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Muhammad Ansar

4PUBLICATIONS

19CO-AUTHORS

Adolescent healthNeurology and neuromuscular diseasesNeurogeneticsGenetics not elsewhere classified

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Publications (4)

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|Jan 12, 2026

Proceedings of the 12<sup>th</sup> International Meeting on Neuroacanthocytosis, Cohen Syndrome, and Other VPS13-Related Disorders.

Fabrizio Vacca, Binnaz Yalcin, Lars Kaestner

|Oct 25, 2022

<i>KIF1A</i> novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IIC.

Saima Ghafoor, Muhammad Arshad Rafiq, Syed Tahir Abbas Shah

|Aug 10, 2022

A new nonsense mutation in <i>HMX1</i> in two siblings with oculoauricular syndrome.

Muhammad Ansar, Samra Javed, Hafiz Muhammad Azhar Baig

|Mar 11, 2021

Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2.

Stylianos E Antonarakis, Aleš Holoubek, Melivoia Rapti

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Frequent Collaborators

1 joint publications

Stylianos E Antonarakis

1 joint publications

Justyna Iwaszkiewicz

1 joint publications

Vincent Zoete

1 joint publications

Callum Wilson

1 joint publications

Christelle Borel

1 joint publications

Olivier Menzel

1 joint publications

Kateřina Kuželová

1 joint publications

Federico A Santoni

1 joint publications

Hafiz Muhammad Azhar Baig

1 joint publications

Mathieu Quinodoz

Frequent Collaborators

1 joint publications

Stylianos E Antonarakis

1 joint publications

Justyna Iwaszkiewicz

1 joint publications

Vincent Zoete

1 joint publications

Callum Wilson

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