Accessibility of Vendor-Created Database Tutorials for People with Disabilities von Oud, Joanne

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Academic Librarians with Disabilities: Job Perceptions and Factors Influencing Positive Workplace Experiences von Oud, Joanne

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Systemic Workplace Barriers for Academic Librarians with Disabilities von Oud, Joanne

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How Well Do Ontario Library Web Sites Meet New Accessibility Requirements? von Oud, Joanne

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Guidelines for effective online instruction using multimedia screencasts von Oud, Joanne

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Adjusting to the Workplace : Transitions Faced by New Academic Librarians von OUD, Joanne

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Usability testing of an online information literacy tutorial von Bury, Sophie, Oud, Joanne

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Eliminating Duplication in A Shared Storage Facility: Practical and Political Issues von Oud, Joanne

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The Insider's Guide to Grantmaking: How Foundations Find, Fund, and Manage Effective Programs von Oud, Joanne

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Eliminating Duplication in A Shared Storage Facility: Practical and Political Issues von Oud, Joanne

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Jumping into the deep end: training for new academic librarians von Oud, Joanne

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Disability and Equity von Oud, Joanne

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Disability and Equity: Librarians with disabilities face barriers to accessibility and inclusion von Oud, Joanne

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Bisexual Identities and Theories (Book Review) von Oud, Joanne

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Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium von Miyagawa, Toji, Brushaber, Danielle, Syrjanen, Jeremy, Kremers, Walter, Fields, Julie, Forsberg, Leah K., Heuer, Hilary W., Knopman, David, Kornak, John, Boxer, Adam, Rosen, Howard J., Boeve, Bradley F., Appleby, Brian, Bordelon, Yvette, Bove, Jessica, Brannelly, Patrick, Caso, Christina, Coppola, Giovanni, Dever, Reilly, Dheel, Christina, Dickerson, Bradford, Dickinson, Susan, Dominguez, Sophia, Domoto‐Reilly, Kimiko, Faber, Kelley, Ferrell, Jessica, Fishman, Ann, Fong, Jamie, Foroud, Tatiana, Gavrilova, Ralitza, Gearhart, Debra, Ghazanfari, Behnaz, Ghoshal, Nupur, Goldman, Jill S., Graff‐Radford, Jonathan, Graff‐Radford, Neill, Grant, Ian, Grossman, Murray, Haley, Dana, Hsiung, Robin, Huey, Edward, Irwin, David, Jones, David, Jones, Lynne, Kantarci, Kejal, Karydas, Anna, Kaufer, Daniel, Kerwin, Diana, Kraft, Ruth, Kramer, Joel, Kukull, Walter, Litvan, Irene, Lucente, Diane, Lungu, Codrin, Mackenzie, Ian, Maldonado, Miranda, Manoochehri, Masood, McGinnis, Scott, McKinley, Emily, Mendez, Mario F., Miller, Bruce, Multani, Namita, Onyike, Chiadi, Padmanabhan, Jaya, Pantelyat, Alexander, Pearlman, Rodney, Petrucelli, Leonard, Potter, Madeline, Rademakers, Rosa, Ramos, Eliana M., Rankin, Kate, Rascovsky, Katya, Roberson, Erik D., Rogalski, Emily, Sengdy, Pheth, Shaw, Leslie, Tartaglia, Maria C., Tatton, Nadine, Taylor, Joanne, Toga, Arthur, Trojanowski, John Q., Wang, Ping, Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew

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DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study von Trinh, Joanne, BSc, Gustavsson, Emil K, MSc, Vilariño-Güell, Carles, PhD, Bortnick, Stephanie, BSc, Latourelle, Jeanne, PhD, McKenzie, Marna B, BSc, Tu, Chelsea Szu, MSc, Nosova, Ekaterina, PhD, Khinda, Jaskaran, BSc, Milnerwood, Austen, PhD, Lesage, Suzanne, PhD, Brice, Alexis, MD, Tazir, Meriem, MD, Aasly, Jan O, MD, Parkkinen, Laura, PhD, Haytural, Hazal, MSc, Foroud, Tatiana, PhD, Myers, Richard H, PhD, Sassi, Samia Ben, MD, Hentati, Emna, MD, Nabli, Fatma, MD, Farhat, Emna, MD, Amouri, Rim, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, Dr

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Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort von Shen, Li, Kim, Sungeun, Risacher, Shannon L., Nho, Kwangsik, Swaminathan, Shanker, West, John D., Foroud, Tatiana, Pankratz, Nathan, Moore, Jason H., Sloan, Chantel D., Huentelman, Matthew J., Craig, David W., DeChairo, Bryan M., Potkin, Steven G., Jack, Clifford R., Weiner, Michael W., Saykin, Andrew J.

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Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families von Cruchaga, Carlos, Haller, Gabe, Chakraverty, Sumitra, Mayo, Kevin, Vallania, Francesco L M, Mitra, Robi D, Faber, Kelley, Williamson, Jennifer, Bird, Tom, Diaz-Arrastia, Ramon, Foroud, Tatiana M, Boeve, Bradley F, Graff-Radford, Neill R, St Jean, Pamela, Lawson, Michael, Ehm, Margaret G, Mayeux, Richard, Goate, Alison M

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C9orf72 Hexanucleotide Repeat Expansions in Clinical Alzheimer Disease von Harms, Matthew, Benitez, Bruno A, Cairns, Nigel, Cooper, Breanna, Cooper, Paul, Mayo, Kevin, Carrell, David, Faber, Kelley, Williamson, Jennifer, Bird, Tom, Diaz-Arrastia, Ramon, Foroud, Tatiana M, Boeve, Bradley F, Graff-Radford, Neill R, Mayeux, Richard, Chakraverty, Sumitra, Goate, Alison M, Cruchaga, Carlos

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Genetic Testing for Parkinson Disease: Are We Ready? von Cook, Lola, Schulze, Jeanine, Kopil, Catherine, Hastings, Tara, Naito, Anna, Wojcieszek, Joanne, Payne, Katelyn, Alcalay, Roy N., Klein, Christine, Saunders-Pullman, Rachel, Simuni, Tatyana, Foroud, Tatiana

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