检索结果 - Amanda Partch
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Reassessment of Risk Genotypes (<i>GRN</i>,<i>TMEM106B</i>, and<i>ABCC9</i>Variants) Associated With Hippocampal Sclerosis of Aging Pathology 由 Peter T. Nelson, Wang‐Xia Wang, Amanda Partch, Sarah E. Monsell, Otto Valladares, Sally R. Ellingson, Bernard R. Wilfred, Adam C. Naj, Li-San Wang, Walter A. Kukull, David W. Fardo
出版 2014Artigo -
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The role of <i>TREM2</i> R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 由 Christina M. Lill, Aina Rengmark, Lasse Pihlstrøm, Isabella Fogh, Aleksey Shatunov, Patrick Sleiman, Li‐San Wang, Tian Liu, Christina Funch Lassen, Esther Meissner, Panagiotis Alexopoulos, Andrea Calvo, Adriano Chió, Nil Dizdar, Frank Faltraco, Lars Forsgren, Julia Kirchheiner, Alexander Kurz, Jan Larsen, Maria Liebsch, Jan Linder, Karen Morrison, Hans Nissbrandt, Markus Otto, Jens Pahnke, Amanda Partch, Gabriella Restagno, Dan Rujescu, Cathrin Schnack, Christopher E. Shaw, Pamela J. Shaw, Hayrettin Tumani, Ole‐Bjørn Tysnes, Otto Valladares, Vincenzo Silani, Leonard H. van den Berg, Wouter van Rheenen, Jan H. Veldink, Ulman Lindenberger, Elisabeth Steinhagen‐Thiessen, Stefan Teipel, Robert Perneczky, Hákon Hákonarson, Harald Hampel, Christine A. F. Von Arnim, Jørgen H. Olsen, Vivianna M. Van Deerlin, Ammar Al‐Chalabi, Mathias Toft, Beate Ritz, Lars Bertram
出版 2015Revisão -
3
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology 由 Peter T. Nelson, Steven Estus, Erin L. Abner, Ishita Parikh, Manasi Malik, Janna H. Neltner, Eseosa T. Ighodaro, Wang‐Xia Wang, Bernard R. Wilfred, Li‐San Wang, Walter A. Kukull, Kannabiran Nandakumar, Mark Farman, Wayne W. Poon, María M. Corrada, Claudia H. Kawas, David H. Cribbs, David A. Bennett, Julie A. Schneider, Eric B. Larson, Paul K. Crane, Otto Valladares, Frederick A. Schmitt, Richard J. Kryscio, Gregory A. Jicha, Charles D. Smith, Stephen W. Scheff, Joshua A. Sonnen, Jonathan L. Haines, Margaret A. Pericak‐Vance, Richard Mayeux, Lindsay A. Farrer, Linda J. Van Eldik, Craig Horbinski, Robert C. Green, Marla Gearing, Leonard W. Poon, Patricia L. Kramer, Randall L. Woltjer, Thomas J. Montine, Amanda Partch, Alexander J. Rajic, KatieRose Richmire, Sarah E. Monsell, Gerard D. Schellenberg, David W. Fardo
出版 2014Revisão -
4
Rarity of the Alzheimer Disease–Protective<i>APP</i>A673T Variant in the United States 由 Li-San Wang, Adam C. Naj, Robert Graham, Paul K. Crane, Brian W. Kunkle, Carlos Cruchaga, Josue D. Gonzalez Murcia, Lisa Cannon‐Albright, Clinton T. Baldwin, Henrik Zetterberg, Kaj Blennow, Walter A. Kukull, Kelley M. Faber, Nicole Schupf, Maria C. Norton, JoAnn T. Tschanz, Ronald G. Munger, Christopher Corcoran, Ekaterina Rogaeva, Chiao‐Feng Lin, Beth A. Dombroski, Laura B. Cantwell, Amanda Partch, Otto Valladares, Hákon Hákonarson, Peter St George‐Hyslop, Robert C. Green, Alison Goate, Tatiana Foroud, Regina M. Carney, Eric B. Larson, Timothy W. Behrens, John Kauwe, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Richard Mayeux, Gerard D. Schellenberg, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Robert W. Barber, M. Michael Barmada, Lisa L. Barnes, Thomas G. Beach, James T. Becker, Gary W. Beecham, Duane Beekly, David A. Bennett, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Joseph D. Buxbaum, Nigel J. Cairns, Chuanhai Cao, Chris Carlson, Steven L. Carroll, Helena C. Chui, David G. Clark, David H. Cribbs, Elizabeth Crocco, Charles DeCarli, Steven T. DeKosky, F. Yesim Demirci, Malcolm Dick, Dennis W. Dickson, Ranjan Duara, Nilüfer Ertekin‐Taner, Kenneth B. Fallon, Martin R. Farlow, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Mary Ganguli, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Jonathan D. Glass, Neill R. Graff‐Radford, John H. Growdon, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Lindy E. Harrell, Elizabeth Head, Lawrence S. Honig, Christine M. Hulette, Bradley T. Hyman, Gail P. Jarvik, Gregory A. Jicha, Lee‐Way Jin, Gyungah Jun, M. Ilyas Kamboh, Anna Karydas, Jeffrey Kaye
出版 2014Artigo
相关主题
Medicine
Biology
Disease
Gene
Genetics
Genotype
Internal medicine
Alzheimer's disease
Dementia
Epilepsy
Genome-wide association study
Hippocampal sclerosis
Odds ratio
Oncology
Pathology
Single-nucleotide polymorphism
Temporal lobe
Allele
Allele frequency
Amyotrophic lateral sclerosis
Case-control study
Cerebrospinal fluid
Cohort
Cohort study
Environmental health
Frontotemporal dementia
Frontotemporal lobar degeneration
Gastroenterology
Genotyping
Gerontology