| Year |
Citation |
Score |
| 2024 |
Akgun B, Feliciano-Astacio BE, Hamilton-Nelson KL, Scott K, Rivero J, Adams LD, Sanchez JJ, Valladares GS, Tejada S, Bussies PL, Silva-Vergara C, Rodriguez VC, Mena PR, Celis K, Whitehead PG, ... ... Beecham GW, et al. Genome-wide association analysis and admixture mapping in a Puerto Rican cohort supports an Alzheimer disease risk locus on chromosome 12. Frontiers in Aging Neuroscience. 16: 1459796. PMID 39295643 DOI: 10.3389/fnagi.2024.1459796 |
0.368 |
|
| 2024 |
Ray NR, Kumar A, Zaman A, Del Rosario P, Mena PR, Manoochehri M, Stein C, De Vito AN, Sweet RA, Hohman TJ, Cuccaro ML, Beecham GW, Huey ED, Reitz C. Disentangling the genetic underpinnings of neuropsychiatric symptoms in Alzheimer's disease in the Alzheimer's Disease Sequencing Project: Study design and methodology. Alzheimer's & Dementia (Amsterdam, Netherlands). 16: e70000. PMID 39183746 DOI: 10.1002/dad2.70000 |
0.302 |
|
| 2024 |
Ray NR, Kunkle BW, Hamilton-Nelson K, Kurup JT, Rajabli F, Qiao M, Vardarajan BN, Cosacak MI, Kizil C, Jean-Francois M, Cuccaro M, Reyes-Dumeyer D, Cantwell L, Kuzma A, Vance JM, ... ... Beecham GW, et al. Extended genome-wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 38958117 DOI: 10.1002/alz.13880 |
0.407 |
|
| 2024 |
Cruchaga C, Bradley J, Western D, Wang C, Fonseca ELD, Neupane A, Kurup J, Ray N, Jean-Francois M, Gorijala P, Bergmann K, Budde J, Martin E, Pericak-Vance M, Cuccaro M, ... ... Beecham G, et al. Novel early-onset Alzheimer-associated genes influence risk through dysregulation of glutamate, immune activation, and intracell signaling pathways. Research Square. PMID 38883718 DOI: 10.21203/rs.3.rs-4480585/v1 |
0.339 |
|
| 2023 |
Nuytemans K, Rajabli F, Jean-Francois M, Kurup JT, Adams LD, Starks TD, Whitehead PL, Kunkle BW, Caban-Holt A, Haines JL, Cuccaro ML, Vance JM, Byrd GS, Beecham GW, Reitz C, et al. Genetic analyses in multiplex families confirms chromosome 5q35 as a risk locus for Alzheimer's Disease in individuals of African Ancestry. Neurobiology of Aging. 133: 125-133. PMID 37952397 DOI: 10.1016/j.neurobiolaging.2023.10.010 |
0.382 |
|
| 2023 |
Ray NR, Kunkle BW, Hamilton-Nelson K, Kurup JT, Rajabli F, Cosacak MI, Kizil C, Jean-Francois M, Cuccaro M, Reyes-Dumeyer D, Cantwell L, Kuzma A, Vance JM, Gao S, Hendrie HC, ... ... Beecham GW, et al. Extended genome-wide association study employing the African Genome Resources Panel identifies novel susceptibility loci for Alzheimer's Disease in individuals of African ancestry. Medrxiv : the Preprint Server For Health Sciences. PMID 37693582 DOI: 10.1101/2023.08.29.23294774 |
0.408 |
|
| 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, ... ... Beecham GW, 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 |
0.39 |
|
| 2023 |
Ray NR, Ayodele T, Jean-Francois M, Baez P, Fernandez V, Bradley J, Crane PK, Dalgard CL, Kuzma A, Nicaretta H, Sims R, Williams J, Cuccaro ML, Pericak-Vance MA, Mayeux R, ... ... Beecham GW, et al. The Early-Onset Alzheimer's Disease Whole-Genome Sequencing Project: Study design and methodology. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37390458 DOI: 10.1002/alz.13370 |
0.382 |
|
| 2023 |
Cochran JN, Acosta-Uribe J, Esposito BT, Madrigal L, Aguillón D, Giraldo MM, Taylor JW, Bradley J, Fulton-Howard B, Andrews SJ, Acosta-Baena N, Alzate D, Garcia GP, Piedrahita F, Lopez HE, ... ... Beecham GW, et al. Genetic associations with age at dementia onset in the PSEN1 E280A Colombian kindred. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 36951251 DOI: 10.1002/alz.13021 |
0.318 |
|
| 2022 |
Rajabli F, Tosto G, Hamilton-Nelson KL, Kunkle BW, Vardarajan BN, Naj A, Whitehead PG, Gardner OK, Bush WS, Sariya S, Mayeux RP, Farrer LA, Cuccaro ML, Vance JM, Griswold AJ, ... ... Beecham GW, et al. Admixture mapping identifies novel Alzheimer's disease risk regions in African Americans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 36539198 DOI: 10.1002/alz.12865 |
0.304 |
|
| 2022 |
Holstege H, Hulsman M, Charbonnier C, Grenier-Boley B, Quenez O, Grozeva D, van Rooij JGJ, Sims R, Ahmad S, Amin N, Norsworthy PJ, Dols-Icardo O, Hummerich H, Kawalia A, Amouyel P, ... Beecham GW, et al. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genetics. PMID 36411364 DOI: 10.1038/s41588-022-01208-7 |
0.372 |
|
| 2022 |
Rajabli F, Beecham GW, Hendrie HC, Baiyewu O, Ogunniyi A, Gao S, Kushch NA, Lipkin-Vasquez M, Hamilton-Nelson KL, Young JI, Dykxhoorn DM, Nuytemans K, Kunkle BW, Wang L, Jin F, et al. A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry. Plos Genetics. 18: e1009977. PMID 35788729 DOI: 10.1371/journal.pgen.1009977 |
0.397 |
|
| 2021 |
Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, et al. Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology. PMID 33938021 DOI: 10.1002/ana.26094 |
0.342 |
|
| 2021 |
Rajabli F, Feliciano-Astacio BE, Cukier HN, Wang L, Griswold AJ, Hamilton-Nelson KL, Adams LD, Rodriguez VC, Mena PR, Tejada S, Celis K, Whitehead PL, Van Booven DJ, Hofmann NK, Bussies PL, ... ... Beecham GW, et al. Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus. Neurobiology of Aging. PMID 33902942 DOI: 10.1016/j.neurobiolaging.2021.02.019 |
0.395 |
|
| 2021 |
Griswold AJ, Celis K, Bussies PL, Rajabli F, Whitehead PL, Hamilton-Nelson KL, Beecham GW, Dykxhoorn DM, Nuytemans K, Wang L, Gardner OK, Dorfsman DA, Bigio EH, Mesulam MM, Weintraub S, et al. Increased APOE ε4 expression is associated with the difference in Alzheimer's disease risk from diverse ancestral backgrounds. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 33522086 DOI: 10.1002/alz.12287 |
0.368 |
|
| 2021 |
Ayodele T, Rogaeva E, Kurup JT, Beecham G, Reitz C. Early-Onset Alzheimer's Disease: What Is Missing in Research? Current Neurology and Neuroscience Reports. 21: 4. PMID 33464407 DOI: 10.1007/s11910-020-01090-y |
0.356 |
|
| 2020 |
Reitz C, Rogaeva E, Beecham GW. Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference? Neurology. Genetics. 6: e512. PMID 33225065 DOI: 10.1212/NXG.0000000000000512 |
0.378 |
|
| 2020 |
Griswold AJ, Sivasankaran SK, Van Booven D, Gardner OK, Rajabli F, Whitehead PL, Hamilton-Nelson KL, Adams LD, Scott AM, Hofmann NK, Vance JM, Cuccaro ML, Bush WS, Martin ER, Byrd GS, ... ... Beecham GW, et al. Immune and Inflammatory Pathways Implicated by Whole Blood Transcriptomic Analysis in a Diverse Ancestry Alzheimer's Disease Cohort. Journal of Alzheimer's Disease : Jad. PMID 32597797 DOI: 10.3233/Jad-190855 |
0.454 |
|
| 2020 |
Bussies PL, Rajabli F, Griswold A, Dorfsman DA, Whitehead P, Adams LD, Mena PR, Cuccaro M, Haines JL, Byrd GS, Beecham GW, Pericak-Vance MA, Young JI, Vance JM. Use of local genetic ancestry to assess -523' and risk for Alzheimer disease. Neurology. Genetics. 6: e404. PMID 32337333 DOI: 10.1212/Nxg.0000000000000404 |
0.471 |
|
| 2020 |
Mock C, Teylan M, Beecham G, Besser L, Cairns NJ, Crary JF, Katsumata Y, Nelson PT, Kukull W. The Utility of the National Alzheimer's Coordinating Center's Database for the Rapid Assessment of Evolving Neuropathologic Conditions. Alzheimer Disease and Associated Disorders. PMID 32304374 DOI: 10.1097/Wad.0000000000000380 |
