Mojgan Babanejad

619 total citations
22 papers, 322 citations indexed

About

Mojgan Babanejad is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Mojgan Babanejad has authored 22 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Sensory Systems and 6 papers in Neurology. Recurrent topics in Mojgan Babanejad's work include Hearing, Cochlea, Tinnitus, Genetics (10 papers), Connexins and lens biology (6 papers) and Vestibular and auditory disorders (6 papers). Mojgan Babanejad is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (10 papers), Connexins and lens biology (6 papers) and Vestibular and auditory disorders (6 papers). Mojgan Babanejad collaborates with scholars based in Iran, United States and Canada. Mojgan Babanejad's co-authors include Hossein Najmabadi, Kimia Kahrizi, Richard J. Smith, Nooshin Nikzat, Niloofar Bazazzadegan, Sanaz Arzhangi, Zohreh Fattahi, Marzieh Mohseni, Kevin T. Booth and Khadijeh Jalalvand and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Genetics and Annals of Otology Rhinology & Laryngology.

In The Last Decade

Mojgan Babanejad

20 papers receiving 320 citations

Peers

Countries citing papers authored by Mojgan Babanejad

Since Specialization

Citations

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

Fields of papers citing papers by Mojgan Babanejad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mojgan Babanejad

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A Novel Candidate Gene MACF1 is Associated with Autosomal Dominant Non-syndromic Hearing Loss in an Iranian Family 2024 ·Archives of Iranian Medicine ·Niloofar Bazazzadegan, Mojgan Babanejad, (unknown), Sanaz Arzhangi, Kimia Kahrizi, Kevin T. Booth, Hossein Najmabadi	0
2	An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene 2023 ·Archives of Iranian Medicine ·Marzieh Mohseni, (unknown), (unknown), (unknown), Khadijeh Jalalvand, Sanaz Arzhangi, Mojgan Babanejad, (unknown), Kimia Kahrizi, Hossein Najmabadi	3
3	Genetic etiology of hearing loss in Iran 2022 ·Human Genetics ·Mojgan Babanejad, Maryam Beheshtian, (unknown), Marzieh Mohseni, Kevin T. Booth, Kimia Kahrizi, Hossein Najmabadi	14
4	When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS) 2020 ·Journal of Human Genetics ·Marzieh Mohseni, (unknown), Kevin T. Booth, Mojgan Babanejad, Héla Azaiez, (unknown), Sanaz Arzhangi, Khadijeh Jalalvand, Nooshin Nikzat, (unknown), Payman Jamali, (unknown), (unknown), Kimia Kahrizi, Hossein Najmabadi	2
5	G130V de novo mutation in an Iranian pedigree with nonsyndromic hearing loss without palmoplantar keratoderma 2019 ·International Journal of Pediatric Otorhinolaryngology ·Mojgan Babanejad, Masoud Motasaddi Zarandy, Nooshin Nikzat, Niloofar Bazazzadegan, Sanaz Arzhangi, Marzieh Mohseni, Kimia Kahrizi, Hossein Najmabadi	1
6	Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases 2019 ·Molecular Genetics & Genomic Medicine ·(unknown), (unknown), (unknown), Masood Bazrgar, (unknown), (unknown), Parvin Rostami, (unknown), Mojgan Babanejad, (unknown), (unknown), Hossein Najmabadi, Roxana Kariminejad	7
7	SLC52A2 mutations cause SCABD2 phenotype: A second report 2017 ·International Journal of Pediatric Otorhinolaryngology ·Mojgan Babanejad, (unknown), Nooshin Nikzat, Maryam Beheshtian, (unknown), (unknown), Marzieh Mohseni, Hossein Najmabadi, Kimia Kahrizi	8
8	C-reactive protein and complement factor H polymorphism interaction in advanced exudative age-related macular degeneration 2016 ·International Ophthalmology ·(unknown), (unknown), Hamid-Reza Moein, Mojgan Babanejad, Alireza Ramezani, Mehdi Yaseri, Masoud Soheilian	4
