Fatemeh Alasti

611 total citations
16 papers, 451 citations indexed

About

Fatemeh Alasti is a scholar working on Sensory Systems, Surgery and Molecular Biology. According to data from OpenAlex, Fatemeh Alasti has authored 16 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Sensory Systems, 4 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in Fatemeh Alasti's work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Hearing Loss and Rehabilitation (4 papers) and Vestibular and auditory disorders (3 papers). Fatemeh Alasti is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (9 papers), Hearing Loss and Rehabilitation (4 papers) and Vestibular and auditory disorders (3 papers). Fatemeh Alasti collaborates with scholars based in Iran, Belgium and United States. Fatemeh Alasti's co-authors include Guy Van Camp, Mohammad Hossein Sanati, Richard J. Smith, Thomas Somers, Mohammad Farhadi, Morteza Hashemzadeh Chaleshtori, Carla Nishimura, Mahdi Malekpour, Arjan P.M. de Brouwer and Hannie Kremer and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Fatemeh Alasti

16 papers receiving 448 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fatemeh Alasti Iran	10	221	176	142	107	98	16	451
Martijn H. Kemperman Netherlands	13	275 1.2×	126 0.7×	59 0.4×	66 0.6×	156 1.6×	16	385
Tomonori Takasaka Japan	9	270 1.2×	224 1.3×	37 0.3×	75 0.7×	82 0.8×	11	450
Nermin Başerer Türkiye	10	239 1.1×	175 1.0×	34 0.2×	63 0.6×	109 1.1×	18	386
Maddalena Martella Italy	11	151 0.7×	215 1.2×	54 0.4×	14 0.1×	40 0.4×	21	372
Soo Kyung Koo South Korea	11	80 0.4×	320 1.8×	108 0.8×	18 0.2×	41 0.4×	26	487
Lingyun Mei China	14	223 1.0×	315 1.8×	39 0.3×	43 0.4×	107 1.1×	61	531
Megan Ealy United States	15	247 1.1×	169 1.0×	34 0.2×	278 2.6×	75 0.8×	16	568
Nele Dieltjens Belgium	9	189 0.9×	112 0.6×	21 0.1×	197 1.8×	76 0.8×	9	415
Nathalie Pallarès-Ruiz France	8	262 1.2×	279 1.6×	23 0.2×	22 0.2×	81 0.8×	13	440
Xiao Ouyang China	7	220 1.0×	238 1.4×	32 0.2×	32 0.3×	86 0.9×	20	380

Countries citing papers authored by Fatemeh Alasti

Since Specialization

Citations

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

Fields of papers citing papers by Fatemeh Alasti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fatemeh Alasti

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

All Works

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16 of 16 papers shown

Alasti, Fatemeh, Guy Van Camp, & Richard J. Smith. (2014). Pendred Syndrome/DFNB4. 2 indexed citations

Brophy, Patrick D., Fatemeh Alasti, Benjamin W. Darbro, et al.. (2013). Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes. Human Genetics. 132(12). 1339–1350. 27 indexed citations

Schrauwen, Isabelle, Fatemeh Alasti, E.P.A. Jorssen, et al.. (2011). A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame. American Journal of Medical Genetics Part A. 155(8). 2021–2023. 9 indexed citations

Alasti, Fatemeh, et al.. (2011). Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss.. PubMed. 40(2). 34–48. 33 indexed citations

Alasti, Fatemeh, Nils Peeters, Wim Wuyts, Mohammad Hossein Sanati, & Guy Van Camp. (2010). Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive.. PubMed. 127(1). 116–116. 1 indexed citations

Sanati, Mohammad Hossein, et al.. (2009). Contribution of GJB2 mutations and Four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran. Iranian Journal of Biotechnology. 7(2). 108–111. 17 indexed citations

Alasti, Fatemeh & Guy Van Camp. (2009). Genetics of microtia and associated syndromes. Journal of Medical Genetics. 46(6). 361–369. 107 indexed citations

Sanati, Mohammad Hossein, et al.. (2009). SHORT COMMUNICATION: CONTRIBUTION OF GJB2 MUTATIONS AND FOUR COMMON DFNB LOCI IN AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING IMPAIRMENT IN MARKAZI AND QOM PROVINCES OF IRAN. 7(2). 108–111. 2 indexed citations

Alasti, Fatemeh, et al.. (2008). A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family. The American Journal of Human Genetics. 82(4). 982–991. 77 indexed citations

10.

Hilgert, Nele, Fatemeh Alasti, Nele Dieltjens, et al.. (2008). Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11. Clinical Genetics. 74(3). 223–232. 55 indexed citations

11.

Alasti, Fatemeh, et al.. (2008). A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family. The American Journal of Human Genetics. 83(3). 424–424. 6 indexed citations

12.

Laer, Lut Van, Nicole C. Meyer, Mahdi Malekpour, et al.. (2007). A novel DFNA5 mutation does not cause hearing loss in an Iranian family. Journal of Human Genetics. 52(6). 549–552. 23 indexed citations

13.

Meyer, Nicole C., Fatemeh Alasti, Carla Nishimura, et al.. (2007). Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus. American Journal of Medical Genetics Part A. 143A(14). 1623–1629. 38 indexed citations

14.

Alasti, Fatemeh, Mohammad Hossein Sanati, Arjan P.M. de Brouwer, et al.. (2007). A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families. International Journal of Pediatric Otorhinolaryngology. 72(2). 249–255. 39 indexed citations

15.

Sanati, Mohammad Hossein, et al.. (2005). Mutation analysis of connexin 26 gene and del(GJB6- D13S1830) in patients with hereditary deafness from two provinces in Iran. Iranian Journal of Biotechnology. 3(4). 255–258. 12 indexed citations

16.

Alasti, Fatemeh, et al.. (2003). Cloning and expression of human gamma-interferon cDNA in E. coli. Iranian Journal of Biotechnology. 1(2). 87–94. 3 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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