0.382 |
|
| 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, ... ... Beecham GW, 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 |
0.447 |
|
| 2020 |
Wang L, Cukier HN, Rajabli F, Hofmann NK, Adams LD, Rodriguez VC, Mena PR, Garcia‐Serje C, Silva C, Feliciano NI, Feliciano‐Astacio BE, Acosta H, Vance JM, Beecham GW, Pericak‐Vance MA. Functional analysis of candidate genes identified through whole genome sequencing in Caribbean Hispanic families for late‐onset Alzheimer disease Alzheimer's & Dementia. 16. DOI: 10.1002/alz.046017 |
0.364 |
|
| 2020 |
Rajabli F, Adams LD, Tejada S, Rodriguez VC, Mena PR, Prough M, Bussies P, Feliciano NI, Silva‐Vergara C, Contreras M, Hamilton‐Nelson KL, Acosta H, Vance JM, Cuccaro ML, Feliciano‐Astacio BE, ... Beecham GW, et al. Southern European genetic ancestry shows reduced APOE E4 risk for Alzheimer disease in Caribbean Hispanic population Alzheimer's & Dementia. 16. DOI: 10.1002/alz.045951 |
0.302 |
|
| 2020 |
Griswold AJ, Gardner OK, Rajabli F, Hamilton‐Nelson KL, Adams LD, Rodriguez VC, Mena PR, Whitehead PL, Hofmann NK, Garcia‐Serje C, Silva‐Vergara C, Feliciano NI, Feliciano‐Astacio BE, Acosta H, Haines JL, ... ... Beecham GW, et al. Transcriptomic characterization of a Puerto Rican Alzheimer disease cohort implicates convergent immune‐related pathways Alzheimer's & Dementia. 16. DOI: 10.1002/alz.045890 |
0.326 |
|
| 2020 |
Cornejo‐Olivas MR, Rajabli F, Veliz‐Otani DM, Whitehead PL, Hofmann NK, Hamilton‐Nelson KL, Illanes‐Manrique M, Milla‐Neyra K, Marca V, Sarapura‐Castro E, Rivera‐Valdivia A, Mejía KK, Adams LD, Mena PR, Vance JM, ... ... Beecham GW, et al. Exploring the role of Amerindian genetic ancestry and
ApoEε4
gene on Alzheimer disease in the Peruvian population Alzheimer's & Dementia. 16. DOI: 10.1002/alz.045012 |
0.309 |
|
| 2019 |
Ganna A, Verweij KJH, Nivard MG, Maier R, Wedow R, Busch AS, Abdellaoui A, Guo S, Sathirapongsasuti JF, Lichtenstein P, Lundström S, Långström N, Auton A, Harris KM, ... Beecham GW, et al. Genome studies must account for history-Response. Science (New York, N.Y.). 366: 1461-1462. PMID 31857477 DOI: 10.1126/Science.Aaz8941 |
0.303 |
|
| 2019 |
Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Bush WS, Gifford KA, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, Montine TJ, et al. Sex differences in the genetic predictors of Alzheimer's pathology. Brain : a Journal of Neurology. 142: 2581-2589. PMID 31497858 DOI: 10.1093/Brain/Awz206 |
0.456 |
|
| 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, ... ... Beecham GW, 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 |
0.306 |
|
| 2019 |
Young JI, Sivasankaran SK, Wang L, Ali A, Mehta A, Davis DA, Dykxhoorn DM, Petito CK, Beecham GW, Martin ER, Mash DC, Pericak-Vance M, Scott WK, Montine TJ, Vance JM. Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease. Neurology. Genetics. 5: e342. PMID 31403079 DOI: 10.1212/Nxg.0000000000000342 |
0.308 |
|
| 2019 |
Feliciano-Astacio BE, Celis K, Ramos J, Rajabli F, Adams LD, Rodriguez A, Rodriguez V, Bussies PL, Sierra C, Manrique P, Mena PR, Grana A, Prough M, Hamilton-Nelson KL, Feliciano N, ... ... Beecham GW, et al. The Puerto Rico Alzheimer Disease Initiative (PRADI): A Multisource Ascertainment Approach. Frontiers in Genetics. 10: 538. PMID 31275353 DOI: 10.3389/Fgene.2019.00538 |
0.46 |
|
| 2019 |
Gardner OK, Wang L, Van Booven D, Whitehead PL, Hamilton-Nelson KL, Adams LD, Starks TD, Hofmann NK, Vance JM, Cuccaro ML, Martin ER, Byrd GS, Haines JL, Bush WS, Beecham GW, et al. RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways. Human Molecular Genetics. PMID 31162550 DOI: 10.1093/Hmg/Ddz110 |
0.351 |
|
| 2019 |
Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, et al. Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Journal of Neuromuscular Diseases. PMID 30958311 DOI: 10.3233/Jnd-190377 |
0.379 |
|
| 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, ... ... Beecham GW, 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 |
0.398 |
|
| 2019 |
Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Morrow JM, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, et al. Variation in SIPA1L2 is Correlated with Phenotype Modification in CMT Type 1A. Annals of Neurology. PMID 30706531 DOI: 10.1002/Ana.25426 |
0.357 |
|
| 2019 |
Gardner OK, Wang L, Booven DV, Whitehead PL, Hamilton-Nelson KL, Adams LD, Starks TD, Hofmann NK, Vance JM, Cuccaro ML, Martin ER, Byrd GS, Haines JL, Bush WS, Beecham GW, et al. O3-13-04: Genetic Variants In Alzheimer'S Disease-Associated Regions Have Different Effects On Rna Editing Rates In African-American And Non-Hispanic White Populations Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4699 |
0.397 |
|
| 2019 |
Jaworski J, Kunkle BW, Rajabli F, Adams LD, Starks TD, Goate AM, Cuccaro ML, Vance JM, Martin ER, Foroud TM, Mayeux R, Reitz C, Byrd GS, Beecham GW, Pericak-Vance MA. O3-13-02: Genome-Wide Linkage Analysis Of African-American Alzheimer Disease Families Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4697 |
0.437 |
|
| 2019 |
Reiman EM, Arboleda-Velasquez JF, Quiroz YT, Huentelman MJ, Beach TG, Farrer LA, Mayeux R, Haines JL, Schellenberg GD, Beecham GW, Montine TJ, Jun GR. P4-259: Exceptionally Low Risk Of Alzheimer'S Dementia In Apoe2 Homozygotes Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3928 |
0.391 |
|
| 2019 |
Griswold AJ, Gardner OK, Booven DV, Jean-Francois M, Hamilton-Nelson KL, Whitehead PL, Adams LD, Starks TD, Hofmann NK, Cuccaro ML, Martin ER, Vance JM, Byrd GS, Haines JL, Bush WS, ... Beecham GW, et al. P4-114: Eqtl Analysis Identifies Ancestry Specific Regulatory Effects Of Alzheimer Disease Associated Variants Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3775 |
0.484 |
|
| 2019 |
Vardarajan BN, Jaworski J, Beecham GW, Barral S, Reyes-Dumeyer D, Medrano M, Lantigua R, Leung YY, Wang L, Naj A, Martin ER, Haines JL, Bush WS, Farrer LA, Schellenberg GD, et al. P4-097: Rare Variants In Familial Late-Onset Alzheimer'S Disease Identified From Large Scale Whole Genome Sequencing Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3757 |
0.482 |
|
| 2019 |
Kunkle BW, Hamilton-Nelson KL, Gomez L, Jean-Francois M, Naj A, Wang L, Kuzma AB, Beecham GW, Bush WS, Hohman TJ, Vardarajan BN, Wang L, Mayeux R, Haines JL, Farrer LA, et al. P4-094: Exome-Wide Analysis Identifies Novel Sex-Specific Candidate Genes For Alzheimer Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3754 |
0.464 |
|
| 2019 |
Cuccaro ML, Celis K, Adams LD, Scott AM, Ayodele T, Martinez I, Starks TD, Vance JM, Byrd GS, Haines JL, Reitz C, Beecham GW, Pericak-Vance MA. P3-311: Neuropsychiatric Features In African American (Aa) And Caucasian (Ca) Individuals With Alzheimer Disease (Ad) Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3343 |
0.395 |
|
| 2019 |
Jean-Francois M, Johnson FS, Baez P, Martinez I, Adams LD, Vance JM, Martin ER, Ayodele T, Pericak-Vance MA, Cuccaro ML, Beecham GW, Reitz C. P2-150: Degree Of Inbreeding In Multiplex Caribbean Hispanic Families Loaded For Early-Onset Alzheimer'S Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2557 |
0.441 |
|
| 2019 |
Rajabli F, Feliciano-Astacio BE, Celis K, Hamilton-Nelson KL, Adams LD, Rodriguez VC, Mena PR, Whitehead PL, Hofmann NK, Bussies P, Prough M, Sierra-Lopez CB, Acosta H, Chinea A, Feliciano NI, ... ... Beecham GW, et al. P2-140: Genome-Wide Linkage Analysis Of Caribbean Hispanic Puerto Rican Families Supports Evidence Of Linkage To C9Orf72 Region Of Chromosome 9 Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2547 |
0.35 |
|
| 2019 |
Starks TD, Byfield G, Naney KB, Luther R, King V, Dykxhoorn DM, Cukier HN, Edwards C, Adams LD, Haines JL, Cuccaro ML, Vance JM, Mayeux R, Reitz C, Beecham GW, et al. P1‐558: Mitigating Complexities In Recruiting And Retaining African American (Aa) Multiplex Families For Alzheimer Disease Research Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.1163 |
0.385 |
|
| 2018 |
Beecham GW, Vardarajan B, Blue E, Bush W, Jaworski J, Barral S, DeStefano A, Hamilton-Nelson K, Kunkle B, Martin ER, Naj A, Rajabli F, Reitz C, Thornton T, van Duijn C, et al. Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease. Neurology. Genetics. 4: e286. PMID 30569016 DOI: 10.1212/Nxg.0000000000000286 |
0.468 |
|
| 2018 |
Rajabli F, Feliciano BE, Celis K, Hamilton-Nelson KL, Whitehead PL, Adams LD, Bussies PL, Manrique CP, Rodriguez A, Rodriguez V, Starks T, Byfield GE, Sierra Lopez CB, McCauley JL, Acosta H, ... ... Beecham GW, et al. Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations. Plos Genetics. 14: e1007791. PMID 30517106 DOI: 10.1371/Journal.Pgen.1007791 |
0.409 |
|
| 2018 |
Zhang X, Zhu C, Beecham G, Vardarajan BN, Ma Y, Lancour D, Farrell JJ, Chung J, Mayeux R, Haines JL, Schellenberg GD, Pericak-Vance MA, Lunetta KL, Farrer LA. A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 30503768 DOI: 10.1016/j.jalz.2018.10.005 |
0.416 |
|
| 2018 |
Cheng R, Tang M, Martinez I, Ayodele T, Baez P, Reyes-Dumeyer D, Lantigua R, Medrano M, Jimenez-Velazquez I, Lee JH, Beecham GW, Reitz C. Linkage analysis of multiplex Caribbean Hispanic families loaded for unexplained early-onset cases identifies novel Alzheimer's disease loci. Alzheimer's & Dementia (Amsterdam, Netherlands). 10: 554-562. PMID 30406174 DOI: 10.1016/J.Dadm.2018.07.007 |
0.473 |
|
| 2018 |
Bis JC, Jian X, Kunkle BW, Chen Y, Hamilton-Nelson KL, Bush WS, Salerno WJ, Lancour D, Ma Y, Renton AE, Marcora E, Farrell JJ, Zhao Y, Qu L, Ahmad S, ... ... Beecham GW, et al. Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry. PMID 30108311 DOI: 10.1038/S41380-018-0112-7 |
0.488 |
|
| 2018 |
Vardarajan BN, Beecham GW, Haines JL. Pedigree Selection and Information Content. Current Protocols in Human Genetics. 97: e56. PMID 30040223 DOI: 10.1002/Cphg.56 |
0.358 |
|
| 2018 |
Hohman TJ, Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Gifford KA, Bush WS, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, et al. Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau. Jama Neurology. PMID 29801024 DOI: 10.1001/Jamaneurol.2018.0821 |
0.409 |
|
| 2018 |
Vardarajan BN, Barral S, Jaworski J, Beecham GW, Blue E, Tosto G, Reyes-Dumeyer D, Medrano M, Lantigua R, Naj A, Thornton T, DeStefano A, Martin E, Wang LS, Brown L, et al. Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease. Annals of Clinical and Translational Neurology. 5: 406-417. PMID 29688227 DOI: 10.1002/Acn3.537 |
0.507 |
|
| 2018 |
Blue EE, Bis JC, Dorschner MO, Tsuang DW, Barral SM, Beecham G, Below JE, Bush WS, Butkiewicz M, Cruchaga C, DeStefano A, Farrer LA, Goate A, Haines J, Jaworski J, et al. Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. Dementia and Geriatric Cognitive Disorders. 45: 1-17. PMID 29486463 DOI: 10.1159/000485503 |
0.483 |
|
| 2018 |
Chung J, Zhang X, Allen M, Wang X, Ma Y, Beecham G, Montine TJ, Younkin SG, Dickson DW, Golde TE, Price ND, Ertekin-Taner N, Lunetta KL, Mez J, et al. Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease. Alzheimer's Research & Therapy. 10: 22. PMID 29458411 DOI: 10.1186/S13195-018-0349-Z |
0.493 |
|
| 2018 |
Rajabli F, Hamilton-Nelson KL, Vance JM, Martin ER, Griswold AJ, Schellenberg GD, Haines JL, Farrer LAA, Wang L, Beecham GW, Pericak-Vance MAA. P2-106: African American Whole Exome Sequencing Suggests Risk Coding Variants In Idh1 Gene Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.792 |
0.345 |
|
| 2018 |
Rajabli F, Vance JM, Feliciano-Astacio BE, Celis K, Adams LD, Hamilton-Nelson KL, Wang L, Nuytemans K, Whitehead PL, Hofmann NK, Rolati S, Haines JL, Byrd GS, Reitz C, Beecham GW, et al. O3-06-06: Identifying A Protective Variant That Lowers The Risk For Developing Ad In Apoe-E4 Carriers Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.2805 |
0.334 |
|
| 2018 |
Gardner OK, Wang L, Whitehead PL, Hamilton-Nelson KL, Adams LD, Rolati S, Hofmann NK, Vance JM, Cuccaro ML, Bush WS, Martin ER, Byrd GS, Haines JL, Beecham GW, Pericak-Vance MA, et al. O2-01-05: Multi-Ethnic Alzheimer'S Disease Related Changes Of Rna Editing Affect Immune Regulation, Endocytosis, And Amyloid Precursor Protein Catabolism Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.2643 |
0.351 |
|
| 2018 |
Vardarajan BN, Barral S, Jaworski J, Beecham GW, Blue E, Tosto G, Reyes-Dumeyer D, Medrano M, Lantigua R, Naj AC, Thornton TA, Destefano AL, Martin ER, Wang L, Brown L, et al. P1-156: Gene-Based Analyses In Whole Genome Sequencing Of Familial Late-Onset Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.160 |
0.495 |
|
| 2018 |
Kunkle BW, Jaworski J, Rajabli F, Adams LD, Cuccaro ML, Vance JM, Goate AM, Martin ER, Foroud TM, Reitz C, Beecham GW, Mayeux R, Pericak-Vance MA. P1-154: Genome-Wide Linkage Analyses Of African American Families Supports Evidence Of Linkage To Chromosome 12 Alzheimers & Dementia. 14: 336. DOI: 10.1016/J.Jalz.2018.06.158 |
0.35 |
|
| 2018 |
Griswold AJ, Sivasankaran SK, Gardner OK, Rajabli F, Hamilton-Nelson KL, Rolati S, Hofmann NK, Whitehead PL, Adams LD, Byrd GS, Martin ER, Cuccaro ML, Bush WS, Haines JL, Vance JM, ... Beecham GW, et al. P1-144: Transcriptomic Analysis Of Whole Blood In African American And Non-Hispanic White Alzheimer Disease Cases And Controls Alzheimers & Dementia. 14: 331. DOI: 10.1016/J.Jalz.2018.06.147 |
0.382 |
|
| 2018 |
Dumitrescu L, Deming Y, Lu Q, Beecham GW, Kunkle BW, Del-Aguila JL, Fernandez MV, Budde JP, Fagan AM, Jager PLD, Albert MS, Moghekar A, Riemenschneider M, Petersen RC, Barnes LL, et al. P1-139: The Contribution Of Sex-Specific Associations In Genetic Studies Of Alzheimer'S Disease Pathology Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.142 |
0.485 |
|
| 2018 |
Byfield G, Starks T, Cuccaro ML, Adams LD, Whitehead PL, Hamilton-Nelson KL, Reitz C, Beecham GW, Reyes-Dumeyer D, Haines JL, Mayeux R, Vance JM, Pericak-Vance MA, Edwards C, Byrd GS. P3-034: Continuous Community Engagement Improves Recruitment Of Older African Americans For Genetic Studies In Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.1389 |
0.404 |
|
| 2017 |
Sanders AR, Beecham GW, Guo S, Dawood K, Rieger G, Badner JA, Gershon ES, Krishnappa RS, Kolundzija AB, Duan J, Gejman PV, Bailey JM, Martin ER. Genome-Wide Association Study of Male Sexual Orientation. Scientific Reports. 7: 16950. PMID 29217827 DOI: 10.1038/S41598-017-15736-4 |
