Naveed Wasif

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 12

Top Venues

Genes

Molecular genetics & genomic medicine

The journal of gene medicine

BMC medical genetics

Universitätsklinikum Schleswig-Holstein

Quaid-i-Azam University Faculty of Biological Sciences (PHD)

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

Affiliation History

Universitätsklinikum Schleswig-Holstein Oct 8o 2018

Germany

Post-Doc :: Institute of Human Genetics

Education History

Quaid-i-Azam University Faculty of Biological Sciences Sep 4o 2007 - Nov 23o 2011

Pakistan

PHD

Publications

Asia Parveen, Muhammad Tariq, Sher Alam Khan, Naseebullah Kakar, Amina Arif, Naveed Wasif
A novel frameshift variant in UBA2 causing split-hand/foot malformations in a Pakistani family. Human genome variation 10 (1) (2023)
Syeda Iqra Hussain, Nazif Muhammad, Niamatullah Khan, Mobeen Khan, Fardous Fardous, Raheel Tahir, Muhammad Yasin, Sher Alam Khan, Shamim Saleha, Noor Muhammad, Naveed Wasif, Saadullah Khan
Molecular insight into CREBBP and TANGO2 variants causing intellectual disability. The journal of gene medicine (2023)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Sher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad, Hina Bashir, Niamat Khan, Noor Muhammad, Rüstem Yilmaz, Saadullah Khan, Naveed Wasif
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family. BMC medical genetics 21 (1) (2020)
Naveed Wasif, Asia Parveen, Hina Bashir, Fareeha Ashraf, Ehtasham Ali, Kashif Raza Khan, Amina Arif
Novel homozygous nonsense variant in MLPH causing Griscelli syndrome type 3 in a consanguineous Pakistani family. The Journal of dermatology 47 (11) (2020)
Asia Parveen, Muhammad Usman Mirza, Michiel Vanmeert, Javed Akhtar, Hina Bashir, Saadullah Khan, Saqib Shehzad, Matheus Froeyen, Wasim Ahmad, Muhammad Ansar, Naveed Wasif
A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations. Molecular genetics & genomic medicine 7 (9) (2019)
Asia Parveen, Sher Alam Khan, Muhammad Usman Mirza, Hina Bashir, Fatima Arshad, Maria Iqbal, Waseem Ahmad, Ahsan Wahab, Amal Fiaz, Sidra Naz, Fareeha Ashraf, Tayyaba Mobeen, Salman Aziz, Syed Shoaib Ahmed, Noor Muhammad, Nehal F Hassib, Mostafa I Mostafa, Nagwa E Gaboon, Roquyya Gul, Saadullah Khan, Matheus Froeyen, Muhammad Shoaib, Naveed Wasif
Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations. International journal of molecular sciences 20 (21) (2019)
Muhammad Umair, Naveed Wasif, Alia M Albalawi, Khushnooda Ramzan, Majid Alfadhel, Wasim Ahmad, Sulman Basit
Exome sequencing revealed a novel loss-of-function variant in the GLI3 transcriptional activator 2 domain underlies nonsyndromic postaxial polydactyly. Molecular genetics & genomic medicine 7 (7) (2019)

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Publication Activity (10 Years)

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Naveed Wasif