Muhammad Sajid Hussain - Dissemin

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All papers authored by Muhammad Sajid Hussain

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2024 Maria Asif, Arwa Ishaq A. Khayyat, Salem Alawbathani, Uzma Abdullah, Anne Sanner

ORCID

, Theodoros Georgomanolis, Judith Haasters, Kerstin Becker, Birgit Budde, Christian Becker, Holger Thiele, Shahid M. Baig, María Isidoro-García, Dominic Winter, Hans-Martin Pogoda and 8 other authors

Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia

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2023 Maria Asif, Uzma Abdullah

ORCID

, Peter Nürnberg

ORCID

, Sigrid Tinschert, Muhammad Sajid Hussain

ORCID

Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic Microcephaly

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2022 Maria Asif, Emrah Kaygusuz, Marwan Shinawi, Anna Nickelsen, Tzung-Chien Hsieh, Prerana Wagle, Birgit S. Budde, Jennifer Hochscherf, Uzma Abdullah, Stefan Höning, Christian Nienberg, Dirk Lindenblatt, Angelika A. Noegel, Janine Altmüller

ORCID

, Holger Thiele and 18 other authors

De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway

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2021 Maria Asif, Ionut Dragos Mocanu, Uzma Abdullah, Wolfgang Höhne, Janine Altmüller

ORCID

, Ehtisham Ul Haq Makhdoom, Holger Thiele, Shahid Mahmood Baig, Peter Nürnberg, Luitgard Graul‐Neumann

ORCID

, Muhammad Sajid Hussain

ORCID

A novel missense variant of SCN4A co‐segregates with congenital essential tremor in a consanguineous Kurdish family

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Syeda Seema Waseem, Abubakar Moawia, Birgit Budde

ORCID

, Muhammad Tariq

ORCID

ORCID

ORCID

ORCID

, Maria Iqbal, Naveed Altaf Malik, Saif ul Haque, Janine Altmüller

ORCID

, Holger Thiele, Muhammad Sajid Hussain

ORCID

, Sebahattin Cirak, Shahid Mahmood Baig and 1 other authors

A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family

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Natalie Young, Maria Asif, Matthew Jackson

ORCID

, Daniel Martín Fernández-Mayoralas, Mar Jimenez de la Peña, Beatriz Calleja-Pérez, Sara Álvarez, Eve Hunter-Featherstone, Angelika A. Noegel

ORCID

, Wolfgang Höhne, Peter Nürnberg

ORCID

, Boguslaw Obara, Muhammad Sajid Hussain

ORCID

, Iakowos Karakesisoglou, Alberto Fernández-Jaén

ORCID

Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism

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Ehtisham Ul Haq Makhdoom, Syeda Seema Waseem, Maria Iqbal, Uzma Abdullah

ORCID

, Ghulam Hussain, Maria Asif, Birgit Budde

ORCID

, Wolfgang Höhne, Sigrid Tinschert, Saadia Maryam Saadi

ORCID

, Hammad Yousaf, Zafar Ali, Ambrin Fatima, Emrah Kaygusuz

ORCID

ORCID

and 10 other authors

Modifier Genes in Microcephaly: A Report on WDR62, CEP63, RAD50 and PCNT Variants Exacerbating Disease Caused by Biallelic Mutations of ASPM and CENPJ

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2020 Muhammad Farooq, Louise Lindbæk, Nicolai Krogh, Canan Doganli, Cecilie Keller, Maren Mönnich, André Brás Gonçalves, Srinivasan Sakthivel, Yuan Mang, Ambrin Fatima, Vivi Søgaard Andersen, Muhammad S. Hussain

ORCID

, Hans Eiberg, Lars Hansen, Klaus Wilbrandt Kjaer and 8 other authors

RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis

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Shaista Ilyas

ORCID

, Nighat K. Ullah, Muhammad Ilyas

ORCID

, Kerstin Wennhold, Maria Iqbal, Hans A. Schlößer, Muhammad S. Hussain

ORCID

, Sanjay Mathur

ORCID

Mediating the Fate of Cancer Cell Uptake: Dual-Targeted Magnetic Nanovectors with Biotin and Folate Surface Ligands

