Daryl A. Scott - Concepedia

Author

Daryl A. Scott

Also Known As

Callens, Tom, Carlos A. Bacino, Catherine H. Sillari, Chunli Zhao, Cynthia J. Tifft, D A Scott, D. A. Scott, D. Scott, D.A. Scott, Daniel Wegner

257

Publications

10.7K

Citations

H-Index

151

Concepts

All Affiliations

Baylor College of Medicine Texas Children's Hospital Baylor Genetics Howard Hughes Medical Institute University of Washington

About

Daryl A. Scott is an author at Baylor College of Medicine specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	34	52	3.6K
2	Engineering	5	5	403
3	Arts	4	4	124
4	Health Sciences	3	3	75
5	Natural Sciences	3	3	242

Daryl A. Scott

117

Publications

8.4K

Citations

H-Index

Page 1

	Year	Citations
Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size Marwan Shinawi, P. Liu, Sung Hae L. Kang, Journal of Medical Genetics	2009	593
The Pendred syndrome gene encodes a chloride-iodide transport protein Daryl A. Scott, Rong Wang, Trisha Kreman, Nature Genetics Pendred Syndrome GeneDisease MechanismMendelian DisorderGenetic DisorderGenetics	1999	564
Use of Exome Sequencing for Infants in Intensive Care Units Linyan Meng, Mohan Pammi, Anirudh Saronwala, JAMA Pediatrics	2017	422
A Pathologic Cascade Leading to Synaptic Dysfunction in -Synuclein-Induced Neurodegeneration Daryl A. Scott, Iustin V. Tabarean, Yong Tang, Journal of Neuroscience	2010	357
<i>Dusp6</i>(<i>Mkp3</i>) is a negative feedback regulator of FGF-stimulated ERK signaling during mouse development Daryl A. Scott, Ekaterina Hatch, Xiaoyan Tian, Development	2006	281
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss Raye Lynn Alford, Kathleen S. Arnos, Michelle Fox, Genetics in Medicine	2014	267
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome Julia Wang, Rami Al‐Ouran, Yanhui Hu, The American Journal of Human Genetics	2017	217
Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics Sau Wai Cheung, Chad A. Shaw, Daryl A. Scott, American Journal of Medical Genetics Part A Genetic TestingCytogeneticsGeneticsPathologyMolecular Genetics	2007	189
Two Frequent Missense Mutations in Pendred Syndrome Peter Van Hauwe, Lorraine A. Everett, Paul Coucke, Human Molecular Genetics	1998	189
The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease Rachel Ramoni, John J. Mulvihill, David R. Adams, The American Journal of Human Genetics Disease DiagnosisNetwork ScienceHealth InformaticsData ScienceData Mining	2017	181

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