Year |
Citation |
Score |
2024 |
Nasello C, Poppi LA, Wu J, Kowalski TF, Thackray JK, Wang R, Persaud A, Mahboob M, Lin S, Spaseska R, Johnson CK, Gordon D, Tissir F, Heiman GA, Tischfield JA, ... ... Tischfield MA, et al. Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice. Proceedings of the National Academy of Sciences of the United States of America. 121: e2307156121. PMID 38683996 DOI: 10.1073/pnas.2307156121 |
0.626 |
|
2023 |
Nasello C, Poppi LA, Wu J, Kowalski TF, Thackray JK, Wang R, Persaud A, Mahboob M, Lin S, Spaseska R, Johnson CK, Gordon D, Tissir F, Heiman GA, Tischfield JA, ... ... Tischfield MA, et al. Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice. Biorxiv : the Preprint Server For Biology. PMID 38077033 DOI: 10.1101/2023.11.28.569034 |
0.621 |
|
2022 |
Wu J, Poppi LA, Tischfield MA. Planar cell polarity and the pathogenesis of Tourette Disorder: New hypotheses and perspectives. Developmental Biology. 489: 14-20. PMID 35644250 DOI: 10.1016/j.ydbio.2022.05.017 |
0.67 |
|
2021 |
Poppi LA, Ho-Nguyen KT, Shi A, Daut CT, Tischfield MA. Recurrent Implication of Striatal Cholinergic Interneurons in a Range of Neurodevelopmental, Neurodegenerative, and Neuropsychiatric Disorders. Cells. 10. PMID 33920757 DOI: 10.3390/cells10040907 |
0.649 |
|
2018 |
Latremoliere A, Cheng L, DeLisle M, Wu C, Chew S, Hutchinson EB, Sheridan A, Alexandre C, Latremoliere F, Sheu SH, Golidy S, Omura T, Huebner EA, Fan Y, Whitman MC, ... ... Tischfield MA, et al. Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration. Cell Reports. 24: 1865-1879.e9. PMID 30110642 DOI: 10.1016/J.Celrep.2018.07.029 |
0.309 |
|
2017 |
Tischfield MA, Robson CD, Gilette NM, Chim SM, Sofela FA, DeLisle MM, Gelber A, Barry BJ, MacKinnon S, Dagi LR, Nathans J, Engle EC. Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura. Developmental Cell. PMID 28844842 DOI: 10.1016/J.Devcel.2017.07.027 |
0.557 |
|
2016 |
Park JG, Tischfield MA, Nugent AA, Cheng L, Di Gioia SA, Chan WM, Maconachie G, Bosley TM, Summers CG, Hunter DG, Robson CD, Gottlob I, Engle EC. Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects. American Journal of Human Genetics. PMID 27181683 DOI: 10.1016/J.Ajhg.2016.03.023 |
0.374 |
|
2015 |
Whitman MC, Andrews C, Chan WM, Tischfield MA, Stasheff SF, Brancati F, Ortiz-Gonzalez X, Nuovo S, Garaci F, MacKinnon SE, Hunter DG, Grant PE, Engle EC. Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development. American Journal of Medical Genetics. Part A. PMID 26639658 DOI: 10.1002/Ajmg.A.37362 |
0.405 |
|
2014 |
Zhou Y, Wang Y, Tischfield M, Williams J, Smallwood PM, Rattner A, Taketo MM, Nathans J. Canonical WNT signaling components in vascular development and barrier formation. The Journal of Clinical Investigation. 124: 3825-46. PMID 25083995 DOI: 10.1172/Jci76431 |
0.528 |
|
2012 |
Cederquist GY, Luchniak A, Tischfield MA, Peeva M, Song Y, Menezes MP, Chan WM, Andrews C, Chew S, Jamieson RV, Gomes L, Flaherty M, Grant PE, Gupta ML, Engle EC. An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation. Human Molecular Genetics. 21: 5484-99. PMID 23001566 DOI: 10.1093/Hmg/Dds393 |
0.372 |
|
2011 |
Tischfield MA, Cederquist GY, Gupta ML, Engle EC. Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations. Current Opinion in Genetics & Development. 21: 286-94. PMID 21292473 DOI: 10.1016/J.Gde.2011.01.003 |
0.481 |
|
2010 |
Tischfield MA, Engle EC. Distinct alpha- and beta-tubulin isotypes are required for the positioning, differentiation and survival of neurons: new support for the 'multi-tubulin' hypothesis. Bioscience Reports. 30: 319-30. PMID 20406197 DOI: 10.1042/Bsr20100025 |
0.301 |
|
2010 |
Tischfield MA, Baris HN, Wu C, Rudolph G, Van Maldergem L, He W, Chan WM, Andrews C, Demer JL, Robertson RL, Mackey DA, Ruddle JB, Bird TD, Gottlob I, Pieh C, et al. Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. Cell. 140: 74-87. PMID 20074521 DOI: 10.1016/J.Cell.2009.12.011 |
0.449 |
|
2008 |
