% alzhub.org library filter % Source: https://alzhub.org/research?journal=Human+Molecular+Genetics % 46 entries, in the order the page lists them. Built from alzhub.org's own records. % 0 entries have no readable author in the source record and carry no author field. @article{grupe2007-17317784, author = {Grupe, A. and Abraham, R. and Li, Y. and Rowland, C. and Hollingworth, P. and Morgan, A. and Jehu, L. and Segurado, R. and others}, title = {{Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants}}, journal = {Human molecular genetics}, year = {2007}, doi = {10.1093/hmg/ddm031}, pmid = {17317784}, url = {https://doi.org/10.1093/hmg/ddm031} } @article{shulman2013-24067533, author = {Shulman, Joshua M and Imboywa, Selina H. and Γιαγτζόγλου, Νικόλαος and Powers, Martin P. and Hu, Yanhui and Devenport, Danelle and Chipendo, Portia I. and Chibnik, Lori Beth and others}, title = {{Functional screening in Drosophila identifies Alzheimer's disease susceptibility genes and implicates Tau-mediated mechanisms}}, journal = {Human Molecular Genetics}, year = {2013}, doi = {10.1093/hmg/ddt478}, pmid = {24067533}, url = {https://doi.org/10.1093/hmg/ddt478} } @article{gass2006-16950801, author = {Gass, J. and Cannon, A. and Mackenzie, I. R. and Boeve, B. and Baker, M. and Adamson, J. and Crook, R. and Melquist, S. and others}, title = {{Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration}}, journal = {Human molecular genetics}, year = {2006}, doi = {10.1093/hmg/ddl241}, pmid = {16950801}, url = {https://doi.org/10.1093/hmg/ddl241} } @article{lagiertourenne2010-20400460, author = {Lagier-Tourenne, C. and Polymenidou, M. and Cleveland, D. W.}, title = {{TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration}}, journal = {Human molecular genetics}, year = {2010}, doi = {10.1093/hmg/ddq137}, pmid = {20400460}, url = {https://doi.org/10.1093/hmg/ddq137} } @article{jin2014-24899047, author = {Jin, S. C. and Benitez, B. A. and Karch, C. M. and Cooper, B. and Skorupa, T. and Carrell, D. and Norton, J. B. and Hsu, S. and others}, title = {{Coding variants in TREM2 increase risk for Alzheimer's disease}}, journal = {Human molecular genetics}, year = {2014}, doi = {10.1093/hmg/ddu277}, pmid = {24899047}, url = {https://doi.org/10.1093/hmg/ddu277} } @article{farg2014-24549040, author = {Farg, M. A. and Sundaramoorthy, V. and Sultana, J. M. and Yang, S. and Atkinson, R. A. and Levina, V. and Halloran, M. A. and Gleeson, P. A. and others}, title = {{C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking}}, journal = {Human molecular genetics}, year = {2014}, doi = {10.1093/hmg/ddu068}, pmid = {24549040}, url = {https://doi.org/10.1093/hmg/ddu068} } @article{rademakers2008-18723524, author = {Rademakers, R. and Eriksen, J. L. and Baker, M. and Robinson, T. and Ahmed, Z. and Lincoln, S. J. and Finch, N. and Rutherford, N. J. and others}, title = {{Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia}}, journal = {Human molecular genetics}, year = {2008}, doi = {10.1093/hmg/ddn257}, pmid = {18723524}, url = {https://doi.org/10.1093/hmg/ddn257} } @article{liu2020-32959884, author = {Liu, W. and Taso, O. and Wang, R. and Bayram, S. and Graham, A. C. and Garcia-Reitboeck, P. and Mallach, A. and Andrews, W. D. and others}, title = {{Trem2 promotes anti-inflammatory responses in microglia and is suppressed under pro-inflammatory conditions}}, journal = {Human molecular genetics}, year = {2020}, doi = {10.1093/hmg/ddaa209}, pmid = {32959884}, url = {https://doi.org/10.1093/hmg/ddaa209} } @article{kabashi2010-19959528, author = {Kabashi, E. and Lin, L. and Tradewell, M. L. and Dion, P. A. and Bercier, V. and Bourgouin, P. and Rochefort, D. and Bel Hadj, S. and others}, title = {{Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo}}, journal = {Human molecular genetics}, year = {2010}, doi = {10.1093/hmg/ddp534}, pmid = {19959528}, url = {https://doi.org/10.1093/hmg/ddp534} } @article{cruts1998-9384602, author = {Cruts, M. and van Duijn, C. M. and Backhovens, H. and Van den Broeck, M. and Wehnert, A. and Serneels, S. and Sherrington, R. and Hutton, M. and others}, title = {{Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease}}, journal = {Human molecular genetics}, year = {1998}, doi = {10.1093/hmg/7.1.43}, pmid = {9384602}, url = {https://doi.org/10.1093/hmg/7.1.43} } @article{bradley2023-37208024, author = {Bradley, J. and Gorijala, P. and Schindler, S. E. and Sung, Y. J. and Ances, B. and {Alzheimer’s Disease Neuroimaging Initiative} and {the Human Connectome Project} and Fernandez, M. V. and others}, title = {{Genetic architecture of plasma Alzheimer disease biomarkers}}, journal = {Human molecular genetics}, year = {2023}, doi = {10.1093/hmg/ddad087}, pmid = {37208024}, url = {https://doi.org/10.1093/hmg/ddad087} } @article{kimura2007-17135279, author = {Kimura, R. and Kamino, K. and Yamamoto, M. and Nuripa, A. and Kida, T. and Kazui, H. and Hashimoto, R. and Tanaka, T. and others}, title = {{The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between beta-amyloid production and tau phosphorylation in Alzheimer disease}}, journal = {Human molecular genetics}, year = {2007}, doi = {10.1093/hmg/ddl437}, pmid = {17135279}, url = {https://doi.org/10.1093/hmg/ddl437} } @article{winkelmann2012-22328086, author = {Winkelmann, J. and Lin, L. and Schormair, B. and Kornum, B. R. and Faraco, J. and Plazzi, G. and Melberg, A. and Cornelio, F. and others}, title = {{Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy}}, journal = {Human molecular genetics}, year = {2012}, doi = {10.1093/hmg/dds035}, pmid = {22328086}, url = {https://doi.org/10.1093/hmg/dds035} } @article{chartierharlin1994-8069300, author = {Chartier‐Harlin, Marie‐Christine and Parfitt, Matthew and Legrain, Sylvie and Pérez‐Tur, Jordi and Brousseau, Thierry and Evans, Alun and Berr, Claudine and Vldal, Odile and others}, title = {{Apolipoprotein E, ɛ4 allele as a major risk factor for sporadic early and late-onset forms of Alzheimer's disease: analysis of the 19q13.2 chromosomal region}}, journal = {Human Molecular Genetics}, year = {1994}, doi = {10.1093/hmg/3.4.569}, pmid = {8069300}, url = {https://doi.org/10.1093/hmg/3.4.569} } @article{smith2013-23297359, author = {Smith, K. R. and Dahl, H. H. and Canafoglia, L. and Andermann, E. and Damiano, J. and Morbin, M. and Bruni, A. C. and Giaccone, G. and others}, title = {{Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis}}, journal = {Human molecular genetics}, year = {2013}, doi = {10.1093/hmg/dds558}, pmid = {23297359}, url = {https://doi.org/10.1093/hmg/dds558} } @article{kang2018-29040522, author = {Kang, S. S. and Kurti, A. and Baker, K. E. and Liu, C. C. and Colonna, M. and Ulrich, J. D. and Holtzman, D. M. and Bu, G. and others}, title = {{Behavioral and transcriptomic analysis of Trem2-null mice: not all knockout mice are created equal}}, journal = {Human molecular genetics}, year = {2018}, doi = {10.1093/hmg/ddx366}, pmid = {29040522}, url = {https://doi.org/10.1093/hmg/ddx366} } @article{ash2010-20530643, author = {Ash, P. E. and Zhang, Y. J. and Roberts, C. M. and Saldi, T. and Hutter, H. and Buratti, E. and Petrucelli, L. and Link, C. 