induced Pluripotent Stem Cells, Stem Cells.34(1): 27-33, 01/2016. PM26373465
Tidball AM, Aboud AA, Kumar KK, Neely MD, Han B, Ess KC, Hong CC, Erikson KM, Hedera P, Bowman AB: PARK2 patient neuroprogenitors show increased mitochondrial sensitivity to copper, Neurobiology of Disease.73: 204-212, 01/2015. PM25315681
Tidball AM, Bryan MR, Uhouse MA, Kumar KK, Aboud AA, Feist JE, Ess KC, Diana Neely M, Aschner M, Bowman AB: A novel manganese dependent ATM-p53 signaling pathway is selectively impaired in patient-based neuroprogenitor and murine striatal models of Huntington's disease, Human Molecular Genetics.24(7): 1929-1944, 10/2014. PM25489053
Aboud AA, Tidball AM, Kumar KK, Neely MD, Ess KC, Erikson KM, Bowman AB: Genetic risk for Parkinson's disease correlates with alterations in neuronal manganese sensitivity between two human subjects, NeuroToxicology.33(6): 1443-1449, 12/2012. PM23099318
Book Chapter
Tidball AM: Disease in a dish: Cellular models to understand human conditions. In Walz K; Young J Ed. 1st, Elsevier Science Publishing Co, (2019) Andrew Tidball 5 09/26/2022