Works by Schellenberg, Gerard D.

Results: 251
    1

    Novel early‐onset Alzheimer‐associated genes influence risk through dysregulation of glutamate, immune activation, and intracellular signaling pathways.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2025, v. 21, n. 6, p. 1, doi. 10.1002/alz.70377
    By:
    • Bradley, Joseph;
    • Pottier, Cyril;
    • da Fonseca, Eder Lucio;
    • Kurup, Jiji Thulaseedhara;
    • Western, Daniel;
    • Wang, Ciyang;
    • Neupane, Achal;
    • Ray, Nicholas R.;
    • Jean‐Francois, Melissa;
    • Ali, Muhammad;
    • Timsina, Jigyasha;
    • Bergmann, Kristy;
    • Budde, John;
    • Martin, Eden R.;
    • Pericak‐Vance, Margaret A.;
    • Cuccaro, Michael;
    • Naj, Adam C.;
    • Kunkle, Brian W.;
    • Schellenberg, Gerard D.;
    • Fernandez, Victoria
    Publication type:
    Article
    2

    Structural variation detection and association analysis of whole‐genome‐sequence data from 16,543 Alzheimer's disease sequencing project subjects.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2025, v. 21, n. 6, p. 1, doi. 10.1002/alz.70277
    By:
    • Wang, Hui;
    • Dombroski, Beth A.;
    • Cheng, Po‐Liang;
    • Tucci, Albert;
    • Si, Ya‐Qin;
    • Farrell, John J.;
    • Tzeng, Jung‐Ying;
    • Leung, Yuk Yee;
    • Malamon, John S.;
    • Wang, Li‐San;
    • Vardarajan, Badri N.;
    • Farrer, Lindsay A.;
    • Schellenberg, Gerard D.;
    • Lee, Wan‐Ping
    Publication type:
    Article
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    The Seattle Alzheimer's disease data set.

    Published in:
    Genetic Epidemiology, 1993, v. 10, n. 6, p. 365, doi. 10.1002/gepi.1370100606
    By:
    • Wijsman, Ellen M.;
    • Bird, Thomas D.;
    • Martin, George M.;
    • Schellenberg, Gerard D.
    Publication type:
    Article
    6

    CXCR4 involvement in neurodegenerative diseases.

    Published in:
    Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-017-0049-7
    By:
    • Bonham, Luke W.;
    • Karch, Celeste M.;
    • Fan, Chun C.;
    • Tan, Chin;
    • Geier, Ethan G.;
    • Wang, Yunpeng;
    • Wen, Natalie;
    • Broce, Iris J.;
    • Li, Yi;
    • Barkovich, Matthew J.;
    • Ferrari, Raffaele;
    • Hardy, John;
    • Momeni, Parastoo;
    • Höglinger, Günter;
    • Müller, Ulrich;
    • Hess, Christopher P.;
    • Sugrue, Leo P.;
    • Dillon, William P.;
    • Schellenberg, Gerard D.;
    • Miller, Bruce L.
    Publication type:
    Article
    7
    8

    Gene-Environment Interactions in Progressive Supranuclear Palsy.

    Published in:
    Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2021.664796
    By:
    • Litvan, Irene;
    • Proudfoot, James A.;
    • Martin, Eden R.;
    • Standaert, David;
    • Riley, David;
    • Hall, Deborah;
    • Marras, Connie;
    • Bayram, Ece;
    • Dubinsky, Richard M.;
    • Bordelon, Yvette;
    • Reich, Stephen;
    • Shprecher, David;
    • Kluger, Benzi;
    • Cunningham, Christopher;
    • Schellenberg, Gerard D.;
    • Jankovic, Joseph
    Publication type:
    Article
    9

    Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability.

