Searching journal content for articles similar to Cheng et al. 9 (10): 936.

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  1. Method: The oligogenic inheritance test GCOD detects risk genes and their interactions in congenital heart defects
    • Maureen Pittman,
    • Kihyun Lee,
    • Franco Felix,
    • Yu Huang,
    • Adrienne Lam,
    • Mauro W. Costa,
    • Deepak Srivastava,
    • and Katherine S. Pollard
    Genome Res. February 2026 36: 330-347; Published in Advance December 12, 2025, doi:10.1101/gr.281141.125
    ...damaging variants in splice sites or regulatory regions, as well as cryptic risk genes that lack statistical evidence of association. The latter can occur owing to incomplete penetrance and variable expressivity of gene lesions, in which carriers differ in the presence and severity of disease symptoms...
    OPEN ACCESS ARTICLE
  2. Review: Contrasting genetic architectures in different mouse reference populations used for studying complex traits
    • David A. Buchner and
    • Joseph H. Nadeau
    Genome Res. June 2015 25: 775-791; Published in Advance May 7, 2015, doi:10.1101/gr.187450.114
    ...functions, and systems properties that underlie phenotypic variation and disease risk in humans, model organisms, agricultural species, and natural populations. The challenges are many, beginning with the seemingly simple tasks of mapping QTLs and identifying their underlying genetic determinants. Various...
  3. LETTER: Sequence Diversity and Large-Scale Typing of SNPs in the Human Apolipoprotein E Gene
    • Deborah A. Nickerson,
    • Scott L. Taylor,
    • Stephanie M. Fullerton,
    • Kenneth M. Weiss,
    • Andrew G. Clark,
    • Jari H. Stengård,
    • Veikko Salomaa,
    • Eric Boerwinkle,
    • and Charles F. Sing
    Genome Res. October 1, 2000 10: 1532-1545; doi:10.1101/gr.146900
    ...from three populations (two of European-descent and one of African descent) currently engaged in epidemiological studies of environmental and genetic factors that influence the risk of cardiovascular disease. This represents a core data set characterizing the relative allele and genotype frequency...
  4. LETTER: New Target Regions for Human Hypertension via Comparative Genomics
    • Monika Stoll,
    • Anne E. Kwitek-Black,
    • Allen W. Cowley, Jr.,
    • Eugenie L. Harris,
    • Stephen B. Harrap,
    • José E. Krieger,
    • Morton P. Printz,
    • Abraham P. Provoost,
    • Jean Sassard,
    • and Howard J. Jacob
    Genome Res. April 1, 2000 10: 473-482; doi:10.1101/gr.10.4.473
    ...– 156 . ↵ Staessen J.A. , Wang J.G. , Ginocchio G. , Petrov V. , Saavedra A.P. , Soubrier F. , Vlietinck R. , Fagard R. ( 1997 ) The deletion/insertion polymorphism of the angiotensin converting enzyme gene and cardiovascular-renal risk. J. Hypertens. 15 : 1579 – 1592 . ↵ Stoll M. , Jacob H...
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