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Paper Details

PEDIA: prioritization of exome data by image analysis.
Genet Med
35
2019
PEDIA, disease-causing gene, dysmorphologists, exome, exomes, genomic variants, monogenic, monogenic disorders
Author NameAffiliation
Saskia BiskupInstitute of Genomic Statistics and Bioinformatics, University of Bonn
Sandra C D??lkenSt Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust Manchester Academic Health Sciences Centre
Sandra C D??lkenUniversity of Manchester
Sofia DouzgouInstitute of Genomic Statistics and Bioinformatics, University of Bonn
Nadja EhmkeMedical University of Innsbruck
Bj??rn Fischer-ZirnsakFDNA Inc.
Luitgard Graul-NeumannA. I. duPont Hospital for Children
Sebastian K??hlerResearch Institute of Medical Genetics of Russian Academy of Medical Sciences
Sebastian K??hlerResearch Institute of Medical Genetics of Russian Academy of Medical Sciences
Uwe KornakCharite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt-Universitat zu Berlin, and Berlin Institute of Health, Institute of Medical Genetics and Human Genetics
Markus M N??thenCharite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt-Universitat zu Berlin, and Berlin Institute of Health, Institute of Medical Genetics and Human Genetics
Markus M N??thenCharite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt-Universitat zu Berlin, and Berlin Institute of Health, Institute of Medical Genetics and Human Genetics
Claus-Eric OttClinical Institute of Medical Genetics, University Medical Centre Ljubljana
Peter N RobinsonCharite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt-Universitat zu Berlin, and Berlin Institute of Health, Institute of Medical Genetics and Human Genetics
Peter N RobinsonCharite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt-Universitat zu Berlin, and Berlin Institute of Health, Institute of Medical Genetics and Human Genetics
Max SchubachFDNA Inc.
Malte SpielmannCenter for Prenatal Diagnosis and Human Genetics
Stefan MundlosCharite - Universitatsmedizin Berlin, corporate member of Freie Universitat Berlin, Humboldt-Universitat zu Berlin, and Berlin Institute of Health, Institute of Medical Genetics and Human Genetics
Denise HornInstitute of Genomic Statistics and Bioinformatics, University of Bonn
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