Year |
Citation |
Score |
2024 |
Simmonds E, Leonenko G, Yaman U, Bellou E, Myers A, Morgan K, Brookes K, Hardy J, Salih D, Escott-Price V. Chromosome X-wide association study in case control studies of pathologically confirmed Alzheimer's disease in a European population. Translational Psychiatry. 14: 358. PMID 39231932 DOI: 10.1038/s41398-024-03058-9 |
0.546 |
|
2023 |
Rajabli F, Benchek P, Tosto G, Kushch N, Sha J, Bazemore K, Zhu C, Lee WP, Haut J, Hamilton-Nelson KL, Wheeler NR, Zhao Y, Farrell JJ, Grunin MA, Leung YY, ... ... Myers AJ, et al. Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences. PMID 37461624 DOI: 10.1101/2023.07.06.23292311 |
0.821 |
|
2023 |
Baker E, Leonenko G, Schmidt KM, Hill M, Myers AJ, Shoai M, de Rojas I, Tesi N, Holstege H, van der Flier WM, Pijnenburg YAL, Ruiz A, Hardy J, van der Lee S, Escott-Price V. What does heritability of Alzheimer's disease represent? Plos One. 18: e0281440. PMID 37115753 DOI: 10.1371/journal.pone.0281440 |
0.575 |
|
2020 |
Reiman EM, Arboleda-Velasquez JF, Quiroz YT, Huentelman MJ, Beach TG, Caselli RJ, Chen Y, Su Y, Myers AJ, Hardy J, Paul Vonsattel J, Younkin SG, Bennett DA, De Jager PL, Larson EB, et al. Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study. Nature Communications. 11: 667. PMID 32015339 DOI: 10.1038/S41467-019-14279-8 |
0.597 |
|
2019 |
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Myers AJ, et al. Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. PMID 31417202 DOI: 10.1038/s41588-019-0495-7 |
0.748 |
|
2019 |
Huentelman M, De Both M, Jepsen W, Piras IS, Talboom JS, Willeman M, Reiman EM, Hardy J, Myers AJ. Common BACE2 Polymorphisms are Associated with Altered Risk for Alzheimer's Disease and CSF Amyloid Biomarkers in APOE ε4 Non-Carriers. Scientific Reports. 9: 9640. PMID 31270419 DOI: 10.1038/S41598-019-45896-4 |
0.604 |
|
2019 |
Talboom JS, Håberg AK, De Both MD, Naymik MA, Schrauwen I, Lewis CR, Bertinelli SF, Hammersland C, Fritz MA, Myers AJ, Hay M, Barnes CA, Glisky E, Ryan L, Huentelman MJ. Family history of Alzheimer's disease alters cognition and is modified by medical and genetic factors. Elife. 8. PMID 31210642 DOI: 10.7554/Elife.46179 |
0.465 |
|
2019 |
Escott-Price V, Baker E, Shoai M, Leonenko G, Myers AJ, Huentelman M, Hardy J. Genetic analysis suggests high misassignment rates in clinical Alzheimer's cases and controls. Neurobiology of Aging. 77: 178-182. PMID 30851568 DOI: 10.1016/J.Neurobiolaging.2018.12.002 |
0.53 |
|
2019 |
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Myers AJ, et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. 51: 414-430. PMID 30820047 DOI: 10.1038/s41588-019-0358-2 |
0.783 |
|
2019 |
Talboom JS, Håberg A, Both MDD, Naymik MA, Schrauwen I, Lewis CR, Bertinelli SF, Hammersland C, Fritz MA, Myers AJ, Hay M, Barnes CA, Glisky E, Ryan L, Huentelman MJ. Author response: Family history of Alzheimer’s disease alters cognition and is modified by medical and genetic factors Elife. DOI: 10.7554/Elife.46179.018 |
0.327 |
|
2018 |
Petyuk VA, Chang R, Ramirez-Restrepo M, Beckmann ND, Henrion MYR, Piehowski PD, Zhu K, Wang S, Clarke J, Huentelman MJ, Xie F, Andreev V, Engel A, Guettoche T, Navarro L, ... ... Myers AJ, et al. The human brainome: network analysis identifies HSPA2 as a novel Alzheimer's disease target. Brain : a Journal of Neurology. PMID 30137212 DOI: 10.1093/Brain/Awy215 |
0.556 |
|
2017 |
