Rong Mao

Summary

Affiliation: Johns Hopkins University
Country: USA

Publications

  1. ncbi request reprint Functional profiling of the Saccharomyces cerevisiae genome
    Guri Giaever
    Stanford Genome Technology Center, Stanford University, Palo Alto, California 94304, USA
    Nature 418:387-91. 2002
  2. ncbi request reprint Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain
    Rong Mao
    Program in Biochemistry, Cellular and Molecular Biology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA
    Genomics 81:457-67. 2003
  3. pmc Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart
    Rong Mao
    Program in Biochemistry, Cellular and Molecular Biology, Johns Hopkins School of Medicine, 1830 East Monument Street, Baltimore, MD 21205, USA
    Genome Biol 6:R107. 2005
  4. pmc Gene expression alterations over large chromosomal regions in cancers include multiple genes unrelated to malignant progression
    Brett G Masayesva
    Department of Otolaryngology Head and Neck Surgery, Head and Neck Cancer Research Division, Johns Hopkins Medical Institutions, 720 Rutland Avenue, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 101:8715-20. 2004
  5. ncbi request reprint The use of genomic microarrays to study chromosomal abnormalities in mental retardation
    Rong Mao
    Program in Biochemistry, Molecular, and Cellular Biology, Johns Hopkins School of Medicine, and Department of Neurology, Kennedy Krieger Institute, Baltimore, Maryland 21205, USA
    Ment Retard Dev Disabil Res Rev 11:279-85. 2005
  6. ncbi request reprint 4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotype
    David A Stevenson
    Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, Utah, USA
    J Pediatr 145:840-2. 2004

Collaborators

  • Joseph Califano
  • Elizabeth Garrett-Mayer
  • David A Stevenson
  • Brett G Masayesva
  • Guri Giaever
  • Traci Speed
  • William H Westra
  • Chul So Moon
  • Jonathan Pevsner
  • Thomas Pilkington
  • Nicole Benoit
  • Pinar Bayrak-Toydemir
  • Arthur R Brothman
  • David Sidransky
  • Patrick Ha
  • John C Carey
  • Brett C Cowley
  • Francoise Foury
  • Sally Dow
  • David J Garfinkel
  • Diane E Kelly
  • Steven L Kelly
  • Jeffrey N Strathern
  • Stefano Campanaro
  • Jose L Revuelta
  • Patrick Flaherty
  • Johannes H Hegemann
  • Keith Anderson
  • Daniel F Jaramillo
  • Bruno Andre
  • Deanna Gotte
  • Marc Lussier
  • Siew Loon Ooi
  • Ronald W Davis
  • Li Ni
  • Patrice Menard
  • Sharon Sookhai-Mahadeo
  • Daniel D Shoemaker
  • Marleen Voet
  • Darlene LaBonte
  • Lucy Liu
  • Hong Liao
  • Bart Scherens
  • Ning Lan
  • Mark Gerstein
  • Karen Davis
  • David C Lamb
  • Ching Yun Wang
  • Elizabeth A Winzeler
  • Reginald K Storms
  • Angela M Chu
  • Petra Ross-Macdonald
  • Linda Riles
  • Jef D Boeke
  • Peter K├Âtter
  • Adam P Arkin
  • Sophie Brachat
  • Zelek Herman
  • Steeve Veronneau
  • Mohamed El-Bakkoury
  • Michael Snyder
  • Mark Johnston
  • Yonghong Yang
  • Rhonda Bangham
  • Matt Curtiss
  • Grace Yen
  • Ankuta Lucau-Danila
  • Rocio Benito
  • Kexin Yu
  • Peter Philippsen
  • Brenda Shafer
  • Adam Deutschbauer
  • Chuanyun Luo
  • Teresa R Ward
  • Matthias Rose
  • Christopher J Roberts
  • Anna Astromoff
  • Julie Wilhelmy
  • Giorgio Valle
  • Guido Volckaert
  • Hong Liang
  • Karl Dieter Entian
  • Carla Connelly
  • Ulrich Guldener
  • Svenja Hempel
  • Elaine Youngman
  • Greg Schimmack
  • Howard Bussey

Detail Information

Publications6

  1. ncbi request reprint Functional profiling of the Saccharomyces cerevisiae genome
    Guri Giaever
    Stanford Genome Technology Center, Stanford University, Palo Alto, California 94304, USA
    Nature 418:387-91. 2002
    ..Our results validate the yeast gene-deletion collection as a valuable resource for functional genomics...
  2. ncbi request reprint Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain
    Rong Mao
    Program in Biochemistry, Cellular and Molecular Biology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA
    Genomics 81:457-67. 2003
    ..However, it is possible that these gene expression changes ultimately relate to the phenotypic variability of DS...
  3. pmc Primary and secondary transcriptional effects in the developing human Down syndrome brain and heart
    Rong Mao
    Program in Biochemistry, Cellular and Molecular Biology, Johns Hopkins School of Medicine, 1830 East Monument Street, Baltimore, MD 21205, USA
    Genome Biol 6:R107. 2005
    ..Also, the statistical significance of differentially expressed genes in human Down syndrome tissues has not been reported...
  4. pmc Gene expression alterations over large chromosomal regions in cancers include multiple genes unrelated to malignant progression
    Brett G Masayesva
    Department of Otolaryngology Head and Neck Surgery, Head and Neck Cancer Research Division, Johns Hopkins Medical Institutions, 720 Rutland Avenue, Baltimore, MD 21205, USA
    Proc Natl Acad Sci U S A 101:8715-20. 2004
    ..Loss and gain of chromosomal material in solid cancers can alter gene expression over large chromosomal regions, including multiple genes unrelated to malignant progression...
  5. ncbi request reprint The use of genomic microarrays to study chromosomal abnormalities in mental retardation
    Rong Mao
    Program in Biochemistry, Molecular, and Cellular Biology, Johns Hopkins School of Medicine, and Department of Neurology, Kennedy Krieger Institute, Baltimore, Maryland 21205, USA
    Ment Retard Dev Disabil Res Rev 11:279-85. 2005
    ..Genomic microarrays offer both a genome-wide perspective of chromosomal aberrations as well as higher resolution (to the level of approximately one megabase) compared to alternative available technologies...
  6. ncbi request reprint 4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotype
    David A Stevenson
    Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, Utah, USA
    J Pediatr 145:840-2. 2004
    ..Terminal 4p deletions cause Wolf-Hirschhorn syndrome, but the phenotype probably was modified by the paternally derived 11p duplication. This emphasizes the clinical utility of genomic microarray...