Benke TA - Search Results

1

Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons.

Camp CR, Vlachos A, Klöckner C, Krey I, Banke TG, Shariatzadeh N, Ruggiero SM, Galer P, Park KL, Caccavano A, Kimmel S, Yuan X, Yuan H, Helbig I, Benke TA, Lemke JR, Pelkey KA, McBain CJ, Traynelis SF. Camp CR, et al. Among authors: benke ta. Commun Biol. 2023 Sep 19;6(1):952. doi: 10.1038/s42003-023-05298-9. Commun Biol. 2023. PMID: 37723282 Free PMC article.

2

Classification of missense variants in the N-methyl-d-aspartate receptor GRIN gene family as gain- or loss-of-function.

Myers SJ, Yuan H, Perszyk RE, Zhang J, Kim S, Nocilla KA, Allen JP, Bain JM, Lemke JR, Lal D, Benke TA, Traynelis SF. Myers SJ, et al. Among authors: benke ta. Hum Mol Genet. 2023 Sep 16;32(19):2857-2871. doi: 10.1093/hmg/ddad104. Hum Mol Genet. 2023. PMID: 37369021 Free PMC article.

3

De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor.

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, Hu C, Kusumoto H, Pecha J, Cappuccio G, Gaitanis J, Sullivan J, Shashi V, Petrovski S, Jauss RT, Lee HK, Bozarth X, Lynch DR, Helbig I, Pierson TM, Boerkoel CF, Myers SJ, Lemke JR, Benke TA, Yuan H, Traynelis SF. Xu Y, et al. Among authors: benke ta. Cell Mol Life Sci. 2024 Mar 28;81(1):153. doi: 10.1007/s00018-023-05069-z. Cell Mol Life Sci. 2024. PMID: 38538865 Free PMC article.

4

Rett syndrome diagnostic odyssey: Limitations of NextGen sequencing.

Abbott M, Angione K, Forbes E, Stoecker M, Saenz M, Neul JL, Marsh ED, Skinner SA, Percy AK, Benke TA. Abbott M, et al. Among authors: benke ta. Am J Med Genet A. 2024 May 22:e63725. doi: 10.1002/ajmg.a.63725. Online ahead of print. Am J Med Genet A. 2024. PMID: 38775384

5

Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study.

Neul JL, Benke TA, Marsh ED, Suter B, Silveira L, Fu C, Peters SU, Percy AK; Rett syndrome Natural History Study Group. Neul JL, et al. Among authors: benke ta. J Neurodev Disord. 2023 Oct 13;15(1):33. doi: 10.1186/s11689-023-09502-z. J Neurodev Disord. 2023. PMID: 37833681 Free PMC article.

6

Analysis of electrocardiograms in individuals with CDKL5 deficiency disorder.

Stansauk J, Fidell A, Benke T, Schaffer M, Demarest ST. Stansauk J, et al. Am J Med Genet A. 2023 Jan;191(1):108-111. doi: 10.1002/ajmg.a.62995. Epub 2022 Nov 13. Am J Med Genet A. 2023. PMID: 36372969 Free PMC article.

7

Expression of hyperpolarization-activated current (I_h) in zonally defined vestibular calyx terminals of the crista.

Meredith FL, Vu TA, Gehrke B, Benke TA, Dondzillo A, Rennie KJ. Meredith FL, et al. Among authors: benke ta. J Neurophysiol. 2023 Jun 1;129(6):1468-1481. doi: 10.1152/jn.00135.2023. Epub 2023 May 17. J Neurophysiol. 2023. PMID: 37198134 Free PMC article.

8

Psychometric properties of QI-Disability in CDKL5 Deficiency Disorder: Establishing readiness for clinical trials.

Saldaris JM, Jacoby P, Leonard H, Benke TA, Demarest S, Marsh ED, Downs J. Saldaris JM, et al. Among authors: benke ta. Epilepsy Behav. 2023 Feb;139:109069. doi: 10.1016/j.yebeh.2022.109069. Epub 2023 Jan 10. Epilepsy Behav. 2023. PMID: 36634535 Free PMC article.

9

A review of the Rett Syndrome Behaviour Questionnaire and its utilization in the assessment of symptoms associated with Rett syndrome.

Percy AK, Neul JL, Benke TA, Marsh ED, Glaze DG. Percy AK, et al. Among authors: benke ta. Front Pediatr. 2023 Jul 28;11:1229553. doi: 10.3389/fped.2023.1229553. eCollection 2023. Front Pediatr. 2023. PMID: 37635789 Free PMC article. Review.

10

Electroencephalographic Correlates of Clinical Severity in the Natural history study of RTT and Related Disorders.

Saby JN, Mulcahey PJ, Benke TA, Peters SU, Standridge SM, Lieberman DN, Key AP, Percy AK, Nelson CA, Roberts TPL, Neul JL, Marsh ED. Saby JN, et al. Among authors: benke ta. Ann Neurol. 2024 May 9. doi: 10.1002/ana.26948. Online ahead of print. Ann Neurol. 2024. PMID: 38721759

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