129 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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