| Year |
Citation |
Score |
| 2023 |
Aslam MM, Fan KH, Lawrence E, Bedison MA, Snitz BE, DeKosky ST, Lopez OL, Feingold E, Kamboh MI. Genome-wide analysis identifies novel loci influencing plasma apolipoprotein E concentration and Alzheimer's disease risk. Molecular Psychiatry. PMID 37666928 DOI: 10.1038/s41380-023-02170-4 |
0.361 |
|
| 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, ... ... Kamboh MI, 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 |
0.394 |
|
| 2023 |
Ali M, Archer DB, Gorijala P, Western D, Timsina J, Fernández MV, Wang TC, Satizabal CL, Yang Q, Beiser AS, Wang R, Chen G, Gordon B, Benzinger TLS, Xiong C, ... ... Kamboh MI, et al. Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer disease. Acta Neuropathologica Communications. 11: 68. PMID 37101235 DOI: 10.1186/s40478-023-01563-4 |
0.375 |
|
| 2023 |
Nho K, Risacher SL, Apostolova L, Bice PJ, Brosch J, Deardorff R, Faber K, Farlow MR, Foroud T, Gao S, Rosewood T, Kim JP, Nudelman K, Yu M, Aisen P, ... ... Kamboh MI, et al. Novel Alzheimer's disease locus identified by genome-wide association analysis of cerebral tau deposition on PET. Medrxiv : the Preprint Server For Health Sciences. PMID 36993271 DOI: 10.1101/2023.02.27.23286048 |
0.371 |
|
| 2022 |
Fan K, Francis L, Aslam MM, Bedison MA, Lawrence E, Acharya V, Snitz BE, Ganguli M, DeKosky ST, Lopez OL, Feingold E, Kamboh MI. Investigation of the independent role of a rare APOE variant (L28P; APOE*4Pittsburgh) in late-onset Alzheimer disease. Neurobiology of Aging. 122: 107-111. PMID 36528961 DOI: 10.1016/j.neurobiolaging.2022.11.007 |
0.367 |
|
| 2022 |
Wu M, Schweitzer N, Iordanova BE, Halligan-Eddy E, Tudorascu DL, Mathis CA, Lopresti BJ, Kamboh MI, Cohen AD, Snitz BE, Klunk WE, Aizenstein HJ. In Pre-Clinical AD Small Vessel Disease is Associated With Altered Hippocampal Connectivity and Atrophy. The American Journal of Geriatric Psychiatry : Official Journal of the American Association For Geriatric Psychiatry. PMID 36274019 DOI: 10.1016/j.jagp.2022.09.011 |
0.307 |
|
| 2022 |
Harper JD, Fan KH, Aslam MM, Snitz BE, DeKosky ST, Lopez OL, Feingold E, Kamboh MI. Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Journal of Alzheimer's Disease : Jad. PMID 35694926 DOI: 10.3233/JAD-220293 |
0.328 |
|
| 2022 |
Khan MJ, Chung NA, Hansen S, Dumitrescu L, Hohman TJ, Kamboh MI, Lopez OL, Robinson RAS. Targeted Lipidomics To Measure Phospholipids and Sphingomyelins in Plasma: A Pilot Study To Understand the Impact of Race/Ethnicity in Alzheimer's Disease. Analytical Chemistry. 94: 4165-4174. PMID 35235294 DOI: 10.1021/acs.analchem.1c03821 |
0.304 |
|
| 2021 |
Kamboh MI. Genomics and Functional Genomics of Alzheimer's Disease. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 19: 152-172. PMID 34935119 DOI: 10.1007/s13311-021-01152-0 |
0.376 |
|
| 2021 |
Kamboh MI. Genomics and Functional Genomics of Alzheimer's Disease. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 19: 152-172. PMID 34935119 DOI: 10.1007/s13311-021-01152-0 |
0.376 |
|
| 2021 |
Kamboh MI. Genomics and Functional Genomics of Alzheimer's Disease. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 19: 152-172. PMID 34935119 DOI: 10.1007/s13311-021-01152-0 |
0.376 |
|
| 2021 |
DeMichele-Sweet MAA, Klei L, Creese B, Harwood JC, Weamer EA, McClain L, Sims R, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Alarcón-Martín E, Valero S, Liu Y, ... ... Kamboh MI, et al. Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. Molecular Psychiatry. PMID 34112972 DOI: 10.1038/s41380-021-01152-8 |
0.388 |
|
| 2021 |
Khan MJ, Desaire H, Lopez OL, Kamboh MI, Robinson RAS. Why Inclusion Matters for Alzheimer's Disease Biomarker Discovery in Plasma. Journal of Alzheimer's Disease : Jad. PMID 33427747 DOI: 10.3233/JAD-201318 |
0.301 |
|
| 2020 |
Kunkle BW, Schmidt M, Klein HU, Naj AC, Hamilton-Nelson KL, Larson EB, Evans DA, De Jager PL, Crane PK, Buxbaum JD, Ertekin-Taner N, Barnes LL, Fallin MD, Manly JJ, Go RCP, ... ... Kamboh MI, et al. Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis. Jama Neurology. PMID 33074286 DOI: 10.1001/jamaneurol.2020.3536 |
0.309 |
|
| 2020 |
Cheema AN, Pirim D, Wang X, Ali J, Bhatti A, John P, Feingold E, Demirci FY, Kamboh MI. Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population. Disease Markers. 2020: 9738567. PMID 32685059 DOI: 10.1155/2020/9738567 |
0.302 |
|
| 2020 |
Fan KH, Feingold E, Rosenthal SL, Demirci FY, Ganguli M, Lopez OL, Kamboh MI. Whole-Exome Sequencing Analysis of Alzheimer's Disease in Non-APOE*4 Carriers. Journal of Alzheimer's Disease : Jad. PMID 32651314 DOI: 10.3233/Jad-200037 |
0.459 |
|
| 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, ... ... Kamboh MI, 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 |
0.36 |
|
| 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, ... ... Kamboh MI, 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 |
0.318 |
|
| 2019 |
Pirim D, Radwan ZH, Wang X, Niemsiri V, Hokanson JE, Hamman RF, Feingold E, Bunker CH, Demirci FY, Kamboh MI. Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups. Plos One. 14: e0214060. PMID 30913229 DOI: 10.1371/Journal.Pone.0214060 |
0.343 |
|
| 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, ... ... Kamboh MI, 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 |
0.361 |
|
| 2019 |
Kamboh MI, Bhatia KK, Ferrell RE. Genetic studies of human apolipoproteins: XII. Population genetics of apolipoproteins in Papua New Guinea. American Journal of Human Biology : the Official Journal of the Human Biology Council. 2: 17-23. PMID 28520258 DOI: 10.1002/Ajhb.1310020103 |
0.392 |
|
| 2018 |
Mukherjee S, Mez J, Trittschuh EH, Saykin AJ, Gibbons LE, Fardo DW, Wessels M, Bauman J, Moore M, Choi SE, Gross AL, Rich J, Louden DKN, Sanders RE, Grabowski TJ, ... ... Kamboh MI, et al. Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. Molecular Psychiatry. PMID 30514930 DOI: 10.1038/S41380-018-0298-8 |
0.318 |
|
| 2018 |
Kamboh MI. A Brief Synopsis on the Genetics of Alzheimer's Disease. Current Genetic Medicine Reports. 6: 133-135. PMID 30460168 DOI: 10.1007/s40142-018-0155-8 |
0.32 |
|
| 2018 |
