Joann N Bodurtha

Professor

1974 …2019

Research output per year

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Research Output

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Review article

Assessment of the newborn with dysmorphic features.

Bodurtha, J., Mar 1999, In : Neonatal network : NN. 18, 2, p. 27-30 4 p.

Research output: Contribution to journalReview article

Café au lait spots: The pediatrician's perspective

Tekin, M., Bodurtha, J. N. & Riccardi, V. M., Jan 1 2001, In : Pediatrics in review. 22, 3, p. 82-90 9 p.

Research output: Contribution to journalReview article

Coffin-Siris syndrome: Review and presentation of new cases from a questionnaire study

Fleck, B. J., Pandya, A., Vanner, L., Kerkering, K. & Bodurtha, J., Feb 15 2001, In : American journal of medical genetics. 99, 1, p. 1-7 7 p.

Research output: Contribution to journalReview article

Congenital central hypoventilation syndrome and Hirschsprung's disease in half sibs

Hamilton, J. & Bodurtha, J. N., Jan 1 1989, In : Journal of medical genetics. 26, 4, p. 272-274 3 p.

Research output: Contribution to journalReview article

DNA testing: diagnostic role in single gene conditions.

Bodurtha, J., Lloyd, J. & Tams, L., Jan 1 1992, In : Virginia medical quarterly : VMQ. 119, 2, p. 95-96 2 p.

Research output: Contribution to journalReview article

Factors influencing men's interest in gene testing for prostate cancer susceptibility

Culler, D. D., Silberg, J., Vanner-Nicely, L., Ware, J. L., Jackson-Cook, C. & Bodurtha, J., Dec 1 2002, In : Journal of Genetic Counseling. 11, 5, p. 383-398 16 p.

Research output: Contribution to journalReview article

Five pediatric cancers – update on genetic implications

Cooper, S., Rubens, J. & Bodurtha, J. N., Feb 1 2017, In : Current Pediatric Reviews. 13, 1, p. 42-48 7 p.

Research output: Contribution to journalReview article

Genomics and perinatal care

Bodurtha, J. & Strauss, J. F., Jan 5 2012, In : New England Journal of Medicine. 366, 1, p. 64-73 10 p.

Research output: Contribution to journalReview article

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

Paznekas, W. A., Karczeski, B., Vermeer, S., Lowry, R. B., Delatycki, M., Laurence, F., Koivisto, P. A., Van Maldergem, L., Boyadjiev, S. A., Bodurtha, J. N. & Jabs, E. W., May 1 2009, In : Human mutation. 30, 5, p. 724-733 10 p.

Research output: Contribution to journalReview article

Goldenhar complex in discordant monozygotic twins: A case report and review of the literature

Boles, D. J., Bodurtha, J. & Nance, W. E., Jan 1 1987, In : American journal of medical genetics. 28, 1, p. 103-109 7 p.

Research output: Contribution to journalReview article

Health information technology in screening and treatment of child obesity: A systematic review

Smith, A. J., Skow, Á., Bodurtha, J. & Kinra, S., Mar 1 2013, In : Pediatrics. 131, 3, p. e894-e902

Research output: Contribution to journalReview article

Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10

Rampersaud, E., Bassuk, A. G., Enterline, D. S., George, T. M., Siegel, D. G., Melvin, E. C., Aben, J., Allen, J., Aylsworth, A., Brei, T., Bodurtha, J., Buran, C., Floyd, L. E., Hammock, P., Iskandar, B., Ito, J., Kessler, J. A., Lasarsky, N., Mack, P., Mackey, J. & 14 others, McLone, D., Meeropol, E., Mehltretter, L., Mitchell, L. E., Oakes, W. J., Nye, J. S., Powell, C., Sawin, K., Stevenson, R., Walker, M., West, S. G., Worley, G., Gilbert, J. R. & Speer, M. C., Dec 1 2005, In : Journal of medical genetics. 42, 12, p. 940-946 7 p.

Research output: Contribution to journalReview article