Coding variants in TREM2 increase risk for Alzheimer's disease
Jin, Sheng Chih, Benitez, Bruno A, Karch, Celeste M, Cooper, Breanna, Skorupa, Tara, Carrell, David, Norton, Joanne B, Hsu, Simon, Harari, Oscar, Cai, Yefei, Bertelsen, Sarah, Goate, Alison M, Cruchaga, Carlos
Published in Human molecular genetics (01.11.2014)
Published in Human molecular genetics (01.11.2014)
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TDP-43 A315T mutation in familial motor neuron disease
Gitcho, Michael A., Baloh, Robert H., Chakraverty, Sumi, Mayo, Kevin, Norton, Joanne B., Levitch, Denise, Hatanpaa, Kimmo J., White III, Charles L., Bigio, Eileen H., Caselli, Richard, Baker, Matt, Al-Lozi, Muhammad T., Morris, John C., Pestronk, Alan, Rademakers, Rosa, Goate, Alison M., Cairns, Nigel J.
Published in Annals of neurology (01.04.2008)
Published in Annals of neurology (01.04.2008)
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Discovery and validation of autosomal dominant Alzheimer's disease mutations
Hsu, Simon, Gordon, Brian A, Hornbeck, Russ, Norton, Joanne B, Levitch, Denise, Louden, Adia, Ziegemeier, Ellen, Laforce, Jr, Robert, Chhatwal, Jasmeer, Day, Gregory S, McDade, Eric, Morris, John C, Fagan, Anne M, Benzinger, Tammie L S, Goate, Alison M, Cruchaga, Carlos, Bateman, Randall J, Karch, Celeste M
Published in Alzheimer's research & therapy (18.07.2018)
Published in Alzheimer's research & therapy (18.07.2018)
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Examination of the Effect of Rare Variants in TREM2, ABI3, and PLCG2 in LOAD Through Multiple Phenotypes
Olive, Claudia, Ibanez, Laura, Farias, Fabiana H Geraldo, Wang, Fengxian, Budde, John P, Norton, Joanne B, Gentsch, Jen, Morris, John C, Li, Zeran, Dube, Umber, Del-Aguila, Jorge, Bergmann, Kristy, Bradley, Joseph, Benitez, Bruno A, Harari, Oscar, Fagan, Anne, Ances, Beau, Cruchaga, Carlos, Fernandez, Maria Victoria
Published in Journal of Alzheimer's disease (01.01.2020)
Published in Journal of Alzheimer's disease (01.01.2020)
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Clinically early-stage CSPα mutation carrier exhibits remarkable terminal stage neuronal pathology with minimal evidence of synaptic loss
Benitez, Bruno A, Cairns, Nigel J, Schmidt, Robert E, Morris, John C, Norton, Joanne B, Cruchaga, Carlos, Sands, Mark S
Published in Acta neuropathologica communications (26.11.2015)
Published in Acta neuropathologica communications (26.11.2015)
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Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation
Behrens, Maria I, Mukherjee, Odity, Tu, Pang-hsien, Liscic, Rajka M, Grinberg, Lea Tenenholz, Carter, Deborah, Paulsmeyer, Katherine, Taylor-Reinwald, Lisa, Gitcho, Michael, Norton, Joanne B, Chakraverty, Sumi, Goate, Alison M, Morris, John C, Cairns, Nigel J
Published in Alzheimer disease and associated disorders (01.01.2007)
Published in Alzheimer disease and associated disorders (01.01.2007)
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Association of TMEM106B Gene Polymorphism With Age at Onset in Granulin Mutation Carriers and Plasma Granulin Protein Levels
Cruchaga, Carlos, Graff, Caroline, Chiang, Huei-Hsin, Wang, Jun, Hinrichs, Anthony L, Spiegel, Noah, Bertelsen, Sarah, Mayo, Kevin, Norton, Joanne B, Morris, John C, Goate, Alison
Published in Archives of neurology (Chicago) (01.05.2011)
Published in Archives of neurology (Chicago) (01.05.2011)
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P3-287: TDP-43 A315T mutation in familial motor neuron disease
Gitcho, Michael A, Baloh, Robert H, Chakraverty, Sumi, Mayo, Kevin, Norton, Joanne B, Levitch, Denise, Hatanpaa, Kimmo J, White, Charles H, Bigio, Eileen H, Caselli, Richard, Baker, Matt, Al-Lozi, Muhammad T, Morris, John C, Pestronk, Alan, Rademakers, Rosa, Goate, Alison M, Cairns, Nigel J
Published in Alzheimer's & dementia (01.07.2008)
Published in Alzheimer's & dementia (01.07.2008)
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Clinically early-stage CSP[alpha] mutation carrier exhibits remarkable terminal stage neuronal pathology with minimal evidence of synaptic loss
Benitez, Bruno A, Cairns, Nigel J, Schmidt, Robert E, Morris, John C, Norton, Joanne B, Cruchaga, Carlos, Sands, Mark S
Published in Acta neuropathologica communications (26.11.2015)
Published in Acta neuropathologica communications (26.11.2015)
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Clinically early-stage CSPAlpha mutation carrier exhibits remarkable terminal stage neuronal pathology with minimal evidence of synaptic loss
Benitez, Bruno A, Cairns, Nigel J, Schmidt, Robert E, Morris, John C, Norton, Joanne B, Cruchaga, Carlos, Sands, Mark S
Published in Acta neuropathologica communications (01.01.2015)
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Published in Acta neuropathologica communications (01.01.2015)
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TMEM106B gene polymorphism is associated with age at onset in granulin mutation carriers and plasma granulin protein levels
Cruchaga, Carlos, Graff, Caroline, Chiang, Huei-Hsin, Wang, Jun, Hinrichs, Anthony L., Spiegel, Noah, Bertelsen, Sarah, Mayo, Kevin, Norton, Joanne B., Morris, John C., Goate, Alison
Published in Archives of neurology (Chicago) (10.01.2011)
Published in Archives of neurology (Chicago) (10.01.2011)
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