Association of Common Genetic Variants in the CPSF7 and SDHAF2 Genes with Canine Idiopathic Pulmonary Fibrosis in the West Highland White Terrier

por Piras, Ignazio S., Bleul, Christiane, Siniard, Ashley, Wolfe, Amanda J., De Both, Matthew D., Hernandez, Alvaro G., Huentelman, Matthew J.
Publicado 2020

Adenosine triphosphate binding cassette subfamily C member 1 (ABCC1) overexpression reduces APP processing and increases alpha- versus beta-secretase activity, in vitro

por Jepsen, Wayne M., De Both, Matthew, Siniard, Ashley L., Ramsey, Keri, Piras, Ignazio S., Naymik, Marcus, Henderson, Adrienne, Huentelman, Matthew J.
Publicado 2021

DNA Methylation and Expression Profiles of Whole Blood in Parkinson’s Disease

por Henderson, Adrienne R., Wang, Qi, Meechoovet, Bessie, Siniard, Ashley L., Naymik, Marcus, De Both, Matthew, Huentelman, Matthew J., Caselli, Richard J., Driver-Dunckley, Erika, Dunckley, Travis
Publicado 2021

Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing

por Szelinger, Szabolcs, Malenica, Ivana, Corneveaux, Jason J., Siniard, Ashley L., Kurdoglu, Ahmet A., Ramsey, Keri M., Schrauwen, Isabelle, Trent, Jeffrey M., Narayanan, Vinodh, Huentelman, Matthew J., Craig, David W.
Publicado 2014

The PKC-β selective inhibitor, Enzastaurin, impairs memory in middle-aged rats

por Willeman, Mari N., Mennenga, Sarah E., Siniard, Ashley L., Corneveaux, Jason J., De Both, Matt, Hewitt, Lauren T., Tsang, Candy W. S., Caselli, Jason, Braden, B. Blair, Bimonte-Nelson, Heather A., Huentelman, Matthew J.
Publicado 2018

Hippocampal Transcriptomic Profiles: Subfield Vulnerability to Age and Cognitive Impairment

por Ianov, Lara, De Both, Matt, Chawla, Monica K., Rani, Asha, Kennedy, Andrew J., Piras, Ignazio, Day, Jeremy J., Siniard, Ashley, Kumar, Ashok, Sweatt, J. David, Barnes, Carol A., Huentelman, Matthew J., Foster, Thomas C.
Publicado 2017

Associations of MAP2K3 Gene Variants With Superior Memory in SuperAgers

por Huentelman, Matthew J., Piras, Ignazio S., Siniard, Ashley L., De Both, Matthew D., Richholt, Ryan F., Balak, Chris D., Jamshidi, Pouya, Bigio, Eileen H., Weintraub, Sandra, Loyer, Emmaleigh T., Mesulam, M.-Marsel, Geula, Changiz, Rogalski, Emily J.
Publicado 2018

A Guide to Single-Cell Transcriptomics in Adult Rodent Brain: The Medium Spiny Neuron Transcriptome Revisited

por Ho, Hanson, Both, Matt De, Siniard, Ashley, Sharma, Sasha, Notwell, James H., Wallace, Michelle, Leone, Dino P., Nguyen, Amy, Zhao, Eric, Lee, Hannah, Zwilling, Daniel, Thompson, Kimberly R., Braithwaite, Steven P., Huentelman, Matthew, Portmann, Thomas
Publicado 2018

A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome

por Schrauwen, Isabelle, Szelinger, Szabolcs, Siniard, Ashley L., Kurdoglu, Ahmet, Corneveaux, Jason J., Malenica, Ivana, Richholt, Ryan, Van Camp, Guy, De Both, Matt, Swaminathan, Shanker, Turk, Mari, Ramsey, Keri, Craig, David W., Narayanan, Vinodh, Huentelman, Matthew J.
Publicado 2015

Total Extracellular Small RNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects

por Yeri, Ashish, Courtright, Amanda, Reiman, Rebecca, Carlson, Elizabeth, Beecroft, Taylor, Janss, Alex, Siniard, Ashley, Richholt, Ryan, Balak, Chris, Rozowsky, Joel, Kitchen, Robert, Hutchins, Elizabeth, Winarta, Joseph, McCoy, Roger, Anastasi, Matthew, Kim, Seungchan, Huentelman, Matthew, Van Keuren-Jensen, Kendall
Publicado 2017

Identification of Novel Genetic Risk Loci in Maltese Dogs with Necrotizing Meningoencephalitis and Evidence of a Shared Genetic Risk across Toy Dog Breeds

por Schrauwen, Isabelle, Barber, Renee M., Schatzberg, Scott J., Siniard, Ashley L., Corneveaux, Jason J., Porter, Brian F., Vernau, Karen M., Keesler, Rebekah I., Matiasek, Kaspar, Flegel, Thomas, Miller, Andrew D., Southard, Teresa, Mariani, Christopher L., Johnson, Gayle C., Huentelman, Matthew J.
Publicado 2014

Extracellular circular RNA profiles in plasma and urine of healthy, male college athletes

por Hutchins, Elizabeth, Reiman, Rebecca, Winarta, Joseph, Beecroft, Taylor, Richholt, Ryan, De Both, Matt, Shahbander, Khalouk, Carlson, Elizabeth, Janss, Alex, Siniard, Ashley, Balak, Chris, Bruhns, Ryan, Whitsett, Timothy G., McCoy, Roger, Anastasi, Matthew, Allen, April, Churas, Brian, Huentelman, Matthew, Van Keuren-Jensen, Kendall
Publicado 2021

