2020
Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus
Panchagnula S, Jin S, Dong W, Kundishora A, Moreno-De-Luca A, Furey C, Allocco A, Walker R, Nelson-Williams C, Smith H, Dunbar A, Conine S, Lu Q, Zen X, Sierant M, Knight J, Sullivan W, Phan D, DeSpenza T, Reeves B, Karimy J, Marlier A, Castaldi C, Tikhonova I, Li B, Peña; H, Broach J, Kabachelor E, Ssenyonga P, Hehnly C, Ge L, Keren B, Timberlake A, Goto J, Mangano F, Johnston J, Butler W, Warf B, Smith E, Schiff S, Limbrick D, Heuer G, Jackson E, Iskandar B, Mane S, Haider S, Guclu B, Bayri Y, Sahin Y, Duncan C, Apuzzo M, DiLuna M, Hoffman E, Sestan N, Ment L, Alper S, Bilguvar K, Geschwind D, Günel M, Lifton R, Kahle K. Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus. Neurosurgery 2020, 67 DOI: 10.1093/neuros/nyaa447_572.Peer-Reviewed Original Research
2019
Exome Sequencing Defines the Molecular Pathogenesis of Vein of Galen Malformation
Kundishora A, Zeng X, Duran D, Allocco A, Choi J, Jin S, Conine S, Nelson-Williams C, Gaillard J, Furey C, Timberlake A, Mansuri M, Sorscher M, Klein J, Lu Q, Montejo J, Vera A, Karimy J, Panchagnula S, Youngblood M, DiLuna M, Matouk C, Mane S, Alper S, Ducruet A, Zabramski J, Aagaard-Kienitz B, Rodesch G, Smith E, Orbach D, Berenstein A, Bilguvar K, Gunel M, Lifton R, Kahle K. Exome Sequencing Defines the Molecular Pathogenesis of Vein of Galen Malformation. Neurosurgery 2019, 66: 310-341. DOI: 10.1093/neuros/nyz310_341.Peer-Reviewed Original Research
2007
Linkage and Copy Number Variation Analysis of Large Families and Sibling Pairs Demonstrates Locus Heterogeneity for Familial Intracranial Aneurysms
Bilguvar K, Bayrakli F, Bayri Y, Ozturk A, DiLuna M, Bydon M, Gunel M. Linkage and Copy Number Variation Analysis of Large Families and Sibling Pairs Demonstrates Locus Heterogeneity for Familial Intracranial Aneurysms. Neurosurgery 2007, 61: 198. DOI: 10.1227/01.neu.0000279890.51914.ec.Peer-Reviewed Original ResearchContributor's List
Berkovic S, Bilguvar K, Blackstone C, Bloch M, Blumenfeld H, Bredesen D, Bressman S, Brucal M, Burton E, Dalmau J, Dawson T, Dawson V, Depondt C, DiLuna M, DiMauro S, Ferrari M, Fink D, Flügel A, Frants R, Glorioso J, Goadsby P, Goldin A, Gunel M, Harel N, Helbig I, Hemmen T, Hisama F, Hyman B, Ingelsson M, Johnson D, Kamholz J, Kaul M, Kocsis J, Lammers G, Leckman J, Li J, Lipton S, Maragakis N, Mehlen P, Morimoto R, Orton K, Overeem S, Ozelius L, Pandolfo M, Pascual J, Paulson H, Peroutka S, Petroff O, Ransom C, Rao R, Rismanchi N, Rothstein J, Savitt J, Scheffer I, Schon E, Shy M, Strittmatter S, Tafti M, Tanriover G, Todi S, van den Maagdenberg A, Vance J, Vincent A, Voisine C, Waxman S, Wekerle H, Williams A, Wood J, Yang Y, Zivin J. Contributor's List. 2007, vii-ix. DOI: 10.1016/b978-012369509-3.50001-9.Chapters13 Hemorrhagic Brain Disease
DiLuna M, Bilguvar K, Tanriover G, Gunel M. 13 Hemorrhagic Brain Disease. 2007, 187-205. DOI: 10.1016/b978-012369509-3.50015-9.Chapters