Gary W. Beecham, Ph.D. - Publications

Affiliations: 
2006 North Carolina State University, Raleigh, NC 
Area:
Genetics, Statistics, Bioinformatics Biology

151 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Sanders AR, Beecham GW, Guo S, Dawood K, Rieger G, Krishnappa RS, Kolundzija AB, Bailey JM, Martin ER. Genome-Wide Linkage and Association Study of Childhood Gender Nonconformity in Males. Archives of Sexual Behavior. PMID 34518958 DOI: 10.1007/s10508-021-02146-x  1
2021 Zietsch BP, Sidari MJ, Abdellaoui A, Maier R, Långström N, Guo S, Beecham GW, Martin ER, Sanders AR, Verweij KJH. Author Correction: Genomic evidence consistent with antagonistic pleiotropy may help explain the evolutionary maintenance of same-sex sexual behaviour in humans. Nature Human Behaviour. PMID 34518664 DOI: 10.1038/s41562-021-01210-9  1
2021 Zietsch BP, Sidari MJ, Abdellaoui A, Maier R, Långström N, Guo S, Beecham GW, Martin ER, Sanders AR, Verweij KJH. Genomic evidence consistent with antagonistic pleiotropy may help explain the evolutionary maintenance of same-sex sexual behaviour in humans. Nature Human Behaviour. PMID 34426668 DOI: 10.1038/s41562-021-01168-8  1
2021 Sanders AR, Beecham GW, Guo S, Badner JA, Bocklandt S, Mustanski BS, Hamer DH, Martin ER. Genome-Wide Linkage Study Meta-Analysis of Male Sexual Orientation. Archives of Sexual Behavior. PMID 34080073 DOI: 10.1007/s10508-021-02035-3  1
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  1
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  1
2021 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. Response to Comment on "Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior". Science (New York, N.Y.). 371. PMID 33766859 DOI: 10.1126/science.aba5693  1
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  1
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  1
2020 Marca-Ysabel MV, Rajabli F, Cornejo-Olivas M, Whitehead PG, Hofmann NK, Illanes Manrique MZ, Veliz Otani DM, Milla Neyra AK, Castro Suarez S, Meza Vega M, Adams LD, Mena PR, Rosario I, Cuccaro ML, Vance JM, ... Beecham GW, et al. Dissecting the role of Amerindian genetic ancestry and the ApoE ε4 allele on Alzheimer disease in an admixed Peruvian population. Neurobiology of Aging. PMID 33541779 DOI: 10.1016/j.neurobiolaging.2020.10.003  1
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  0.01
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  1
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  1
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  0.01
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  1
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  1
2019 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. Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry. PMID 31636380 DOI: 10.1038/s41380-019-0529-7  1
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  1
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. Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. Science (New York, N.Y.). 365. PMID 31467194 DOI: 10.1126/Science.Aat7693  1
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  1
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  1
2019 Beecham AH, Amezcua L, Chinea A, Manrique CP, Rubi C, Isobe N, Lund BT, Santaniello A, Beecham GW, Burchard EG, Comabella M, Patsopoulos N, Fitzgerald K, Calabresi PA, De Jager P, et al. The genetic diversity of multiple sclerosis risk among Hispanic and African American populations living in the United States. Multiple Sclerosis (Houndmills, Basingstoke, England). 1352458519863764. PMID 31368393 DOI: 10.1177/1352458519863764  1
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  1
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  1
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  1
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  1
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  1
2019 Chauhan G, Adams HHH, Satizabal CL, Bis JC, Teumer A, Sargurupremraj M, Hofer E, Trompet S, Hilal S, Smith AV, Jian X, Malik R, Traylor M, Pulit SL, Amouyel P, ... ... Beecham GW, et al. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting. Neurology. PMID 30651383 DOI: 10.1212/Wnl.0000000000006851  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2018 Wedow R, Abdellaoui A, Beecham G, Day F, Ganna A, Guo S, Maier R, Martin E, Neale B, Nivard M, Perry J, Sanders A, Verweij K, Zietsch B. Results from the largest genetic study of sexual orientation Behavior Genetics. 48: 454-526. PMID 30284061 DOI: 10.1007/S10519-018-9929-8  1
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  1
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  1
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  1
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  1
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  1
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  1
2018 Celis K, Feliciano-Astacio BE, Acosta H, Chinea A, Adams LD, Beecham GW, Pericak-Vance MAA, Vance JM, Cuccaro ML. P2-121: Apolipoprotein E And Phenotypic Features In Hispanics Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.807  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2017 Martin ER, Tunc I, Liu Z, Slifer SH, Beecham AH, Beecham GW. Properties of global- and local-ancestry adjustments in genetic association tests in admixed populations. Genetic Epidemiology. PMID 29288582 DOI: 10.1002/Gepi.22103  1
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  1
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  1
