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Myers KC, Bolyard AA, Otto B, Wong TE, Jones A, Harris RE, MD, Davies SM, Dale DC, and Shimamura A. Variable Clinical Presentation of Shwachman-Diamond Syndrome: Update From the North-American Shwachman-Diamond Syndrome Registry. J Pediatr. 2013 Dec 31.

Myers KC, Rose SR, Rutter MM, Mehta PA, Khoury JC, Cole T, Harris RE. Endocrine Evaluation of Children with and without Shwachman-Bodian-Diamond Syndrome Gene Mutations and Shwachman-Diamond Syndrome. J Pediatr. 2013 Jun;162(6):1235-40.

Myers KC, Lawrence J, Marsh RA, Davies SM, Jodele S. High-Dose Methylprednisolone for Veno-Occlusive Disease of the Liver in Pediatric Hematopoietic Stem Cell Transplantation Recipients. Biol Blood Marrow Transplant. 2013 Mar;19(3):500-3.

Myers KC, Davies SM, Shimamura A. Clinical and Molecular Pathophysiology of Shwachman–Diamond Syndrome: An Update. Hematol Oncol Clin North Am. 2013 Feb;27(1):117-28.

Myers KC, Davies SM, Shimamura A. Clinical and Molecular Pathophysiology of Shwachman–Diamond Syndrome: An Update. Hematol Oncol Clin North Am. 2013 Feb;27(1):117-28.

Rose RS, Myers K, Rutter MM, Mueller R, Khoury JC, Mehta PA, Harris RE, Davies SM, Endocrine Phenotype of Children and Adults with Fanconi Anemia. Pediatr Blood Cancer. 2012 Oct;59(4):690-6.

Du W, Rani R, Sipple J, Schick J, Myers KC, Mehta P, Andreassen PR, Davies SM, Pang Q, The FA pathway counteracts oxidative stress through selective protection of antioxidant defense gene promoters. Blood. 2012 May 3;119(18):4142-51.

Myers K, Davies SM, Harris RE, Spunt SL, Smolarek TA, Zimmerman S, McMasters R, Wagner L, Mueller R, Auerbach AD, Mehta PA. The Clinical Phenotype of Children with Fanconi Anemia Caused by Biallelic FANCD1/BRCA2 Mutations. Pediatric Blood and Cancer. 2012 Mar;58(3): 462-5.

Myers KC, Bleesing JJ, Davies, SM, Zhang X, Martin LJ, Mueller R, Harris RE, Filipovich AH, Butsch Kovacic M, Wells SI, Mehta PA. Impaired Immune Function in Children with Fanconi Anemia. Br J Haematol. 2011 Jul;154(2):234-40.

Mehta PA, Harris RE, Davies SM, Kim MO, Mueller R, Lampkin B, Mo J, Myers K, Smolarek TA. Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia. Cancer Genet Cytogenet. 2010 Dec;203(2):180-6.