Concepedia

Author

Susanne Lützkendorf

Charité - Universitätsmedizin Berlin

Also Known As

S. Lützkendorf, Susanne Lützkendorf, Susanne Lützkendorf

8

Publications

1.5K

Citations

8

H-Index

21

Concepts

All Affiliations

Charité - Universitätsmedizin BerlinNewcastle UniversityInstitut de Biologie ValroseInsermMSB Medical School Berlin
SL

About

Susanne Lützkendorf is an author at Charité - Universitätsmedizin Berlin specializing in medicine, genetics, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

713

2

Pathology

2

2

294

3

Health Sciences

1

1

236

4

Cell Biology

1

1

419

5

Cardiovascular Genetics

1

1

236

Susanne Lützkendorf

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6

Publications

1.5K

Citations

6

H-Index

YearCitations

Functional analysis of <i>Sox8</i> and <i>Sox9</i> during sex determination in the mouse

Marie‐Christine Chaboissier, Akio Kobayashi, Valerie I. P. Vidal,

Development

2004

542

Sox9 Is Essential for Outer Root Sheath Differentiation and the Formation of the Hair Stem Cell Compartment

Valérie Vidal, Marie‐Christine Chaboissier, Susanne Lützkendorf,

Current Biology

2005

419

Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to PTRF-CAVIN Mutations

Anna Rajab, Volker Straub, Liza McCann,

PLoS Genetics

2010

236

EXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia

Veronika Boczonadi, Juliane Müller, Angela Pyle,

Nature Communications

2014

154

Clinical variability in distal spinal muscular atrophy type 1 (DSMA1): determination of steady-state IGHMBP2 protein levels in five patients with infantile and juvenile disease

Ulf‐Peter Guenther, Lusy Handoko, Raymonda Varon,

Journal of Molecular Medicine

2008

58

<i>POMK</i> mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination, mild hearing deficit and intellectual disability

Anja von Renesse, Mina Petkova, Susanne Lützkendorf,

Journal of Medical Genetics

2014

51

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