Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants Journal Articles uri icon

Overview

Authors

  • Authorship

    • PIZZO L
    • VAN DIJCK A
    • POPE K
    • VOORHOEVE E
    • YOON J
    • STANKIEWICZ P
    • CHEUNG SW
    • PAZUCHANICS D
    • HUBER E
    • KUMAR V
    • KEMBER RL
    • JENSEN M
    • MARI F
    • CURRÓ A
    • CASTIGLIA L
    • GALESI O
    • AVOLA E
    • MATTINA T
    • FICHERA M
    • MANDARÀ L
    • VINCENT M
    • NIZON M
    • POLYAK A
    • MERCIER S
    • BÉNÉTEAU C
    • BLESSON S
    • MARTIN-COIGNARD D
    • MOSCA-BOIDRON AL
    • CABERG JH
    • BUCAN M
    • ZEESMAN S
    • NOWACZYK MJM
    • LEFEBVRE M
    • ROSENFELD JA
    • FAIVRE L
    • CALLIER P
    • SKINNER C
    • KEREN B
    • PERRINE C
    • PRONTERA P
    • MARLE N
    • RENIERI A
    • REYMOND A
    • KOOY RF
    • MANNIK K
    • ISIDOR B
    • SCHWARTZ C
    • ROMANO C
    • SISTERMANS E
    • PROF David Amor
    • ANDRIEUX J
    • GIRIRAJAN S
    • KRISHNAN A
    • MCCREADY E
    • PICHON O
    • LE CAIGNEC C

Published in

  • Genetics in Medicine

Time

Date/time value

  • 2018

Identity

Digital Object Identifier (DOI)

  • 10.1038/s41436-018-0266-3

Additional Document Info

Parent Title

  • Genetics in Medicine

Publisher

  • Lippincott Williams & Wilkins