Laura P.W. Ranum - Concepedia

Author

Laura P.W. Ranum

Also Known As

L P Ranum, L P W Ranum, L Ranum, L. P. W. Ranum, L. P.W. Ranum, L. Ranum, L.P. W. Ranum, L.P.W. Ranum, LAURA P.W. RANUM, Laura P W Ranum

158

Publications

16.7K

Citations

H-Index

119

Concepts

All Affiliations

University of Minnesota University of Florida Florida College Institute of Human Genetics Johns Hopkins University

About

Laura P.W. Ranum is an author at University of Minnesota specializing in medicine, genetics, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	45	8.9K
2	Natural Sciences	13	13	1.4K
3	Health Sciences	4	4	576
4	Engineering	2	2	28
5	Public Health	1	1	83

Laura P.W. Ranum

Publications

14.2K

Citations

H-Index

Page 1

	Year	Citations
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1 Harry T. Orr, Ming‐Yi Chung, Sandro Banfi, Nature Genetics Molecular NeuroscienceGeneticsMolecular BiologyMolecular GeneticsNeuroscience	1993	1.6K
Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of <i>ZNF9</i> Christina L. Liquori, K. Ricker, Melinda L. Moseley, Science	2001	1.2K
Non-ATG–initiated translation directed by microsatellite expansions Tao Zu, Brian B. Gibbens, Noelle S. Doty, Proceedings of the National Academy of Sciences Trinucleotide ExpansionsNeurodegenerative DiseasesAllelic VariantGenetic DisorderMedicine	2010	896
RAN proteins and RNA foci from antisense transcripts in <i>C9ORF72</i> ALS and frontotemporal dementia Tao Zu, Yuanjing Liu, Mónica Báñez-Coronel, Proceedings of the National Academy of Sciences GeneticsAntisense TranscriptsDisease Gene IdentificationSocial SciencesNeurobiology Of Disease	2013	772
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8) Michael D. Koob, Melinda L. Moseley, Lawrence J. Schut, Nature Genetics Molecular NeuroscienceNeurological DisorderNeuroanatomyGeneticsSpinocerebellar Ataxia	1999	636
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I Ming‐Yi Chung, Laura P.W. Ranum, Lisa Duvick, Nature Genetics Neurodegenerative DiseasesGenetic DisorderGeneticsSpinocerebellar Ataxia TypeDegenerative Disease	1993	482
Myotonic dystrophy type 2 John Day, K. Ricker, Jennifer F. Jacobsen, Neurology	2003	456
Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8 Melinda L. Moseley, Tao Zu, Yoshio Ikeda, Nature Genetics Neurodegenerative DiseasesMolecular NeuroscienceCag Expansion TranscriptsBidirectional ExpressionNeuroscience	2006	419
Spectrin mutations cause spinocerebellar ataxia type 5 Yoshio Ikeda, Katherine A. Dick, Marcy R. Weatherspoon, Nature Genetics Molecular NeuroscienceMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2006	382
C9orf72 BAC Mouse Model with Motor Deficits and Neurodegenerative Features of ALS/FTD Yuanjing Liu, Amrutha Pattamatta, Tao Zu, Neuron Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurodegenerative FeaturesDegenerative DiseaseDegenerative Pathology	2016	369

Page 1