Elham Alehabib

488 total citations
24 papers, 181 citations indexed

About

Elham Alehabib is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Elham Alehabib has authored 24 papers receiving a total of 181 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in Elham Alehabib's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and RNA regulation and disease (4 papers). Elham Alehabib is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and RNA regulation and disease (4 papers). Elham Alehabib collaborates with scholars based in Iran, United States and Australia. Elham Alehabib's co-authors include Hossein Darvish, Abbas Tafakhori, Javad Jamshidi, Coro Paisán‐Ruiz, Narsis Daftarian, Hamid Ghaedi, Luís Azcona, Babak Emamalizadeh, Sakineh Ranji‐Burachaloo and Saghar Ghasemi Firouzabadi and has published in prestigious journals such as Annals of Neurology, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Elham Alehabib

24 papers receiving 180 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elham Alehabib Iran 9 114 51 41 24 19 24 181
Amy Gerrish United Kingdom 10 112 1.0× 61 1.2× 74 1.8× 23 1.0× 46 2.4× 18 289
Tim M. Strom Germany 3 224 2.0× 62 1.2× 24 0.6× 45 1.9× 33 1.7× 3 293
Lance P. Doucette Canada 9 136 1.2× 39 0.8× 141 3.4× 21 0.9× 8 0.4× 13 283
Annick Cabot France 5 167 1.5× 52 1.0× 78 1.9× 49 2.0× 16 0.8× 5 240
Qing Fu China 5 156 1.4× 51 1.0× 57 1.4× 25 1.0× 15 0.8× 7 180
Ryea Maswood United Kingdom 8 195 1.7× 34 0.7× 73 1.8× 49 2.0× 68 3.6× 10 263
Margaret J. Ochocinska United States 5 191 1.7× 40 0.8× 9 0.2× 19 0.8× 37 1.9× 5 260
Keren Yosovich Israel 10 148 1.3× 35 0.7× 14 0.3× 40 1.7× 51 2.7× 24 231
Alejandro Estrada‐Cuzcano Peru 7 275 2.4× 131 2.6× 93 2.3× 57 2.4× 44 2.3× 13 325
Michael Nahmou United States 11 217 1.9× 21 0.4× 58 1.4× 23 1.0× 86 4.5× 17 301

Countries citing papers authored by Elham Alehabib

Since Specialization
Citations

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

Fields of papers citing papers by Elham Alehabib

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elham Alehabib

This figure shows the co-authorship network connecting the top 25 collaborators of Elham Alehabib. A scholar is included among the top collaborators of Elham Alehabib 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 Elham Alehabib. Elham Alehabib 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.
Alehabib, Elham, et al.. (2024). A Novel Ornithine Aminotransferase Splice Site Mutation Causes Vitamin B6-Responsive Gyrate Atrophy. Journal of Ophthalmic and Vision Research. 19(1). 118–132. 1 indexed citations
2.
Bahmanpour, Zahra, Somayeh Kazeminasab, Elham Alehabib, et al.. (2022). A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 24(1-2). 148–151. 2 indexed citations
3.
Emamalizadeh, Babak, et al.. (2021). Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations. International Ophthalmology. 41(10). 3269–3276. 3 indexed citations
4.
Alehabib, Elham, et al.. (2021). Clinical and molecular spectrum of P/Q type calcium channel Cav2.1 in epileptic patients. Orphanet Journal of Rare Diseases. 16(1). 461–461. 8 indexed citations
5.
Darvish, Hossein, Luís Azcona, Saghar Ghasemi Firouzabadi, et al.. (2021). ANXA1 with Anti‐Inflammatory Properties Might Contribute to Parkinsonism. Annals of Neurology. 90(2). 319–323. 8 indexed citations
6.
Alehabib, Elham, Sakineh Ranji‐Burachaloo, Abbas Tafakhori, et al.. (2021). Leu226Trp CACNA1A variant associated with juvenile myoclonic epilepsy with and without intellectual disability. Clinical Neurology and Neurosurgery. 213. 107108–107108. 4 indexed citations
7.
Langeslag, Michiel, John Manion, Elham Alehabib, et al.. (2021). PRDM12 Is Transcriptionally Active and Required for Nociceptor Function Throughout Life. Frontiers in Molecular Neuroscience. 14. 720973–720973. 8 indexed citations
8.
Alehabib, Elham, et al.. (2020). Incomplete penetrance of MITF gene c.943C>T mutation in an extended family with Waardenburg syndrome type II. International Journal of Pediatric Otorhinolaryngology. 135. 110014–110014. 6 indexed citations
9.
Bahmanpour, Zahra, et al.. (2020). A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome. International Ophthalmology. 41(2). 389–397. 5 indexed citations
10.
Darvish, Hossein, Luís Azcona, Abbas Tafakhori, et al.. (2020). Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes. Scientific Reports. 10(1). 968–968. 11 indexed citations
11.
Ghaedi, Hamid, et al.. (2019). Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome. Genes & Diseases. 7(4). 614–619. 2 indexed citations
12.
Alehabib, Elham, et al.. (2019). The rs1986112 Variant is Associated with Increased RAB8B Gene Expression in Schizophrenic Patients. Clinical Laboratory. 65(04/2019). 2 indexed citations
13.
Ghaedi, Hamid, Abbas Tafakhori, Elham Alehabib, et al.. (2019). Homozygous Mutation in TWNK Cases Ataxia, Sensorineural Hearing Loss and Optic Nerve Atrophy.. Archives of Iranian Medicine. 22(12). 728–730. 6 indexed citations
14.
Sabbaghi, Hamideh, Elham Alehabib, Javad Jamshidi, et al.. (2019). Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy. Ophthalmic Genetics. 40(3). 259–266. 15 indexed citations
15.
Alehabib, Elham, et al.. (2019). Expression analysis and genotyping of DGKZ: a GWAS-derived risk gene for schizophrenia. Molecular Biology Reports. 46(4). 4105–4111. 7 indexed citations
16.
Yazdani, Shahin, Narsis Daftarian, M R Jafarinasab, et al.. (2018). COL18A1 is a candidate eye iridocorneal angle-closure gene in humans. Human Molecular Genetics. 27(21). 3772–3786. 29 indexed citations
17.
Alehabib, Elham, Ehsan Esmaili Shandiz, Javad Jamshidi, et al.. (2017). Support for “Disease-Only” Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia. Genetic Testing and Molecular Biomarkers. 21(8). 485–490. 14 indexed citations
18.
Jamshidi, Javad, et al.. (2017). A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome. European Journal of Medical Genetics. 60(11). 578–582. 8 indexed citations
19.
Lima, Behnam Safarpour, Hamid Ghaedi, Narsis Daftarian, et al.. (2016). c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness. European Journal of Medical Genetics. 59(2). 65–69. 6 indexed citations
20.
Daftarian, Narsis, Hamid Ahmadieh, Babak Emamalizadeh, et al.. (2016). A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome. Eye. 30(11). 1424–1432. 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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