Bosley TM, Alorainy IA, Salih MA, Aldhalaan HM, Abu-Amero KK, Oystreck DT, Tischfield MA, Engle EC, Erickson RP. The clinical spectrum of homozygous HOXA1 mutations. American Journal of Medical Genetics. Part A. 146: 1235-40. PMID 18412118 DOI: 10.1002/Ajmg.A.32262 |
0.341 |
|
2007 |
Bosley TM, Salih MA, Alorainy IA, Oystreck DT, Nester M, Abu-Amero KK, Tischfield MA, Engle EC. Clinical characterization of the HOXA1 syndrome BSAS variant. Neurology. 69: 1245-53. PMID 17875913 DOI: 10.1212/01.Wnl.0000276947.59704.Cf |
0.418 |
|
2006 |
Tischfield MA, Chan WM, Grunert JF, Andrews C, Engle EC. HOXA1 mutations are not a common cause of Duane anomaly. American Journal of Medical Genetics. Part A. 140: 900-2. PMID 16528738 DOI: 10.1002/Ajmg.A.31167 |
0.325 |
|
2005 |
Tischfield MA, Bosley TM, Salih MA, Alorainy IA, Sener EC, Nester MJ, Oystreck DT, Chan WM, Andrews C, Erickson RP, Engle EC. Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Nature Genetics. 37: 1035-7. PMID 16155570 DOI: 10.1038/Ng1636 |
0.455 |
|
Low-probability matches (unlikely to be authored by this person) |
2017 |
Michalak SM, Whitman MC, Park JG, Tischfield MA, Nguyen EH, Engle EC. Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle. Investigative Ophthalmology & Visual Science. 58: 2388-2396. PMID 28437527 DOI: 10.1167/Iovs.16-21268 |
0.271 |
|
2017 |
Agarwal A, Wu PH, Hughes EG, Fukaya M, Tischfield MA, Langseth AJ, Wirtz D, Bergles DE. Transient Opening of the Mitochondrial Permeability Transition Pore Induces Microdomain Calcium Transients in Astrocyte Processes. Neuron. PMID 28132831 DOI: 10.1016/J.Neuron.2016.12.034 |
0.261 |
|
2010 |
Demer JL, Clark RA, Tischfield MA, Engle EC. Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations. Investigative Ophthalmology & Visual Science. 51: 4600-11. PMID 20393110 DOI: 10.1167/Iovs.10-5438 |
0.256 |
|
2023 |
Jain A, Ang PS, Matrongolo MJ, Tischfield MA. Understanding the development, pathogenesis, and injury response of meningeal lymphatic networks through the use of animal models. Cellular and Molecular Life Sciences : Cmls. 80: 332. PMID 37872442 DOI: 10.1007/s00018-023-04984-5 |
0.232 |
|
2023 |
Matrongolo MJ, Ho-Nguyen KT, Jain M, Ang PS, Reddy A, Schaper S, Tischfield MA. Loss of Twist1 and balanced retinoic acid signaling from the meninges causes cortical folding in mice. Development (Cambridge, England). PMID 37590085 DOI: 10.1242/dev.201381 |
0.209 |
|
2022 |
Ang PS, Matrongolo MJ, Zietowski ML, Nathan SL, Reid RR, Tischfield MA. Cranium growth, patterning and homeostasis. Development (Cambridge, England). 149. PMID 36408946 DOI: 10.1242/dev.201017 |
0.194 |
|
2022 |
Whitman MC, Gilette NM, Bell JL, Kim S, Tischfield M, Engle EC. TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse. Developmental Biology. PMID 35944701 DOI: 10.1016/j.ydbio.2022.07.010 |
0.174 |
|
2023 |
Matrongolo MJ, Ang PS, Wu J, Jain A, Thackray JK, Reddy AG, Sung CC, Barbet G, Hong YK, Tischfield MA. Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice. The Journal of Clinical Investigation. PMID 37917195 DOI: 10.1172/JCI171468 |
0.157 |
|
2023 |
Matrongolo MJ, Ang PS, Wu J, Jain A, Thackray JK, Reddy A, Sung CC, Barbet G, Hong YK, Tischfield MA. Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice. Biorxiv : the Preprint Server For Biology. PMID 37808775 DOI: 10.1101/2023.09.27.559761 |
0.157 |
|
2022 |
Ang PS, Matrongolo MJ, Tischfield MA. The growth and expansion of meningeal lymphatic networks are affected in craniosynostosis. Development (Cambridge, England). 149. PMID 34908123 DOI: 10.1242/dev.200065 |
0.154 |
|
2023 |
Bohic M, Pattison LA, Jhumka ZA, Rossi H, Thackray JK, Ricci M, Mossazghi N, Foster W, Ogundare S, Twomey CR, Hilton H, Arnold J, Tischfield MA, Yttri EA, St John Smith E, et al. Mapping the neuroethological signatures of pain, analgesia, and recovery in mice. Neuron. PMID 37442132 DOI: 10.1016/j.neuron.2023.06.008 |
0.132 |
|
Hide low-probability matches. |