Uzma Abdullah

602 citations

23 papers · 152 indexed · h-index 8

Co-authors: Shahid Mahmood Baig Muhammad Tariq Niklas Dahl Joakim Klar Zafar Ali Ambrin Fatima Peter Nürnberg Muhammad Sajid Hussain
Topics: Genetics and Neurodevelopmental Disorders (8 papers)Genomics and Rare Diseases (7 papers)Microtubule and mitosis dynamics (5 papers)
Cited by: Neurology Genetics Sensory Systems
Journals: Cells Human Mutation Human Genetics
Partner nations: Pakistan Germany Sweden

In The Last Decade

Uzma Abdullah

23 papers receiving 152 citations

Peers

Countries citing papers authored by Uzma Abdullah

Since Specialization

Citations

This map shows the geographic impact of Uzma Abdullah's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Uzma Abdullah with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Uzma Abdullah more than expected).

Fields of papers citing papers by Uzma Abdullah

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Uzma Abdullah. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Uzma Abdullah. The network helps show where Uzma Abdullah may publish in the future.

Co-authorship network of co-authors of Uzma Abdullah

This figure shows the co-authorship network connecting the top 25 collaborators of Uzma Abdullah. A scholar is included among the top collaborators of Uzma Abdullah based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Uzma Abdullah. Uzma Abdullah is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Computational advances in the design and discovery of artemis inhibitors for radiosensitization in cancer therapy 2025 ·Frontiers in Chemistry ·(unknown),Uzma Abdullah,Sadia Nazir,Farhan Siddique,Nasir Jalal	1
2	Nanostructured lipid carriers applications in cosmeceuticals: structure, formulation, safety profile and market trends 2025 ·(unknown),Sadaf Ahmad,Muneeb Ur Rahman,(unknown),Uzma Abdullah	3
3	Whole exome sequencing identifies variable expressivity of CLN6 variants in Progressive myoclonic epilepsy affected families 2023 ·Epilepsy Research ·(unknown),(unknown),(unknown),Umme Habiba,(unknown),Sadiq Noor Khan,Yasir Ali,(unknown),Stéphanie Efthymiou,Uzma Abdullah,Ghazala Kaukab Raja,(unknown)	1
4	Whole-Exome sequencing identifies GYS2 biallelic variants in individuals with suspected epilepsy 2023 ·Seizure ·(unknown),(unknown),(unknown),Yasir Ali,Umme Habiba,(unknown),Sadia Saeed,Uzma Abdullah,Sadiq Noor Khan,(unknown),Ghazala Kaukab Raja,(unknown),Walid Fazeli,Wolfram S. Kunz,(unknown)	2
5	Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic Microcephaly 2023 ·Cells ·Maria Asif,Uzma Abdullah,Peter Nürnberg,Sigrid Tinschert,Muhammad Sajid Hussain	7
6	Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders 2023 ·Genes ·(unknown),(unknown),(unknown),(unknown),(unknown),Haq Nawaz Khan,(unknown),Barbara Vona,Uzma Abdullah,Naveed Altaf Malik,Joakim Klar,Stéphanie Efthymiou,Niklas Dahl,Henry Houlden,Mathias Toft,Shahid Mahmood Baig,Ambrin Fatima,Zafar Iqbal	4
7	Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability 2022 ·Genes ·Maria Asif,(unknown),(unknown),(unknown),(unknown),Christian Becker,Kerstin Becker,Holger Thiele,(unknown),(unknown),Shahid Mahmood Baig,Peter Nürnberg,Muhammad Sajid Hussain,Ghazala Kaukab Raja,Uzma Abdullah	6
8	A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family 2022 ·Cells ·(unknown),Leon Tejwani,Uzma Abdullah,Sadia Saeed,(unknown),(unknown),Jungmin Choi,Weilai Dong,Carol Nelson‐Williams,Richard P. Lifton,Janghoo Lim,Ghazala Kaukab Raja	2
9	Identification of a novel variant in GPR56/ADGRG1 gene through whole exome sequencing in a consanguineous Pakistani family 2021 ·Journal of Clinical Neuroscience ·(unknown),Muhammad Tariq,(unknown),(unknown),(unknown),Zafar Ali,Niklas Dahl,Uzma Abdullah,Shahid Mahmood Baig	3