Escott-Price V, Myers AJ, Huentelman M, Hardy J. Polygenic Risk Score Analysis of Pathologically Confirmed Alzheimer's Disease. Annals of Neurology. PMID 28727176 DOI: 10.1002/Ana.24999 |
0.543 |
|
2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Myers AJ, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.795 |
|
2014 |
Naj AC, Jun G, Reitz C, Kunkle BW, Perry W, Park YS, Beecham GW, Rajbhandary RA, Hamilton-Nelson KL, Wang LS, Kauwe JS, Huentelman MJ, Myers AJ, Bird TD, Boeve BF, et al. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. Jama Neurology. 71: 1394-404. PMID 25199842 DOI: 10.1001/Jamaneurol.2014.1491 |
0.784 |
|
2014 |
Beecham GW, Hamilton K, Naj AC, Martin ER, Huentelman M, Myers AJ, Corneveaux JJ, Hardy J, Vonsattel JP, Younkin SG, Bennett DA, De Jager PL, Larson EB, Crane PK, Kamboh MI, et al. Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Plos Genetics. 10: e1004606. PMID 25188341 DOI: 10.1371/Journal.Pgen.1004606 |
0.6 |
|
2014 |
Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, ... ... Myers AJ, et al. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Plos One. 9: e94661. PMID 24922517 DOI: 10.1371/Journal.Pone.0094661 |
0.818 |
|
2013 |
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-Wells TA, Jones N, Smith AV, Chouraki V, ... ... Myers AJ, et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nature Genetics. 45: 1452-8. PMID 24162737 DOI: 10.1038/Ng.2802 |
0.823 |
|
2013 |
Zhang B, Gaiteri C, Bodea LG, Wang Z, McElwee J, Podtelezhnikov AA, Zhang C, Xie T, Tran L, Dobrin R, Fluder E, Clurman B, Melquist S, Narayanan M, Suver C, ... ... Myers AJ, et al. Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's disease. Cell. 153: 707-20. PMID 23622250 DOI: 10.1016/J.Cell.2013.03.030 |
0.384 |
|
2013 |
Lim AS, Myers AJ, Yu L, Buchman AS, Duffy JF, De Jager PL, Bennett DA. Sex difference in daily rhythms of clock gene expression in the aged human cerebral cortex. Journal of Biological Rhythms. 28: 117-29. PMID 23606611 DOI: 10.1177/0748730413478552 |
0.302 |
|
2013 |
Giraldo M, Lopera F, Siniard AL, Corneveaux JJ, Schrauwen I, Carvajal J, Muñoz C, Ramirez-Restrepo M, Gaiteri C, Myers AJ, Caselli RJ, Kosik KS, Reiman EM, Huentelman MJ. Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease. Neurobiology of Aging. 34: 2077.e11-8. PMID 23582655 DOI: 10.1016/J.Neurobiolaging.2013.02.016 |
0.548 |
|
2013 |
Holton P, Ryten M, Nalls M, Trabzuni D, Weale ME, Hernandez D, Crehan H, Gibbs JR, Mayeux R, Haines JL, Farrer LA, Pericak-Vance MA, Schellenberg GD, Ramirez-Restrepo M, ... ... Myers AJ, et al. Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci. Annals of Human Genetics. 77: 85-105. PMID 23360175 DOI: 10.1111/Ahg.12000 |
0.608 |
|
2013 |
Myers AJ. AD gene 3-D: moving past single layer genetic information to map novel loci involved in Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 33: S15-22. PMID 22659613 DOI: 10.3233/JAD-2012-129013 |
0.428 |
|
2012 |
Swaminathan S, Huentelman MJ, Corneveaux JJ, Myers AJ, Faber KM, Foroud T, Mayeux R, Shen L, Kim S, Turk M, Hardy J, Reiman EM, Saykin AJ. Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Plos One. 7: e50640. PMID 23227193 DOI: 10.1371/Journal.Pone.0050640 |
0.642 |
|
2012 |
Lim AS, Chang AM, Shulman JM, Raj T, Chibnik LB, Cain SW, Rothamel K, Benoist C, Myers AJ, Czeisler CA, Buchman AS, Bennett DA, Duffy JF, Saper CB, De Jager PL. A common polymorphism near PER1 and the timing of human behavioral rhythms. Annals of Neurology. 72: 324-34. PMID 23034908 DOI: 10.1002/Ana.23636 |
