T. F. Wienker

Quantitative Analysis of Survival Motor Neuron Copies: Identification of Subtle SMN1 Mutations in Patients with Spinal Muscular Atrophy, Genotype-Phenotype Correlation, and Implications for Genetic Counseling

Micaela A. Godoy Herz, A Wetter, S. Moskau et al. · The American Journal of Human Genetics · 1999 · 364 citations · Full text

Medicine, Genetics, Molecular Genetics +17

A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function

Andreas Reif, Sarah Herterich, Alexander Strobel et al. · Molecular Psychiatry · 2006 · 210 citations

Medicine, Neuroscience, Psychiatry +14

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

Michael Steffens, Costin Leu, Ann‐Kathrin Ruppert et al. · Human Molecular Genetics · 2012 · 151 citations · Full text

Life Sciences, Genetics, Human Genetics +15

β-2 Adrenoceptor genetic variation is associated with genetic predisposition to essential hypertension: The Bergen Blood Pressure Study

Bernd Timmermann, Friedrich C. Luft, Eva Gerdts et al. · Kidney International · 1998 · 144 citations · Full text

Medicine, Cardiology, Genetics +15

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

M. Rietschel, Manuel Mattheisen, F. Degenhardt et al. · Molecular Psychiatry · 2011 · 116 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15