注册 | 登录 | FAQ      [?] 
Recent | Unread | Search | Authors | Tags | Export

waszak's cnv [27 articles]

当前文献位于 waszak's 文献库 标签分类为 cnv. You can also see everyone's cnv.
  • Copy-number variations associated with neuropsychiatric conditions
    Nature, Vol. 455, No. 7215. (16 October 2008), pp. 919-923.
    by Cook, Stephen W Scherer
    posted to schizophrenia review neuropsychiatric microarray cnv autism by waszak on 2008-10-17 14:05:37 as ** along with 2 people psique jdbowes
  • Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability
    Nat Rev Genet, Vol. 8, No. 8. (2007), pp. 639-646.
    by Jacques S Beckmann, Xavier Estivill, Stylianos E Antonarakis
    posted to review genetics cnv by waszak on 2008-10-08 15:13:51 as ** along with 3 people and 1 group frohike rdiaz ryanraaum Bioinformatics
  • Copy-number variation and association studies of human disease.
    Nat Genet, Vol. 39, No. 7 Suppl. (July 2007)
    by SA McCarroll, DM Altshuler
    posted to review human disease cnv cnp by waszak on 2008-10-08 15:12:44 as ** along with 7 people and 1 group jo_davies vplagnol jyuh mrkrause balicea rdiaz jasonflannick Bioinformatics
  • Integrated detection and population-genetic analysis of SNPs and copy number variation.
    Nature genetics (7 September 2008)
    by Steven A A McCarroll, Finny G G Kuruvilla, Joshua M M Korn, Simon Cawley, James Nemesh, Alec Wysoker, Michael H H Shapero, Paul I W I de Bakker, Julian B B Maller, Andrew Kirby, Amanda L L Elliott, Melissa Parkin, Earl Hubbell, Teresa Webster, Rui Mei, James Veitch, Patrick J J Collins, Robert Handsaker, Steve Lincoln, Marcia Nizzari, John Blume, Keith W W Jones, Rich Rava, Mark J J Daly, Stacey B B Gabriel, David Altshuler
    posted to snp hapmap genetics cnv affymetrix by waszak on 2008-10-08 15:11:10 as ** along with 13 people and 1 group pdexheimer madreach caseybrown rsantana Zephyrus psique jbsaltz Ema misonneh djkt daed rdiaz jyuh Roswell Cancer Crosstalk
  • A robust statistical method for case-control association testing with copy number variation.
    Nature genetics (7 September 2008)
    by Chris Barnes, Vincent Plagnol, Tomas Fitzgerald, Richard Redon, Jonathan Marchini, David Clayton, Matthew E E Hurles
    posted to software snp r ld gmm em cnv associationstudy algorithm affymetrix by waszak on 2008-10-08 15:01:08 as ** along with 12 people and 1 group pengchy ptrobajo vplagnol caseybrown Zephyrus dakelley buyske misonneh djkt rdiaz Stew jyuh Roswell Cancer Crosstalk
  • Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome
    Proceedings of the National Academy of Sciences, Vol. 104, No. 24. (12 June 2007), pp. 10110-10115.
    by Jan O Korbel, Alexander E Urban, Fabian Grubert, Jiang Du, Thomas E Royce, Peter Starr, Guoneng Zhong, Beverly S Emanuel, Sherman M Weissman, Michael Snyder, Mark B Gerstein
    posted to human hmm genome cnv breakpoints by waszak on 2008-10-08 14:58:45 as ** along with 2 people caldavis oelemento
  • QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.
    Nucleic Acids Res (27 March 2007)
    by Stefano Colella, Christopher Yau, Jennifer M M Taylor, Ghazala Mirza, Helen Butler, Penny Clouston, Anne S S Bassett, Anneke Seller, Christopher C C Holmes, Jiannis Ragoussis
    posted to snp microarray hmm genotyping cnv bayes algorithm by waszak on 2008-10-08 14:42:05 as ** along with 4 people and 2 groups druvus psique caldavis jfr parkinson's disease references Bioinformatics
  • Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
    Genome Res., Vol. 16, No. 12. (1 December 2006), pp. 1575-1584.
    by Daisuke Komura, Fan Shen, Shumpei Ishikawa, Karen R Fitch, Wenwei Chen, Jane Zhang, Guoying Liu, Sigeo Ihara, Hiroshi Nakamura, Matthew E Hurles, Charles Lee, Stephen W Scherer, Keith W Jones, Michael H Shapero, Jing Huang, Hiroyuki Aburatani
    posted to snp microarray human genome cnv algorithm affymetrix by waszak on 2008-10-08 14:40:40 as ** along with 8 people and 4 groups jfr dchughes giovanni jeremymiller frohike vpschulz shigepong debasis Bioinformatics G4ID GeschwindLab Genetics-of-Gambling
  • Mutational and selective effects on copy-number variants in the human genome.
    Nat Genet, Vol. 39, No. 7 Suppl. (July 2007)
    by GM Cooper, DA Nickerson, EE Eichler
    posted to ld human genome cnv by waszak on 2008-10-08 14:39:07 as ** along with 3 people and 1 group daed mrkrause rdiaz Bioinformatics
  • Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
    Am J Hum Genet, Vol. 79, No. 2. (August 2006), pp. 275-290.
    by DP Locke, AJ Sharp, SA McCarroll, SD McGrath, TL Newman, Z Cheng, S Schwartz, DG Albertson, D Pinkel, DM Altshuler, EE Eichler
    posted to snp ld human hapmap genome cnv cnp by waszak on 2008-10-08 14:36:13 as ** along with 1 person lp2
  • Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
    PLoS Genetics, Vol. 3, No. 10. (1 October 2007), e190.
    by Xavier Estivill, Lluís Armengol
    posted to snp gwas genome cnv by waszak on 2008-10-08 14:32:56 as ** along with 2 people jfr giovanni
  • Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
    Science (27 March 2008), 1155174.
    by Tom Walsh, Jon M Mcclellan, Shane E Mccarthy, Anjene M Addington, Sarah B Pierce, Greg M Cooper, Alex S Nord, Mary Kusenda, Dheeraj Malhotra, Abishek Bhandari, Sunday M Stray, Caitlin F Rippey, Patricia Roccanova, Vlad Makarov, B Lakshmi, Robert L Findling, Linmarie Sikich, Thomas Stromberg, Barry Merriman, Nitin Gogtay, Philip Butler, Kristen Eckstrand, Laila Noory, Peter Gochman, Robert Long, Zugen Chen, Sean Davis, Carl Baker, Evan E Eichler, Paul S Meltzer, Stanley F Nelson, Andrew B Singleton, Ming K Lee, Judith L Rapoport, Mary-Claire King, Jonathan Sebat
    posted to sv schizophrenia neurodevelopment cnv by waszak on 2008-10-08 14:29:39 as ** along with 8 people and 1 group sekulerlab GustavoLacerda MWagner applebyb giovanni djkt lisa1 renatomilani VisionLab
  • Diet and the evolution of human amylase gene copy number variation.
    Nat Genet (9 September 2007)
    by George H H Perry, Nathaniel J J Dominy, Katrina G G Claw, Arthur S S Lee, Heike Fiegler, Richard Redon, John Werner, Fernando A A Villanea, Joanna L L Mountain, Rajeev Misra, Nigel P P Carter, Charles Lee, Anne C C Stone
    posted to human disease cnv by waszak on 2008-10-08 14:27:55 as ** along with 5 people bpb balicea dchughes saru ajw
  • Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
    Nature Genetics, Vol. 38, No. 9. (13 August 2006), pp. 1038-1042.
    by Andrew J Sharp, Sierra Hansen, Rebecca R Selzer, Ze Cheng, Regina Regan, Jane A Hurst, Helen Stewart, Sue M Price, Edward Blair, Raoul C Hennekam, Carrie A Fitzpatrick, Rick Segraves, Todd A Richmond, Cheryl Guiver, Donna G Albertson, Daniel Pinkel, Peggy S Eis, Stuart Schwartz, Samantha JL Knight, Evan E Eichler
    posted to human cnv cnp by waszak on 2008-10-08 14:26:09 as **
  • The Influence of CCL3L1 Gene-Containing Segmental Duplications on HIV-1/AIDS Susceptibility
    Science, Vol. 307, No. 5714. (04 March 2005), pp. 1434-1440.
