Sex-stratified RNA-seq analysis reveals traumatic brain injury-induced transcriptional changes in the female hippocampus conducive to dementia

por Fiorini, Michael R., Dilliott, Allison A., Farhan, Sali M. K.
Publicado 2022

Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes

por Dilliott, Allison A, Kwon, Seulki, Rouleau, Guy A, Iqbal, Sumaiya, Farhan, Sali M K
Publicado 2023

A De Novo POLD1 Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner Syndrome

por Wang, Linda R., Radonjic, Aleksandar, Dilliott, Allison A., McIntyre, Adam D., Hegele, Robert A.
Publicado 2018

DnaJC7 in Amyotrophic Lateral Sclerosis

por Dilliott, Allison A., Andary, Catherine M., Stoltz, Meaghan, Petropavlovskiy, Andrey A., Farhan, Sali M. K., Duennwald, Martin L.
Publicado 2022

The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration

por Farhan, Sali M K, Dilliott, Allison A, Ghani, Mahdi, Sato, Christine, Liang, Eric, Zhang, Ming, McIntyre, Adam D, Cao, Henian, Racacho, Lemuel, Robinson, John F, Strong, Michael J, Masellis, Mario, St George-Hyslop, Peter, Bulman, Dennis E, Rogaeva, Ekaterina, Hegele, Robert A
Publicado 2016

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

por Dilliott, Allison A., Farhan, Sali M.K., Ghani, Mahdi, Sato, Christine, Liang, Eric, Zhang, Ming, McIntyre, Adam D., Cao, Henian, Racacho, Lemuel, Robinson, John F., Strong, Michael J., Masellis, Mario, Bulman, Dennis E., Rogaeva, Ekaterina, Lang, Anthony, Tartaglia, Carmela, Finger, Elizabeth, Zinman, Lorne, Turnbull, John, Freedman, Morris, Swartz, Rick, Black, Sandra E., Hegele, Robert A.
Publicado 2018

Soluble Epoxide Hydrolase Derived Linoleic Acid Oxylipins, Small Vessel Disease Markers, and Neurodegeneration in Stroke

por Yu, Di, Liang, Nuanyi, Zebarth, Julia, Shen, Qing, Ozzoude, Miracle, Goubran, Maged, Rabin, Jennifer S., Ramirez, Joel, Scott, Christopher J. M., Gao, Fuqiang, Bartha, Robert, Symons, Sean, Haddad, Seyyed Mohammad Hassan, Berezuk, Courtney, Tan, Brian, Kwan, Donna, Hegele, Robert A., Dilliott, Allison A., Nanayakkara, Nuwan D., Binns, Malcolm A., Beaton, Derek, Arnott, Stephen R., Lawrence‐Dewar, Jane M., Hassan, Ayman, Dowlatshahi, Dar, Mandzia, Jennifer, Sahlas, Demetrios, Casaubon, Leanne, Saposnik, Gustavo, Otoki, Yurika, Lanctôt, Krista L., Masellis, Mario, Black, Sandra E., Swartz, Richard H., Taha, Ameer Y., Swardfager, Walter
Publicado 2022

Association of Dual-Task Gait Cost and White Matter Hyperintensity Burden Poststroke: Results From the ONDRI

por Pieruccini-Faria, Frederico, Cornish, Benjamin, Binns, Malcolm, Fraser, Julia, Haddad, Seyyed M. H., Sunderland, Kelly, Ramirez, Joel, Beaton, Derek, Kwan, Donna, Dilliott, Allison A., Scott, Christopher, Sarquis-Adamson, Yanina, Black, Alanna, Van Ooteghem, Karen, Casaubon, Leanne, Dowlatshahi, Dar, Hassan, Ayman, Mandzia, Jennifer, Sahlas, Demetrios, Saposnik, Gustavo, Tan, Brian, Hegele, Robert, Bulman, Dennis, Ghani, Mahdi, Robinson, John, Rogaeva, Ekaterina, Farhan, Sali, Symons, Sean, Nanayakkara, Nuwan, Arnott, Stephen R., Berezuk, Courtney, Holmes, Melissa, Adamo, Sabrina, Ozzoude, Miracle, Zamyadi, Mojdeh, Lou, Wendy, Sujanthan, Sujeevini, Bartha, Robert, Black, Sandra E., Swartz, Richard H., McIlroy, William, Montero-Odasso, Manuel
Publicado 2023

Targeted copy number variant identification across the neurodegenerative disease spectrum

por Dilliott, Allison A., Zhang, Kristina K., Wang, Jian, Abrahao, Agessandro, Binns, Malcolm A., Black, Sandra E., Borrie, Michael, Dowlatshahi, Dar, Finger, Elizabeth, Fischer, Corinne E., Frank, Andrew, Freedman, Morris, Grimes, David, Hassan, Ayman, Jog, Mandar, Kumar, Sanjeev, Lang, Anthony E., Mandzia, Jennifer, Masellis, Mario, Pasternak, Stephen H., Pollock, Bruce G., Rajji, Tarek K., Rogaeva, Ekaterina, Sahlas, Demetrios J., Saposnik, Gustavo, Sato, Christine, Seitz, Dallas, Shoesmith, Christen, Steeves, Thomas D. L., Swartz, Richard H., Tan, Brian, Tang‐Wai, David F., Tartaglia, Maria C., Turnbull, John, Zinman, Lorne, Hegele, Robert A.
Publicado 2022

Contribution of rare variant associations to neurodegenerative disease presentation

por Dilliott, Allison A., Abdelhady, Abdalla, Sunderland, Kelly M., Farhan, Sali M. K., Abrahao, Agessandro, Binns, Malcolm A., Black, Sandra E., Borrie, Michael, Casaubon, Leanne K., Dowlatshahi, Dar, Finger, Elizabeth, Fischer, Corinne E., Frank, Andrew, Freedman, Morris, Grimes, David, Hassan, Ayman, Jog, Mandar, Kumar, Sanjeev, Kwan, Donna, Lang, Anthony E., Mandzia, Jennifer, Masellis, Mario, McIntyre, Adam D., Pasternak, Stephen H., Pollock, Bruce G., Rajji, Tarek K., Rogaeva, Ekaterina, Sahlas, Demetrios J., Saposnik, Gustavo, Sato, Christine, Seitz, Dallas, Shoesmith, Christen, Steeves, Thomas D. L., Swartz, Richard H., Tan, Brian, Tang-Wai, David F., Tartaglia, Maria C., Turnbull, John, Zinman, Lorne, Hegele, Robert A.
Publicado 2021