Lindsay C. Burrage - Concepedia

Author

Lindsay C. Burrage

Also Known As

Ashok Balasubramanyam, Brendan Lee, Brent L. Fogel, Bret L. Bostwick, Burrage, Lindsay C., Carlos Bacino, Elizabeth A Burke, Elizabeth A. Burke, Gary Clark, Heather A. Colley

230

Publications

7.3K

Citations

H-Index

160

Concepts

All Affiliations

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

About

Lindsay C. Burrage is an author at Baylor College of Medicine specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	58	3.7K
2	Health Sciences	9	9	390
3	Public Health	6	6	944
4	Natural Sciences	4	4	107
5	Engineering	2	2	261

Lindsay C. Burrage

Publications

5.9K

Citations

H-Index

Page 1

	Year	Citations
Use of Exome Sequencing for Infants in Intensive Care Units Linyan Meng, Mohan Pammi, Anirudh Saronwala, JAMA Pediatrics	2017	422
Genetic Dissection of Complex Traits with Chromosome Substitution Strains of Mice Jonathan B. Singer, Annie E. Hill, Lindsay C. Burrage, Science GeneticsGenomicsGenotype-phenotype AssociationMolecular EcologyChromosome Substitution Strains	2004	351
Genetic architecture of complex traits: Large phenotypic effects and pervasive epistasis Haifeng Shao, Lindsay C. Burrage, David S. Sinasac, Proceedings of the National Academy of Sciences Phenotypic VariationGeneticsGenetic FoundationPervasive EpistasisEpistasis	2008	266
The genetic basis of DOORS syndrome: an exome-sequencing study Philippe M. Campeau, Dalia Kasperavičiūtė, James T. Lu, The Lancet Neurology	2013	227
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
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism Marcus J. Miller, Adam D. Kennedy, Andrea D. Eckhart, Journal of Inherited Metabolic Disease	2015	214
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
Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing David R. Murdock, Hongzheng Dai, Lindsay C. Burrage, Journal of Clinical Investigation	2020	168
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms Hyung-Lok Chung, Michael F. Wangler, Paul C. Marcogliese, Neuron Reductive StressGenome InstabilityDifferent MechanismsRedox RegulatorGenetics	2020	153
Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase Philippe M. Campeau, Guy M. Lenk, James T. Lu, The American Journal of Human Genetics Mendelian DisorderPhosphoinositide PhosphataseGenetic DisorderGeneticsPathogenesis	2013	139

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