0.36 |
|
| 2017 |
Beecham GW, Bis JC, Martin ER, Choi SH, DeStefano AL, van Duijn CM, Fornage M, Gabriel SB, Koboldt DC, Larson DE, Naj AC, Psaty BM, Salerno W, Bush WS, Foroud TM, et al. The Alzheimer's Disease Sequencing Project: Study design and sample selection. Neurology. Genetics. 3: e194. PMID 29184913 DOI: 10.1212/Nxg.0000000000000194 |
0.484 |
|
| 2017 |
Kunkle BW, Vardarajan BN, Naj AC, Whitehead PL, Rolati S, Slifer S, Carney RM, Cuccaro ML, Vance JM, Gilbert JR, Wang LS, Farrer LA, Reitz C, Haines JL, Beecham GW, et al. Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport. Jama Neurology. PMID 28738127 DOI: 10.1001/Jamaneurol.2017.1518 |
0.458 |
|
| 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, ... ... Beecham GW, 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 |
0.49 |
|
| 2017 |
Damas OM, Gomez L, Quintero MA, Rampersaud E, Slifer S, Beecham GW, Kerman DH, Deshpande AR, Sussman DA, Abreu MT, McCauley JL. Genetic Characterization and Influence on Inflammatory Bowel Disease Expression in a Diverse Hispanic South Florida Cohort. Clinical and Translational Gastroenterology. 8: e87. PMID 28406493 DOI: 10.1038/Ctg.2017.13 |
0.371 |
|
| 2017 |
Kunkle BW, Carney RM, Kohli MA, Naj AC, Hamilton-Nelson KL, Whitehead PL, Wang L, Lang R, Cuccaro ML, Vance JM, Byrd GS, Beecham GW, Gilbert JR, Martin ER, Haines JL, et al. Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease. Neuroscience Letters. PMID 28400126 DOI: 10.1016/J.Neulet.2017.04.014 |
0.453 |
|
| 2017 |
Jun GR, Chung J, Mez J, Barber R, Beecham GW, Bennett DA, Buxbaum JD, Byrd GS, Carrasquillo MM, Crane PK, Cruchaga C, De Jager P, Ertekin-Taner N, Evans D, Fallin MD, et al. Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 28183528 DOI: 10.1016/J.Jalz.2016.12.012 |
0.489 |
|
| 2017 |
Beecham GW, Vardarajan BN, Blue E, Barral S, Haines JL, Bush WS, Duijn CMv, Martin ER, Schellenberg GD, Mayeux R, Wijsman E, Pericak-Vance MA. Whole-Genome Sequencing In Familial Late-Onset Alzheimer’S Disease Identifies Rare Variation In Ad Candidate Genes Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.07.188 |
0.48 |
|
| 2017 |
Chung J, Ma Y, Zhang X, Yang Q, Beecham GW, Lunetta KL, Mez J, Haines JL, Pericak-Vance MA, Schellenberg GD, Jun GR, Farrer LA. Bivariate Genome-Wide Association Study Of Neuropathologic Features Of Alzheimer’S Disease Alzheimers & Dementia. 13: 217. DOI: 10.1016/J.Jalz.2017.07.094 |
0.426 |
|
| 2017 |
Naj AC, Below J, Zhao Y, Chen H, Lee SJvd, Hamilton-Nelson KL, Petty L, Kunkle BW, Kuzma AB, Valladares O, Reitz C, Beecham GW, Martin ER, Wang L, Haines JL, et al. Genome-Wide Rare Variant Imputation And Tissue-Specific Transcriptomic Analysis Identify Novel Rare Variant Candidate Loci In Late-Onset Alzheimer’S Disease: The Alzheimer’S Disease Genetics Consortium Alzheimers & Dementia. 13: 189. DOI: 10.1016/J.Jalz.2017.07.045 |
0.467 |
|
| 2017 |
Celis K, Feliciano-Astacio BE, Adams LD, Bussies P, Sierra C, Hamilton-Nelson KL, Rajabli F, Acosta H, Chinea A, McCauley JL, Vance JM, Cuccaro ML, Beecham GW, Pericak-Vance MA. The Puerto Rican Alzheimer Disease Initiative (Pradi): Initial Clinical Findings Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.774 |
0.402 |
|
| 2017 |
Rajabli F, Hamilton-Nelson KL, Feliciano-Astacio BE, Celis K, Adams LD, Bussies P, Sierra C, Chinea A, Acosta H, McCauley JL, Vance JM, Cuccaro ML, Haines JL, Bush WS, Beecham GW, et al. The Relevance Of Apoe4 To Alzheimer’S Disease In The Presence Of Local Ancestry Differences Alzheimers & Dementia. 13: 650. DOI: 10.1016/J.Jalz.2017.06.763 |
0.377 |
|
| 2017 |
Reitz C, Tang M, Reyes-Dumeyer D, Kunkle BW, Hamilton-Nelson KL, Lantigua R, Medrano M, Martin ER, Jimenez-Velazquez IZ, Pericak-Vance MA, Mayeux R, Beecham GW. [P2-105]: COLLECTION OF MULTIPLEX FAMILIES WITH UNEXPLAINED EARLY-ONSET ALZHEIMER's DISEASE FOR GENOMIC RESEARCH Alzheimer's & Dementia. 13: P647-P647. DOI: 10.1016/J.Jalz.2017.06.755 |
0.476 |
|
| 2017 |
Feliciano‐Astacio BE, Celis K, Deon Adams L, Hamilton‐Nelson KL, Bussies P, Sierra C, Feliciano N, Chinea A, Acosta H, McCauley JL, Vance JM, Cuccaro ML, Beecham GW, Pericak‐Vance MA. [P2–102]: THE PUERTO RICO ALZHEIMER DISEASE INITIATIVE (PRADI): A MULTISOURCE ASCERTAINMENT APPROACH Alzheimer's & Dementia. 13. DOI: 10.1016/j.jalz.2017.06.751 |
0.31 |
|
| 2017 |
Cuccaro ML, Reitz C, Beecham GW, Cukier HN, Celis K, Adams LD, Starks T, Joseph N, Whitehead PL, Hamilton-Nelson KL, Reyes-Dumeyer D, Byfield G, Bennett DA, Rosenberg RN, Boeve BF, et al. Resource Of Multiplex African American Families For Whole-Genome Sequencing Alzheimers & Dementia. 13: 970. DOI: 10.1016/J.Jalz.2017.06.1304 |
0.333 |
|
| 2016 |
Beecham AH, Wang L, Vasudeva N, Liu Z, Dong C, Goldschmidt-Clermont PJ, Pericak-Vance MA, Rundek T, Seo D, Blanton SH, Sacco RL, Beecham GW. Utility of blood pressure genetic risk score in admixed Hispanic samples. Journal of Human Hypertension. PMID 27251080 DOI: 10.1038/Jhh.2016.29 |
0.311 |
|
| 2016 |
Cukier HN, Kunkle BW, Vardarajan BN, Rolati S, Hamilton-Nelson KL, Kohli MA, Whitehead PL, Dombroski BA, Van Booven D, Lang R, Dykxhoorn DM, Farrer LA, Cuccaro ML, Vance JM, Gilbert JR, ... Beecham GW, et al. ABCA7 frameshift deletion associated with Alzheimer disease in African Americans. Neurology. Genetics. 2: e79. PMID 27231719 DOI: 10.1016/J.Jalz.2016.06.305 |
0.477 |
|
| 2016 |
Wang L, Maldonado L, Beecham GW, Martin ER, Evatt ML, Ritchie JC, Haines JL, Zabetian CP, Payami H, Pericak-Vance MA, Vance JM, Scott WK. DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient. Neurology. Genetics. 2: e72. PMID 27123490 DOI: 10.1212/Nxg.0000000000000072 |
0.323 |
|
| 2016 |
Mez J, Mukherjee S, Thornton T, Fardo DW, Trittschuh E, Sutti S, Sherva R, Kauwe JS, Naj AC, Beecham GW, Gross A, Saykin AJ, Green RC, Crane PK, et al. The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable. Neurobiology of Aging. 41: 115-21. PMID 27103524 DOI: 10.1016/J.Neurobiolaging.2016.02.015 |
0.382 |
|
| 2016 |
Nuytemans K, Maldonado L, Ali A, John-Williams K, Beecham GW, Martin E, Scott WK, Vance JM. Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants. Neurology. Genetics. 2: e44. PMID 27066581 DOI: 10.1212/Nxg.0000000000000044 |
0.433 |
|
| 2016 |
Kohli MA, Cukier HN, Hamilton-Nelson KL, Rolati S, Kunkle BW, Whitehead PL, Züchner SL, Farrer LA, Martin ER, Beecham GW, Haines JL, Vance JM, Cuccaro ML, Gilbert JR, Schellenberg GD, et al. Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease. Neurology. Genetics. 2: e41. PMID 27066578 DOI: 10.1212/Nxg.0000000000000041 |
0.471 |
|
| 2016 |
Chung J, Ma Y, Lunetta KL, Mez J, Beecham GW, Pericak-Vance MA, Haines JL, Mayeux R, Schellenberg GD, Jun GR, Farrer LA. Multivariate Phenotypes Association Study Of Neuropathological Features Of Alzheimer'S Disease And Related Dementias Alzheimers & Dementia. 12: 450. DOI: 10.1016/J.Jalz.2016.06.838 |
0.447 |
|
| 2016 |
