Connection

BERNHARD SUTER to Rett Syndrome

This is a "connection" page, showing publications BERNHARD SUTER has written about Rett Syndrome.
Connection Strength

4.560
  1. Comprehensive assessment reveals numerous clinical and neurophysiological differences between MECP2-allelic disorders. Ann Clin Transl Neurol. 2025 02; 12(2):433-447.
    View in: PubMed
    Score: 0.734
  2. Sensory experiences questionnaire unravels differences in sensory profiles between MECP2-related disorders. Autism Res. 2024 04; 17(4):775-784.
    View in: PubMed
    Score: 0.691
  3. Kinematics associated with treadmill walking in Rett syndrome. Disabil Rehabil. 2021 06; 43(11):1585-1593.
    View in: PubMed
    Score: 0.510
  4. Current clinical evidence does not support a link between TBL1XR1 and Rett syndrome: Description of one patient with Rett features and a novel mutation in TBL1XR1, and a review of TBL1XR1 phenotypes. Am J Med Genet A. 2018 07; 176(7):1683-1687.
    View in: PubMed
    Score: 0.462
  5. Brief report: MECP2 mutations in people without Rett syndrome. J Autism Dev Disord. 2014 Mar; 44(3):703-11.
    View in: PubMed
    Score: 0.345
  6. Gait Analysis in Rett Syndrome: Integrating Linear and Nonlinear Techniques. J Child Neurol. 2026 May; 41(5):647-665.
    View in: PubMed
    Score: 0.192
  7. A randomized, placebo-controlled, cross-over trial of ketamine in Rett syndrome. J Neurodev Disord. 2025 Jan 24; 17(1):4.
    View in: PubMed
    Score: 0.184
  8. International workshop: what is needed to ensure outcome measures for Rett syndrome are fit-for-purpose for clinical trials? June 7, 2023, Nashville, USA. Trials. 2024 Dec 21; 25(1):845.
    View in: PubMed
    Score: 0.183
  9. Clinical Features and Disease Progression in Older Individuals with Rett Syndrome. Genes (Basel). 2024 Aug 22; 15(8).
    View in: PubMed
    Score: 0.178
  10. Adapting a measure of gross motor skills for individuals with CDKL5 deficiency disorder: A psychometric study. Epilepsy Res. 2024 02; 200:107287.
    View in: PubMed
    Score: 0.171
  11. Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study. J Neurodev Disord. 2023 10 13; 15(1):33.
    View in: PubMed
    Score: 0.168
  12. Exploring gastrointestinal health in MECP2 duplication syndrome. Neurogastroenterol Motil. 2023 08; 35(8):e14601.
    View in: PubMed
    Score: 0.163
  13. Gastrointestinal Health Questionnaire for Rett Syndrome: Tool Development. J Pediatr Gastroenterol Nutr. 2021 03 01; 72(3):354-360.
    View in: PubMed
    Score: 0.140
  14. Characteristic behaviors associated with gait of individuals with Rett syndrome. Disabil Rehabil. 2022 04; 44(8):1508-1515.
    View in: PubMed
    Score: 0.136
  15. The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2. Am J Med Genet B Neuropsychiatr Genet. 2019 01; 180(1):55-67.
    View in: PubMed
    Score: 0.120
  16. Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale. J Child Neurol. 2015 Nov; 30(13):1743-8.
    View in: PubMed
    Score: 0.093
  17. Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levels. Hum Mol Genet. 2024 11 08; 33(22):1986-2001.
    View in: PubMed
    Score: 0.045
  18. MECP2 Variants in Males: More Common than Previously Appreciated. Pediatr Neurol. 2024 Dec; 161:263-267.
    View in: PubMed
    Score: 0.045
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.