María Isabel Behrens

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

Life Sciences, Genetics, Molecular Genetics +16

The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

Robert Clark, M. Hutton, M. Fuldner et al. · Nature Genetics · 1995 · 476 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Alzheimer disease and cancer

Catherine M. Roe, María Isabel Behrens, Chengjie Xiong et al. · Neurology · 2005 · 230 citations

Medicine, Oncology, Cancer Epidemiology +10

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin

Odity Mukherjee, Pau Pástor, Nigel J. Cairns et al. · Annals of Neurology · 2006 · 188 citations · Full text

Life Sciences, Genetics, Neurology +17

Inner membrane protease I, an enzyme mediating intramitochondrial protein sorting in yeast.

Achim Schneider, María Isabel Behrens, Philipp E. Scherer et al. · The EMBO Journal · 1991 · 187 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +10