Anees Muhammad

Peshawar, KP, Pakistan

Last Updated: 09/26/2026

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Found 14 publications

Expanding the genetic spectrum of autosomal recessive microcephaly in Pakistani families.

Expanding the genetic spectrum of autosomal recessive microcephaly in Pakistani families.

Journal: BMC neurology

Published: December 23, 2025

Isolated absence epilepsy associated with a de novo FBXW7 missense variant in the F-box domain.

Isolated absence epilepsy associated with a de novo FBXW7 missense variant in the F-box domain.

Journal: Epilepsia open

Published: October 24, 2025

Identification of a Novel Homozygous SCN1B Splice-Site Variant in a Consanguineous Families With Early-Onset Epilepsy: A Case Series and Review of Literature.

Identification of a Novel Homozygous SCN1B Splice-Site Variant in a Consanguineous Families With Early-Onset Epilepsy: A Case Series and Review of Literature.

Journal: Molecular genetics & genomic medicine

Published: August 15, 2025

Genomic insights into autosomal recessive epilepsy: novel pathogenic variants in ITPA and CLN5 identified in consanguineous families.

Genomic insights into autosomal recessive epilepsy: novel pathogenic variants in ITPA and CLN5 identified in consanguineous families.

Journal: Molecular biology reports

Published: July 17, 2025

Biallelic COL4A2 Variants Associated With Brain Small Vessel Disease and Brain Malformations.

Biallelic COL4A2 Variants Associated With Brain Small Vessel Disease and Brain Malformations.

Journal: Clinical genetics

Published: April 16, 2025

Challenges in Genomic Variant Interpretation Within Pakistani Populations due to Genomic Healthcare Inequalities.

Challenges in Genomic Variant Interpretation Within Pakistani Populations due to Genomic Healthcare Inequalities.

Journal: American journal of medical genetics. Part A

Published: January 30, 2025

Exome Sequencing of Consanguineous Pashtun Families With Familial Epilepsy Reveals Causative and Candidate Variants in TSEN54, MOCS2, and OPHN1.

Exome Sequencing of Consanguineous Pashtun Families With Familial Epilepsy Reveals Causative and Candidate Variants in TSEN54, MOCS2, and OPHN1.

Journal: Clinical genetics

Published: July 25, 2024

Pathogenic variants identification in primary congenital glaucoma patients using whole exome sequencing.

Pathogenic variants identification in primary congenital glaucoma patients using whole exome sequencing.

Journal: Scientific reports

Published: July 07, 2024

Prevalence Of Human Adenovirus In Paediatric Patients Presenting With Acute Respiratory Symptoms At Different Hospitals Of Pakistan.

Prevalence Of Human Adenovirus In Paediatric Patients Presenting With Acute Respiratory Symptoms At Different Hospitals Of Pakistan.

Journal: Journal of Ayub Medical College, Abbottabad : JAMC

Published: February 27, 2023

Antibiotic resistance genes in the gut microbiota of mothers and linked neonates with or without sepsis from low- and middle-income countries.

Antibiotic resistance genes in the gut microbiota of mothers and linked neonates with or without sepsis from low- and middle-income countries.

Journal: Nature microbiology

Published: May 04, 2021

Bacterial Spectrum and Antimicrobial Profile of Pediatric Blood Stream Infection at a Tertiary Care Hospital in Pakistan.

Bacterial Spectrum and Antimicrobial Profile of Pediatric Blood Stream Infection at a Tertiary Care Hospital in Pakistan.

Journal: Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih

Published: January 08, 2021

Serological Screening of Suspected COVID-19 Patients in Pakistan.

Serological Screening of Suspected COVID-19 Patients in Pakistan.

Journal: Journal of the College of Physicians and Surgeons--Pakistan : JCPSP

Published: September 08, 2020

Showing 1-12 of 14

Last Updated: 09/26/2026