Yan Q, Nho K, Del-Aguila JL, Wang X, Risacher SL, Fan KH, Snitz BE, Aizenstein HJ, Mathis CA, Lopez OL, Demirci FY, Feingold E, Klunk WE, Saykin AJ, ... ... Kamboh MI, et al. Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging. Molecular Psychiatry. PMID 30361487 DOI: 10.1038/S41380-018-0246-7 |
0.328 |
|
| 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, ... ... Kamboh MI, 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 |
0.397 |
|
| 2017 |
DeMichele-Sweet MAA, Weamer EA, Klei L, Vrana DT, Hollingshead DJ, Seltman HJ, Sims R, Foroud T, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Ruiz A, Williams J, Mayeux R, ... ... Kamboh MI, et al. Genetic risk for schizophrenia and psychosis in Alzheimer disease. Molecular Psychiatry. PMID 28461698 DOI: 10.1038/Mp.2017.81 |
0.366 |
|
| 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, ... ... Kamboh MI, 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 |
0.381 |
|
| 2016 |
Mez J, Chung J, Jun G, Kriegel J, Bourlas AP, Sherva R, Logue MW, Barnes LL, Bennett DA, Buxbaum JD, Byrd GS, Crane PK, Ertekin-Taner N, Evans D, Fallin MD, ... ... Kamboh MI, et al. Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 27770636 DOI: 10.1016/J.Jalz.2016.09.002 |
0.322 |
|
| 2015 |
Ghani M, Reitz C, Cheng R, Vardarajan BN, Jun G, Sato C, Naj A, Rajbhandary R, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, ... ... Kamboh MI, et al. Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals. Jama Neurology. PMID 26366463 DOI: 10.1001/Jamaneurol.2015.1700 |
0.404 |
|
| 2015 |
Barral S, Vardarajan BN, Reyes-Dumeyer D, Faber KM, Bird TD, Tsuang D, Bennett DA, Rosenberg R, Boeve BF, Graff-Radford NR, Goate AM, Farlow M, Lantigua R, Medrano MZ, Wang X, ... Kamboh MI, et al. Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer's disease families. Neurobiology of Aging. 36: 3116.e9-3116.e16. PMID 26359528 DOI: 10.1016/J.Neurobiolaging.2015.08.006 |
0.307 |
|
| 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, ... ... Kamboh MI, 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 |
0.383 |
|
| 2015 |
Rosenthal SL, Bamne MN, Wang X, Berman S, Snitz BE, Klunk WE, Sweet RA, Demirci FY, Lopez OL, Kamboh MI. More evidence for association of a rare TREM2 mutation (R47H) with Alzheimer's disease risk. Neurobiology of Aging. 36: 2443.e21-6. PMID 26058841 DOI: 10.1016/J.Neurobiolaging.2015.04.012 |
0.353 |
|
| 2015 |
Zheng X, Demirci FY, Barmada MM, Richardson GA, Lopez OL, Sweet RA, Kamboh MI, Feingold E. Genome-wide copy-number variation study of psychosis in Alzheimer's disease. Translational Psychiatry. 5: e574. PMID 26035058 DOI: 10.1038/Tp.2015.64 |
0.369 |
|
| 2015 |
Cheema AN, Bhatti A, Wang X, Ali J, Bamne MN, Demirci FY, Kamboh MI. APOE gene polymorphism and risk of coronary stenosis in Pakistani population. Biomed Research International. 2015: 587465. PMID 25883965 DOI: 10.1155/2015/587465 |
0.373 |
|
| 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, ... ... Kamboh MI, et al. A novel Alzheimer disease locus located near the gene encoding tau protein. Molecular Psychiatry. PMID 25778476 DOI: 10.1038/Mp.2015.23 |
0.408 |
|
| 2015 |
Wang X, Lopez O, Sweet RA, Becker JT, DeKosky ST, Barmada MM, Feingold E, Demirci FY, Kamboh MI. Genetic Determinants of Survival in Patientswith Alzheimer’s Disease. Journal of Alzheimer's Disease : Jad. 45: 651-8. PMID 25649651 DOI: 10.3233/Jad-142442 |
0.398 |
|
| 2015 |
Pirim D, Wang X, Radwan ZH, Niemsiri V, Bunker CH, Barmada MM, Kamboh MI, Demirci FY. Resequencing of LPL in African Blacks and associations with lipoprotein-lipid levels. European Journal of Human Genetics : Ejhg. 23: 1244-53. PMID 25626708 DOI: 10.1038/Ejhg.2014.268 |
0.318 |
|
| 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, ... ... Kamboh MI, 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 |
0.385 |
|
| 2015 |
Chaudhry M, Wang X, Bamne MN, Hasnain S, Demirci FY, Lopez OL, Kamboh MI. Genetic variation in imprinted genes is associated with risk of late-onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 44: 989-94. PMID 25391383 DOI: 10.3233/Jad-142106 |
0.401 |
|
| 2015 |
Wang X, Lopez OL, Sweet RA, Becker JT, DeKosky ST, Barmada MM, Demirci FY, Kamboh MI. Genetic determinants of disease progression in Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 43: 649-55. PMID 25114068 DOI: 10.3233/Jad-140729 |
0.459 |
|
| 2014 |
Floudas CS, Um N, Kamboh MI, Barmada MM, Visweswaran S. Identifying genetic interactions associated with late-onset Alzheimer's disease. Biodata Mining. 7: 35. PMID 25649863 DOI: 10.1186/s13040-014-0035-z |
0.326 |
|
| 2014 |
Zheng X, Demirci FY, Barmada MM, Richardson GA, Lopez OL, Sweet RA, Kamboh MI, Feingold E. A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease. Plos One. 9: e111462. PMID 25379732 DOI: 10.1371/Journal.Pone.0111462 |
0.317 |
|
| 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, ... ... Kamboh MI, 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 |
0.349 |
|
| 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 |
0.372 |
|
| 2014 |
Logue MW, Schu M, Vardarajan BN, Farrell J, Bennett DA, Buxbaum JD, Byrd GS, Ertekin-Taner N, Evans D, Foroud T, Goate A, Graff-Radford NR, Kamboh MI, Kukull WA, Manly JJ, et al. Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 609-618.e11. PMID 25172201 DOI: 10.1016/J.Jalz.2014.06.010 |
0.365 |
|
| 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, ... ... Kamboh MI, 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 |
0.366 |
|
| 2014 |
Rosenthal SL, Kamboh MI. Late-Onset Alzheimer's Disease Genes and the Potentially Implicated Pathways. Current Genetic Medicine Reports. 2: 85-101. PMID 24829845 DOI: 10.1007/s40142-014-0034-x |
0.306 |
|
| 2014 |
Rosenthal SL, Barmada MM, Wang X, Demirci FY, Kamboh MI. Connecting the dots: potential of data integration to identify regulatory SNPs in late-onset Alzheimer's disease GWAS findings. Plos One. 9: e95152. PMID 24743338 DOI: 10.1371/journal.pone.0095152 |
0.325 |
|
| 2014 |
Bamne MN, Demirci FY, Berman S, Snitz BE, Rosenthal SL, Wang X, Lopez OL, Kamboh MI. Investigation of an amyloid precursor protein protective mutation (A673T) in a North American case-control sample of late-onset Alzheimer's disease. Neurobiology of Aging. 35: 1779.e15-6. PMID 24529499 DOI: 10.1016/J.Neurobiolaging.2014.01.020 |
0.382 |
|
| 2014 |
Cruchaga C, Karch CM, Jin SC, Benitez BA, Cai Y, Guerreiro R, Harari O, Norton J, Budde J, Bertelsen S, Jeng AT, Cooper B, Skorupa T, Carrell D, Levitch D, ... ... Kamboh MI, et al. Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease. Nature. 505: 550-4. PMID 24336208 DOI: 10.1038/Nature12825 |
0.364 |
|
| 2014 |
Wang MH, Fiocchi C, Zhu X, Ripke S, Kamboh MI, Rebert N, Duerr RH, Achkar JP. Gene-gene and gene-environment interactions in ulcerative colitis. Human Genetics. 133: 547-58. PMID 24241240 DOI: 10.1007/s00439-013-1395-z |
0.325 |
|
| 2014 |
Pirim D, Wang X, Radwan ZH, Niemsiri V, Hokanson JE, Hamman RF, Barmada MM, Demirci FY, Kamboh MI. Lipoprotein lipase gene sequencing and plasma lipid profile. Journal of Lipid Research. 55: 85-93. PMID 24212298 DOI: 10.1194/jlr.M043265 |
0.316 |
|
| 2014 |
Hughes TM, Lopez OL, Evans RW, Kamboh MI, Williamson JD, Klunk WE, Mathis CA, Price JC, Cohen AD, Snitz BE, Dekosky ST, Kuller LH. Markers of cholesterol transport are associated with amyloid deposition in the brain. Neurobiology of Aging. 35: 802-7. PMID 24199960 DOI: 10.1016/J.Neurobiolaging.2013.09.040 |
0.314 |
|
| 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, ... ... Kamboh MI, 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 |
0.37 |
|
| 2013 |
Reitz C, Jun G, Naj A, Rajbhandary R, Vardarajan BN, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, Crane PK, Buxbaum JD, Murrell JR, ... ... Kamboh MI, et al. Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. Jama. 309: 1483-92. PMID 23571587 DOI: 10.1001/Jama.2013.2973 |
0.457 |
|
| 2012 |
Christie D, Shofer J, Millard SP, Li E, Demichele-Sweet MA, Weamer EA, Kamboh MI, Lopez OL, Sweet RA, Tsuang D. Genetic association between APOE*4 and neuropsychiatric symptoms in patients with probable Alzheimer's disease is dependent on the psychosis phenotype. Behavioral and Brain Functions : Bbf. 8: 62. PMID 23270420 DOI: 10.1186/1744-9081-8-62 |
0.324 |
|
| 2012 |
Elbers CC, Guo Y, Tragante V, van Iperen EP, Lanktree MB, Castillo BA, Chen F, Yanek LR, Wojczynski MK, Li YR, Ferwerda B, Ballantyne CM, Buxbaum SG, Chen YD, Chen WM, ... ... Kamboh MI, et al. Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations. Plos One. 7: e50198. PMID 23236364 DOI: 10.1371/Journal.Pone.0050198 |
0.318 |
|
| 2012 |
Rosenthal SL, Wang X, Demirci FY, Barmada MM, Ganguli M, Lopez OL, Kamboh MI. Beta-amyloid toxicity modifier genes and the risk of Alzheimer's disease. American Journal of Neurodegenerative Disease. 1: 191-8. PMID 22984654 |
0.403 |
|
| 2012 |
Kamboh MI, Demirci FY, Wang X, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ, Jun G, Baldwin C, Logue MW, Buros J, Farrer L, Pericak-Vance MA, et al. Genome-wide association study of Alzheimer's disease. Translational Psychiatry. 2: e117. PMID 22832961 DOI: 10.1038/Tp.2012.45 |
0.441 |
|
| 2012 |
Allen M, Zou F, Chai HS, Younkin CS, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN, Nair AA, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus KG, Palusak R, ... ... Kamboh MI, et al. Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology. 79: 221-8. PMID 22722634 DOI: 10.1212/Wnl.0B013E3182605801 |
0.373 |
|
| 2012 |
Kamboh MI, Barmada MM, Demirci FY, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ, Sweet RA, Feingold E, DeKosky ST, Lopez OL. Genome-wide association analysis of age-at-onset in Alzheimer's disease. Molecular Psychiatry. 17: 1340-6. PMID 22005931 DOI: 10.1038/Mp.2011.135 |
0.457 |
|
| 2012 |
Hollingworth P, Sweet R, Sims R, Harold D, Russo G, Abraham R, Stretton A, Jones N, Gerrish A, Chapman J, Ivanov D, Moskvina V, Lovestone S, Priotsi P, Lupton M, ... ... Kamboh MI, et al. Genome-wide association study of Alzheimer's disease with psychotic symptoms. Molecular Psychiatry. 17: 1316-27. PMID 22005930 DOI: 10.1016/J.Jalz.2011.05.516 |
0.415 |
|
| 2012 |
Kamboh MI, Minster RL, Demirci FY, Ganguli M, Dekosky ST, Lopez OL, Barmada MM. Association of CLU and PICALM variants with Alzheimer's disease. Neurobiology of Aging. 33: 518-21. PMID 20570404 DOI: 10.1016/J.Neurobiolaging.2010.04.015 |
0.41 |
|
| 2012 |
Rosenthal SL, Wang X, Demirci FY, Barmada MM, Ganguli M, Lopez OL, Kamboh MI. Beta-amyloid toxicity modifier genes and the risk of Alzheimer’s disease American Journal of Neurodegenerative Diseases. 1: 191-198. |
0.388 |
|
| 2011 |
Genin E, Hannequin D, Wallon D, Sleegers K, Hiltunen M, Combarros O, Bullido MJ, Engelborghs S, De Deyn P, Berr C, Pasquier F, Dubois B, Tognoni G, Fiévet N, Brouwers N, ... ... Kamboh MI, et al. APOE and Alzheimer disease: a major gene with semi-dominant inheritance. Molecular Psychiatry. 16: 903-7. PMID 21556001 DOI: 10.1038/Mp.2011.52 |
0.385 |
|
| 2011 |
Burns LC, Minster RL, Demirci FY, Barmada MM, Ganguli M, Lopez OL, DeKosky ST, Kamboh MI. Replication study of genome-wide associated SNPs with late-onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 507-12. PMID 21480501 DOI: 10.1002/Ajmg.B.31194 |
0.417 |
|
| 2011 |
Taylor KE, Chung SA, Graham RR, Ortmann WA, Lee AT, Langefeld CD, Jacob CO, Kamboh MI, Alarcón-Riquelme ME, Tsao BP, Moser KL, Gaffney PM, Harley JB, Petri M, Manzi S, et al. Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes. Plos Genetics. 7: e1001311. PMID 21379322 DOI: 10.1371/Journal.Pgen.1001311 |
0.335 |
|
| 2011 |
Dasgupta S, Demirci FY, Dressen AS, Kao AH, Rhew EY, Ramsey-Goldman R, Manzi S, Kammerer CM, Kamboh MI. Association analysis of PON2 genetic variants with serum paraoxonase activity and systemic lupus erythematosus. Bmc Medical Genetics. 12: 7. PMID 21223581 DOI: 10.1186/1471-2350-12-7 |
0.59 |
|
| 2011 |
Reitz C, Cheng R, Rogaeva E, Lee JH, Tokuhiro S, Zou F, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Arai H, Kamboh MI, Prince JA, Maier W, et al. Meta-analysis of the association between variants in SORL1 and Alzheimer disease. Archives of Neurology. 68: 99-106. PMID 21220680 DOI: 10.1001/Archneurol.2010.346 |
0.413 |
|
| 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, ... ... Kamboh MI, 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 |
0.488 |
|
| 2010 |
Hansmannel F, Sillaire A, Kamboh MI, Lendon C, Pasquier F, Hannequin D, Laumet G, Mounier A, Ayral AM, DeKosky ST, Hauw JJ, Berr C, Mann D, Amouyel P, Campion D, et al. Is the urea cycle involved in Alzheimer's disease? Journal of Alzheimer's Disease : Jad. 21: 1013-21. PMID 20693631 DOI: 10.3233/Jad-2010-100630 |
