Searching journal content for articles similar to Paulsen et al. 15 (1): 146.

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  1. Review: The superpowers of imprinting control regions
    • Bertille Montibus,
    • Franck Court,
    • and Philippe Arnaud
    Genome Res. January 2026 36: 1-19; Published in Advance December 10, 2025, doi:10.1101/gr.281215.125
  2. Resource: High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation
    • Jonas A. Gustafson,
    • Sophia B. Gibson,
    • Nikhita Damaraju,
    • Miranda P.G. Zalusky,
    • Kendra Hoekzema,
    • David Twesigomwe,
    • Lei Yang,
    • Anthony A. Snead,
    • Phillip A. Richmond,
    • Wouter De Coster,
    • Nathan D. Olson,
    • Andrea Guarracino,
    • Qiuhui Li,
    • Angela L. Miller,
    • Joy Goffena,
    • Zachary B. Anderson,
    • Sophie H.R. Storz,
    • Sydney A. Ward,
    • Maisha Sinha,
    • Claudia Gonzaga-Jauregui,
    • Wayne E. Clarke,
    • Anna O. Basile,
    • André Corvelo,
    • Catherine Reeves,
    • Adrienne Helland,
    • Rajeeva Lochan Musunuri,
    • Mahler Revsine,
    • Karynne E. Patterson,
    • Cate R. Paschal,
    • Christina Zakarian,
    • Sara Goodwin,
    • Tanner D. Jensen,
    • Esther Robb,
    • The 1000 Genomes ONT Sequencing Consortium,
    • University of Washington Center for Rare Disease Research (UW-CRDR),
    • Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium,
    • William Richard McCombie,
    • Fritz J. Sedlazeck,
    • Justin M. Zook,
    • Stephen B. Montgomery,
    • Erik Garrison,
    • Mikhail Kolmogorov,
    • Michael C. Schatz,
    • Richard N. McLaughlin, Jr.,
    • Harriet Dashnow,
    • Michael C. Zody,
    • Matt Loose,
    • Miten Jain,
    • Evan E. Eichler,
    • and Danny E. Miller
    Genome Res. November 2024 34: 2061-2073; Published in Advance October 2, 2024, doi:10.1101/gr.279273.124
    ...patterns at two disease-associated loci: 11p15.5, which is associated with both Beckwith–Wiedemann syndrome (BWS, MIM #130650) and Silver–Russell syndrome (SRS, MIM #180860) (Saal et al. 1993; Shuman et al. 1993); and 15q11.2-q13, associated with Prader–Willi syndrome (PWS, MIM #176270) and Angelman...
    OPEN ACCESS ARTICLE
  3. LETTER: Phylogenetic Footprint Analysis of IGF2 in Extant Mammals
    • Jennifer R. Weidman,
    • Susan K. Murphy,
    • Catherine M. Nolan,
    • Fred S. Dietrich,
    • and Randy L. Jirtle
    Genome Res. September 2004 14: 1726-1732; doi:10.1101/gr.2774804
    ...chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. Eur. J. Hum. Genet. 2 : 3 -23. ↵ Murphy, S.K. and Jirtle, R.L. 2003 . Imprinting evolution and the price of silence. BioEssays 25 : 577 -588. ↵ Murphy, W.J., Eizirik, E., Johnson, W.E., Zhang, Y.P., Ryder...
  4. Chicken Special/Letters: Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2–Igf2–H19 region
    • Takaaki Yokomine,
    • Hisao Shirohzu,
    • Wahyu Purbowasito,
    • Atsushi Toyoda,
    • Hisakazu Iwama,
    • Kazuho Ikeo,
    • Tetsuya Hori,
    • Shigeki Mizuno,
    • Masaoki Tsudzuki,
    • Yoh-ichi Matsuda,
    • Masahira Hattori,
    • Yoshiyuki Sakaki,
    • and Hiroyuki Sasaki
    Genome Res. January 2005 15: 154-165; Published in Advance December 8, 2004, doi:10.1101/gr.2609605
    ...11 in humans ( Reik and Maher 1997 ). The human domain is responsible for Beckwith-Wiedemann syndrome (BWS), an imprinting-associated fetal overgrowth syndrome. The domain is ∼1 Mb in size and contains 13 imprinted genes. Evidence indicates that the domain is composed of two subdomains, which are...
