Year |
Citation |
Score |
2024 |
Xu Y, Song R, Perszyk RE, Chen W, Kim S, Park KL, Allen JP, Nocilla KA, Zhang J, XiangWei W, Tankovic A, McDaniels ED, Sheikh R, Mizu RK, Karamchandani MM, ... ... Kusumoto H, et al. De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor. Cellular and Molecular Life Sciences : Cmls. 81: 153. PMID 38538865 DOI: 10.1007/s00018-023-05069-z |
0.487 |
|
2019 |
XiangWei W, Kannan V, Xu Y, Kosobucki GJ, Schulien AJ, Kusumoto H, Moufawad El Achkar C, Bhattacharya S, Lesca G, Nguyen S, Helbig KL, Cuisset JM, Fenger CD, Marjanovic D, Schuler E, et al. Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy. Brain : a Journal of Neurology. PMID 31504254 DOI: 10.1093/Brain/Awz232 |
0.667 |
|
2019 |
Li J, Zhang J, Tang W, Mizu RK, Kusumoto H, XiangWei W, Xu Y, Chen W, Amin JB, Perozo E, Hu C, Kannan V, Keller SR, Wilcox WR, Lemke JR, et al. De Novo GRIN Variants in NMDA Receptor M2 Channel Pore-Forming Loop Are Associated with Neurological Diseases. Human Mutation. PMID 31429998 DOI: 10.1002/Humu.23895 |
0.659 |
|
2018 |
Wells G, Yuan H, McDaniel MJ, Kusumoto H, Snyder JP, Liotta DC, Traynelis SF. The GluN2B-Glu413Gly NMDA receptor variant arising from a de novo GRIN2B mutation promotes ligand-unbinding and domain opening. Proteins. PMID 30168177 DOI: 10.1002/Prot.25595 |
0.656 |
|
2018 |
Perszyk R, Katzman BM, Kusumoto H, Kell SA, Epplin MP, Tahirovic YA, Moore RL, Menaldino D, Burger P, Liotta DC, Traynelis SF. An NMDAR positive and negative allosteric modulator series share a binding site and are interconverted by methyl groups. Elife. 7. PMID 29792594 DOI: 10.7554/Elife.34711 |
0.609 |
|
2018 |
Fernández-Marmiesse A, Kusumoto H, Rekarte S, Roca I, Zhang J, Myers SJ, Traynelis SF, Couce ML, Gutierrez-Solana L, Yuan H. A novel missense mutation in GRIN2A causes a nonepileptic neurodevelopmental disorder. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29644724 DOI: 10.1002/Mds.27315 |
0.649 |
|
2018 |
Fry AE, Fawcett KA, Zelnik N, Yuan H, Thompson BAN, Shemer-Meiri L, Cushion TD, Mugalaasi H, Sims D, Stoodley N, Chung SK, Rees MI, Patel CV, Brueton LA, Layet V, ... ... Kusumoto H, et al. De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : a Journal of Neurology. PMID 29365063 DOI: 10.1093/Brain/Awx358 |
0.667 |
|
2018 |
Perszyk R, Katzman BM, Kusumoto H, Kell SA, Epplin MP, Tahirovic YA, Moore RL, Menaldino D, Burger P, Liotta DC, Traynelis SF. Author response: An NMDAR positive and negative allosteric modulator series share a binding site and are interconverted by methyl groups Elife. DOI: 10.7554/Elife.34711.058 |
0.529 |
|
2017 |
Kaiser TM, Kell SA, Kusumoto H, Shaulsky G, Bhattacharya S, Epplin MP, Strong KL, Miller EJ, Cox BD, Menaldino DS, Liotta DC, Traynelis SF, Burger PB. The bioactive protein-ligand conformation of GluN2C-selective positive allosteric modulators bound to the NMDA receptor. Molecular Pharmacology. PMID 29242355 DOI: 10.1124/Mol.117.110940 |
0.646 |
|
2017 |
