Search Results - author:"Bauer, Peter" OR author2:"Bauer, Peter" OR author_corporate:"Bauer, Peter"

AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia by Terhal, Paulien (Author) , Venhuizen, Anton J. (Author) , Lessel, Davor (Author) , Tan, Wen-Hann (Author) , Alswaid, Abdulrahman (Author) , Grün, Regina (Author) , Alzaidan, Hamad I. (Author) , von Kroge, Simon (Author) , Ragab, Nada (Author) , Hempel, Maja (Author) , Kubisch, Christian (Author) , Novais, Eduardo (Author) , Cristobal, Alba (Author) , Tripolszki, Kornelia (Author) , Bauer, Peter (Author) , Fischer-Zirnsak, Björn (Author) , Nievelstein, Rutger A. J. (Author) , van Dijk, Atty (Author) , Nikkels, Peter (Author) , Oheim, Ralf (Author) , Hahn, Heidi (Author) , Bertoli-Avella, Aida (Author) , Maurice, Madelon M. (Author) , Kornak, Uwe (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women by Sepahi, Ilnaz (Author) , Faust, Ulrike (Author) , Sturm, Marc (Author) , Bosse, Kristin (Author) , Kehrer, Martin (Author) , Heinrich, Tilman (Author) , Grundman-Hauser, Kathrin (Author) , Bauer, Peter (Author) , Ossowski, Stephan (Author) , Susak, Hana (Author) , Varon, Raymonda (Author) , Schröck, Evelin (Author) , Niederacher, Dieter (Author) , Auber, Bernd (Author) , Sutter, Christian (Author) , Nguyen, Huu Phuc (Author) ,

• Resolving-System, kostenfrei
• Resolving-System, kostenfrei
• Verlag, kostenfrei, Volltext

Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias by Jacobi, Heike (Author) , Tezenas du Montcel, Sophie (Author) , Bauer, Peter (Author) ,

• Verlag, Volltext

Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study by Diallo, Alhassane (Author) , Jacobi, Heike (Author) , Cook, Arron (Author) , Labrum, Robyn (Author) , Durr, Alexandra (Author) , Schmitz-Hübsch, Tanja (Author) , Schöls, Ludger (Author) , Hengel, Holger (Author) , Schulz, Jörg B. (Author) , Bauer, Peter (Author) , Kang, Jun-Suk (Author) , Tezenas du Montcel, Sophie (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

LRRK2 contributes to monocyte dysregulation in Parkinson’s disease: letter to the editor by Bliederhäuser, Corinna (Author) , Zondler, Lisa (Author) , Grozdanov, Veselin (Author) , Ruf, Wolfgang P. (Author) , Brenner, David (Author) , Melrose, Heather L. (Author) , Bauer, Peter (Author) , Ludolph, Albert C. (Author) , Gillardon, Frank (Author) , Kassubek, Jan Rainer (Author) , Weishaupt, Jochen H. (Author) , Danzer, Karin M. (Author) ,

• Verlag, lizenzpflichtig, Volltext

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients by Schüle-Freyer, Rebecca (Author) , Wiethoff, Sarah (Author) , Martus, Peter (Author) , Karle, Kathrin Nora (Author) , Otto, Susanne (Author) , Klebe, Stephan (Author) , Klimpe, Sven (Author) , Gallenmüller, Constanze (Author) , Kurzwelly, Delia (Author) , Henkel, Dorothea (Author) , Rimmele, Florian D. (Author) , Stolze, Henning Wolfgang (Author) , Kohl, Zacharias (Author) , Kassubek, Jan Rainer (Author) , Klockgether, Thomas (Author) , Vielhaber, Stefan (Author) , Kamm, Christoph (Author) , Klopstock, Thomas (Author) , Bauer, Peter (Author) , Züchner, Stephan (Author) , Liepelt-Scarfone, Inga (Author) , Schöls, Ludger (Author) ,

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients by Schüle-Freyer, Rebecca (Author) , Wiethoff, Sarah (Author) , Martus, Peter (Author) , Karle, Kathrin Nora (Author) , Otto, Susanne (Author) , Klebe, Stephan (Author) , Klimpe, Sven (Author) , Gallenmüller, Constanze (Author) , Kurzwelly, Delia (Author) , Henkel, Dorothea (Author) , Rimmele, Florian D. (Author) , Stolze, Henning Wolfgang (Author) , Kohl, Zacharias (Author) , Kassubek, Jan Rainer (Author) , Klockgether, Thomas (Author) , Vielhaber, Stefan (Author) , Kamm, Christoph (Author) , Klopstock, Thomas (Author) , Bauer, Peter (Author) , Züchner, Stephan (Author) , Liepelt-Scarfone, Inga (Author) , Schöls, Ludger (Author) ,

• Resolving-System, Volltext

A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes

De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation by Grasshoff, Ute (Author) , Bonin, Michael (Author) , Goehring, Ina (Author) , Ekici, Arif (Author) , Dufke, Andreas (Author) , Cremer, Kirsten (Author) , Wagner, Nicholas (Author) , Rossier, Eva (Author) , Jauch, Anna (Author) , Walter, Michael (Author) , Bauer, Claudia (Author) , Bauer, Peter (Author) , Horber, Karl (Author) , Beck-Woedl, Stefanie (Author) , Wieczorek, Dagmar (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

The effects of COMT (Val108/158Met) and DRD4 (SNP -521) dopamine genotypes on brain activations related to valence and magnitude of rewards by Càmara, Estela (Author) , Krämer, Ulrike M. (Author) , Cunillera, Toni (Author) ,

Genetic variability in the dopamine system (dopamine receptor D4, catechol-O-methyltransferase) modulates neurophysiological responses to gains and losses by Marco-Pallarés, Josep (Author) , Cucurell, David (Author) , Cunillera, Toni (Author) ,

• Resolving-System

The impact of catechol-O-methyltransferase and dopamine D4 receptor genotypes on neurophysiological markers of performance monitoring by Krämer, Ulrike M. (Author) , Cunillera, Toni (Author) , Càmara, Estela (Author) ,

• Resolving-System, lizenzpflichtig, Volltext