James M. Killian - Concepedia

Concepedia

Author

James M. Killian

Baylor College of Medicine

Also Known As

J Killian, J M Killian, J. Killian, J. M. Killian, J.M. Killian, JAMES M. KILLIAN, James Killian, James M Killian, James M. Killian

55

Publications

4.6K

Citations

28

H-Index

105

Concepts

All Affiliations

Baylor College of Medicine Multiple Sclerosis Center of Atlanta Texas Children's Hospital Tulane University Shanghai Institutes for Biological Sciences

JM

About

James M. Killian is an author at Baylor College of Medicine specializing in medicine, neurology, and health sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	18	3.1K
2	Health Sciences	7	7	944
3	Social Sciences	3	3	141
4	Natural Sciences	1	1	69
5	Anesthesia	1	1	329

James M. Killian

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33

Publications

4.6K

Citations

28

H-Index

	Year	Citations
DNA duplication associated with Charcot-Marie-Tooth disease type 1A James R. Lupski, Roberto Montes‐de‐Oca‐Luna, Susan Slaugenhaupt, Cell Mendelian DisorderGenetic DisorderGeneticsDna DuplicationPathology	1991	1.3K
Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination Laura E. Warner, Max J. Hilz, Stanley H. Appel, Neuron	1996	362
Carbamazepine in the Treatment of Neuralgia James M. Killian Archives of Neurology Pain MedicinePsychotropic MedicationNeuropathic PainPharmacotherapyEpilepsy	1968	329
Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2) Frank Greenberg, Richard A. Lewis, Lorraine Potocki, American Journal of Medical Genetics Neurological DisorderDiagnosisPathologyHuman PathologyClinical Genetics	1996	325
Diagnosis of acute cerebral infarction: comparison of CT and MR imaging. R. Nick Bryan, L. M. Levy, W. D. Whitlow, PubMed	1991	276
Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1A Benjamin B. Roa, Carlos A. Garcia, Pentao Liu, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathology	1993	159
Increased CD8+ Cytotoxic T Cell Responses to Myelin Basic Protein in Multiple Sclerosis Ying C. Q. Zang, Sufang Li, Víctor M. Rivera, The Journal of Immunology	2004	142
CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1 Amanda J. Ward, Mendell Rimer, James M. Killian, Human Molecular Genetics Muscle FunctionMolecular RegulationGeneticsPathologyCugbp1 Overexpression	2010	142
GSK3β mediates muscle pathology in myotonic dystrophy Karlie Jones, Christina Wei, Polina Iakova, Journal of Clinical Investigation Muscle FunctionMolecular RegulationNeuromusculoskeletal DisorderSkeletal Muscle WeaknessCellular Physiology	2012	127
Interferon beta induces T-helper 2 immune deviation in MS M Kozovska, Jian Hong, Ying C. Q. Zang, Neurology	1999	112

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