Search Results - Chines, Peter S.

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  1. 1
    Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene

    Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene by DuBose, Amanda J., Lichtenstein, Stephen T., Narisu, Narisu, Bonnycastle, Lori L., Swift, Amy J., Chines, Peter S., Collins, Francis S.

    Published 2013
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  2. 2
    BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues

    BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues by Zou, Luli S., Erdos, Michael R., Taylor, D. Leland, Chines, Peter S., Varshney, Arushi, Parker, Stephen C. J., Collins, Francis S., Didion, John P.

    Published 2018
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  3. 3
    Correlated alterations in genome organization, histone methylation, and DNA–lamin A/C interactions in Hutchinson-Gilford progeria syndrome

    Correlated alterations in genome organization, histone methylation, and DNA–lamin A/C interactions in Hutchinson-Gilford progeria syndrome by McCord, Rachel Patton, Nazario-Toole, Ashley, Zhang, Haoyue, Chines, Peter S., Zhan, Ye, Erdos, Michael R., Collins, Francis S., Dekker, Job, Cao, Kan

    Published 2013
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  4. 4
    LocusZoom: regional visualization of genome-wide association scan results

    LocusZoom: regional visualization of genome-wide association scan results by 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.

    Published 2010
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  5. 5
    Linkage Disequilibrium Between Microsatellite Markers Extends Beyond 1 cM on Chromosome 20 in Finns

    Linkage Disequilibrium Between Microsatellite Markers Extends Beyond 1 cM on Chromosome 20 in Finns by Mohlke, Karen L., Lange, Ethan M., Valle, Timo T., Ghosh, Soumitra, Magnuson, Victoria L., Silander, Kaisa, Watanabe, Richard M., Chines, Peter S., Bergman, Richard N., Tuomilehto, Jaakko, Collins, Francis S., Boehnke, Michael

    Published 2001
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  6. 6
    A Systems Genetics Approach Identifies CXCL14, ITGAX, and LPCAT2 as Novel Aggressive Prostate Cancer Susceptibility Genes

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

    Published 2014
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  7. 7
    Integrative Genetic Analysis of Allergic Inflammation in the Murine Lung

    Integrative Genetic Analysis of Allergic Inflammation in the Murine Lung by Kelada, Samir N. P., Carpenter, Danielle E., Aylor, David L., Chines, Peter, Rutledge, Holly, Chesler, Elissa J., Churchill, Gary A., Pardo-Manuel de Villena, Fernando, Schwartz, David A., Collins, Francis S.

    Published 2014
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  8. 8
    A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome

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

    Published 2017
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  9. 9
    Genetic Regulation of Zfp30, CXCL1, and Neutrophilic Inflammation in Murine Lung

    Genetic Regulation of Zfp30, CXCL1, and Neutrophilic Inflammation in Murine Lung by Rutledge, Holly, Aylor, David L., Carpenter, Danielle E., Peck, Bailey C., Chines, Peter, Ostrowski, Lawrence E., Chesler, Elissa J., Churchill, Gary A., de Villena, Fernando Pardo-Manuel, Kelada, Samir N. P.

    Published 2014
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  10. 10
    Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium

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

    Published 2005
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  11. 11
    Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype

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

    Published 2017
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  12. 12
    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 traits

    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... by 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

    Published 2005
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  13. 13
    Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing

    Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing by Teer, Jamie K., Bonnycastle, Lori L., Chines, Peter S., Hansen, Nancy F., Aoyama, Natsuyo, Swift, Amy J., Abaan, Hatice Ozel, Albert, Thomas J., Margulies, Elliott H., Green, Eric D., Collins, Francis S., Mullikin, James C., Biesecker, Leslie G.

    Published 2010
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  14. 14
    Global epigenomic analysis of primary human pancreatic islets provides insights into type 2 diabetes susceptibility loci

    Global epigenomic analysis of primary human pancreatic islets provides insights into type 2 diabetes susceptibility loci by Stitzel, Michael L., Sethupathy, Praveen, Pearson, Daniel S., Chines, Peter S., Song, Lingyun, Erdos, Michael R., Welch, Ryan, Parker, Stephen C. J., Boyle, Alan P., Scott, Laura J., Margulies, Elliott H., Boehnke, Michael, Furey, Terrence S., Crawford, Gregory E., Collins, Francis S.

    Published 2010
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  15. 15
    Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation

    Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation by 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

    Published 2013
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  16. 16
    Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study

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

    Published 2017
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  17. 17
    Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle

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

    Published 2019
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  18. 18
    Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes

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

    Published 2008
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  19. 19
    The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine

    The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine by Biesecker, Leslie G., Mullikin, James C., Facio, Flavia M., Turner, Clesson, Cherukuri, Praveen F., Blakesley, Robert W., Bouffard, Gerard G., Chines, Peter S., Cruz, Pedro, Hansen, Nancy F., Teer, Jamie K., Maskeri, Baishali, Young, Alice C., Manolio, Teri A., Wilson, Alexander F., Finkel, Toren, Hwang, Paul, Arai, Andrew, Remaley, Alan T., Sachdev, Vandana, Shamburek, Robert, Cannon, Richard O., Green, Eric D.

    Published 2009
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  20. 20
    Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects

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

    Published 2012
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