These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

80 related articles for article (PubMed ID: 12446872)

  • 21. [Structural variation in the human genome contributes to variation of traits].
    Barøy T; Misceo D; Frengen E
    Tidsskr Nor Laegeforen; 2008 Sep; 128(17):1951-5. PubMed ID: 18787571
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Sequencing errors or SNPs at splice-acceptor guanines in dbSNP?
    Platzer M; Hiller M; Szafranski K; Jahn N; Hampe J; Schreiber S; Backofen R; Huse K
    Nat Biotechnol; 2006 Sep; 24(9):1068-70. PubMed ID: 16964207
    [No Abstract]   [Full Text] [Related]  

  • 23. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping.
    Maniatis N; Collins A; Morton NE
    Genet Epidemiol; 2007 Apr; 31(3):179-88. PubMed ID: 17285621
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genome search reveals gene variants associated with low bone mineral density and fractures in osteoporosis.
    Johnson J; Wang MY
    Neurosurgery; 2008 Oct; 63(4):N12. PubMed ID: 18981868
    [No Abstract]   [Full Text] [Related]  

  • 25. Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.
    Kozyrev SV; Abelson AK; Wojcik J; Zaghlool A; Linga Reddy MV; Sanchez E; Gunnarsson I; Svenungsson E; Sturfelt G; Jönsen A; Truedsson L; Pons-Estel BA; Witte T; D'Alfonso S; Barizzone N; Danieli MG; Gutierrez C; Suarez A; Junker P; Laustrup H; González-Escribano MF; Martin J; Abderrahim H; Alarcón-Riquelme ME
    Nat Genet; 2008 Feb; 40(2):211-6. PubMed ID: 18204447
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genomics. The HapMap gold rush: researchers mine a rich deposit.
    Couzin J
    Science; 2006 May; 312(5777):1131. PubMed ID: 16728611
    [No Abstract]   [Full Text] [Related]  

  • 27. On transferability of genome-wide tagSNPs.
    Gu CC; Yu K; Ketkar S; Templeton AR; Rao DC
    Genet Epidemiol; 2008 Feb; 32(2):89-97. PubMed ID: 17896344
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Evolution. Where we're hot, they're not.
    Jorde LB
    Science; 2005 Apr; 308(5718):60-2. PubMed ID: 15802591
    [No Abstract]   [Full Text] [Related]  

  • 29. Conjuring SNPs to detect associations.
    Clark AG; Li J
    Nat Genet; 2007 Jul; 39(7):815-6. PubMed ID: 17597769
    [No Abstract]   [Full Text] [Related]  

  • 30. Toxicology. Tying genetics to the risk of environmental diseases.
    Kaiser J
    Science; 2003 Apr; 300(5619):563. PubMed ID: 12714715
    [No Abstract]   [Full Text] [Related]  

  • 31. Genome-wide analysis of transcript isoform variation in humans.
    Kwan T; Benovoy D; Dias C; Gurd S; Provencher C; Beaulieu P; Hudson TJ; Sladek R; Majewski J
    Nat Genet; 2008 Feb; 40(2):225-31. PubMed ID: 18193047
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome.
    Tsunoda T; Lathrop GM; Sekine A; Yamada R; Takahashi A; Ohnishi Y; Tanaka T; Nakamura Y
    Hum Mol Genet; 2004 Aug; 13(15):1623-32. PubMed ID: 15190013
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Direct detection of null alleles in SNP genotyping data.
    Carlson CS; Smith JD; Stanaway IB; Rieder MJ; Nickerson DA
    Hum Mol Genet; 2006 Jun; 15(12):1931-7. PubMed ID: 16644863
    [TBL] [Abstract][Full Text] [Related]  

  • 34. In silico discrimination of single nucleotide polymorphisms and pathological mutations in human gene promoter regions by means of local DNA sequence context and regularity.
    Khan IA; Mort M; Buckland PR; O'Donovan MC; Cooper DN; Chuzhanova NA
    In Silico Biol; 2006; 6(1-2):23-34. PubMed ID: 16789908
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Strand bias in complementary single-nucleotide polymorphisms of transcribed human sequences: evidence for functional effects of synonymous polymorphisms.
    Qu HQ; Lawrence SG; Guo F; Majewski J; Polychronakos C
    BMC Genomics; 2006 Aug; 7():213. PubMed ID: 16916449
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genetic variation of FUT2 in Ovambos, Turks, and Mongolians.
    Soejima M; Nakajima T; Fujihara J; Takeshita H; Koda Y
    Transfusion; 2008 Jul; 48(7):1423-31. PubMed ID: 18422843
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Looking at genetics in general and racism in particular].
    Nau JY
    Rev Med Suisse; 2006 Dec; 2(90):2826. PubMed ID: 17225696
    [No Abstract]   [Full Text] [Related]  

  • 38. Diversity of human copy number variation and multicopy genes.
    Sudmant PH; Kitzman JO; Antonacci F; Alkan C; Malig M; Tsalenko A; Sampas N; Bruhn L; Shendure J; ; Eichler EE
    Science; 2010 Oct; 330(6004):641-6. PubMed ID: 21030649
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Challenges for the 21st century.
    Nat Genet; 2001 Dec; 29(4):353-4. PubMed ID: 11726913
    [No Abstract]   [Full Text] [Related]  

  • 40. Three-dimensional genome structure of a single cell.
    Tan L
    Science; 2019 Nov; 366(6468):964-965. PubMed ID: 31753992
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.