0.38 |
|
2012 |
Allen M, Zou F, Chai HS, Younkin CS, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN, Nair AA, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus KG, Palusak R, ... ... Myers AJ, et al. Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology. 79: 221-8. PMID 22722634 DOI: 10.1212/Wnl.0B013E3182605801 |
0.77 |
|
2012 |
Myers AJ, Nemeroff CB. APOE: a risk factor for multiple disorders. The American Journal of Geriatric Psychiatry : Official Journal of the American Association For Geriatric Psychiatry. 20: 545-8. PMID 22627179 DOI: 10.1097/Jgp.0B013E318259B9A5 |
0.333 |
|
2012 |
Andreev VP, Petyuk VA, Brewer HM, Karpievitch YV, Xie F, Clarke J, Camp D, Smith RD, Lieberman AP, Albin RL, Nawaz Z, El Hokayem J, Myers AJ. Label-free quantitative LC-MS proteomics of Alzheimer's disease and normally aged human brains. Journal of Proteome Research. 11: 3053-67. PMID 22559202 DOI: 10.1021/Pr3001546 |
0.396 |
|
2012 |
Keenan BT, Shulman JM, Chibnik LB, Raj T, Tran D, Sabuncu MR, Allen AN, Corneveaux JJ, Hardy JA, Huentelman MJ, Lemere CA, Myers AJ, Nicholson-Weller A, Reiman EM, et al. A coding variant in CR1 interacts with APOE-ε4 to influence cognitive decline. Human Molecular Genetics. 21: 2377-88. PMID 22343410 DOI: 10.1093/Hmg/Dds054 |
0.535 |
|
2012 |
Myers AJ. The age of the "ome": genome, transcriptome and proteome data set collection and analysis. Brain Research Bulletin. 88: 294-301. PMID 22142972 DOI: 10.1016/J.Brainresbull.2011.11.015 |
0.401 |
|
2012 |
De Jager PL, Shulman JM, Chibnik LB, Keenan BT, Raj T, Wilson RS, Yu L, Leurgans SE, Tran D, Aubin C, Anderson CD, Biffi A, Corneveaux JJ, Huentelman MJ, ... ... Myers AJ, et al. A genome-wide scan for common variants affecting the rate of age-related cognitive decline. Neurobiology of Aging. 33: 1017.e1-15. PMID 22054870 DOI: 10.1016/J.Neurobiolaging.2011.09.033 |
0.424 |
|
2012 |
Myers A, Ramirez-Restrepo M, Engel A. O3-11-02: eQTL regulation by NATs in Alzheimer's disease Alzheimer's & Dementia. 8: P451-P451. DOI: 10.1016/J.Jalz.2012.05.1201 |
0.398 |
|
2012 |
Swaminathan S, Huentelman M, Corneveaux J, Myers A, Faber K, Foroud T, Mayeux R, Shen L, Kim S, Turk M, Hardy J, Reiman E, Saykin A. Replication and meta-analysis of the CHRFAM7A copy number variant in a cohort of clinically characterized and neuropathologically verified individuals Alzheimers & Dementia. 8: 678. DOI: 10.1016/J.Jalz.2012.05.101 |
0.462 |
|
2011 |
Naj AC, Jun G, Beecham GW, Wang LS, Vardarajan BN, Buros J, Gallins PJ, Buxbaum JD, Jarvik GP, Crane PK, Larson EB, Bird TD, Boeve BF, Graff-Radford NR, De Jager PL, ... ... Myers AJ, et al. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nature Genetics. 43: 436-41. PMID 21460841 DOI: 10.1038/Ng.801 |
0.739 |
|
2011 |
Chibnik LB, Shulman JM, Leurgans SE, Schneider JA, Wilson RS, Tran D, Aubin C, Buchman AS, Heward CB, Myers AJ, Hardy JA, Huentelman MJ, Corneveaux JJ, Reiman EM, Evans DA, et al. CR1 is associated with amyloid plaque burden and age-related cognitive decline. Annals of Neurology. 69: 560-9. PMID 21391232 DOI: 10.1002/Ana.22277 |
0.56 |
|
2011 |
Liang WS, Chen K, Lee W, Sidhar K, Corneveaux JJ, Allen AN, Myers A, Villa S, Meechoovet B, Pruzin J, Bandy D, Fleisher AS, Langbaum JB, Huentelman MJ, Jensen K, et al. Association between GAB2 haplotype and higher glucose metabolism in Alzheimer's disease-affected brain regions in cognitively normal APOEε4 carriers. Neuroimage. 54: 1896-902. PMID 20888920 DOI: 10.1016/J.Neuroimage.2010.09.066 |
