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Connection

Christopher M. Gomez to Spinocerebellar Ataxias

This is a "connection" page, showing publications Christopher M. Gomez has written about Spinocerebellar Ataxias.
Connection Strength

11.552
  1. Genotypic Differences in Networks Supporting Regional Predictors of Speech Rate in Spinocerebellar Ataxia: Preliminary Observations. Brain Connect. 2021 08; 11(6):408-417.
    View in: PubMed
    Score: 0.706
  2. Commentary to: "The Pathophysiology and Clinical Manifestations of Spinocerebellar Ataxia Type 6" by Rentiya et al., Cerebellum 2020;19(3):459-464). Cerebellum. 2021 06; 20(3):484-485.
    View in: PubMed
    Score: 0.677
  3. a1ACT Is Essential for Survival and Early Cerebellar Programming in a Critical Neonatal Window. Neuron. 2019 05 22; 102(4):770-785.e7.
    View in: PubMed
    Score: 0.604
  4. Targeting the CACNA1A IRES as a Treatment for Spinocerebellar Ataxia Type 6. Cerebellum. 2018 02; 17(1):72-77.
    View in: PubMed
    Score: 0.558
  5. Spinocerebellar [corrected] Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics. Adv Exp Med Biol. 2018; 1049:147-173.
    View in: PubMed
    Score: 0.555
  6. Evaluation of parkinsonism and striatal dopamine transporter loss in patients with spinocerebellar ataxia type 6. J Neurol. 2016 Nov; 263(11):2302-2307.
    View in: PubMed
    Score: 0.504
  7. An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron. Sci Transl Med. 2016 07 13; 8(347):347ra94.
    View in: PubMed
    Score: 0.501
  8. The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability. J Neurol Neurosurg Psychiatry. 2015 May; 86(5):554-61.
    View in: PubMed
    Score: 0.439
  9. Revelations from a bicistronic calcium channel gene. Cell Cycle. 2014; 13(6):875-6.
    View in: PubMed
    Score: 0.424
  10. Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6. Cell. 2013 Jul 03; 154(1):118-33.
    View in: PubMed
    Score: 0.406
  11. A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult. Hum Mol Genet. 2012 Dec 15; 21(26):5472-83.
    View in: PubMed
    Score: 0.385
  12. Spinocerebellar ataxia type 6. Handb Clin Neurol. 2012; 103:461-73.
    View in: PubMed
    Score: 0.366
  13. Loss of intrinsic organization of cerebellar networks in spinocerebellar ataxia type 1: correlates with disease severity and duration. Cerebellum. 2011 Jun; 10(2):218-32.
    View in: PubMed
    Score: 0.351
  14. Impaired eye movements in presymptomatic spinocerebellar ataxia type 6. Arch Neurol. 2008 Apr; 65(4):530-6.
    View in: PubMed
    Score: 0.282
  15. Molecular pathogenesis of spinocerebellar ataxia type 6. Neurotherapeutics. 2007 Apr; 4(2):285-94.
    View in: PubMed
    Score: 0.263
  16. Evaluation of sleep and daytime somnolence in spinocerebellar ataxia type 6 (SCA6). Neurology. 2006 May 09; 66(9):1430-1.
    View in: PubMed
    Score: 0.247
  17. Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes. Mov Disord. 2005 Nov; 20(11):1405-12.
    View in: PubMed
    Score: 0.239
  18. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6. Ann Neurol. 2005 Mar; 57(3):349-54.
    View in: PubMed
    Score: 0.228
  19. Intermuscular Coherence in Spinocerebellar Ataxias 3 and 6: a Preliminary Study. Cerebellum. 2024 Apr; 23(2):601-608.
    View in: PubMed
    Score: 0.203
  20. Spinocerebellar ataxia in monozygotic twins. Arch Neurol. 2002 Dec; 59(12):1945-51.
    View in: PubMed
    Score: 0.195
  21. The vestibulo-ocular reflex and velocity storage in spinocerebellar ataxia 8. Arch Ital Biol. 2002 Oct; 140(4):323-9.
    View in: PubMed
    Score: 0.193
  22. Gait Variability in Spinocerebellar Ataxia Assessed Using Wearable Inertial Sensors. Mov Disord. 2021 12; 36(12):2922-2931.
    View in: PubMed
    Score: 0.178
  23. Polyglutamine aggregates in SCA6 Purkinje cells: a tail of two toxicities. Neurology. 2001 Jun 26; 56(12):1618-9.
    View in: PubMed
    Score: 0.176
