| Year |
Citation |
Score |
| 2021 |
de Vries PJ, Leclezio L, Gardner-Lubbe S, Krueger D, Sahin M, Sparagana S, De Waele L, Jansen A. Multivariate data analysis identifies natural clusters of Tuberous Sclerosis Complex Associated Neuropsychiatric Disorders (TAND). Orphanet Journal of Rare Diseases. 16: 447. PMID 34689816 DOI: 10.1186/s13023-021-02076-w |
0.568 |
|
| 2021 |
Capal JK, Williams ME, Pearson DA, Kissinger R, Horn PS, Murray D, Currans K, Kent B, Bebin M, Northrup H, Wu JY, Sahin M, Krueger DA. Profile of Autism Spectrum Disorder in Tuberous Sclerosis Complex: Results from a longitudinal, prospective, multi-site study. Annals of Neurology. PMID 34668231 DOI: 10.1002/ana.26249 |
0.618 |
|
| 2021 |
Ihnen SKZ, Capal JK, Horn PS, Griffith M, Sahin M, Bebin EM, Wu JY, Northrup H, Krueger DA. Epilepsy Is Heterogeneous in Early-Life Tuberous Sclerosis Complex. Pediatric Neurology. 123: 1-9. PMID 34343869 DOI: 10.1016/j.pediatrneurol.2021.06.012 |
0.768 |
|
| 2021 |
Cable J, Purcell RH, Robinson E, Vorstman JAS, Chung WK, Constantino JN, Sanders SJ, Sahin M, Dolmetsch RE, Shah BM, Thurm A, Martin CL, Bearden CE, Mulle JG. Harnessing rare variants in neuropsychiatric and neurodevelopment disorders-a Keystone Symposia report. Annals of the New York Academy of Sciences. PMID 34342000 DOI: 10.1111/nyas.14658 |
0.598 |
|
| 2021 |
Mariscal MG, Berry-Kravis E, Buxbaum JD, Ethridge LE, Filip-Dhima R, Foss-Feig JH, Kolevzon A, Modi ME, Mosconi MW, Nelson CA, Powell CM, Siper PM, Soorya L, Thaliath A, Thurm A, ... ... Sahin M, et al. Shifted phase of EEG cross-frequency coupling in individuals with Phelan-McDermid syndrome. Molecular Autism. 12: 29. PMID 33910615 DOI: 10.1186/s13229-020-00411-9 |
0.707 |
|
| 2021 |
Cohen AL, Mulder BP, Prohl AK, Soussand L, Davis P, Kroeck MR, McManus P, Gholipour A, Scherrer B, Bebin EM, Wu JY, Northrup H, Krueger DA, Sahin M, Warfield SK, et al. Tuber locations associated with infantile spasms map to a common brain network. Annals of Neurology. PMID 33410532 DOI: 10.1002/ana.26015 |
0.769 |
|
| 2020 |
Farach LS, Richard MA, Lupo PJ, Sahin M, Krueger DA, Wu JY, Bebin EM, Au KS, Northrup H. Epilepsy Risk Prediction Model for Patients With Tuberous Sclerosis Complex. Pediatric Neurology. 113: 46-50. PMID 33011641 DOI: 10.1016/J.Pediatrneurol.2020.07.015 |
0.761 |
|
| 2020 |
Karimi D, Peters JM, Ouaalam A, Prabhu SP, Sahin M, Krueger DA, Kolevzon A, Eng C, Warfield SK, Gholipour A. LEARNING TO DETECT BRAIN LESIONS FROM NOISY ANNOTATIONS. Proceedings. Ieee International Symposium On Biomedical Imaging. 2020: 1910-1914. PMID 32879655 DOI: 10.1109/isbi45749.2020.9098599 |
0.661 |
|
| 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 |
0.706 |
|
| 2020 |
Grayson LE, Peters JM, McPherson T, Krueger DA, Sahin M, Wu JY, Northrup HA, Porter B, Cutter GR, O'Kelley SE, Krefting J, Stone SS, Madsen JR, Fallah A, Blount JP, et al. Pilot Study of Neurodevelopmental Impact of Early Epilepsy Surgery in Tuberous Sclerosis Complex. Pediatric Neurology. PMID 32418847 DOI: 10.1016/J.Pediatrneurol.2020.04.002 |
0.762 |
|
| 2020 |
Gonçalves IDCG, Brecht J, Thelen MP, Rehorst WA, Peters M, Lee HJ, Motameny S, Torres-Benito L, Ebrahimi-Fakhari D, Kononenko NL, Altmüller J, Vilchez D, Sahin M, Wirth B, Kye MJ. Author Correction: Neuronal activity regulates DROSHA via autophagy in spinal muscular atrophy. Scientific Reports. 10: 8206. PMID 32398663 DOI: 10.1038/s41598-020-64694-x |