0.412 |
|
2011 |
Liang WS, Chen K, Lee W, Sidhar K, Corneveaux JJ, Allen AN, Myers A, Villa S, Meechoovet B, Pruzin J, Bandy D, Fleisher AS, Langbaum JBS, Huentelman MJ, Jensen K, et al. Corrigendum to "Association between GAB2 haplotype and higher glucose metabolism in Alzheimer's disease-affected brain regions in cognitively normal APOEε4 carriers" [NeuroImage 54/3 (2011) 1896-1902] Neuroimage. 58: 974. DOI: 10.1016/J.Neuroimage.2011.07.055 |
0.389 |
|
2011 |
Keenan B, Shulman J, Chibnik L, Corneveaux J, Allen A, Myers A, Hardy J, Huentelman M, Reiman E, Evans D, Bennett D, Jager PD. A candidate causal variant in the CR1 locus Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.2389 |
0.44 |
|
2010 |
Webster J, Reiman EM, Zismann VL, Joshipura KD, Pearson JV, Hu-Lince D, Huentelman MJ, Craig DW, Coon KD, Beach T, Rohrer KC, Zhao AS, Leung D, Bryden L, Marlowe L, ... ... Myers A, et al. Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis. International Journal of Molecular Epidemiology and Genetics. 1: 19-30. PMID 21537449 |
0.551 |
|
2010 |
Corneveaux JJ, Myers AJ, Allen AN, Pruzin JJ, Ramirez M, Engel A, Nalls MA, Chen K, Lee W, Chewning K, Villa SE, Meechoovet HB, Gerber JD, Frost D, Benson HL, et al. Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Human Molecular Genetics. 19: 3295-301. PMID 20534741 DOI: 10.1093/Hmg/Ddq221 |
0.619 |
|
2010 |
Corneveaux JJ, Liang WS, Reiman EM, Webster JA, Myers AJ, Zismann VL, Joshipura KD, Pearson JV, Hu-Lince D, Craig DW, Coon KD, Dunckley T, Bandy D, Lee W, Chen K, et al. Evidence for an association between KIBRA and late-onset Alzheimer's disease. Neurobiology of Aging. 31: 901-9. PMID 18789830 DOI: 10.1016/J.Neurobiolaging.2008.07.014 |
0.514 |
|
2010 |
Huentelman M, Corneveaux J, Myers A, Allen A, Pruzin J, Nalls M, Chibnik L, Singleton A, Craig D, Van Keuren-Jensen K, Dunckley T, Bennett D, DeJager P, Hardy J, Reiman E. S4-03-02: Genome-Wide Association Study for Alzheimer's Disease Risk in a Large Cohort Of Clinically Characterized And Neuropathologically Verified Subjects Alzheimer's & Dementia. 6: e13-e13. DOI: 10.1016/J.Jalz.2010.08.041 |
0.575 |
|
2009 |
Webster JA, Gibbs JR, Clarke J, Ray M, Zhang W, Holmans P, Rohrer K, Zhao A, Marlowe L, Kaleem M, McCorquodale DS, Cuello C, Leung D, Bryden L, Nath P, ... ... Myers AJ, et al. Genetic control of human brain transcript expression in Alzheimer disease. American Journal of Human Genetics. 84: 445-58. PMID 19361613 DOI: 10.1016/J.Ajhg.2009.03.011 |
0.569 |
|
2008 |
Hong MG, Myers AJ, Magnusson PK, Prince JA. Transcriptome-wide assessment of human brain and lymphocyte senescence. Plos One. 3: e3024. PMID 18714388 DOI: 10.1371/Journal.Pone.0003024 |
0.302 |
|
2008 |
Webster JA, Myers AJ, Pearson JV, Craig DW, Hu-Lince D, Coon KD, Zismann VL, Beach T, Leung D, Bryden L, Halperin RF, Marlowe L, Kaleem M, Huentelman MJ, Joshipura K, et al. Sorl1 as an Alzheimer's disease predisposition gene? Neuro-Degenerative Diseases. 5: 60-4. PMID 17975299 DOI: 10.1159/000110789 |
0.566 |
|
2008 |
Myers AJ. S2-03-02: The Tau top 10: 10 things you need to know about the genetics of MAPT and cognitive decline Alzheimer's & Dementia. 4: T126-T126. DOI: 10.1016/J.Jalz.2008.05.284 |
0.341 |
|
2008 |
McCorquodale DS, Myers AJ, Lemmon V. P3-241: Assigning biological significance to eQTLs in late-onset Alzheimer's disease Alzheimer's & Dementia. 4: T591-T591. DOI: 10.1016/J.Jalz.2008.05.1808 |
