खोज परिणाम - Chines, Peter

परिणाम को परिष्कृत करें
  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 द्वारा DuBose, Amanda J., Lichtenstein, Stephen T., Narisu, Narisu, Bonnycastle, Lori L., Swift, Amy J., Chines, Peter S., Collins, Francis S.

    प्रकाशित 2013
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा Zou, Luli S., Erdos, Michael R., Taylor, D. Leland, Chines, Peter S., Varshney, Arushi, Parker, Stephen C. J., Collins, Francis S., Didion, John P.

    प्रकाशित 2018
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा McCord, Rachel Patton, Nazario-Toole, Ashley, Zhang, Haoyue, Chines, Peter S., Zhan, Ye, Erdos, Michael R., Collins, Francis S., Dekker, Job, Cao, Kan

    प्रकाशित 2013
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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  4. 4
    LocusZoom: regional visualization of genome-wide association scan results

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

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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

    प्रकाशित 2001
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 2014
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 2014
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 2014
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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

    प्रकाशित 2005
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 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... द्वारा 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

    प्रकाशित 2005
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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

    प्रकाशित 2013
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 2019
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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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 द्वारा 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.

    प्रकाशित 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 द्वारा 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.

    प्रकाशित 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 द्वारा 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

    प्रकाशित 2012
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
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