Hussain Muhammad Sajid - University of Cologne, University of Cologne

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Bio

Group leader at Cologne Center for Genomics (CCG), University of Cologne, in the field of human molecular genetics and biochemistry with an interest in exploring human disease biology and mechanism of disease pathogenesis (especially of inherited disorders like autosomal recessive primary microcephaly, intellectual disability, primordial dwarfism, Filippi syndrome, and essential tremors).

Research Interests

Papers共 66 篇Author StatisticsCo-AuthorSimilar Experts

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Molecular Genetics, Neuroimaging Outcomes, and Structural Analyses of Novel and Recurrent Variants of WDR62 Gene in Two Consanguineous Pakistani Families with Autosomal Recessive Primary Microcephaly

Komal Aslam,Aysha Saeed,Hafiza Iqra Saeed,Rasheeda Bashir, Hanna Abid, Roeha Akhtar, Nida Habib, Ramisha Khan, Roha Asif, Shereen Rafiq,Maria Asif,Ehtisham Ul Haq Makhdoom,Muhammad Sajid Hussain,Shahid Mahmood Baig,Iram Anjum

Molecular Biology Reportsno. 1 (2024): 1-11

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Biocompatible Hollow Gadolinium Oxide Nanocarriers for the Transport of Bioactive Molecules to Cells

Shifaa M. Siribbal,Anna Jurewicz, Menna Hassan,Sumiya Iqbal,Zhangjun Hu,Kajsa Uvdal,Muhammad S. Hussain,Sanjay Mathur,Shaista Ilyas

ACS Applied Nano Materialsno. 11 (2024): 12408-12419

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Investigating the Effects of a Single ASPM Variant (c.8508_8509) on Brain Architecture among Siblings in a Consanguineous Pakistani Family

Komal Aslam,Aysha Saeed, Iffat Jamil,Hafiza Iqra Saeed, Ramisha Khan,Samina Hassan, Shereen Rafiq,Maria Asif,Ehtisham Ul Haq Makhdoom,Rasheeda Bashir,Muhammad Sajid Hussain,Shahid Mahmood Baig,Iram Anjum

Molecular Biology Reportsno. 1 (2024)

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Recurrence Mutation in RBBP8 Gene Causing Non-Syndromic Autosomal Recessive Primary Microcephaly; Geometric Simulation Approach for Insight into Predicted Computational Models

Tahira Batool,Saba Irshad, Muhammad Riaz,Shahid Mahmood Baig,Peter Nuernberg,Muhammad Sajid Hussain

JOURNAL OF HUMAN GENETICS（2023）

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Targeted Next Generation Sequencing (NGS) identified novel mutations in rare neurodevelopmental disorders

Ammara Maryam,Maria Asif, Muhammad Ijaz, Urooj Fatima, Atir Raza, Nimra Maheen,Muhammad Sajid Hussain,Farooq Muhammad

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 200-200

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Biallelic mutations in CACTIN encoding component of spliceosome machinery cause severe intellectual disability, speech impairment and epilepsy

Uzma Abdullah,Maria Asif, Maryam Anayat, Ghulam Nasseer Udin,Muhammad Sajid Hussain

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 465-465

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RNA-Seq Analysis of Mung Bean (vigna Radiata L.) Roots Shows Differential Gene Expression and Predicts Regulatory Pathways Responding to Taxonomically Different Rhizobia

Sughra Hakim,Asma Imran,Muhammad Sajid Hussain,M. Sajjad Mirza

Microbiological research (2023): 127451-127451

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