Platzer K, Yuan H, Schütz H, Winschel A, Chen W, Hu C, Kusumoto H, Heyne HO, Helbig KL, Tang S, Willing MC, Tinkle BT, Adams DJ, Depienne C, Keren B, et al. GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects. Journal of Medical Genetics. PMID 28377535 DOI: 10.1136/Jmedgenet-2016-104509 |
0.506 |
|
2017 |
Gao K, Tankovic A, Zhang Y, Kusumoto H, Zhang J, Chen W, XiangWei W, Shaulsky GH, Hu C, Traynelis SF, Yuan H, Jiang Y. A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia. Plos One. 12: e0170818. PMID 28182669 DOI: 10.1371/Journal.Pone.0170818 |
0.64 |
|
2017 |
Chen W, Tankovic A, Burger PB, Kusumoto H, Traynelis SF, Yuan H. Functional Evaluation of a De Novo GRIN2A Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy. Molecular Pharmacology. PMID 28126851 DOI: 10.1124/Mol.116.106781 |
0.697 |
|
2017 |
Ogden KK, Chen W, Swanger SA, McDaniel MJ, Fan LZ, Hu C, Tankovic A, Kusumoto H, Kosobucki GJ, Schulien AJ, Su Z, Pecha J, Bhattacharya S, Petrovski S, Cohen AE, et al. Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology. Plos Genetics. 13: e1006536. PMID 28095420 DOI: 10.1371/Journal.Pgen.1006536 |
0.693 |
|
2016 |
Swanger SA, Chen W, Wells G, Burger PB, Tankovic A, Bhattacharya S, Strong KL, Hu C, Kusumoto H, Zhang J, Adams DR, Millichap JJ, Petrovski S, Traynelis SF, Yuan H. Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains. American Journal of Human Genetics. PMID 27839871 DOI: 10.1016/J.Ajhg.2016.10.002 |
0.652 |
|
2016 |
Li D, Yuan H, Ortiz-Gonzalez XR, Marsh ED, Tian L, McCormick EM, Kosobucki GJ, Chen W, Schulien AJ, Chiavacci R, Tankovic A, Naase C, Brueckner F, von Stülpnagel-Steinbeis C, Hu C, ... Kusumoto H, et al. GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers. American Journal of Human Genetics. PMID 27616483 DOI: 10.1016/J.Ajhg.2016.07.013 |
0.682 |
|
Low-probability matches (unlikely to be authored by this person) |
2020 |
Kusumoto H, Ta C, Brown SM, Mulcahey MK. Factors Contributing to Diurnal Variation in Athletic Performance and Methods to Reduce Within-Day Performance Variation: A Systematic Review. Journal of Strength and Conditioning Research. PMID 32868676 DOI: 10.1519/JSC.0000000000003758 |
0.095 |
|
2021 |
Kusumoto H, Hasegawa K, Ishibuchi K, Otsuji S. A novel treatment using a guide extension catheter and distal protection device for refractory coronary embolism: case report. European Heart Journal. Case Reports. 5: ytaa507. PMID 34263112 DOI: 10.1093/ehjcr/ytaa507 |
0.049 |
|
2019 |
Yamamoto W, Fujii K, Otsuji S, Takiuchi S, Kakishita M, Ibuki M, Hasegawa K, Ishibuchi K, Tamaru H, Yasuda S, Ishii R, Nakabayashi S, Kusumoto H, Higashino Y. Optical coherence tomography characteristics of in-stent restenosis after drug-eluting stent implantation: a novel classification and its clinical significance. Heart and Vessels. PMID 31250131 DOI: 10.1007/s00380-019-01461-7 |
0.042 |
|
2020 |
Hill KL, Wu VJ, Kusumoto H, Sherman WF, Savoie FH. Management of Orthopaedic Emergencies During a Pandemic: Compartment Syndrome of the Hand in a Patient with COVID-19: A Case Report. Jbjs Case Connector. 10: e2000377. PMID 32960013 DOI: 10.2106/JBJS.CC.20.00377 |
0.037 |
|
2020 |