0.486 |
|
2007 |
Myers AJ, Gibbs JR, Webster JA, Rohrer K, Zhao A, Marlowe L, Kaleem M, Leung D, Bryden L, Nath P, Zismann VL, Joshipura K, Huentelman MJ, Hu-Lince D, Coon KD, et al. A survey of genetic human cortical gene expression. Nature Genetics. 39: 1494-9. PMID 17982457 DOI: 10.1038/Ng.2007.16 |
0.501 |
|
2007 |
Hamshere ML, Holmans PA, Avramopoulos D, Bassett SS, Blacker D, Bertram L, Wiener H, Rochberg N, Tanzi RE, Myers A, Wavrant-De Vrièze F, Go R, Fallin D, Lovestone S, Hardy J, et al. Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Human Molecular Genetics. 16: 2703-12. PMID 17725986 DOI: 10.1093/Hmg/Ddm224 |
0.647 |
|
2007 |
Kaleem M, Zhao A, Hamshere M, Myers AJ. Identification of a novel valosin-containing protein polymorphism in late-onset Alzheimer's disease. Neuro-Degenerative Diseases. 4: 376-81. PMID 17622780 DOI: 10.1159/000105158 |
0.488 |
|
2007 |
Reiman EM, Webster JA, Myers AJ, Hardy J, Dunckley T, Zismann VL, Joshipura KD, Pearson JV, Hu-Lince D, Huentelman MJ, Craig DW, Coon KD, Liang WS, Herbert RH, Beach T, et al. GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. Neuron. 54: 713-20. PMID 17553421 DOI: 10.1016/J.Neuron.2007.05.022 |
0.625 |
|
2007 |
De Ferrari GV, Papassotiropoulos A, Biechele T, Wavrant De-Vrieze F, Avila ME, Major MB, Myers A, Sáez K, HenrÃquez JP, Zhao A, Wollmer MA, Nitsch RM, Hock C, Morris CM, Hardy J, et al. Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 104: 9434-9. PMID 17517621 DOI: 10.1073/Pnas.0603523104 |
0.627 |
|
2007 |
Hollingworth P, Hamshere ML, Holmans PA, O'Donovan MC, Sims R, Powell J, Lovestone S, Myers A, DeVrieze FW, Hardy J, Goate A, Owen M, Williams J. Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 841-8. PMID 17492769 DOI: 10.1002/Ajmg.B.30515 |
0.658 |
|
2007 |
Coon KD, Myers AJ, Craig DW, Webster JA, Pearson JV, Lince DH, Zismann VL, Beach TG, Leung D, Bryden L, Halperin RF, Marlowe L, Kaleem M, Walker DG, Ravid R, et al. A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. The Journal of Clinical Psychiatry. 68: 613-8. PMID 17474819 DOI: 10.4088/Jcp.V68N0419 |
0.656 |
|
2007 |
Hardy J, Myers A. Genetic variability in expression of proteins and the risk of sporadic neurologic diseases Neurology. 68: 632-633. PMID 17325268 DOI: 10.1212/01.Wnl.0000256793.58438.C4 |
0.564 |
|
2007 |
Myers AJ, Pittman AM, Zhao AS, Rohrer K, Kaleem M, Marlowe L, Lees A, Leung D, McKeith IG, Perry RH, Morris CM, Trojanowski JQ, Clark C, Karlawish J, Arnold S, et al. The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts. Neurobiology of Disease. 25: 561-70. PMID 17174556 DOI: 10.1016/J.Nbd.2006.10.018 |
0.582 |
|
2006 |
Marlowe L, Peila R, Benke KS, Hardy J, White LR, Launer LJ, Myers A. Insulin-degrading enzyme haplotypes affect insulin levels but not dementia risk. Neuro-Degenerative Diseases. 3: 320-6. PMID 17192720 DOI: 10.1159/000097300 |
0.402 |
|
2006 |
Hardy J, Pittman A, Myers A, Fung HC, de Silva R, Duckworth J. Tangle diseases and the tau haplotypes. Alzheimer Disease and Associated Disorders. 20: 60-2. PMID 16493238 DOI: 10.1097/01.Wad.0000201853.54493.D8 |
0.57 |
|
2006 |
Grupe A, Li Y, Rowland C, Nowotny P, Hinrichs AL, Smemo S, Kauwe JS, Maxwell TJ, Cherny S, Doil L, Tacey K, van Luchene R, Myers A, Wavrant-De Vrièze F, Kaleem M, et al. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. American Journal of Human Genetics. 78: 78-88. PMID 16385451 DOI: 10.1086/498851 |
0.748 |
