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Page 1
Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.
Verscaj CP, Velez-Bartolomei F, Bodle E, Chan K, Lyons MJ, Thorson W, Tan WH, Rodig N, Graham JM Jr, Peron A, Quintero-Rivera F, Zackai EH, Thomas MA, Stevens CA, Adam MP, Bird LM, Jones MC, Matalon DR. Verscaj CP, et al. Among authors: bodle e. Prenat Diagn. 2024 Feb;44(2):237-246. doi: 10.1002/pd.6424. Epub 2023 Aug 26. Prenat Diagn. 2024. PMID: 37632214 Review.
ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis.
Deisseroth CA, Birgmeier J, Bodle EE, Kohler JN, Matalon DR, Nazarenko Y, Genetti CA, Brownstein CA, Schmitz-Abe K, Schoch K, Cope H, Signer R; Undiagnosed Diseases Network; Martinez-Agosto JA, Shashi V, Beggs AH, Wheeler MT, Bernstein JA, Bejerano G. Deisseroth CA, et al. Among authors: bodle ee. Genet Med. 2019 Jul;21(7):1585-1593. doi: 10.1038/s41436-018-0381-1. Epub 2018 Dec 5. Genet Med. 2019. PMID: 30514889 Free PMC article.
Acute leukemia in a patient with 15q overgrowth syndrome.
Bodle EE, Gupta R, Cherry AM, Muffly L, Manning MA. Bodle EE, et al. Am J Med Genet A. 2019 Jun;179(6):1025-1029. doi: 10.1002/ajmg.a.61115. Epub 2019 Mar 12. Am J Med Genet A. 2019. PMID: 30861314
Effects of dose, administration route, and/or vehicle on decabromodiphenyl ether concentrations in plasma of maternal, fetal, and neonatal rats and in milk of maternal rats.
Biesemeier JA, Beck MJ, Silberberg H, Myers NR, Ariano JM, Bodle ES, Sved DW, Jacobi S, Stump DG, Hardy M, Stedeford T. Biesemeier JA, et al. Among authors: bodle es. Drug Metab Dispos. 2010 Oct;38(10):1648-54. doi: 10.1124/dmd.110.033431. Epub 2010 Jun 25. Drug Metab Dispos. 2010. PMID: 20581093
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