Jian X, Bis JC, Kunkle BW, Hamilton KL, Beecham GW, Bush WS, Salerno W, Lancour D, Ma Y, Chen Y, DeStefano AL, Dupuis J, Boerwinkle E, Schellenberg GD, Seshadri S, et al. Rare Deleterious And Loss-Of-Function Variants In Oprl1 And Gas2L2 Contribute To The Risk Of Late-Onset Alzheimer’S Disease: Alzheimer’S Disease Sequencing Project Case-Control Study Alzheimers & Dementia. 12: 163. DOI: 10.1016/J.Jalz.2016.06.765 |
0.421 |
|
| 2016 |
Beecham GW, Vardarajan BN, Blue E, Barral S, Haines JL, Bush WS, Duijn CMv, Martin ER, Schellenberg GD, Mayeux R, Wijsman E, Pericak-Vance MA. Whole Genome Sequencing In Familial Late-Onset Alzheimer’S Disease Identifies Variations In Ttc3 And Fsip2 Alzheimers & Dementia. 12: 197. DOI: 10.1016/J.Jalz.2016.06.343 |
0.437 |
|
| 2016 |
Cukier HN, Kunkle BW, Rolati S, Whitehead PL, Vance JM, Cuccaro ML, Carney RM, Gilbert JR, Martin ER, Beecham GW, Haines JL, Pericak-Vance MA, Hamilton-Nelson KL. O1-09-02: Whole Exome Sequencing of Late Onset Multiplex Families Identifies Rare Coding Variants in Known and Novel Alzheimer’s Disease Genes Alzheimer's & Dementia. 12: P196-P197. DOI: 10.1016/J.Jalz.2016.06.342 |
0.399 |
|
| 2016 |
Naj AC, Zhao Y, Lee SJvd, Hamilton KL, Kunkle BW, Partch AB, Valladares O, Beecham GW, Martin ER, Wang L, Haines JL, Mayeux R, Farrer LA, Pericak-Vance MA, Schellenberg GD. High-Resolution Imputation In Genome-Wide Association Studies Of Late-Onset Alzheimer'S Disease Identifies Novel Rare Variant Associations Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.308 |
0.481 |
|
| 2016 |
Kunkle BW, Vardarajan BN, Naj AC, Cukier HN, Dykxhoorn DM, Rolati S, Whitehead PL, Carney RM, Cuccaro ML, Vance JM, Genetics Consortium AD, Farrer LA, Haines JL, Schellenberg GD, Martin ER, ... ... Beecham GW, et al. O1-03-03: Identification of Novel Candidate Genes for Early-Onset Alzheimer's Disease Through Integrated Whole-Exome Sequencing and Exome Chip Array Association Analysis Alzheimer's & Dementia. 12: P177-P178. DOI: 10.1016/J.Jalz.2016.06.306 |
0.439 |
|
| 2016 |
Marcora E, Renton AE, Beecham GW, Boerwinkle E, Cantwell L, Cruchaga C, Cweibel R, Felsenfeld A, Fornage M, Kapoor M, Kauwe K, Khaladkar M, Kobolt D, Ma Y, Mayeux R, et al. F1-01-02: Alzheimer's Disease Sequencing Project: Search for Alzheimer's Disease Resilience Genes That May Modify Disease Susceptibility in Specific Apoe Genotype Backgrounds Alzheimer's & Dementia. 12: P162-P163. DOI: 10.1016/J.Jalz.2016.06.272 |
0.466 |
|
| 2016 |
Marcora E, Renton AE, Beecham GW, Boerwinkle E, Cantwell L, Cruchaga C, Cweibel R, Felsenfeld A, Fornage M, Kapoor M, Kauwe K, Khaladkar M, Kobolt D, Ma Y, Mayeux R, et al. P2-077: Alzheimer's Disease Sequencing Project: Search for Alzheimer's Disease Resilience Genes That May Modify Disease Susceptibility in Specific Apoe
Genotype Backgrounds Alzheimer's & Dementia. 12: P638-P638. DOI: 10.1016/j.jalz.2016.06.1282 |
0.399 |
|
| 2015 |
Barral S, Cheng R, Reitz C, Vardarajan B, Lee J, Kunkle B, Beecham G, Cantwell LS, Pericak-Vance MA, Farrer LA, Haines JL, Goate AM, Foroud T, Boerwinkle E, Schellenberg GD, et al. Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26433351 DOI: 10.1016/J.Jalz.2015.07.487 |
0.479 |
|
| 2015 |
Kunkle BW, Jaworski J, Barral S, Vardarajan B, Beecham GW, Martin ER, Cantwell LS, Partch A, Bird TD, Raskind WH, DeStefano AL, Carney RM, Cuccaro M, Vance JM, Farrer LA, et al. Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26365416 DOI: 10.1016/J.Jalz.2015.05.020 |
0.486 |
|
| 2015 |
Hohman TJ, Cooke-Bailey JN, Reitz C, Jun G, Naj A, Beecham GW, Liu Z, Carney RM, Vance JM, Cuccaro ML, Rajbhandary R, Vardarajan BN, Wang LS, Valladares O, Lin CF, et al. Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26092349 DOI: 10.1016/J.Jalz.2015.02.012 |
0.481 |
|
| 2015 |
Jun G, Ibrahim-Verbaas CA, Vronskaya M, Lambert JC, Chung J, Naj AC, Kunkle BW, Wang LS, Bis JC, Bellenguez C, Harold D, Lunetta KL, Destefano AL, Grenier-Boley B, Sims R, ... Beecham GW, et al. A novel Alzheimer disease locus located near the gene encoding tau protein. Molecular Psychiatry. PMID 25778476 DOI: 10.1038/Mp.2015.23 |
0.431 |
|
| 2015 |
Beecham GW, Dickson DW, Scott WK, Martin ER, Schellenberg G, Nuytemans K, Larson EB, Buxbaum JD, Trojanowski JQ, Van Deerlin VM, Hurtig HI, Mash DC, Beach TG, Troncoso JC, Pletnikova O, et al. PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease. Neurology. 84: 972-80. PMID 25663231 DOI: 10.1212/Wnl.0000000000001332 |
0.401 |
|
| 2015 |
Wang LS, Naj AC, Graham RR, Crane PK, Kunkle BW, Cruchaga C, Murcia JD, Cannon-Albright L, Baldwin CT, Zetterberg H, Blennow K, Kukull WA, Faber KM, Schupf N, Norton MC, ... ... Beecham GW, et al. Rarity of the Alzheimer disease-protective APP A673T variant in the United States. Jama Neurology. 72: 209-16. PMID 25531812 DOI: 10.1001/Jamaneurol.2014.2157 |
0.444 |
|
| 2015 |
Humphries CE, Kohli MA, Nathanson L, Whitehead P, Beecham G, Martin E, Mash DC, Pericak-Vance MA, Gilbert J. Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 44: 977-87. PMID 25380588 DOI: 10.3233/Jad-141989 |
0.324 |
|
| 2015 |
Beecham GW, Kunkle BW, Vardarajan B, Whitehead PL, Rolati S, Martin ER, Gilbert JR, Mayeux R, Haines JL, Pericak-Vance MA. O3-13-02: Whole-exome sequencing in early-onset Alzheimer disease cases identifies novel candidate genes Alzheimer's & Dementia. 11: P251-P251. DOI: 10.1016/J.Jalz.2015.07.310 |
0.427 |
|
| 2015 |
Cukier HN, Kunkle BW, Rolati S, Hamilton-Nelson KL, Kohli MA, Dombroski BA, Vardarajan BN, Whitehead PL, Booven DJV, Martin ER, Beecham GW, Farrer LA, Cuccaro ML, Vance JM, Mayeux R, et al. ABCA7 deletion associated with Alzheimer's disease in african americans Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.06.549 |
0.451 |
|
| 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 |
0.471 |
|
| 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 |
0.455 |
|
| 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, ... ... Beecham GW, 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 |
0.496 |
|
| 2014 |
Brewer MH, Ma KH, Beecham GW, Gopinath C, Baas F, Choi BO, Reilly MM, Shy ME, Züchner S, Svaren J, Antonellis A. Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2. Human Molecular Genetics. 23: 5171-87. PMID 24833716 DOI: 10.1093/Hmg/Ddu240 |
0.335 |
|
| 2014 |
Nuytemans K, Inchausti V, Beecham GW, Wang L, Dickson DW, Trojanowski JQ, Lee VM, Mash DC, Frosch MP, Foroud TM, Honig LS, Montine TJ, Dawson TM, Martin ER, Scott WK, et al. Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 827-30. PMID 24573903 DOI: 10.1002/Mds.25838 |
0.354 |
|
| 2014 |
O'Neill B, Lindman B, Castillo J, Seo P, Cohen M, Heldman A, Zajarias A, Lasala J, Slifer S, Vasudeva N, Beecham G, Goldschmidt-Clermont P, O'Neill W, Seo D. NOTCH1 IS ASSOCIATED WITH THE DEVELOPMENT OF TRI-LEAFLET CALCIFIC AORTIC STENOSIS Journal of the American College of Cardiology. 63: A1757. DOI: 10.1016/S0735-1097(14)61760-5 |
0.335 |
|
| 2014 |
Pericak-Vance M, Reitz C, Kunkle BW, Vardarajan BN, Kohli MA, Naj AC, Whitehead PL, Perry W, Martin E, Beecham G, Gilbert J, Farrer LA, Haines J, Schellenberg GD, Mayeux R. P2-131: WHOLE-EXOME SEQUENCING OF HISPANIC EARLY-ONSET ALZHEIMER DISEASE FAMILIES IDENTIFIES RARE VARIANTS IN MULTIPLE ALZHEIMER'S-RELATED GENES Alzheimer's & Dementia. 10: P518-P519. DOI: 10.1016/J.Jalz.2014.05.806 |