0.682 |
|
| 2020 |
Modi ME, Sahin M. Tau: A Novel Entry Point for mTOR-Based Treatments in Autism Spectrum Disorder? Neuron. 106: 359-361. PMID 32380047 DOI: 10.1016/J.Neuron.2020.04.019 |
0.704 |
|
| 2020 |
Sánchez Fernández I, Yang E, Calvachi P, Amengual-Gual M, Wu JY, Krueger D, Northrup H, Bebin ME, Sahin M, Yu KH, Peters JM. Deep learning in rare disease. Detection of tubers in tuberous sclerosis complex. Plos One. 15: e0232376. PMID 32348367 DOI: 10.1371/Journal.Pone.0232376 |
0.743 |
|
| 2020 |
O'Brien AM, Bayet L, Riley K, Nelson CA, Sahin M, Modi ME. Auditory Processing of Speech and Tones in Children With Tuberous Sclerosis Complex. Frontiers in Integrative Neuroscience. 14: 14. PMID 32327979 DOI: 10.3389/Fnint.2020.00014 |
0.683 |
|
| 2020 |
Behne R, Teinert J, Wimmer M, D'Amore A, Davies AK, Scarrott JM, Eberhardt K, Brechmann B, Chen IP, Buttermore ED, Barrett L, Dwyer S, Chen T, Hirst J, Wiesener A, ... ... Sahin M, et al. Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein trafficking. Human Molecular Genetics. PMID 31915823 DOI: 10.1093/Hmg/Ddz310 |
0.732 |
|
| 2019 |
Schoenberger A, Capal JK, Ondracek A, Horn PS, Murray D, Byars AW, Pearson DA, Williams ME, Bebin M, Northrup H, Wu JY, Sahin M, Krueger DA. Language predictors of autism spectrum disorder in young children with tuberous sclerosis complex. Epilepsy & Behavior : E&B. 106844. PMID 31864941 DOI: 10.1016/J.Yebeh.2019.106844 |
0.766 |
|
| 2019 |
Prohl AK, Scherrer B, Tomas-Fernandez X, Davis PE, Filip-Dhima R, Prabhu SP, Peters JM, Bebin EM, Krueger DA, Northrup H, Wu JY, Sahin M, Warfield SK. Early white matter development is abnormal in tuberous sclerosis complex patients who develop autism spectrum disorder. Journal of Neurodevelopmental Disorders. 11: 36. PMID 31838998 DOI: 10.1186/S11689-019-9293-X |
0.77 |
|
| 2019 |
Scherrer B, Prohl AK, Taquet M, Kapur K, Peters JM, Tomas-Fernandez X, Davis PE, M Bebin E, Krueger DA, Northrup H, Y Wu J, Sahin M, Warfield SK. The Connectivity Fingerprint of the Fusiform Gyrus Captures the Risk of Developing Autism in Infants with Tuberous Sclerosis Complex. Cerebral Cortex (New York, N.Y. : 1991). PMID 31812987 DOI: 10.1093/Cercor/Bhz233 |
0.757 |
|
| 2019 |
Cook IA, Wilson AC, Peters JM, Goyal MN, Bebin EM, Northrup H, Krueger D, Leuchter AF, Sahin M. EEG Spectral Features in Sleep of Autism Spectrum Disorders in Children with Tuberous Sclerosis Complex. Journal of Autism and Developmental Disorders. PMID 31811616 DOI: 10.1007/S10803-019-04326-0 |
0.752 |
|
| 2019 |
Wu JY, Goyal M, Peters JM, Krueger D, Sahin M, Northrup H, Au KS, O'Kelley S, Williams M, Pearson DA, Hanson E, Byars AW, Krefting J, Beasley M, Cutter G, et al. Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study. Epilepsia. PMID 31691264 DOI: 10.1111/Epi.16379 |
0.752 |
|
| 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 |
0.783 |
|
| 2019 |
Sanders SJ, Sahin M, Hostyk J, Thurm A, Jacquemont S, Avillach P, Douard E, Martin CL, Modi ME, Moreno-De-Luca A, Raznahan A, Anticevic A, Dolmetsch R, Feng G, Geschwind DH, et al. A framework for the investigation of rare genetic disorders in neuropsychiatry. Nature Medicine. PMID 31548702 DOI: 10.1038/S41591-019-0581-5 |
0.786 |
|
