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Page 1
The heritability and genetics of frontotemporal lobar degeneration.
Rohrer JD, Guerreiro R, Vandrovcova J, Uphill J, Reiman D, Beck J, Isaacs AM, Authier A, Ferrari R, Fox NC, Mackenzie IR, Warren JD, de Silva R, Holton J, Revesz T, Hardy J, Mead S, Rossor MN. Rohrer JD, et al. Neurology. 2009 Nov 3;73(18):1451-6. doi: 10.1212/WNL.0b013e3181bf997a. Neurology. 2009. PMID: 19884572 Free PMC article.
Presymptomatic studies in genetic frontotemporal dementia.
Rohrer JD, Warren JD, Fox NC, Rossor MN. Rohrer JD, et al. Rev Neurol (Paris). 2013 Oct;169(10):820-4. doi: 10.1016/j.neurol.2013.07.010. Epub 2013 Sep 4. Rev Neurol (Paris). 2013. PMID: 24012408 Free PMC article. Review.
An Automated Toolbox to Predict Single Subject Atrophy in Presymptomatic Granulin Mutation Carriers.
Premi E, Costa T, Gazzina S, Benussi A, Cauda F, Gasparotti R, Archetti S, Alberici A, van Swieten JC, Sanchez-Valle R, Moreno F, Santana I, Laforce R, Ducharme S, Graff C, Galimberti D, Masellis M, Tartaglia C, Rowe JB, Finger E, Tagliavini F, de Mendonça A, Vandenberghe R, Gerhard A, Butler CR, Danek A, Synofzik M, Levin J, Otto M, Ghidoni R, Frisoni G, Sorbi S, Peakman G, Todd E, Bocchetta M, Rohrer JD, Borroni B; GENFI Consortium Members. Premi E, et al. Among authors: rohrer jd. J Alzheimers Dis. 2022;86(1):205-218. doi: 10.3233/JAD-215447. J Alzheimers Dis. 2022. PMID: 35068455
Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation.
Alner K, Hyare H, Mead S, Rudge P, Wroe S, Rohrer JD, Ridgway GR, Ourselin S, Clarkson M, Hunt H, Fox NC, Webb T, Collinge J, Cipolotti L. Alner K, et al. Among authors: rohrer jd. J Neurol Neurosurg Psychiatry. 2012 Jan;83(1):109-14. doi: 10.1136/jnnp-2011-300167. Epub 2011 Aug 17. J Neurol Neurosurg Psychiatry. 2012. PMID: 21849340
A practical approach to diagnosing adult onset leukodystrophies.
Ahmed RM, Murphy E, Davagnanam I, Parton M, Schott JM, Mummery CJ, Rohrer JD, Lachmann RH, Houlden H, Fox NC, Chataway J. Ahmed RM, et al. Among authors: rohrer jd. J Neurol Neurosurg Psychiatry. 2014 Jul;85(7):770-81. doi: 10.1136/jnnp-2013-305888. Epub 2013 Dec 19. J Neurol Neurosurg Psychiatry. 2014. PMID: 24357685 No abstract available.
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases.
Ferrari R, Wang Y, Vandrovcova J, Guelfi S, Witeolar A, Karch CM, Schork AJ, Fan CC, Brewer JB; International FTD-Genomics Consortium (IFGC),; International Parkinson's Disease Genomics Consortium (IPDGC),; International Genomics of Alzheimer's Project (IGAP),; Momeni P, Schellenberg GD, Dillon WP, Sugrue LP, Hess CP, Yokoyama JS, Bonham LW, Rabinovici GD, Miller BL, Andreassen OA, Dale AM, Hardy J, Desikan RS. Ferrari R, et al. J Neurol Neurosurg Psychiatry. 2017 Feb;88(2):152-164. doi: 10.1136/jnnp-2016-314411. Epub 2016 Nov 29. J Neurol Neurosurg Psychiatry. 2017. PMID: 27899424 Free PMC article.
386 results