Genetic Differentiation among Wild Populations of Tribolium castaneum Estimated Using Microsatellite Markers

por Drury, Douglas W., Siniard, Ashley L., Wade, Michael J.
Publicado em 2009

MECP2 impairs neuronal structure by regulating KIBRA

por Williams, Alison A., White, Robin, Siniard, Ashley, Corneveaux, Jason, Huentelman, Matt, Duch, Carsten
Publicado no Neurobiol Dis (2016)

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 no Genes (Basel) (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 no Biol Open (2021)

A Cellular Model of Amyloid Precursor Protein Processing and Amyloid-β Peptide Production

por Macias, MiMi P., Gonzales, Amanda M., Siniard, Ashley L., Walker, Aaron W., Corneveaux, Jason J., Huentelman, Matthew J., Sabbagh, Marwan N., Decourt, Boris
Publicado em 2013

Rare Variants in Cardiomyopathy Genes Associated With Stress-Induced Cardiomyopathy

por Kalani, M. Yashar S., Siniard, Ashley L., Corneveaux, Jason J., Bruhns, Ryan, Richholt, Ryan, Forseth, James, Zabramski, Joseph M., Nakaji, Peter, Spetzler, Robert F., Huentelman, Matthew J.
Publicado no Neurosurgery (2016)

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 no Front Genet (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 no PLoS One (2014)

Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer’s disease

por Giraldo, Margarita, Lopera, Francisco, Siniard, Ashley, Corneveaux, Jason J., Schrauwen, Isabelle, Carvajal, Julian, Muñoz, Claudia, Ramirez-Restrepo, Manuel, Myers, Amanda J., Caselli, Richard J., Kosik, Kenneth S., Reiman, Eric M., Huentelman, Matthew J.
Publicado em 2013

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 no PLoS One (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 no Front Aging Neurosci (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 no Front Aging Neurosci (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 no Front Cell Neurosci (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 no PLoS One (2015)

A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex

por You, Jing, Sobreira, Nara L., Gable, Dustin L., Jurgens, Julie, Grange, Dorothy K., Belnap, Newell, Siniard, Ashley, Szelinger, Szabolcs, Schrauwen, Isabelle, Richholt, Ryan F., Vallee, Stephanie E., Dinulos, Mary Beth P., Valle, David, Armanios, Mary, Hoover-Fong, Julie
Publicado no Am J Hum Genet (2016)

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 no Sci Rep (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 no PLoS One (2014)

Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2: Potential modifying effect of BRCA1/BRCA2 mutation carrier status

por Figueiredo, Jane C., Brooks, Jennifer D., Conti, David V., Poynter, Jenny N., Teraoka, Sharon N., Malone, Kathleen E., Bernstein, Leslie, Lee, Won D., Duggan, David J., Siniard, Ashley, Concannon, Patrick, Capanu, Marinela, Lynch, Charles F., Olsen, Jørgen H., Haile, Robert W., Bernstein, Jonine L.
Publicado em 2010

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 em 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 no Cold Spring Harb Mol Case Stud (2016)