Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq ProjectRobert C. Green, Alan H. Beggs, Nidhi Shah et al.|The American Journal of Human Genetics|2023Cited by 55
Mutation analysis of BRCA1/2 mutations with special reference to polymorphic SNPs in Indian breast cancer patientsNidhi Shah, Mandava V. Rao, Parth Shah et al.|The Application of Clinical Genetics|2018Cited by 18
Mutation analysis of β-thalassemia in East-Western Indian population: a recent molecular approachParth Shah, Mandava V. Rao, Hari Shankar P Ray et al.|The Application of Clinical Genetics|2017Cited by 17
Bi‐allelic loss of function variants in <scp>GOLGA2</scp> are associated with a complex neurological phenotype: Report of a second familyUdhaya Kotecha, Vandana Gupta, Mehul Mistri et al.|Clinical Genetics|2021Cited by 8
Single-day HER2neu amplification assessment using chip-based digital PCR in formalin-fixed paraffin-embedded breast carcinoma tissueParth Shah, Jacob Sands, Shiva Murarka et al.|Breast Cancer Targets and Therapy|2018Cited by 5