Aziz Mhanni

753 total citations
10 papers, 102 citations indexed

About

Aziz Mhanni is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Aziz Mhanni has authored 10 papers receiving a total of 102 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Rheumatology. Recurrent topics in Aziz Mhanni's work include Genomics and Rare Diseases (2 papers), Craniofacial Disorders and Treatments (2 papers) and RNA modifications and cancer (1 paper). Aziz Mhanni is often cited by papers focused on Genomics and Rare Diseases (2 papers), Craniofacial Disorders and Treatments (2 papers) and RNA modifications and cancer (1 paper). Aziz Mhanni collaborates with scholars based in Canada, Germany and United States. Aziz Mhanni's co-authors include Mubeen F. Rafay, Atul Sharma, Martin Bunge, Brandy Wicklow, Monica Hrynchak, Eloi Mercier, Christine Tyson, Diana Alcantara, M. E. Suzanne Lewis and Sandra L. Marles and has published in prestigious journals such as Human Molecular Genetics, Frontiers in Immunology and Orphanet Journal of Rare Diseases.

In The Last Decade

Aziz Mhanni

9 papers receiving 100 citations

Peers

Aziz Mhanni

GENET

MB

PPCH

SURGE

EDM

Suliman Khan Pakistan

Resham Ejaz Canada

Daniel Doherty United States

Sophia Kitsiou Greece

Federica Tamburrino Italy

Jazmín Arteaga‐Vázquez Mexico

Renchao Liu China

Abdulrahman Swaid Saudi Arabia

Shivarajan Amudhavalli United States

Fabienne Prieur France

Suliman Khan Pakistan

Aziz Mhanni

36 ×0.7

GENET

59 ×1.2

MB

26 ×0.9

PPCH

8 ×0.6

SURGE

5 ×0.5

EDM

Citations per year, relative to Aziz Mhanni Aziz Mhanni (= 1×) peers Suliman Khan

Countries citing papers authored by Aziz Mhanni

Since Specialization

Citations

This map shows the geographic impact of Aziz Mhanni'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 Aziz Mhanni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aziz Mhanni more than expected).

Fields of papers citing papers by Aziz Mhanni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aziz Mhanni. 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 Aziz Mhanni. The network helps show where Aziz Mhanni may publish in the future.

Co-authorship network of co-authors of Aziz Mhanni

This figure shows the co-authorship network connecting the top 25 collaborators of Aziz Mhanni. A scholar is included among the top collaborators of Aziz Mhanni 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 Aziz Mhanni. Aziz Mhanni is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Rubin, Tamar, Lum Peng Lim, Michael S. Salman, et al.. (2025). Two rare mutations in homozygosity synergize to silence TREX1 in Aicardi-Goutières syndrome. Frontiers in Immunology. 16. 1557632–1557632.

2.

Greenberg, Cheryl R., et al.. (2022). Impact of discontinuing 5 years of enzyme replacement treatment in a cohort of 6 adults with hypophosphatasia: A case series. Bone Reports. 17. 101617–101617. 7 indexed citations

3.

Marshall, Aren E., Xiaomin Dong, Aziz Mhanni, et al.. (2021). Compound heterozygous variants in SHQ1 are associated with a spectrum of neurological features, including early-onset dystonia. Human Molecular Genetics. 31(4). 614–624. 10 indexed citations

4.

Mhanni, Aziz, et al.. (2020). Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba: 1980–2020. Molecular Genetics and Metabolism Reports. 25. 100666–100666. 1 indexed citations

5.

Dawson, Angelika J., Karine Hovanes, Jing Liu, et al.. (2020). Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly. Clinical Dysmorphology. 30(2). 83–88. 3 indexed citations

6.

Shamsi, Aisha Al, et al.. (2020). A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature review. Molecular Genetics & Genomic Medicine. 8(11). e1514–e1514. 5 indexed citations

7.

Bunge, Martin, et al.. (2017). Increasing incidence of optic nerve hypoplasia/septo-optic dysplasia spectrum: Geographic clustering in Northern Canada. Paediatrics & Child Health. 22(8). 445–453. 24 indexed citations

8.

Harvard, Chansonette, Eloi Mercier, Rita Colnaghi, et al.. (2011). Understanding the impact of 1q21.1 copy number variant. Orphanet Journal of Rare Diseases. 6(1). 54–54. 43 indexed citations

9.

Mhanni, Aziz, et al.. (2011). Variable expressivity of a novel mutation in the SCN1A gene leading to an autosomal dominant seizure disorder. Seizure. 20(9). 711–712. 3 indexed citations

10.

Greenberg, C. R., et al.. (2008). Genetic Testing of Children at Risk for Adult Onset Conditions: When is Testing Indicated?. Journal of Genetic Counseling. 17(6). 523–525. 6 indexed citations

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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