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Connection

Shanlee Davis to Child, Preschool

This is a "connection" page, showing publications Shanlee Davis has written about Child, Preschool.

 
Connection Strength
 
 
 
0.533
 
  1. Davis SM, Marshall TE, Swenson KS, Bothwell S, Nokoff NJ, Middleton A, Furniss A, Alkhdour M, Christakis DA, Elliott VA, Heeley J, Ikomi C, Ross J, Stone SI, Vogiatzi MG, Tartaglia NR. Reference Growth Charts for Children With 47,XXY/Klinefelter Syndrome. Pediatrics. 2025 Dec 01; 156(6).
    View in: PubMed
    Score: 0.080
  2. Hutaff-Lee C, Jolliffe M, Swenson KS, Wakeman H, Swain D, Furniss A, Nokoff N, Hansen-Moore J, Ikomi C, Bamba V, Lean RE, Leonard S, Davis SM. Neurodevelopmental and Mental Health Diagnoses Among Pediatric Patients With Turner Syndrome: A PEDSnet Study. Am J Med Genet A. 2026 02; 200(2):308-315.
    View in: PubMed
    Score: 0.079
  3. Hall A, Furniss A, Tartaglia NN, Janusz J, Wilson R, Middleton C, Martin S, Frazier J, Martinez-Chadrom M, Hansen-Moore J, Ikomi C, Ross J, Vogiaski MG, Morrow L, Christakis DA, Lean RE, Nokoff N, Pyle L, Davis SM. Neurodevelopmental and Mental Health Outcomes in a National Clinical Sample of Youth With Sex Chromosome Trisomies Compared With Matched Controls. J Dev Behav Pediatr. 2025 Mar-Apr 01; 46(2):e208-e215.
    View in: PubMed
    Score: 0.075
  4. Klamut N, Bothwell S, Carl AE, Bamba V, Law JR, Brickman WJ, Klein KO, Kanakatti Shankar R, Pinnaro CT, Fechner PY, Prakash SK, Gutmark-Little I, Howell S, Tartaglia N, Good M, Ranallo KC, Davis SM. Prevalence, diagnostic features, and medical outcomes of females with Turner syndrome with a trisomy X cell line (45,X/47,XXX): Results from the InsighTS Registry. Am J Med Genet A. 2024 12; 194(12):e63819.
    View in: PubMed
    Score: 0.073
  5. Davis SM, Lahlou N, Cox-Martin M, Kowal K, Zeitler PS, Ross JL. Oxandrolone Treatment Results in an Increased Risk of Gonadarche in Prepubertal Boys With Klinefelter Syndrome. J Clin Endocrinol Metab. 2018 09 01; 103(9):3449-3455.
    View in: PubMed
    Score: 0.048
  6. Davis SM, Katusic SK, Barbaresi WJ, Killian J, Weaver AL, Ottman R, Wirrell EC. Epilepsy in children with attention-deficit/hyperactivity disorder. Pediatr Neurol. 2010 May; 42(5):325-30.
    View in: PubMed
    Score: 0.027
  7. Thodberg HH, Aksglaede L, Juul A, Davis SM, Ross J. High-precision automated bone age: a clinically useful tool in monitoring of treatment effects in children and adolescents. Sci Rep. 2026 Apr 27; 16(1).
    View in: PubMed
    Score: 0.021
  8. Chen LM, Valentine A, Davis SM, Graber E, Fechner PY, Furniss A, Nahata L, Pyle L, Vyas AK, Vogiatzi MG, Nokoff NJ. Multicenter Analysis of Cardiometabolic-Related Diagnoses in Youth With Congenital Adrenal Hyperplasia: A PEDSnet Study. J Clin Endocrinol Metab. 2025 Mar 17; 110(4):e1009-e1016.
    View in: PubMed
    Score: 0.019
  9. Pham TT, Davis SM, Tong S, Campa KA, Friedman NR, Gitomer SA. High Prevalence of Obstructive Sleep-Disordered Breathing in Pediatric Patients With Turner Syndrome. Otolaryngol Head Neck Surg. 2024 03; 170(3):905-912.
    View in: PubMed
    Score: 0.017
  10. Kremen J, Davis SM, Nahata L, Kapa HM, Dattilo TM, Liu E, Hutaff-Lee C, Tishelman AC, Crerand CE. Neuropsychological and mental health concerns in a multicenter clinical sample of youth with turner syndrome. Am J Med Genet A. 2023 04; 191(4):962-976.
    View in: PubMed
    Score: 0.016
  11. Howell S, Buchanan C, Davis SM, Miyazawa H, Furuta GT, Tartaglia NR, Nguyen N. Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implications. Mol Genet Genomic Med. 2021 12; 9(12):e1833.
    View in: PubMed
    Score: 0.015
  12. Hsu SC, Bartz S, Pyle L, Fete M, Davis S, Ohman-Hanson R, Fete TJ, Motil KJ. Growth failure in focal dermal hypoplasia. Am J Med Genet A. 2019 04; 179(4):628-633.
    View in: PubMed
    Score: 0.012
  13. Martin S, Cordeiro L, Richardson P, Davis S, Tartaglia N. The Association of Motor Skills and Adaptive Functioning in XXY/Klinefelter and XXYY Syndromes. Phys Occup Ther Pediatr. 2019; 39(4):446-459.
    View in: PubMed
    Score: 0.012
  14. Tartaglia NR, Wilson R, Miller JS, Rafalko J, Cordeiro L, Davis S, Hessl D, Ross J. Autism Spectrum Disorder in Males with Sex Chromosome Aneuploidy: XXY/Klinefelter Syndrome, XYY, and XXYY. J Dev Behav Pediatr. 2017 Apr; 38(3):197-207.
    View in: PubMed
    Score: 0.011
  15. Ross JL, Kushner H, Kowal K, Bardsley M, Davis S, Reiss AL, Tartaglia N, Roeltgen D. Androgen Treatment Effects on Motor Function, Cognition, and Behavior in Boys with Klinefelter Syndrome. J Pediatr. 2017 06; 185:193-199.e4.
    View in: PubMed
    Score: 0.011
  16. Poppy A, Retamal-Munoz C, Cree-Green M, Wood C, Davis S, Clements SA, Majidi S, Steck AK, Alonso GT, Chambers C, Rewers A. Reduction of Insulin Related Preventable Severe Hypoglycemic Events in Hospitalized Children. Pediatrics. 2016 07; 138(1).
    View in: PubMed
    Score: 0.010
  17. Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. A new look at XXYY syndrome: medical and psychological features. Am J Med Genet A. 2008 Jun 15; 146A(12):1509-22.
    View in: PubMed
    Score: 0.006
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.

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