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Paper Details

A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases.
Cell
264
2014
165 genes, Drosophila, Drosophila X chromosome, Mendelian disease, brain dysgenesis, drosophila, evolutionarily conserved genes, fly genes, genetic diseases, human, human homologs, microcephaly, rare variant alleles
Author NameAffiliation
Shinya YamamotoBaylor College of Medicine (BCM), USA Jan and Dan Duncan Neurological Research Institute
Tomasz GambinUSA Institute of Computer Science, Warsaw University of Technology
Ghayda M MirzaaUniversity of Washington, USA Center for Integrative Brain Research, Seattle Children's Research Institute
Wojciech WiszniewskiUSA Texas Children's Hospital
Ke Zhang
Shalini N Jhangiani
Donna M Muzny
Donna M Muzny
Ying-Wooi WanJan and Dan Duncan Neurological Research Institute
Zhandong LiuJan and Dan Duncan Neurological Research Institute
Robin D ClarkLoma Linda University Medical Center
Nichole Link
Eric BoerwinkleUniversity of Texas
Eric BoerwinkleUniversity of Texas
William B DobynsUniversity of Washington, USA Center for Integrative Brain Research, Seattle Children's Research Institute
Rando AllikmetsColumbia University College of Physicians and Surgeons
Richard A Gibbs
Richard A Gibbs
Rui ChenBaylor College of Medicine (BCM)
James R LupskiUSA Texas Children's Hospital
James R LupskiUSA Texas Children's Hospital
Michael F WanglerUSA Texas Children's Hospital
Hugo J BellenBaylor College of Medicine (BCM), USA Jan and Dan Duncan Neurological Research Institute, USA Howard Hughes Medical Institute
Hugo J BellenBaylor College of Medicine (BCM), USA Jan and Dan Duncan Neurological Research Institute, USA Howard Hughes Medical Institute
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