| 2019 |
Prohl AK, Scherrer B, Tomas-Fernandez X, Filip-Dhima R, Kapur K, Velasco-Annis C, Clancy S, Carmody E, Dean M, Valle M, Prabhu SP, Peters JM, Bebin EM, Krueger DA, Northrup H, ... ... Sahin M, et al. Reproducibility of Structural and Diffusion Tensor Imaging in the TACERN Multi-Center Study. Frontiers in Integrative Neuroscience. 13: 24. PMID 31417372 DOI: 10.3389/Fnint.2019.00024 |
0.767 |
|
| 2019 |
Ahtam B, Dehaes M, Sliva DD, Peters JM, Krueger DA, Bebin EM, Northrup H, Wu JY, Warfield SK, Sahin M, Grant PE. Resting-State fMRI Networks in Children with Tuberous Sclerosis Complex. Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging. PMID 31304656 DOI: 10.1111/Jon.12653 |
0.757 |
|
| 2019 |
Davis PE, Kapur K, Filip-Dhima R, Trowbridge SK, Little E, Wilson A, Leuchter A, Bebin EM, Krueger D, Northrup H, Wu JY, Sahin M, Peters JM. Increased electroencephalography connectivity precedes epileptic spasm onset in infants with tuberous sclerosis complex. Epilepsia. PMID 31297797 DOI: 10.1111/Epi.16284 |
0.754 |
|
| 2019 |
Farach LS, Pearson DA, Woodhouse JP, Schraw JM, Sahin M, Krueger DA, Wu JY, Bebin EM, Lupo PJ, Au KS, Northrup H. Tuberous Sclerosis Complex Genotypes and Developmental Phenotype. Pediatric Neurology. PMID 31005478 DOI: 10.1016/J.Pediatrneurol.2019.03.003 |
0.761 |
|
| 2019 |
Williams ME, Pearson DA, Capal JK, Byars AW, Murray DS, Kissinger R, O'Kelley SE, Hanson E, Bing NM, Kent B, Wu JY, Northrup H, Bebin EM, Sahin M, Krueger D, et al. Impacting development in infants with tuberous sclerosis complex: Multidisciplinary research collaboration. The American Psychologist. 74: 356-367. PMID 30945897 DOI: 10.1037/Amp0000436 |
0.774 |
|
| 2018 |
Charupanit K, Nunez MD, Bernardo D, Bebin M, Krueger DA, Northrup H, Sahin M, Wu JY, Lopour BA. Automated Detection of High Frequency Oscillations in Human Scalp Electroencephalogram. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2018: 3116-3119. PMID 30441054 DOI: 10.1109/EMBC.2018.8513033 |
0.751 |
|
| 2018 |
Peters JM, Prohl A, Kapur K, Nath A, Scherrer B, Clancy S, Prabhu SP, Sahin M, Franz DN, Warfield SK, Krueger DA. Longitudinal Effects of Everolimus on White Matter Diffusion in Tuberous Sclerosis Complex. Pediatric Neurology. PMID 30424962 DOI: 10.1016/J.Pediatrneurol.2018.10.005 |
0.676 |
|
| 2018 |
Purtell H, Dhamne SC, Gurnani S, Bainbridge E, Modi ME, Lammers SHT, Super CE, Hameed MQ, Johnson EL, Sahin M, Rotenberg A. Electrographic spikes are common in wildtype mice. Epilepsy & Behavior : E&B. 89: 94-98. PMID 30399547 DOI: 10.1016/J.Yebeh.2018.09.003 |
0.763 |
|
| 2018 |
Tsai PT, Rudolph S, Guo C, Ellegood J, Gibson JM, Schaeffer SM, Mogavero J, Lerch JP, Regehr W, Sahin M. Sensitive Periods for Cerebellar-Mediated Autistic-like Behaviors. Cell Reports. 25: 357-367.e4. PMID 30304677 DOI: 10.1016/J.Celrep.2018.09.039 |
0.782 |
|
| 2018 |
Hussain SA, Schmid E, Peters JM, Goyal M, Bebin EM, Northrup H, Sahin M, Krueger DA, Wu JY. High vigabatrin dosage is associated with lower risk of infantile spasms relapse among children with tuberous sclerosis complex. Epilepsy Research. 148: 1-7. PMID 30296632 DOI: 10.1016/J.Eplepsyres.2018.09.016 |
0.768 |
|
| 2018 |
Modi ME, Sahin M. A Unified Circuit for Social Behavior. Neurobiology of Learning and Memory. PMID 30149055 DOI: 10.1016/J.Nlm.2018.08.010 |
0.683 |
|
| 2018 |
Modi ME, Sahin M. The Way Forward for Mechanism-Based Therapeutics in Genetically Defined Neurodevelopmental Disorders. Clinical Pharmacology and Therapeutics. PMID 30101418 DOI: 10.1002/Cpt.1181 |
0.713 |
|
| 2018 |
Gonçalves IDCG, Brecht J, Thelen MP, Rehorst WA, Peters M, Lee HJ, Motameny S, Torres-Benito L, Ebrahimi-Fakhari D, Kononenko NL, Altmüller J, Vilchez D, Sahin M, Wirth B, Kye MJ. Author Correction: Neuronal activity regulates DROSHA via autophagy in spinal muscular atrophy. Scientific Reports. 8: 10294. PMID 29967434 DOI: 10.1038/S41598-018-28202-6 |
0.681 |
|
| 2018 |
Gonçalves IDCG, Brecht J, Thelen MP, Rehorst WA, Peters M, Lee HJ, Motameny S, Torres-Benito L, Ebrahimi-Fakhari D, Kononenko NL, Altmüller J, Vilchez D, Sahin M, Wirth B, Kye MJ. Neuronal activity regulates DROSHA via autophagy in spinal muscular atrophy. Scientific Reports. 8: 7907. PMID 29784949 DOI: 10.1038/S41598-018-26347-Y |
0.69 |
|
| 2018 |
Bernardo D, Nariai H, Hussain SA, Sankar R, Salamon N, Krueger DA, Sahin M, Northrup H, Bebin EM, Wu JY. Visual and semi-automatic non-invasive detection of interictal fast ripples: A potential biomarker of epilepsy in children with tuberous sclerosis complex. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. PMID 29673547 DOI: 10.1016/J.Clinph.2018.03.010 |
0.749 |
|
| 2018 |
Srivastava S, Prohl AK, Scherrer B, Kapur K, Krueger DA, Warfield SK, Sahin M. Cerebellar volume as an imaging marker of development in infants with tuberous sclerosis complex. Neurology. PMID 29572283 DOI: 10.1212/Wnl.0000000000005352 |
0.677 |
|
| 2017 |
Krueger DA, Sadhwani A, Byars AW, de Vries PJ, Franz DN, Whittemore VH, Filip-Dhima R, Murray D, Kapur K, Sahin M. Everolimus for treatment of tuberous sclerosis complex-associated neuropsychiatric disorders. Annals of Clinical and Translational Neurology. 4: 877-887. PMID 29296616 DOI: 10.1002/Acn3.494 |
0.681 |
|
| 2017 |
Yuskaitis CJ, Jones BM, Wolfson RL, Super CE, Dhamne SC, Rotenberg A, Sabatini DM, Sahin M, Poduri A. A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility. Neurobiology of Disease. PMID 29274432 DOI: 10.1016/J.Nbd.2017.12.010 |
0.775 |
|
| 2017 |
Kelly E, Schaeffer SM, Dhamne SC, Lipton JO, Lindemann L, Honer M, Jaeschke G, Super CE, Lammers SH, Modi ME, Silverman JL, Dreier JR, Kwiatkowski DJ, Rotenberg A, Sahin M. mGluR5 Modulation of Behavioral and Epileptic Phenotypes in a Mouse Model of Tuberous Sclerosis Complex. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 29206810 DOI: 10.1038/Npp.2017.295 |
0.77 |
|
| 2017 |
Davis PE, Filip-Dhima R, Sideridis G, Peters JM, Au KS, Northrup H, Bebin EM, Wu JY, Krueger D, Sahin M. Presentation and Diagnosis of Tuberous Sclerosis Complex in Infants. Pediatrics. PMID 29101226 DOI: 10.1542/Peds.2016-4040 |
0.762 |
|
| 2017 |
Capal JK, Horn PS, Murray DS, Byars AW, Bing NM, Kent B, Bucher LA, Williams ME, O'Kelley S, Pearson DA, Sahin M, Krueger DA. Utility of the Autism Observation Scale for Infants in Early Identification of Autism in Tuberous Sclerosis Complex. Pediatric Neurology. PMID 28844798 DOI: 10.1016/J.Pediatrneurol.2017.06.010 |
0.691 |
|
| 2017 |
Lipton JO, Boyle LM, Yuan ED, Hochstrasser KJ, Chifamba FF, Nathan A, Tsai PT, Davis F, Sahin M. Aberrant Proteostasis of BMAL1 Underlies Circadian Abnormalities in a Paradigmatic mTOR-opathy. Cell Reports. 20: 868-880. PMID 28746872 DOI: 10.1016/J.Celrep.2017.07.008 |
