Handedness genetics: considering the phenotype

Por Ocklenburg, Sebastian, Beste, Christian, Arning, Larissa
Publicado no Front Psychol (2014)

Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)

Por Schlang, Katharina J, Arning, Larissa, Epplen, Joerg T, Stemmler, Susanne
Publicado em 2008

Age at onset of Huntington disease is not modulated by the R72P variation in TP53 and the R196K variation in the gene coding for the human caspase activated DNase (hCAD)

Por Arning, Larissa, Kraus, Peter H, Saft, Carsten, Andrich, Jürgen, Epplen, Jörg T
Publicado em 2005

Genomic NGFB variation and multiple sclerosis in a case control study

Por Akkad, Denis A, Kruse, Niels, Arning, Larissa, Gold, Ralf, Epplen, Jörg T
Publicado em 2008

PGC-1alpha as modifier of onset age in Huntington disease

Por Taherzadeh-Fard, Elahe, Saft, Carsten, Andrich, Jürgen, Wieczorek, Stefan, Arning, Larissa
Publicado em 2009

Glutathione S-Transferase Ω 1 variation does not influence age at onset of Huntington's disease

Por Arning, Larissa, Jagiello, Peter, Wieczorek, Stefan, Saft, Carsten, Andrich, Jürgen, Epplen, Jörg T
Publicado em 2004

Cholecystokinin A Receptor (CCKAR) Gene Variation Is Associated with Language Lateralization

Por Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian
Publicado em 2013

Failure to confirm influence of Methyltetrahydrofolate reductase (MTHFR) polymorphisms on age at onset of Huntington disease

Por Hansen, Wiebke, Saft, Carsten, Andrich, Jürgen, Müller, Thomas, Wieczorek, Stefan, Epplen, Jörg T, Arning, Larissa
Publicado em 2005

On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors

Por Wagenleiter, Sonja EN, Jagiello, Peter, Akkad, Denis A, Arning, Larissa, Griga, Thomas, Klein, Wolfram, Epplen, Jörg T
Publicado em 2005

Hepatic mitochondrial dysfunction in Friedreich Ataxia

Por Stüwe, Sven H, Goetze, Oliver, Arning, Larissa, Banasch, Matthias, Schmidt, Wolfgang E, Schöls, Ludger, Saft, Carsten
Publicado em 2011

PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease

Por Haghikia Aiden, Wieczorek Stefan, Akkad Denis A, Saft Carsten, Taherzadeh-Fard Elahe, Chan Andrew, Epplen Jörg T, Arning Larissa
Publicado em 2011-05-01

No association between polymorphisms in the BDNF gene and age at onset in Huntington disease

Por Mai, Maren, Akkad, Amer D, Wieczorek, Stefan, Saft, Carsten, Andrich, Jürgen, Kraus, Peter H, Epplen, Jörg T, Arning, Larissa
Publicado em 2006

PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease

Por Taherzadeh-Fard, Elahe, Saft, Carsten, Akkad, Denis A, Wieczorek, Stefan, Haghikia, Aiden, Chan, Andrew, Epplen, Jörg T, Arning, Larissa
Publicado em 2011

Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1

Por Steinemann, Doris, Arning, Larissa, Praulich, Inka, Stuhrmann, Manfred, Hasle, Henrik, Starý, Jan, Schlegelberger, Brigitte, Niemeyer, Charlotte M., Flotho, Christian
Publicado em 2010

Efficacy of Fumaric Acid Esters in the R6/2 and YAC128 Models of Huntington's Disease

Por Ellrichmann, Gisa, Petrasch-Parwez, Elisabeth, Lee, De-Hyung, Reick, Christiane, Arning, Larissa, Saft, Carsten, Gold, Ralf, Linker, Ralf A.
Publicado em 2011

PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness

Por Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M., Hengstler, Jan G., Falkenstein, Michael, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian
Publicado em 2013

Handedness and the X chromosome: The role of androgen receptor CAG-repeat length

Por Arning, Larissa, Ocklenburg, Sebastian, Schulz, Stefanie, Ness, Vanessa, Gerding, Wanda M., Hengstler, Jan G., Falkenstein, Michael, Epplen, Jörg T., Güntürkün, Onur, Beste, Christian
Publicado no Sci Rep (2015)

NMDA receptor gene variations as modifiers in Huntington disease: a replication study

Por Saft, Carsten, Epplen, Jörg T., Wieczorek, Stefan, Landwehrmeyer, G. Bernhard, Roos, Raymund A.C., de Yebenes, Justo Garcia, Dose, Matthias, Tabrizi, Sarah J, Craufurd, David, Arning, Larissa
Publicado em 2011

Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene

Por D'Adamo, Maria C., Gallenmüller, Constanze, Servettini, Ilenio, Hartl, Elisabeth, Tucker, Stephen J., Arning, Larissa, Biskup, Saskia, Grottesi, Alessandro, Guglielmi, Luca, Imbrici, Paola, Bernasconi, Pia, Di Giovanni, Giuseppe, Franciolini, Fabio, Catacuzzeno, Luigi, Pessia, Mauro, Klopstock, Thomas
Publicado no Front Physiol (2015)