Natalia K. Hofmann

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

Holly N. Cukier, Nicole Dueker, Susan H. Slifer et al. · Molecular Autism · 2014 · 329 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy

Arthur van den Wijngaard, Paul G.A. Volders, J. Peter van Tintelen et al. · Netherlands Heart Journal · 2011 · 63 citations · Full text

Medicine, Cardiology, Genetics +9

RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways

Olivia K. Gardner, Lily Wang, Derek Van Booven et al. · Human Molecular Genetics · 2019 · 30 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

Dissecting the role of Amerindian genetic ancestry and the ApoE ε4 allele on Alzheimer disease in an admixed Peruvian population

Maria Victoria Marca-Ysabel, Farid Rajabli, Mario Cornejo‐Olivas et al. · Neurobiology of Aging · 2020 · 26 citations · Full text

Medicine, Genetics, Neurology +17

Identifying differential regulatory control of <i>APOE</i> ɛ4 on African versus European haplotypes as potential therapeutic targets

Karen Nuytemans, Marina Lipkin Vasquez, Liyong Wang et al. · Alzheimer s & Dementia · 2022 · 21 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16