0.386 |
|
| 2010 |
Suresh S, Demirci FY, Lefterov I, Kammerer CM, Ramsey-Goldman R, Manzi S, Kamboh MI. Functional and genetic characterization of the promoter region of apolipoprotein H (beta2-glycoprotein I). The Febs Journal. 277: 951-63. PMID 20089041 DOI: 10.1111/J.1742-4658.2009.07538.X |
0.539 |
|
| 2010 |
Fukumoto N, Fujii T, Combarros O, Kamboh MI, Tsai SJ, Matsushita S, Nacmias B, Comings DE, Arboleda H, Ingelsson M, Hyman BT, Akatsu H, Grupe A, Nishimura AL, Zatz M, et al. Sexually dimorphic effect of the Val66Met polymorphism of BDNF on susceptibility to Alzheimer's disease: New data and meta-analysis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 235-42. PMID 19504537 DOI: 10.1002/Ajmg.B.30986 |
0.419 |
|
| 2010 |
Heng CK, He X, Saha N, Low PS, Demirci FY, Kamboh MI. Association of three lipoprotein lipase polymorphisms with coronary artery disease in Chinese and Asian Indians. International Journal of Cardiology. 144: 142-3. PMID 19167106 DOI: 10.1016/j.ijcard.2008.12.121 |
0.304 |
|
| 2009 |
Chapuis J, Hot D, Hansmannel F, Kerdraon O, Ferreira S, Hubans C, Maurage CA, Huot L, Bensemain F, Laumet G, Ayral AM, Fievet N, Hauw JJ, DeKosky ST, Lemoine Y, ... ... Kamboh MI, et al. Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease. Molecular Psychiatry. 14: 1004-16. PMID 19204726 DOI: 10.1038/Mp.2009.10 |
0.414 |
|
| 2009 |
Minster RL, Demirci FY, DeKosky ST, Kamboh MI. No association between CALHM1 variation and risk of Alzheimer disease. Human Mutation. 30: E566-9. PMID 19191331 DOI: 10.1002/Humu.20989 |
0.449 |
|
| 2009 |
Suresh S, Demirci FY, Jacobs E, Kao AH, Rhew EY, Sanghera DK, Selzer F, Sutton-Tyrrell K, McPherson D, Bontempo FA, Kammerer CM, Ramsey-Goldman R, Manzi S, Kamboh MI. Apolipoprotein H promoter polymorphisms in relation to lupus and lupus-related phenotypes. The Journal of Rheumatology. 36: 315-22. PMID 19132787 DOI: 10.3899/Jrheum.080482 |
0.609 |
|
| 2009 |
Conley YP, Mukherjee A, Kammerer C, DeKosky ST, Kamboh MI, Finegold DN, Ferrell RE. Evidence supporting a role for the calcium-sensing receptor in Alzheimer disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 703-9. PMID 19035514 DOI: 10.1002/Ajmg.B.30896 |
0.379 |
|
| 2009 |
Figgins JA, Minster RL, Demirci FY, Dekosky ST, Kamboh MI. Association studies of 22 candidate SNPs with late-onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 520-6. PMID 18780302 DOI: 10.1002/Ajmg.B.30851 |
0.466 |
|
| 2009 |
Minster RL, DeKosky ST, Kamboh MI. No association of DAPK1 and ABCA2 SNPs on chromosome 9 with Alzheimer's disease. Neurobiology of Aging. 30: 1890-1. PMID 18336955 DOI: 10.1016/J.Neurobiolaging.2008.01.006 |
0.437 |
|
| 2008 |
Shih PB, Manzi S, Shaw P, Kenney M, Kao AH, Bontempo F, Barmada MM, Kammerer C, Kamboh MI. Genetic variation in C-reactive protein (CRP) gene may be associated with risk of systemic lupus erythematosus and CRP concentrations. The Journal of Rheumatology. 35: 2171-8. PMID 18793001 DOI: 10.3899/Jrheum.080262 |
0.307 |
|
| 2008 |
Sanghera DK, Ortega L, Han S, Singh J, Ralhan SK, Wander GS, Mehra NK, Mulvihill JJ, Ferrell RE, Nath SK, Kamboh MI. Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk. Bmc Medical Genetics. 9: 59. PMID 18598350 DOI: 10.1186/1471-2350-9-59 |
0.329 |
|
| 2008 |
Minster RL, DeKosky ST, Kamboh MI. No association of SORL1 SNPs with Alzheimer's disease. Neuroscience Letters. 440: 190-2. PMID 18562096 DOI: 10.1016/J.Neulet.2008.05.082 |
0.447 |
|
| 2008 |
Taylor KE, Remmers EF, Lee AT, Ortmann WA, Plenge RM, Tian C, Chung SA, Nititham J, Hom G, Kao AH, Demirci FY, Kamboh MI, Petri M, Manzi S, Kastner DL, et al. Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus. Plos Genetics. 4: e1000084. PMID 18516230 DOI: 10.1371/Journal.Pgen.1000084 |
0.36 |
|
| 2008 |
Sanghera DK, Nath SK, Ortega L, Gambarelli M, Kim-Howard X, Singh JR, Ralhan SK, Wander GS, Mehra NK, Mulvihill JJ, Kamboh MI. TCF7L2 polymorphisms are associated with type 2 diabetes in Khatri Sikhs from North India: genetic variation affects lipid levels. Annals of Human Genetics. 72: 499-509. PMID 18397358 DOI: 10.1111/j.1469-1809.2008.00443.x |
0.349 |
|
| 2008 |
Chen Q, Razzaghi H, Demirci FY, Kamboh MI. Functional significance of lipoprotein lipase HindIII polymorphism associated with the risk of coronary artery disease. Atherosclerosis. 200: 102-8. PMID 18242618 DOI: 10.1016/j.atherosclerosis.2007.12.011 |
0.345 |
|
| 2008 |
Hom G, Graham RR, Modrek B, Taylor KE, Ortmann W, Garnier S, Lee AT, Chung SA, Ferreira RC, Pant PV, Ballinger DG, Kosoy R, Demirci FY, Kamboh MI, Kao AH, et al. Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. The New England Journal of Medicine. 358: 900-9. PMID 18204098 DOI: 10.1056/Nejmoa0707865 |
0.305 |
|
| 2008 |
Sanghera DK, Manzi S, Minster RL, Shaw P, Kao A, Bontempo F, Kamboh MI. Genetic variation in the paraoxonase-3 (PON3) gene is associated with serum PON1 activity. Annals of Human Genetics. 72: 72-81. PMID 17900266 DOI: 10.1111/J.1469-1809.2007.00400.X |
0.382 |
|
| 2008 |
Minster RL, DeKosky ST, Kamboh MI. No association of dynamin binding protein (DNMBP) gene SNPs and Alzheimer's disease. Neurobiology of Aging. 29: 1602-4. PMID 17442457 DOI: 10.1016/J.Neurobiolaging.2007.03.010 |
0.369 |
|
| 2007 |
Lambert JC, Ferreira S, Gussekloo J, Christiansen L, Brysbaert G, Slagboom E, Cottel D, Petit T, Hauw JJ, DeKosky ST, Richard F, Berr C, Lendon C, Kamboh MI, Mann D, et al. Evidence for the association of the S100beta gene with low cognitive performance and dementia in the elderly. Molecular Psychiatry. 12: 870-80. PMID 17579612 DOI: 10.1038/Sj.Mp.4001974 |
0.365 |
|
| 2007 |
Ozturk A, Minster RL, DeKosky ST, Kamboh MI. Association of tagSNPs in the urokinase-plasminogen activator (PLAU) gene with Alzheimer's disease and associated quantitative traits. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 79-82. PMID 16967469 DOI: 10.1002/Ajmg.B.30403 |
0.721 |
|
| 2007 |
Sundar PD, Feingold E, Minster RL, DeKosky ST, Kamboh MI. Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease. Neurobiology of Aging. 28: 856-62. PMID 16725228 DOI: 10.1016/J.Neurobiolaging.2006.04.005 |
0.482 |
|
| 2006 |
