Salman Kirmani

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 4

Top Topics

Duchenne Muscular Dystrophy

Dna Methylation

Top Venues

Case reports in genetics

American journal of medical genetics. Part A

JMIR research protocols

Journal of genetic counseling

This page only lists publications with an associated author ORCID identifier.

Publications

Fizza Akbar, Shafaq Muhammad Saleem, Ehtesham Khalid, Shahnaz Ibrahim, Bushra Afroze, Salman Kirmani, Sara Khan
The spectrum of hereditary neuromuscular disorders in the Pakistani population. American journal of medical genetics. Part A (2023)
Zul Qarnain, Fatima Khan, Fizza Akbar, Salman Kirmani
Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report). Case reports in genetics 2022 (2022)
Lubaina Ehsan, Muhammad Talha Waheed, Fizza Akbar, Zahraa Siddiqui, Abida K Sattar, Salman Kirmani
Challenges and opportunities in the establishment of a hereditary breast cancer clinic at an academic medical center in a low-middle income country. Journal of genetic counseling 31 (4) (2022)
Ayat Siddiqui, Laila Akbar Ladak, Abdul Momin Kazi, Sidra Kaleem Jafri, Fizza Akbar, Salman Kirmani
Assessing Health-Related Quality of Life, Morbidity, and Survival Status for Individuals With Down Syndrome in Pakistan (DS-Pak): Protocol for a Web-Based Collaborative Registry. JMIR research protocols 10 (6) (2021)