Jill A. Morris - Concepedia

Author

Jill A. Morris

National Institute of Neurological Disorders and Stroke ORCID

Also Known As

Codrin I. Lungu, J A Morris, J. A. Morris, J. Morris, J.A Morris, J.A. Morris, Jill A Morris, Jill A. Morris, Jill Morris

Publications

5.3K

Citations

H-Index

Concepts

All Affiliations

National Institute of Neurological Disorders and Stroke National Institutes of Health United States Military Academy National Human Genome Research Institute Massachusetts General Hospital

About

Jill A. Morris is an author at National Institute of Neurological Disorders and Stroke specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	19	1.3K
2	Social Sciences	5	5	261
3	Natural Sciences	4	4	451
4	Health Sciences	3	3	185
5	Engineering	1	2	44

Jill A. Morris

Publications

Citations

H-Index

Page 1

	Year	Citations
Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis Eugene D. Carstea, Jill A. Morris, Katherine Coleman, Science	1997	1.5K
Murine Model of Niemann-Pick C Disease: Mutation in a Cholesterol Homeostasis Gene Stacie K. Loftus, Jill A. Morris, Eugene D. Carstea, Science	1997	804
DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation Jill A. Morris Human Molecular Genetics Centrosome-associated ProteinMolecular BiologySynaptic SignalingPsychiatric GeneticsDisrupted-in-schizophrenia 1	2003	375
The Niemann-Pick C1 Protein Resides in a Vesicular Compartment Linked to Retrograde Transport of Multiple Lysosomal Cargo Edward B. Neufeld, Meryl E. Wastney, Shutish C. Patel, Journal of Biological Chemistry	1999	374
Immunoglobulin Binding Protein (BiP) Function Is Required to Protect Cells from Endoplasmic Reticulum Stress but Is Not Required for the Secretion of Selective Proteins Jill A. Morris, Andrew J. Dorner, Chris Edwards, Journal of Biological Chemistry	1997	350
Niemann-Pick C1 Disease: The I1061T Substitution Is a Frequent Mutant Allele in Patients of Western European Descent and Correlates with a Classic Juvenile Phenotype Gilles Millat, Christophe Marçais, Mohammad A. Rafi, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathogenesisInherited Metabolic Disease	1999	204
Differential Interaction of Coagulation Factor VIII and Factor V with Protein Chaperones Calnexin and Calreticulin Steven W. Pipe, Jill A. Morris, Jay Shah, Journal of Biological Chemistry	1998	147
Mutagenesis of the putative sterol-sensing domain of yeast Niemann Pick C–related protein reveals a primordial role in subcellular sphingolipid distribution Krishnamurthy Malathi, Katsumi Higaki, Arthur H. Tinkelenberg, The Journal of Cell Biology	2004	142
Expression of disrupted-in-schizophrenia-1, a schizophrenia-associated gene, is prominent in the mouse hippocampus throughout brain development Christopher P. Austin, Betty Ky, Lan Ma, Neuroscience Developmental BiologySchizophrenia-associated GeneBrain DevelopmentGeneticsPsychiatric Genetics	2004	139
Cloning and Characterization of Disc1, the Mouse Ortholog of DISC1 (Disrupted-in-Schizophrenia 1) Lei Ma, Yuan Liu, Betty Ky, Genomics Developmental BiologyMolecular NeuroscienceMouse OrthologMedicinePsychiatric Genetics	2002	99

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