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Basavaraj V. Hooli, Ph.D. - Publications

Affiliations: 
2011 Drexel University, Philadelphia, PA, United States 
Area:
Genetics, Neurobiology Biology, Neuroscience Biology
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24 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
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, ... ... Hooli B, 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  0.482
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, ... Hooli B, 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  0.442
2019 Suh J, Romano DM, Nitschke L, Herrick SP, DiMarzio BA, Dzhala V, Bae JS, Oram MK, Zheng Y, Hooli B, Mullin K, Gennarino VA, Wasco W, Schmahmann JD, Albers MW, et al. Loss of Ataxin-1 Potentiates Alzheimer's Pathogenesis by Elevating Cerebral BACE1 Transcription. Cell. 178: 1159-1175.e17. PMID 31442405 DOI: 10.1016/J.Ibror.2019.07.707  0.512
2017 Li A, Hooli B, Mullin K, Tate RE, Bubnys A, Kirchner R, Chapman B, Hofmann O, Hide W, Tanzi RE. Silencing Of The Drosophila Ortholog Of Sox5 Leads To Abnormal Neuronal Development And Behavioral Impairment. Human Molecular Genetics. PMID 28186563 DOI: 10.1093/Hmg/Ddx051  0.512
2016 Song W, Hooli B, Mullin K, Jin SC, Cella M, Ulland TK, Wang Y, Tanzi R, Colonna M. Alzheimer's disease-associated TREM2 variants exhibit either decreased or increased ligand-dependent activation. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 27520774 DOI: 10.1016/J.Jalz.2016.07.004  0.506
2016 Alfonso SI, Callender JA, Hooli B, Antal CE, Mullin K, Sherman MA, Lesné SE, Leitges M, Newton AC, Tanzi RE, Malinow R. Gain-of-function mutations in protein kinase Cα (PKCα) may promote synaptic defects in Alzheimer's disease. Science Signaling. 9: ra47. PMID 27165780 DOI: 10.1126/Scisignal.Aaf6209  0.522
2016 Herold C, Hooli BV, Mullin K, Liu T, Roehr JT, Mattheisen M, Parrado AR, Bertram L, Lange C, Tanzi RE. Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. Molecular Psychiatry. PMID 26830138 DOI: 10.1038/Mp.2015.218  0.499
2015 Park S, Lee S, Lee Y, Herold C, Hooli B, Mullin K, Park T, Park C, Bertram L, Lange C, Tanzi R, Won S. Adjusting heterogeneous ascertainment bias for genetic association analysis with extended families. Bmc Medical Genetics. 16: 62. PMID 26286599 DOI: 10.1186/S12881-015-0198-6  0.38
2015 Hooli BV, Lill CM, Mullin K, Qiao D, Lange C, Bertram L, Tanzi RE. PLD3 gene variants and Alzheimer's disease. Nature. 520: E7-8. PMID 25832413 DOI: 10.1038/Nature14040  0.51
2014 Choi SH, Kim YH, Hebisch M, Sliwinski C, Lee S, D'Avanzo C, Chen H, Hooli B, Asselin C, Muffat J, Klee JB, Zhang C, Wainger BJ, Peitz M, Kovacs DM, et al. A three-dimensional human neural cell culture model of Alzheimer's disease. Nature. 515: 274-8. PMID 25307057 DOI: 10.1038/Nature13800  0.435
2014 Hooli BV, Parrado AR, Mullin K, Yip WK, Liu T, Roehr JT, Qiao D, Jessen F, Peters O, Becker T, Ramirez A, Lange C, Bertram L, Tanzi RE. The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk. Neurology. 83: 1353-8. PMID 25186855 DOI: 10.1212/Wnl.0000000000000855  0.558
2014 Hooli BV, Kovacs-Vajna ZM, Mullin K, Blumenthal MA, Mattheisen M, Zhang C, Lange C, Mohapatra G, Bertram L, Tanzi RE. Rare autosomal copy number variations in early-onset familial Alzheimer's disease. Molecular Psychiatry. 19: 676-81. PMID 23752245 DOI: 10.1038/Mp.2013.77  0.626
