David Dimmock - Concepedia

Author

David Dimmock

Also Known As

Catherine A. McCarty, D Dimmock, D P Dimmock, D. Dimmock, D. P. Dimmock, D.P Dimmock, David Dimmock, David M. Dimmock, David P Dimmock, David P. Dimmock

206

Publications

13.5K

Citations

H-Index

149

Concepts

All Affiliations

Children’s Institute Medical College of Wisconsin University of California San Diego Baylor College of Medicine Rady Children's Hospital-San Diego

About

David Dimmock is an author at Children’s Institute specializing in medicine, pediatrics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	32	46	4.6K
2	Natural Sciences	4	4	273
3	Health Sciences	3	3	132
4	Engineering	2	2	253
5	Nursing	1	1	48

David Dimmock

Publications

10.9K

Citations

H-Index

Page 1

	Year	Citations
Guidelines for investigating causality of sequence variants in human disease Daniel G. MacArthur, Teri A. Manolio, David Dimmock, Nature	2014	1.3K
Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma Lauren Fishbein, Ignaty Leshchiner, Vonn Walter, Cancer Cell MedicineComprehensive Molecular CharacterizationPathologyAdrenal DiseaseMolecular Diagnostics	2017	750
Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease Elizabeth A. Worthey, Alan N. Mayer, Grant Syverson, Genetics in Medicine	2010	704
Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases Michelle M. Clark, Zornitza Stark, Lauge Farnaes, npj Genomic Medicine	2018	614
Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission Smruthi Karthikeyan, Joshua I. Levy, Peter De Hoff, Nature	2022	482
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization Lauge Farnaes, Amber Hildreth, Nathaly M. Sweeney, npj Genomic Medicine	2018	438
Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis Shiran Rabinovich, Lital N. Adler, Keren Yizhak, Nature Ass1-deficient Tumours FostersEndocrine-related CancerOncogenic AgentMedicineMolecular Biology	2015	378
Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study Derralynn Hughes, Suma P. Shankar, Gere Sunder‐Plassmann, Journal of Medical Genetics	2016	370
A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants Stephen F. Kingsmore, Julie A. Cakici, Michelle M. Clark, The American Journal of Human Genetics Neonatal GenomicsNewborn ScreeningRapid GenomeExome SequencingGenetics	2019	348
Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation Michelle M. Clark, Amber Hildreth, Serge Batalov, Science Translational Medicine	2019	288

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