| Year |
Citation |
Score |
| 2020 |
Giannikou K, Zhu Z, Kim J, Winden KD, Tyburczy ME, Marron D, Parker JS, Hebert Z, Bongaarts A, Taing L, Long HW, Pisano WV, Alexandrescu S, Godlewski B, Nellist M, ... ... Sahin M, et al. Subependymal giant cell astrocytomas are characterized by mTORC1 hyperactivation, a very low somatic mutation rate, and a unique gene expression profile. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. PMID 33051600 DOI: 10.1038/s41379-020-00659-9 |
1 |
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| 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 |
1 |
|
| 2020 |
Ebrahimi-Fakhari D, Teinert J, Behne R, Wimmer M, D'Amore A, Eberhardt K, Brechmann B, Ziegler M, Jensen DM, Nagabhyrava P, Geisel G, Carmody E, Shamshad U, Dies KA, Yuskaitis CJ, ... ... Sahin M, et al. Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia. Brain : a Journal of Neurology. PMID 32979048 DOI: 10.1093/brain/awz307 |
1 |
|
| 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 |
1 |
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| 2020 |
Srivastava S, Love-Nichols JA, Dies KA, Ledbetter DH, Martin CL, Chung WK, Firth HV, Frazier T, Hansen RL, Prock L, Brunner H, Hoang N, Scherer SW, Sahin M, Miller DT, et al. Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32728138 DOI: 10.1038/s41436-020-0913-3 |
1 |
|
| 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 |
1 |
|
| 2020 |
Sundberg M, Sahin M. Modeling Neurodevelopmental Deficits in Tuberous Sclerosis Complex with Stem Cell Derived Neural Precursors and Neurons. Advances in Neurobiology. 25: 1-31. PMID 32578142 DOI: 10.1007/978-3-030-45493-7_1 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 2020 |
D'Amore A, Tessa A, Naef V, Bassi MT, Citterio A, Romaniello R, Fichi G, Galatolo D, Mero S, Battini R, Bertocci G, Baldacci J, Sicca F, Gemignani F, Ricca I, ... ... Sahin M, et al. Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52. Annals of Clinical and Translational Neurology. PMID 32216065 DOI: 10.1002/acn3.51018 |
1 |
|
| 2020 |
Bassell J, Srivastava S, Prohl AK, Scherrer B, Kapur K, Filip-Dhima R, Berry-Kravis E, Soorya L, Thurm A, Powell CM, Bernstein JA, Buxbaum JD, Kolevzon A, Warfield SK, Sahin M, et al. Diffusion Tensor Imaging Abnormalities in the Uncinate Fasciculus and Inferior Longitudinal Fasciculus in Phelan-McDermid Syndrome. Pediatric Neurology. PMID 32107139 DOI: 10.1016/j.pediatrneurol.2020.01.006 |
1 |
|
| 2020 |
Kodani A, Kenny C, Lai A, Gonzalez DM, Stronge E, Sejourne GM, Isacco L, Partlow JN, O'Donnell A, McWalter K, Byrne AB, Barkovich AJ, Yang E, Hill RS, Gawlinski P, ... ... Sahin M, et al. Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5. Neuron. PMID 32097629 DOI: 10.1016/j.neuron.2020.01.030 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 2019 |
Teinert J, Behne R, D'Amore A, Wimmer M, Dwyer S, Chen T, Buttermore ED, Chen IP, Sahin M, Ebrahimi-Fakhari D. Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4B1-associated hereditary spastic paraplegia (SPG47). Stem Cell Research. 40: 101575. PMID 31525725 DOI: 10.1016/j.scr.2019.101575 |
1 |
|
| 2019 |
Dickinson A, Varcin KJ, Sahin M, Nelson CA, Jeste SS. Early patterns of functional brain development associated with autism spectrum disorder in tuberous sclerosis complex. Autism Research : Official Journal of the International Society For Autism Research. PMID 31419043 DOI: 10.1002/aur.2193 |
1 |
|
| 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 |
1 |
|
| 2019 |
Peters JM, Struyven RR, Prohl AK, Vasung L, Stajduhar A, Taquet M, Bushman JJ, Lidov H, Singh JM, Scherrer B, Madsen JR, Prabhu SP, Sahin M, Afacan O, Warfield SK. White matter mean diffusivity correlates with myelination in tuberous sclerosis complex. Annals of Clinical and Translational Neurology. 6: 1178-1190. PMID 31353853 DOI: 10.1002/acn3.793 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 2019 |
