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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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David A. Stevenson

University of Utah

Division of Medical Genetics

2C412 SOM

Salt Lake City

USA

[email]@hsc.utah.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • University of Utah, Division of Medical Genetics, 2C412 SOM, Salt Lake City, USA. 2012
  • Department of Pediatrics, University of Utah, Salt Lake City, UT 84132, USA. 2004 - 2011
  • Division of Medical Genetics, Department of Pediatrics, University of Utah, 2C412 School of Medicine. 2009 - 2011

References

  1. Peripheral muscle weakness in RASopathies. Stevenson, D.A., Allen, S., Tidyman, W.E., Carey, J.C., Viskochil, D.H., Stevens, A., Hanson, H., Sheng, X., Thompson, B.A., Okumura, M.J., Reinker, K., Johnson, B., Rauen, K.A. Muscle. Nerve (2012) [Pubmed]
  2. Bone resorption in syndromes of the Ras/MAPK pathway. Stevenson, D.A., Schwarz, E.L., Carey, J.C., Viskochil, D.H., Hanson, H., Bauer, S., Weng, H.Y., Greene, T., Reinker, K., Swensen, J., Chan, R.J., Yang, F.C., Senbanjo, L., Yang, Z., Mao, R., Pasquali, M. Clin. Genet. (2011) [Pubmed]
  3. Pediatric 25-hydroxyvitamin D concentrations in neurofibromatosis type 1. Stevenson, D.A., Viskochil, D.H., Carey, J.C., Sheng, X., Murray, M., Moyer-Mileur, L., Shelton, J., Roberts, W.L., Bunker, A.M., Hanson, H., Bauer, S., D'Astous, J.L. J. Pediatr. Endocrinol. Metab. (2011) [Pubmed]
  4. Familial clustering of hemangiomas. Grimmer, J.F., Williams, M.S., Pimentel, R., Mineau, G., Wood, G.M., Bayrak-Toydemir, P., Stevenson, D.A. Arch. Otolaryngol. Head Neck Surg. (2011) [Pubmed]
  5. Analysis of radiographic characteristics of anterolateral bowing of the leg before fracture in neurofibromatosis type 1. Stevenson, D.A., Carey, J.C., Viskochil, D.H., Moyer-Mileur, L.J., Slater, H., Murray, M.A., D'Astous, J.L., Murray, K.A. J. Pediatr. Orthop (2009) [Pubmed]
  6. Familial predisposition to developmental dysplasia of the hip. Stevenson, D.A., Mineau, G., Kerber, R.A., Viskochil, D.H., Schaefer, C., Roach, J.W. J. Pediatr. Orthop (2009) [Pubmed]
  7. Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomography. Stevenson, D.A., Viskochil, D.H., Carey, J.C., Slater, H., Murray, M., Sheng, X., D'Astous, J., Hanson, H., Schorry, E., Moyer-Mileur, L.J. Bone (2009) [Pubmed]
  8. Health-related quality of life measures in genetic disorders: an outcome variable for consideration in clinical trials. Stevenson, D.A., Carey, J.C. American J. Medical Genetics. C, Seminars Medical Genetics (2009) [Pubmed]
  9. Evidence of increased bone resorption in neurofibromatosis type 1 using urinary pyridinium crosslink analysis. Stevenson, D.A., Schwarz, E.L., Viskochil, D.H., Moyer-Mileur, L.J., Murray, M., Firth, S.D., D'Astous, J.L., Carey, J.C., Pasquali, M. Pediatr. Res. (2008) [Pubmed]
  10. Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement. Stevenson, D.A., Carey, J.C., Coburn, S.P., Ericson, K.L., Byrne, J.L., Mumm, S., Whyte, M.P. J. Clin. Endocrinol. Metab. (2008) [Pubmed]
  11. Deaths due to choking in Prader-Willi syndrome. Stevenson, D.A., Heinemann, J., Angulo, M., Butler, M.G., Loker, J., Rupe, N., Kendell, P., Clericuzio, C.L., Scheimann, A.O. Am. J. Med. Genet. A (2007) [Pubmed]
  12. Bone mineral density in children and adolescents with neurofibromatosis type 1. Stevenson, D.A., Moyer-Mileur, L.J., Murray, M., Slater, H., Sheng, X., Carey, J.C., Dube, B., Viskochil, D.H. J. Pediatr. (2007) [Pubmed]
  13. Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene cluster. Stevenson, D.A., Bleyl, S.B., Maxwell, T., Brothman, A.R., South, S.T. Am. J. Med. Genet. A (2007) [Pubmed]
  14. Gastric rupture and necrosis in Prader-Willi syndrome. Stevenson, D.A., Heinemann, J., Angulo, M., Butler, M.G., Loker, J., Rupe, N., Kendell, P., Cassidy, S.B., Scheimann, A. J. Pediatr. Gastroenterol. Nutr. (2007) [Pubmed]
  15. Familial congenital non-immune hydrops, chylothorax, and pulmonary lymphangiectasia. Stevenson, D.A., Pysher, T.J., Ward, R.M., Carey, J.C. Am. J. Med. Genet. A (2006) [Pubmed]
  16. Double inactivation of NF1 in tibial pseudarthrosis. Stevenson, D.A., Zhou, H., Ashrafi, S., Messiaen, L.M., Carey, J.C., D'Astous, J.L., Santora, S.D., Viskochil, D.H. Am. J. Hum. Genet. (2006) [Pubmed]
  17. A new distal arthrogryposis syndrome characterized by plantar flexion contractures. Stevenson, D.A., Swoboda, K.J., Sanders, R.K., Bamshad, M. Am. J. Med. Genet. A (2006) [Pubmed]
  18. Case-control study of the muscular compartments and osseous strength in neurofibromatosis type 1 using peripheral quantitative computed tomography. Stevenson, D.A., Moyer-Mileur, L.J., Carey, J.C., Quick, J.L., Hoff, C.J., Viskochil, D.H. J. Musculoskelet. Neuronal. Interact (2005) [Pubmed]
  19. Unexpected death and critical illness in Prader-Willi syndrome: report of ten individuals. Stevenson, D.A., Anaya, T.M., Clayton-Smith, J., Hall, B.D., Van Allen, M.I., Zori, R.T., Zackai, E.H., Frank, G., Clericuzio, C.L. Am. J. Med. Genet. A (2004) [Pubmed]
  20. 6q subtelomeric deletion: is there a recognizable syndrome?. Stevenson, D.A., Brothman, A.R., Carey, J.C., Chen, Z., Dent, K.M., Bale, J.F., Longo, N. Clin. Dysmorphol. (2004) [Pubmed]
  21. Paternal uniparental disomy of chromosome 14: confirmation of a clinically-recognizable phenotype. Stevenson, D.A., Brothman, A.R., Chen, Z., Bayrak-Toydemir, P., Longo, N. Am. J. Med. Genet. A (2004) [Pubmed]
 
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