  24. Prodromal Spinocerebellar Ataxia Type 2 Subjects Have Quantifiable Gait and Postural Sway Deficits. Mov Disord. 2021 02; 36(2):471-480.
    View in: PubMed
    Score: 0.169
  25. Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean. Cerebellum. 2020 Jun; 19(3):446-458.
    View in: PubMed
    Score: 0.164
  26. Dysphagia in spinocerebellar ataxias type 1, 2, 3 and 6. J Neurol Sci. 2020 Aug 15; 415:116878.
    View in: PubMed
    Score: 0.163
  27. Tremor in the Degenerative Cerebellum: Towards the Understanding of Brain Circuitry for Tremor. Cerebellum. 2019 Jun; 18(3):519-526.
    View in: PubMed
    Score: 0.153
  28. Neurochemical abnormalities in premanifest and early spinocerebellar ataxias. Ann Neurol. 2018 04; 83(4):816-829.
    View in: PubMed
    Score: 0.141
  29. C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias. Mov Disord. 2018 03; 33(3):497-498.
    View in: PubMed
    Score: 0.138
  30. Dystonia and ataxia progression in spinocerebellar ataxias. Parkinsonism Relat Disord. 2017 Dec; 45:75-80.
    View in: PubMed
    Score: 0.137
  31. Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias. Tremor Other Hyperkinet Mov (N Y). 2017; 7:492.
    View in: PubMed
    Score: 0.136
  32. The Initial Symptom and Motor Progression in Spinocerebellar Ataxias. Cerebellum. 2017 06; 16(3):615-622.
    View in: PubMed
    Score: 0.133
  33. Trial-to-trial Adaptation: Parsing out the Roles of Cerebellum and BG in Predictive Motor Timing. J Cogn Neurosci. 2016 Jul; 28(7):920-34.
    View in: PubMed
    Score: 0.122
  34. Depression and clinical progression in spinocerebellar ataxias. Parkinsonism Relat Disord. 2016 Jan; 22:87-92.
    View in: PubMed
    Score: 0.120
  35. Early Cerebellar Network Shifting in Spinocerebellar Ataxia Type 6. Cereb Cortex. 2016 07; 26(7):3205-18.
    View in: PubMed
    Score: 0.117
  36. Cerebrospinal Fluid Biomarkers in Spinocerebellar Ataxia: A Pilot Study. Dis Markers. 2015; 2015:413098.
    View in: PubMed
    Score: 0.117
  37. DnaJ-1 and karyopherin a3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6. Hum Mol Genet. 2015 Aug 01; 24(15):4385-96.
    View in: PubMed
    Score: 0.115
  38. Clinical evaluation of eye movements in spinocerebellar ataxias: a prospective multicenter study. J Neuroophthalmol. 2015 Mar; 35(1):16-21.
    View in: PubMed
    Score: 0.114
  39. Coenzyme Q10 and spinocerebellar ataxias. Mov Disord. 2015 Feb; 30(2):214-20.
    View in: PubMed
    Score: 0.112
  40. Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study. Orphanet J Rare Dis. 2013 Nov 13; 8:177.
    View in: PubMed
    Score: 0.104
  41. Distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy. Cerebellum. 2011 Jun; 10(2):208-17.
    View in: PubMed
    Score: 0.088
  42. The neural substrate of predictive motor timing in spinocerebellar ataxia. Cerebellum. 2011 Jun; 10(2):233-44.
    View in: PubMed
    Score: 0.088
  43. Speech characteristics associated with three genotypes of ataxia. J Commun Disord. 2011 Jul-Aug; 44(4):478-92.
    View in: PubMed
    Score: 0.087
  44. Ophthalmologic features of the common spinocerebellar ataxias. Curr Opin Ophthalmol. 2010 Nov; 21(6):447-53.
    View in: PubMed
    Score: 0.084
  45. Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status. Mov Disord. 2010 Jul 15; 25(9):1253-61.
    View in: PubMed
    Score: 0.083
  46. Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels. Proc Natl Acad Sci U S A. 2008 Aug 19; 105(33):11987-92.
    View in: PubMed
    Score: 0.072
  47. Dominantly inherited ataxias. Semin Pediatr Neurol. 2003 Sep; 10(3):210-22.
    View in: PubMed
    Score: 0.051
  48. The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes. J Neurosci. 2000 Sep 01; 20(17):6394-403.
    View in: PubMed
    Score: 0.042
  49. Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13). PLoS One. 2011 Mar 29; 6(3):e17811.
    View in: PubMed
    Score: 0.022
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.