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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 17, 2025
Immunofluorescence and Electron Microscopy in Genetically Engineered Pig-to-Human Kidney Xenotransplantation: A Case ReportHuma Fatima, Isam-Eldin Eltoum, Vineeta Kumar, et al.BMC Infectious Diseases|November 8, 2019
Occurrence and seasonal variation of human Plasmodium infection in Punjab Province, PakistanNaveeda Akhtar Qureshi, Huma Fatima, Muhammad Afzal, et al.Journal of Photochemistry and Photobiology. B, Biology|November 21, 2020
In vitro anti-leishmanial activity of Prunus armeniaca fractions on Leishmania tropica and molecular docking studiesNargis Shaheen, Naveeda Akhter Qureshi, Asma Ashraf, et al.Journal of Medical Genetics|March 9, 2018
Homozygous CHST11 mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactylyRana Muhammad Kamran Shabbir, Gökhan Nalbant, Nafees Ahmad, et al.American Journal of Medical Genetics. Part A|September 4, 2015
RBBP8 syndrome with microcephaly, intellectual disability, short stature and brachydactylySara Mumtaz, Esra Yıldız, Saliha Jabeen, et al.Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|July 22, 2025
Assessment of menstrual knowledge, beliefs and hygiene practices among ethnic groups in isolated populations in PakistanSaif Ullah, Maryam Bibi, Anila Parveen, et al.Anti-Cancer Agents in Medicinal Chemistry|February 24, 2025
Recurrent Missense Driver STAT5B N642H Mutation in Children Transiting into Adolescence, with Acute Lymphoid Leukemia and its In silico InhibitionRehana Yasmin, Rashda Abbasi, Tajdar Jahangir Gohar, et al.The Yale Journal of Biology and Medicine|October 2, 2023
Expanding OBSL1 Mutation Phenotype: Disproportionate Short Stature, Barrel Chest, Thoracic Kyphoscoliosis, Hypogonadism, and HypospadiasMine Koprulu, Rana Muhammad Kamran Shabbir, Sara Mumtaz, et al.European Journal of Medical Genetics|June 1, 2017
Novel splice mutation in LRP4 causes severe type of Cenani-Lenz syndactyly syndrome with oro-facial and skeletal symptomsMuhammad Afzal, Qamar Zaman, Uwe Kornak, et al.Pakistan Journal of Medical Sciences|March 19, 2025
Congenital anomalies in Okara District of Pakistan: Epidemiology, spectrum and ethno-demographic inequalitiesAqeela Nawaz, Ayesha Siddiqui, Mahnoor Mughal, et al.Pageof 18