Concepedia

Author

Elizabeth Scott

Emory University

Also Known As

E. Scott, Elizabeth H. Scott, Elizabeth Scott

8

Publications

645

Citations

8

H-Index

29

Concepts

All Affiliations

Emory UniversityGerman Centre for Cardiovascular ResearchUniversity of NottinghamUniversität HamburgUniversity Medical Center Hamburg-Eppendorf
ES

About

Elizabeth Scott is an author at Emory University specializing in medicine, genetics, and fragile x spectrum.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

4

4

285

2

Public Health

2

2

209

3

Natural Sciences

1

1

22

4

Social Sciences

1

1

54

5

Cognitive Science

1

1

54

Elizabeth Scott

×

8

Publications

645

Citations

8

H-Index

YearCitations

CRISPR/Cas9 editing in human pluripotent stem cell-cardiomyocytes highlights arrhythmias, hypocontractility, and energy depletion as potential therapeutic targets for hypertrophic cardiomyopathy

Diogo Mosqueira, Ingra Mannhardt, Jamie R. Bhagwan,

European Heart Journal

2018

242

Prevalence of the fragile X syndrome in African‐Americans

Dana C. Crawford, Kellen L. Meadows, James L. Newman,

American Journal of Medical Genetics

2002

145

Isogenic Pairs of hiPSC-CMs with Hypertrophic Cardiomyopathy/LVNC-Associated ACTC1 E99K Mutation Unveil Differential Functional Deficits

James G.W. Smith, Thomas J. Owen, Jamie R. Bhagwan,

Stem Cell Reports

2018

74

Paternally Transmitted FMR1 Alleles Are Less Stable than Maternally Transmitted Alleles in the Common and Intermediate Size Range

Amy K. Sullivan, Dana C. Crawford, Elizabeth Scott,

The American Journal of Human Genetics

2002

64

Examination of the Effect of the Polymorphic CGG Repeat in the FMR1 Gene on Cognitive Performance

Emily G. Allen, Stephanie L. Sherman, Ann Abramowitz,

Behavior Genetics

2005

54

Trinucleotide repeat expansion in the FRAXE locus is not common among institutionalized individuals with non-specific developmental disabilities

Jeanette J. A. Holden, Colin Julien-Inalsingh, Maryse Chalifoux,

American Journal of Medical Genetics

1996

25

Rare Disease Mechanisms Identified by Genealogical Proteomics of Copper Homeostasis Mutant Pedigrees

Stephanie A. Zlatic, Alysia D. Vrailas‐Mortimer, Avanti Gokhale,

Cell Systems

2018

22

Cognitive and behavioral performance among FMR1 high‐repeat allele carriers surveyed from special education classes

Stephanie L. Sherman, Frederick Marsteller, Ann Abramowitz,

American Journal of Medical Genetics

2002

19

Page 1