Minster RL, DeKosky ST, Kamboh MI. Lack of association of two chromosome 10q24 SNPs with Alzheimer's disease. Neuroscience Letters. 408: 170-2. PMID 17000046 DOI: 10.1016/J.Neulet.2006.08.081 |
0.323 |
|
| 2006 |
Ozturk A, DeKosky ST, Kamboh MI. Lack of association of 5 SNPs in the vicinity of the insulin-degrading enzyme (IDE) gene with late-onset Alzheimer's disease. Neuroscience Letters. 406: 265-9. PMID 16914266 DOI: 10.1016/J.Neulet.2006.07.054 |
0.701 |
|
| 2006 |
Kamboh MI, Minster RL, Feingold E, DeKosky ST. Genetic association of ubiquilin with Alzheimer's disease and related quantitative measures. Molecular Psychiatry. 11: 273-9. PMID 16302009 DOI: 10.1038/Sj.Mp.4001775 |
0.478 |
|
| 2006 |
Ozturk A, DeKosky ST, Kamboh MI. Genetic variation in the choline acetyltransferase (CHAT) gene may be associated with the risk of Alzheimer's disease. Neurobiology of Aging. 27: 1440-4. PMID 16223550 DOI: 10.1016/J.Neurobiolaging.2005.08.024 |
0.727 |
|
| 2006 |
Kamboh MI, Minster RL, Kenney M, Ozturk A, Desai PP, Kammerer CM, DeKosky ST. Alpha-1-antichymotrypsin (ACT or SERPINA3) polymorphism may affect age-at-onset and disease duration of Alzheimer's disease. Neurobiology of Aging. 27: 1435-9. PMID 16137793 DOI: 10.1016/J.Neurobiolaging.2005.07.015 |
0.796 |
|
| 2005 |
Ozturk A, Desai PP, Minster RL, Dekosky ST, Kamboh MI. Three SNPs in the GSTO1, GSTO2 and PRSS11 genes on chromosome 10 are not associated with age-at-onset of Alzheimer's disease. Neurobiology of Aging. 26: 1161-5. PMID 15917099 DOI: 10.1016/J.Neurobiolaging.2004.11.001 |
0.788 |
|
| 2005 |
Desai PP, Ikonomovic MD, Abrahamson EE, Hamilton RL, Isanski BA, Hope CE, Klunk WE, DeKosky ST, Kamboh MI. Apolipoprotein D is a component of compact but not diffuse amyloid-beta plaques in Alzheimer's disease temporal cortex. Neurobiology of Disease. 20: 574-82. PMID 15916898 DOI: 10.1016/J.Nbd.2005.04.012 |
0.686 |
|
| 2005 |
Desai P, Nebes R, DeKosky ST, Kamboh MI. Investigation of the effect of brain-derived neurotrophic factor (BDNF) polymorphisms on the risk of late-onset Alzheimer's disease (AD) and quantitative measures of AD progression. Neuroscience Letters. 379: 229-34. PMID 15843069 DOI: 10.1016/J.Neulet.2005.01.008 |
0.732 |
|
| 2005 |
Tsuang DW, Wilson RK, Lopez OL, Luedecking-Zimmer EK, Leverenz JB, DeKosky ST, Kamboh MI, Hamilton RL. Genetic association between the APOE*4 allele and Lewy bodies in Alzheimer disease. Neurology. 64: 509-13. PMID 15699383 DOI: 10.1212/01.Wnl.0000150892.81839.D1 |
0.39 |
|
| 2004 |
Sanghera DK, Manzi S, Bontempo F, Nestlerode C, Kamboh MI. Role of an intronic polymorphism in the PDCD1 gene with the risk of sporadic systemic lupus erythematosus and the occurrence of antiphospholipid antibodies Human Genetics. 115: 393-398. PMID 15322919 DOI: 10.1007/s00439-004-1172-0 |
0.317 |
|
| 2004 |
Kamboh MI. Molecular genetics of late-onset Alzheimer's disease Annals of Human Genetics. 68: 381-404. PMID 15225164 DOI: 10.1046/j.1529-8817.2004.00110.x |
0.423 |
|
| 2004 |
Heng CK, Lal S, Saha N, Low PS, Kamboh MI. The impact of factor XIIIa V34L polymorphism on plasma factor XIII activity in the Chinese and Asian Indians from Singapore. Human Genetics. 114: 186-91. PMID 14593529 DOI: 10.1007/s00439-003-1040-3 |
0.309 |
|
| 2004 |
Ozturk A, Desai PP, Minster RL, Scott T, Kammerer CM, DeKosky ST, Kamboh MI. P4-078 Alpha-1 antichymotrypsin (ACT or serpina3) may affect age-at-onset of Alzheimer's disease Neurobiology of Aging. 25: S496. DOI: 10.1016/S0197-4580(04)81636-1 |
0.739 |
|
| 2003 |
Hokanson JE, Kamboh MI, Scarboro S, Eckel RH, Hamman RF. Effects of the hepatic lipase gene and physical activity on coronary heart disease risk. American Journal of Epidemiology. 158: 836-43. PMID 14585761 DOI: 10.1093/Aje/Kwg230 |
0.308 |
|
| 2003 |
Chen Q, Reis SE, Kammerer CM, McNamara DM, Holubkov R, Sharaf BL, Sopko G, Pauly DF, Bairey Merz CN, Kamboh MI. APOE polymorphism and angiographic coronary artery disease severity in the Women's Ischemia Syndrome Evaluation (WISE) study. Atherosclerosis. 169: 159-67. PMID 12860263 DOI: 10.1016/S0021-9150(03)00160-6 |
0.391 |
|
| 2003 |
Chen Q, Reis SE, Kammerer C, Craig WY, LaPierre SE, Zimmer EL, McNamara DM, Pauly DF, Sharaf B, Holubkov R, Bairey Merz CN, Sopko G, Bontempo F, Kamboh MI. Genetic variation in lectin-like oxidized low-density lipoprotein receptor 1 (LOX1) gene and the risk of coronary artery disease. Circulation. 107: 3146-51. PMID 12810610 DOI: 10.1161/01.Cir.0000074207.85796.36 |
0.66 |
|
| 2003 |
Lambert JC, Luedecking-Zimmer E, Merrot S, Hayes A, Thaker U, Desai P, Houzet A, Hermant X, Cottel D, Pritchard A, Iwatsubo T, Pasquier F, Frigard B, Conneally PM, Chartier-Harlin MC, ... ... Kamboh MI, et al. Association of 3'-UTR polymorphisms of the oxidised LDL receptor 1 (OLR1) gene with Alzheimer's disease. Journal of Medical Genetics. 40: 424-30. PMID 12807963 DOI: 10.1136/Jmg.40.6.424 |
0.456 |
|
| 2003 |
Wang GQ, DiPietro M, Roeder K, Heng CK, Bunker CH, Hamman RF, Kamboh MI. Cladistic analysis of human apolipoprotein a4 polymorphisms in relation to quantitative plasma lipid risk factors of coronary heart disease. Annals of Human Genetics. 67: 107-24. PMID 12675687 DOI: 10.1046/J.1469-1809.2003.00023.X |
0.373 |
|
| 2003 |
Mehdi H, Manzi S, Desai P, Chen Q, Nestlerode C, Bontempo F, Strom SC, Zarnegar R, Kamboh MI. A functional polymorphism at the transcriptional initiation site in beta2-glycoprotein I (apolipoprotein H) associated with reduced gene expression and lower plasma levels of beta2-glycoprotein I. European Journal of Biochemistry / Febs. 270: 230-8. PMID 12605674 DOI: 10.1046/J.1432-1033.2003.03379.X |
0.679 |
|
| 2003 |
Luedecking-Zimmer E, DeKosky ST, Nebes R, Kamboh MI. Association of the 3' UTR transcription factor LBP-1c/CP2/LSF polymorphism with late-onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 117: 114-7. PMID 12555245 DOI: 10.1002/Ajmg.B.10026 |
0.467 |
|
| 2003 |
DeKosky ST, Ikonomovic MD, Wang X, Farlow M, Wisniewski S, Lopez OL, Becker JT, Saxton J, Klunk WE, Sweet R, Kaufer DI, Kamboh MI. Plasma and cerebrospinal fluid alpha1-antichymotrypsin levels in Alzheimer's disease: correlation with cognitive impairment. Annals of Neurology. 53: 81-90. PMID 12509851 DOI: 10.1002/Ana.10414 |
0.325 |
|
| 2003 |
