Linear Decay of Retrotransposon Antisense Bias across Genes Is Contingent upon Tissue Specificity

por Linker, Sara, Hedges, Dale
Publicado 2013

Correction: Linear Decay of Retrotransposon Antisense Bias across Genes Is Contingent upon Tissue Specificity

por Linker, Sara, Hedges, Dale J.
Publicado 2014

LINE-1 RNA splicing and influences on mammalian gene expression

por Belancio, Victoria P., Hedges, Dale J., Deininger, Prescott
Publicado 2006

Analysis of the human Alu Ye lineage

por Salem, Abdel-Halim, Ray, David A, Hedges, Dale J, Jurka, Jerzy, Batzer, Mark A
Publicado 2005

Sequencing, identification and mapping of primed L1 elements (SIMPLE) reveals significant variation in full length L1 elements between individuals

por Streva, Vincent A, Jordan, Vallmer E, Linker, Sara, Hedges, Dale J, Batzer, Mark A, Deininger, Prescott L
Publicado 2015

Modeling the Amplification Dynamics of Human Alu Retrotransposons

por Hedges, Dale J, Cordaux, Richard, Xing, Jinchuan, Witherspoon, David J, Rogers, Alan R, Jorde, Lynn B, Batzer, Mark A
Publicado 2005

The Contribution of Alu Elements to Mutagenic DNA Double-Strand Break Repair

por Morales, Maria E., White, Travis B., Streva, Vincent A., DeFreece, Cecily B., Hedges, Dale J., Deininger, Prescott L.
Publicado 2015

Rescuing Alu: Recovery of New Inserts Shows LINE-1 Preserves Alu Activity through A-Tail Expansion

por Wagstaff, Bradley J., Hedges, Dale J., Derbes, Rebecca S., Campos Sanchez, Rebeca, Chiaromonte, Francesca, Makova, Kateryna D., Roy-Engel, Astrid M.
Publicado 2012

Alu repeats increase local recombination rates

por Witherspoon, David J, Watkins, W Scott, Zhang, Yuhua, Xing, Jinchuan, Tolpinrud, Whitney L, Hedges, Dale J, Batzer, Mark A, Jorde, Lynn B
Publicado 2009

CovidExpress: an interactive portal for intuitive investigation on SARS-CoV-2 related transcriptomes

por Djekidel, Mohamed Nadhir, Rosikiewicz, Wojciech, Peng, Jamy C., Kanneganti, Thirumala-Devi, Hui, Yawei, Jin, Hongjian, Hedges, Dale, Schreiner, Patrick, Fan, Yiping, Wu, Gang, Xu, Beisi
Publicado 2021

Methylation profiling reveals novel molecular classes of rhabdomyosarcoma

por Clay, Michael R., Patel, Anand, Tran, Quynh, Hedges, Dale J., Chang, Ti-Cheng, Stewart, Elizabeth, Charville, Greg, Cline, Cynthia, Dyer, Michael A., Orr, Brent A.
Publicado 2021

Genome-wide analysis of the human Alu Yb-lineage

por Carter, Anthony B, Salem, Abdel-Halim, Hedges, Dale J, Keegan, Catherine Nguyen, Kimball, Beth, Walker, Jerilyn A, Watkins, W Scott, Jorde, Lynn B, Batzer, Mark A
Publicado 2004

Exome Sequencing of a Multigenerational Human Pedigree

por Hedges, Dale, Burges, Dan, Powell, Eric, Almonte, Cherylyn, Huang, Jia, Young, Stuart, Boese, Benjamin, Schmidt, Mike, Pericak-Vance, Margaret A., Martin, Eden, Zhang, Xinmin, Harkins, Timothy T., Züchner, Stephan
Publicado 2009

Correction: Exome Sequencing of a Multigenerational Human Pedigree

por Hedges, Dale J., Burges, Dan, Powell, Eric, Almonte, Cherylyn, Huang, Jia, Young, Stuart, Boese, Benjamin, Schmidt, Mike, Pericak-Vance, Margaret A., Martin, Eden, Zhang, Xinmin, Harkins, Timothy T., Züchner, Stephan
Publicado 2009

A comprehensive approach to expression of L1 loci

por Deininger, Prescott, Morales, Maria E., White, Travis B., Baddoo, Melody, Hedges, Dale J., Servant, Geraldine, Srivastav, Sudesh, Smither, Madison E., Concha, Monica, DeHaro, Dawn L., Flemington, Erik K., Belancio, Victoria P.
Publicado 2017

Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform

por Hedges, Dale J., Guettouche, Toumy, Yang, Shan, Bademci, Guney, Diaz, Ashley, Andersen, Ashley, Hulme, William F., Linker, Sara, Mehta, Arpit, Edwards, Yvonne J. K., Beecham, Gary W., Martin, Eden R., Pericak-Vance, Margaret A., Zuchner, Stephan, Vance, Jeffery M., Gilbert, John R.
Publicado 2011

An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males

por Chung, Ren-Hua, Ma, Deqiong, Wang, Kai, Hedges, Dale J, Jaworski, James M, Gilbert, John R, Cuccaro, Michael L, Wright, Harry H, Abramson, Ruth K, Konidari, Ioanna, Whitehead, Patrice L, Schellenberg, Gerard D, Hakonarson, Hakon, Haines, Jonathan L, Pericak-Vance, Margaret A, Martin, Eden R
Publicado 2011

Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia

por Ryan, Sarra L., Peden, John F., Kingsbury, Zoya, Schwab, Claire J., James, Terena, Polonen, Petri, Mijuskovic, Martina, Becq, Jenn, Yim, Richard, Cranston, Ruth E., Hedges, Dale J., Roberts, Kathryn G., Mullighan, Charles G., Vora, Ajay, Russell, Lisa J., Bain, Robert, Moorman, Anthony V., Bentley, David R., Harrison, Christine J., Ross, Mark T.
Publicado 2023

Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci

por Hedges, Dale J, Hamilton-Nelson, Kara L, Sacharow, Stephanie J, Nations, Laura, Beecham, Gary W, Kozhekbaeva, Zhanna M, Butler, Brittany L, Cukier, Holly N, Whitehead, Patrice L, Ma, Deqiong, Jaworski, James M, Nathanson, Lubov, Lee, Joycelyn M, Hauser, Stephen L, Oksenberg, Jorge R, Cuccaro, Michael L, Haines, Jonathan L, Gilbert, John R, Pericak-Vance, Margaret A
Publicado 2012

Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants

por Edmonson, Michael N., Patel, Aman N., Hedges, Dale J., Wang, Zhaoming, Rampersaud, Evadnie, Kesserwan, Chimene A., Zhou, Xin, Liu, Yanling, Newman, Scott, Rusch, Michael C., McLeod, Clay L., Wilkinson, Mark R., Rice, Stephen V., Soussi, Thierry, Taylor, J. Paul, Benatar, Michael, Becksfort, Jared B., Nichols, Kim E., Robison, Leslie L., Downing, James R., Zhang, Jinghui
Publicado 2019