de Groen AC, Bolton J, Bergin AM, Sahin M, Peters JM. The Evolution of Subclinical Seizures in Children With Tuberous Sclerosis Complex. Journal of Child Neurology. 883073819860640. PMID 31290714 DOI: 10.1177/0883073819860640 |
1 |
|
| 2019 |
Peters JM, Hyde DE, Chu CJ, Boom M, Scherrer B, Madsen JR, Stone SS, Ouaalam H, Prabhu SP, Sahin M, Warfield SK. Lesion-Constrained Electrical Source Imaging: A Novel Approach in Epilepsy Surgery for Tuberous Sclerosis Complex. Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society. PMID 31261349 DOI: 10.1097/WNP.0000000000000615 |
1 |
|
| 2019 |
Srivastava S, Love-Nichols JA, Dies KA, Ledbetter DH, Martin CL, Chung WK, Firth HV, Frazier T, Hansen RL, Prock L, Brunner H, Hoang N, Scherer SW, Sahin M, Miller DT, et al. Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31182824 DOI: 10.1038/s41436-019-0554-6 |
1 |
|
| 2019 |
Yuskaitis CJ, Rossitto LA, Gurnani S, Bainbridge E, Poduri A, Sahin M. Chronic mTORC1 inhibition rescues behavioral and biochemical deficits resulting from neuronal Depdc5 loss in mice. Human Molecular Genetics. PMID 31174205 DOI: 10.1093/hmg/ddz123 |
1 |
|
| 2019 |
Giannikou K, Lasseter KD, Grevelink JM, Tyburczy ME, Dies KA, Zhu Z, Hamieh L, Wollison BM, Thorner AR, Ruoss SJ, Thiele EA, Sahin M, Kwiatkowski DJ. Low-level mosaicism in tuberous sclerosis complex: prevalence, clinical features, and risk of disease transmission. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31160751 DOI: 10.1038/s41436-019-0562-6 |
1 |
|
| 2019 |
Salussolia CL, Klonowska K, Kwiatkowski DJ, Sahin M. Genetic Etiologies, Diagnosis, and Treatment of Tuberous Sclerosis Complex. Annual Review of Genomics and Human Genetics. PMID 31018109 DOI: 10.1146/annurev-genom-083118-015354 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 2018 |
Marami B, Scherrer B, Khan S, Afacan O, Prabhu SP, Sahin M, Warfield SK, Gholipour A. Motion-robust diffusion compartment imaging using simultaneous multi-slice acquisition. Magnetic Resonance in Medicine. PMID 30443929 DOI: 10.1002/mrm.27613 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 2018 |
Srivastava S, Scherrer B, Prohl AK, Filip-Dhima R, Kapur K, Kolevzon A, Buxbaum JD, Berry-Kravis E, Soorya L, Thurm A, Powell CM, Bernstein JA, Warfield SK, Sahin M. Volumetric Analysis of the Basal Ganglia and Cerebellar Structures in Patients with Phelan-McDermid Syndrome. Pediatric Neurology. PMID 30396833 DOI: 10.1016/j.pediatrneurol.2018.09.008 |
1 |
|
| 2018 |
Jülich K, Neuberger I, Sahin M, Takeoka M, Pinto A, Prabhu SP. Yield of Emergent Neuroimaging in Patients With Sturge-Weber Syndrome Presenting With Acute Neurologic Symptoms. Journal of Child Neurology. 883073818801635. PMID 30378435 DOI: 10.1177/0883073818801635 |
1 |
|
| 2018 |
Yu KH, Miron O, Palmer N, Lemos D, Fox K, Kou SC, Sahin M, Kohane IS. Data-driven analyses revealed the comorbidity landscape of tuberous sclerosis complex. Neurology. PMID 30333165 DOI: 10.1212/WNL.0000000000006546 |
1 |
|
| 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 |
0.44 |
|
| 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 |
1 |
|
| 2018 |
Howe JR, Bear MF, Golshani P, Klann E, Lipton SA, Mucke L, Sahin M, Silva AJ. The mouse as a model for neuropsychiatric drug development. Current Biology : Cb. 28: R909-R914. PMID 30205056 DOI: 10.1016/j.cub.2018.07.046 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 2018 |
Di Nardo A, Sahin M. mTOR'ing across the Cortex by Chopping the Cilia. Neuron. 99: 3-5. PMID 30001510 DOI: 10.1016/j.neuron.2018.06.042 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 2018 |
