Gertrud Eckstein - Concepedia

Author

Gertrud Eckstein

Also Known As

Eckstein, Gertrud, G Eckstein, G N Eckstein, G. Eckstein, G. N. Eckstein, G.N. Eckstein, Gertrud Eckstein, Gertrud N. Eckstein, Gertrud N. Eckstein

Publications

3.7K

Citations

H-Index

Concepts

All Affiliations

Helmholtz Zentrum München Ludwig-Maximilians-Universität München Technical University of Munich Klinikum rechts der Isar University of Bonn

About

Gertrud Eckstein is an author at Helmholtz Zentrum München specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	19	3.2K
2	Public Health	4	4	180
3	Biology	3	3	117
4	Health Sciences	1	1	273
5	Social Sciences	1	1	842

Gertrud Eckstein

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, The Lancet ChannelopathiesNeurophysiologyNeurotransmissionNeurologyNeuroscience	2005	842
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions Juliane Winkelmann, Barbara Schormair, Peter Lichtner, Nature Genetics Genome-wide Association StudyGenetic DisorderGeneticsDisease Gene IdentificationGenomic Regions	2007	690
Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3 Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Gertrud Eckstein, The American Journal of Human Genetics UrologySodium HomeostasisHypercalciuria IsGeneticsInherited Metabolic Disease	2006	367
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome Barbara Schormair, David Kemlink, Darina Roeske, Nature Genetics Clinical DisordersSignal TransductionPhysiologyRestless LegsNeurology	2008	273
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations Elin Org, S. Eyheramendy, Peeter Juhanson, Human Molecular Genetics	2009	187
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6 Sibylle G. Schwab, Joachim Hallmayer, Margot Albus, Molecular Psychiatry PsychiatryGenetic DisorderGeneticsPsychiatric GeneticsSchizophrenia	2000	169
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 Sibylle G. Schwab, Gertrud Eckstein, Joachim Hallmayer, Molecular Psychiatry Israeli FamiliesPsychiatryGenetic DisorderGeneticsPsychiatric Genetics	1997	158
Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island Alice Hadchouel, Thomas Wieland, Matthias Griese, The American Journal of Human Genetics Biallelic MutationsAdvanced Lung DiseaseMethionyl-trna Synthetase CauseGeneticsPulmonary Alveolar Proteinosis	2015	124
Congenital heart disease risk loci identified by genome-wide association study in European patients Harald Lahm, Meiwen Jia, Martina Dreßen, Journal of Clinical Investigation GeneticsGenetic EpidemiologyHuman PolymorphismGenomicsCongenital Heart Anomaly	2020	107
Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy Laura S. Kremer, Felix Distelmaier, Bader Alhaddad, The American Journal of Human Genetics CardiomyopathyGenetic DisorderGeneticsMolecular GeneticsBi-allelic Truncating Mutations	2016	105

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