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Sajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, Ilyas Ahmad, Maria Iqbal, Syeda Seema Waseem, Maria Asif, Uzma Abdullah, Ehtisham Ul Haq Makhdoom, Emrah Kaygusuz, Muhammad Zakaria, Shafaq Ramzan, Saif ul Haque, Asif Mir, Iram Anjum and 12 other authors

An update of pathogenic variants in ASPM , WDR62, CDK5RAP2 , STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

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Daniel Bamborschke

ORCID

, Hülya‐Sevcan Daimagüler, Andreas Hahn, Muhammad S. Hussain

ORCID

, Peter Nürnberg, Sebahattin Cirak

Mutation in CEP135 causing primary microcephaly and subcortical heterotopia

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Sajida Rasool, Saba Irshad, Neelam Saba, Fiaz Mehak, Muhammad Sajid Hussain

ORCID

, Muhammad Wajid Hussain, Peter Nürnberg

A Novel Homozygous Nonsense Variant in BICD2 Underlies Hereditary Spastic Paraplegia Complex Type

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2019 Ilknur Sur-Erdem

ORCID

, Muhammed Sajid Hussain

ORCID

, Maria Asif, Nareg Pınarbası, Ali Cenk Aksu, Angelika A. Noegel

Nesprin-1 impact on tumorigenic cell phenotypes

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Thomas M. Kinfe

ORCID

, Maria Asif, Krishnan V. Chakravarthy, Timothy R. Deer, Jeffery M. Kramer, Thomas L. Yearwood, Rene Hurlemann

ORCID

, Muhammad Sajid Hussain

ORCID

, Susanne Motameny, Prerana Wagle, Peter Nürnberg, Sascha Gravius, Thomas Randau, Nadine Gravius, Shafqat R. Chaudhry and 1 other authors

Unilateral L4-dorsal root ganglion stimulation evokes pain relief in chronic neuropathic postsurgical knee pain and changes of inflammatory markers: part II whole transcriptome profiling

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2017 Muhammad Sajid Hussain

ORCID

Mutations of KIF14 Cause Primary Microcephaly by Impairing Cytokinesis.

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A. Moawia, S. Waseem, B. Budde, A. Noegel, P. Nürnberg, S. Baig, A. Hahn, M. Hussain

ORCID

Mutations in KIF14, Encoding Kinesin-Like Protein KIF14, Cause Primary and Syndromic Microcephaly

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I. Ahmad, S. M. Baig, A. R. Abdulkareem, M. S. Hussain

ORCID

, I. Sur

ORCID

, M. R. Toliat, G. Nürnberg, N. Dalibor, A. Moawia, S. S. Waseem, M. Asif, H. Nagra, M. Sher, M. M. A. Khan, I. Hassan and 5 other authors

Genetic heterogeneity in Pakistani microcephaly families revisited

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This paper is made freely available by the publisher.

2016 Salil K. Sukumaran, Maria Stumpf, Sarah Salamon, Ilyas Ahmad, Kurchi Bhattacharya, Sarah Fischer, Rolf Müller, Janine Altmüller

ORCID

, Birgit Budde, Holger Thiele, Muhammad Tariq, Naveed Altaf Malik, Peter Nürnberg, Shahid Mahmood Baig, Muhammad Sajid Hussain

ORCID

and 1 other authors

CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly

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2015 Sandra Szczepanski, Muhammad Sajid Hussain

ORCID

ORCID

, Janine Altmüller

ORCID

, Holger Thiele, Uzma Abdullah, Syeda Seema Waseem, Abubakar Moawia, Gudrun Nürnberg, Angelika Anna Noegel, Shahid Mahmood Baig, Peter Nürnberg

A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family

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This paper is available in a repository.

2014 Muhammad Sajid Hussain

ORCID

, Agatino Battaglia, Sandra Szczepanski, Emrah Kaygusuz, Mohammad Reza Toliat, Shin-Ichi Sakakibara, Janine Altmüller

ORCID

, Holger Thiele, Gudrun Nürnberg, Shahida Moosa, Gökhan Yigit, Filippo Beleggia, Sigrid Tinschert, Jill Clayton-Smith, Pradeep Vasudevan and 13 other authors

Mutations in CKAP2L, the Human Homolog of the Mouse Radmis Gene, Cause Filippi Syndrome

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