Torthaí cuardaigh - Arning, Larissa

Handedness genetics: considering the phenotype de réir Ocklenburg, Sebastian, Beste, Christian, Arning, Larissa

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31) de réir Schlang, Katharina J, Arning, Larissa, Epplen, Joerg T, Stemmler, Susanne

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

DRD1 and DRD2 Genotypes Modulate Processing Modes of Goal Activation Processes during Action Cascading de réir Stock, Ann-Kathrin, Arning, Larissa, Epplen, Jörg T., Beste, Christian

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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) de réir Arning, Larissa, Kraus, Peter H, Saft, Carsten, Andrich, Jürgen, Epplen, Jörg T

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Genomic NGFB variation and multiple sclerosis in a case control study de réir Akkad, Denis A, Kruse, Niels, Arning, Larissa, Gold, Ralf, Epplen, Jörg T

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

PGC-1alpha as modifier of onset age in Huntington disease de réir Taherzadeh-Fard, Elahe, Saft, Carsten, Andrich, Jürgen, Wieczorek, Stefan, Arning, Larissa

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Glutathione S-Transferase Ω 1 variation does not influence age at onset of Huntington's disease de réir Arning, Larissa, Jagiello, Peter, Wieczorek, Stefan, Saft, Carsten, Andrich, Jürgen, Epplen, Jörg T

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

A large-scale estimate on the relationship between language and motor lateralization de réir Packheiser, Julian, Schmitz, Judith, Arning, Larissa, Beste, Christian, Güntürkün, Onur, Ocklenburg, Sebastian

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Author Correction: A large-scale estimate on the relationship between language and motor lateralization de réir Packheiser, Julian, Schmitz, Judith, Arning, Larissa, Beste, Christian, Güntürkün, Onur, Ocklenburg, Sebastian

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Cholecystokinin A Receptor (CCKAR) Gene Variation Is Associated with Language Lateralization de réir Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes de réir Aydin, Gülsah, Dekomien, Gabriele, Hoffjan, Sabine, Gerding, Wanda Maria, Epplen, Jörg T., Arning, Larissa

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

The Role of DRD1 and DRD2 Receptors for Response Selection Under Varying Complexity Levels: Implications for Metacontrol Processes de réir Zink, Nicolas, Bensmann, Wiebke, Arning, Larissa, Colzato, Lorenza S, Stock, Ann-Kathrin, Beste, Christian

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Failure to confirm influence of Methyltetrahydrofolate reductase (MTHFR) polymorphisms on age at onset of Huntington disease de réir Hansen, Wiebke, Saft, Carsten, Andrich, Jürgen, Müller, Thomas, Wieczorek, Stefan, Epplen, Jörg T, Arning, Larissa

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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 de réir Wagenleiter, Sonja EN, Jagiello, Peter, Akkad, Denis A, Arning, Larissa, Griga, Thomas, Klein, Wolfram, Epplen, Jörg T

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Hepatic mitochondrial dysfunction in Friedreich Ataxia de réir Stüwe, Sven H, Goetze, Oliver, Arning, Larissa, Banasch, Matthias, Schmidt, Wolfgang E, Schöls, Ludger, Saft, Carsten

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

No association between polymorphisms in the BDNF gene and age at onset in Huntington disease de réir Mai, Maren, Akkad, Amer D, Wieczorek, Stefan, Saft, Carsten, Andrich, Jürgen, Kraus, Peter H, Epplen, Jörg T, Arning, Larissa

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease de réir Taherzadeh-Fard, Elahe, Saft, Carsten, Akkad, Denis A, Wieczorek, Stefan, Haghikia, Aiden, Chan, Andrew, Epplen, Jörg T, Arning, Larissa

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Genetic variation in dopamine availability modulates the self-reported level of action control in a sex-dependent manner de réir Schlüter, Caroline, Arning, Larissa, Fraenz, Christoph, Friedrich, Patrick, Pinnow, Marlies, Güntürkün, Onur, Beste, Christian, Ocklenburg, Sebastian, Genc, Erhan

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Polygenic scores for handedness and their association with asymmetries in brain structure de réir Ocklenburg, Sebastian, Metzen, Dorothea, Schlüter, Caroline, Fraenz, Christoph, Arning, Larissa, Streit, Fabian, Güntürkün, Onur, Kumsta, Robert, Genç, Erhan

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1 de réir Steinemann, Doris, Arning, Larissa, Praulich, Inka, Stuhrmann, Manfred, Hasle, Henrik, Starý, Jan, Schlegelberger, Brigitte, Niemeyer, Charlotte M., Flotho, Christian

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán