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Narayanan Veeraraghavan, Ph.D.

Affiliations: 
2011 Pennsylvania State University, State College, PA, United States 
Area:
theoretical and computational methods for describing chemical reactions in condensed phases and at interfaces
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"Narayanan Veeraraghavan"
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Sharon Hammes-Schiffer grad student 2011 Penn State
 (Catalytic and structural roles of nucleobases and metal ions in small ribozymes: New insights from calculations and comparison to experiments.)

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Publications

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James KN, Clark MM, Camp B, et al. (2020) Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses. Npj Genomic Medicine. 5: 33
Kingsmore SF, Cakici JA, Clark MM, et al. (2019) A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants. American Journal of Human Genetics
Clark MM, Hildreth A, Batalov S, et al. (2019) Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation. Science Translational Medicine. 11
Berg JS, Agrawal PB, Bailey DB, et al. (2017) Newborn Sequencing in Genomic Medicine and Public Health. Pediatrics
Huang Z, Rustagi N, Veeraraghavan N, et al. (2016) A hybrid computational strategy to address WGS variant analysis in >5000 samples. Bmc Bioinformatics. 17: 361
Polfus LM, Khajuria RK, Schick UM, et al. (2016) Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 785
Polfus LM, Khajuria RK, Schick UM, et al. (2016) Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 481-488
English AC, Salerno WJ, Hampton OA, et al. (2015) Assessing structural variation in a personal genome-towards a human reference diploid genome. Bmc Genomics. 16: 286
Yang Y, Muzny DM, Xia F, et al. (2014) Molecular findings among patients referred for clinical whole-exome sequencing. Jama. 312: 1870-9
Naccache SN, Federman S, Veeraraghavan N, et al. (2014) A cloud-compatible bioinformatics pipeline for ultrarapid pathogen identification from next-generation sequencing of clinical samples. Genome Research. 24: 1180-92
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