Michael Nalls

Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

Jean-François Dartigues, Günther Deuschl, Yoav Ben-Shlomo, 2017, Genome Biology.

Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

Sonja W. Scholz, Hannah A. Pliner, John D. Eicher, 2019, Annals of neurology.

Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein

Ahmad Al Khleifat, M. Nalls, M. Daly, 2019, Nature Neuroscience.

Creating the Pick’s disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick’s disease

Derek H. Oakley, A. Singleton, D. Vitale, 2023, medRxiv.

omicSynth: an Open Multi-omic Community Resource for Identifying Druggable Targets across Neurodegenerative Diseases

A. Singleton, Mary B Makarious, H. Leonard, 2023, medRxiv.

Longitudinal Risk Factors For Developing Depression in Parkinson’s Disease

A. Singleton, H. Leonard, H. Iwaki, 2021 .

Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinsons Disease in African and African Admixed Populations

D. Hernandez, A. Singleton, H. Leonard, 2023, medRxiv.

Parallel CRISPR-Cas9 screens identify mechanisms of PLIN2 and lipid droplet regulation.

Sayed Hadi Hashemi, F. Faghri, J. Olzmann, 2023, Developmental cell.