Muzammil Ahmad Khan (Muzammil A Khan)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 10

Top Venues

Genes

Molecular genetics & genomic medicine

Molecular genetics and genomics : MGG

Annals of human genetics

Gomal University

Quaid-i-Azam University (PHD)

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

Affiliation History

Gomal University - Nov 14 2011

Pakistan

Assistant Professor :: Gomal Centre of Biochemistry and Biotechnology

Education History

Quaid-i-Azam University Mar 10 2007 - Oct 27 2011

Pakistan

PHD :: Biochemistry

Publications

Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal, Amjad Ullah Khan, Muhammad Ikram, Mari Muurinen, Shabir Hussain, Petra Loid, Muzammil Ahmad Khan, Outimaija Mäkitie
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly. Genes 14 (4) (2023)
Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal, Amjad Ullah Khan, Muhammad Ikram, Mari Muurinen, Shabir Hussain, Petra Loid, Muzammil Ahmad Khan, Outimaija Mäkitie
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly. Genes 14 (4) (2023)
Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal, Amjad Ullah Khan, Muhammad Ikram, Mari Muurinen, Shabir Hussain, Petra Loid, Muzammil Ahmad Khan, Outimaija Mäkitie
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly. Genes 14 (4) (2023)
Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal, Amjad Ullah Khan, Muhammad Ikram, Mari Muurinen, Shabir Hussain, Petra Loid, Muzammil Ahmad Khan, Outimaija Mäkitie
Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly. Genes 14 (4) (2023)
Muhammad Zeeshan Ali, Arshad Farid, Safeer Ahmad, Muhammad Muzammal, Mohammad Al Mohaini, Abdulkhaliq J Alsalman, Maitham A Al Hawaj, Yousef N Alhashem, Abdulmonem A Alsaleh, Eman M Almusalami, Mahpara Maryam, Muzammil Ahmad Khan
In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in Human SLITRK1 Gene. Genes 13 (4) (2022)
Safeer Ahmad, Muhammad Zeeshan Ali, Muhammad Muzammal, Fayaz Ahmad Mir, Muzammil Ahmad Khan
The molecular genetics of human appendicular skeleton. Molecular genetics and genomics : MGG 297 (5) (2022)
Muhammad Muzammal, Alessandro di Cerbo, Eman M Almusalami, Arshad Farid, Muzammil Ahmad Khan, Shakira Ghazanfar, Mohammad Al Mohaini, Abdulkhaliq J Alsalman, Yousef N Alhashem, Maitham A Al Hawaj, Abdulmonem A Alsaleh
In Silico Analysis of the L-2-Hydroxyglutarate Dehydrogenase Gene Mutations and Their Biological Impact on Disease Etiology. Genes 13 (4) (2022)
Muhammad Z Ali, Jasmin Blatterer, Muzammil Ahmad Khan, Erich Schaflinger, Erwin Petek, Safeer Ahmad, Ejazullah Khan, Christian Windpassinger
Identification of a novel protein truncating mutation p.Asp98* in XPC associated with xeroderma pigmentosum in a consanguineous Pakistani family. Molecular genetics & genomic medicine 8 (2) (2020)
Hadia Gul, Abdul Haleem Shah, Ricardo Harripaul, Anna Mikhailov, Kamalben Prajapati, Ejazullah Khan, Farman Ullah, Muhammad Zubair, Muhammad Zeeshan Ali, Ayesha Haleem Shah, Said Salman, Saadullah Khan, John B Vincent, Muzammil Ahmad Khan
Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations. Annals of human genetics 83 (4) (2019)
Muhammad Muzammal, Muhammad Zubair, Sophie Bierbaumer, Jasmin Blatterer, Ricarda Graf, Aisha Gul, Safdar Abbas, Muhammad Badar, Ansar Ahmad Abbasi, Muzammil Ahmad Khan, Christian Windpassinger
Exome sequence analysis in consanguineous Pakistani families inheriting Bardet-Biedle syndrome determined founder effect of mutation c.299delC (p.Ser100Leufs*24) in BBS9 gene. Molecular genetics & genomic medicine 7 (8) (2019)

Muzammil Ahmad Khan.css-eqlu8i{font-size:small;padding-left:4px;} (Muzammil A Khan)

Publication Activity (10 Years)

Top Topics

Top Venues

Muzammil Ahmad Khan (Muzammil A Khan)