Manfred Wehnert

Universität Greifswald — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

33h-index4.6kcitations120works5.02yr avg
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Research Topics

Nuclear Structure and Function(62), RNA Research and Splicing(58), Genomics and Chromatin Dynamics(17), RNA regulation and disease(17), Hemophilia Treatment and Research(12)

Publications120 total

Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomere
Journal of Biological Chemistry·2024· 5 citedOpen Access
A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism
EBioMedicine·2019· 35 citedOpen Access
A Multistage Sequencing Strategy Pinpoints Many Novel and Candidate Disease Alleles for Orphan Disease Emery-Dreifuss Muscular Dystrophy and Supports Gene Misregulation as its Pathomechanism
2019· 2 citedOpen Access
Immunohistochemistry on a panel of Emery–Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology
Neuromuscular Disorders·2016· 15 citedOpen Access
AB091. Analysis of LA2 as a functional candidate gene for Emery Dreifuss muscular dystrophy and dilated cardiomyopathy.
PubMed Central·2015Open Access
Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cells
Nucleus·2015· 41 citedOpen Access
Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery–Dreifuss muscular dystrophy
Neuromuscular Disorders·2014· 20 citedOpen Access
Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization
PLoS Genetics·2014· 179 citedOpen Access
Rapamycin treatment of Mandibuloacral Dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics
Aging·2014· 34 citedOpen Access
Contribution of SUN1 Mutations to the Pathomechanism in Muscular Dystrophies
Human Mutation·2013· 26 cited
New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update
European Journal of Human Genetics·2013· 59 citedOpen Access
Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C
Aging·2013· 19 citedOpen Access
Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutation
Neuromuscular Disorders·2013· 6 cited
Li <scp>NC</scp> Complex and Human Genetic Muscular Disease
Encyclopedia of Life Sciences·2012· 2 cited
Progeroide Laminopathien zwischen Hutchinson-Gilford-Syndrom, restriktiver Dermopathie und mandibuloakraler Dysplasie
Medizinische Genetik·2012
Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution
Cell Cycle·2012· 30 citedOpen Access
LINC complex alterations in DMD and EDMD/CMT fibroblasts
European Journal of Cell Biology·2012· 60 citedOpen Access
The LINC complex and human disease
Biochemical Society Transactions·2011· 95 cited
Distinct association of the nuclear pore protein Nup153 with A- and B-type lamins
Nucleus·2011· 84 citedOpen Access
Prelamin A processing and functional effects in restrictive dermopathy
Cell Cycle·2010· 22 citedOpen Access
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Frequent Co-authors

Giovanna Lattanzi(9), Gisèle Bonne(8), Vittoria Cenni(7), Peter Meinke(7), Cristina Capanni(6), Elisabetta Mattioli(6), Marta Columbaro(6), Stefano Squarzoni(6), Nadir M. Maraldi(5), Nguyễn Thùy Dương(5), Luciano Merlini(4), Angelika A. Noegel(4), W. Schröder(4), K. Wulff(4), Juliet A. Ellis(3), Matthias Vorgerd(3), Antoine Muchir(3), B. Eymard(3), Denis Duboc(3), Xavier Ferrer(3)