HeatmapGenerator: high performance RNAseq and microarray visualization software suite to examine differential gene expression levels using an R and C++ hybrid computational pipelin...

Por Khomtchouk, Bohdan B, Van Booven, Derek J, Wahlestedt, Claes
Publicado no Source Code Biol Med (2014)

Epigenomic and metabolic responses of hypothalamic POMC neurons to gestational nicotine exposure in adult offspring

Por Silva, Jose P., Lambert, Guerline, van Booven, Derek, Wahlestedt, Claes
Publicado no Genome Med (2016)

RISC RNA sequencing for context-specific identification of in vivo miR targets

Por Matkovich, Scot J, Van Booven, Derek J, Eschenbacher, William H, Dorn, Gerald W
Publicado em 2010

articles: Association of An Intronic, but Not Any Exonic, FRMD4B Sequence Variant and Heart Failure

Por Matkovich, Scot J., Van Booven, Derek J., Cappola, Thomas P., Dorn II, Gerald W.
Publicado em 2010

High-throughput analysis reveals novel maternal germline RNAs crucial for primordial germ cell preservation and proper migration

Por Owens, Dawn A., Butler, Amanda M., Aguero, Tristan H., Newman, Karen M., Van Booven, Derek, King, Mary Lou
Publicado no Development (2017)

Cytochrome P450 2C9-CYP2C9

Por Van Booven, Derek, Marsh, Sharon, McLeod, Howard, Carrillo, Michelle Whirl, Sangkuhl, Katrin, Klein, Teri E., Altman, Russ B.
Publicado em 2010

Pharmacogenomic assessment of Mexican and Peruvian populations

Por Marsh, Sharon, King, Cristi R, Van Booven, Derek J, Revollo, Jane Y, Gilman, Robert H, McLeod, Howard L
Publicado no Pharmacogenomics (2015)

Epigenetic reprogramming of melanoma cells by vitamin C treatment

Por Gustafson, Christopher B, Yang, Cuixia, Dickson, Kevin M, Shao, Hongwei, Van Booven, Derek, Harbour, J William, Liu, Zhao-Jun, Wang, Gaofeng
Publicado no Clin Epigenetics (2015)

Identification of Copy Number Variants Through Whole-Exome Sequencing in Autosomal Recessive Nonsyndromic Hearing Loss

Por Bademci, Guney, Diaz-Horta, Oscar, Guo, Shengru, Duman, Duygu, Van Booven, Derek, Foster II, Joseph, Cengiz, Filiz Basak, Blanton, Susan, Tekin, Mustafa
Publicado em 2014

Whole Genome Sequencing and a New Bioinformatics Platform Allow for Rapid Gene Identification in D. melanogaster EMS Screens

Por Gonzalez, Michael A., Van Booven, Derek, Hulme, William, Ulloa, Rick H., Lebrigio, Rafael F. Acosta, Osterloh, Jeannette, Logan, Mary, Freeman, Marc, Zuchner, Stephan
Publicado em 2012

GEnomes Management Application (GEM.app): A new software tool for large-scale collaborative genome analysis

Por Gonzalez, Michael A., Acosta Lebrigio, Rafael F., Van Booven, Derek, Ulloa, Rick H., Powell, Eric, Speziani, Fiorella, Tekin, Mustafa, Schule, Rebecca, Zuchner, Stephan
Publicado no Hum Mutat (2013)

An Improved Workflow for miRNA Expression Profiling Using Ion Semiconductor Sequencing

Por Clarke, Jennifer, Andersen, Ashley, Navarro, Loida, Cardentey, Yoslayma, Hulme, William, Bademci, Guney, van Booven, Derek, Hedges, Dale, Pericak-Vance, Margaret, Gilbert, John, Guettouche, Toumy
Publicado em 2012

Ischemic Preconditioning Confers Epigenetic Repression of Mtor and Induction of Autophagy Through G9a‐Dependent H3K9 Dimethylation

Por Gidlöf, Olof, Johnstone, Andrea L., Bader, Kerstin, Khomtchouk, Bohdan B., O'Reilly, Jiaqi J., Celik, Selvi, Van Booven, Derek J., Wahlestedt, Claes, Metzler, Bernhard, Erlinge, David
Publicado no J Am Heart Assoc (2016)

Reciprocal regulation of myocardial miR and mRNA in human cardiomyopathy and reversal of the miR signature by biomechanical support

Por Matkovich, Scot J, Van Booven, Derek J, Youker, Keith A, Torre-Amione, Guillermo, Diwan, Abhinav, Eschenbacher, William H, Dorn, Lisa E, Watson, Mark A, Margulies, Kenneth B, Dorn, Gerald W
Publicado em 2009

Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease

Por Matkovich, Scot J., Van Booven, Derek J., Hindes, Anna, Kang, Min Young, Druley, Todd E., Vallania, Francesco L.M., Mitra, Robi D., Reilly, Muredach P., Cappola, Thomas P., Dorn, Gerald W.
Publicado em 2009

Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation

Por Cappola, Thomas P., Matkovich, Scot J., Wang, Wei, van Booven, Derek, Li, Mingyao, Wang, Xuexia, Qu, Liming, Sweitzer, Nancy K., Fang, James C., Reilly, Muredach P., Hakonarson, Hakon, Nerbonne, Jeanne M., Dorn, Gerald W.
Publicado em 2011

Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants

Por Griswold, Anthony J., Dueker, Nicole D., Van Booven, Derek, Rantus, Joseph A., Jaworski, James M., Slifer, Susan H., Schmidt, Michael A., Hulme, William, Konidari, Ioanna, Whitehead, Patrice L., Cuccaro, Michael L., Martin, Eden R., Haines, Jonathan L., Gilbert, John R., Hussman, John P., Pericak-Vance, Margaret A.
Publicado no Mol Autism (2015)

ABCA7 frameshift deletion associated with Alzheimer disease in African Americans

Por Cukier, Holly N., Kunkle, Brian W., Vardarajan, Badri N., Rolati, Sophie, Hamilton-Nelson, Kara L., Kohli, Martin A., Whitehead, Patrice L., Dombroski, Beth A., Van Booven, Derek, Lang, Rosalyn, Dykxhoorn, Derek M., Farrer, Lindsay A., Cuccaro, Michael L., Vance, Jeffery M., Gilbert, John R., Beecham, Gary W., Martin, Eden R., Carney, Regina M., Mayeux, Richard, Schellenberg, Gerard D., Byrd, Goldie S., Haines, Jonathan L., Pericak-Vance, Margaret A.
Publicado no Neurol Genet (2016)