    Published in:
    Science Translational Medicine, 2010, v. 2, n. 49, p. 1, doi. 10.1126/scitranslmed.3001267
    By:
    • Noor, Abdul;
    • Whibley, Annabel;
    • Marshall, Christian R.;
    • Gianakopoulos, Peter J.;
    • Piton, Amelie;
    • Carson, Andrew R.;
    • Orlic-Milacic, Marija;
    • Lionel, Anath C.;
    • Sato, Daisuke;
    • Estes, Annette M.;
    • Fiebig, Andreas;
    • Franke, Andre;
    • Schreiber, Stefan;
    • Stewart, Alexandre F. R.;
    • Roberts, Robert;
    • McPherson, Ruth;
    • Guter, Stephen J.;
    • Cook Jr., Edwin H.;
    • Dawson, Geraldine;
    • Schellenberg, Gerard D.
    Publication type:
    Article
    10
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    GWAS‐informed variant‐to‐gene mapping integration with microglial single‐cell non‐coding CRISPRi screen illuminates genetic etiology of Alzheimer's disease.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. S8, p. 1, doi. 10.1002/alz.095581
    By:
    • Laub, Shannon;
    • Tulina, Natalia;
    • Ramachandran, Sandhya;
    • Murali, Svathi;
    • Boateng, Louisa;
    • Faryean, J. Bormeh;
    • Hoffman, Matthew;
    • Cook, Kieona;
    • Pippin, James A.;
    • Conery, Mitchell;
    • Burton, Elizabeth A;
    • Wells, Andrew D.;
    • Wang, Li‐San;
    • Schellenberg, Gerard D.;
    • Anderson, Stewart A.;
    • Grant, Struan F.A.;
    • Chesi, Alessandra
    Publication type:
    Article
    12

    Novel rare variant associations with late‐life cognitive performance.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. S8, p. 1, doi. 10.1002/alz.095364
    By:
    • Regelson, Alexandra N.;
    • Archer, Derek B.;
    • Durant, Alaina;
    • Mukherjee, Shubhabrata;
    • Lee, Michael L.;
    • Choi, Seo‐Eun;
    • Scollard, Phoebe;
    • Trittschuh, Emily H.;
    • Mez, Jesse;
    • Bush, William S.;
    • Kuzma, Amanda B;
    • Cuccaro, Michael L.;
    • Cruchaga, Carlos;
    • Farrer, Lindsay A.;
    • Wang, Li‐San;
    • Schellenberg, Gerard D.;
    • Mayeux, Richard;
    • Kukull, Walter A.;
    • Keene, C. Dirk;
    • Saykin, Andrew J.
    Publication type:
    Article
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    Indian‐enriched genetic variants are associated with cognitive function.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.093199
    By:
    • Abu‐Amara, Hasan;
    • Zhao, Wei;
    • Li, Zheng;
    • Leung, Yuk Yee;
    • Schellenberg, Gerard D.;
    • Wang, Li‐San;
    • Moorjani, Priya;
    • Dey, A.B;
    • Dey, Sharmistha;
    • Zhou, Xiang;
    • Gross, Alden L.;
    • Lee, Jinkook;
    • Kardia, Sharon L R;
    • Smith, Jennifer A
    Publication type:
    Article
    15

    The Alzheimer's Disease Sequencing Project – Discovery, Discovery Extension and Follow Up Study (ADSP‐FUS): APOE genotype status and demographic characteristics across datasets.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.092629
    By:
    • Mena, Pedro R.;
    • Zaman, Andrew F;
    • Faber, Kelley M.;
    • Adams, Larry D.;
    • Inciute, Jovita D.;
    • Whitehead, Patrice L.;
    • Foroud, Tatiana M.;
    • Reyes‐Dumeyer, Dolly;
    • Kuzma, Amanda B;
    • Nicaretta, Heather Issen;
    • Naj, Adam C.;
    • Martin, Eden R.;
    • Dalgard, Clifton L.;
    • Schellenberg, Gerard D.;
    • Wang, Li‐San;
    • Mayeux, Richard;
    • Vardarajan, Badri N.;
    • Vance, Jeffery M.;
    • Cuccaro, Michael L.;
    • Kunkle, Brain
    Publication type:
    Article
    16

