C. Becker

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

K Hasselbacher, Roger C. Wiggins, Verena Matejas et al. · Kidney International · 2006 · 214 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Hypomorphic mutations in meckelin (<i>MKS3/TMEM67</i>) cause nephronophthisis with liver fibrosis (NPHP11)

Edgar A. Otto, Kálmán Tory, Massimo Attanasio et al. · Journal of Medical Genetics · 2009 · 129 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Mutations of NPHP2 and NPHP3 in infantile nephronophthisis

Kálmán Tory, Caroline Rousset‐Rouvière, Marie-Claire Gübler et al. · Kidney International · 2009 · 120 citations

Medicine, Genetics, Nephrology +5

Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays

Juliane Hoyer, Alexander Dreweke, C. Becker et al. · Journal of Medical Genetics · 2007 · 118 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21‐q23

Manfred Stuhrmann, HC Hennies, Kai Brakensiek et al. · Clinical Genetics · 2008 · 62 citations

Life Sciences, Dermatology, Genetics +14