Yamamoto W, Otsuji S, Takiuchi S, Kakishita M, Shimatani Y, Hasegawa K, Ishibuchi K, Tamaru H, Ishii R, Yasuda S, Taniguchi Y, Nakabayashi S, Kusumoto H, Higashino Y. Successful percutaneous removal of dislodged ring-marker of optical coherence tomography catheter using the twisted wire technique with a guide-extension catheter: A case report. Journal of Cardiology Cases. 22: 242-245. PMID 33133319 DOI: 10.1016/j.jccase.2020.07.011 |
0.034 |
|
2022 |
Kusumoto H, Ishibuchi K, Hasegawa K, Otsuji S. Trans-coronary pacing via Rota wire prevents bradycardia during rotational atherectomy: a case report. European Heart Journal. Case Reports. 6: ytac013. PMID 35295733 DOI: 10.1093/ehjcr/ytac013 |
0.032 |
|
2020 |
Yamamoto W, Fujii K, Otsuji S, Takiuchi S, Kakishita M, Shimatani Y, Hasegawa K, Ishibuchi K, Tamaru H, Ishii R, Yasuda S, Taniguchi Y, Nakabayashi S, Kusumoto H, Higashino Y. Effect of neointimal tissue morphology on vascular response to balloon angioplasty in lesions with in-stent restenosis after drug-eluting stent deployment: an optical coherence tomography analysis. Heart and Vessels. PMID 32253529 DOI: 10.1007/s00380-020-01595-z |
0.031 |
|
2019 |
Ishibuchi K, Fujii K, Otsuji S, Takiuchi S, Hasegawa K, Tamaru H, Ishii R, Yasuda S, Nakabayashi S, Yamamoto W, Kusumoto H, Taniguchi Y, Kakishita M, Shimatani Y, Higashino Y. Utility and Validity of Intracoronary Administration of Nicorandil Alone for the Measurement of Fractional Flow Reserve in Patients With Intermediate Coronary Stenosis. Circulation Journal : Official Journal of the Japanese Circulation Society. PMID 31413232 DOI: 10.1253/circj.CJ-19-0421 |
0.031 |
|
2022 |
Kusumoto H, Ishibuchi K, Takiuchi S, Otsuji S. Usefulness of transpedal intervention for inferior epigastric artery bleeding following catheter ablation: a case report. European Heart Journal. Case Reports. 6: ytac181. PMID 35542825 DOI: 10.1093/ehjcr/ytac181 |
0.025 |
|
2021 |
Tamaru H, Fujii K, Otsuji S, Takiuchi S, Hasegawa K, Ishibuchi K, Ishii R, Yamamoto W, Nakabayashi S, Yasuda S, Kusumoto H, Taniguchi Y, Kakishita M, Shimatani Y, Higashino Y. Late peri-stent contrast staining appearance due to rupture of atherogenic neointima following drug-eluting stent. Journal of Cardiology Cases. 23: 210-213. PMID 33995698 DOI: 10.1016/j.jccase.2020.11.004 |
0.021 |
|
2021 |
Yamamoto W, Otsuji S, Takiuchi S, Kakishita M, Shimatani Y, Hasegawa K, Ishibuchi K, Tamaru H, Ishii R, Yasuda S, Taniguchi Y, Nakabayashi S, Kusumoto H, Higashino Y. Acute myocardial infarction in a patient with uncorrected tetralogy of Fallot accompanied by coronary artery ectasia: A case report. Journal of Cardiology Cases. 23: 119-122. PMID 33717376 DOI: 10.1016/j.jccase.2020.10.009 |
0.016 |
|
2021 |
Fletcher ND, Murphy JS, Austin TM, Bruce RW, Harris H, Bush P, Yu A, Kusumoto H, Schmitz ML, Devito DP, Fabregas JA, Miyanji F. Short term outcomes of an enhanced recovery after surgery (ERAS) pathway versus a traditional discharge pathway after posterior spinal fusion for adolescent idiopathic scoliosis. Spine Deformity. PMID 33460022 DOI: 10.1007/s43390-020-00282-3 |
0.015 |
|
Hide low-probability matches. |