Ingrid Goebel

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

Alfredo Ramı́rez, André Heimbach, Jan Gründemann et al. · Nature Genetics · 2006 · 1.2K citations

Alzheimer's Disease, P-type Atpase, Hereditary Parkinsonism +10

Dynamic m ⁶ A methylation facilitates mRNA triaging to stress granules

Maximilian Anders, Irina Chelysheva, Ingrid Goebel et al. · Life Science Alliance · 2018 · 185 citations · Full text

Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

Guntram Borck, Atteeq U. Rehman, Kwanghyuk Lee et al. · The American Journal of Human Genetics · 2011 · 119 citations · Full text

Genetics, Audiology, Auditory Physiology +7

Rare missense variants inATP1A2 in families with clustering of common forms of migraine

Unda Todt, Martin Dichgans, Karin Jurkat‐Rott et al. · Human Mutation · 2005 · 92 citations

Atpase Activity, Cluster Headache, Molecular Neuroscience +14

Identification of a novel mutation in the coding region of the grey-lethal gene<i>OSTM1</i>in human malignant infantile osteopetrosis

Alfredo Ramı́rez, Julia Faupel, Ingrid Goebel et al. · Human Mutation · 2004 · 78 citations · Full text

Sclerostin, Engineering, Genetics +18