    Genetic factors modify the effect of chronic viral infections on Alzheimer disease risk.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.091644
    By:
    • Tejeda, Marlene;
    • Farrell, John J.;
    • Zhu, Congcong;
    • Wetzler, Lee;
    • Lunetta, Kathryn L.;
    • Bush, William S.;
    • Martin, Eden R.;
    • Wang, Li‐San;
    • Schellenberg, Gerard D.;
    • Pericak‐Vance, Margaret A;
    • Haines, Jonathan L.;
    • Farrer, Lindsay A.;
    • Sherva, Richard
    Publication type:
    Article
    17

    Genome‐wide Interaction and Stratified Study with Smoking Identifies Association of APAF1 and MIXL1/LIN9 with Alzheimer's Disease.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.091434
    By:
    • Dacey, Ryan;
    • Han, Xudong;
    • Moore, Mackenzie R;
    • Chung, Jaeyoon;
    • Durape, Shruti;
    • Rosenthaler, Max;
    • Uretsky, Madeline;
    • Abdolmohammadi, Bobak;
    • Lee, Annie J.;
    • Brickman, Adam M.;
    • Hohman, Timothy J.;
    • Cuccaro, Michael L.;
    • Bennett, David A.;
    • Crane, Paul K.;
    • Kamboh, M. Ilyas;
    • Kukull, Walter A.;
    • Au, Rhoda;
    • Haines, Jonathan L.;
    • Pericak‐Vance, Margaret A.;
    • Schellenberg, Gerard D.
    Publication type:
    Article
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    Variant‐to‐function mapping of late‐onset Alzheimer's disease GWAS loci in human microglial models implicates RTFDC1 as an effector gene at the CASS4 locus.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.089683
    By:
    • Burton, Elizabeth A;
    • Argenziano, Mariana;
    • Cook, Kieona;
    • Ridler, Molly;
    • Su, Chun;
    • Manduchi, Elisabetta;
    • Hodge, Kenyaita M;
    • Wang, Li‐San;
    • Schellenberg, Gerard D.;
    • Pippin, James A.;
    • Wells, Andrew D.;
    • Anderson, Stewart A.;
    • Brown, Christopher D.;
    • Grant, Struan F.A.;
    • Chesi, Alessandra
    Publication type:
    Article
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    Variant‐gene pair in silico analyses and functional validation of LOAD GWAS loci in human brain‐relevant cell types identify EGFR as a target gene for potential drug repurposing.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.087633
    By:
    • Leung, Yuk Yee;
    • Kuksa, Pavel P.;
    • Cifello, Jeffrey;
    • Greenfest‐Allen, Emily;
    • Boateng, Louisa;
    • Laub, Shannon;
    • Tulina, Natalia;
    • Schellenberg, Gerard D.;
    • Chesi, Alessandra;
    • Wang, Li‐San
    Publication type:
    Article
    22

    Longitudinal change in memory performance as a strong endophenotype for Alzheimer's disease.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 2, p. 1268, doi. 10.1002/alz.13508
    By:
    • Archer, Derek B.;
    • Eissman, Jaclyn M.;
    • Mukherjee, Shubhabrata;
    • Lee, Michael L.;
    • Choi, Seo‐Eun;
    • Scollard, Phoebe;
    • Trittschuh, Emily H.;
    • Mez, Jesse B.;
    • Bush, William S.;
    • Kunkle, Brian W.;
    • Naj, Adam C.;
    • Gifford, Katherine A.;
    • Cuccaro, Michael L.;
    • Pericak‐Vance, Margaret A.;
    • Farrer, Lindsay A.;
    • Wang, Li‐San;
    • Schellenberg, Gerard D.;
    • Mayeux, Richard P.;
    • Haines, Jonathan L.;
    • Jefferson, Angela L.
    Publication type:
    Article
    23