Pinto ALR, Ou Y, Sahin M, Grant PE. Quantitative Apparent Diffusion Coefficient Mapping May Predict Seizure Onset in Children With Sturge-Weber Syndrome. Pediatric Neurology. PMID 29753575 DOI: 10.1016/j.pediatrneurol.2018.04.004 |
1 |
|
| 2018 |
van der Poest Clement EA, Sahin M, Peters JM. Vigabatrin for Epileptic Spasms and Tonic Seizures in Tuberous Sclerosis Complex. Journal of Child Neurology. 883073818768309. PMID 29687739 DOI: 10.1177/0883073818768309 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 2018 |
O'Leary HM, Kaufmann WE, Barnes KV, Rakesh K, Kapur K, Tarquinio DC, Cantwell NG, Roche KJ, Rose SA, Walco AC, Bruck NM, Bazin GA, Holm IA, Alexander ME, Swanson LC, ... ... Sahin M, et al. Placebo-controlled crossover assessment of mecasermin for the treatment of Rett syndrome. Annals of Clinical and Translational Neurology. 5: 323-332. PMID 29560377 DOI: 10.1002/acn3.533 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
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| 2017 |
Baumer FM, Peters JM, Clancy S, Prohl AK, Prabhu SP, Scherrer B, Jansen FE, Braun KPJ, Sahin M, Stamm A, Warfield SK. Corpus Callosum White Matter Diffusivity Reflects Cumulative Neurological Comorbidity in Tuberous Sclerosis Complex. Cerebral Cortex (New York, N.Y. : 1991). PMID 29939236 DOI: 10.1093/cercor/bhx247 |
1 |
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| 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 |
1 |
|
| 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 |
1 |
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| 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 |
1 |
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| 2017 |
Ebrahimi-Fakhari D, Cheng C, Dies K, Diplock A, Pier DB, Ryan CS, Lanpher BC, Hirst J, Chung WK, Sahin M, Rosser E, Darras B, Bennett JT. Clinical and genetic characterization of AP4B1-associated SPG47. American Journal of Medical Genetics. Part A. PMID 29193663 DOI: 10.1002/ajmg.a.38561 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 2017 |
Dy ME, Waugh JL, Sharma N, O'Leary H, Kapur K, D'Gama AM, Sahin M, Urion DK, Kaufmann WE. Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective. Pediatric Neurology. PMID 28838622 DOI: 10.1016/j.pediatrneurol.2017.05.025 |
1 |
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| 2017 |
McDonald NM, Varcin KJ, Bhatt R, Wu JY, Sahin M, Nelson CA, Jeste SS. Early autism symptoms in infants with tuberous sclerosis complex. Autism Research : Official Journal of the International Society For Autism Research. PMID 28801991 DOI: 10.1002/aur.1846 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 2017 |
Agulnik A, Kelly DP, Bruccoleri R, Yuskaitis C, Ebrahimi-Fakhari D, Sahin M, Burns MM, Kohane DS. Combination Clearance Therapy and Barbiturate Coma for Severe Carbamazepine Overdose. Pediatrics. 139. PMID 28557718 DOI: 10.1542/peds.2016-1560 |
1 |
|
| 2017 |
Lam HC, Baglini CV, Llorente Lope A, Parkhitko A, Liu HJ, Alesi N, Malinowska IA, Ebrahimi-Fakhari D, Saffari A, Yu JJ, Pereira A, Khabibullin D, Ogorek B, Nijmeh JS, Kavanagh T, ... ... Sahin M, et al. p62/SQSTM1 cooperates with hyperactive mTORC1 to regulate glutathione production, maintain mitochondrial integrity and promote tumorigenesis. Cancer Research. PMID 28512249 DOI: 10.1158/0008-5472.CAN-16-2458 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 2017 |
Ebrahimi-Fakhari D, Saffari A, Wahlster L, Sahin M. Using tuberous sclerosis complex to understand the impact of MTORC1 signaling on mitochondrial dynamics and mitophagy in neurons. Autophagy. 0. PMID 28121223 DOI: 10.1080/15548627.2016.1277310 |
1 |
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| 2016 |
