Monika Hartig

Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Monika Hartig, Arcangela Iuso, Tobias B. Haack et al. · The American Journal of Human Genetics · 2011 · 262 citations · Full text

Neurodegenerative Diseases, Alzheimer's Disease, Mitochondrial Function +14

Genotypic and phenotypic spectrum of <i>PANK2</i> mutations in patients with neurodegeneration with brain iron accumulation

Monika Hartig, Konstanze Hörtnagel, Barbara Garavaglia et al. · Annals of Neurology · 2006 · 182 citations

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy

Tobias B. Haack, Erika Ignatius, Javier Calvo‐Garrido et al. · The American Journal of Human Genetics · 2016 · 117 citations · Full text

Neurodegenerative Diseases, Neurological Disorder, Autophagy +8

The role of verbal self-instructions in children's resistance to temptation.

Monika Hartig, Frederick H. Kanfer · Journal of Personality and Social Psychology · 1973 · 111 citations

Behavioural Psychology, Child Psychology, Cognitive Science +10

Mitochondrial membrane protein associated neurodegenration: A novel variant of neurodegeneration with brain iron accumulation

Eva C. Schulte, Malte Christian Claussen, Angela Jochim et al. · Movement Disorders · 2012 · 47 citations