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Page 1
Tuberous Sclerosis Complex Genotypes and Developmental Phenotype.
Farach LS, Pearson DA, Woodhouse JP, Schraw JM, Sahin M, Krueger DA, Wu JY, Bebin EM, Lupo PJ, Au KS, Northrup H; TACERN Study Group. Farach LS, et al. Among authors: woodhouse jp. Pediatr Neurol. 2019 Jul;96:58-63. doi: 10.1016/j.pediatrneurol.2019.03.003. Epub 2019 Mar 13. Pediatr Neurol. 2019. PMID: 31005478 Free PMC article.
Risk factors and time trends for isolated craniosynostosis.
Schraw JM, Woodhouse JP, Langlois PH, Canfield MA, Scheuerle AE, Agopian AJ, Benjamin RH, Lupo PJ. Schraw JM, et al. Among authors: woodhouse jp. Birth Defects Res. 2021 Jan 1;113(1):43-54. doi: 10.1002/bdr2.1824. Epub 2020 Oct 22. Birth Defects Res. 2021. PMID: 33091229
Factors associated with nonsyndromic anotia and microtia, Texas, 1999-2014.
Schraw JM, Woodhouse JP, Benjamin RH, Shumate CJ, Nguyen J, Canfield MA, Agopian AJ, Lupo PJ. Schraw JM, et al. Among authors: woodhouse jp. Birth Defects Res. 2023 Jan 1;115(1):67-78. doi: 10.1002/bdr2.2130. Epub 2022 Nov 17. Birth Defects Res. 2023. PMID: 36398384 Free PMC article.
Epigenomic signature of major congenital heart defects in newborns with Down syndrome.
Mouat JS, Li S, Myint SS, Laufer BI, Lupo PJ, Schraw JM, Woodhouse JP, de Smith AJ, LaSalle JM. Mouat JS, et al. Among authors: woodhouse jp. medRxiv [Preprint]. 2023 May 5:2023.05.02.23289417. doi: 10.1101/2023.05.02.23289417. medRxiv. 2023. Update in: Hum Genomics. 2023 Oct 6;17(1):92. doi: 10.1186/s40246-023-00540-1 PMID: 37205408 Free PMC article. Updated. Preprint.