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VERNON SUTTON to Middle Aged

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This is a "connection" page, showing publications VERNON SUTTON has written about Middle Aged.
VERNON SUTTON
Connection Strength
0.306
Middle Aged
  1. Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome). Am J Med Genet A. 2020 01; 182(1):38-52.
    View in: PubMed
    Score: 0.037
  2. A cross-sectional multicenter study of osteogenesis imperfecta in North America - results from the linked clinical research centers. Clin Genet. 2015 Feb; 87(2):133-40.
    View in: PubMed
    Score: 0.026
  3. Longitudinal Characterization of Males With X-Linked Creatine Transporter Deficiency: Final Results of a Multiyear Observational Study. Pediatr Neurol. 2026 Feb; 175:8-18.
    View in: PubMed
    Score: 0.014
  4. Two commonly reported incidental variants in OTC are associated with late-onset disease. HGG Adv. 2026 Jan 15; 7(1):100531.
    View in: PubMed
    Score: 0.014
  5. Detecting mitochondrial electron transport chain enzyme defects in low-heteroplasmy single large-scale mtDNA deletion syndromes (SLSMDSs). Mol Genet Metab. 2025 Nov; 146(3):109260.
    View in: PubMed
    Score: 0.014
  6. Mindful Self-Compassion to Reduce Pain Interference Among Adults with Osteogenesis Imperfecta. J Clin Psychol Med Settings. 2026 Jun; 33(2):248-258.
    View in: PubMed
    Score: 0.014
  7. Osteogenesis imperfecta and the family: A qualitative analysis of the experiences of family and caregivers. Fam Syst Health. 2025 09; 43(3):482-499.
    View in: PubMed
    Score: 0.014
  8. Setrusumab for the treatment of osteogenesis imperfecta: 12-month results from the phase 2b asteroid study. J Bone Miner Res. 2024 09 02; 39(9):1215-1228.
    View in: PubMed
    Score: 0.013
  9. Resilience and coping: a qualitative analysis of cognitive and behavioral factors in adults with osteogenesis Imperfecta. Disabil Rehabil. 2025 Feb; 47(3):709-718.
    View in: PubMed
    Score: 0.013
  10. Psychosocial Outcomes of Pain and Pain Management in Adults with Osteogenesis Imperfecta: A Qualitative Study. J Clin Psychol Med Settings. 2024 Sep; 31(3):614-627.
    View in: PubMed
    Score: 0.012
  11. Comparison of Untargeted Metabolomic Profiling vs Traditional Metabolic Screening to Identify Inborn Errors of Metabolism. JAMA Netw Open. 2021 07 01; 4(7):e2114155.
    View in: PubMed
    Score: 0.010
  12. Health-related quality of life in adults with osteogenesis imperfecta. Clin Genet. 2021 06; 99(6):772-779.
    View in: PubMed
    Score: 0.010
  13. Craniofacial phenotypes associated with Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3606-3612.
    View in: PubMed
    Score: 0.010
  14. Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3576-3583.
    View in: PubMed
    Score: 0.010
  15. Characterization of the Robinow syndrome skeletal phenotype, bone micro-architecture, and genotype-phenotype correlations with the osteosclerotic form. Am J Med Genet A. 2020 11; 182(11):2632-2640.
    View in: PubMed
    Score: 0.010
  16. Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profiles. Bone. 2020 11; 140:115547.
    View in: PubMed
    Score: 0.010
  17. Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study. Am J Med Genet A. 2020 04; 182(4):697-704.
    View in: PubMed
    Score: 0.009
  18. Mobility in osteogenesis imperfecta: a multicenter North American study. Genet Med. 2019 10; 21(10):2311-2318.
    View in: PubMed
    Score: 0.009
  19. Caries prevalence and experience in individuals with osteogenesis imperfecta: A cross-sectional multicenter study. Spec Care Dentist. 2019 Mar; 39(2):214-219.
    View in: PubMed
    Score: 0.009
  20. Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type V. Eur J Med Genet. 2019 Dec; 62(12):103606.
    View in: PubMed
    Score: 0.009
  21. Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies. Am J Hum Genet. 2018 05 03; 102(5):985-994.
    View in: PubMed
    Score: 0.008
  22. WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome. Am J Hum Genet. 2018 01 04; 102(1):27-43.
    View in: PubMed
    Score: 0.008
  23. Quantitation of phenylbutyrate metabolites by UPLC-MS/MS demonstrates inverse correlation of phenylacetate:phenylacetylglutamine ratio with plasma glutamine levels. Mol Genet Metab. 2017 11; 122(3):39-45.
    View in: PubMed
    Score: 0.008
  24. Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum. Am J Med Genet A. 2014 Jul; 164A(7):1713-33.
    View in: PubMed
    Score: 0.006
  25. Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA. Nat Genet. 2012 Jun 24; 44(8):928-33.
    View in: PubMed
    Score: 0.006
  26. Cytologic differential diagnosis of papillary pattern in breast aspirates: correlation with histology. Ann Diagn Pathol. 2001 Feb; 5(1):34-42.
    View in: PubMed
    Score: 0.003
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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.