Correlated conformational fluctuations during enzymatic catalysis: Implications for catalytic rate enhancement

Por Alper, Kutay O., Singla, Manish, Stone, Jennifer L., Bagdassarian, Carey K.
Publicado em 2001

The relationship between glaucoma medication adherence, eye drop technique, and visual field defect severity

Por Sleath, B, Blalock, Susan, Covert, David, Stone, Jennifer L., Skinner, Asheley Cockrell, Muir, Kelly, Robin, Alan L.
Publicado em 2011

Evidence for Sex-Specific Risk Alleles in Autism Spectrum Disorder

Por Stone, Jennifer L., Merriman, Barry, Cantor, Rita M., Yonan, Amanda L., Gilliam, T. Conrad, Geschwind, Daniel H., Nelson, Stanley F.
Publicado em 2004

DNA double-strand breaks relieve USF-mediated repression of Dβ2 germline transcription in developing thymocytes

Por Stone, Jennifer L., McMillan, Ruth E., Skaar, David A., Bradshaw, Justin M., Jirtle, Randy L., Sikes, Michael L.
Publicado em 2012

“High Density SNP Association Study of the 17q21 Chromosomal Region Linked to Autism Identifies CACNA1G as a Novel Candidate Gene”

Por Strom, Samuel P., Stone, Jennifer L., Bosch, John R. ten, Merriman, Barry, Cantor, Rita M., Geschwind, Daniel H., Nelson, Stanley F.
Publicado em 2009

Replication of Autism Linkage: Fine-Mapping Peak at 17q21

Por Cantor, Rita M., Kono, Naoko, Duvall, Jackie A., Alvarez-Retuerto, Ana, Stone, Jennifer L., Alarcón, Maricela, Nelson, Stanley F., Geschwind, Daniel H.
Publicado em 2005

Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

Por Alarcón, Maricela, Abrahams, Brett S., Stone, Jennifer L., Duvall, Jacqueline A., Perederiy, Julia V., Bomar, Jamee M., Sebat, Jonathan, Wigler, Michael, Martin, Christa L., Ledbetter, David H., Nelson, Stanley F., Cantor, Rita M., Geschwind, Daniel H.
Publicado em 2008

Genetic Linkage of Attention-Deficit/Hyperactivity Disorder on Chromosome 16p13, in a Region Implicated in Autism

Por Smalley, Susan L., Kustanovich, Vlad, Minassian, Sonia L., Stone, Jennifer L., Ogdie, Matthew N., McGough, James J., McCracken, James T., MacPhie, I. Laurence, Francks, Clyde, Fisher, Simon E., Cantor, Rita M., Monaco, Anthony P., Nelson, Stanley F.
Publicado em 2002

Copy number variations on chromosome 12q14 in patients with normal tension glaucoma

Por Fingert, John H., Robin, Alan L., Stone, Jennifer L., Roos, Ben R., Davis, Lea K., Scheetz, Todd E., Bennett, Steve R., Wassink, Thomas H., Kwon, Young H., Alward, Wallace L.M., Mullins, Robert F., Sheffield, Val C., Stone, Edwin M.
Publicado em 2011

Improved Imputation of Common and Uncommon Single Nucleotide Polymorphisms (SNPs) with a New Reference Set

Por Wang, Zhaoming, Jacobs, Kevin B., Yeager, Meredith, Hutchinson, Amy, Sampson, Joshua, Chatterjee, Nilanjan, Albanes, Demetrius, Berndt, Sonja I., Chung, Charles C., Diver, W. Ryan, Gapstur, Susan M., Teras, Lauren R., Haiman, Christopher A., Henderson, Brian E., Stram, Daniel, Deng, Xiang, Hsing, Ann W., Virtamo, Jarmo, Eberle, Michael A., Stone, Jennifer L., Purdue, Mark P., Taylor, Phil, Tucker, Margaret, Chanock, Stephen J.
Publicado em 2011