|
2006 |
Smemo S, Nowotny P, Hinrichs AL, Kauwe JS, Cherny S, Erickson K, Myers AJ, Kaleem M, Marlowe L, Gibson AM, Hollingworth P, O'Donovan MC, Morris CM, Holmans P, Lovestone S, et al. Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. Annals of Neurology. 59: 21-6. PMID 16278862 DOI: 10.1002/Ana.20673 |
0.753 |
|
2006 |
Wollmer MA, Nitsch RM, Hock C, Papassotiropoulos A, Marlowe L, Peila R, Benke KS, Figueiredo-Pereira ME, Robakis NK, Hardy J, White LR, Wu YR, Arnaud L, Gibbs JR, Launer LJ, ... Myers A, et al. Contents Vol. 3, 2006 Neurodegenerative Diseases. 3: 359-360. DOI: 10.1159/000098410 |
0.324 |
|
2006 |
Wollmer MA, Nitsch RM, Hock C, Papassotiropoulos A, Marlowe L, Peila R, Benke KS, Figueiredo-Pereira ME, Robakis NK, Hardy J, White LR, Wu YR, Arnaud L, Gibbs JR, Launer LJ, ... Myers A, et al. Subject Index Vol. 3, 2006 Complexus. 3: 254-254. DOI: 10.1159/000098409 |
0.331 |
|
2006 |
Escott-Price V, Baker EA, Myers A, Huentelman MJ, Hardy J. P2-307: GENETIC ANALYSIS SUGGESTS HIGH MISASSIGNMENT RATE IN BOTH ALZHEIMER'S DISEASE CASES AND CONTROLS Alzheimer's & Dementia. 14: P800-P800. DOI: 10.1016/J.Jalz.2018.06.997 |
0.571 |
|
2006 |
Hollingworth P, Hamshere M, Holmans P, Jones L, O'Donavan M, Myers A, Hardy J, Goate A, Lovestone S, Owen M, Williams J. P1-331: Familiality and linkage analysis of behavioral symptoms and age at disease onset in late-onset Alzheimer's disease Alzheimer's & Dementia. 2: S194-S194. DOI: 10.1016/J.Jalz.2006.05.709 |
0.618 |
|
2006 |
Pittman A, Myers AJ, Hardy J, Wood NW, Lees A, de Silva R. P3-161: Increased MAPT
expression is associated with progressive supranuclear palsy Alzheimer's & Dementia. 2: S421-S421. DOI: 10.1016/J.Jalz.2006.05.1429 |
0.439 |
|
2006 |
Myers AJ, Pittman AM, Rohrer K, Zhao A, Leung D, Bryden L, Kaleem M, Marlowe L, Chung Fung H, Lees A, Morris CM, de Silva R, Hardy JA. O2-02-02 Alzheimer's & Dementia. 2: S32. DOI: 10.1016/J.Jalz.2006.05.112 |
0.439 |
|
2005 |
Hardy J, Pittman A, Myers A, Gwinn-Hardy K, Fung HC, de Silva R, Hutton M, Duckworth J. Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens. Biochemical Society Transactions. 33: 582-5. PMID 16042549 DOI: 10.1042/Bst0330582 |
0.404 |
|
2005 |
Myers AJ, Kaleem M, Marlowe L, Pittman AM, Lees AJ, Fung HC, Duckworth J, Leung D, Gibson A, Morris CM, de Silva R, Hardy J. The H1c haplotype at the MAPT locus is associated with Alzheimer's disease. Human Molecular Genetics. 14: 2399-404. PMID 16000317 DOI: 10.1093/Hmg/Ddi241 |
0.627 |
|
2005 |
Nowotny P, Hinrichs AL, Smemo S, Kauwe JS, Maxwell T, Holmans P, Hamshere M, Turic D, Jehu L, Hollingworth P, Moore P, Bryden L, Myers A, Doil LM, Tacey KM, et al. Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 136: 62-8. PMID 15858813 DOI: 10.1002/Ajmg.B.30186 |
0.766 |
|
2005 |
Pittman AM, Myers AJ, Abou-Sleiman P, Fung HC, Kaleem M, Marlowe L, Duckworth J, Leung D, Williams D, Kilford L, Thomas N, Morris CM, Dickson D, Wood NW, Hardy J, et al. Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration. Journal of Medical Genetics. 42: 837-46. PMID 15792962 DOI: 10.1136/Jmg.2005.031377 |
0.518 |
|
2005 |
Fung HC, Evans J, Evans W, Duckworth J, Pittman A, de Silva R, Myers A, Hardy J. The architecture of the tau haplotype block in different ethnicities. Neuroscience Letters. 377: 81-4. PMID 15740841 DOI: 10.1016/J.Neulet.2004.11.072 |
0.473 |
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2005 |
