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Page 1
IGF1R variants associated with isolated single suture craniosynostosis.
Cunningham ML, Horst JA, Rieder MJ, Hing AV, Stanaway IB, Park SS, Samudrala R, Speltz ML. Cunningham ML, et al. Among authors: horst ja. Am J Med Genet A. 2011 Jan;155A(1):91-7. doi: 10.1002/ajmg.a.33781. Am J Med Genet A. 2011. PMID: 21204214 Free PMC article.
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.
Rieder MJ, Green GE, Park SS, Stamper BD, Gordon CT, Johnson JM, Cunniff CM, Smith JD, Emery SB, Lyonnet S, Amiel J, Holder M, Heggie AA, Bamshad MJ, Nickerson DA, Cox TC, Hing AV, Horst JA, Cunningham ML. Rieder MJ, et al. Among authors: horst ja. Am J Hum Genet. 2012 May 4;90(5):907-14. doi: 10.1016/j.ajhg.2012.04.002. Am J Hum Genet. 2012. PMID: 22560091 Free PMC article.
Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.
Smith JD, Hing AV, Clarke CM, Johnson NM, Perez FA, Park SS, Horst JA, Mecham B, Maves L, Nickerson DA; University of Washington Center for Mendelian Genomics; Cunningham ML. Smith JD, et al. Among authors: horst ja. Am J Hum Genet. 2014 Aug 7;95(2):235-40. doi: 10.1016/j.ajhg.2014.07.008. Am J Hum Genet. 2014. PMID: 25105228 Free PMC article.
Novel paradigms for drug discovery: computational multitarget screening.
Jenwitheesuk E, Horst JA, Rivas KL, Van Voorhis WC, Samudrala R. Jenwitheesuk E, et al. Among authors: horst ja. Trends Pharmacol Sci. 2008 Feb;29(2):62-71. doi: 10.1016/j.tips.2007.11.007. Epub 2008 Jan 10. Trends Pharmacol Sci. 2008. PMID: 18190973 Free PMC article. Review.
55 results