Weisleder P, Gospe SM, Ng YT, Sahin M. The Pediatric Neurology Trainee Publication Award for 2015. Pediatric Neurology. 63: 1-2. PMID 28847386 DOI: 10.1016/j.pediatrneurol.2016.07.004 |
1 |
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| 2016 |
Huang L, Couto JA, Pinto A, Alexandrescu S, Madsen JR, Greene AK, Sahin M, Bischoff J. Somatic GNAQ Mutation is Enriched in Brain Endothelial Cells in Sturge-Weber Syndrome. Pediatric Neurology. PMID 27919468 DOI: 10.1016/j.pediatrneurol.2016.10.010 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 2016 |
Arslan MS, Tutal E, Sahin M, Karakose M, Ucan B, Ozturk G, Cakal E, Biyikli Gencturk Z, Ozbek M, Delibasi T. Effect of lifestyle interventions with or without metformin therapy on serum levels of osteoprotegerin and receptor activator of nuclear factor kappa B ligand in patients with prediabetes. Endocrine. PMID 27743302 DOI: 10.1007/s12020-016-1121-4 |
1 |
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| 2016 |
Yormaz S, Yılmaz H, Ece I, Yılmaz F, Sahin M. Midterm Clinical Outcomes of Antrum Resection Margin at Laparoscopic Sleeve Gastrectomy for Morbid Obesity. Obesity Surgery. PMID 27696100 DOI: 10.1007/s11695-016-2384-9 |
1 |
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| 2016 |
Canovic EP, Qing B, Mijailovic AS, Jagielska A, Whitfield MJ, Kelly E, Turner D, Sahin M, Van Vliet KJ. Characterizing Multiscale Mechanical Properties of Brain Tissue Using Atomic Force Microscopy, Impact Indentation, and Rheometry. Journal of Visualized Experiments : Jove. PMID 27684097 DOI: 10.3791/54201 |
1 |
|
| 2016 |
Weisleder P, Gospe SM, Ng YT, Sahin M. The Pediatric Neurology Trainee Publication Award for 2015. Pediatric Neurology. PMID 27543367 DOI: 10.1016/j.pediatrneurol.2016.07.004 |
1 |
|
| 2016 |
Jeste SS, Varcin KJ, Hellemann GS, Gulsrud AC, Bhatt R, Kasari C, Wu JY, Sahin M, Nelson CA. Symptom profiles of autism spectrum disorder in tuberous sclerosis complex. Neurology. PMID 27440144 DOI: 10.1212/WNL.0000000000003002 |
1 |
|
| 2016 |
Crall C, Valle M, Kapur K, Dies KA, Liang MG, Sahin M, Huang JT. Effect of Angiofibromas on Quality of Life and Access to Care in Tuberous Sclerosis Patients and Their Caregivers. Pediatric Dermatology. PMID 27436143 DOI: 10.1111/pde.12933 |
1 |
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| 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 |
1 |
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| 2016 |
Comi AM, Sahin M, Hammill A, Kaplan EH, Juhász C, North P, Ball KL, Levin AV, Cohen B, Morris J, Lo W, Roach ES. Leveraging a Sturge-Weber Gene Discovery: An Agenda for Future Research. Pediatric Neurology. 58: 12-24. PMID 27268758 DOI: 10.1016/j.pediatrneurol.2015.11.009 |
1 |
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| 2016 |
Sahin M, Henske EP, Manning BD, Ess KC, Bissler JJ, Klann E, Kwiatkowski DJ, Roberds SL, Silva AJ, Hillaire-Clarke CS, Young LR, Zervas M, Mamounas LA. Advances and Future Directions for Tuberous Sclerosis Complex Research: Recommendations From the 2015 Strategic Planning Conference. Pediatric Neurology. PMID 27267556 DOI: 10.1016/j.pediatrneurol.2016.03.015 |
1 |
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| 2016 |
Dölen G, Sahin M. Editorial: Essential Pathways and Circuits of Autism Pathogenesis. Frontiers in Neuroscience. 10: 182. PMID 27199644 DOI: 10.3389/fnins.2016.00182 |
1 |
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| 2016 |
Pinto A, Sahin M, Pearl PL. Epileptogenesis in neurocutaneous disorders with focus in Sturge Weber syndrome. F1000research. 5. PMID 27019697 DOI: 10.12688/f1000research.7605.1 |
0.01 |
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| 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 |
1 |
