E. Tilch

发表

Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice

A. Altmann, B. Pütz, B. Müller-Myhsok, 2015, PloS one.

Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon

C. Gieger, M. Waldenberger, H. Fuchs, 2014, Genome research.

Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.

C. Gieger, A. Peters, W. Oertel, 2014, American journal of human genetics.

Using the MCF10A/MCF10CA1a Breast Cancer Progression Cell Line Model to Investigate the Effect of Active, Mutant Forms of EGFR in Breast Cancer Development and Treatment Using Gefitinib

Sean M. Grimmond, Peter T. Simpson, Georgia Chenevix-Trench, 2015, PloS one.

Mutations in EGFR, BRAF and RAS are rare in triple-negative and basal-like breast cancers from Caucasian women

S. Fox, A. Vargas, S. Lakhani, 2013, Breast Cancer Research and Treatment.

Identification of Restless Legs Syndrome Genes by Mutational Load Analysis

C. Gieger, A. Peters, A. Hoischen, 2019, Annals of neurology.

Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry

Stephen H. Bell, J. Danesh, C. Gieger, 2022 .

alters enhancer function in the developing telencephalon Meis 1 Restless Legs Syndrome-associated intronic common variant in Material Supplemental

C. Gieger, M. Waldenberger, H. Fuchs, 2014 .

ExomeChip-based rare variant association study in restless legs syndrome.

M. Nöthen, M. Müller-Nurasyid, B. Müller-Myhsok, 2022, Sleep medicine.

Genetics of Restless Legs Syndrome

E. Tilch, 2017 .

Episignature analysis of moderate effects and mosaics

R. Jech, B. Haslinger, J. Winkelmann, 2023, European Journal of Human Genetics.

Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis

J. Danesh, C. Gieger, A. Auton, 2017, The Lancet Neurology.

Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice

A. Altmann, B. Pütz, B. Müller-Myhsok, 2015, PloS one.

Phenotypic and genome-wide studies on dicarbonyls: major associations to glomerular filtration rate and gamma-glutamyltransferase activity

C. Gieger, B. Schormair, K. Oexle, 2024, EBioMedicine.

Restless Legs Syndrome-associated intronic common-variant in Meis 1 alters enhancer function in the developing telencephalon Supplemental Material

Wolfgang, C. Gieger, M. Waldenberger, 2014 .