2013 Griciuc A, Serrano-Pozo A, Parrado AR, Lesinski AN, Asselin CN, Mullin K, Hooli B, Choi SH, Hyman BT, Tanzi RE. Alzheimer's disease risk gene CD33 inhibits microglial uptake of amyloid beta. Neuron. 78: 631-43. PMID 23623698 DOI: 10.1016/J.Neuron.2013.04.014  0.4
2013 Schjeide B, Borovecki F, Clarimón J, Faltraco F, Giedraitis V, Ingelsson M, Hampel H, Hooli B, Kilander L, Kirchheiner J, Klepac N, Kurz A, Lannfelt L, Lill C, Lleó A, et al. Assessment of Alzheimer's disease risk genes with CSF-biomarker levels Alzheimers & Dementia. 9: 179. DOI: 10.1016/J.Jalz.2013.05.294  0.43
2012 Hooli BV, Mohapatra G, Mattheisen M, Parrado AR, Roehr JT, Shen Y, Gusella JF, Moir R, Saunders AJ, Lange C, Tanzi RE, Bertram L. Role of common and rare APP DNA sequence variants in Alzheimer disease. Neurology. 78: 1250-7. PMID 22491860 DOI: 10.1212/Wnl.0B013E3182515972  0.609
2011 Hooli B, Bertram L, Parrado A, Tanzi R, Mullin K, Gotta L. RETRACTED: Genome-wide assessment of copy number variations in early-onset Alzheimer's disease Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.228  0.442
2011 Parrado T, Hooli B, Mullin K, Gotta L, Bertram L, Lange C, Tanzi R. Significant association of coding (Missense) SNPs with familial LOAD based on a functional genome-wide association screen Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.1040  0.326
2009 Hooli BV, Tanzi RE. A current view of Alzheimer's disease. F1000 Biology Reports. 1: 54. PMID 20948630 DOI: 10.3410/B1-54  0.534
2009 Kim M, Suh J, Romano D, Truong MH, Mullin K, Hooli B, Norton D, Tesco G, Elliott K, Wagner SL, Moir RD, Becker KD, Tanzi RE. Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate {alpha}-secretase activity. Human Molecular Genetics. 18: 3987-96. PMID 19608551 DOI: 10.1093/Hmg/Ddp323  0.557
2009 Schjeide BM, Hooli B, Parkinson M, Hogan MF, DiVito J, Mullin K, Blacker D, Tanzi RE, Bertram L. GAB2 as an Alzheimer disease susceptibility gene: follow-up of genomewide association results. Archives of Neurology. 66: 250-4. PMID 19204163 DOI: 10.1001/Archneurol.2008.552  0.553
2009 Schjeide BM, McQueen MB, Mullin K, DiVito J, Hogan MF, Parkinson M, Hooli B, Lange C, Blacker D, Tanzi RE, Bertram L. Assessment of Alzheimer's disease case-control associations using family-based methods. Neurogenetics. 10: 19-25. PMID 18830724 DOI: 10.1007/S10048-008-0151-3  0.609
2008 Bertram L, Schjeide BM, Hooli B, Mullin K, Hiltunen M, Soininen H, Ingelsson M, Lannfelt L, Blacker D, Tanzi RE. No association between CALHM1 and Alzheimer's disease risk. Cell. 135: 993-4; author reply . PMID 19070563 DOI: 10.1016/J.Cell.2008.11.030  0.519
2008 Bertram L, Lange C, Mullin K, Parkinson M, Hsiao M, Hogan MF, Schjeide BM, Hooli B, Divito J, Ionita I, Jiang H, Laird N, Moscarillo T, Ohlsen KL, Elliott K, et al. Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. American Journal of Human Genetics. 83: 623-32. PMID 18976728 DOI: 10.1016/J.Ajhg.2008.10.008  0.591
2006 Hooli B, Hsiao M, Mullin K, Parkinson M, Patel S, Saunders AJ, Blacker D, Tanzi RE, Bertram L. P1-274: In search of novel Alzheimer’s disease genes on chromosome 19 Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.651  0.342
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