Preeti Paliwal

Shree Guru Gobind Singh Tricentenary University — India

Medicine · Health Sciences

15h-index706citations47works5.02yr avg
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Research Topics

Prenatal Screening and Diagnostics(10), Genomic variations and chromosomal abnormalities(9), Corneal surgery and disorders(6), Corneal Surgery and Treatments(6), Fetal and Pediatric Neurological Disorders(5)

Publications47 total

Synthesis and in vitro antimicrobial evaluation of 2,4-diamino-8,8-dimethyl-6-oxo-5-(heteroaryl)-6,7,8,9-tetrahydro-5H-chromeno[2,3-b] pyridine-3-carbonitrile
International Journal of Drug Design and Discovery·2025
Unveiling the Genetic and Immunophenotypic Landscape of Chronic Lymphocytic Leukemia in Indian Cohort
Indian Journal of Hematology and Blood Transfusion·2025Open Access
Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of 300 Indian Patients
The Indian Journal of Pediatrics·2025· 1 cited
58P NSCLC genomic complexity: Insights from comprehensive molecular profiling in the era of precision medicine
ESMO Open·2024Open Access
Bright and enlarged fetal kidneys: One phenotype different genotypes, and counseling dilemmas
Journal of Clinical Ultrasound·2024
Revisiting Utility of Fetal Autopsy in Genomic Era
Fetal and Pediatric Pathology·2024
Aficamten is a small-molecule cardiac myosin inhibitor designed to treat hypertrophic cardiomyopathy
Nature Cardiovascular Research·2024· 46 citedOpen Access
In vitro treatment with liposome-encapsulated Mannose-1-phosphate restores N-glycosylation in PMM2-CDG patient-derived fibroblasts
Molecular Genetics and Metabolism·2024· 3 cited
Beyond Binary: Biomarkers Reveal the Coexistence of Acute Motor Axonal Neuropathy (AMAN) and Acute Inflammatory Demyelinating Polyneuropathy (AIDP) in Guillain-Barré Syndrome (P9-11.001)
Neurology·2024
Comprehensive post-mortem evaluation in Intrauterine deaths /still births in improving uptake of autopsy and future pregnancy outcomes
2024Open Access
A Rare Case of Mosaic 3pter and 5pter Deletion-Duplication with Autism Spectrum Disorder and Dyskinesia
Case Reports in Genetics·2023· 1 citedOpen Access
Practical Applications of Chromosomal Microarray in Prenatal Diagnosis
Journal of Fetal Medicine·2023Open Access
Regions of homozygosity and a novel variant in Steel syndrome: An added dilemma to diagnosis
Journal of Postgraduate Medicine·2023· 1 citedOpen Access
Phosphofurin Acidic Cluster Sorting Protein 1 Syndrome: Insights Gained on the Multisystem Involvement Reviewing Encoded Protein Interactions?
Journal of Pediatric Genetics·2022Open Access
Prenatal Diagnosis by Chromosome Microarray Analysis, An Indian Experience
The Journal of Obstetrics and Gynecology of India·2021· 9 citedOpen Access
Severe Polyhydramnios with Consistent Fetal Full Bladder: A Novel Sign of Antenatal Bartter's Disease
Journal of Pediatric Genetics·2020· 3 citedOpen Access
Characterization of the Cardiac Myosin Inhibitor CK-3773274: a Potential Therapeutic Approach for Hypertrophic Cardiomyopathy
Biophysical Journal·2020· 9 citedOpen Access
Abstract 332: Pharmacologic Characterization of the Cardiac Myosin Inhibitor, CK-3773274: A Potential Therapeutic Approach for Hypertrophic Cardiomyopathy
Circulation Research·2019· 3 cited
Molecular characterization of supernumerary marker chromosomes found as unexpected chromosome abnormalities in nine prenatal and nine postnatal samples
Obstetrics & Gynecology International Journal·2019· 3 citedOpen Access
The changing scenario in prenatal diagnosis of genetic disorders: Genetics to genomics
Current Medicine Research and Practice·2018· 18 cited
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Frequent Co-authors

Arundhati Sharma(14), Radhika Tandon(9), Meena Lall(8), Pushpa Saviour(8), Ishwar C. Verma(7), Seema Thakur(7), Seema Sen(6), Rasik B. Vajpayee(6), Ratna Dua Puri(6), Surbhi Mahajan(6), Namrata Sharma(5), Sunita Bijarnia‐Mahay(5), Anju Joshi(5), Shruti Agarwal(4), Irina M. Conboy(3), Jeevan S. Titiyal(3), James J. Hartman(3), Darren T. Hwee(3), Chih-Yuan Chuang(3), Eva R. Chin(3)