Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene

por DuBose, Amanda J., Lichtenstein, Stephen T., Narisu, Narisu, Bonnycastle, Lori L., Swift, Amy J., Chines, Peter S., Collins, Francis S.
Publicado 2013

Addressing Bias in Small RNA Library Preparation for Sequencing: A New Protocol Recovers MicroRNAs that Evade Capture by Current Methods

por Baran-Gale, Jeanette, Kurtz, C. Lisa, Erdos, Michael R., Sison, Christina, Young, Alice, Fannin, Emily E., Chines, Peter S., Sethupathy, Praveen
Publicado 2015

BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues

por Zou, Luli S., Erdos, Michael R., Taylor, D. Leland, Chines, Peter S., Varshney, Arushi, Parker, Stephen C. J., Collins, Francis S., Didion, John P.
Publicado 2018

Correlated alterations in genome organization, histone methylation, and DNA–lamin A/C interactions in Hutchinson-Gilford progeria syndrome

por McCord, Rachel Patton, Nazario-Toole, Ashley, Zhang, Haoyue, Chines, Peter S., Zhan, Ye, Erdos, Michael R., Collins, Francis S., Dekker, Job, Cao, Kan
Publicado 2013

Putative Prostate Cancer Risk SNP in an Androgen Receptor‐Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites

por Bu, Huajie, Narisu, Narisu, Schlick, Bettina, Rainer, Johannes, Manke, Thomas, Schäfer, Georg, Pasqualini, Lorenza, Chines, Peter, Schweiger, Michal R., Fuchsberger, Christian, Klocker, Helmut
Publicado 2015

LocusZoom: regional visualization of genome-wide association scan results

por Pruim, Randall J., Welch, Ryan P., Sanna, Serena, Teslovich, Tanya M., Chines, Peter S., Gliedt, Terry P., Boehnke, Michael, Abecasis, Gonçalo R., Willer, Cristen J.
Publicado 2010

A Systems Genetics Approach Identifies CXCL14, ITGAX, and LPCAT2 as Novel Aggressive Prostate Cancer Susceptibility Genes

por Williams, Kendra A., Lee, Minnkyong, Hu, Ying, Andreas, Jonathan, Patel, Shashank J., Zhang, Suiyuan, Chines, Peter, Elkahloun, Abdel, Chandrasekharappa, Settara, Gutkind, J. Silvio, Molinolo, Alfredo A., Crawford, Nigel P. S.
Publicado 2014

A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome

por Bar, Daniel Z, Arlt, Martin F, Brazier, Joan F, Norris, Wendy E, Campbell, Susan E, Chines, Peter, Larrieu, Delphine, Jackson, Stephen P, Collins, Francis S, Glover, Thomas W, Gordon, Leslie B
Publicado 2017

Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium

por Duggal, Priya, Gillanders, Elizabeth M, Mathias, Rasika A, Ibay, Grace P, Klein, Alison P, Baffoe-Bonnie, Agnes B, Ou, Liang, Dusenberry, Ian P, Tsai, Ya-Yu, Chines, Peter S, Doan, Betty Q, Bailey-Wilson, Joan E
Publicado 2005

Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype

por Asur, Rajalakshmi S., Kimble, Danielle C., Lach, Francis P., Jung, Moonjung, Donovan, Frank X., Kamat, Aparna, Noonan, Raymond J., Thomas, James W., Park, Morgan, Chines, Peter, Vlachos, Adrianna, Auerbach, Arleen D., Smogorzewska, Agata, Chandrasekharappa, Settara C.
Publicado 2017

Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative...

por Klein, Alison P, Tsai, Ya-Yu, Duggal, Priya, Gillanders, Elizabeth M, Barnhart, Michael, Mathias, Rasika A, Dusenberry, Ian P, Turiff, Amy, Chines, Peter S, Goldstein, Janet, Wojciechowski, Robert, Hening, Wayne, Pugh, Elizabeth W, Bailey-Wilson, Joan E
Publicado 2005

Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation

por Bonnycastle, Lori L., Chines, Peter S., Hara, Takashi, Huyghe, Jeroen R., Swift, Amy J., Heikinheimo, Pirkko, Mahadevan, Jana, Peltonen, Sirkku, Huopio, Hanna, Nuutila, Pirjo, Narisu, Narisu, Goldfeder, Rachel L., Stitzel, Michael L., Lu, Simin, Boehnke, Michael, Urano, Fumihiko, Collins, Francis S., Laakso, Markku
Publicado 2013

Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study

por Davis, James P., Huyghe, Jeroen R., Locke, Adam E., Jackson, Anne U., Sim, Xueling, Stringham, Heather M., Teslovich, Tanya M., Welch, Ryan P., Fuchsberger, Christian, Narisu, Narisu, Chines, Peter S., Kangas, Antti J., Soininen, Pasi, Ala-Korpela, Mika, Kuusisto, Johanna, Collins, Francis S., Laakso, Markku, Boehnke, Michael, Mohlke, Karen L.
Publicado 2017

Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle

por Taylor, D. Leland, Jackson, Anne U., Narisu, Narisu, Hemani, Gibran, Erdos, Michael R., Chines, Peter S., Swift, Amy, Idol, Jackie, Didion, John P., Welch, Ryan P., Kinnunen, Leena, Saramies, Jouko, Lakka, Timo A., Laakso, Markku, Tuomilehto, Jaakko, Parker, Stephen C. J., Koistinen, Heikki A., Davey Smith, George, Boehnke, Michael, Scott, Laura J., Birney, Ewan, Collins, Francis S.
Publicado 2019

Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes

por Gaulton, Kyle J., Willer, Cristen J., Li, Yun, Scott, Laura J., Conneely, Karen N., Jackson, Anne U., Duren, William L., Chines, Peter S., Narisu, Narisu, Bonnycastle, Lori L., Luo, Jingchun, Tong, Maurine, Sprau, Andrew G., Pugh, Elizabeth W., Doheny, Kimberly F., Valle, Timo T., Abecasis, Gonçalo R., Tuomilehto, Jaakko, Bergman, Richard N., Collins, Francis S., Boehnke, Michael, Mohlke, Karen L.
Publicado 2008

Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects

por Pangilinan, Faith, Molloy, Anne M, Mills, James L, Troendle, James F, Parle-McDermott, Anne, Signore, Caroline, O’Leary, Valerie B, Chines, Peter, Seay, Jessica M, Geiler-Samerotte, Kerry, Mitchell, Adam, VanderMeer, Julia E, Krebs, Kristine M, Sanchez, Angelica, Cornman-Homonoff, Joshua, Stone, Nicole, Conley, Mary, Kirke, Peadar N, Shane, Barry, Scott, John M, Brody, Lawrence C
Publicado 2012

Multiomic Profiling Identifies cis-Regulatory Networks Underlying Human Pancreatic β Cell Identity and Function

por Lawlor, Nathan, Márquez, Eladio J., Orchard, Peter, Narisu, Narisu, Shamim, Muhammad Saad, Thibodeau, Asa, Varshney, Arushi, Kursawe, Romy, Erdos, Michael R., Kanke, Matt, Gu, Huiya, Pak, Evgenia, Dutra, Amalia, Russell, Sheikh, Li, Xingwang, Piecuch, Emaly, Luo, Oscar, Chines, Peter S., Fuchbserger, Christian, Sethupathy, Praveen, Aiden, Aviva Presser, Ruan, Yijun, Aiden, Erez Lieberman, Collins, Francis S., Ucar, Duygu, Parker, Stephen C.J., Stitzel, Michael L.
Publicado 2019

Interactions between genetic variation and cellular environment in skeletal muscle gene expression

por Taylor, D. Leland, Knowles, David A., Scott, Laura J., Ramirez, Andrea H., Casale, Francesco Paolo, Wolford, Brooke N., Guan, Li, Varshney, Arushi, Albanus, Ricardo D’Oliveira, Parker, Stephen C. J., Narisu, Narisu, Chines, Peter S., Erdos, Michael R., Welch, Ryan P., Kinnunen, Leena, Saramies, Jouko, Sundvall, Jouko, Lakka, Timo A., Laakso, Markku, Tuomilehto, Jaakko, Koistinen, Heikki A., Stegle, Oliver, Boehnke, Michael, Birney, Ewan, Collins, Francis S.
Publicado 2018

The genetic regulatory signature of type 2 diabetes in human skeletal muscle

por Scott, Laura J., Erdos, Michael R., Huyghe, Jeroen R., Welch, Ryan P., Beck, Andrew T., Wolford, Brooke N., Chines, Peter S., Didion, John P., Narisu, Narisu, Stringham, Heather M., Taylor, D. Leland, Jackson, Anne U., Vadlamudi, Swarooparani, Bonnycastle, Lori L., Kinnunen, Leena, Saramies, Jouko, Sundvall, Jouko, Albanus, Ricardo D'Oliveira, Kiseleva, Anna, Hensley, John, Crawford, Gregory E., Jiang, Hui, Wen, Xiaoquan, Watanabe, Richard M., Lakka, Timo A., Mohlke, Karen L., Laakso, Markku, Tuomilehto, Jaakko, Koistinen, Heikki A., Boehnke, Michael, Collins, Francis S., Parker, Stephen C. J.
Publicado 2016

A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome

por Di Gioia, Silvio Alessandro, Connors, Samantha, Matsunami, Norisada, Cannavino, Jessica, Rose, Matthew F., Gilette, Nicole M., Artoni, Pietro, de Macena Sobreira, Nara Lygia, Chan, Wai-Man, Webb, Bryn D., Robson, Caroline D., Cheng, Long, Van Ryzin, Carol, Ramirez-Martinez, Andres, Mohassel, Payam, Leppert, Mark, Scholand, Mary Beth, Grunseich, Christopher, Ferreira, Carlos R., Hartman, Tyler, Hayes, Ian M., Morgan, Tim, Markie, David M., Fagiolini, Michela, Swift, Amy, Chines, Peter S., Speck-Martins, Carlos E., Collins, Francis S., Jabs, Ethylin Wang, Bönnemann, Carsten G., Olson, Eric N., Carey, John C., Robertson, Stephen P., Manoli, Irini, Engle, Elizabeth C.
Publicado 2017