Connection

STEVEN SCHERER to Base Sequence

This is a "connection" page, showing publications STEVEN SCHERER has written about Base Sequence.
Connection Strength

0.256
  1. Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study. Genet Med. 2022 05; 24(5):1062-1072.
    View in: PubMed
    Score: 0.035
  2. Accuracy and applications of sequencing and genotyping approaches for CYP2A6 and homologous genes. Pharmacogenet Genomics. 2022 06 01; 32(4):159-172.
    View in: PubMed
    Score: 0.035
  3. A massive expansion of effector genes underlies gall-formation in the wheat pest Mayetiola destructor. Curr Biol. 2015 Mar 02; 25(5):613-20.
    View in: PubMed
    Score: 0.022
  4. Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1). Hum Mol Genet. 2013 Nov 01; 22(21):4329-38.
    View in: PubMed
    Score: 0.019
  5. Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy. Am J Hum Genet. 2010 Mar 12; 86(3):343-52.
    View in: PubMed
    Score: 0.015
  6. Identification of two novel HLA alleles, HLA-A*02010103 and HLA-B*4455, and characterization of the complete genomic sequence of HLA-A*290201. Tissue Antigens. 2008 Oct; 72(4):397-400.
    View in: PubMed
    Score: 0.014
  7. The genetic structure of mouse ornithine transcarbamylase. Nucleic Acids Res. 1988 Feb 25; 16(4):1593-601.
    View in: PubMed
    Score: 0.013
  8. Identification and characterization of three novel HLA alleles, HLA-A*240214, HLA-A*3215 and HLA-DQB1*060302. Tissue Antigens. 2007 Dec; 70(6):511-4.
    View in: PubMed
    Score: 0.013
  9. Characterization of a new HLA-B allele, HLA-B*5312, and re-evaluation of the published sequences of the untranslated regions of HLA-B*35 and HLA-B*53. Tissue Antigens. 2007 Oct; 70(4):319-23.
    View in: PubMed
    Score: 0.013
  10. Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia. Proc Natl Acad Sci U S A. 2007 Aug 21; 104(34):13732-7.
    View in: PubMed
    Score: 0.013
  11. Recurrent duplication-driven transposition of DNA during hominoid evolution. Proc Natl Acad Sci U S A. 2006 Nov 21; 103(47):17626-31.
    View in: PubMed
    Score: 0.012
  12. The DNA sequence, annotation and analysis of human chromosome 3. Nature. 2006 Apr 27; 440(7088):1194-8.
    View in: PubMed
    Score: 0.012
  13. Description and characterization of two new HLA alleles, B*4051 and DRB1*1364, identified by sequence-based typing. Tissue Antigens. 2005 Aug; 66(2):151-5.
    View in: PubMed
    Score: 0.011
  14. Reversion of a promoter deletion in yeast. Nature. 1982 Aug 26; 298(5877):815-9.
    View in: PubMed
    Score: 0.009
  15. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat Genet. 1999 Aug; 22(4):336-45.
    View in: PubMed
    Score: 0.007
  16. A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis. Nat Genet. 1998 Dec; 20(4):358-61.
    View in: PubMed
    Score: 0.007
  17. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science. 1993 Dec 24; 262(5142):2039-42.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.