Goate AM - Search Results

1

Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.

Ghani M, Reitz C, Cheng R, Vardarajan BN, Jun G, Sato C, Naj A, Rajbhandary R, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, Crane PK, Buxbaum JD, Murrell JR, Raj T, Ertekin-Taner N, Logue M, Baldwin CT, Green RC, Barnes LL, Cantwell LB, Fallin MD, Go RC, Griffith PA, Obisesan TO, Manly JJ, Lunetta KL, Kamboh MI, Lopez OL, Bennett DA, Hendrie H, Hall KS, Goate AM, Byrd GS, Kukull WA, Foroud TM, Haines JL, Farrer LA, Pericak-Vance MA, Lee JH, Schellenberg GD, St George-Hyslop P, Mayeux R, Rogaeva E; Alzheimer’s Disease Genetics Consortium. Ghani M, et al. Among authors: goate am. JAMA Neurol. 2015 Nov;72(11):1313-23. doi: 10.1001/jamaneurol.2015.1700. JAMA Neurol. 2015. PMID: 26366463 Free PMC article.

2

Molecular genetics of Alzheimer's disease.

Clark RF, Goate AM. Clark RF, et al. Among authors: goate am. Arch Neurol. 1993 Nov;50(11):1164-72. doi: 10.1001/archneur.1993.00540110044004. Arch Neurol. 1993. PMID: 8215975 Review.

3

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

4

Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation.

Lopera F, Ardilla A, Martínez A, Madrigal L, Arango-Viana JC, Lemere CA, Arango-Lasprilla JC, Hincapíe L, Arcos-Burgos M, Ossa JE, Behrens IM, Norton J, Lendon C, Goate AM, Ruiz-Linares A, Rosselli M, Kosik KS. Lopera F, et al. Among authors: goate am. JAMA. 1997 Mar 12;277(10):793-9. JAMA. 1997. PMID: 9052708

5

Exploring the etiology of Alzheimer disease using molecular genetics.

Lendon CL, Ashall F, Goate AM. Lendon CL, et al. Among authors: goate am. JAMA. 1997 Mar 12;277(10):825-31. JAMA. 1997. PMID: 9052714 Review.

6

Genetic association studies between dementia of the Alzheimer's type and three receptors for apolipoprotein E in a Caucasian population.

Lendon CL, Talbot CJ, Craddock NJ, Han SW, Wragg M, Morris JC, Goate AM. Lendon CL, et al. Among authors: goate am. Neurosci Lett. 1997 Feb 7;222(3):187-90. doi: 10.1016/s0304-3940(97)13381-x. Neurosci Lett. 1997. PMID: 9148246

7

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.

8

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

9

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

10

Failure to replicate a protective effect of allele 2 of NACP/alpha-synuclein polymorphism in Alzheimer's disease: an association study.

Hellman NE, Grant EA, Goate AM. Hellman NE, et al. Among authors: goate am. Ann Neurol. 1998 Aug;44(2):278-81. doi: 10.1002/ana.410440223. Ann Neurol. 1998. PMID: 9708555

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