Denise Levitch

<i>TDP‐43</i> A315T mutation in familial motor neuron disease

Michael A. Gitcho, Robert H. Baloh, Sumi Chakraverty et al. · Annals of Neurology · 2008 · 610 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

Carlos Cruchaga, Celeste M. Karch, Sheng Chih Jin et al. · Nature · 2013 · 476 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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

Genotype patterns at<i>PICALM, CR1, BIN1, CLU</i>, and<i>APOE</i>genes are associated with episodic memory

Sandra Barral, Thomas D. Bird, Alison Goate et al. · Neurology · 2012 · 104 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

TYROBP genetic variants in early-onset Alzheimer's disease

Cyril Pottier, Thomas A. Ravenscroft, Patricia H. Brown et al. · Neurobiology of Aging · 2016 · 103 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14