0.777 |
|
| 2017 |
Dhamne SC, Silverman JL, Super CE, Lammers SHT, Hameed MQ, Modi ME, Copping NA, Pride MC, Smith DG, Rotenberg A, Crawley JN, Sahin M. Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism. Molecular Autism. 8: 26. PMID 28638591 DOI: 10.1186/S13229-017-0142-Z |
0.78 |
|
| 2017 |
Capal JK, Bernardino-Cuesta B, Horn PS, Murray D, Byars AW, Bing NM, Kent B, Pearson DA, Sahin M, Krueger DA. Influence of seizures on early development in tuberous sclerosis complex. Epilepsy & Behavior : E&B. 70: 245-252. PMID 28457992 DOI: 10.1016/J.Yebeh.2017.02.007 |
0.682 |
|
| 2017 |
Modi ME, Sahin M. Translational use of event-related potentials to assess circuit integrity in ASD. Nature Reviews. Neurology. PMID 28211449 DOI: 10.1038/Nrneurol.2017.15 |
0.694 |
|
| 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 |
0.405 |
|
| 2016 |
Ebrahimi-Fakhari D, Saffari A, Wahlster L, DiNardo A, Turner D, Lewis TL, Conrad C, Rothberg JM, Lipton JO, Kölker S, Hoffmann GF, Han MJ, Polleux F, Sahin M. Impaired Mitochondrial Dynamics And Mitophagy In Neuronal Models Of Tuberous Sclerosis Complex. Cell Reports. 17: 2162. PMID 27851977 DOI: 10.1016/j.celrep.2016.10.051 |
0.721 |
|
| 2016 |
Ebrahimi-Fakhari D, Saffari A, Wahlster L, Di Nardo A, Turner D, Lewis TL, Conrad C, Rothberg JM, Lipton JO, Kölker S, Hoffmann GF, Han MJ, Polleux F, Sahin M. Impaired Mitochondrial Dynamics and Mitophagy in Neuronal Models of Tuberous Sclerosis Complex. Cell Reports. 17: 1053-1070. PMID 27760312 DOI: 10.1016/J.Celrep.2016.09.054 |
0.712 |
|
| 2016 |
Alexander MS, Gasperini MJ, Tsai PT, Gibbs DE, Spinazzola JM, Marshall JL, Feyder MJ, Pletcher MT, Chekler EL, Morris CA, Sahin M, Harms JF, Schmidt CJ, Kleiman RJ, Kunkel LM. Reversal of neurobehavioral social deficits in dystrophic mice using inhibitors of phosphodiesterases PDE5A and PDE9A. Translational Psychiatry. 6: e901. PMID 27676442 DOI: 10.1038/Tp.2016.174 |
0.551 |
|
| 2016 |
Sun Y, Lipton JO, Boyle LM, Madsen JR, Goldenberg MC, Pascual-Leone A, Sahin M, Rotenberg A. Direct current stimulation induces mGluR5-dependent neocortical plasticity. Annals of Neurology. PMID 27315032 DOI: 10.1002/Ana.24708 |
0.698 |
|
| 2015 |
Tyburczy ME, Dies KA, Glass J, Camposano S, Chekaluk Y, Thorner AR, Lin L, Krueger D, Franz DN, Thiele EA, Sahin M, Kwiatkowski DJ. Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing. Plos Genetics. 11: e1005637. PMID 26540169 DOI: 10.1371/Journal.Pgen.1005637 |
0.675 |
|
| 2015 |
Wu JY, Peters JM, Goyal M, Krueger D, Sahin M, Northrup H, Au KS, Cutter G, Bebin EM. Clinical Electroencephalographic Biomarker for Impending Epilepsy in Asymptomatic Tuberous Sclerosis Complex Infants. Pediatric Neurology. PMID 26498039 DOI: 10.1016/J.Pediatrneurol.2015.09.013 |
0.754 |
|
| 2015 |
Kloth AD, Badura A, Li A, Cherskov A, Connolly SG, Giovannucci A, Bangash MA, Grasselli G, Peñagarikano O, Piochon C, Tsai PT, Geschwind DH, Hansel C, Sahin M, Takumi T, et al. Cerebellar associative sensory learning defects in five mouse autism models. Elife. 4. PMID 26158416 DOI: 10.7554/Elife.06085 |
0.591 |
|
| 2015 |
Davis PE, Peters JM, Krueger DA, Sahin M. Tuberous Sclerosis: A New Frontier in Targeted Treatment of Autism. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 12: 572-83. PMID 25986747 DOI: 10.1007/S13311-015-0359-5 |
