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Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome.
Jolly A, Du H, Borel C, Chen N, Zhao S, Grochowski CM, Duan R, Fatih JM, Dawood M, Salvi S, Jhangiani SN, Muzny DM, Koch A, Rouskas K, Glentis S, Deligeoroglou E, Bacopoulou F, Wise CA, Dietrich JE, Van den Veyver IB, Dimas AS, Brucker S, Sutton VR, Gibbs RA, Antonarakis SE, Wu N, Coban-Akdemir ZH, Zhu L, Posey JE, Lupski JR. Jolly A, et al. Among authors: sutton vr. HGG Adv. 2023 Mar 29;4(3):100188. doi: 10.1016/j.xhgg.2023.100188. eCollection 2023 Jul 13. HGG Adv. 2023. PMID: 37124138 Free PMC article.
Neuroimaging aspects of Aicardi syndrome.
Hopkins B, Sutton VR, Lewis RA, Van den Veyver I, Clark G. Hopkins B, et al. Among authors: sutton vr. Am J Med Genet A. 2008 Nov 15;146A(22):2871-8. doi: 10.1002/ajmg.a.32537. Am J Med Genet A. 2008. PMID: 18925666 Free PMC article.
Non-random X chromosome inactivation in Aicardi syndrome.
Eble TN, Sutton VR, Sangi-Haghpeykar H, Wang X, Jin W, Lewis RA, Fang P, Van den Veyver IB. Eble TN, et al. Among authors: sutton vr. Hum Genet. 2009 Mar;125(2):211-6. doi: 10.1007/s00439-008-0615-4. Epub 2009 Jan 1. Hum Genet. 2009. PMID: 19116729 Free PMC article.
A genome-wide screen for copy number alterations in Aicardi syndrome.
Wang X, Sutton VR, Eble TN, Lewis RA, Gunaratne P, Patel A, Van den Veyver IB. Wang X, et al. Among authors: sutton vr. Am J Med Genet A. 2009 Oct;149A(10):2113-21. doi: 10.1002/ajmg.a.32976. Am J Med Genet A. 2009. PMID: 19760649 Free PMC article.
The gender medicine team: "it takes a village".
Axelrad ME, Berg JS, Coker LA, Dietrich J, Adcock L, French SL, Gunn S, Ligon BL, McCullough LB, Sutton VR, Karaviti LP. Axelrad ME, et al. Among authors: sutton vr. Adv Pediatr. 2009;56:145-64. doi: 10.1016/j.yapd.2009.08.001. Adv Pediatr. 2009. PMID: 19968947 No abstract available.
283 results