Daniel Moreno de Lucca

Summary

Affiliation: Emory University
Country: USA

Publications

  1. pmc Common genetic variants, acting additively, are a major source of risk for autism
    Lambertus Klei
    Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA
    Mol Autism 3:9. 2012
  2. pmc 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
  3. pmc 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
  4. pmc 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
  5. pmc 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
  • Sarah T South
  • Daniel Moreno-De-Luca
  • David H Ledbetter
  • Erin B Kaminsky
  • Lambertus Klei
  • Pauline Chaste
  • Stephan J Sanders
  • Warren G Sanger
  • Arthur R Brothman
  • John A Crolla
  • Christa L Martin
  • Emily Aston
  • Erik C Thorland
  • Todd Ackley
  • JENNIFER G MULLE
  • Swaroop Aradhya
  • Shuwen Huang
  • Diane L Pickering
  • Stephen T Warren
  • Troy J Gliem
  • Denae M Golden
  • Richard Delorme
  • Norma C Serrano
  • Bernie Devlin
  • Kathryn Roeder
  • Timothy W Yu
  • Michael T Murtha
  • Donna M Martin
  • Matthew W State
  • James S Sutcliffe
  • Dorothy E Grice
  • Vanessa Hus
  • A Jeremy Willsey
  • Catherine Lord
  • Nadine M Melhem
  • Eric M Morrow
  • Jennifer K Lowe
  • Edwin H Cook
  • Christopher A Walsh
  • Eric Fombonne
  • Daniel Geschwind
  • Shrikant M Mane
  • Christa Lese Martin
  • Shashirekha Shetty
  • Dawn Kunig
  • Justin Paschall
  • Morag N Collinson
  • Heidi Whitby
  • Michael R Rossi
  • Ramaswamy K Iyer
  • Vineith Kaul
  • Amy E Fuller
  • Brian Bunke
  • Andres Moreno-De-Luca
  • Deanna M Church
  • M Katharine Rudd
  • John G Compton
  • Sarah J Beal
  • Juan P Casas
  • Catalina Betancur
  • Rainald Mossner
  • Peter Falkai
  • Michael Wagner
  • Marion Leboyer
  • Ram Iyer
  • Melanie E Care
  • María C Páez
  • Kim Uhas
  • Margaret P Adam
  • LuAnn Weik
  • Marie Christine Mouren
  • Lisa Guy
  • Ashadeep Chandrareddy
  • Aurélie Gennetier
  • Aroon D Hingorani
  • Daniel Moreno de Lucca
  • John C Barber
  • Charlotte Boni
  • Nancy J Eisenhauer
  • Stephan Ruhrmann
  • Chantal F Morel
  • Wolfgang Maier
  • Bonnie Anne Salbert
  • Luis A Diaz
  • Laurie A Demmer
  • Amy T Pakula
  • Hans Jörgen Grabe
  • Urvashi Surti

Detail Information

Publications5

  1. pmc Common genetic variants, acting additively, are a major source of risk for autism
    Lambertus Klei
    Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA
    Mol Autism 3:9. 2012
    ..abstract:..
  2. pmc 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...
  3. pmc 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...
  4. pmc 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...
  5. pmc 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
    ....