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| 2016 |
Tai DJ, Ragavendran A, Manavalan P, Stortchevoi A, Seabra CM, Erdin S, Collins RL, Blumenthal I, Chen X, Shen Y, Sahin M, Zhang C, Lee C, Gusella JF, Talkowski ME. Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR. Nature Neuroscience. PMID 26829649 DOI: 10.1038/nn.4235 |
1 |
|
| 2015 |
Ebrahimi-Fakhari D, Saffari A, Wahlster L, Lu J, Byrne S, Hoffmann GF, Jungbluth H, Sahin M. Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism. Brain : a Journal of Neurology. PMID 26715604 DOI: 10.1093/brain/awv371 |
1 |
|
| 2015 |
Pinto AL, Chen L, Friedman R, Grant PE, Poduri A, Takeoka M, Prabhu SP, Sahin M. Sturge-Weber Syndrome: Brain Magnetic Resonance Imaging and Neuropathology Findings. Pediatric Neurology. PMID 26706049 DOI: 10.1016/j.pediatrneurol.2015.11.005 |
1 |
|
| 2015 |
Gholipour A, Afacan O, Aganj I, Scherrer B, Prabhu SP, Sahin M, Warfield SK. Super-resolution reconstruction in frequency, image, and wavelet domains to reduce through-plane partial voluming in MRI. Medical Physics. 42: 6919. PMID 26632048 DOI: 10.1118/1.4935149 |
1 |
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| 2015 |
Dies KA, Sahin M. Genetics of neurocutaneous disorders: basic principles of inheritance as they apply to neurocutaneous syndromes. Handbook of Clinical Neurology. 132: 3-8. PMID 26564068 DOI: 10.1016/B978-0-444-62702-5.00001-9 |
1 |
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| 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 |
1 |
|
| 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 |
1 |
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| 2015 |
Sahin M, Sur M. Genes, circuits, and precision therapies for autism and related neurodevelopmental disorders. Science (New York, N.Y.). PMID 26472761 DOI: 10.1126/science.aab3897 |
1 |
|
| 2015 |
Peters JM, Prohl AK, Tomas-Fernandez XK, Taquet M, Scherrer B, Prabhu SP, Lidov HG, Singh JM, Jansen FE, Braun KP, Sahin M, Warfield SK, Stamm A. Tubers are neither static nor discrete: Evidence from serial diffusion tensor imaging. Neurology. 85: 1536-45. PMID 26432846 DOI: 10.1212/WNL.0000000000002055 |
1 |
|
| 2015 |
Scherrer B, Schwartzman A, Taquet M, Sahin M, Prabhu SP, Warfield SK. Characterizing brain tissue by assessment of the distribution of anisotropic microstructural environments in diffusion-compartment imaging (DIAMOND). Magnetic Resonance in Medicine. PMID 26362832 DOI: 10.1002/mrm.25912 |
1 |
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| 2015 |
Sundberg M, Sahin M. Cerebellar Development and Autism Spectrum Disorder in Tuberous Sclerosis Complex. Journal of Child Neurology. PMID 26303409 DOI: 10.1177/0883073815600870 |
1 |
|
| 2015 |
Nie D, Chen Z, Ebrahimi-Fakhari D, Di Nardo A, Julich K, Robson VK, Cheng YC, Woolf CJ, Heiman M, Sahin M. The Stress-Induced Atf3-Gelsolin Cascade Underlies Dendritic Spine Deficits in Neuronal Models of Tuberous Sclerosis Complex. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 10762-72. PMID 26224859 DOI: 10.1523/JNEUROSCI.4796-14.2015 |
1 |
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| 2015 |
Wertz MH, Sahin M. Developing therapies for spinal muscular atrophy. Annals of the New York Academy of Sciences. PMID 26173388 DOI: 10.1111/nyas.12813 |
1 |
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| 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 |
0.44 |
|
| 2015 |
Neul JL, Sahin M. Therapeutic Advances in Autism and Other Neurodevelopmental Disorders. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 12: 519-20. PMID 26076992 DOI: 10.1007/s13311-015-0364-8 |
1 |
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| 2015 |