0.508 |
|
| 2014 |
Reitz C, Cheng R, Kunkle BW, Beecham G, Pericak-Vance MA, Farrer LA, Haines J, Schellenberg GD, Mayeux R. P1-054: LINKAGE ANALYSES OF EXTENDED CARIBBEAN HISPANIC FAMILIES INDICATES NOVEL LOCI ASSOCIATED WITH FAMILIAL LATE-ONSET ALZHEIMER'S DISEASE Alzheimer's & Dementia. 10: P323-P323. DOI: 10.1016/J.Jalz.2014.05.290 |
0.383 |
|
| 2014 |
Carney R, Kohli MA, Kunkle BW, Martin ER, Beecham GW, Gilbert JR, Pericak-Vance MA. P1-036: CLINICAL CHARACTERISTICS OF LATE ONSET ALZHEIMER DISEASE IN AN EXTENDED FAMILY WITH A MISSENSE VARIANT IN TTC3 Alzheimer's & Dementia. 10: P316-P316. DOI: 10.1016/J.Jalz.2014.05.271 |
0.448 |
|
| 2014 |
Kunkle BW, Naj AC, Hamilton-Nelson K, Perry WR, Partch A, Valladares O, Chung J, Jun G, Schmidt M, Beecham G, Wang L, Martin E, Mayeux R, Haines J, Farrer LA, et al. Low-Frequency Variant Imputation Identifies Novel Disease-Associated Loci In A Genome-Wide Association Study Of Late-Onset Alzheimer'S Disease Alzheimers & Dementia. 10: 135. DOI: 10.1016/J.Jalz.2014.04.076 |
0.498 |
|
| 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, 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 |
0.505 |
|
| 2013 |
Nuytemans K, Bademci G, Kohli MM, Beecham GW, Wang L, Young JI, Nahab F, Martin ER, Gilbert JR, Benatar M, Haines JL, Scott WK, Züchner S, Pericak-Vance MA, Vance JM. C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Annals of Human Genetics. 77: 351-63. PMID 23845100 DOI: 10.1111/Ahg.12033 |
0.332 |
|
| 2013 |
Nuytemans K, Bademci G, Inchausti V, Dressen A, Kinnamon DD, Mehta A, Wang L, Züchner S, Beecham GW, Martin ER, Scott WK, Vance JM. Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease. Neurology. 80: 982-9. PMID 23408866 DOI: 10.1212/Wnl.0B013E31828727D4 |
0.4 |
|
| 2013 |
Kohli MA, John-Williams K, Rajbhandary R, Naj A, Whitehead P, Hamilton K, Carney RM, Wright C, Crocco E, Gwirtzman HE, Lang R, Beecham G, Martin ER, Gilbert J, Benatar M, et al. Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians. Neurobiology of Aging. 34: 1519.e5-12. PMID 23107433 DOI: 10.1016/J.Neurobiolaging.2012.10.003 |
0.459 |
|
| 2013 |
Humphries C, Whitehead PL, Mash D, Beecham G, Pericak-Vance M, Gilbert J. P1-053: Genome-wide analysis of DNA methylation differentiates late-onset Alzheimer's disease from dementia with Lewy bodies Alzheimer's & Dementia. 9: P171-P172. DOI: 10.1016/J.Jalz.2013.05.274 |
0.434 |
|
| 2013 |
Pericak-Vance M, Kunkle B, Kholi M, Naj A, Perry W, Hamilton K, Whitehead PL, Levin B, Carney R, Crocco E, Wright C, Beecham G, Martin E, Wang L, Gilbert J, et al. P3-021: Variant-domain mapping in confirmed late-onset Alzheimer disease (LOAD) loci identifies multiple genomic regions with potentially functional variants Alzheimer's & Dementia. 9: P557-P557. DOI: 10.1016/J.Jalz.2013.05.1090 |
0.445 |
|
| 2013 |
Trittschuh E, Mukherjee S, Thornton T, Fardo D, Waterston L, Crane P, Mez J, Sherva R, Kauwe J, Naj A, Beecham G, Gross A, Saykin A, Green R. P3-003: Genome-wide SNP analysis finds executive-prominent late-onset Alzheimer's disease is highly heritable Alzheimer's & Dementia. 9: P550-P551. DOI: 10.1016/J.Jalz.2013.05.1072 |
0.41 |
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| 2013 |
Beecham G, Hamilton-Nelson K, Naj A, Wang L, Martin E, Mayeux R, Haines J, Farrer L, Schellenberg G, Pericak-Vance M, Montine T. O4-06-04: Late-onset Alzheimer's disease neuropathology genomic screen identifies novel loci for neuritic plaque and other Alzheimer's neuropathology features Alzheimer's & Dementia. 9: P693-P693. DOI: 10.1016/J.Jalz.2013.04.368 |
0.458 |
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| 2013 |
Kohli M, Kunkle B, Naj A, Carney RM, Hamilton-Nelson K, Rolati S, Whitehead PL, Gilbert J, Martin E, Beecham G, Wang L, Mayeux R, Haines J, Farrer L, Schellenberg G, et al. The identification of rare variants in late-onset Alzheimer’s disease using extended families Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.04.239 |
0.424 |
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| 2012 |
Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, et al. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Annals of Neurology. 71: 370-84. PMID 22451204 DOI: 10.1002/Ana.22687 |
0.36 |
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| 2012 |
Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. Plos Genetics. 8: e1002548. PMID 22438815 DOI: 10.1371/Journal.Pgen.1002548 |
0.419 |
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| 2012 |
Wang L, Hara K, Van Baaren JM, Price JC, Beecham GW, Gallins PJ, Whitehead PL, Wang G, Lu C, Slifer MA, Züchner S, Martin ER, Mash D, Haines JL, Pericak-Vance MA, et al. Vitamin D receptor and Alzheimer's disease: a genetic and functional study. Neurobiology of Aging. 33: 1844.e1-9. PMID 22306846 DOI: 10.1016/J.Neurobiolaging.2011.12.038 |
0.401 |
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| 2012 |
Cai G, Atzmon G, Naj AC, Beecham GW, Barzilai N, Haines JL, Sano M, Pericak-Vance M, Buxbaum JD. Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease. Neurobiology of Aging. 33: 416-417.e3. PMID 20381196 DOI: 10.1016/J.Neurobiolaging.2010.03.003 |
0.403 |
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| 2012 |
Zuchner S, Gonzalez M, Schuele R, Siskind C, Powell E, Montenegro G, Shengru G, Blanton S, Beecham G, Speziani F, Deconinck T, Young P, Kennerson M, Nicholson G, De Jonghe P, et al. Gene Identification in Axonopathies by Applying Massive Whole Exome Sequencing (S27.005) Neurology. 78: S27.005-S27.005. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S27.005 |
0.324 |
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| 2012 |
Vance J, Bademci G, Nuytemans K, Beecham G, Edwards Y, Singer C, Nahab F, Rhodes S, Ritz B, Zuchner S, Haines J, Scott W. Identification of Rare Variants in Parkinson Disease Using Next-Generation Sequencing (S22.007) Neurology. 78: S22.007-S22.007. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S22.007 |
0.425 |
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| 2012 |
Pericak-Vance M, Zuchner S, Kohli M, John-Williams K, Naj A, Rajbhandary R, Whitehead PL, Hamilton-Nelson K, Carney R, Wright C, Crocco E, Gwirtzman H, Lang R, Beecham G, Martin E, et al. Large repeat expansions in the C9ORF72 gene contribute to a spectrum of neurodegenerative disorders including Alzheimer's disease in Caucasians, but not African-Americans Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2013.08.277 |
0.424 |
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| 2012 |
Haines J, Naj A, Kohli M, Hamilton-Nelson K, Rajbhandary R, Whitehead PL, Carney R, Crocco E, Wright C, Beecham G, Martin E, Gilbert J, Zuchner S, Pericak-Vance M, Levin B. O5-03-01: Deep resequencing of 9 confirmed late-onset Alzheimer's disease (LOAD) loci identifies multiple genomic regions with potentially functional variants Alzheimer's & Dementia. 8: P734-P735. DOI: 10.1016/J.Jalz.2012.05.1981 |
0.458 |
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| 2012 |
