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KS

Karen Schmidt

Medical Genetics / Clinical Genetics (M.D.)

Credentials: · ·

History

Pediatrics

Research

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
Molecular Cytogenetics · 2008 · 192 citations
Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability
Journal of Medical Genetics · 2011 · 140 citations
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region
Human Molecular Genetics · 2009 · 59 citations

BB
Bassem Bejjani
2 papers
Elaine Zackai
2 papers
AA
Alexander Asamoah
1 paper
Amanda DeCrow
1 paper · 1 as a resident
AL
Andres Moreno De Luca
1 paper · 1 as a resident
BD
Barbara Dupont
1 paper
BP
Berkley Powell
1 paper
Chad Haldeman-Englert
1 paper
CF
Christopher Friedrich
1 paper
David Weaver
1 paper
DW
Dieter Wefuan
1 paper
Donna McDonald-McGinn
1 paper