0.703 |
|
| 2015 |
Lipton JO, Yuan ED, Boyle LM, Ebrahimi-Fakhari D, Kwiatkowski E, Nathan A, Güttler T, Davis F, Asara JM, Sahin M. The Circadian Protein BMAL1 Regulates Translation in Response to S6K1-Mediated Phosphorylation. Cell. 161: 1138-51. PMID 25981667 DOI: 10.1016/J.Cell.2015.04.002 |
0.702 |
|
| 2014 |
Lipton JO, Sahin M. The neurology of mTOR. Neuron. 84: 275-91. PMID 25374355 DOI: 10.1016/J.Neuron.2014.09.034 |
0.728 |
|
| 2014 |
Greene-Colozzi EA, Sadowski AR, Chadwick E, Tsai PT, Sahin M. Both maternal and pup genotype influence ultrasonic vocalizations and early developmental milestones in tsc2 (+/-) mice. Epilepsy Research and Treatment. 2014: 784137. PMID 25165580 DOI: 10.1155/2014/784137 |
0.557 |
|
| 2014 |
Kye MJ, Niederst ED, Wertz MH, Gonçalves Ido C, Akten B, Dover KZ, Peters M, Riessland M, Neveu P, Wirth B, Kosik KS, Sardi SP, Monani UR, Passini MA, Sahin M. SMN regulates axonal local translation via miR-183/mTOR pathway. Human Molecular Genetics. 23: 6318-31. PMID 25055867 DOI: 10.1093/Hmg/Ddu350 |
0.736 |
|
| 2014 |
Olson H, Shen Y, Avallone J, Sheidley BR, Pinsky R, Bergin AM, Berry GT, Duffy FH, Eksioglu Y, Harris DJ, Hisama FM, Ho E, Irons M, Jacobsen CM, James P, ... ... Sahin M, et al. Copy number variation plays an important role in clinical epilepsy. Annals of Neurology. 75: 943-58. PMID 24811917 DOI: 10.1002/Ana.24178 |
0.793 |
|
| 2014 |
Di Nardo A, Wertz MH, Kwiatkowski E, Tsai PT, Leech JD, Greene-Colozzi E, Goto J, Dilsiz P, Talos DM, Clish CB, Kwiatkowski DJ, Sahin M. Neuronal Tsc1/2 complex controls autophagy through AMPK-dependent regulation of ULK1. Human Molecular Genetics. 23: 3865-74. PMID 24599401 DOI: 10.1093/Hmg/Ddu101 |
0.566 |
|
| 2013 |
Fogarasi A, Loddenkemper T, Mellado C, Tuxhorn I, Evers G, Sarco D, Burgess RC, Halász P, Barsis P, Gyorsok Z, Gyimesi C, Kóbor J, Siegler Z, Janszky J, Jakus R, ... ... Sahin M, et al. Sturge-Weber syndrome: clinical and radiological correlates in 86 patients. Ideggyã³Gyã¡Szati Szemle. 66: 53-7. PMID 23607230 |
0.273 |
|
| 2013 |
Dimitriadi M, Kye MJ, Kalloo G, Yersak JM, Sahin M, Hart AC. The neuroprotective drug riluzole acts via small conductance Ca2+-activated K+ channels to ameliorate defects in spinal muscular atrophy models. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 6557-62. PMID 23575853 DOI: 10.1523/Jneurosci.1536-12.2013 |
0.698 |
|
| 2013 |
Lipton J, Sahin M. Fragile X syndrome therapeutics: translation, meet translational medicine. Neuron. 77: 212-3. PMID 23352156 DOI: 10.1016/J.Neuron.2013.01.009 |
0.728 |
|
| 2013 |
Weisenfeld NI, Peters JM, Tsai PT, Prabhu SP, Dies KA, Sahin M, Warfield SK. A magnetic resonance imaging study of cerebellar volume in tuberous sclerosis complex. Pediatric Neurology. 48: 105-10. PMID 23337002 DOI: 10.1016/J.Pediatrneurol.2012.10.011 |
0.569 |
|
| 2013 |
Tsai PT, Greene-Colozzi E, Goto J, Anderl S, Kwiatkowski DJ, Sahin M. Prenatal rapamycin results in early and late behavioral abnormalities in wildtype C57BL/6 mice. Behavior Genetics. 43: 51-9. PMID 23229624 DOI: 10.1007/S10519-012-9571-9 |
0.566 |
|
| 2012 |
Tsai PT, Hull C, Chu Y, Greene-Colozzi E, Sadowski AR, Leech JM, Steinberg J, Crawley JN, Regehr WG, Sahin M. Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice. Nature. 488: 647-51. PMID 22763451 DOI: 10.1038/Nature11310 |
