Ahm M. Huq

492 total citations
16 papers, 319 citations indexed

About

Ahm M. Huq is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Ahm M. Huq has authored 16 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Psychiatry and Mental health. Recurrent topics in Ahm M. Huq's work include Genomic variations and chromosomal abnormalities (3 papers), Ion channel regulation and function (3 papers) and Epilepsy research and treatment (3 papers). Ahm M. Huq is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Ion channel regulation and function (3 papers) and Epilepsy research and treatment (3 papers). Ahm M. Huq collaborates with scholars based in United States, Australia and Germany. Ahm M. Huq's co-authors include Fatema Serajee, Harry T. Chugani, Senthil K. Sundaram, Benjamin J. Wilson, Ram S. Verma, B Shan, John A. Lewis, Keisuke Ueda, Harvey Dosik and Lynne Hobson and has published in prestigious journals such as Journal of Biological Chemistry, Neurology and PEDIATRICS.

In The Last Decade

Ahm M. Huq

15 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ahm M. Huq United States 10 132 89 82 75 60 16 319
Ana Florencia Vega-Benedetti Italy 9 128 1.0× 98 1.1× 109 1.3× 17 0.2× 11 0.2× 13 338
Haruka Yamamoto Japan 11 196 1.5× 31 0.3× 27 0.3× 48 0.6× 16 0.3× 31 357
Katy Sterling-Levis Australia 8 64 0.5× 55 0.6× 121 1.5× 53 0.7× 25 0.4× 11 323
Heidi Mateus Colombia 11 165 1.3× 119 1.3× 33 0.4× 7 0.1× 21 0.3× 32 362
Aaron D. Besterman United States 10 110 0.8× 130 1.5× 52 0.6× 18 0.2× 11 0.2× 24 338
Anna Erlandson Sweden 9 248 1.9× 141 1.6× 75 0.9× 21 0.3× 68 1.1× 13 327
Lise-Andrée Gobeil Canada 8 271 2.1× 178 2.0× 25 0.3× 9 0.1× 73 1.2× 9 512
Christine Windemuth Germany 9 77 0.6× 102 1.1× 27 0.3× 30 0.4× 165 2.8× 14 402
Iain Fotheringham United Kingdom 4 111 0.8× 255 2.9× 185 2.3× 42 0.6× 42 0.7× 11 358
Vinayak Rayannavar United States 7 111 0.8× 16 0.2× 12 0.1× 36 0.5× 40 0.7× 9 267

Countries citing papers authored by Ahm M. Huq

Since Specialization
Citations

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

Fields of papers citing papers by Ahm M. Huq

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ahm M. Huq. 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 Ahm M. Huq. The network helps show where Ahm M. Huq may publish in the future.

Co-authorship network of co-authors of Ahm M. Huq

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

All Works

16 of 16 papers shown
1.
2.
Li, Yang, et al.. (2022). Posterior reversible encephalopathy syndrome and autoimmunity. Autoimmunity Reviews. 22(2). 103239–103239. 7 indexed citations
3.
Serajee, Fatema, et al.. (2018). Clinical Reasoning: Siblings with progressive weakness, hypotonia, nystagmus, and hearing loss. Neurology. 90(7). e625–e631. 6 indexed citations
4.
Ueda, Keisuke, Fatema Serajee, & Ahm M. Huq. (2018). Clinical Benefit of NMDA Receptor Antagonists in a Patient With ATP1A2 Gene Mutation. PEDIATRICS. 141(Supplement_5). S390–S394. 17 indexed citations
5.
Serajee, Fatema, Marie Shaw, Lynne Hobson, et al.. (2018). O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling. Journal of Biological Chemistry. 293(27). 10810–10824. 49 indexed citations
6.
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Serajee, Fatema, Ahm M. Huq, & Keisuke Ueda. (2016). Exome Sequencing Identifying Dual Mutations in Calcium Signaling Genes GNAO1 and ATP2B3 in a Patient with Early Infantile Epileptic Encephalopathy. Journal of Pediatric Neurology. 15(4). 183–186. 2 indexed citations
8.
9.
Sundaram, Senthil K., et al.. (2013). Exome sequencing and diffusion tensor imaging in developmental disabilities. Pediatric Research. 75(3). 443–447. 8 indexed citations
10.
Sundaram, Senthil K., Ahm M. Huq, Zhen Sun, et al.. (2011). Exome sequencing of a pedigree with tourette syndrome or chronic tic disorder. Annals of Neurology. 69(5). 901–904. 34 indexed citations
11.
Sundaram, Senthil K., Ahm M. Huq, Benjamin J. Wilson, & Harry T. Chugani. (2010). Tourette syndrome is associated with recurrent exonic copy number variants. Neurology. 74(20). 1583–1590. 75 indexed citations
12.
Zhong, Hailang, et al.. (2003). No association between single nucleotide polymorphisms in DLX6 and piccolo genes at 7q21‐q22 and autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 119B(1). 98–101. 12 indexed citations
13.
Lewis, John A., Ahm M. Huq, & B Shan. (1989). Beta and gamma interferons act synergistically to produce an antiviral state in cells resistant to both interferons individually. Journal of Virology. 63(11). 4569–4578. 34 indexed citations
14.
Verma, Ram S. & Ahm M. Huq. (1987). Sex ratio of children with trisomy 21 or Down syndrome.. PubMed. 51(206-207). 145–8. 15 indexed citations
15.
Verma, Ram S., Ahm M. Huq, & Harvey Dosik. (1983). Racial variation of a non-fluorescent segment of the Y chromosome in East Indians.. Journal of Medical Genetics. 20(2). 102–106. 9 indexed citations
16.
Verma, Ram S., et al.. (1982). Higher Incidence of Small Y Chromosome in Humans with Trisomy 21 (Down Syndrome). Pediatric Research. 16(9). 769–770. 11 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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