Gabrielle C. Geddes - Concepedia

Author

Gabrielle C. Geddes

Also Known As

G C GEDDES, G C Geddes, G Geddes, G. Geddes, Gabrielle C Geddes, Gabrielle C. Geddes, Gabrielle Geddes, Gabrielle C. Geddes

Publications

696

Citations

H-Index

Concepts

All Affiliations

Medical College of Wisconsin Indiana University – Purdue University Indianapolis Children's Hospital of Wisconsin Indiana University School of Medicine Indiana University Bloomington

About

Gabrielle C. Geddes is an author at Medical College of Wisconsin specializing in cardiology, medicine, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	163
2	Molecular Genetics	2	2	44
3	Public Health	1	1	15
4	Cell Biology	1	1	26
5	Molecular Biology	1	1	18

Gabrielle C. Geddes

Publications

431

Citations

H-Index

Page 1

	Year	Citations
The spectrum of manifestations in desmoplakin gene (DSP) spectrin repeat 6 domain mutations: Immunophenotyping and response to ustekinumab Amy S. Paller, Tali Czarnowicki, Yael Renert‐Yuval, Journal of the American Academy of Dermatology	2017	75
BAG3 myofibrillar myopathy presenting with cardiomyopathy Chamindra G. Konersman, Brett J. Bordini, Gunter Scharer, Neuromuscular Disorders Mitochondrial MyopathyCardiomyopathyHeart FailureBag3 Myofibrillar MyopathyPathology	2015	72
Large granular lymphocyte expansions in patients with Felty's syndrome: analysis using anti-T cell receptor Vβ-specific monoclonal antibodies Simon Bowman, M. Bhavnani, Gabrielle C. Geddes, Clinical & Experimental Immunology	1995	49
Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease Gabrielle C. Geddes, Donald Basel, Peter C. Frommelt, Pediatric Cardiology	2017	40
Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy Jeffrey Schubert, Muhammad Tariq, Gabrielle C. Geddes, Human Mutation Cardiac MuscleGeneticsPathologyRcm FamiliesMolecular Genetics	2018	26
Pompe disease treatment with twice a week high dose alglucoside alfa in a patient with severe dilated cardiomyopathy Jesa L. Landis, Holly Hyland, Steven J. Kindel, Molecular Genetics and Metabolism Reports Heart FailureU.s. FoodPediatricsPediatric Lung DiseasePaediatric Medicine	2018	20
Pathogenic variants in MRPL44 cause infantile cardiomyopathy due to a mitochondrial translation defect Marisa W. Friederich, Gabrielle C. Geddes, Saskia B. Wortmann, Molecular Genetics and Metabolism CardiomyopathyMitochondrial Translation DefectMitochondrial BiogenesisMitochondrial FunctionGenetics	2021	18
Redox signaling in colonial hydroids: many pathways for peroxide Neil W. Blackstone, Matthew J. Bivins, Kimberly S. Cherry, Journal of Experimental Biology	2005	17
A case of Coffin–Siris syndrome with severe congenital heart disease and a novel <i>SMARCA4</i> variant Nikita R. Dsouza, Michael T. Zimmermann, Gabrielle C. Geddes Molecular Case Studies	2019	16
Novel <i>KLHL26</i> variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction Sai Suma K. Samudrala, Lauren M. North, Karl Stamm, Molecular Genetics & Genomic Medicine	2020	16

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