0.571 |
|
| 2012 |
Yuan E, Tsai PT, Greene-Colozzi E, Sahin M, Kwiatkowski DJ, Malinowska IA. Graded loss of tuberin in an allelic series of brain models of TSC correlates with survival, and biochemical, histological and behavioral features. Human Molecular Genetics. 21: 4286-300. PMID 22752306 DOI: 10.1093/Hmg/Dds262 |
0.556 |
|
| 2012 |
Ehninger D, Sano Y, de Vries PJ, Dies K, Franz D, Geschwind DH, Kaur M, Lee YS, Li W, Lowe JK, Nakagawa JA, Sahin M, Smith K, Whittemore V, Silva AJ. Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice. Molecular Psychiatry. 17: 62-70. PMID 21079609 DOI: 10.1038/Mp.2010.115 |
0.418 |
|
| 2012 |
Ehninger D, Sano Y, De Vries PJ, Dies K, Franz D, Geschwind DH, Kaur M, Lee YS, Li W, Lowe JK, Nakagawa JA, Sahin M, Smith K, Whittemore V, Silva AJ. Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult mice (Molecular Psychiatry (2012) 17, (62-70) DOI:10.1038/mp.2010.115) Molecular Psychiatry. 17: 469-470. DOI: 10.1038/Mp.2011.39 |
0.387 |
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| 2011 |
Kye MJ, Neveu P, Lee YS, Zhou M, Steen JA, Sahin M, Kosik KS, Silva AJ. NMDA mediated contextual conditioning changes miRNA expression. Plos One. 6: e24682. PMID 21931811 DOI: 10.1371/Journal.Pone.0024682 |
0.726 |
|
| 2011 |
Akten B, Kye MJ, Hao le T, Wertz MH, Singh S, Nie D, Huang J, Merianda TT, Twiss JL, Beattie CE, Steen JA, Sahin M. Interaction of survival of motor neuron (SMN) and HuD proteins with mRNA cpg15 rescues motor neuron axonal deficits. Proceedings of the National Academy of Sciences of the United States of America. 108: 10337-42. PMID 21652774 DOI: 10.1073/Pnas.1104928108 |
0.692 |
|
| 2011 |
Tsai P, Sahin M. Mechanisms of neurocognitive dysfunction and therapeutic considerations in tuberous sclerosis complex Current Opinion in Neurology. 24: 106-113. PMID 21301339 DOI: 10.1097/Wco.0B013E32834451C4 |
0.589 |
|
| 2010 |
Neveu P, Kye MJ, Qi S, Buchholz DE, Clegg DO, Sahin M, Park IH, Kim KS, Daley GQ, Kornblum HI, Shraiman BI, Kosik KS. MicroRNA profiling reveals two distinct p53-related human pluripotent stem cell states. Cell Stem Cell. 7: 671-81. PMID 21112562 DOI: 10.1016/J.Stem.2010.11.012 |
0.726 |
|
| 2010 |
Margolis SS, Salogiannis J, Lipton DM, Mandel-Brehm C, Wills ZP, Mardinly AR, Hu L, Greer PL, Bikoff JB, Ho HY, Soskis MJ, Sahin M, Greenberg ME. EphB-mediated degradation of the RhoA GEF Ephexin5 relieves a developmental brake on excitatory synapse formation. Cell. 143: 442-55. PMID 21029865 DOI: 10.1016/J.Cell.2010.09.038 |
0.766 |
|
| 2010 |
Nie D, Di Nardo A, Han JM, Baharanyi H, Kramvis I, Huynh T, Dabora S, Codeluppi S, Pandolfi PP, Pasquale EB, Sahin M. Tsc2-Rheb signaling regulates EphA-mediated axon guidance. Nature Neuroscience. 13: 163-72. PMID 20062052 DOI: 10.1038/Nn.2477 |
0.753 |
|
| 2009 |
Di Nardo A, Kramvis I, Cho N, Sadowski A, Meikle L, Kwiatkowski DJ, Sahin M. Tuberous sclerosis complex activity is required to control neuronal stress responses in an mTOR-dependent manner. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 5926-37. PMID 19420259 DOI: 10.1523/Jneurosci.0778-09.2009 |
0.752 |
|
| 2008 |
