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International Journal of Neonatal Screening|September 22, 2022
dbRUSP: An Interactive Database to Investigate Inborn Metabolic Differences for Improved Genetic Disease ScreeningGang Peng, Yunxuan Zhang, Hongyu Zhao, et al.
Metabolites|January 26, 2024
Association of Maternal Age and Blood Markers for Metabolic Disease in NewbornsYuhan Xie, Gang Peng, Hongyu Zhao, et al.
Molecules (Basel, Switzerland)|November 7, 2012
Forward chemical genetics in yeast for discovery of chemical probes targeting metabolismRobert St Onge, Ulrich Schlecht, Curt Scharfe, et al.
Communications Engineering|March 14, 2025
Allele-specific electrical genotyping for diagnosis of transthyretin amyloidosisMuhammad Tayyab, Neeru Gandotra, Jianye Sui, et al.
Genetics in Medicine Open|March 3, 2025
CFTR haplotype phasing using long-read genome sequencing from ultralow input DNANeeru Gandotra, Antariksh Tyagi, Irina Tikhonova, et al.
Frontiers in Pediatrics|February 8, 2021
Timing of Newborn Blood Collection Alters Metabolic Disease Screening PerformanceGang Peng, Yishuo Tang, Tina M Cowan, et al.
Forensic Science International. Genetics|June 13, 2022
A multipurpose panel of microhaplotypes for use with STR markers in caseworkKenneth K Kidd, Andrew J Pakstis, Neeru Gandotra, et al.
Scientific Reports|March 23, 2021
Multi-frequency impedance sensing for detection and sizing of DNA fragmentsJianye Sui, Neeru Gandotra, Pengfei Xie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 7, 2009
Mitochondrial DNA analysis by multiplex denaturing high-performance liquid chromatography and selective sequencing in pediatric patients with cardiomyopathyIris Schrijver, Lynn M Pique, Ilana Traynis, et al.
Bioinformatics (Oxford, England)|May 15, 2012
SRMA: an R package for resequencing array data analysisNianxiang Zhang, Yan Xu, Martin O'Hely, et al.
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