    Sex‐specific genetic architecture of late‐life memory performance.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 2, p. 1250, doi. 10.1002/alz.13507
    By:
    • Eissman, Jaclyn M.;
    • Archer, Derek B.;
    • Mukherjee, Shubhabrata;
    • Lee, Michael L.;
    • Choi, Seo‐Eun;
    • Scollard, Phoebe;
    • Trittschuh, Emily H.;
    • Mez, Jesse B.;
    • Bush, William S.;
    • Kunkle, Brian W.;
    • Naj, Adam C.;
    • Gifford, Katherine A.;
    • Cuccaro, Michael L.;
    • Cruchaga, Carlos;
    • Pericak‐Vance, Margaret A.;
    • Farrer, Lindsay A.;
    • Wang, Li‐San;
    • Schellenberg, Gerard D.;
    • Mayeux, Richard P.;
    • Haines, Jonathan L.
    Publication type:
    Article
    24

    DNA from multiple viral species is associated with Alzheimer's disease risk.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 1, p. 253, doi. 10.1002/alz.13414
    By:
    • Tejeda, Marlene;
    • Farrell, John;
    • Zhu, Congcong;
    • Wetzler, Lee;
    • Lunetta, Kathryn L.;
    • Bush, William S.;
    • Martin, Eden R.;
    • Wang, Li‐San;
    • Schellenberg, Gerard D.;
    • Pericak‐Vance, Margaret A.;
    • Haines, Jonathan L.;
    • Farrer, Lindsay A.;
    • Sherva, Richard
    Publication type:
    Article
    25

    Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007791
    By:
    • Rajabli, Farid;
    • Feliciano, Briseida E.;
    • Celis, Katrina;
    • Hamilton-Nelson, Kara L.;
    • Whitehead, Patrice L.;
    • Adams, Larry D.;
    • Bussies, Parker L.;
    • Manrique, Clara P.;
    • Rodriguez, Alejandra;
    • Rodriguez, Vanessa;
    • Starks, Takiyah;
    • Byfield, Grace E.;
    • Sierra Lopez, Carolina B.;
    • McCauley, Jacob L.;
    • Acosta, Heriberto;
    • Chinea, Angel;
    • Kunkle, Brian W.;
    • Reitz, Christiane;
    • Farrer, Lindsay A.;
    • Schellenberg, Gerard D.
    Publication type:
    Article
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    LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.

    Published in:
    Movement Disorders, 2009, v. 24, n. 7, p. 1034, doi. 10.1002/mds.22514
    By:
    • Zabetian, Cyrus P.;
    • Yamamoto, Mitsutoshi;
    • Lopez, Alexis N.;
    • Ujike, Hiroshi;
    • Mata, Ignacio F.;
    • Izumi, Yuishin;
    • Kaji, Ryuji;
    • Maruyama, Hirofumi;
    • Morino, Hiroyuki;
    • Oda, Masaya;
    • Hutter, Carolyn M.;
    • Edwards, Karen L.;
    • Schellenberg, Gerard D.;
    • Tsuang, Debby W.;
    • Yearout, Dora;
    • Larson, Eric B.;
    • Kawakami, Hideshi
    Publication type:
    Article
    28

    A comparative study of structural variant calling in WGS from Alzheimer's disease families.

    Published in:
    Life Science Alliance, 2024, v. 7, n. 5, p. 1, doi. 10.26508/lsa.202302181
    By:
    • Malamon, John S.;
    • Farrell, John J.;
    • Li Charlie Xia;
    • Dombroski, Beth A.;
    • Das, Rueben G.;
    • Way, Jessica;
    • Kuzma, Amanda B.;
    • Valladares, Otto;
    • Yuk Yee Leung;
    • Scanlon, Allison J.;
    • Lopez, Irving Antonio Barrera;
    • Brehony, Jack;
    • Worley, Kim C.;
    • Zhang, Nancy R.;
    • Li-San Wang;
    • Farrer, Lindsay A.;
    • Schellenberg, Gerard D.;
    • Wan-Ping Lee;
    • Vardarajan, Badri N.
    Publication type:
    Article
    29
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    Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau.

