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BMC Genetics|October 26, 2018
Correction to: Application of geographic population structure (GPS) algorithm for biogeographical analyses of populations with complex ancestries: a case study of South Asians from 1000 genomes projectRanajit Das, Priyanka Upadhyai
Genome Biology and Evolution|June 9, 2017
Unraveling the Population History of Indian SiddisRanajit Das, Priyanka Upadhyai
Peerj|September 5, 2020
Characterization of primary cilia features reveal cell-type specific variability in in vitro models of osteogenic and chondrogenic differentiationPriyanka Upadhyai, Vishal Singh Guleria, Prajna Udupa
Life (Basel, Switzerland)|September 28, 2021
Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European DescentPriyanka Upadhyai, Gokul Suresh, Rahul Parit, et al.
Gene|November 11, 2019
Novel splice site and nonsense variants in INVS cause infantile nephronophthisisPuneeth H Somashekar, Priyanka Upadhyai, Anju Shukla, et al.
Clinical Genetics|December 5, 2024
Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological DisorderPeriyasamy Radhakrishnan, Neha Quadri, Florian Erger, et al.
BMC Genetics|October 23, 2020
The story of the lost twins: decoding the genetic identities of the Kumhar and Kurcha populations from the Indian subcontinentRanajit Das, Vladimir A Ivanisenko, Anastasia A Anashkina, et al.
European Journal of Medical Genetics|December 4, 2016
Autosomal recessive spinocerebellar ataxia 20: Report of a new patient and review of literatureAnju Shukla, Priyanka Upadhyai, Jhanvi Shah, et al.
Bone|November 9, 2018
Phenotyping and genotyping of skeletal dysplasias: Evolution of a center and a decade of experience in IndiaAnusha Uttarilli, Hitesh Shah, Gandham SriLakshmi Bhavani, et al.
Clinical Dysmorphology|May 28, 2020
Recurrent 1q21.1 deletion syndrome: report on variable expression, nonpenetrance and review of literaturePriyanka Upadhyai, Eram Fatima Amiri, Vishal Singh Guleria, et al.
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