Zuchner S, Kohli M, Naj A, Hamilton K, Rajbhandary R, Plitnik T, John-Williams K, Whitehead PL, Gilbert J, Martin E, Beecham G, Haines J, Pericak-Vance M. Exome sequencing of extended late-onset Alzheimer's disease families identifies a variant in the TTC3 gene Alzheimers & Dementia. 8: 679. DOI: 10.1016/J.Jalz.2012.05.1839 |
0.486 |
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| 2012 |
Kohli M, John-Williams K, Bademci G, Plitnik T, Whitehead PL, Rajbhandary R, Hamilton-Nelson K, Naj A, Wang L, Carney R, Martin E, Beecham G, Vance J, Small G, Gilbert J, et al. Identification of C9ORF72 repeat-expansions in Alzheimer's sample collections Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1823 |
0.345 |
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| 2012 |
Beecham G, Montine T, Rajbhandary R, Hamilton-Nelson K, Naj A, Martin E, Mayeux R, Haines J, Farrer L, Schellenberg G, Pericak-Vance M. P4-102: APP associated with late-onset Alzheimer's disease in an autopsy-confirmed dataset Alzheimer's & Dementia. 8: P668-P668. DOI: 10.1016/J.Jalz.2012.05.1805 |
0.48 |
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| 2012 |
Naj A, Park Y, Rajbhandary R, Hamilton-Nelson K, Beecham G, Martin E, Mayeux R, Haines J, Farrer L, Schellenberg G, Pericak-Vance M. Genome-wide association analyses of onset age in late-onset Alzheimer's disease (LOAD) demonstrate no strong effect outside of the apolipoprotein region Alzheimers & Dementia. 8: 554. DOI: 10.1016/J.Jalz.2012.05.1785 |
0.324 |
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| 2011 |
Hedges DJ, Guettouche T, Yang S, Bademci G, Diaz A, Andersen A, Hulme WF, Linker S, Mehta A, Edwards YJ, Beecham GW, Martin ER, Pericak-Vance MA, Zuchner S, Vance JM, et al. Comparison of three targeted enrichment strategies on the SOLiD sequencing platform. Plos One. 6: e18595. PMID 21559511 DOI: 10.1371/Journal.Pone.0018595 |
0.304 |
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| 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, 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 |
0.351 |
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| 2011 |
Edwards YJ, Beecham GW, Scott WK, Khuri S, Bademci G, Tekin D, Martin ER, Jiang Z, Mash DC, ffrench-Mullen J, Pericak-Vance MA, Tsinoremas N, Vance JM. Identifying consensus disease pathways in Parkinson's disease using an integrative systems biology approach. Plos One. 6: e16917. PMID 21364952 DOI: 10.1371/Journal.Pone.0016917 |
0.371 |
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| 2011 |
Züchner S, Dallman J, Wen R, Beecham G, Naj A, Farooq A, Kohli MA, Whitehead PL, Hulme W, Konidari I, Edwards YJ, Cai G, Peter I, Seo D, Buxbaum JD, et al. Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa. American Journal of Human Genetics. 88: 201-6. PMID 21295283 DOI: 10.1016/J.Ajhg.2011.01.001 |
0.348 |
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| 2011 |
Montenegro G, Powell E, Huang J, Speziani F, Edwards YJ, Beecham G, Hulme W, Siskind C, Vance J, Shy M, Züchner S. Exome sequencing allows for rapid gene identification in a Charcot-Marie-Tooth family. Annals of Neurology. 69: 464-70. PMID 21254193 DOI: 10.1002/Ana.22235 |
0.348 |
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| 2011 |
Beecham GW, Weir BS. Confidence interval of the likelihood ratio associated with mixed stain DNA evidence. Journal of Forensic Sciences. 56: S166-71. PMID 21198611 DOI: 10.1111/J.1556-4029.2010.01600.X |
0.46 |
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| 2011 |
Ortel TL, Beecham G, Hedges D, Whitehead P, Beecham A, Hahn S, Lawson JW, Erkan D, Brandao LR, James AH, Manco-Johnson MJ, Kulkarni R, Kitchens CS, Pericak-Vance M, Vance JM. Whole-Exome Sequencing Identifies Novel Risk Variant for Thrombotic Storm Blood. 118: 1229-1229. DOI: 10.1182/Blood.V118.21.1229.1229 |
0.36 |
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| 2011 |
Patel AA, Goldschmidt-Clermont PJ, Sikka N, Hamilton K, Pericak-Vance M, Beecham GW, Seo D. GENOME-WIDE ASSOCIATION FOR HYPERTENSION: RESULTS FROM THE MIAMI CARDIOVASCULAR REGISTRY Journal of the American College of Cardiology. 57: E1196. DOI: 10.1016/S0735-1097(11)61196-0 |
0.321 |
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| 2011 |
Kohli M, Naj A, Van Baaren J, Hulme W, Beecham G, Buxbaum J, Zuchner S, Haines J, Gilbert J, Pericak‐Vance M. P1‐242: Comprehensive Variant Discovery in the Late‐Onset Alzheimer's Disease Susceptibility Gene MTHFD1L Using Next Generation Sequencing Technology Alzheimer's & Dementia. 7. DOI: 10.1016/j.jalz.2011.05.522 |
0.34 |
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| 2011 |
Beecham G. Alzheimer's disease genetics consortium: new Alzheimer's disease genes and gene interactions Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.201 |
0.457 |
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| 2010 |
Naj AC, Beecham GW, Martin ER, Gallins PJ, Powell EH, Konidari I, Whitehead PL, Cai G, Haroutunian V, Scott WK, Vance JM, Slifer MA, Gwirtsman HE, Gilbert JR, Haines JL, et al. Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. Plos Genetics. 6: e1001130. PMID 20885792 DOI: 10.1371/Journal.Pgen.1001130 |
0.394 |
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| 2010 |
Lambert JC, Sleegers K, González-Pérez A, Ingelsson M, Beecham GW, Hiltunen M, Combarros O, Bullido MJ, Brouwers N, Bettens K, Berr C, Pasquier F, Richard F, Dekosky ST, Hannequin D, et al. The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. Journal of Alzheimer's Disease : Jad. 22: 247-55. PMID 20847397 DOI: 10.3233/Jad-2010-100933 |
0.456 |
|
| 2010 |
Jun G, Naj AC, Beecham GW, Wang LS, Buros J, Gallins PJ, Buxbaum JD, Ertekin-Taner N, Fallin MD, Friedland R, Inzelberg R, Kramer P, Rogaeva E, St George-Hyslop P, et al. Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. Archives of Neurology. 67: 1473-84. PMID 20697030 DOI: 10.1001/Archneurol.2010.201 |
0.396 |
|
| 2010 |
Beecham GW, Martin ER, Gilbert JR, Haines JL, Pericak-Vance MA. APOE is not associated with Alzheimer disease: a cautionary tale of genotype imputation. Annals of Human Genetics. 74: 189-94. PMID 20529013 DOI: 10.1111/J.1469-1809.2010.00573.X |
0.405 |
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| 2010 |
Beecham GW, Naj AC, Gilbert JR, Haines JL, Buxbaum JD, Pericak-Vance MA. PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility. Psychiatric Genetics. 20: 321-4. PMID 20523261 DOI: 10.1097/Ypg.0B013E32833B635D |
0.371 |
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| 2010 |
Seo D, Goldschidt-Clermont P, Velazquez O, Beecham G. Genomics of premature atherosclerotic vascular disease. Current Atherosclerosis Reports. 12: 187-193. PMID 20425258 DOI: 10.1007/S11883-010-0104-9 |
0.382 |
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| 2010 |
Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, Beecham GW, Wang L, Züchner S, Konidari I, Wang G, Singer C, Nahab F, Scott B, Stajich JM, Pericak-Vance M, et al. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Annals of Human Genetics. 74: 97-109. PMID 20070850 DOI: 10.1111/J.1469-1809.2009.00560.X |
0.422 |
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| 2010 |
