Juvianee Estrada‐Veras

Author

National Human Genome Research Institute ORCID

Also Known As

Juvianee Estrada-Veras, Juvianee Estrada‐Veras, Juvianee I Estrada-Veras, Juvianee I. Estrada-Veras, Juvianee I. Estrada‐Veras, Kevin O'Brien

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

National Human Genome Research Institute National Institutes of Health Walter Reed National Military Medical Center Henry M. Jackson Foundation National Institutes of Health Clinical Center

About

Juvianee Estrada‐Veras is an author at National Human Genome Research Institute specializing in medicine, radiology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	228
2	Social Sciences	2	2	125
3	Health Sciences	1	1	19
4	Natural Sciences	1	1	24
5	Biology	1	1	24

Juvianee Estrada‐Veras

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Consensus guidelines for the diagnosis and clinical management of Erdheim-Chester disease Eli L. Diamond, Lorenzo Dagna, David M. Hyman, Blood	2014	579
Diverse and Targetable Kinase Alterations Drive Histiocytic Neoplasms Eli L. Diamond, Benjamin H. Durham, Julien Haroche, Cancer Discovery	2015	518
The clinical spectrum of Erdheim-Chester disease: an observational cohort study Juvianee Estrada‐Veras, Kevin O’Brien, Louisa C. Boyd, Blood Advances	2017	242
Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus Phan Q. Duy, Stefan Weise, Claudia Marini, Nature Neuroscience NeuroregenerationDevelopmental BiologyBrain StructureNeuroanatomyNeuroprogenitor-based Genetic Subtype	2022	96
Neurological manifestations of Erdheim–Chester Disease Louisa C. Boyd, Kevin O’Brien, Neval Özkaya, Annals of Clinical and Translational Neurology	2020	43
Novel findings and expansion of phenotype in a mosaic <scp>RASopathy</scp> caused by somatic <scp><i>KRAS</i></scp> variants Caitlin A. Chang, Renée Perrier, Kyle C. Kurek, American Journal of Medical Genetics Part A	2021	38
Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness Anne Slavotinek, Doriana Misceo, Stephanie Htun, Human Molecular Genetics	2020	34
Abdominal involvement in Erdheim-Chester disease (ECD): MRI and CT imaging findings and their association with BRAFV600E mutation Moozhan Nikpanah, Lauren Kim, S. Mojdeh Mirmomen, European Radiology Abdominal InvolvementHistopathologyGastroenterologyPathologyErdheim-chester Disease	2018	32
Thoracic involvement in Erdheim-Chester disease: computed tomography imaging findings and their association with the BRAFV600E mutation S. Mojdeh Mirmomen, Arlene Sirajuddin, Moozhan Nikpanah, European Radiology PathologyErdheim-chester DiseaseThoracic InvolvementRadiologyBrafv600e Mutation	2018	30
Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish Sheng‐Jia Lin, Barbara Vona, Patrícia Gonçalves Barbalho, Genetics in Medicine Neurodevelopmental DisordersKnockout ZebrafishDevelopmental BiologyBiallelic VariantsGenetic Disorder	2021	29

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