Gertrud Eckstein
Helmholtz Zentrum München(DE)
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Mitochondrial Function and Pathology, Genetic Neurodegenerative Diseases, Parkinson's Disease Mechanisms and Treatments, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine(2005)842 cited
- → Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions(2007)699 cited
- → Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3(2006)369 cited
- → PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome(2008)281 cited
- → Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations(2009)189 cited
- → A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6(2000)169 cited
- → Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis(1997)158 cited
- → Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island(2015)124 cited
- → Congenital heart disease risk loci identified by genome-wide association study in European patients(2020)112 cited
- → Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy(2016)105 cited