Holmans P, Hamshere M, Hollingworth P, Rice F, Tunstall N, Jones S, Moore P, Wavrant DeVrieze F, Myers A, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, et al. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 135: 24-32. PMID 15729734 DOI: 10.1002/Ajmg.B.30114 |
0.602 |
|
2005 |
Myers AJ, Kaleem M, Marlowe L, Pittman A, Fung HC, Duckworth J, Gibson A, Morris CM, de Silva R, Hardy JA. [P-085]: The H1c haplotype of the MAPT locus is associated with autopsy confirmed late onset Alzheimer's disease Alzheimer's & Dementia. 1: S34-S35. DOI: 10.1016/J.Jalz.2005.06.159 |
0.541 |
|
2004 |
Hardy J, Myers A, Wavrant-De Vrieze F. Problems and solutions in the genetic analysis of late-onset Alzheimer's disease Neurodegenerative Diseases. 1: 213-217. PMID 16908992 DOI: 10.1159/000080988 |
0.569 |
|
2004 |
Evans W, Fung HC, Steele J, Eerola J, Tienari P, Pittman A, Silva RD, Myers A, Vrieze FWD, Singleton A, Hardy J. The tau H2 haplotype is almost exclusively Caucasian in origin Neuroscience Letters. 369: 183-185. PMID 15464261 DOI: 10.1016/J.Neulet.2004.05.119 |
0.411 |
|
2004 |
Pittman AM, Myers AJ, Duckworth J, Bryden L, Hanson M, Abou-Sleiman P, Wood NW, Hardy J, Lees A, de Silva R. The structure of the tau haplotype in controls and in progressive supranuclear palsy. Human Molecular Genetics. 13: 1267-74. PMID 15115761 DOI: 10.1093/Hmg/Ddh138 |
0.545 |
|
2004 |
Busby V, Goossens S, Nowotny P, Hamilton G, Smemo S, Harold D, Turic D, Jehu L, Myers A, Womick M, Woo D, Compton D, Doil LM, Tacey KM, Lau KF, et al. Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease. Neuromolecular Medicine. 5: 133-46. PMID 15075440 DOI: 10.1385/Nmm:5:2:133 |
0.659 |
|
2004 |
Singleton A, Myers A, Hardy J. The law of mass action applied to neurodegenerative disease: A hypothesis concerning the etiology and pathogenesis of complex diseases Human Molecular Genetics. 13: R123-R126. PMID 14976159 DOI: 10.1093/Hmg/Ddh093 |
0.541 |
|
2004 |
Myers AJ, Marshall H, Holmans P, Compton D, Crook RJ, Mander AP, Nowotny P, Smemo S, Dunstan M, Jehu L, Wang JC, Hamshere M, Morris JC, Norton J, Chakraventy S, et al. Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 124: 29-37. PMID 14681909 DOI: 10.1002/Ajmg.B.20036 |
0.646 |
|
2004 |
Braungart E, Gerlach M, Riederer P, Baumeister R, Hoener MC, Silva OABdCe, Vieira SI, Silva EFdCe, Froelich-Fabre S, Skoglund L, Ostojic J, Kilander L, Lindau M, Rebelo S, Hartmann D, ... ... Myers A, et al. DIADEM / Participants Directory Neurodegenerative Diseases. 1: 243-244. DOI: 10.1159/000082213 |
0.33 |
|
2004 |
Leung DG, Gibbs R, Wood WH, Teichberg D, Hardy JA, Becker KG, Myers AJ. P4-165 Microarray analysis of gene expression in the frontal cortex of patients with frontotemporal dementia Neurobiology of Aging. 25: S522. DOI: 10.1016/S0197-4580(04)81723-8 |
0.333 |
|
2004 |
Fung HC, Evans W, Steele J, Morris H, Myers A, Singleton A, Vrièze FW, Hardy J. P4-157 Genetic analysis of a the tau haplotype in the CEPH diversity panel and in Guam disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81715-9 |
0.557 |
|
2004 |
Myers AJ, Gibbs R, Leung D, Wood WH, Teichberg D, Hardy JA, Becker KG. P4-094 Microarray profiling of Alzheimer's disease: findings based on segregation by APOE genotype Neurobiology of Aging. 25: S501. DOI: 10.1016/S0197-4580(04)81652-X |
0.511 |
|
2004 |
Holmans P, Nowotny P, Smemo S, Myers A, Wavrant-DeVrieze F, Hardy J, Lovestone S, Jones L, Williams J, Owen M, Goate A. O3-02-06 Linkage analysis of AD SIB pairs indicates evidence of interaction between genes regulating beta-amyloid degradation Neurobiology of Aging. 25: S55-S56. DOI: 10.1016/S0197-4580(04)80188-X |
