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Publications by Maria Hoeltzenbein
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
American Journal of Human Genetics
Genetics
Mutations in the ZNF41 Gene Are Associated With Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation
American Journal of Human Genetics
Genetics
Hereditary Spastic Paraplegia Caused by Mutations in the SPG4 Gene
European Journal of Human Genetics
Genetics
New Alström Syndrome Phenotypes Based on the Evaluation of 182 Cases
Archives of Internal Medicine
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Recent Human Adaptation: Genomic Approaches, Interpretation and Insights
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ChIP–seq and Beyond: New and Improved Methodologies to Detect and Characterize Protein–DNA Interactions
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Sex and the Singular DM Domain: Insights Into Sexual Regulation, Evolution and Plasticity
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Putting Gene Essentiality Into Context
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Promoter-Proximal Pausing of RNA Polymerase II: Emerging Roles in Metazoans
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Stress and the Epigenetic Landscape: A Link to the Pathobiology of Human Diseases?
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Autoimmune Diseases — Connecting Risk Alleles With Molecular Traits of the Immune System
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Bayesian Molecular Clock Dating of Species Divergences in the Genomics Era
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