    Published in:
    JAMA Neurology, 2018, v. 75, n. 8, p. 989, doi. 10.1001/jamaneurol.2018.0821
    By:
    • Hohman, Timothy J.;
    • Dumitrescu, Logan;
    • Barnes, Lisa L.;
    • Thambisetty, Madhav;
    • Beecham, Gary;
    • Kunkle, Brian;
    • Gifford, Katherine A.;
    • Bush, William S.;
    • Chibnik, Lori B.;
    • Mukherjee, Shubhabrata;
    • De Jager, Philip L.;
    • Kukull, Walter;
    • Crane, Paul K.;
    • Resnick, Susan M.;
    • Keene, C. Dirk;
    • Montine, Thomas J.;
    • Schellenberg, Gerard D.;
    • Haines, Jonathan L.;
    • Zetterberg, Henrik;
    • Blennow, Kaj
    Publication type:
    Article
    31

    Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.

    Published in:
    JAMA Neurology, 2018, v. 75, n. 7, p. 860, doi. 10.1001/jamaneurol.2018.0372
    By:
    • Karch, Celeste M.;
    • Wen, Natalie;
    • Fan, Chun C.;
    • Yokoyama, Jennifer S.;
    • Kouri, Naomi;
    • Ross, Owen A.;
    • Höglinger, Gunter;
    • Müller, Ulrich;
    • Ferrari, Raffaele;
    • Hardy, John;
    • Schellenberg, Gerard D.;
    • Sleiman, Patrick M.;
    • Momeni, Parastoo;
    • Hess, Christopher P.;
    • Miller, Bruce L.;
    • Sharma, Manu;
    • Van Deerlin, Vivianna;
    • Smeland, Olav B.;
    • Andreassen, Ole A.;
    • Dale, Anders M.
    Publication type:
    Article
    32

    Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.

    Published in:
    JAMA Neurology, 2017, v. 74, n. 9, p. 1113, doi. 10.1001/jamaneurol.2017.1518
    By:
    • Kunkle, Brian W.;
    • Vardarajan, Badri N.;
    • Naj, Adam C.;
    • Whitehead, Patrice L.;
    • Rolati, Sophie;
    • Slifer, Susan;
    • Carney, Regina M.;
    • Cuccaro, Michael L.;
    • Vance, Jeffery M.;
    • Gilbert, John R.;
    • Li-San Wang;
    • Farrer, Lindsay A.;
    • Reitz, Christiane;
    • Haines, Jonathan L.;
    • Beecham, GaryW.;
    • Martin, Eden R.;
    • Schellenberg, Gerard D.;
    • Mayeux, Richard P.;
    • Pericak-Vance, Margaret A.
    Publication type:
    Article
    33

    Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci.

    Published in:
    Annals of Human Genetics, 2013, v. 77, n. 2, p. 85, doi. 10.1111/ahg.12000
    By:
    • Holton, Patrick;
    • Ryten, Mina;
    • Nalls, Michael;
    • Trabzuni, Daniah;
    • Weale, Michael E.;
    • Hernandez, Dena;
    • Crehan, Helen;
    • Gibbs, J. Raphael;
    • Mayeux, Richard;
    • Haines, Jonathan L.;
    • Farrer, Lindsay A.;
    • Pericak‐Vance, Margaret A.;
    • Schellenberg, Gerard D.;
    • Ramirez‐Restrepo, Manuel;
    • Engel, Anzhelika;
    • Myers, Amanda J.;
    • Corneveaux, Jason J.;
    • Huentelman, Matthew J.;
    • Dillman, Allissa;
    • Cookson, Mark R.
    Publication type:
    Article
    34

    Genome-wide association study of brain arteriolosclerosis.

