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Douglas Stewart, Ph.D.

Adjunct Investigator, Genetic Disease Research Branch, National Human Genome Research Institute (NHGRI)
Investigator, Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI)

Select publications

Stewart DR, Huang A, Zackai EH, Anderlid BM, Medne L, Russell K, Kaur M, Rossi E, Tenconi R, Nordenskjöld M, Gripp K, Nicholson L, Meschino WS, Capua E, Quarrell OWJ, Flint J, Irons M, Giampietro PF, Schowalter DB, Zeleski CA, Malacarre M, Faravelli F, Spinner NB, Krantz ID. Subtelomeric deletions of chromosome 9q: A novel microdeletion syndrome. American Journal of Medical Genetics, 128A (4): 340-351. 2004. [PubMed]

Ho CKM, Wood JR, Stewart DR, Ewens K, Ankener W, Wickenheisser J, Nelson-Delgrave V, Zhang Z, Legro RS, Dunaif A, McAllister JM, Spielman R, Strauss, JF. Increased transcription and increased mRNA stability contribute to increased GATA6 mRNA abundance in PCOS theca cells. Journal of Clinical Endocrinology and Metabolism, 90 (12): 6596-6602. 2005. [PubMed]

Stewart DR, Dombroski B, Urbanek M, Ankener W, Ewens KE, Wood JR, Legro RS, Strauss JF, Dunaif A, Spielman RS. Fine mapping of genetic susceptibility to polycystic ovary syndrome on chromosome 19p13.2 and tests for regulatory activity. Journal of Clinical Endocrinology and Metabolism, 91 (10): 4112-4117. 2006. [PubMed]

Stewart DR, Corless CL, Rubin BP, Heinrich MC, Messiaen LM, Kessler LJ, Zhang PJ, Brooks DG. Mitotic recombination as evidence of alternative pathogenesis of gastrointestinal stromal tumors (GISTs) in neurofibromatosis type 1. Journal of Medical Genetics, 44: e61. 2007. [PubMed]

Stewart DR, Cogan JD, Kramer MR, Miller WT Jr., Christiansen LE, Pauciulo MW, Messiaen LM, Tu GS, Thompson WH, Pyeritz RE, Ryo JH, Nichols WC, Kodama M, Meyrick BO, Ross DJ. Is pulmonary arterial hypertension in neurofibromatosis type 1 secondary to a plexogenic arteriopathy? Chest, 132 (3): 798-808. 2007. [PubMed]

Stewart DR and Kleefstra T. The chromosome 9q subtelomere deletion syndrome. American Journal of Medical Genetics Part C Seminar in Medical Genetics, 145C: 383-392. 2007. [PubMed]

Boley S, Sloan JL, Pemov A, Stewart DR. A quantitative assessment of the burden and distribution of Lisch nodules in adults with neurofibromatosis type 1. Investigative Ophthalmology and Visual Science, 50: 5035-5043. 2009. [PubMed]

Brems H, Park C, Maertens O, Pemov A, Messiaen L, Upadhyaya M, Claes K, Beert E, Peeters K, Mautner V, Sloan JL, Yao L, Lee CR, Sciot R, De Smet L, Legius E, Stewart DR. Glomus tumors in neurofibromatosis type 1: genetic, functional and clinical evidence of a novel association. Cancer Research, 69 (18): 7393-7401. 2009. [PubMed]

Pemov A, Park C, Reilly KM, Stewart DR. Evidence of perturbations of cell cycle and DNA repair pathways as a consequence of human and murine NF1-haploinsufficiency. BMC Genomics, 11(1): 194. 2010. [PubMed]

Ewens KG, Stewart DR, Ankener W, Urbanek M, McAllister JM, Chen C, Baig KM, Parker SCJ, Margulies EH, Legro RS, Duanif A, Strauss JF, Spielman RS (posthumously). Family-based analysis of candidate genes for polycystic ovary syndrome. Journal of Clinical Endocrinology and Metabolism, 95(5): 2306-2315. 2010. [PubMed]

Stewart DR, Sloan JL, Yao L, Mannes AJ, Moshyedi A, Lee CR, Sciot R, De Smet L, Mautner V-F, Legius E. Diagnosis, management, and complications of glomus tumors of the fingers in neurofibromatosis type 1. Journal of Medical Genetics, 47 (8): 525-32. 2010. [PubMed]

Denayer E, Descheemaeker M-J, Stewart DR, Keymolen K, Coombes SL, Snow J, Thurm AE, Joseph LA, Fryns J-P, Legius E. Observations on Intelligence and Behavior in 15 Patients with Legius Syndrome. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 157(2): 123-8. 2011. [PubMed]

Soto E, Stewart DR, Mannes AJ, Ruppert SL, Baker K, Zlott D, Phillips J, Wroblewski GA, Handel D, Berger AM. Oral ketamine in a palliative care setting: A review of the literature and case report of a patient with NF1 and glomus tumor-associated CRPS. American Journal of Hospice and Palliative Medicine, 2011. [PubMed]

Stewart DR, Pemov A, Van Loo P, Beert E, Brems H, Sciot R, Claes K, Pak E, Dutra A, Lee CR and Legius E. Mitotic Recombination of Chromosome Arm 17q as a Cause of Loss of Heterozygosity of NF1 in Neurofibromatosis type 1-associated Glomus Tumors. Genes, Chromosomes and Cancer. [PubMed]

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Posted: February 14, 2012