Joline Dalton - Concepedia

Author

Joline Dalton

Also Known As

J C Dalton, J. C. Dalton, J. Dalton, J.C. Dalton, Joline C Dalton, Joline C. Dalton, Joline Dalton, Sarcoplasmic/endoplasmic Reticulum Ca -atpase, V Moriondo

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

University of Minnesota University of Washington UNSW Sydney University of Iowa Stanford University

About

Joline Dalton is an author at University of Minnesota specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	1.1K
2	Health Sciences	1	1	162
3	Social Sciences	1	1	106
4	Biology	1	1	96
5	Child Development	1	1	106

Joline Dalton

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Myotonic dystrophy type 2 John Day, K. Ricker, Jennifer F. Jacobsen, Neurology	2003	456
Spectrin mutations cause spinocerebellar ataxia type 5 Yoshio Ikeda, Katherine A. Dick, Marcy R. Weatherspoon, Nature Genetics Molecular NeuroscienceMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2006	382
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort Kevin M. Flanigan, Diane M. Dunn, Andrew von Niederhausern, Human Mutation	2009	308
Insulin Receptor Splicing Alteration in Myotonic Dystrophy Type 2 Rajesh S. Savkur, Anne V. Philips, Thomas A. Cooper, The American Journal of Human Genetics Metabolic SyndromePhysiologyDiabetesEndocrinologyMedicine	2004	162
MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain Marianne Goodwin, Apoorva Mohan, Ranjan Batra, Cell Reports	2015	151
Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures Slavé Petrovski, Sébastien Küry, Candace T. Myers, The American Journal of Human Genetics Mendelian DisorderBrain DevelopmentGenetic DisorderGeneticsNeurology	2016	116
Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network Anne M. Connolly, Julaine Florence, Mary Michaeleen Cradock, Neuromuscular Disorders Neuropsychological FunctioningNeuropsychologyDevelopmental Cognitive NeuroscienceDuchenne Muscular DystrophyMotor Development	2013	106
Myotonic Dystrophy Type 2: Human Founder Haplotype and Evolutionary Conservation of the Repeat Tract Christina L. Liquori, Yoshio Ikeda, Marcy R. Weatherspoon, The American Journal of Human Genetics BiologyRare DiseasesRepeat TractMendelian DisorderGenetic Disorder	2003	96
A focal domain of extreme demethylation within D4Z4 in FSHD2 Lynn M. Hartweck, Lindsey Anderson, Richard J.L.F. Lemmers, Neurology	2013	84
Spinocerebellar Ataxia Type 8: Molecular Genetic Comparisonsand Haplotype Analysis of 37 Families with Ataxia Yoshio Ikeda, Joline Dalton, Melinda L. Moseley, The American Journal of Human Genetics Genetic DisorderGeneticsClinical GeneticsGenetic FactorNeurology	2004	84

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