9	Similarity in the Amino Acid Sequences of Mycobacterium tuberculosis Protein Targets Involved in Binding Sites of Docking with Thiacetazone 2016 ·Pharmaceutica Analytica Acta ·Mojgan Babanejad, Setareh Soroush	1
10	Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review. 2016 ·PubMed ·Maryam Beheshtian, Mojgan Babanejad, Héla Azaiez, Niloofar Bazazzadegan, Diana L. Kolbe, Christina Sloan-Heggen, Sanaz Arzhangi, Kevin T. Booth, Marzieh Mohseni, Kathy Frees, (unknown), Ahmad Daneshi, Mohammad Farhadi, Kimia Kahrizi, Richard J. Smith, Hossein Najmabadi	26
11	Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa. 2015 ·PubMed ·Maryam Beheshtian, (unknown), Mojgan Babanejad, Marzieh Mohseni, Hassan Hashemi, (unknown), Fedra Hajizadeh, Mohammad R. Akbari, Kimia Kahrizi, Mohammad Riazi Esfahani, Hossein Najmabadi	18
12	Investigating Seven Recently Identified Genes in 100 Iranian Families with Autosomal Recessive Non-syndromic Hearing Loss 2015 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Mojgan Babanejad, Niloofar Bazazzadegan, Hossein Najmabadi, Kimia Kahrizi	1
13	PDZD7 and hearing loss: More than just a modifier 2015 ·American Journal of Medical Genetics Part A ·Kevin T. Booth, Héla Azaiez, Kimia Kahrizi, Allen C. Simpson, (unknown), Christina M. Sloan, Nicole C. Meyer, Mojgan Babanejad, (unknown), Sanaz Arzhangi, Michael J. Schnieders, Hossein Najmabadi, Richard J. Smith	46
14	Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families 2015 ·Journal of Genetics ·(unknown), Mojgan Babanejad, Kimia Kahrizi, Hossein Najmabadi	11
15	Association of polymorphisms at LDLR locus with coronary artery disease independently from lipid profile. 2014 ·PubMed ·(unknown), Mojgan Babanejad, (unknown), Nooshin Nikzat, Khadijeh Jalalvand, (unknown), (unknown), Farshad Shakerian, Mahdi Afshari, Kimia Kahrizi, Hossein Najmabadi	11
16	Analysis of the association Hind III Polymorphism of Lipoprotein Lipase gene on the risk of coronary artery disease 2013 ·(unknown), Mandana Hasanzad, Tahereh Naji, (unknown), Mojgan Babanejad, (unknown), (unknown), (unknown), (unknown), (unknown)	2
17	A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran 2012 ·American Journal of Medical Genetics Part A ·Mojgan Babanejad, Zohreh Fattahi, Niloofar Bazazzadegan, Carla Nishimura, Nicole C. Meyer, Nooshin Nikzat, (unknown), (unknown), (unknown), (unknown), Richard J. Smith, Kimia Kahrizi, Hossein Najmabadi	48
18	Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population 2012 ·American Journal of Medical Genetics Part A ·Zohreh Fattahi, A. Eliot Shearer, Mojgan Babanejad, Niloofar Bazazzadegan, (unknown), Nooshin Nikzat, Khadijeh Jalalvand, Sanaz Arzhangi, Fatemehsadat Esteghamat, (unknown), (unknown), Richard J. Smith, Kimia Kahrizi, Hossein Najmabadi	48
19	Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss 2011 ·International Journal of Pediatric Otorhinolaryngology ·Behzad Davarnia, Mojgan Babanejad, Zohreh Fattahi, Nooshin Nikzat, Niloofar Bazazzadegan, (unknown), (unknown), Carla Nishimura, Khadijeh Jalalvand, Sanaz Arzhangi, Kimia Kahrizi, Richard J. Smith, Hossein Najmabadi	22
20	Mutations in TMC1 are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population 2010 ·Annals of Otology Rhinology & Laryngology ·Michael S. Hildebrand, Kimia Kahrizi, Catherine Bromhead, A. Eliot Shearer, Jennifer Webster, (unknown), (unknown), Niloofar Bazazzadegan, Mojgan Babanejad, Nooshin Nikzat, William J. Kimberling, Dietrich Stephan, P.L.M. Huygen, Melanie Bahlo, Richard J. Smith, Hossein Najmabadi	24

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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