Concepedia

Author

Johannes Egerer

Max Planck Institute for Molecular Genetics

Also Known As

Egerer, Johannes, J. Egerer, Johannes Egerer

12

Publications

807

Citations

9

H-Index

22

Concepts

All Affiliations

Max Planck Institute for Molecular GeneticsCharité - Universitätsmedizin BerlinUniversity of ManchesterBerlin-Brandenburger Centrum für Regenerative TherapienMax Planck Institute of Biochemistry
JE

About

Johannes Egerer is an author at Max Planck Institute for Molecular Genetics specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

6

6

374

2

Engineering

1

1

21

3

Biology

1

1

156

4

Cell Biology

1

1

45

5

Immunology

1

1

23

Johannes Egerer

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8

Publications

753

Citations

8

H-Index

YearCitations

Functional dissection of Rab GTPases involved in primary cilium formation

Shin‐ichiro Yoshimura, Johannes Egerer, Evelyn Fuchs,

The Journal of Cell Biology

2007

361

Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin

Hans Christian Hennies, Uwe Kornak, Haikuo Zhang,

Nature Genetics

2008

156

Further characterization of ATP6V0A2-related autosomal recessive cutis laxa

Björn Fischer‐Zirnsak, Aikaterini Dimopoulou, Johannes Egerer,

Human Genetics

2012

93

Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplastica

Wing Lee Chan, Magdalena Steiner, Tomasz M. Witkos,

PLoS Genetics

2018

45

GORAB Missense Mutations Disrupt RAB6 and ARF5 Binding and Golgi Targeting

Johannes Egerer, Denise Emmerich, Björn Fischer‐Zirnsak,

Journal of Investigative Dermatology

2015

36

A major resistance gene from Russian apple ‘Antonovka’ conferring field immunity against apple scab is closely linked to the Vf locus

F. Dunemann, Johannes Egerer

Tree Genetics & Genomes

2010

23

TRANSFORMATION IN APPLE FOR INCREASED DISEASE RESISTANCE

Ines Hiller, G. Klotzsche, Katrin Winkler,

Acta Horticulturae

2000

21

An overlapping phenotype of Osteogenesis imperfecta and Ehlers–Danlos syndrome due to a heterozygous mutation in <i>COL1A1</i> and biallelic missense variants in <i>TNXB</i> identified by whole exome sequencing

Luisa Mackenroth, Björn Fischer‐Zirnsak, Johannes Egerer,

American Journal of Medical Genetics Part A

2016

18

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