Ng YT, Gospe SM, Sahin M. Pediatric Neurology 2014 Trainee Publication Award Winner: Dr. Mitchel T. Williams. Pediatric Neurology. PMID 26047694 DOI: 10.1016/j.pediatrneurol.2015.04.010 |
1 |
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| 2015 |
Aad G, Abbott B, Abdallah J, Abdinov O, Aben R, Abolins M, AbouZeid OS, Abramowicz H, Abreu H, Abreu R, Abulaiti Y, Acharya BS, Adamczyk L, Adams DL, Adelman J, ... ... Sahin MÖ, et al. Combined Measurement of the Higgs Boson Mass in pp Collisions at sqrt[s]=7 and 8 TeV with the ATLAS and CMS Experiments. Physical Review Letters. 114: 191803. PMID 26024162 DOI: 10.1103/PhysRevLett.114.191803 |
1 |
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| 2015 |
DiMario FJ, Sahin M, Ebrahimi-Fakhari D. Tuberous sclerosis complex. Pediatric Clinics of North America. 62: 633-48. PMID 26022167 DOI: 10.1016/j.pcl.2015.03.005 |
1 |
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| 2015 |
Varcin KJ, Nelson CA, Ko J, Sahin M, Wu JY, Jeste SS. Visual Evoked Potentials as a Readout of Cortical Function in Infants With Tuberous Sclerosis Complex. Journal of Child Neurology. PMID 26018199 DOI: 10.1177/0883073815587328 |
1 |
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| 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 |
1 |
|
| 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 |
1 |
|
| 2015 |
Baumer FM, Song JW, Mitchell PD, Pienaar R, Sahin M, Grant PE, Takahashi E. Longitudinal changes in diffusion properties in white matter pathways of children with tuberous sclerosis complex. Pediatric Neurology. 52: 615-23. PMID 25817702 DOI: 10.1016/j.pediatrneurol.2015.02.004 |
1 |
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| 2015 |
Akula JD, Noonan ER, Di Nardo A, Favazza TL, Zhang N, Sahin M, Hansen RM, Fulton AB. Vigabatrin can enhance electroretinographic responses in pigmented and albino rats. Documenta Ophthalmologica. Advances in Ophthalmology. 131: 1-11. PMID 25761928 DOI: 10.1007/s10633-015-9491-0 |
1 |
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| 2015 |
Im K, Ahtam B, Haehn D, Peters JM, Warfield SK, Sahin M, Ellen Grant P. Altered Structural Brain Networks in Tuberous Sclerosis Complex. Cerebral Cortex (New York, N.Y. : 1991). PMID 25750257 DOI: 10.1093/cercor/bhv026 |
1 |
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| 2015 |
Ebrahimi-Fakhari D, Sahin M. Autism and the synapse: emerging mechanisms and mechanism-based therapies. Current Opinion in Neurology. 28: 91-102. PMID 25695134 DOI: 10.1097/WCO.0000000000000186 |
1 |
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| 2015 |
Leech JD, Lammers SH, Goldman S, Auricchio N, Bronson RT, Kwiatkowski DJ, Sahin M. A vascular model of Tsc1 deficiency accelerates renal tumor formation with accompanying hemangiosarcomas. Molecular Cancer Research : McR. 13: 548-55. PMID 25548102 DOI: 10.1158/1541-7786.MCR-14-0178 |
1 |
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| 2015 |
de Vries PJ, Whittemore VH, Leclezio L, Byars AW, Dunn D, Ess KC, Hook D, King BH, Sahin M, Jansen A. Tuberous sclerosis associated neuropsychiatric disorders (TAND) and the TAND Checklist. Pediatric Neurology. 52: 25-35. PMID 25532776 DOI: 10.1016/j.pediatrneurol.2014.10.004 |
1 |
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| 2014 |
Sahin M. Gene therapy for childhood neurological disease. Pediatric Neurology. 51: 595-6. PMID 25439574 DOI: 10.1016/j.pediatrneurol.2014.08.005 |
1 |
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| 2014 |
Lipton JO, Sahin M. The neurology of mTOR. Neuron. 84: 275-91. PMID 25374355 DOI: 10.1016/j.neuron.2014.09.034 |
1 |
|
| 2014 |
Ebrahimi-Fakhari D, Wahlster L, Sahin M. Parkinson's disease: A disorder of axonal mitophagy? Movement Disorders : Official Journal of the Movement Disorder Society. 29: 1582. PMID 25256171 DOI: 10.1002/mds.26047 |