Seo D, Goldschmidt-Clermont PJ, Hamilton K, Pericak-Vance M, Beecham G. GENOME-WIDE ASSOCIATION OF CORONARY ARTERY DISEASE Journal of the American College of Cardiology. 55: A174.E1632. DOI: 10.1016/S0735-1097(10)61633-6 |
0.335 |
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| 2010 |
Kohli MA, Griswold A, Naj AC, Beecham G, Haines JL, Gilbert J, Pericak-Vance MA. Comprehensive variant discovery in the Late-Onset Alzheimer Disease susceptibility gene Clusterin using next generation sequencing technology Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.610 |
0.441 |
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| 2010 |
Beecham GW, Schnetz-Boutaud N, Bartlett J, Naj A, Gilbert J, Martin ER, Buxbaum J, Haines JL, Pericak-Vance MA. Copy number polymorphism at chromosome 19 locus associated with late-onset Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.349 |
0.389 |
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| 2010 |
Naj AC, Beecham GW, Martin ER, Gallins PJ, Powell EH, Konidari I, Whitehead PL, Cai G, Kajiwara Y, Haroutunian V, Scott WK, Vance JM, Slifer MA, Gwirtsman HE, Gilbert JR, et al. O1‐03‐03: Dementia revealed: Novel chromosome 6 locus for late‐onset Alzheimer's disease provides genetic evidence for folate‐pathway abnormalities Alzheimer's & Dementia. 6. DOI: 10.1016/j.jalz.2010.05.219 |
0.326 |
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| 2010 |
Zuchner S, Beecham G, Haines J, Pericak-Vance M. O1-03-02: Exome sequencing of late-onset extended Alzheimer families Alzheimer's & Dementia. 6: S74-S74. DOI: 10.1016/J.Jalz.2010.05.218 |
0.347 |
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| 2010 |
Seo D, Goldschmidt-Clermont P, Velazquez O, Beecham G. Erratum to: Genomics of Premature Atherosclerotic Vascular Disease Current Atherosclerosis Reports. 12: 355-355. DOI: 10.1007/S11883-010-0127-2 |
0.392 |
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| 2009 |
Beecham GW, Schnetz-Boutaud N, Haines JL, Pericak-Vance MA. CALHM1 polymorphism is not associated with late-onset Alzheimer disease. Annals of Human Genetics. 73: 379-81. PMID 19472444 DOI: 10.1111/J.1469-1809.2009.00509.X |
0.403 |
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| 2009 |
Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, et al. A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Annals of Human Genetics. 73: 263-73. PMID 19456320 DOI: 10.1111/J.1469-1809.2009.00523.X |
0.395 |
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| 2009 |
Kajiwara Y, Akram A, Katsel P, Haroutunian V, Schmeidler J, Beecham G, Haines JL, Pericak-Vance MA, Buxbaum JD. FE65 binds Teashirt, inhibiting expression of the primate-specific caspase-4. Plos One. 4: e5071. PMID 19343227 DOI: 10.1371/Journal.Pone.0005071 |
0.355 |
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| 2009 |
Beecham GW, Martin ER, Li YJ, Slifer MA, Gilbert JR, Haines JL, Pericak-Vance MA. Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. American Journal of Human Genetics. 84: 35-43. PMID 19118814 DOI: 10.1016/J.Ajhg.2008.12.008 |
0.413 |
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| 2009 |
Edwards T, Scott W, Almonte C, Burt A, Powell E, Beecham G, Wang L, Zuchner S, Konidari I, Wang G, Pericak-Vance M, Haines J, Vance J, Martin E. P3.116 Genome-wide signiflcant conflrmation of SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease Parkinsonism & Related Disorders. 15: S178. DOI: 10.1016/S1353-8020(09)70680-7 |
0.328 |
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| 2009 |
Chung R, Edwards T, Scott W, Almonte C, Burt A, Powell E, Beecham G, Konidari I, Pericak-Vance M, Haines J, Zuchner S, Wang G, Wang L, Vance J, Martin E. P1.126 Developing a risk model for Parkinson disease Parkinsonism & Related Disorders. 15: S61. DOI: 10.1016/S1353-8020(09)70248-2 |
0.621 |
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| 2009 |
Naj AC, Beecham GW, Slifer MA, Martin ER, Gallins PJ, Konidari I, Whitehead PL, Cai G, Kajiwara Y, Haroutunian V, Gwirtsman HE, Gilbert JR, Haines JL, Buxbaum JD, Pericak-Vance MA. Genome-wide association study validates associations in APOE, VDR, SORL1, WWC1, and ELAVL4 and identifies novel candidate genes for late-onset Alzheimer's disease Alzheimers & Dementia. 5. DOI: 10.1016/J.Jalz.2009.05.519 |
0.498 |
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| 2009 |
Beecham GW, Naj AC, Cai G, Kajiwara Y, Haroutunian V, Konidari I, Gallins P, Whitehead P, Gilbert JR, Slifer MA, Gwirstman H, Martin ER, Buxbaum J, Haines JL, Pericak-Vance MA. GRB-associated binding protein 2 (GAB2) interacts with APOE to alter risk of late-onset Alzheimer's disease Alzheimers & Dementia. 5: 111. DOI: 10.1016/J.Jalz.2009.05.348 |
0.416 |
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| 2009 |
Slifer MA, Naj A, Beecham G, Martin E, Konidari I, Whitehead P, Gallins P, Cai G, Kajiwara Y, Haroutunian V, Vance J, Haines J, Buxbaum J, Pericak-Vance M. ELAVL4 locus confirmed in depression of Alzheimer's disease Alzheimers & Dementia. 5: 468. DOI: 10.1016/J.Jalz.2009.04.793 |
0.376 |
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| 2008 |
Slifer MA, Beecham GW, Martin ER, Wang G, Gilbert JR, Haines JL, Vance J, Pericak-Vance MA. O2-06-02: A genetic susceptibility locus for depression of Alzheimer's disease and Parkinson's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.350 |
0.424 |
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| 2008 |
Martin ER, Turner SD, Beecham GW, Gilbert JR, Haines JL, Pericak-Vance MA, Ritchie MD. P3-240: Genome-wide analysis of gene-gene interaction in Alzheimer's disease Alzheimer's & Dementia. 4: T591-T591. DOI: 10.1016/J.Jalz.2008.05.1807 |
0.446 |
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| 2008 |
Hara K, Gilbert J, Gallins P, Whitehead P, Beecham G, Slifer M, Martin E, Haines J, Pericak-Vance M. P3-228: Genetic association of vitamin D receptor gene on chromosome 12q with late-onset Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1795 |
0.391 |
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| 2008 |
Gilbert JR, Beecham G, Gallins P, Slifer M, Martin ER, Haines J, Pericak-Vance MA. P3-223: Genome-wide association analysis of the age-at-onset for individuals with Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1790 |
0.479 |
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| 2008 |
Beecham GW, Slifer MA, Martin ER, Li Y, Carney RM, Gilbert JR, Haines JL, Pericak-Vance MA. P3-200: Genomic convergence of late-onset Alzheimer's disease candidate genes Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1766 |
0.497 |
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| 2006 |
Beecham GW, Vardarajan BN, Blue E, Bush WS, Jaworski J, Barral S, Kunkle BW, Martin ER, Reitz C, van Duijn CM, Haines JL, Schellenberg GD, Mayeux R, Wijsman E, Pericak-Vance MA. P2-108: WHOLE-GENOME SEQUENCING IN NON-HISPANIC WHITE FAMILIES IMPLICATES RARE VARIATION IN LATE-ONSET ALZHEIMER'S DISEASE RISK Alzheimer's & Dementia. 14: P710-P710. DOI: 10.1016/J.Jalz.2018.06.794 |
0.495 |
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