Grace Yoon - Concepedia

Author

Grace Yoon

Hospital for Sick Children ORCID

Also Known As

Andrew Skalsky, Carlo Wilke, Carolyn Solomon, G Yoon, G. Yoon, Grace Yoon, Jennie Murray, Yoon, Grace

182

Publications

Citations

H-Index

106

Concepts

All Affiliations

Hospital for Sick Children University of Toronto SickKids Foundation Children's Hospital of Eastern Ontario McGill University

About

Grace Yoon is an author at Hospital for Sick Children specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	35	1.6K
2	Public Health	4	4	94
3	Social Sciences	2	2	48
4	Cell Biology	2	2	64
5	Biochemistry	1	1	36

Grace Yoon

Publications

4.1K

Citations

H-Index

Page 1

	Year	Citations
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia Nícolas C. Hoch, Hana Hanzlíková, Stuart L. Rulten, Nature Xrcc1 MutationMolecular NeuroscienceGenetic DisorderGeneticsFragile X Spectrum	2016	263
Cognitive and Neurobehavioral Profile in Boys With Duchenne Muscular Dystrophy Rudaina Banihani, Sharon Smile, Grace Yoon, Journal of Child Neurology	2015	217
Critically Ill Children During the 2009–2010 Influenza Pandemic in the United States Adrienne G. Randolph, Frances L. Vaughn, Ryan M. Sullivan, PEDIATRICS	2011	216
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III Isabelle Thiffault, Nicole I. Wolf, Diane Forget, Nature Communications	2015	176
The genetic landscape of familial congenital hydrocephalus Ranad Shaheen, Mohammed Adeeb Sebai, Nisha Patel, Annals of Neurology	2017	144
Progression of Friedreich ataxia: quantitative characterization over 5 years Maya Patel, Charles J. Isaacs, Lauren Seyer, Annals of Clinical and Translational Neurology	2016	134
Neurological complications of cardio‐facio‐cutaneous syndrome Grace Yoon, Jodine Rosenberg, Susan Blasér, Developmental Medicine & Child Neurology	2007	130
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia Ziv Gan‐Or, Naïma Bouslam, Nazha Birouk, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsMolecular Genetics	2016	113
Andersen‐Tawil syndrome: Prospective cohort analysis and expansion of the phenotype Grace Yoon, Snehlata Oberoi, Martin Tristani‐Firouzi, American Journal of Medical Genetics Part A	2006	111
Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism John J. Reynolds, Louise S. Bicknell, Paula Carroll, Nature Genetics Genome InstabilityDevelopmental BiologyGenetic DisorderGeneticsGenomic Mechanism	2017	109

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