B. Miterski

发表

Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data

Ansgar Steland, Stefan Böhringer, A. Steland, 2003, European Journal of Human Genetics.

Polymerase chain reaction—single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes

M. Kauth, J. Epplen, F. Tschentscher, 1998, Electrophoresis.

Neurophysiological findings in SPG4 patients differ from other types of spastic paraplegia

L. Schöls, H. Przuntek, J. Epplen, 2003, Neurology.

SCA2 alleles are not general predisposition factors for multiple sclerosis

J. Epplen, D. Poehlau, B. Miterski, 2000, Neurogenetics.

New Mutations of EXT1 and EXT2 Genes in German Patients with Multiple Osteochondromas

C. Zweier, A. Bohring, W. Heinritz, 2009, Annals of human genetics.

Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene

Wei Li, R. Spritz, D. Bennett, 2002, Nature Genetics.

Inhibitors in the NFκB cascade comprise prime candidate genes predisposing to multiple sclerosis, especially in selected combinations

S. Böhringer, J. Epplen, W. Klein, 2002, Genes and Immunity.

Association of a common polymorphism in the promoter of UCP2 with susceptibility to multiple sclerosis

R. Gold, P. Rieckmann, U. Zettl, 2005, Journal of Molecular Medicine.

A genome screen for linkage disequilibrium in HLA-DRB1*15-positive Germans with multiple sclerosis based on 4666 microsatellite markers

S. Sawcer, A. Compston, Stefan Boehringer, 2002, Human Genetics.

The interferon gene cluster: a candidate region for MS predisposition?

C. Hardt, B. Miterski, J. Epplen, 1999, Genes and Immunity.

Complex genetic predisposition in adult and juvenile rheumatoid arthritis

J. Epplen, W. Klein, B. Miterski, 2004, BMC Genetics.

Multiple Sclerosis Severity Score: Using disability and disease duration to rate disease severity

G. Salemi, M. Trojano, G. Edan, 2005, Neurology.

Does the tuberous sclerosis complex include clivus chordoma? A case report

J. Epplen, J. Börgel, B. Miterski, 2001, European Journal of Pediatrics.

PTPRC (CD45) is not associated with multiple sclerosis in a large cohort of German patients

J. Epplen, S. Schimrigk, B. Miterski, 2002, BMC Medical Genetics.

Differential stability of the (GAA)n tract in the Friedreich ataxia (STM7) gene

L. Schöls, J. Epplen, B. Miterski, 1997, Human Genetics.

Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia

L. Schöls, W. Engel, J. Epplen, 2002, Human mutation.

Mutation analysis and association studies of nuclear factor-κB1 in sporadic Parkinson's disease patients

H. Przuntek, R. Krüger, L. Schöls, 2002, Journal of Neural Transmission.

The multiple sclerosis severity score

S. Sawcer, X. Montalban, E. Celius, 2003 .