    by Enrique Gonzalez, Hemant Kulkarni, Hector Bolivar, Andrea Mangano, Racquel Sanchez, Gabriel Catano, Robert J Nibbs, Barry I Freedman, Marlon P Quinones, Michael J Bamshad, Krishna K Murthy, Brad H Rovin, William Bradley, Robert A Clark, Stephanie A Anderson, Robert J O'Connell, Brian K Agan, Seema S Ahuja, Rosa Bologna, Luisa Sen, Matthew J Dolan, Sunil K Ahuja
    posted to hiv cnv aids by waszak on 2008-10-08 14:23:46 as ** along with 3 people mercaptan tkershaw vplagnol
  • alpha-Synuclein Locus Triplication Causes Parkinson's Disease
    Science, Vol. 302, No. 5646. (October 2003), 841.
    by AB Singleton
    posted to parkinson cnv by waszak on 2008-10-08 14:22:21 as **
  • Systematic assessment of copy number variant detection via genome-wide SNP genotyping.
    Nature genetics (7 September 2008)
    by Gregory M M Cooper, Troy Zerr, Jeffrey M M Kidd, Evan E E Eichler, Deborah A A Nickerson
    posted to snp human genotyping cnv by waszak on 2008-10-08 13:54:15 as ** along with 8 people and 1 group pengchy vplagnol caseybrown Zephyrus psique misonneh rdiaz jyuh Roswell Cancer Crosstalk
  • Global variation in copy number in the human genome
    Nature, Vol. 444, No. 7118. (23 November 2006), pp. 444-454.
    by Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, Daniel T Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen, Eun K Cho, Stephanie Dallaire, Jennifer L Freeman, Juan R Gonzalez, Monica Gratacos, Jing Huang, Dimitrios Kalaitzopoulos, Daisuke Komura, Jeffrey R Macdonald, Christian R Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, Kohji Okamura, Fan Shen, Martin J Somerville, Joelle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluis Armengol, Donald F Conrad, Xavier Estivill, Chris Tyler-Smith, Nigel P Carter, Hiroyuki Aburatani, Charles Lee, Keith W Jones, Stephen W Scherer, Matthew E Hurles
    posted to human cnv by waszak on 2008-10-08 13:53:04 as ** along with 28 people and 7 groups jo_davies psique bpb jfr balajis pradiptaray dpollard mtagaya adepace aswin rdiaz qfwills ealloza vplagnol giovanni jeremymiller frohike vpschulz raiyar ramensky ccr azazello dbgrant colinveal xingxu srp33 Ema daed parkinson's disease references Bioinformatics EisenLab BioinfoCIPF GeschwindLab steinmetzlab MBLAB
  • Fine-scale structural variation of the human genome
    Nature Genetics, Vol. 37, No. 7. (15 May 2005), pp. 727-732.
    by Eray Tuzun, Andrew J Sharp, Jeffrey A Bailey, Rajinder Kaul, Anne V Morrison, Lisa M Pertz, Eric Haugen, Hillary Hayden, Donna Albertson, Daniel Pinkel, Maynard V Olson, Evan E Eichler
    posted to human cnv by waszak on 2008-10-08 13:51:54 as ** along with 4 people matthewsuderman bpb pcahan1 Neeperando
  • Large-Scale Copy Number Polymorphism in the Human Genome
    Science, Vol. 305, No. 5683. (23 July 2004), pp. 525-528.
    by Jonathan Sebat, B Lakshmi, Jennifer Troge, Joan Alexander, Janet Young, Par Lundin, Susanne Maner, Hillary Massa, Megan Walker, Maoyen Chi, Nicholas Navin, Robert Lucito, John Healy, James Hicks, Kenny Ye, Andrew Reiner, Conrad C Gilliam, Barbara Trask, Nick Patterson, Anders Zetterberg, Michael Wigler
    posted to human genetics cnv cnp by waszak on 2008-10-08 13:50:55 as ** along with 9 people and 2 groups krokicki mercaptan pcahan1 mrkrause rdiaz jeremymiller massivemayhem jpdemuth Ema Bioinformatics GeschwindLab
  • Reduction of endogenous angiogenesis inhibitors in Bruch's membrane of the submacular region in eyes with age-related macular degeneration.
