FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Karin Wiegers

Research Profile

Chemicals & Drugs

Procedures

DNA Mutational Analysis

Physiology

Concepts & Ideas

Disorders

Genes & Molecular Sequences

Dominant Genes

Co-author Network

Publications

TOP 3
Alexander Schmidt; Karin Wiegers; Eckart Altenmüller; Hans-Christian Jabusch; Christine Klein; André Lee; Katja Lohmann
The GAG deletion in Tor1A (DYT1) is a rare cause of complex musician's dystonia.
Norbert Brüggemann; Manfred Mitterer; Andrea J Lanthaler; Ana Djarmati; Johann Hagenah; Karin Wiegers; Susen Winkler; Heike Pawlack; Thora Lohnau; Peter P Pramstaller; Christine Klein; Katja Lohmann
Frequency of heterozygous Parkin mutations in healthy subjects: need for careful prospective follow-up examination of mutation carriers.
Anne Grünewald; Ana Djarmati; Katja Lohmann-Hedrich; K Farrell; J A Zeller; Niels Allert; F Papengut; B Petersen; Victor S C Fung; C M Sue; D O'Sullivan; N Mahant; Andreas Kupsch; R S Chuang; Karin Wiegers; H Pawlack; Johann Hagenah; Laurie J Ozelius; Ulrich Stephani; Robert Schuit; Anthony E Lang; Jens Volkmann; Alexander Münchau; Christine Klein
Myoclonus-dystonia: significance of large SGCE deletions.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Karin Wiegers (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Alexander Schmidt; Karin Wiegers; Eckart Altenmüller; Hans-Christian Jabusch; Christine Klein; André Lee; Katja Lohmann
The GAG deletion in Tor1A (DYT1) is a rare cause of complex musician's dystonia.
Parkinsonism & related disorders 2012;18(5):690-1.
2009: Norbert Brüggemann; Manfred Mitterer; Andrea J Lanthaler; Ana Djarmati; Johann Hagenah; Karin Wiegers; Susen Winkler; Heike Pawlack; Thora Lohnau; Peter P Pramstaller; Christine Klein; Katja Lohmann
Frequency of heterozygous Parkin mutations in healthy subjects: need for careful prospective follow-up examination of mutation carriers.
Parkinsonism & related disorders 2009;15(6):425-9.
2008: Anne Grünewald; Ana Djarmati; Katja Lohmann-Hedrich; K Farrell; J A Zeller; Niels Allert; F Papengut; B Petersen; Victor S C Fung; C M Sue; D O'Sullivan; N Mahant; Andreas Kupsch; R S Chuang; Karin Wiegers; H Pawlack; Johann Hagenah; Laurie J Ozelius; Ulrich Stephani; Robert Schuit; Anthony E Lang; Jens Volkmann; Alexander Münchau; Christine Klein
Myoclonus-dystonia: significance of large SGCE deletions.
Human mutation 2008;29(2):331-2.
2005: Christine Klein; Ana Djarmati; Katja Hedrich; Nora Schäfer; Cesa Scaglione; Roberta Marchese; Norman Kock; Birgitt Schuele; Anja Hiller; Thora Lohnau; Susen Winkler; Karin Wiegers; Robert Hering; Peter Bauer; Olaf Riess; Giovanni Abbruzzese; Paolo Martinelli; Peter P Pramstaller
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.
European journal of human genetics : EJHG 2005;13(9):1086-93.
2005: Johann Hagenah; Rachel Saunders-Pullman; Katja Hedrich; Kemal Kabakci; K Habermann; Karin Wiegers; Kathrin Mohrmann; Thora Lohnau; Deborah Raymond; Peter Vieregge; TG Nygaard; Laurie J Ozelius; Susan Bressman; Christine Klein
High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening.
Neurology 2005;64(5):908-11.
2004: Katja Hedrich; E-M Meyer; Birgitt Schuele; Norman Kock; Patricia de Carvalho Aguiar; Karin Wiegers; J H T M Koelman; Jennifer Garrels; R Dürr; Liu Liu; Eberhard Schwinger; Laurie J Ozelius; B Landwehrmeyer; A Jon Stoessl; Marina A J Tijssen; Christine Klein
Myoclonus-dystonia: detection of novel, recurrent, and de novo SGCE mutations.
Neurology 2004;62(7):1229-31.
2004: Norman Kock; Meike Kasten; Birgitt Schuele; Katja Hedrich; Karin Wiegers; Kemal Kabakci; Johann Hagenah; Peter P Pramstaller; Matthias F Nitschke; Alexander Münchau; Jürgen Sperner; Christine Klein
Clinical and genetic features of myoclonus-dystonia in 3 cases: a video presentation.
Movement disorders : official journal of the Movement Disorder Society 2004;19(2):231-4.
2002: Christine Klein; Katja Hedrich; K Kabakçi; Kathrin Mohrmann; Karin Wiegers; Olfert Landt; Johann Hagenah; Eberhard Schwinger; Peter P Pramstaller; Laurie J Ozelius; K Gucuyener; Sabiha Aysun; E Demir
Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia.
Neurology 2002;59(11):1783-6.
2002: Martin Kann; Helfried Jacobs; Kathrin Mohrmann; Kirsten Schumacher; Katja Hedrich; Jennifer Garrels; Karin Wiegers; Eberhard Schwinger; Peter P Pramstaller; Xandra O Breakefield; Laurie J Ozelius; Peter Vieregge; Christine Klein
Role of parkin mutations in 111 community-based patients with early-onset parkinsonism.
Annals of neurology 2002;51(5):621-5.