Rana K. Shabbir
Rawalpindi, PB, Pakistan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 21 publications
Homozygous PTRHD1 Mutation in Intellectual Disability and Atypical Parkinsonism.
Journal: The Yale journal of biology and medicine
Published: April 01, 2026
Comparative study of extraction methods and process parameters of polyphenolic content obtained from Celosia argentea L. Flower for herbal sunscreen.
Journal: Natural product research
Published: November 08, 2025
Retrospective Evaluation of the Incidence of Cystic Echinococcosis in Humans Between 2012-2023 in Pakistan.
Journal: Turkiye parazitolojii dergisi
Published: September 09, 2025
Prevalence, knowledge, attitude, and practices regarding tick infestation in large ruminants of district Sheikhupura, Punjab, Pakistan.
Journal: Journal of parasitic diseases : official organ of the Indian Society for Parasitology
Published: April 09, 2024
In-silico analysis of potential anticancer drug for NEK7 and PPP1CA proteins overexpressed in pancreatic ductal adenocarcinoma.
Journal: Journal of biomolecular structure & dynamics
Published: March 12, 2024
Expanding OBSL1 Mutation Phenotype: Disproportionate Short Stature, Barrel Chest, Thoracic Kyphoscoliosis, Hypogonadism, and Hypospadias.
Journal: The Yale journal of biology and medicine
Published: October 02, 2023
A Recurrent Mutation in Growth Hormone Receptor (GHR) Gene Underlying Laron-type Dwarfism in a Pakistani Family.
Journal: The Yale journal of biology and medicine
Published: October 02, 2023
Prevalence of different tick species on livestock and associated equines and canine from different agro-ecological zones of Pakistan.
Journal: Frontiers in veterinary science
Published: November 04, 2022
A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family.
Journal: Genetic testing and molecular biomarkers
Published: January 28, 2022
KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies.
KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies.
Journal: European journal of human genetics : EJHG
Published: August 30, 2021
Demographic Attributes of Knowledge, Attitude, Practices, and One Health Perspective Regarding Diarrhea in Pakistan.
Journal: Frontiers in public health
Published: June 26, 2021
Last Updated: 09/26/2026