Desai PP, Hendrie HC, Evans RM, Murrell JR, DeKosky ST, Kamboh MI. Genetic variation in apolipoprotein D affects the risk of Alzheimer disease in African-Americans. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 116: 98-101. PMID 12497622 DOI: 10.1002/Ajmg.B.10798 |
0.758 |
|
| 2003 |
Chen Q, Reis SE, Kammerer CM, McNamara DM, Holubkov R, Sharaf BL, Sopko G, Pauly DF, Merz CN, Kamboh MI. Association between the severity of angiographic coronary artery disease and paraoxonase gene polymorphisms in the National Heart, Lung, and Blood Institute-sponsored Women's Ischemia Syndrome Evaluation (WISE) study. American Journal of Human Genetics. 72: 13-22. PMID 12454802 DOI: 10.1086/345312 |
0.356 |
|
| 2002 |
Luedecking-Zimmer E, DeKosky ST, Chen Q, Barmada MM, Kamboh MI. Investigation of oxidized LDL-receptor 1 (OLR1) as the candidate gene for Alzheimer's disease on chromosome 12. Human Genetics. 111: 443-51. PMID 12384789 DOI: 10.1007/S00439-002-0802-7 |
0.466 |
|
| 2002 |
Desai P, DeKosky ST, Kamboh MI. Genetic variation in the cholesterol 24-hydroxylase (CYP46) gene and the risk of Alzheimer's disease. Neuroscience Letters. 328: 9-12. PMID 12123847 DOI: 10.1016/S0304-3940(02)00443-3 |
0.779 |
|
| 2002 |
Desai PP, Bunker CH, Ukoli FA, Kamboh MI. Genetic variation in the apolipoprotein D gene among African blacks and its significance in lipid metabolism. Atherosclerosis. 163: 329-38. PMID 12052480 DOI: 10.1016/S0021-9150(02)00012-6 |
0.73 |
|
| 2002 |
Wang X, DeKosky ST, Ikonomovic MD, Kamboh MI. Distribution of plasma alpha 1-antichymotrypsin levels in Alzheimer disease patients and controls and their genetic controls. Neurobiology of Aging. 23: 377-82. PMID 11959399 DOI: 10.1016/S0197-4580(01)00322-0 |
0.43 |
|
| 2002 |
Wang X, DeKosky ST, Luedecking-Zimmer E, Ganguli M, Kamboh MI. Genetic variation in alpha(1)-antichymotrypsin and its association with Alzheimer's disease. Human Genetics. 110: 356-65. PMID 11941486 DOI: 10.1007/S00439-002-0697-3 |
0.395 |
|
| 2002 |
Sweet RA, Kamboh MI, Wisniewski SR, Lopez OL, Klunk WE, Kaufer DI, DeKosky ST. Apolipoprotein E and alpha-1-antichymotrypsin genotypes do not predict time to psychosis in Alzheimer's disease. Journal of Geriatric Psychiatry and Neurology. 15: 24-30. PMID 11936240 DOI: 10.1177/089198870201500106 |
0.395 |
|
| 2001 |
Bhojak TJ, DeKosky ST, Ganguli M, Kamboh MI. Genetic polymorphism in the cathepsin G gene and the risk of Alzheimer's disease. Neuroscience Letters. 309: 138-40. PMID 11502364 DOI: 10.1016/S0304-3940(01)02033-X |
0.467 |
|
| 2001 |
Wang X, Luedecking EK, Minster RL, Ganguli M, DeKosky ST, Kamboh MI. Lack of association between alpha2-macroglobulin polymorphisms and Alzheimer's disease. Human Genetics. 108: 105-8. PMID 11281447 DOI: 10.1007/S004390000445 |
0.439 |
|
| 2001 |
Parra EJ, Kittles RA, Argyropoulos G, Pfaff CL, Hiester K, Bonilla C, Sylvester N, Parrish-Gause D, Garvey WT, Jin L, McKeigue PM, Kamboh MI, Ferrell RE, Pollitzer WS, Shriver MD. Ancestral proportions and admixture dynamics in geographically defined African Americans living in South Carolina. American Journal of Physical Anthropology. 114: 18-29. PMID 11150049 DOI: 10.1002/1096-8644(200101)114:1<18::Aid-Ajpa1002>3.0.Co;2-2 |
0.376 |
|
| 2001 |
Pfaff CL, Parra EJ, Bonilla C, Hiester K, McKeigue PM, Kamboh MI, Hutchinson RG, Ferrell RE, Boerwinkle E, Shriver MD. Population structure in admixed populations: effect of admixture dynamics on the pattern of linkage disequilibrium. American Journal of Human Genetics. 68: 198-207. PMID 11112661 DOI: 10.1086/316935 |
0.318 |
|
| 2000 |
Lopez OL, Becker JT, Klunk W, Saxton J, Hamilton RL, Kaufer DI, Sweet RA, Cidis Meltzer C, Wisniewski S, Kamboh MI, DeKosky ST. Research evaluation and diagnosis of possible Alzheimer's disease over the last two decades: II. Neurology. 55: 1863-9. PMID 11134386 DOI: 10.1212/Wnl.55.12.1863 |
0.301 |
|
| 2000 |
Johnston JM, Nazar-Stewart V, Kelsey SF, Kamboh MI, Ganguli M. Relationships between cerebrovascular events, APOE polymorphism and Alzheimer's disease in a community sample Neuroepidemiology. 19: 320-326. PMID 11060506 |
0.305 |
|
| 2000 |
Luedecking EK, DeKosky ST, Mehdi H, Ganguli M, Kamboh MI. Analysis of genetic polymorphisms in the transforming growth factor-beta1 gene and the risk of Alzheimer's disease. Human Genetics. 106: 565-9. PMID 10914688 DOI: 10.1007/S004390000313 |
0.416 |
|
| 2000 |
Bhojak TJ, DeKosky ST, Ganguli M, Kamboh MI. Genetic polymorphisms in the cathespin D and interleukin-6 genes and the risk of Alzheimer's disease. Neuroscience Letters. 288: 21-4. PMID 10869806 DOI: 10.1016/S0304-3940(00)01185-X |
0.441 |
|
| 2000 |
Ganguli M, Chandra V, Kamboh MI, Johnston JM, Dodge HH, Thelma BK, Juyal RC, Pandav R, Belle SH, DeKosky ST. Apolipoprotein E polymorphism and Alzheimer disease: The Indo-US Cross-National Dementia Study. Archives of Neurology. 57: 824-30. PMID 10867779 DOI: 10.1001/Archneur.57.6.824 |
0.384 |
|
| 1999 |
Saha N, Sanghera DK, Kamboh MI. The p22 phox polymorphism C242T is not associated with CHD risk in Asian Indians and Chinese European Journal of Clinical Investigation. 29: 999-1002. PMID 10583446 DOI: 10.1046/j.1365-2362.1999.00575.x |
0.355 |
|
| 1999 |
Mehdi H, Aston CE, Sanghera DK, Hamman RF, Kamboh MI. Genetic variation in the apolipoprotein H (β2-glycoprotein I) gene affects plasma apolipoprotein H concentrations Human Genetics. 105: 63-71. PMID 10480357 DOI: 10.1007/s004390051065 |
0.304 |
|
| 1999 |
Nestlerode CS, Bunker CH, Sanghera DK, Aston CE, Ukoli FA, Kamboh MI. Apolipoprotein J polymorphisms and serum HDL cholesterol levels in African blacks Human Biology. 71: 197-218. PMID 10222643 |
0.315 |
|
| 1999 |
Kamboh MI, Aston CE, Perez-Tur J, Kokmen E, Ferrell RE, Hardy J, DeKosky ST. A novel mutation in the apolipoprotein E gene (APOE*4 Pittsburgh) is associated with the risk of late-onset Alzheimer's disease. Neuroscience Letters. 263: 129-32. PMID 10213152 DOI: 10.1016/S0304-3940(99)00129-9 |
0.371 |
|
| 1999 |
Luedecking EK, Ganguli M, DeKosky ST, Kamboh MI. Genetic polymorphism in the persyn (gamma-synuclein) gene and the risk of Alzheimer's disease. Neuroscience Letters. 261: 186-8. PMID 10081980 DOI: 10.1016/S0304-3940(99)00025-7 |
0.5 |
|
| 1999 |
