A Functional Interaction between the Carboxy-Terminal Domain of RNA Polymerase II and Pre-mRNA Splicing

by Du, Lei, Warren, Stephen L.
Published 1997

Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP

by Suhl, Joshua A., Warren, Stephen T.
Published 2015

Splicing Factors Associate with Hyperphosphorylated RNA Polymerase II in the Absence of Pre-mRNA

by Kim, Euikyung, Du, Lei, Bregman, David B., Warren, Stephen L.
Published 1997

Robust Regression Analysis of Copy Number Variation Data based on a Univariate Score

by Satten, Glen A., Allen, Andrew S., Ikeda, Morna, Mulle, Jennifer G., Warren, Stephen T.
Published 2014

Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus

by Alisch, Reid S, Wang, Tao, Chopra, Pankaj, Visootsak, Jeannie, Conneely, Karen N, Warren, Stephen T
Published 2013

Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome

by Xie, Nina, Gong, He, Suhl, Joshua A., Chopra, Pankaj, Wang, Tao, Warren, Stephen T.
Published 2016

Identification of consensus binding sites clarifies FMRP binding determinants

by Anderson, Bart R., Chopra, Pankaj, Suhl, Joshua A., Warren, Stephen T., Bassell, Gary J.
Published 2016

Quality-Control Culture System Restores Diabetic Endothelial Progenitor Cell Vasculogenesis and Accelerates Wound Closure

by Tanaka, Rica, Vaynrub, Max, Masuda, Haruchika, Ito, Rie, Kobori, Michiru, Miyasaka, Muneo, Mizuno, Hiroshi, Warren, Stephen M., Asahara, Takayuki
Published 2013

Combination Therapy Accelerates Diabetic Wound Closure

by Allen Jr., Robert J., Soares, Marc A., Haberman, Ilyse D., Szpalski, Caroline, Schachar, Jeffrey, Lin, Clarence D., Nguyen, Phuong D., Saadeh, Pierre B., Warren, Stephen M.
Published 2014

Array-based assay detects genome-wide 5-mC and 5-hmC in the brains of humans, non-human primates, and mice

by Chopra, Pankaj, Papale, Ligia A, White, Andrew T J, Hatch, Andrea, Brown, Ryan M, Garthwaite, Mark A, Roseboom, Patrick H, Golos, Thaddeus G, Warren, Stephen T, Alisch, Reid S
Published 2014

Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

by Girirajan, Santhosh, Brkanac, Zoran, Coe, Bradley P., Baker, Carl, Vives, Laura, Vu, Tiffany H., Shafer, Neil, Bernier, Raphael, Ferrero, Giovanni B., Silengo, Margherita, Warren, Stephen T., Moreno, Carlos S., Fichera, Marco, Romano, Corrado, Raskind, Wendy H., Eichler, Evan E.
Published 2011

Coordination of Engineered Factors with TET1/2 Promotes Early-Stage Epigenetic Modification during Somatic Cell Reprogramming

by Zhu, Gengzhen, Li, Yujing, Zhu, Fei, Wang, Tao, Jin, Wensong, Mu, Wei, Lin, Wei, Tan, Weiqi, Li, Wenqi, Street, R. Craig, Peng, Siying, Zhang, Jian, Feng, Yue, Warren, Stephen T., Sun, Qinmiao, Jin, Peng, Chen, Dahua
Published 2014

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS

by McDonald-McGinn, Donna M, Fahiminiya, Somayyeh, Revil, Timothée, Nowakowska, Beata A, Suhl, Joshua, Bailey, Alice, Mlynarski, Elisabeth, Lynch, David R, Yan, Albert C, Bilaniuk, Larissa T, Sullivan, Kathleen E, Warren, Stephen T, Emanuel, Beverly S, Vermeesch, Joris R, Zackai, Elaine H, Jerome-Majewska, Loydie A
Published 2013

Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency

by Wang, Tao, Wu, Hao, Li, Yujing, Szulwach, Keith E., Lin, Li, Li, Xuekun, Chen, I-Ping, Goldlust, Ian S., Chamberlain, Stormy J., Dodd, Ann, Gong, He, Ananiev, Gene, Han, Ji Woong, Yoon, Young-sup, Rudd, M. Katharine, Yu, Miao, Song, Chun-Xiao, He, Chuan, Chang, Qiang, Warren, Stephen T., Jin, Peng
Published 2013

A catalog of hemizygous variation in 127 22q11 deletion patients

by Hestand, Matthew S, Nowakowska, Beata A, Vergaelen, Elfi, Van Houdt, Jeroen, Dehaspe, Luc, Suhl, Joshua A, Del-Favero, Jurgen, Mortier, Geert, Zackai, Elaine, Swillen, Ann, Devriendt, Koenraad, Gur, Raquel E, McDonald-McGinn, Donna M, Warren, Stephen T, Emanuel, Beverly S, Vermeesch, Joris R
Published 2016

A Genome-Wide Scan of Ashkenazi Jewish Crohn's Disease Suggests Novel Susceptibility Loci

by Kenny, Eimear E., Pe'er, Itsik, Karban, Amir, Ozelius, Laurie, Mitchell, Adele A., Ng, Sok Meng, Erazo, Monica, Ostrer, Harry, Abraham, Clara, Abreu, Maria T., Atzmon, Gil, Barzilai, Nir, Brant, Steven R., Bressman, Susan, Burns, Edward R., Chowers, Yehuda, Clark, Lorraine N., Darvasi, Ariel, Doheny, Dana, Duerr, Richard H., Eliakim, Rami, Giladi, Nir, Gregersen, Peter K., Hakonarson, Hakon, Jones, Michelle R., Marder, Karen, McGovern, Dermot P. B., Mulle, Jennifer, Orr-Urtreger, Avi, Proctor, Deborah D., Pulver, Ann, Rotter, Jerome I., Silverberg, Mark S., Ullman, Thomas, Warren, Stephen T., Waterman, Matti, Zhang, Wei, Bergman, Aviv, Mayer, Lloyd, Katz, Seymour, Desnick, Robert J., Cho, Judy H., Peter, Inga
Published 2012