  5. LETTER: Antisense Transcripts With FANTOM2 Clone Set and Their Implications for Gene Regulation
    • Hidenori Kiyosawa,
    • Itaru Yamanaka,
    • Naoki Osato,
    • Shinji Kondo,
    • RIKEN GER Group,
    • GSLMembers,
    • and Yoshihide Hayashizaki
    Genome Res. June 2003 13: 1324-1334; doi:10.1101/gr.982903
    ...., Paulsen, M., Franck, O., Reinhardt, R., Lane, N., Reik, W., and Walter, J. 2000 . Sequence and functional comparison in the Beckwith-Wiedemann region: Implications for a novel imprinting centre and extended imprinting. Mol. Genet. 9 : 2691 -2706. ↵ Ewing, B. and Green, P. 2000 . Analysis of expressed...
  6. Research: Effects of sequence variation on differential allelic transcription factor occupancy and gene expression
    • Timothy E. Reddy,
    • Jason Gertz,
    • Florencia Pauli,
    • Katerina S. Kucera,
    • Katherine E. Varley,
    • Kimberly M. Newberry,
    • Georgi K. Marinov,
    • Ali Mortazavi,
    • Brian A. Williams,
    • Lingyun Song,
    • Gregory E. Crawford,
    • Barbara Wold,
    • Huntington F. Willard,
    • and Richard M. Myers
    Genome Res. May 2012 22: 860-869; Published in Advance February 2, 2012, doi:10.1101/gr.131201.111
  7. PERSPECTIVE: The opossum genome: Insights and opportunities from an alternative mammal
    • Paul B. Samollow
    Genome Res. August 2008 18: 1199-1215; doi:10.1101/gr.065326.107
    ...between recombination rate, nucleotide composition, and the genomic distributions of repetitive elements. The genome sequence is also beginning to enlarge our understanding of the evolution and function of the vertebrate immune system, and it provides an alternative model for investigating mechanisms...
  8. ARTICLE: Identification of Putative Noncoding RNAs Among the RIKEN Mouse Full-Length cDNA Collection
    • Koji Numata,
    • Akio Kanai,
    • Rintaro Saito,
    • Shinji Kondo,
    • Jun Adachi,
    • Laurens G. Wilming,
    • David A. Hume,
    • RIKEN GER Group,
    • GSL Members,
    • Yoshihide Hayashizaki,
    • and Masaru Tomita
    Genome Res. June 2003 13: 1301-1306; doi:10.1101/gr.1011603
    ...methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. Proc. Natl. Acad. Sci. 96 : 8064 -8069. ↵ Smith, C.M. and Steitz, J.A. 1998 . Classification of gas5 as a multi-small-nucleolar-RNA (snoRNA) host gene and a member...
  9. LETTER: Novel Imprinted DLK1/GTL2 Domain on Human Chromosome 14 Contains Motifs that Mimic Those Implicated in IGF2/H19 Regulation
    • Andrew A. Wylie,
    • Susan K. Murphy,
    • Terry C. Orton,
    • and Randy L. Jirtle
    Genome Res. November 1, 2000 10: 1711-1718; doi:10.1101/gr.161600
    ...ago ( Killian et al. 2000 ) possibly because of an interparental genetic conflict to control maternal-dependent growth of the offspring ( Haig and Graham 1991 ). Imprinted genes have been linked to a number of human behavioral and developmental disorders, including Angelman, Prader-Willi, and Beckwith-Wiedemann...
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