10	A GDF5 frameshift mutation segregating with Grebe type chondrodysplasia and brachydactyly type C+ in a 6 generations family: Clinical report and mini review 2021 ·European Journal of Medical Genetics ·(unknown),Muhammad Farooq,Uzma Abdullah,Zafar Ali,(unknown),Farid Ullah,(unknown),Yasra Sarwar,(unknown),(unknown),Niels Tommerup,Shahid Mahmood Baig	4
11	Rare Pathogenic Variants in Genes Implicated in Glutamatergic Neurotransmission Pathway Segregate with Schizophrenia in Pakistani Families 2021 ·Genes ·Ambrin Fatima,Uzma Abdullah,Muhammad Farooq,Yuan Mang,Mana M. Mehrjouy,Maria Asif,Zafar Ali,Niels Tommerup,Shahid Mahmood Baig	4
12	A novel missense variant of SCN4A co‐segregates with congenital essential tremor in a consanguineous Kurdish family 2021 ·American Journal of Medical Genetics Part A ·Maria Asif,(unknown),Uzma Abdullah,Wolfgang Höhne,Janine Altmüller,(unknown),Hölger Thiele,Shahid Mahmood Baig,Peter Nürnberg,Luitgard Graul‐Neumann,Muhammad Sajid Hussain	2
13	Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families 2020 ·BMC Medical Genetics ·Yingjie Zhou,Muhammad Tariq,(unknown),Uzma Abdullah,Jianguo Zhang,Shahid Mahmood Baig	12
14	Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families 2019 ·Journal of Clinical Neuroscience ·(unknown),Muhammad Tariq,Zafar Ali,Ambrin Fatima,Joakim Klar,Uzma Abdullah,Aamir Ali,(unknown),(unknown),Jianguo Zhang,(unknown),(unknown),(unknown),(unknown),Jens Schuster,Niklas Dahl,Shahid Mahmood Baig	9
15	Primary microcephaly, primordial dwarfism, and brachydactyly in adult cases with biallelic skipping of RTTN exon 42 2019 ·Human Mutation ·(unknown),Ambrin Fatima,Joakim Klar,Johan Wikström,Uzma Abdullah,Zafar Ali,(unknown),Muhammad Tariq,Habib Ahmad,Jens Schuster,Shahid Mahmood Baig,Niklas Dahl	1
16	A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family 2017 ·European Journal of Medical Genetics ·Uzma Abdullah,Muhammad Farooq,Yuan Mang,Syeda Marriam Bakhtiar,Ambrin Fatima,Lars Hestbjerg Hansen,Klaus Kjaer,Lars Allan Larsen,(unknown),Niels Tommerup,Shahid Mahmood Baig	8
17	Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features 2017 ·BMC Medical Genetics ·Zafar Ali,(unknown),Joakim Klar,Johan Wikström,Farid Ullah,(unknown),Uzma Abdullah,Shahid Mahmood Baig,Niklas Dahl	19
18	Incidental Thyroid Carcinoma in Patients Treated Surgically for Presumably Benign Thyroid Disease. 2017 ·PubMed ·(unknown),Uzma Abdullah,(unknown),(unknown),(unknown),Ranjit Sah	2
19	A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family 2015 ·Human Genetics ·(unknown),Muhammad Sajid Hussain,İlknur Sur‐Erdem,Janine Altmüller,Hölger Thiele,Uzma Abdullah,(unknown),(unknown),Gudrun Nürnberg,Angelika A. Noegel,Shahid Mahmood Baig,Peter Nürnberg	25
20	A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency 2014 ·BMC Medical Genetics ·(unknown),Joakim Klar,Muhammad Tariq,(unknown),Naveed Altaf Malik,(unknown),Uzma Abdullah,Tahir Naeem Khan,Raili Raininko,Shahid Mahmood Baig,Niklas Dahl	21

About Uzma Abdullah

Uzma Abdullah is a scholar working on Genetics, Neurology and Cell Biology, having authored 23 papers that have together received 152 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (7 papers) and Microtubule and mitosis dynamics (5 papers). The work is most often cited by research in Neurology (25 citations), Genetics (65 citations) and Sensory Systems (11 citations). Uzma Abdullah has collaborated with scholars based in Pakistan, Germany and Sweden. Frequent co-authors include Shahid Mahmood Baig, Muhammad Tariq, Niklas Dahl, Joakim Klar, Zafar Ali, Ambrin Fatima, Peter Nürnberg, Muhammad Sajid Hussain, Jianguo Zhang and Farid Ullah. Their work appears in journals such as Cells, Human Mutation and Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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