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H. and Mayo, K. and Bertelsen, S. and Hinrichs, A. and others}, title = {{Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimer's disease}}, journal = {Human molecular genetics}, year = {2012}, doi = {10.1093/hmg/dds296}, pmid = {22821396}, url = {https://doi.org/10.1093/hmg/dds296} } @article{miyagawa2016-27179792, author = {Miyagawa, T. and Ebinuma, I. and Morohashi, Y. and Hori, Y. and Young Chang, M. and Hattori, H. and Maehara, T. and Yokoshima, S. and others}, title = {{BIN1 regulates BACE1 intracellular trafficking and amyloid-β production}}, journal = {Human molecular genetics}, year = {2016}, doi = {10.1093/hmg/ddw146}, pmid = {27179792}, url = {https://doi.org/10.1093/hmg/ddw146} } @article{cruts2005-15888485, author = {Cruts, M. and Rademakers, R. and Gijselinck, I. and van der Zee, J. and Dermaut, B. and de Pooter, T. and de Rijk, P. and Del-Favero, J. and others}, title = {{Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region}}, journal = {Human molecular genetics}, year = {2005}, doi = {10.1093/hmg/ddi182}, pmid = {15888485}, url = {https://doi.org/10.1093/hmg/ddi182} } @article{carlson1997-9302276, author = {Carlson, G. 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E. and Zondervan, K. T. and others}, title = {{Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis}}, journal = {Human molecular genetics}, year = {2013}, doi = {10.1093/hmg/dds491}, pmid = {23193196}, url = {https://doi.org/10.1093/hmg/dds491} } @article{chen2009-19808793, author = {Chen, H. and Chan, D. C.}, title = {{Mitochondrial dynamics--fusion, fission, movement, and mitophagy--in neurodegenerative diseases}}, journal = {Human molecular genetics}, year = {2009}, doi = {10.1093/hmg/ddp326}, pmid = {19808793}, url = {https://doi.org/10.1093/hmg/ddp326} } @article{wiseman2009-19297404, author = {Wiseman, F. K. and Alford, K. A. and Tybulewicz, V. L. and Fisher, E. M.}, title = {{Down syndrome--recent progress and future prospects}}, journal = {Human molecular genetics}, year = {2009}, doi = {10.1093/hmg/ddp010}, pmid = {19297404}, url = {https://doi.org/10.1093/hmg/ddp010} } @article{morabito2020-32803238, author = {Morabito, Samuel and Miyoshi, Emily and Michael, Neethu and Swarup, Vivek}, title = {{Integrative genomics approach identifies conserved transcriptomic networks in Alzheimer's disease}}, journal = {Human molecular genetics}, year = {2020}, doi = {10.1093/hmg/ddaa182}, pmid = {32803238}, url = {https://doi.org/10.1093/hmg/ddaa182} } @article{tapias2018-29860433, author = {Tapias, V. and Jainuddin, S. and Ahuja, M. and Stack, C. and Elipenahli, C. and Vignisse, J. and Gerges, M. and Starkova, N. and others}, title = {{Benfotiamine treatment activates the Nrf2/ARE pathway and is neuroprotective in a transgenic mouse model of tauopathy}}, journal = {Human molecular genetics}, year = {2018}, doi = {10.1093/hmg/ddy201}, pmid = {29860433}, url = {https://doi.org/10.1093/hmg/ddy201} } @article{lambert2019-31363735, author = {Lambert, S. 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