W. Schröder

Prevalence of factor V Leiden mutation in various populations

F. H. Herrmann, M. Koesling, W. Schröder et al. · Genetic Epidemiology · 1997 · 102 citations · Full text

High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one‐third of probands are minors

Stefanie Spiegler, Juliane Najm, Jian Liu et al. · Molecular Genetics & Genomic Medicine · 2014 · 71 citations · Full text

Factor V Leiden, Prothrombin Gene G20210A Variant, and Methylenetetrahydrofolate Reductase C677T Genotype in Young Adults With Ischemic Stroke

K. Bykowska, Hubert Kwieciński, Anatol Mickielewicz et al. · Clinical and Applied Thrombosis/Hemostasis · 2001 · 64 citations

Young Adults, Genetic Epidemiology, Pathology +21

New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update

Claire Navarro, Vera Esteves‐Vieira, Sébastien Courrier et al. · European Journal of Human Genetics · 2013 · 59 citations · Full text

Restrictive Dermopathy, Autoimmune Disease, Mendelian Disorder +10

Detection of <i>TSPY</i> protein in a unilateral microscopic gonadoblastoma of a Turner mosaic patient with a Y‐derived marker chromosome

Ralf Hildenbrand, W. Schröder, E. Brude et al. · The Journal of Pathology · 1999 · 46 citations

Marker Chromosome, Cytogenetics, Genetics +19