    Archives of ophthalmology, Vol. 126, No. 5. (May 2008), pp. 670-678.
    by IA Bhutto, K Uno, C Merges, L Zhang, DS McLeod, GA Lutty
    posted to microarray cnv by waszak on 2008-10-08 13:30:49 as *****
  • Expression of endostatin in human choroidal neovascular membranes secondary to age-related macular degeneration.
    Experimental eye research, Vol. 83, No. 2. (August 2006), pp. 329-338.
    by O Tatar, K Shinoda, A Adam, JM Rohrbach, K Lucke, S Henke-Fahle, KU Bartz-Schmidt, S Grisanti
    posted to cnv by waszak on 2008-10-08 13:23:51 as **
  • Implications of bevacizumab on VEGF and endostatin in human choroidal neovascularization.
    The British journal of ophthalmology (6 October 2008)
    by Olcay Tatar, Kei Shinoda, Edwin Kaiserling, Carl Claes, Claus Eckardt, Tillmann Eckert, Vicky Boeyden, Grazia Pertile, Efdal Yoeruek, Peter Szurman, Karl U U Bartz-Schmidt, Salvatore Grisanti
    posted to microarray cnv by waszak on 2008-10-08 13:21:49 as **
  • Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes
    Science, Vol. 315, No. 5813. (9 February 2007), pp. 848-853.
    by Barbara E Stranger, Matthew S Forrest, Mark Dunning, Catherine E Ingle, Claude Beazley, Natalie Thorne, Richard Redon, Christine P Bird, Anna de Grassi, Charles Lee, Chris Tyler-Smith, Nigel Carter, Stephen W Scherer, Simon Tavare, Panagiotis Deloukas, Matthew E Hurles, Emmanouil T Dermitzakis
    posted to tiling microarray embl cnv by waszak on 2008-10-07 21:05:05 as ** along with 19 people and 3 groups daed psique jo_davies srp33 jyuh jfr dpollard balicea rdiaz qfwills djkt vplagnol shigepong jlangdon xingxu cisevol caseybrown frohike jandot Bioinformatics EisenLab cis-regulatory-evolution
  • Hidden copy number variation in the HapMap population.
    Proceedings of the National Academy of Sciences of the United States of America, Vol. 105, No. 29. (22 July 2008), pp. 10067-10072.
    by JC Marioni, M White, S Tavaré, AG Lynch
    posted to cnv hapmap by waszak on 2008-07-24 10:09:47 as ** along with 4 people and 1 group Zephyrus jfr jyuh Stew Roswell Cancer Crosstalk
  • Copy Number Variation Detection via High-Density SNP Genotyping
    Cold Spring Harbor Protocols, Vol. 2008, No. 7. (1 June 2008), pdb.top46.
    by Kai Wang, Maja Bucan
    posted to cnv genotyping snp by waszak on 2008-07-19 22:21:28 as **
  • Hidden copy number variation in the HapMap population
    Proccedings of the national science
    by John
    posted to cnv hapmap by waszak on 2008-07-16 20:51:20 as **
    • ◇温馨提示◇本页的引用地址为： http://www.citeulike.org/user/waszak/tag/cnv

    RIS BibTeX
    CiteULike organises scholarly (or academic) papers or literature and provides bibliographic (which means it makes bibliographies) for universities and higher education establishments. It helps undergraduates and postgraduates. People studying for PhDs or in postdoctoral (postdoc) positions. The service is similar in scope to EndNote or RefWorks or any other reference manager like BibTeX, but it is a social bookmarking service for scientists and humanities researchers.