Aizeddin A. Mhanni

877 total citations
27 papers, 501 citations indexed

About

Aizeddin A. Mhanni is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Aizeddin A. Mhanni has authored 27 papers receiving a total of 501 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Rheumatology. Recurrent topics in Aizeddin A. Mhanni's work include Epigenetics and DNA Methylation (5 papers), Metabolism and Genetic Disorders (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Aizeddin A. Mhanni is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Metabolism and Genetic Disorders (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Aizeddin A. Mhanni collaborates with scholars based in Canada, United States and Netherlands. Aizeddin A. Mhanni's co-authors include Ross McGowan, Cheryl R. Greenberg, Albert E. Chudley, Michael S. Salman, Charuta Joshi, Patrick H. Krone, Hal Landy, Michael P. Whyte, Martin H. Reed and Edward Leung and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Bone.

In The Last Decade

Aizeddin A. Mhanni

25 papers receiving 481 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Aizeddin A. Mhanni Canada 12 310 116 67 63 58 27 501
Kinga Hadzsiev Hungary 14 316 1.0× 212 1.8× 55 0.8× 43 0.7× 58 1.0× 73 624
Kiriko Kaneko Japan 13 402 1.3× 30 0.3× 67 1.0× 94 1.5× 25 0.4× 20 624
Takafumi Yoshioka Japan 15 223 0.7× 53 0.5× 61 0.9× 57 0.9× 22 0.4× 60 627
Chupong Ittiwut Thailand 14 261 0.8× 151 1.3× 45 0.7× 19 0.3× 60 1.0× 53 496
Bret L. Bostwick United States 9 225 0.7× 215 1.9× 29 0.4× 27 0.4× 35 0.6× 17 414
Göran Brandberg Sweden 8 244 0.8× 116 1.0× 71 1.1× 22 0.3× 74 1.3× 10 442
Chutaro Yamanaka Japan 14 222 0.7× 175 1.5× 123 1.8× 252 4.0× 42 0.7× 32 683
Mikołaj Łabuda Canada 10 384 1.2× 141 1.2× 32 0.5× 25 0.4× 15 0.3× 13 594
M Poissonnier France 14 324 1.0× 317 2.7× 114 1.7× 54 0.9× 29 0.5× 20 712
Toshikatsu Shinka Japan 18 505 1.6× 419 3.6× 58 0.9× 34 0.5× 150 2.6× 56 894

Countries citing papers authored by Aizeddin A. Mhanni

Since Specialization
Citations

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

Fields of papers citing papers by Aizeddin A. Mhanni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aizeddin A. Mhanni

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

All Works

20 of 20 papers shown
1.
Mhanni, Aizeddin A., Christiane Auray‐Blais, Michel Boutin, et al.. (2020). Therapeutic challenges in two adolescent male patients with Fabry disease and high antibody titres. Molecular Genetics and Metabolism Reports. 24. 100618–100618. 6 indexed citations
2.
Mhanni, Aizeddin A., et al.. (2020). Isolated sulfite oxidase deficiency: a founder mutation. Molecular Case Studies. 6(6). a005900–a005900. 5 indexed citations
3.
Mhanni, Aizeddin A., et al.. (2015). Successful therapy for protein-losing enteropathy caused by chronic neuronopathic Gaucher disease. SHILAP Revista de lepidopterología. 6. 13–15. 10 indexed citations
4.
Spriggs, Elizabeth, et al.. (2014). Germline mosaicism in X-linked periventricular nodular heterotopia. BMC Neurology. 14(1). 125–125. 5 indexed citations
5.
Leung, Edward, Aizeddin A. Mhanni, Martin H. Reed, et al.. (2013). Outcome of Perinatal Hypophosphatasia in Manitoba Mennonites: A Retrospective Cohort Analysis. JIMD Reports. 11. 73–78. 55 indexed citations
6.
Whyte, Michael P., Priya S. Kishnani, C. R. Greenberg, et al.. (2012). Hypophosphatasia: Enzyme Replacement Therapy (Asfotase Alfa) Decreases TNSALP Substrate Accumulation And Improves Functional Outcomes In Affected Adolescents And Adults.. 51(1). 35. 6 indexed citations
7.
Doherty, Dan, Albert E. Chudley, Gail Coghlan, et al.. (2012). GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome. The American Journal of Human Genetics. 91(1). 209–209. 2 indexed citations
8.
Udow, Sean, Martin Bunge, Lawrence Ryner, Aizeddin A. Mhanni, & Michael S. Salman. (2012). Prolonged Survival and Serial Magnetic Resonance Imaging/Magnetic Resonance Spectroscopy Changes in Infantile Krabbe Disease. Pediatric Neurology. 47(4). 299–302. 9 indexed citations
9.
Whyte, Michael P., Cheryl R. Greenberg, Katherine L. Madson, et al.. (2012). Enzyme replacement therapy (ENB-0040) in hypophosphatasia improves functional outcome and decreases TNSALP substrates in adolescents and adults. Bone. 50. S39–S39.
10.
Frosk, Patrick, Aizeddin A. Mhanni, & Mubeen F. Rafay. (2012). SCN1A Mutation Associated With Intractable Myoclonic Epilepsy and Migraine Headache. Journal of Child Neurology. 28(3). 389–391. 13 indexed citations
11.
Doherty, Dan, Albert E. Chudley, Gail Coghlan, et al.. (2012). GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome. The American Journal of Human Genetics. 90(6). 1088–1093. 81 indexed citations
12.
Mhanni, Aizeddin A., et al.. (2011). Recurrent Acute Necrotizing Encephalopathy in a Canadian Aboriginal Child. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 38(6). 925–928. 3 indexed citations
13.
Joshi, Charuta, Cheryl R. Greenberg, Aizeddin A. Mhanni, & Michael S. Salman. (2009). Ketogenic Diet in Alpers-Huttenlocher Syndrome. Pediatric Neurology. 40(4). 314–316. 47 indexed citations
14.
Tyson, Christine, Angelika J. Dawson, Todd J. Anderson, et al.. (2009). Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability. American Journal of Medical Genetics Part A. 149A(3). 490–495. 14 indexed citations
15.
Mhanni, Aizeddin A., et al.. (2005). Novel splice variants associated with one of the zebrafish dnmt3genes. BMC Developmental Biology. 5(1). 23–23. 14 indexed citations
16.
Mhanni, Aizeddin A. & Ross McGowan. (2004). Global changes in genomic methylation levels during early development of the zebrafish embryo. Development Genes and Evolution. 214(8). 412–417. 97 indexed citations
17.
Mhanni, Aizeddin A. & Ross McGowan. (2002). Variations in DNA (cytosine-5)-methyltransferase-1 expression during oogenesis and early development of the zebrafish. Development Genes and Evolution. 212(11). 530–533. 19 indexed citations
18.
Mhanni, Aizeddin A., et al.. (2001). Cloning and sequence analysis of a zebrafish cDNA encoding DNA (cytosine‐5)‐methyltransferase‐1. genesis. 30(4). 213–219. 14 indexed citations
19.
Mhanni, Aizeddin A. & Albert E. Chudley. (1999). Genetic landmarks through philately – Kabuki theater and Kabuki syndrome. Clinical Genetics. 56(2). 116–117. 6 indexed citations
20.
Mhanni, Aizeddin A., Angelika J. Dawson, & Albert E. Chudley. (1998). Vertical transmission of the Ohdo blepharophimosis syndrome. American Journal of Medical Genetics. 77(2). 144–148. 9 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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