Connection

Co-Authors

This is a "connection" page, showing publications co-authored by DANIEL GLAZE and BERNHARD SUTER.
Connection Strength

1.376
  1. Gastrointestinal Health Questionnaire for Rett Syndrome: Tool Development. J Pediatr Gastroenterol Nutr. 2021 03 01; 72(3):354-360.
    View in: PubMed
    Score: 0.193
  2. Kinematics associated with treadmill walking in Rett syndrome. Disabil Rehabil. 2021 06; 43(11):1585-1593.
    View in: PubMed
    Score: 0.175
  3. 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: 0.159
  4. Temporal Gait Measures Associated With Overground and Treadmill Walking in Rett Syndrome. J Child Neurol. 2018 Jan 01; 883073818780471.
    View in: PubMed
    Score: 0.155
  5. Brief report: MECP2 mutations in people without Rett syndrome. J Autism Dev Disord. 2014 Mar; 44(3):703-11.
    View in: PubMed
    Score: 0.119
  6. Development and validation of parent-reported gastrointestinal health scale in MECP2 duplication syndrome. Orphanet J Rare Dis. 2024 Feb 09; 19(1):52.
    View in: PubMed
    Score: 0.059
  7. Distribution of hand function by age in individuals with Rett syndrome. Ann Child Neurol Soc. 2023 Sep; 1(3):228-238.
    View in: PubMed
    Score: 0.057
  8. Exploring gastrointestinal health in MECP2 duplication syndrome. Neurogastroenterol Motil. 2023 08; 35(8):e14601.
    View in: PubMed
    Score: 0.056
  9. Exploring the characteristics and most bothersome symptoms in MECP2 duplication syndrome to pave the path toward developing parent-oriented outcome measures. Mol Genet Genomic Med. 2022 08; 10(8):e1989.
    View in: PubMed
    Score: 0.053
  10. Assessing the Burden on Caregivers of MECP2 Duplication Syndrome. Pediatr Neurol. 2022 08; 133:1-8.
    View in: PubMed
    Score: 0.053
  11. Multisystem comorbidities in classic Rett syndrome: a scoping review. BMJ Paediatr Open. 2020; 4(1):e000731.
    View in: PubMed
    Score: 0.047
  12. Characteristic behaviors associated with gait of individuals with Rett syndrome. Disabil Rehabil. 2022 04; 44(8):1508-1515.
    View in: PubMed
    Score: 0.047
  13. Consensus guidelines on managing Rett syndrome across the lifespan. BMJ Paediatr Open. 2020; 4(1):e000717.
    View in: PubMed
    Score: 0.047
  14. Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. Clin Genet. 2019 05; 95(5):575-581.
    View in: PubMed
    Score: 0.042
  15. Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 2019 01 08; 92(2):e108-e114.
    View in: PubMed
    Score: 0.041
  16. 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: 0.041
  17. 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: 0.032
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.