Kamboh MI, Bunker CH, Aston CE, Nestlerode CS, McAllister AE, Ukoli FA. Genetic association of five apolipoprotein polymorphisms with serum lipoprotein-lipid levels in African blacks Genetic Epidemiology. 16: 205-222. PMID 10030402 DOI: 10.1002/(Sici)1098-2272(1999)16:2<205::Aid-Gepi7>3.0.Co;2-P |
0.321 |
|
| 1998 |
Kim HS, Kamboh MI. Genetic polymorphisms of apolipoproteins A-IV, E and H in Koreans Human Heredity. 48: 313-317. PMID 9813452 DOI: 10.1159/000022822 |
0.35 |
|
| 1998 |
Sweet RA, Nimgaonkar VL, Kamboh MI, Lopez OL, Zhang F, DeKosky ST. Dopamine receptor genetic variation, psychosis, and aggression in Alzheimer disease. Archives of Neurology. 55: 1335-40. PMID 9779662 DOI: 10.1001/Archneur.55.10.1335 |
0.333 |
|
| 1998 |
Wang X, DeKosky ST, Wisniewski S, Aston, Kamboh MI. Genetic association of two chromosome 14 genes (presenilin 1 and alpha 1-antichymotrypsin) with Alzheimer's disease. Annals of Neurology. 44: 387-90. PMID 9749607 DOI: 10.1002/Ana.410440316 |
0.436 |
|
| 1998 |
Styren SD, Kamboh MI, DeKosky ST. Expression of differential immune factors in temporal cortex and cerebellum: the role of alpha-1-antichymotrypsin, apolipoprotein E, and reactive glia in the progression of Alzheimer's disease. The Journal of Comparative Neurology. 396: 511-20. PMID 9651008 DOI: 10.1002/(Sici)1096-9861(19980713)396:4<511::Aid-Cne7>3.0.Co;2-4 |
0.302 |
|
| 1998 |
Lopez OL, Lopez-Pousa S, Kamboh MI, Adroer R, Oliva R, Lozano-Gallego M, Becker JT, DeKosky ST. Apolipoprotein E polymorphism in Alzheimer's disease: a comparative study of two research populations from Spain and the United States. European Neurology. 39: 229-33. PMID 9635474 DOI: 10.1159/000007939 |
0.413 |
|
| 1998 |
Kamboh MI, Ferrell RE, DeKosky ST. Genetic association studies between Alzheimer's disease and two polymorphisms in the low density lipoprotein receptor-related protein gene. Neuroscience Letters. 244: 65-8. PMID 9572586 DOI: 10.1016/S0304-3940(98)00141-4 |
0.486 |
|
| 1998 |
Harris MR, Bunker CH, Hamman RF, Sanghera DK, Aston CE, Kamboh MI. Racial differences in the distribution of a low density lipoprotein receptor-related protein (LRP) polymorphism and its association with serum lipoprotein, lipid and apolipoprotein levels Atherosclerosis. 137: 187-195. PMID 9568751 DOI: 10.1016/S0021-9150(97)00230-X |
0.304 |
|
| 1998 |
Sanghera DK, Saha N, Kamboh MI. The codon 55 polymorphism in the paraoxonase 1 gene is not associated with the risk of coronary heart disease in Asian Indians and Chinese Atherosclerosis. 136: 217-223. PMID 9543091 DOI: 10.1016/S0021-9150(97)00206-2 |
0.406 |
|
| 1998 |
Kamboh MI, Aston CE, Dekosky ST. Association between ACT polymorphism and Alzheimer's disease. Neurology. 50: 574-6. PMID 9508644 DOI: 10.1212/Wnl.50.2.574-A |
0.391 |
|
| 1998 |
Montoya SE, Aston CE, DeKosky ST, Kamboh MI, Lazo JS, Ferrell RE. Bleomycin hydrolase is associated with risk of sporadic Alzheimer's disease. Nature Genetics. 18: 211-2. PMID 9500538 DOI: 10.1038/ng0398-211 |
0.335 |
|
| 1998 |
Sanghera DK, Aston CE, Saha N, Kamboh MI. DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease American Journal of Human Genetics. 62: 36-44. PMID 9443862 DOI: 10.1086/301669 |
0.419 |
|
| 1997 |
Lopez OL, Kamboh MI, Becker JT, Kaufer DI, DeKosky ST. The apolipoprotein E epsilon 4 allele is not associated with psychiatric symptoms or extrapyramidal signs in probable Alzheimer's disease. Neurology. 49: 794-7. PMID 9305342 DOI: 10.1212/Wnl.49.3.794 |
0.324 |
|
| 1997 |
Sanghera DK, Saha N, Aston CE, Kamboh MI. Genetic polymorphism of paraoxonase and the risk of coronary heart disease. Arteriosclerosis, Thrombosis, and Vascular Biology. 17: 1067-73. PMID 9194756 DOI: 10.1161/01.ATV.17.6.1067 |
0.377 |
|
| 1997 |
Kamboh MI, Sanghera DK, Aston CE, Bunker CH, Hamman RF, Ferrell RE, Dekosky ST. Gender-specific nonrandom association between the α1-antichymotrypsin and apolipoprotein E polymorphisms in the general population and its implication for the risk of Alzheimer's disease Genetic Epidemiology. 14: 169-180. PMID 9129962 DOI: 10.1002/(Sici)1098-2272(1997)14:2<169::Aid-Gepi6>3.0.Co;2-2 |
0.379 |
|
| 1997 |
Sanghera DK, Ferrell RE, Aston CE, McAllister AE, Kamboh MI, Kimm SY. Quantitative effects of the apolipoprotein E polymorphism in a biracial sample of 9-10-year-old girls. Atherosclerosis. 126: 35-42. PMID 8879432 DOI: 10.1016/0021-9150(96)05891-1 |
0.367 |
|
| 1996 |
Kamboh MI, Aston CE, Nestlerode CM, McAllister AE, Hamman RF. Haplotype analysis of two APOA1/MspI polymorphisms in relation to plasma levels of Apo A-I and HDL-cholesterol Atherosclerosis. 127: 255-262. PMID 9125316 DOI: 10.1016/S0021-9150(96)05966-7 |
0.306 |
|
| 1996 |
DeKosky ST, Aston CE, Kamboh MI. Polygenic determinants of Alzheimer's disease: Modulation of the risk by α-1-antichymotrypsin Annals of the New York Academy of Sciences. 802: 27-34. PMID 8993481 DOI: 10.1111/j.1749-6632.1996.tb32595.x |
0.402 |
|
| 1996 |
Kamboh MI, Crawford MH, Aston CE, Leonard WR. Population distributions of APOE, APOH, and APOA4 polymorphisms and their relationships with quantitative plasma lipid levels among the Evenki Herders of Siberia Human Biology. 68: 231-243. PMID 8838914 |
0.356 |
|
| 1996 |
Kamboh MI, Evans RW, Aston CE. Genetic effect of apolipoprotein(a) and apolipoprotein E polymorphisms on plasma quantitative risk factors for coronary heart disease in American black women. Atherosclerosis. 117: 73-81. PMID 8546757 DOI: 10.1016/0021-9150(95)05559-F |
0.353 |
|
| 1996 |
Kamboh MI, DeKosky ST. Apolipoprotein E genotyping in the diagnosis of Alzheimer's disease. Annals of Neurology. 38: 967-70. PMID 8526476 DOI: 10.1002/Ana.410380626 |
0.301 |
|
| 1995 |
Kamboh MI. Apolipoprotein E polymorphism and susceptibility to Alzheimer's disease. Human Biology. 67: 195-215. PMID 7729825 |
0.456 |
|
| 1995 |
Kamboh MI, Sanghera DK, Ferrell RE, DeKosky ST. APOE*4-associated Alzheimer's disease risk is modified by alpha 1-antichymotrypsin polymorphism. Nature Genetics. 10: 486-8. PMID 7670501 DOI: 10.1038/ng0895-486 |
0.462 |
|
| 1995 |
Ganguli M, Cauley JA, DeKosky ST, Kamboh MI. Dementia among elderly apolipoprotein E type 4/4 homozygotes: a prospective study. Genetic Epidemiology. 12: 309-11. PMID 7557352 DOI: 10.1002/Gepi.1370120308 |
0.33 |
|
| 1994 |
