Author

Parminder Kaur

Institution: Post Graduate Institute of Medical Education and Research

Observed institution: Post Graduate Institute of Medical Education and Research

ORCID: 0000-0002-3817-7122

Observed ORCID: 0000-0002-3817-7122

OpenAlex ID: A5045832121

A case control study and one year follow-up of registered epilepsy cases in a resettlement colony of North India, a developing tropical country

1999 · I.M.S Sawhney, Amarjeet Singh, et al. · Journal of the Neurological Sciences · 40

Ayme gripp syndrome in an Indian patient

2021 · Chakshu Chaudhry, Parminder Kaur, et al. · American Journal of Medical Genetics Part A · 6

Pattern Recognition of Common Multiple Congenital Malformation Syndromes with Underlying Chromatinopathy

2022 · Anupriya Kaur, Chakshu Chaudhry, et al. · Journal of Pediatric Genetics · 4

Short Stature Syndromes: Case Series from India

2021 · Inusha Panigrahi, Parminder Kaur, et al. · Journal of Pediatric Genetics · 3

Genetics of idiopathic short stature: Insights into growth regulation

2025 · Parminder Kaur, Jaivinder Yadav, et al. · Journal of Pediatric Endocrinology and Diabetes · 2

Intellectual Disability and Blended Phenotypes: Insights from a Centre in North India

2024 · Inusha Panigrahi, Sudha Rao, et al. · Case Reports in Genetics · 1

Severity Scoring Cutoff for MLPA and Its Diagnostic Yield in 332 North Indian Children with Developmental Delay

2022 · Priyanka Srivastava, Parminder Kaur, et al. · Journal of Pediatric Genetics · 1

Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India

2021 · Chakshu Chaudhry, Parminder Kaur, et al. · Congenital Anomalies · 1

Utility of Tele-Genetic Counselling in Prenatal Diagnosis: Experience from the eSanjeevani Hub-and-Spoke Model

2026 · Parminder Kaur, Richa Gupta, et al. · The Journal of Obstetrics and Gynecology of India

Whole Exome Sequencing in Neonates and Clinical Associations in Antenatally Diagnosed Fetal Growth Retardation Due to Idiopathic Cause and Pre-eclampsia and Associated Placental Abnormalities

2026 · Kanya Mukhopadhyay, Priyanka Srivastava, et al. · Placenta

Microcephaly with or without chorioretinopathy, lymphedema, and mental retardation syndrome as a rare cause of chorio-retinal atrophy in a young child – A case report and review of literature

2026 · Parminder Kaur, Anu Kumari, et al. · Indian Journal of Ophthalmology - Case Reports

Prenatal and postnatal diagnosis of congenital ichthyosis: Three Asian-Indian cases

2025 · Parminder Kaur, Inusha Panigrahi, et al. · Cosmoderma

Elective Termination of Pregnancies Due to Fetal Congenital Anomalies: Utility of Various Investigating Modalities for Etiological Diagnosis of Congenital Anomalies

2025 · Roshan Daniel, Inusha Panigrahi, et al. · Fetal and Pediatric Pathology

Ductus Venosus Anomalies: Genetic Associations and Fetal Outcomes

2025 · Vishali, Snigdha Kumari, et al. · Journal of Fetal Medicine

A Novel Variant in Heparan Sulfate Proteoglycan 2 Gene Causing Schwartz–Jampel Syndrome – A Case Report from India

2025 · Parminder Kaur, Sumita Manhori, et al. · Genetic Clinics

Works count: 15

Citation count: 58

H-index: 3

I10-index: 1