1 |
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| 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 |
0.44 |
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| 2014 |
Jamuar SS, Lam AT, Kircher M, D'Gama AM, Wang J, Barry BJ, Zhang X, Hill RS, Partlow JN, Rozzo A, Servattalab S, Mehta BK, Topcu M, Amrom D, Andermann E, ... ... Sahin M, et al. Somatic mutations in cerebral cortical malformations. The New England Journal of Medicine. 371: 733-43. PMID 25140959 DOI: 10.1056/NEJMoa1314432 |
1 |
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| 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 |
1 |
|
| 2014 |
Spurling Jeste S, Wu JY, Senturk D, Varcin K, Ko J, McCarthy B, Shimizu C, Dies K, Vogel-Farley V, Sahin M, Nelson CA. Early developmental trajectories associated with ASD in infants with tuberous sclerosis complex. Neurology. 83: 160-8. PMID 24920850 DOI: 10.1212/WNL.0000000000000568 |
1 |
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| 2014 |
Kawasaki J, Aegerter S, Fevurly RD, Mammoto A, Mammoto T, Sahin M, Mably JD, Fishman SJ, Chan J. RASA1 functions in EPHB4 signaling pathway to suppress endothelial mTORC1 activity. The Journal of Clinical Investigation. 124: 2774-84. PMID 24837431 DOI: 10.1172/JCI67084 |
1 |
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| 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 |
1 |
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| 2014 |
Roach ES, Gospe S, Ng YT, Sahin M. Trust but verify: the introduction of plagiarism detection software. Pediatric Neurology. 50: 287. PMID 24630278 DOI: 10.1016/j.pediatrneurol.2013.12.021 |
1 |
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| 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 |
1 |
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| 2014 |
Kong SW, Sahin M, Collins CD, Wertz MH, Campbell MG, Leech JD, Krueger D, Bear MF, Kunkel LM, Kohane IS. Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis. Molecular Autism. 5: 16. PMID 24564913 DOI: 10.1186/2040-2392-5-16 |
1 |
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| 2014 |
Taquet M, Scherrer B, Commowick O, Peters JM, Sahin M, Macq B, Warfield SK. A mathematical framework for the registration and analysis of multi-fascicle models for population studies of the brain microstructure. Ieee Transactions On Medical Imaging. 33: 504-17. PMID 24235301 DOI: 10.1109/TMI.2013.2289381 |
1 |
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| 2013 |
Scherrer B, Schwartzman A, Taquet M, Prabhu SP, Sahin M, Akhondi-Asl A, Warfield SK. Characterizing the distribution of anisotropic micro-structural environments with diffusion-weighted imaging (DIAMOND). Medical Image Computing and Computer-Assisted Intervention : Miccai ... International Conference On Medical Image Computing and Computer-Assisted Intervention. 16: 518-26. PMID 24505801 DOI: 10.1007/978-3-642-40760-4_65 |
1 |
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| 2013 |
Peters JM, Taquet M, Prohl AK, Scherrer B, van Eeghen AM, Prabhu SP, Sahin M, Warfield SK. Diffusion tensor imaging and related techniques in tuberous sclerosis complex: review and future directions. Future Neurology. 8: 583-597. PMID 24489482 DOI: 10.2217/fnl.13.37 |
1 |
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| 2013 |
Zhang J, Kim J, Alexander A, Cai S, Tripathi DN, Dere R, Tee AR, Tait-Mulder J, Di Nardo A, Han JM, Kwiatkowski E, Dunlop EA, Dodd KM, Folkerth RD, Faust PL, ... ... Sahin M, et al. A tuberous sclerosis complex signalling node at the peroxisome regulates mTORC1 and autophagy in response to ROS. Nature Cell Biology. 15: 1186-96. PMID 23955302 DOI: 10.1038/ncb2822 |
1 |
