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Ключевое слово association_studies [26 articles]

Recent papers classified by the tag association_studies.
  • Ranks of genuine associations in whole-genome scans.
    Genetics, Vol. 171, No. 2. (October 2005), pp. 813-823.
    posted to association_studies by ramensky on 2007-02-24 02:45:48 as **** along with 1 person jbsaltz
  • Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration
    Nature Genetics, Vol. 38, No. 9. (27 August 2006), pp. 1055-1059.
    by Julian Maller, Sarah George, Shaun Purcell, Jes Fagerness, David Altshuler, Mark J Daly, Johanna M Seddon
    posted to association_studies by ramensky on 2007-07-11 09:01:07 as **** along with 1 person jasonbobe
  • Transferability of tag SNPs in genetic association studies in multiple populations
    Nature Genetics, Vol. 38, No. 11. (22 October 2006), pp. 1298-1303.
    by Paul IW de Bakker, Noël P Burtt, Robert R Graham, Candace Guiducci, Roman Yelensky, Jared A Drake, Todd Bersaglieri, Kathryn L Penney, Johannah Butler, Stanton Young, Robert C Onofrio, Helen N Lyon, Daniel O Stram, Christopher A Haiman, Matthew L Freedman, Xiaofeng Zhu, Richard Cooper, Leif Groop, Laurence N Kolonel, Brian E Henderson, Mark J Daly, Joel N Hirschhorn, David Altshuler
    posted to association_studies haplotypes by ramensky on 2007-02-24 02:38:17 as ** along with 1 person jasonbobe
  • Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol
    Science, Vol. 305, No. 5685. (6 August 2004), pp. 869-872.
    by Jonathan C Cohen, Robert S Kiss, Alexander Pertsemlidis, Yves L Marcel, Ruth Mcpherson, Helen H Hobbs
  • Balancing claims for balancing selection
    Trends in Genetics, Vol. 20, No. 7. (July 2004), pp. 300-304.
    by Martin Kreitman, Anna Di Rienzo
    posted to association_studies nssnps by ramensky on 2008-01-29 00:38:03 as **
  • Genetics of hypertension.
    Genet Med, Vol. 5, No. 6. (c 2003), pp. 413-429.
    by PN Hopkins, SC Hunt
    posted to association_studies by ramensky on 2007-08-28 02:43:21 as **
  • The amino-acid mutational spectrum of human genetic disease.
    Genome Biol, Vol. 4, No. 11. (2003)
    by D Vitkup, C Sander, GM Church
  • Highly consistent patterns for inherited human diseases at the molecular level
    Bioinformatics, Vol. 22, No. 3. (1 February 2006), pp. 269-277.
    by Nuria Lopez-Bigas, Benjamin J Blencowe, Christos A Ouzounis
    posted to association_studies nssnps by ramensky on 2007-10-19 17:17:09 as ****
  • Medical sequencing at the extremes of human body mass.
    Am J Hum Genet, Vol. 80, No. 4. (April 2007), pp. 779-791.
    posted to association_studies nssnps by ramensky on 2007-05-28 20:39:10 as **** along with 2 people balicea lp2
  • Unraveling the genetics of human obesity.
    PLoS Genet, Vol. 2, No. 12. (29 December 2006)
    by DM Mutch, K Clément
    posted to association_studies by ramensky on 2007-08-28 02:38:07 as **
  • Most rare missense alleles are deleterious in humans: implications for complex disease and association studies.
    Am J Hum Genet, Vol. 80, No. 4. (April 2007), pp. 727-739.
    by GV Kryukov, LA Pennacchio, SR Sunyaev
    posted to association_studies nssnps by ramensky on 2007-05-28 20:39:53 as ****
  • Human Genetics: Variants in common diseases
    Nature (11 February 2007)
    by Nelson B Freimer, Chiara Sabatti
    posted to association_studies by ramensky on 2008-03-18 11:54:25 as ** along with 1 person jd222
  • Inflammatory bowel disease: Genetic and epidemiologic considerations.
