| Year |
Citation |
Score |
| 2023 |
Afshar-Saber W, Teaney NA, Winden KD, Jumo H, Shi X, McGinty G, Hubbs J, Chen C, Latzer IT, Gasparoli F, Ebrahimi-Fakhari D, Buttermore ED, Roullet JB, Pearl PL, Sahin M. ALDH5A1-deficient iPSC-derived excitatory and inhibitory neurons display cell type specific alterations. Neurobiology of Disease. 106386. PMID 38110041 DOI: 10.1016/j.nbd.2023.106386 |
0.384 |
|
| 2023 |
Winden KD, Pham TT, Teaney NA, Ruiz J, Chen R, Chen C, Sahin M. Increased degradation of FMRP contributes to neuronal hyperexcitability in tuberous sclerosis complex. Cell Reports. 42: 112838. PMID 37494191 DOI: 10.1016/j.celrep.2023.112838 |
0.335 |
|
| 2022 |
Buttermore ED, Anderson NC, Chen PF, Makhortova NR, Kim KH, Wafa SMA, Dwyer S, Micozzi JM, Winden KD, Zhang B, Han MJ, Kleiman RJ, Brownstein CA, Sahin M, Gonzalez-Heydrich J. 16p13.11 deletion variants associated with neuropsychiatric disorders cause morphological and synaptic changes in induced pluripotent stem cell-derived neurons. Frontiers in Psychiatry. 13: 924956. PMID 36405918 DOI: 10.3389/fpsyt.2022.924956 |
0.353 |
|
| 2021 |
Sundberg M, Pinson H, Smith RS, Winden KD, Venugopal P, Tai DJC, Gusella JF, Talkowski ME, Walsh CA, Tegmark M, Sahin M. 16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro. Nature Communications. 12: 2897. PMID 34006844 DOI: 10.1038/s41467-021-23113-z |
0.31 |
|
| 2020 |
Di Nardo A, Lenoël I, Winden KD, Rühmkorf A, Modi ME, Barrett L, Ercan-Herbst E, Venugopal P, Behne R, Lopes CAM, Kleiman RJ, Bettencourt-Dias M, Sahin M. Phenotypic Screen with TSC-Deficient Neurons Reveals Heat-Shock Machinery as a Druggable Pathway for mTORC1 and Reduced Cilia. Cell Reports. 31: 107780. PMID 32579942 DOI: 10.1016/J.Celrep.2020.107780 |
0.392 |
|
| 2019 |
Winden KD, Sundberg M, Yang C, Wafa SMA, Dwyer S, Chen PF, Buttermore ED, Sahin M. Biallelic mutations in lead to abnormalities associated with cortical tubers in human iPSC-derived neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 31591157 DOI: 10.1523/Jneurosci.0642-19.2019 |
0.482 |
|
| 2018 |
Winden KD, Ebrahimi-Fakhari D, Sahin M. Abnormal mTOR Activation in Autism. Annual Review of Neuroscience. PMID 29490194 DOI: 10.1146/Annurev-Neuro-080317-061747 |
0.351 |
|
| 2018 |
Sundberg M, Tochitsky I, Buchholz DE, Winden K, Kujala V, Kapur K, Cataltepe D, Turner D, Han MJ, Woolf CJ, Hatten ME, Sahin M. Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin. Molecular Psychiatry. PMID 29449635 DOI: 10.1038/S41380-018-0018-4 |
0.421 |
|
| 2017 |
Ercan E, Han JM, Di Nardo A, Winden K, Han MJ, Hoyo L, Saffari A, Leask A, Geschwind DH, Sahin M. Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex. The Journal of Experimental Medicine. PMID 28183733 DOI: 10.1084/Jem.20160446 |
0.547 |
|
| 2016 |
Wertz MH, Winden K, Neveu P, Ng SY, Ercan E, Sahin M. Cell type-specific miR-431 dysregulation in a motor neuron model of Spinal Muscular Atrophy. Human Molecular Genetics. PMID 27005422 DOI: 10.1093/Hmg/Ddw084 |
0.348 |
|
| 2015 |
Winden KD, Yuskaitis CJ, Poduri A. Megalencephaly and Macrocephaly. Seminars in Neurology. 35: 277-87. PMID 26060907 DOI: 10.1055/S-0035-1552622 |
0.391 |
|
| 2015 |
Winden KD, Bragin A, Engel J, Geschwind DH. Molecular alterations in areas generating fast ripples in an animal model of temporal lobe epilepsy. Neurobiology of Disease. 78: 35-44. PMID 25818007 DOI: 10.1016/J.Nbd.2015.02.011 |
0.639 |
|
| 2012 |
Konopka G, Friedrich T, Davis-Turak J, Winden K, Oldham MC, Gao F, Chen L, Wang GZ, Luo R, Preuss TM, Geschwind DH. Human-specific transcriptional networks in the brain. Neuron. 75: 601-17. PMID 22920253 DOI: 10.1016/J.Neuron.2012.05.034 |
0.714 |
|
| 2012 |
Voineagu I, Huang L, Winden K, Lazaro M, Haan E, Nelson J, McGaughran J, Nguyen LS, Friend K, Hackett A, Field M, Gecz J, Geschwind D. CCDC22: a novel candidate gene for syndromic X-linked intellectual disability. Molecular Psychiatry. 17: 4-7. PMID 21826058 DOI: 10.1038/Mp.2011.95 |
0.542 |
|
| 2011 |
Peñagarikano O, Abrahams BS, Herman EI, Winden KD, Gdalyahu A, Dong H, Sonnenblick LI, Gruver R, Almajano J, Bragin A, Golshani P, Trachtenberg JT, Peles E, Geschwind DH. Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits. Cell. 147: 235-46. PMID 21962519 DOI: 10.1016/J.Cell.2011.08.040 |
0.697 |
|
| 2011 |
Rosen EY, Wexler EM, Versano R, Coppola G, Gao F, Winden KD, Oldham MC, Martens LH, Zhou P, Farese RV, Geschwind DH. Functional genomic analyses identify pathways dysregulated by progranulin deficiency, implicating Wnt signaling. Neuron. 71: 1030-42. PMID 21943601 DOI: 10.1016/J.Neuron.2011.07.021 |
0.706 |
|
| 2011 |
Winden KD, Karsten SL, Bragin A, Kudo LC, Gehman L, Ruidera J, Geschwind DH, Engel J. A systems level, functional genomics analysis of chronic epilepsy. Plos One. 6: e20763. PMID 21695113 DOI: 10.1371/Journal.Pone.0020763 |
0.7 |
|
| 2009 |
Konopka G, Bomar JM, Winden K, Coppola G, Jonsson ZO, Gao F, Peng S, Preuss TM, Wohlschlegel JA, Geschwind DH. Human-specific transcriptional regulation of CNS development genes by FOXP2. Nature. 462: 213-7. PMID 19907493 DOI: 10.1038/Nature08549 |
0.664 |
|
| 2009 |
Winden KD, Oldham MC, Mirnics K, Ebert PJ, Swan CH, Levitt P, Rubenstein JL, Horvath S, Geschwind DH. The organization of the transcriptional network in specific neuronal classes. Molecular Systems Biology. 5: 291. PMID 19638972 DOI: 10.1038/Msb.2009.46 |
0.615 |
|
| 2009 |
Coppola G, Winden K, Konopka G, Gao F, Geschwind D. Expression and network analysis of Illumina microarray data Nature Protocols. DOI: 10.1038/Nprot.2009.215 |
0.628 |
|
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