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| 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 |
1 |
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| 2013 |
Peters JM, Taquet M, Vega C, Jeste SS, Fernández IS, Tan J, Nelson CA, Sahin M, Warfield SK. Brain functional networks in syndromic and non-syndromic autism: a graph theoretical study of EEG connectivity. Bmc Medicine. 11: 54. PMID 23445896 DOI: 10.1186/1741-7015-11-54 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 2013 |
Sahin M, Kocak N, Arslan U, Sahin O, Yilmaz M. Bis-schiff base derivatives of 2,5-dihydroxybenzaldehyde: Synthesis, characterization and antimicrobial activity of their Cu(II), Co(II) and Zn(II) complexes Journal of Macromolecular Science, Part a: Pure and Applied Chemistry. 50: 821-827. DOI: 10.1080/10601325.2013.802154 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 2012 |
Elmasri H, Ghelfi E, Yu CW, Traphagen S, Cernadas M, Cao H, Shi GP, Plutzky J, Sahin M, Hotamisligil G, Cataltepe S. Endothelial cell-fatty acid binding protein 4 promotes angiogenesis: Role of stem cell factor/c-kit pathway Angiogenesis. 15: 457-468. PMID 22562362 DOI: 10.1007/s10456-012-9274-0 |
1 |
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| 2012 |
Nie D, Sahin M. A genetic model to dissect the role of Tsc-mTORC1 in neuronal cultures Methods in Molecular Biology. 821: 393-405. PMID 22125080 DOI: 10.1007/978-1-61779-430-8_25 |
1 |
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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 |
1 |
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| 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 |
1 |
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| 2011 |
Han JM, Sahin M. TSC1/TSC2 signaling in the CNS. Febs Letters. 585: 973-80. PMID 21329690 DOI: 10.1016/j.febslet.2011.02.001 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 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 |
1 |
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| 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 |
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| 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 |
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| 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 |
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| 2008 |
Ozcan U, Ozcan L, Yilmaz E, Düvel K, Sahin M, Manning BD, Hotamisligil GS. Loss of the tuberous sclerosis complex tumor suppressors triggers the unfolded protein response to regulate insulin signaling and apoptosis. Molecular Cell. 29: 541-51. PMID 18342602 DOI: 10.1016/j.molcel.2007.12.023 |
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| 2007 |
Meikle L, Talos DM, Onda H, Pollizzi K, Rotenberg A, Sahin M, Jensen FE, Kwiatkowski DJ. A mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survival. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 5546-58. PMID 17522300 DOI: 10.1523/JNEUROSCI.5540-06.2007 |
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| 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 |
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| 2006 |
Zhang HH, Lipovsky AI, Dibble CC, Sahin M, Manning BD. S6K1 regulates GSK3 under conditions of mTOR-dependent feedback inhibition of Akt. Molecular Cell. 24: 185-97. PMID 17052453 DOI: 10.1016/j.molcel.2006.09.019 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 1992 |
Sahin M, Bowen WD, Donoghue JP. Location of nicotinic and muscarinic cholinergic and mu-opiate receptors in rat cerebral neocortex: evidence from thalamic and cortical lesions. Brain Research. 579: 135-47. PMID 1320443 DOI: 10.1016/0006-8993(92)90752-U |
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