Single nucleotide polymorphisms associated with risk for contralateral breast cancer in the Women's Environment, Cancer, and Radiation Epidemiology (WECARE) Study

por Teraoka, Sharon N, Bernstein, Jonine L, Reiner, Anne S, Haile, Robert W, Bernstein, Leslie, Lynch, Charles F, Malone, Kathleen E, Stovall, Marilyn, Capanu, Marinela, Liang, Xiaolin, Smith, Susan A, Mychaleckyj, Josyf, Hou, Xuanlin, Mellemkjaer, Lene, Boice, John D, Siniard, Ashley, Duggan, David, Thomas, Duncan C
Publicado 2011

A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia

por Moskowitz, Abby M., Belnap, Newell, Siniard, Ashley L., Szelinger, Szabolcs, Claasen, Ana M., Richholt, Ryan F., De Both, Matt, Corneveaux, Jason J., Balak, Chris, Piras, Ignazio S., Russell, Megan, Courtright, Amanda L., Rangasamy, Sampath, Ramsey, Keri, Craig, David W., Narayanan, Vinodh, Huentelman, Matt J., Schrauwen, Isabelle
Publicado 2016

Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disabilit...

por Banuelos, Erika, Ramsey, Keri, Belnap, Newell, Krishnan, Malavika, Balak, Chris, Szelinger, Szabolcs, Siniard, Ashley L., Russell, Megan, Richholt, Ryan, De Both, Matt, Piras, Ignazio, Naymik, Marcus, Claasen, Ana M., Rangasamy, Sampathkumar, Huentelman, Matthew J., Craig, David W., Campeau, Philippe M., Narayanan, Vinodh, Schrauwen, Isabelle
Publicado 2017

Feasibility of implementing molecular-guided therapy for the treatment of patients with relapsed or refractory neuroblastoma

por Saulnier Sholler, Giselle L, Bond, Jeffrey P, Bergendahl, Genevieve, Dutta, Akshita, Dragon, Julie, Neville, Kathleen, Ferguson, William, Roberts, William, Eslin, Don, Kraveka, Jacqueline, Kaplan, Joel, Mitchell, Deanna, Parikh, Nehal, Merchant, Melinda, Ashikaga, Takamaru, Hanna, Gina, Lescault, Pamela Jean, Siniard, Ashley, Corneveaux, Jason, Huentelman, Matthew, Trent, Jeffrey
Publicado 2015

De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy

por Fassio, Anna, Esposito, Alessandro, Kato, Mitsuhiro, Saitsu, Hirotomo, Mei, Davide, Marini, Carla, Conti, Valerio, Nakashima, Mitsuko, Okamoto, Nobuhiko, Olmez Turker, Akgun, Albuz, Burcu, Semerci Gündüz, C Nur, Yanagihara, Keiko, Belmonte, Elisa, Maragliano, Luca, Ramsey, Keri, Balak, Chris, Siniard, Ashley, Narayanan, Vinodh, Ohba, Chihiro, Shiina, Masaaki, Ogata, Kazuhiro, Matsumoto, Naomichi, Benfenati, Fabio, Guerrini, Renzo
Publicado 2018

Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms

por Hutchins, Elizabeth D., Markov, Glenn J., Eckalbar, Walter L., George, Rajani M., King, Jesse M., Tokuyama, Minami A., Geiger, Lauren A., Emmert, Nataliya, Ammar, Michael J., Allen, April N., Siniard, Ashley L., Corneveaux, Jason J., Fisher, Rebecca E., Wade, Juli, DeNardo, Dale F., Rawls, J. Alan, Huentelman, Matthew J., Wilson-Rawls, Jeanne, Kusumi, Kenro
Publicado 2014

Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1

por Szelinger, Szabolcs, Krate, Jonida, Ramsey, Keri, Strom, Samuel P., Shieh, Perry B., Lee, Hane, Belnap, Newell, Balak, Chris, Siniard, Ashley L., Russell, Megan, Richholt, Ryan, Both, Matt De, Claasen, Ana M., Schrauwen, Isabelle, Nelson, Stanley F., Huentelman, Matthew J., Craig, David W., Yang, Samuel P., Moore, Steven A., Sivakumar, Kumaraswamy, Narayanan, Vinodh, Rangasamy, Sampathkumar
Publicado 2020

Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders

por Frankel, Eric, Podder, Avijit, Sharifi, Megan, Pillai, Roshan, Belnap, Newell, Ramsey, Keri, Dodson, Julius, Venugopal, Pooja, Brzezinski, Molly, Llaci, Lorida, Gerald, Brittany, Mills, Gabrielle, Sanchez-Castillo, Meredith, Balak, Chris D., Szelinger, Szabolcs, Jepsen, Wayne M., Siniard, Ashley L., Richholt, Ryan, Naymik, Marcus, Schrauwen, Isabelle, Craig, David W., Piras, Ignazio S., Huentelman, Matthew J., Schork, Nicholas J., Narayanan, Vinodh, Rangasamy, Sampathkumar
Publicado 2023