Julia Stadler

Author PubWeight™ 17.25^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	Atlastin GTPases are required for Golgi apparatus and ER morphogenesis.	Hum Mol Genet	2008	2.28
2	Intra- and intermolecular domain interactions of the C-terminal GTPase effector domain of the multimeric dynamin-like GTPase Drp1.	J Biol Chem	2004	2.19
3	L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system.	J Biol Chem	2003	2.12
4	Comparison of porcine epidemic diarrhea viruses from Germany and the United States, 2014.	Emerg Infect Dis	2015	2.08
5	Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin.	J Biol Chem	2003	2.07
6	SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development.	Hum Mol Genet	2006	1.59
7	A lethal de novo mutation in the middle domain of the dynamin-related GTPase Drp1 impairs higher order assembly and mitochondrial division.	J Biol Chem	2010	1.56
8	SUMOylation of the mitochondrial fission protein Drp1 occurs at multiple nonconsensus sites within the B domain and is linked to its activity cycle.	FASEB J	2009	1.45
9	Characterization of a novel SPG3A deletion in a French-Canadian family.	Ann Neurol	2007	0.99
10	Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling.	Hum Mol Genet	2012	0.92
11	Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons.	Neurogenetics	2010	0.82