Kamboh MI, Svitko CM, Williams ER, Ferrell RE, Pollitzer WS. Hypervariable polymorphism of APO(a) in blacks and whites as reflected by phenotyping. Chemistry and Physics of Lipids. 67: 283-92. PMID 8187225 DOI: 10.1016/0009-3084(94)90148-1 |
0.303 |
|
| 1994 |
Ahn YI, Kamboh MI, Aston CE, Ferrell RE, Hamman RF. Role of common genetic polymorphisms in the LDL receptor gene in affecting plasma cholesterol levels in the general population. Arteriosclerosis and Thrombosis : a Journal of Vascular Biology. 14: 663-70. PMID 8172843 DOI: 10.1161/01.Atv.14.5.663 |
0.334 |
|
| 1994 |
Kamboh MI, Friedlaender JS, Ahn YI, Ferrell RE. A common deletion polymorphism in the apolipoprotein A4 gene and its significance in lipid metabolism Arteriosclerosis and Thrombosis. 14: 656-662. PMID 8172842 DOI: 10.1161/01.Atv.14.5.656 |
0.316 |
|
| 1993 |
Crews DE, Bindon JR, Kamboh MI. Apolipoprotein polymorphisms and phenotypic variability in American Samoans: Preliminary data. American Journal of Human Biology : the Official Journal of the Human Biology Council. 5: 39-48. PMID 28524424 DOI: 10.1002/Ajhb.1310050108 |
0.375 |
|
| 1993 |
Crews DE, Kamboh MI, Mancilha-Carvalho JJ, Kottke B. Population genetics of apolipoprotein A-4, E, and H polymorphisms in Yanomami Indians of northwestern Brazil: associations with lipids, lipoproteins, and carbohydrate metabolism Human Biology. 65: 211-224. PMID 8449482 |
0.327 |
|
| 1993 |
Ahn YI, Kamboh MI, Hamman RF, Cole SA, Ferrell RE. Two DNA polymorphisms in the lipoprotein lipase gene and their associations with factors related to cardiovascular disease. Journal of Lipid Research. 34: 421-8. PMID 8096867 |
0.308 |
|
| 1992 |
Kamboh MI, Harmony JA, Sepehrnia B, Nwankwo M, Ferrell RE. Genetic studies of human apolipoproteins. XX. Genetic polymorphism of apolipoprotein J and its impact on quantitative lipid traits in normolipidemic subjects. American Journal of Human Genetics. 49: 1167-73. PMID 1746550 |
0.318 |
|
| 1992 |
Eichner JE, Ferrell RE, Kamboh MI, Kuller LH, Becker DJ, Drash AL, Stein EA, Orchard TJ. The impact of the apolipoprotein E polymorphism on the lipoprotein profile in insulin-dependent diabetes: the Pittsburgh Epidemiology of Diabetes Complications Study IX. Metabolism: Clinical and Experimental. 41: 347-51. PMID 1556940 DOI: 10.1016/0026-0495(92)90066-J |
0.34 |
|
| 1991 |
Crews DE, Kamboh MI, Bindon JR, Ferrell RE. Genetic studies of human apolipoproteins. XVII: Population genetics of apolipoprotein polymorphisms in American Samoa American Journal of Physical Anthropology. 84: 165-170. PMID 2021192 DOI: 10.1002/Ajpa.1330840206 |
0.422 |
|
| 1991 |
Kamboh MI, Serjeantson SW, Ferrell RE. Genetic studies of human apolipoproteins. XVIII. Apolipoprotein polymorphisms in Australian Aborigines. Human Biology. 63: 179-86. PMID 2019410 |
0.347 |
|
| 1991 |
Kamboh MI, Weiss KM, Ferrell RE. Genetic studies of human apolipoproteins. XVI. APOE polymorphism and cholesterol levels in the Mayans of the Yucatan Peninsula, Mexico. Clinical Genetics. 39: 26-32. PMID 1997212 DOI: 10.1111/J.1399-0004.1991.Tb02981.X |
0.443 |
|
| 1991 |
Kaprio J, Ferrell RE, Kottke BA, Kamboh MI, Sing CF. Effects of polymorphisms in apolipoproteins E, A-IV, and H on quantitative traits related to risk for cardiovascular disease. Arteriosclerosis and Thrombosis : a Journal of Vascular Biology. 11: 1330-48. PMID 1911720 DOI: 10.1161/01.Atv.11.5.1330 |
0.312 |
|
| 1990 |
Kamboh MI, Kelly LJ, Ferrell RE. Genetic studies of human apolipoproteins: XIV. A simple agarose isoelectric focusing gel method for apolipoprotein E phenotyping. Electrophoresis. 11: 314-8. PMID 2340826 DOI: 10.1002/Elps.1150110408 |
0.302 |
|
| 1990 |
Kamboh MI, Ferrell RE. Genetic studies of human apolipoproteins. XV. An overview of IEF immunoblotting methods to screen apolipoprotein polymorphisms. Human Heredity. 40: 193-207. PMID 2199367 DOI: 10.1159/000153931 |
0.41 |
|
| 1989 |
Eichner JE, Kuller LH, Kamboh MI, Ferrell RE. Phenotypic effects of apolipoprotein structural variation on lipid profiles. I. APO H and quantitative lipid measures in the healthy women study. Genetic Epidemiology. 6: 311-8. PMID 2721926 DOI: 10.1002/Gepi.1370060202 |
0.379 |
|
| 1989 |
Kamboh MI, Ferrell RE. Genetic studies of low-abundance human plasma proteins. X. Coagulation factor XIIIB variants in blacks. Electrophoresis. 10: 53-7. PMID 2714240 DOI: 10.1002/Elps.1150100113 |
0.356 |
|
| 1989 |
Eichner JE, Kuller LH, Ferrell RE, Kamboh MI. Phenotypic effects of apolipoprotein structural variation on lipid profiles. IV. Apolipoprotein polymorphisms in a small group of black women from the healthy women study. Genetic Epidemiology. 6: 681-9. PMID 2606341 DOI: 10.1002/Gepi.1370060605 |
0.367 |
|
| 1989 |
Eichner JE, Kamboh MI, Cook T, Ferrell RE. Genetic studies of low-abundance human plasma proteins. XII. A new variant of corticosteroid-binding globulin detected by isoelectric focusing/immunoblotting. Human Heredity. 39: 170-3. PMID 2591981 DOI: 10.1159/000153854 |
0.303 |
|
| 1989 |
Lyons LA, Kamboh MI, Ferrell RE. Genetic studies of low-abundance human plasma proteins. XI. Linkage analysis and population genetics of the C1S subcomponent of the first complement component Complement and Inflammation. 6: 81-87. PMID 2541966 DOI: 10.1159/000463078 |
0.34 |
|
| 1988 |
Ferrell RE, Kamboh MI, Sepehrnia BS, Adams-Campbell LL, Weiss KM. Genetic variation in the apolipoproteins C-II and C-III Advances in Experimental Medicine and Biology. 243: 81-85. PMID 3223425 DOI: 10.1007/978-1-4613-0733-4_11 |
0.337 |
|
| 1988 |
Sepehrnia B, Kamboh MI, Adams-Campbell LL, Nwankwo M, Ferrell RE. Genetic studies of human apolipoproteins. VII. Population distribution of polymorphisms of apolipoproteins A-I, A-II, A-IV, C-II, E, and H in Nigeria American Journal of Human Genetics. 43: 847-853. PMID 3143263 |
0.319 |
|
| 1987 |
Kamboh MI, Ferrell RE. Genetic studies of human apolipoproteins. I. Polymorphism of apolipoprotein A-IV. American Journal of Human Genetics. 41: 119-27. PMID 3618592 |
0.324 |
|
| 1987 |
Kamboh MI, Ferrell RE. Genetic studies of low-abundance human plasma proteins. I. Microheterogeneity of zinc-alpha 2-glycoprotein in biological fluids. Biochemical Genetics. 24: 849-57. PMID 3541891 DOI: 10.1007/Bf00554524 |
0.308 |
|
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