Daniel Moreno de Lucca

Summary

Affiliation: Emory University
Country: USA

Publications

  1. ncbi Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
    Richard Delorme
    INSERM, U955, Institut Mondor de Recherche Biomedicale, PsychiatricGenetics, Creteil, France
    BMC Med Genet 11:100. 2010
  2. ncbi Frequency of eNOS polymorphisms in the Colombian general population
    Norma C Serrano
    Biomedical Research Centre, Universidad Autonoma de Bucaramanga, Colombia
    BMC Genet 11:54. 2010
  3. ncbi Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
    Daniel Moreno-De-Luca
    Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
    Am J Hum Genet 87:618-30. 2010
  4. ncbi An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
    Erin B Kaminsky
    Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA
    Genet Med 13:777-84. 2011

Collaborators

  • Gabriele Richard
  • Eva W C Chow
  • Margaret P Adam
  • Sarah T South
  • Daniel Moreno-De-Luca
  • Erin B Kaminsky
  • Erik C Thorland
  • John A Crolla
  • Warren G Sanger
  • Stephen T Warren
  • Troy J Gliem
  • Emily Aston
  • Todd Ackley
  • Shuwen Huang
  • David H Ledbetter
  • Christa L Martin
  • Denae M Golden
  • JENNIFER G MULLE
  • Swaroop Aradhya
  • Diane L Pickering
  • Arthur R Brothman
  • Norma C Serrano
  • Richard Delorme
  • Ramaswamy K Iyer
  • Michael R Rossi
  • John G Compton
  • Dawn Kunig
  • Andres Moreno-De-Luca
  • Vineith Kaul
  • M Katharine Rudd
  • Shashirekha Shetty
  • Sarah J Beal
  • Justin Paschall
  • Deanna M Church
  • Morag N Collinson
  • Amy E Fuller
  • Brian Bunke
  • Heidi Whitby
  • Kim Uhas
  • Ram Iyer
  • Ashadeep Chandrareddy
  • María C Páez
  • Juan P Casas
  • Marion Leboyer
  • LuAnn Weik
  • Rainald Mossner
  • Bonnie Anne Salbert
  • Amy T Pakula
  • Nancy J Eisenhauer
  • Urvashi Surti
  • Lisa Guy
  • Pauline Chaste
  • Daniel Moreno de Lucca
  • Marie Christine Mouren
  • Aurélie Gennetier
  • Aroon D Hingorani
  • Scott M Myers
  • Stephan Ruhrmann
  • Melanie E Care
  • John C Barber
  • Michael Wagner
  • Laurie A Demmer
  • Hans Jörgen Grabe
  • Catalina Betancur
  • Chantal F Morel
  • Wolfgang Maier
  • Stephan J Sanders
  • Peter Falkai
  • Charlotte Boni
  • Luis A Diaz

Detail Information

Publications4

  1. ncbi Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder
    Richard Delorme
    INSERM, U955, Institut Mondor de Recherche Biomedicale, PsychiatricGenetics, Creteil, France
    BMC Med Genet 11:100. 2010
    ..Therefore, the aim of this study was to search for microrearrangements in these two regions in OCD patients...
  2. ncbi Frequency of eNOS polymorphisms in the Colombian general population
    Norma C Serrano
    Biomedical Research Centre, Universidad Autonoma de Bucaramanga, Colombia
    BMC Genet 11:54. 2010
    ..The objective of the present study was to determine the presence of G894T (rs1799983), intron-4 (27-bp TR) and -T786C (rs2070744) polymorphisms in the eNOS gene among the Colombian general population...
  3. ncbi Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
    Daniel Moreno-De-Luca
    Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA
    Am J Hum Genet 87:618-30. 2010
    ..In addition, the phenotypic features of patients with this CNV are consistent with a contiguous gene syndrome that extends beyond RCAD, which is caused by HNF1B mutations only...
  4. ncbi An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
    Erin B Kaminsky
    Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA
    Genet Med 13:777-84. 2011
    ....