0.566 |
|
2004 |
Goate AM, Nowotny P, Hinrichs T, Smemo S, Kawe K, Williams J, Owen M, Holmans P, Jones L, Myers A, De Vrieze FW, Grupe J. S2-01-04 Progress toward the identification of novel genetic risk factors for late onset Alzheimer's disease Neurobiology of Aging. 25: S25-S26. DOI: 10.1016/S0197-4580(04)80082-4 |
0.597 |
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2003 |
Harold D, Peirce T, Moskvina V, Myers A, Jones S, Hollingworth P, Moore P, Lovestone S, Powell J, Foy C, Archer N, Walter S, Edmonson A, McIlroy S, Craig D, et al. Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. Human Genetics. 113: 258-67. PMID 12759818 DOI: 10.1007/S00439-003-0960-2 |
0.686 |
|
2002 |
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, et al. Full genome screen for Alzheimer disease: stage II analysis. American Journal of Medical Genetics. 114: 235-44. PMID 11857588 DOI: 10.1002/Ajmg.10183 |
0.623 |
|
2001 |
Abraham R, Myers A, Wavrant-DeVrieze F, Hamshere ML, Thomas HV, Marshall H, Compton D, Spurlock G, Turic D, Hoogendoorn B, Kwon JM, Petersen RC, Tangalos E, Norton J, Morris JC, et al. Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease. Human Genetics. 109: 646-52. PMID 11810277 DOI: 10.1007/S00439-001-0614-1 |
0.648 |
|
2001 |
Myers AJ, Goate AM. The genetics of late-onset Alzheimer's disease. Current Opinion in Neurology. 14: 433-40. PMID 11470958 DOI: 10.1097/00019052-200108000-00002 |
0.658 |
|
2001 |
Jones L, Abraham R, Myers A, DeVrieze FW, Hamshere MV, Thomas HM, Marshall H, Compton D, Spurlock G, Turic D, Hoogendorn B, Kwon JM, Petersen RC, Tanaglos E, Norton J, et al. Substantial linkage disequilibrium across the insulin degrading enzyme locus but no association with late-onset Alzheimer's disease American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 627-628. |
0.323 |
|
2000 |
Myers A, Holmans P, Marshall H, Kwon J, Meyer D, Ramic D, Shears S, Booth J, DeVrieze FW, Crook R, Hamshere M, Abraham R, Tunstall N, Rice F, Carty S, et al. Susceptibility locus for Alzheimer's disease on chromosome 10. Science (New York, N.Y.). 290: 2304-5. PMID 11125144 DOI: 10.1126/Science.290.5500.2304 |
0.711 |
|
2000 |
Myers AJ, Goate AM, Holmans P, Williams J, Owen MJ, Crook R, Wavrant-De Vrieze F, Hardy JA. Susceptibility locus for late onset Alzheimer's disease on chromosome 10 Neurobiology of Aging. 21: 103. DOI: 10.1016/S0197-4580(00)82261-7 |
0.596 |
|
1997 |
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, et al. E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles. Human Mutation. 10: 186-95. PMID 9298817 DOI: 10.1002/(Sici)1098-1004(1997)10:3<186::Aid-Humu2>3.0.Co;2-H |
0.573 |
|
1997 |
Lendon CL, Myers A, Cumming A, Goate AM, St Clair D. A polymorphism in the presenilin 1 gene does not modify risk for Alzheimer's disease in a cohort with sporadic early onset. Neuroscience Letters. 228: 212-4. PMID 9218645 DOI: 10.1016/S0304-3940(97)00393-5 |
0.65 |
|
1995 |
Clark RF, Hutton M, Fuldner RA, Froelich S, Karran E, Talbot C, Crook R, Lendon C, Prihar G, He C, Korenblat K, Martinez A, Wragg M, Busfield F, Behrens MI, ... Myers A, et al. The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families Nature Genetics. 11: 219-222. PMID 7550356 DOI: 10.1038/Ng1095-219 |
0.661 |
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