Scott E. Hickey - Concepedia

Author

Scott E. Hickey

Also Known As

Bret L. Bostwick, Hickey, Scott, Hickey, Scott., S Hickey, S. E. Hickey, S. Hickey, S.E. Hickey, SCOTT E. HICKEY, Scott E Hickey, Scott E. Hickey

101

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Nationwide Children's Hospital The Ohio State University Baylor College of Medicine Massachusetts General Hospital Baylor Genetics

About

Scott E. Hickey is an author at Nationwide Children's Hospital specializing in medicine, genetics, and systems biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	844
2	Engineering	2	2	62
3	Health Sciences	2	2	34
4	Law	1	1	38
5	Public Health	1	1	162

Scott E. Hickey

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Use of an Automated, Load-Distributing Band Chest Compression Device for Out-of-Hospital Cardiac Arrest Resuscitation Marcus Eng Hock Ong, Joseph P. Ornato, D. P. Edwards, JAMA	2006	242
Recurrent De Novo and Biallelic Variation of ATAD3A , Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes Tamar Harel, Wan Hee Yoon, Caterina Garone, The American Journal of Human Genetics Distinct Neurological SyndromesNeurodegenerative DiseasesRecurrent De NovoMitochondrial FunctionGenetics	2016	186
ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing Scott E. Hickey, Cynthia J. Curry, Helga V. Toriello Genetics in Medicine Acmg Practice GuidelineGenetic TestingGenotype-phenotype AssociationGeneticsGenetic Epidemiology	2013	162
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies Bo Yuan, Juanita Neira, Davut Pehli̇van, Genetics in Medicine BioinformaticsMendelian DisorderGenetic DisorderMedicineGenetics	2018	87
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype Vandana Shashi, Loren D.M. Peña, Katherine Kim, The American Journal of Human Genetics Allelic VariantSystems BiologySomatic VariantGenetic DisorderGenetics	2016	86
Phenotypic expansion in <i> <scp>DDX</scp> 3X </i> – a common cause of intellectual disability in females Xia Wang, Jennifer E. Posey, Jill A. Rosenfeld, Annals of Clinical and Translational Neurology	2018	86
Single-cell multi-omics defines the cell-type-specific impact of splicing aberrations in human hematopoietic clonal outgrowths Mariela Cortés-López, Paulina Chamely, Allegra G. Hawkins, Cell stem cell Developmental BiologySingle Cell SequencingSingle-cell Multi-omicsMedicineHematology	2023	59
Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis Kusumika Mukherjee, Kana Ishii, Vamsee Pillalamarri, Human Molecular Genetics Neural Crest CellsMaxillofacial GrowthCytoskeletonCell SpecializationAnimal Craniofacial Growth	2016	55
Ancestral polymorphisms shape the adaptive radiation of<i>Metrosideros</i>across the Hawaiian Islands Jae Young Choi, Xiaoguang Dai, Ornob Alam, Proceedings of the National Academy of Sciences	2021	52
Cerebral organoids containing an <i>AUTS2</i> missense variant model microcephaly Summer Fair, Wesley N. Schwind, Dominic Julian, Brain	2022	51

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