Goate AM - Search Results

1

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.

Behrens MI, Mukherjee O, Tu PH, Liscic RM, Grinberg LT, Carter D, Paulsmeyer K, Taylor-Reinwald L, Gitcho M, Norton JB, Chakraverty S, Goate AM, Morris JC, Cairns NJ. Behrens MI, et al. Among authors: goate am. Alzheimer Dis Assoc Disord. 2007 Jan-Mar;21(1):1-7. doi: 10.1097/WAD.0b013e31803083f2. Alzheimer Dis Assoc Disord. 2007. PMID: 17334266

2

No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant.

Wragg MA, Talbot CJ, Morris JC, Lendon CL, Goate AM. Wragg MA, et al. Among authors: goate am. Neurosci Lett. 1995 Dec 8;201(2):107-10. doi: 10.1016/0304-3940(95)12146-3. Neurosci Lett. 1995. PMID: 8848229

3

E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.

Lendon CL, Martinez A, Behrens IM, Kosik KS, Madrigal L, Norton J, Neuman R, Myers A, Busfield F, Wragg M, Arcos M, Arango Viana JC, Ossa J, Ruiz A, Goate AM, Lopera F. Lendon CL, et al. Among authors: goate am. Hum Mutat. 1997;10(3):186-95. doi: 10.1002/(SICI)1098-1004(1997)10:3<186::AID-HUMU2>3.0.CO;2-H. Hum Mutat. 1997. PMID: 9298817

4

Notch3 mutations and the potential for diagnostic testing for CADASIL.

Goate AM, Morris JC. Goate AM, et al. Lancet. 1997 Nov 22;350(9090):1490. doi: 10.1016/S0140-6736(97)22047-7. Lancet. 1997. PMID: 9388391 No abstract available.

5

Clinicopathologic studies in cognitively healthy aging and Alzheimer's disease: relation of histologic markers to dementia severity, age, sex, and apolipoprotein E genotype.

Berg L, McKeel DW Jr, Miller JP, Storandt M, Rubin EH, Morris JC, Baty J, Coats M, Norton J, Goate AM, Price JL, Gearing M, Mirra SS, Saunders AM. Berg L, et al. Among authors: goate am. Arch Neurol. 1998 Mar;55(3):326-35. doi: 10.1001/archneur.55.3.326. Arch Neurol. 1998. PMID: 9520006

6

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

Lendon CL, Lynch T, Norton J, McKeel DW Jr, Busfield F, Craddock N, Chakraverty S, Gopalakrishnan G, Shears SD, Grimmett W, Wilhelmsen KC, Hansen L, Morris JC, Goate AM. Lendon CL, et al. Among authors: goate am. Neurology. 1998 Jun;50(6):1546-55. doi: 10.1212/wnl.50.6.1546. Neurology. 1998. PMID: 9633693

7

Tau polymorphisms are not associated with Alzheimer's disease.

Kwon JM, Nowotny P, Shah PK, Chakraverty S, Norton J, Morris JC, Goate AM. Kwon JM, et al. Among authors: goate am. Neurosci Lett. 2000 Apr 21;284(1-2):77-80. doi: 10.1016/s0304-3940(00)00972-1. Neurosci Lett. 2000. PMID: 10771166

8

Association studies using novel polymorphisms in BACE1 and BACE2.

Nowotny P, Kwon JM, Chakraverty S, Nowotny V, Morris JC, Goate AM. Nowotny P, et al. Among authors: goate am. Neuroreport. 2001 Jul 3;12(9):1799-802. doi: 10.1097/00001756-200107030-00008. Neuroreport. 2001. PMID: 11435901

9

Full genome screen for Alzheimer disease: stage II analysis.

Myers A, Wavrant De-Vrieze F, Holmans P, Hamshere M, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, Ramic D, Knowles H, Morris JC, Williams N, Norton N, Abraham R, Kehoe P, Williams H, Rudrasingham V, Rice F, Giles P, Tunstall N, Jones L, Lovestone S, Williams J, Owen MJ, Hardy J, Goate A. Myers A, et al. Am J Med Genet. 2002 Mar 8;114(2):235-44. doi: 10.1002/ajmg.10183. Am J Med Genet. 2002. PMID: 11857588

10

Apolipoprotein Eepsilon4 modifies Alzheimer's disease onset in an E280A PS1 kindred.

Pastor P, Roe CM, Villegas A, Bedoya G, Chakraverty S, García G, Tirado V, Norton J, Ríos S, Martínez M, Kosik KS, Lopera F, Goate AM. Pastor P, et al. Among authors: goate am. Ann Neurol. 2003 Aug;54(2):163-9. doi: 10.1002/ana.10636. Ann Neurol. 2003. PMID: 12891668

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