Detail page

Knowledge Web

Person

Alexej Knaus

Wissenschaftlicher Mitarbeiter

Name	Alexej Knaus
Place	Kiew (Geburtsort) Ukraine Deutschland
Gender	männlich
Profession	Wissenschaftlicher Mitarbeiter (characteristic profession)
Related	Universitätsklinikum Bonn Biotechnologie (Studienfach)
Further information	Dissertation, Freie Universität Berlin, Fachbereich Biologie, Chemie, Pharmazie, 2019
Record type	Person
GND-Identifier	1194586341
Record ID	1194586341
Involved in show all Enhancing Variant Prioritization in VarFish through On-Premise Computational Facial Analysis Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings PEDIA: prioritization of exome data by image analysis Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report Phenotypic characterization of pathogenic mutations in GPIBDs Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis

Please note

The beta version does not yet contain all functions and information of the DNB portal catalogue. If you are missing information or want to order a medium, please visit the page in the DNB portal catalogue via the following link:

Katalog der Deutschen Nationalbibliothek

Alexej Knaus

Enhancing Variant Prioritization in VarFish through On-Premise Computational Facial Analysis

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

PEDIA: prioritization of exome data by image analysis

Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report

Phenotypic characterization of pathogenic mutations in GPIBDs

Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis