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Naveed Wasif

10PUBLICATIONS

33CO-AUTHORS

Polymerisation mechanismsNeonatologyCancer geneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)

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Publications (10)

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|Apr 14, 2025

Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of <i>PGAP2</i> Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3).

Seda Susgun, Afif Ben-Mahmoud, Franz Rüschendorf

|Mar 06, 2025

A Novel Biallelic Variant in IHH Causing Acrocapitofemoral Dysplasia in a Pakistani Family.

Tayyaba Saeed, Nousheen Bibi, Ashfaq Ahmad

|Sep 18, 2023

Molecular insight into CREBBP and TANGO2 variants causing intellectual disability.

Syeda Iqra Hussain, Nazif Muhammad, Niamatullah Khan

|May 23, 2023

A novel frameshift variant in UBA2 causing split-hand/foot malformations in a Pakistani family.

Asia Parveen, Muhammad Tariq, Sher Alam Khan

|Dec 23, 2022

The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (<i>ARMC3</i>).

Adil U Rehman, Malaika Hamid, Sher Alam Khan

|Sep 01, 2020

Novel homozygous nonsense variant in MLPH causing Griscelli syndrome type 3 in a consanguineous Pakistani family.

Naveed Wasif, Asia Parveen, Hina Bashir

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Frequent Collaborators

2 joint publications

Sulman Basit

2 joint publications

Asia Parveen

2 joint publications

Muhammad Usman Mirza

2 joint publications

Saadullah Khan

2 joint publications

Sher Alam Khan

1 joint publications

Michiel Vanmeert

1 joint publications

Matheus Froeyen

1 joint publications

Wasim Ahmed

1 joint publications

Hyung-Goo Kim

1 joint publications

Syed Shoaib Ahmed

Frequent Collaborators

2 joint publications

Sulman Basit

2 joint publications

Asia Parveen

2 joint publications

Muhammad Usman Mirza

2 joint publications

Saadullah Khan

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