2017 Liu Z, Pericak-Vance MA, Goldschmidt-Clermont P, Seo D, Wang L, Rundek T, Beecham GW. Coronary collateralization shows sex and racial-ethnic differences in obstructive artery disease patients. Plos One. 12: e0183836. PMID 29016599 DOI: 10.1371/Journal.Pone.0183836  1
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  1
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  1
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  0.01
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2017 Byfield G, Starks T, Byrd GS, Cuccaro ML, Adams LD, Whitehead PL, Reitz C, Beecham GW, Reyes-Dumeyer D, Haines JL, Mayeux R, Vance JM, Pericak-Vance MA, Edwards C, Hamilton-Nelson KL. Influence Of Community Engaged Family Connector In Recruiting And Ascertaining African Americans’ Family Members For Genomic Research Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.724  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2016 Ridge PG, Hoyt KB, Boehme K, Mukherjee S, Crane PK, Haines JL, Mayeux R, Farrer LA, Pericak-Vance MA, Schellenberg GD, Kauwe JS. Assessment of the genetic variance of late-onset Alzheimer's disease. Neurobiology of Aging. PMID 27036079 DOI: 10.1016/J.Neurobiolaging.2016.02.024  1
2016 Traylor M, Adib-Samii P, Harold D, Dichgans M, Williams J, Lewis CM, Markus HS. Shared genetic contribution to Ischaemic Stroke and Alzheimer's Disease. Annals of Neurology. PMID 26913989 DOI: 10.1002/Ana.24621  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2015 Wang L, Evatt ML, Maldonado LG, Perry WR, Ritchie JC, Beecham GW, Martin ER, Haines JL, Pericak-Vance MA, Vance JM, Scott WK. Vitamin D from different sources is inversely associated with Parkinson disease. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 560-6. PMID 25545356 DOI: 10.1002/Mds.26117  1
2015 . Convergent genetic and expression data implicate immunity in Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 11: 658-71. PMID 25533204 DOI: 10.1016/J.Jalz.2014.05.1757  1
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  1
2015 Sanders AR, Martin ER, Beecham GW, Guo S, Dawood K, Rieger G, Badner JA, Gershon ES, Krishnappa RS, Kolundzija AB, Duan J, Gejman PV, Bailey JM. Genome-wide scan demonstrates significant linkage for male sexual orientation. Psychological Medicine. 45: 1379-88. PMID 25399360 DOI: 10.1017/S0033291714002451  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2013 Humphries C, Gilbert J, Kohli M, Whitehead PL, Mash D, Beecham G, Pericak-Vance M. RNA transcription and editing in Alzheimer’s disease Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.04.474  1
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  1
2012 Whitcomb DC, LaRusch J, Krasinskas AM, Klei L, Smith JP, Brand RE, Neoptolemos JP, Lerch MM, Tector M, Sandhu BS, Guda NM, Orlichenko L, Alkaade S, Amann ST, et al. Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nature Genetics. 44: 1349-54. PMID 23143602 DOI: 10.1038/Ng.2466  1
2012 Liu ZJ, Tan Y, Beecham GW, Seo DM, Tian R, Li Y, Vazquez-Padron RI, Pericak-Vance M, Vance JM, Goldschmidt-Clermont PJ, Livingstone AS, Velazquez OC. Notch activation induces endothelial cell senescence and pro-inflammatory response: implication of Notch signaling in atherosclerosis. Atherosclerosis. 225: 296-303. PMID 23078884 DOI: 10.1016/J.Atherosclerosis.2012.04.010  1
2012 Hedges DJ, Hamilton-Nelson KL, Sacharow SJ, Nations L, Beecham GW, Kozhekbaeva ZM, Butler BL, Cukier HN, Whitehead PL, Ma D, Jaworski JM, Nathanson L, Lee JM, Hauser SL, Oksenberg JR, et al. Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci. Molecular Autism. 3: 2. PMID 22472195 DOI: 10.1186/2040-2392-3-2  1
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  1
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  1
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  1
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  1
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  1
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  1
2012 Carney R, Kohli M, Naj A, Beecham G, Hamilton-Nelson K, Haines J, Gilbert J, Zuchner S, Pericak-Vance M. Parkinsonian symptoms and lack of prominent frontal atrophy in a family with early-onset dementia and the MAPT R406W mutation Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1832  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2011 Liu Z, Tan Y, Tian R, Li Y, Beecham GW, Seo DM, Vazquez-Padron RI, Pericak-Vance M, Vance J, Goldschmidt-Clermont P, Livingstone AS, Velazquez O. PS200. Notch Activation Induces Endothelial Cell Senescence and Pro-Inflammatory Response: Implication of Notch Signaling in Atherosclerosis Journal of Vascular Surgery. 53. DOI: 10.1016/J.Jvs.2011.03.157  1
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  0.01
2010 Goldschmidt-Clermont PJ, Seo DM, Wang L, Beecham GW, Liu ZJ, Vazquez-Padron RI, Dong C, Hare JM, Kapiloff MS, Bishopric NH, Pericak-Vance M, Vance JM, Velazquez OC. Inflammation, stem cells and atherosclerosis genetics. Current Opinion in Molecular Therapeutics. 12: 712-23. PMID 21154163  1
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  1
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  1
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  1
2010 . IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci. Genes and Immunity. 11: 397-405. PMID 20555355 DOI: 10.1038/Gene.2010.28  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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