    World J Gastroenterol, Vol. 14, No. 3. (21 January 2008), pp. 338-347.
    by JH Cho
    posted to association_studies nssnps by ramensky on 2008-02-01 18:19:23 as ** along with 1 person shikin
  • Hypertension genetics, single nucleotide polymorphisms, and the common disease:common variant hypothesis.
    Hypertension, Vol. 39, No. 2 Pt 2. (February 2002), pp. 323-331.
    by PA Doris
    posted to association_studies by ramensky on 2007-02-24 02:21:40 as *****
  • Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.
    Am J Hum Genet, Vol. 67, No. 4. (October 2000), pp. 881-900.
    posted to association_studies haplotypes nssnps by ramensky on 2008-01-28 20:14:32 as **
  • Selection of SNP subsets for association studies in candidate genes: comparison of the power of different strategies to detect single disease susceptibility locus effects.
    BMC Genet, Vol. 7 (2006)
    by E Cousin, JF Deleuze, E Genin
    posted to association_studies by ramensky on 2007-02-24 02:36:55 as ***
  • Common Single-Nucleotide Polymorphisms Act in Concert to Affect Plasma Levels of High-Density Lipoprotein Cholesterol.
    Am J Hum Genet, Vol. 81, No. 6. (19 October 2007)
    by Victor Spirin, Steffen Schmidt, Alexander Pertsemlidis, Richard S S Cooper, Jonathan C C Cohen, Shamil R R Sunyaev
    posted to association_studies by ramensky on 2008-03-03 21:37:48 as **
  • Proportionally more deleterious genetic variation in European than in African populations
    Nature, Vol. 451, No. 7181. (21 February 2008), pp. 994-997.
    by Kirk E Lohmueller, Amit R Indap, Steffen Schmidt, Adam R Boyko, Ryan D Hernandez, Melissa J Hubisz, John J Sninsky, Thomas J White, Shamil R Sunyaev, Rasmus Nielsen, Andrew G Clark, Carlos D Bustamante
  • Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.
    Am J Hum Genet, Vol. 82, No. 1. (January 2008), pp. 100-112.
    by IP Gorlov, OY Gorlova, SR Sunyaev, MR Spitz, CI Amos
    posted to association_studies nssnps by ramensky on 2008-03-08 23:48:12 as ** along with 1 person jyuh
  • Population genetics models of common diseases
    Current Opinion in Genetics & Development, Vol. 16, No. 6. (December 2006), pp. 630-636.
    by Anna Di Rienzo
    posted to association_studies nssnps by ramensky on 2008-01-29 00:46:21 as ** along with 1 person ryanraaum
  • The structure of common genetic variation in United States populations.
    Am J Hum Genet, Vol. 81, No. 6. (December 2007), pp. 1221-1231.
  • Genetic susceptibility to age-related macular degeneration: a paradigm for dissecting complex disease traits.
    Human molecular genetics, Vol. 16 Spec No. 2 (15 October 2007)
    by A Swaroop, KE Branham, W Chen, G Abecasis
    posted to association_studies by ramensky on 2008-07-24 15:55:08 as **
  • Assessing the function of genetic variants in candidate gene association studies
    Nat Rev Genet, Vol. 5, No. 8. (2004), pp. 589-597.
    by Timothy R Rebbeck, Margaret Spitz, Xifeng Wu
    posted to association_studies nssnps by ramensky on 2008-03-08 23:42:37 as ** along with 1 person raiyar
  • Multiple genes for essential-hypertension susceptibility on chromosome 1q.
    Am J Hum Genet, Vol. 80, No. 2. (February 2007), pp. 253-264.
    by YP Chang, X Liu, JD Kim, MA Ikeda, MR Layton, AB Weder, RS Cooper, SL Kardia, DC Rao, SC Hunt, A Luke, E Boerwinkle, A Chakravarti
    posted to association_studies by ramensky on 2007-08-28 02:42:30 as ** along with 1 person qmwwallace
  • The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology.
    Nat Genet, Vol. 36, No. 10. (October 2004), pp. 1045-1051.
    posted to association_studies by ramensky on 2008-03-18 11:53:55 as **
  • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    Nature, Vol. 447, No. 7145. (7 June 2007), pp. 661-678.
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