Searching journal content for Stephen W. Scherer in author.

Displaying results 1-8 of 8
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  1. Research: Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing
    • Jesper Eisfeldt,
    • Edward J. Higginbotham,
    • Felix Lenner,
    • Jennifer Howe,
    • Bridget A. Fernandez,
    • Anna Lindstrand,
    • Stephen W. Scherer,
    • and Lars Feuk
    Genome Res. November 2024 34: 1763-1773; Published in Advance October 29, 2024, doi:10.1101/gr.279263.124
    OPEN ACCESS ARTICLE
  2. Method: Sequencing of isolated sperm cells for direct haplotyping of a human genome
    • Ewen F. Kirkness,
    • Rashel V. Grindberg,
    • Joyclyn Yee-Greenbaum,
    • Christian R. Marshall,
    • Stephen W. Scherer,
    • Roger S. Lasken,
    • and J. Craig Venter
    Genome Res. May 2013 23: 826-832; Published in Advance January 2, 2013, doi:10.1101/gr.144600.112
  3. Method: A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes
    • Sanaa Choufani,
    • Jonathan S. Shapiro,
    • Martha Susiarjo,
    • Darci T. Butcher,
    • Daria Grafodatskaya,
    • Youliang Lou,
    • Jose C. Ferreira,
    • Dalila Pinto,
    • Stephen W. Scherer,
    • Lisa G. Shaffer,
    • Philippe Coullin,
    • Isabella Caniggia,
    • Joseph Beyene,
    • Rima Slim,
    • Marisa S. Bartolomei,
    • and Rosanna Weksberg
    Genome Res. March 2011 21: 465-476; Published in Advance February 7, 2011, doi:10.1101/gr.111922.110
  4. LETTER: Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing
    • David Monk,
    • Alexandre Wagschal,
    • Philippe Arnaud,
    • Pari-Sima Müller,
    • Layla Parker-Katiraee,
    • Déborah Bourc’his,
    • Stephen W. Scherer,
    • Robert Feil,
    • Philip Stanier,
    • and Gudrun E. Moore
    Genome Res. August 2008 18: 1270-1281; Published in Advance May 14, 2008, doi:10.1101/gr.077115.108
  5. Methods: Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
    • 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,
    • and Hiroyuki Aburatani
    Genome Res. December 2006 16: 1575-1584; Published in Advance November 22, 2006, doi:10.1101/gr.5629106
  6. Methods: Accurate and reliable high-throughput detection of copy number variation in the human genome
    • Heike Fiegler,
    • Richard Redon,
    • Dan Andrews,
    • Carol Scott,
    • Robert Andrews,
    • Carol Carder,
    • Richard Clark,
    • Oliver Dovey,
    • Peter Ellis,
    • Lars Feuk,
    • Lisa French,
    • Paul Hunt,
    • Dimitrios Kalaitzopoulos,
    • James Larkin,
    • Lyndal Montgomery,
    • George H. Perry,
    • Bob W. Plumb,
    • Keith Porter,
    • Rachel E. Rigby,
    • Diane Rigler,
    • Armand Valsesia,
    • Cordelia Langford,
    • Sean J. Humphray,
    • Stephen W. Scherer,
    • Charles Lee,
    • Matthew E. Hurles,
    • and Nigel P. Carter
    Genome Res. December 2006 16: 1566-1574; Published in Advance November 22, 2006, doi:10.1101/gr.5630906
    OPEN ACCESS ARTICLE
  7. REVIEW: Copy number variation: New insights in genome diversity
    • Jennifer L. Freeman,
    • George H. Perry,
    • Lars Feuk,
    • Richard Redon,
    • Steven A. McCarroll,
    • David M. Altshuler,
    • Hiroyuki Aburatani,
    • Keith W. Jones,
    • Chris Tyler-Smith,
    • Matthew E. Hurles,
    • Nigel P. Carter,
    • Stephen W. Scherer,
    • and Charles Lee
    Genome Res. August 2006 16: 949-961; Published in Advance June 29, 2006, doi:10.1101/gr.3677206
  8. LETTER: Large-Scale Sequencing of Two Regions in Human Chromosome 7q22: Analysis of 650 kb of Genomic Sequence around the EPO and CUTL1 Loci Reveals 17 Genes
    • Gernot Glöckner,
    • Stephen Scherer,
    • Ruben Schattevoy,
    • Andrew Boright,
    • Jacqueline Weber,
    • Lap-Chee Tsui,
    • and André Rosenthal
    Genome Res. October 1, 1998 8: 1060-1073; doi:10.1101/gr.8.10.1060
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