Synaptic Signaling and Aberrant RNA Splicing in Autism Spectrum Disorders

por Smith, Ryan M., Sadee, Wolfgang
Publicado 2011

A Pilot Study of Symptoms of Major Depressive Disorder in Medical Students at an Osteopathic Medical School Before and After High-Stakes Examinations

por Arabatzis, Taxiarhia J, Doroshenko, Justin, Ashraf, Muhammad A, Smith, Ryan M
Publicado 2023

Genetic influences on nicotinic α5 receptor (CHRNA5) CpG methylation and mRNA expression in brain and adipose tissue

por Ramsay, Jessica E., Rhodes, C. Harker, Thirtamara-Rajamani, Keerthi, Smith, Ryan M.
Publicado 2015

Resources That Improve Medical Board Licensing Examination Performance

por Jackson, Frank, Duane, Ethan, Harmon, Robert, Kollar, Ryan A, Rainville, Nicole M, Smith, Ryan M
Publicado 2019

Investigating SH-SY5Y Neuroblastoma Cell Surfaceome as a Model for Neuronal-Targeted Novel Therapeutic Modalities

por Gangras, Pooja, Gelfanova, Valentina, Williams, Graham D., Handelman, Samuel K., Smith, Ryan M., Debets, Marjoke F.
Publicado 2022

Analyzing allele specific RNA expression using mixture models

por Lu, Rong, Smith, Ryan M, Seweryn, Michal, Wang, Danxin, Hartmann, Katherine, Webb, Amy, Sadee, Wolfgang, Rempala, Grzegorz A
Publicado 2015

Conditional entropy in variation-adjusted windows detects selection signatures associated with expression quantitative trait loci (eQTLs)

por Handelman, Samuel K, Seweryn, Michal, Smith, Ryan M, Hartmann, Katherine, Wang, Danxin, Pietrzak, Maciej, Johnson, Andrew D, Kloczkowski, Andrzej, Sadee, Wolfgang
Publicado 2015

Whole transcriptome RNA-Seq allelic expression in human brain

por Smith, Ryan M, Webb, Amy, Papp, Audrey C, Newman, Leslie C, Handelman, Samuel K, Suhy, Adam, Mascarenhas, Roshan, Oberdick, John, Sadee, Wolfgang
Publicado 2013

Allele-Selective Transcriptome Recruitment to Polysomes Primed for Translation: Protein-Coding and Noncoding RNAs, and RNA Isoforms

por Mascarenhas, Roshan, Pietrzak, Maciej, Smith, Ryan M., Webb, Amy, Wang, Danxin, Papp, Audrey C., Pinsonneault, Julia K., Seweryn, Michal, Rempala, Grzegorz, Sadee, Wolfgang
Publicado 2015

A Genotype–Phenotype Analysis of Glutathione Peroxidase 4 in Human Atrial Myocardium and Its Association with Postoperative Atrial Fibrillation

por Berdaweel, Islam A., Hart, Alexander A., Jatis, Andrew J., Karlan, Nathan, Akhter, Shahab A., Gaine, Marie E., Smith, Ryan M., Anderson, Ethan J.
Publicado 2022

Brain Changes in Responders vs. Non-Responders in Chronic Migraine: Markers of Disease Reversal

por Hubbard, Catherine S., Becerra, Lino, Smith, Jonathan H., DeLange, Justin M., Smith, Ryan M., Black, David F., Welker, Kirk M., Burstein, Rami, Cutrer, Fred M., Borsook, David
Publicado 2016

Genomic structure and expression of the human serotonin 2A receptor gene (HTR2A) locus: identification of novel HTR2A and antisense (HTR2A-AS1) exons

por Ruble, Cara L., Smith, Ryan M., Calley, John, Munsie, Leanne, Airey, David C., Gao, Yuan, Shin, Joo Heon, Hyde, Thomas M., Straub, Richard E., Weinberger, Daniel R., Nisenbaum, Laura K.
Publicado 2016

DRD2/CHRNA5 Interaction on Prefrontal Biology and Physiology during Working Memory

por Di Giorgio, Annabella, Smith, Ryan M., Fazio, Leonardo, D'Ambrosio, Enrico, Gelao, Barbara, Tomasicchio, Aldo, Selvaggi, Pierluigi, Taurisano, Paolo, Quarto, Tiziana, Masellis, Rita, Rampino, Antonio, Caforio, Grazia, Popolizio, Teresa, Blasi, Giuseppe, Sadee, Wolfgang, Bertolino, Alessandro
Publicado 2014

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry

por Grant, Struan FA, Petri, Michelle, Bradfield, Jonathan P, Kim, Cecilia E, Santa, Erin, Annaiah, Kiran, Frackelton, Edward C, Glessner, Joseph T, Otieno, F George, Shaner, Julie L, Smith, Ryan M, Eckert, Andrew W, Chiavacci, Rosetta M, Imielinski, Marcin, Sullivan, Kathleen E, Hakonarson, Hakon
Publicado 2009

Association Analysis of the FTO Gene with Obesity in Children of Caucasian and African Ancestry Reveals a Common Tagging SNP

por Grant, Struan F. A., Li, Mingyao, Bradfield, Jonathan P., Kim, Cecilia E., Annaiah, Kiran, Santa, Erin, Glessner, Joseph T., Casalunovo, Tracy, Frackelton, Edward C., Otieno, F. George, Shaner, Julie L., Smith, Ryan M., Imielinski, Marcin, Eckert, Andrew W., Chiavacci, Rosetta M., Berkowitz, Robert I., Hakonarson, Hakon
Publicado 2008

Follow-Up Analysis of Genome-Wide Association Data Identifies Novel Loci for Type 1 Diabetes

por Grant, Struan F.A., Qu, Hui-Qi, Bradfield, Jonathan P., Marchand, Luc, Kim, Cecilia E., Glessner, Joseph T., Grabs, Rosemarie, Taback, Shayne P., Frackelton, Edward C., Eckert, Andrew W., Annaiah, Kiran, Lawson, Margaret L., Otieno, F. George, Santa, Erin, Shaner, Julie L., Smith, Ryan M., Skraban, Robert, Imielinski, Marcin, Chiavacci, Rosetta M., Grundmeier, Robert W., Stanley, Charles A., Kirsch, Susan E., Waggott, Daryl, Paterson, Andrew D., Monos, Dimitri S., Polychronakos, Constantin, Hakonarson, Hakon
Publicado 2009