Park KK, Liu K, Hu Y, Smith PD, Wang C, Cai B, Xu B, Connolly L, Kramvis I, Sahin M, He Z. Promoting axon regeneration in the adult CNS by modulation of the PTEN/mTOR pathway. Science (New York, N.Y.). 322: 963-6. PMID 18988856 DOI: 10.1126/Science.1161566 |
0.743 |
|
| 2008 |
Choi YJ, Di Nardo A, Kramvis I, Meikle L, Kwiatkowski DJ, Sahin M, He X. Tuberous sclerosis complex proteins control axon formation. Genes & Development. 22: 2485-95. PMID 18794346 DOI: 10.1101/Gad.1685008 |
0.755 |
|
| 2008 |
Meikle L, Pollizzi K, Egnor A, Kramvis I, Lane H, Sahin M, Kwiatkowski DJ. Response of a neuronal model of tuberous sclerosis to mammalian target of rapamycin (mTOR) inhibitors: effects on mTORC1 and Akt signaling lead to improved survival and function. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 5422-32. PMID 18495876 DOI: 10.1523/Jneurosci.0955-08.2008 |
0.765 |
|
| 2007 |
Fu WY, Chen Y, Sahin M, Zhao XS, Shi L, Bikoff JB, Lai KO, Yung WH, Fu AK, Greenberg ME, Ip NY. Cdk5 regulates EphA4-mediated dendritic spine retraction through an ephexin1-dependent mechanism. Nature Neuroscience. 10: 67-76. PMID 17143272 DOI: 10.1038/Nn1811 |
0.765 |
|
| 2005 |
Egea J, Nissen UV, Dufour A, Sahin M, Greer P, Kullander K, Mrsic-Flogel TD, Greenberg ME, Kiehn O, Vanderhaeghen P, Klein R. Regulation of EphA 4 kinase activity is required for a subset of axon guidance decisions suggesting a key role for receptor clustering in Eph function. Neuron. 47: 515-28. PMID 16102535 DOI: 10.1016/J.Neuron.2005.06.029 |
0.768 |
|
| 2005 |
Cowan CW, Shao YR, Sahin M, Shamah SM, Lin MZ, Greer PL, Gao S, Griffith EC, Brugge JS, Greenberg ME. Vav family GEFs link activated Ephs to endocytosis and axon guidance. Neuron. 46: 205-17. PMID 15848800 DOI: 10.1016/J.Neuron.2005.03.019 |
0.762 |
|
| 2005 |
Sahin M, Greer PL, Lin MZ, Poucher H, Eberhart J, Schmidt S, Wright TM, Shamah SM, O'connell S, Cowan CW, Hu L, Goldberg JL, Debant A, Corfas G, Krull CE, et al. Eph-dependent tyrosine phosphorylation of ephexin1 modulates growth cone collapse. Neuron. 46: 191-204. PMID 15848799 DOI: 10.1016/J.Neuron.2005.01.030 |
0.767 |
|
| 2001 |
Shamah SM, Lin MZ, Goldberg JL, Estrach S, Sahin M, Hu L, Bazalakova M, Neve RL, Corfas G, Debant A, Greenberg ME. EphA receptors regulate growth cone dynamics through the novel guanine nucleotide exchange factor ephexin. Cell. 105: 233-44. PMID 11336673 DOI: 10.1016/S0092-8674(01)00314-2 |
0.732 |
|
| 1995 |
Sahin M, Dowling JJ, Hockfield S. Seven protein tyrosine phosphatases are differentially expressed in the developing rat brain. The Journal of Comparative Neurology. 351: 617-31. PMID 7721987 DOI: 10.1002/Cne.903510410 |
0.548 |
|
| 1995 |
Sahin M, Slaugenhaupt SA, Gusella JF, Hockfield S. Expression of PTPH1, a rat protein tyrosine phosphatase, is restricted to the derivatives of a specific diencephalic segment. Proceedings of the National Academy of Sciences of the United States of America. 92: 7859-63. PMID 7644504 DOI: 10.1073/Pnas.92.17.7859 |
0.535 |
|
| 1993 |
Sahin M, Hockfield S. Protein tyrosine phosphatases expressed in the developing rat brain. The Journal of Neuroscience. 13: 4968-4978. DOI: 10.1523/Jneurosci.13-11-04968.1993 |
0.554 |
|
| 1990 |
Sahin M, Hockfield S. Molecular identification of the Lugaro cell in the cat cerebellar cortex. The Journal of Comparative Neurology. 301: 575-84. PMID 2273099 DOI: 10.1002/Cne.903010407 |
0.536 |
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