    Published in:
    Journal of Cerebral Blood Flow & Metabolism, 2022, v. 42, n. 8, p. 1437, doi. 10.1177/0271678X211066299
    By:
    • Shade, Lincoln MP;
    • Katsumata, Yuriko;
    • Hohman, Timothy J;
    • Nho, Kwangsik;
    • Saykin, Andrew J;
    • Mukherjee, Shubhabrata;
    • Boehme, Kevin L;
    • Kauwe, John SK;
    • Farrer, Lindsay A;
    • Schellenberg, Gerard D;
    • Haines, Jonathan L;
    • Mayeux, Richard P;
    • Schneider, Julie A;
    • Nelson, Peter T;
    • Fardo, David W
    Publication type:
    Article
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    Replication of progressive supranuclear palsy genome-wide association study identifies <italic>SLCO1A2</italic> and <italic>DUSP10</italic> as new susceptibility loci.

    Published in:
    Molecular Neurodegeneration, 2018, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13024-018-0267-3
    By:
    • Sanchez-Contreras, Monica Y.;
    • Kouri, Naomi;
    • Cook, Casey N.;
    • Serie, Daniel J.;
    • Heckman, Michael G.;
    • Finch, NiCole A.;
    • Caselli, Richard J.;
    • Uitti, Ryan J.;
    • Wszolek, Zbigniew K.;
    • Graff-Radford, Neill;
    • Petrucelli, Leonard;
    • Wang, Li-San;
    • Schellenberg, Gerard D.;
    • Dickson, Dennis W.;
    • Rademakers, Rosa;
    • Ross, Owen A.
    Publication type:
    Article
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    High copy wildtype human 1N4R tau expression promotes early pathological tauopathy accompanied by cognitive deficits without progressive neurofibrillary degeneration.

    Published in:
    Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0210-6
    By:
    • Wheeler, Jeanna M.;
    • McMillan, Pamela J.;
    • Hawk, Michele;
    • Iba, Michiyo;
    • Robinson, Linda;
    • Xu, George J.;
    • Dombroski, Beth A.;
    • Doori Jeong;
    • Dichter, Marc A.;
    • Halvor Juul;
    • Loomis, Elaine;
    • Raskind, Murray;
    • Leverenz, James B.;
    • Trojanowski, John Q.;
    • Lee, Virginia M. Y.;
    • Schellenberg, Gerard D.;
    • Kraemer, Brian C.
    Publication type:
    Article
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    Homozygous and Compound Heterozygous Mutations at the Werner Syndrome Locus.

    Published in:
    Human Molecular Genetics, 1996, v. 5, n. 12, p. 1909, doi. 10.1093/hmg/5.12.1909
    By:
    • Oshima, Junko;
    • Yu, Chang-En;
    • Piussan, Charles;
    • Klein, Georg;
    • Jabkowski, Jörg;
    • Balci, Sevim;
    • Miki, Tetsuro;
    • Nakura, Jun;
    • Ogihara, Toshio;
    • Ells, James;
    • Smith, Marilia de A. C.;
    • Melaragno, Maria I.;
    • Fraccaro, Marco;
    • Scappaticci, Susi;
    • Matthews, John;
    • Ouais, Samir;
    • Jarzebowicz, Amy;
    • Schellenberg, Gerard D.;
    • Martin, George M.
    Publication type:
    Article
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    Caspase-8, association with Alzheimer’s Disease and functional analysis of rare variants.

    Published in:
    PLoS ONE, 2017, v. 12, n. 10, p. 1, doi. 10.1371/journal.pone.0185777
    By:
    • Rehker, Jan;
    • Rodhe, Johanna;
    • Nesbitt, Ryan R.;
    • Boyle, Evan A.;
    • Martin, Beth K.;
    • Lord, Jenny;
    • Karaca, Ilker;
    • Naj, Adam;
    • Jessen, Frank;
    • Helisalmi, Seppo;
    • Soininen, Hilkka;
    • Hiltunen, Mikko;
    • Ramirez, Alfredo;
    • Scherer, Martin;
    • Farrer, Lindsay A.;
    • Haines, Jonathan L.;
    • Pericak-Vance, Margaret A.;
    • Raskind, Wendy H.;
    • Cruchaga, Carlos;
    • Schellenberg, Gerard D.
    Publication type:
    Article
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