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Biallelic mutations in human DCC cause developmental split-brain syndrome.
Jamuar SS, Schmitz-Abe K, D'Gama AM, Drottar M, Chan WM, Peeva M, Servattalab S, Lam AN, Delgado MR, Clegg NJ, Zayed ZA, Dogar MA, Alorainy IA, Jamea AA, Abu-Amero K, Griebel M, Ward W, Lein ES, Markianos K, Barkovich AJ, Robson CD, Grant PE, Bosley TM, Engle EC, Walsh CA, Yu TW. Jamuar SS, et al. Among authors: drottar m. Nat Genet. 2017 Apr;49(4):606-612. doi: 10.1038/ng.3804. Epub 2017 Feb 27. Nat Genet. 2017. PMID: 28250456 Free PMC article.
Altered White Matter Organization in the TUBB3 E410K Syndrome.
Grant PE, Im K, Ahtam B, Laurentys CT, Chan WM, Brainard M, Chew S, Drottar M, Robson CD, Drmic I, Engle EC. Grant PE, et al. Among authors: drottar m. Cereb Cortex. 2019 Jul 22;29(8):3561-3576. doi: 10.1093/cercor/bhy231. Cereb Cortex. 2019. PMID: 30272120 Free PMC article.
White Matter Alterations in Infants at Risk for Developmental Dyslexia.
Langer N, Peysakhovich B, Zuk J, Drottar M, Sliva DD, Smith S, Becker BL, Grant PE, Gaab N. Langer N, et al. Among authors: drottar m. Cereb Cortex. 2017 Feb 1;27(2):1027-1036. doi: 10.1093/cercor/bhv281. Cereb Cortex. 2017. PMID: 26643353 Free PMC article.
Can cerebellar and brainstem apparent diffusion coefficient (ADC) values predict neuromotor outcome in term neonates with hypoxic-ischemic encephalopathy (HIE) treated with hypothermia?
Arca-Díaz G, Re TJ, Drottar M, Fortuno CR, De Macedo-Rodrigues K, Im K, Figueras-Aloy J, Grant PE. Arca-Díaz G, et al. Among authors: drottar m. PLoS One. 2017 Jul 7;12(7):e0178510. doi: 10.1371/journal.pone.0178510. eCollection 2017. PLoS One. 2017. PMID: 28686592 Free PMC article.
Commissural axons of the mouse cochlear nucleus.
Brown MC, Drottar M, Benson TE, Darrow K. Brown MC, et al. Among authors: drottar m. J Comp Neurol. 2013 May 1;521(7):1683-96. doi: 10.1002/cne.23257. J Comp Neurol. 2013. PMID: 23124982 Free PMC article.