Mohammad‐Sadegh Fallah

917 total citations
25 papers, 344 citations indexed

About

Mohammad‐Sadegh Fallah is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Mohammad‐Sadegh Fallah has authored 25 papers receiving a total of 344 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Hematology. Recurrent topics in Mohammad‐Sadegh Fallah's work include Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Mohammad‐Sadegh Fallah is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Genomics and Rare Diseases (2 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Mohammad‐Sadegh Fallah collaborates with scholars based in Iran, United States and Poland. Mohammad‐Sadegh Fallah's co-authors include Fariborz Mansour‐Ghanaei, Fereidoun Azizi, Kamran Guity, Maryam S. Daneshpour, Bahareh Sedaghati-khayat, Ali Akbar Haghdoost, Sirous Zeinali, Ahmad Ebrahimi, Farhad Hosseinpanah and Mohammad Movahedi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Gene.

In The Last Decade

Mohammad‐Sadegh Fallah

23 papers receiving 331 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mohammad‐Sadegh Fallah Iran 12 93 57 54 53 49 25 344
Gunnar Skeppner Sweden 9 74 0.8× 112 2.0× 62 1.1× 57 1.1× 73 1.5× 10 341
Ananda Rajitha Wickramasinghe Sri Lanka 11 58 0.6× 18 0.3× 86 1.6× 109 2.1× 45 0.9× 20 433
José Antônio de Azevedo Magalhães Brazil 13 48 0.5× 51 0.9× 30 0.6× 86 1.6× 73 1.5× 35 469
Isabella Viani Italy 13 78 0.8× 97 1.7× 121 2.2× 64 1.2× 78 1.6× 24 570
Michael Frey United States 8 72 0.8× 70 1.2× 79 1.5× 38 0.7× 33 0.7× 9 307
Chizuko Suzuki Japan 9 35 0.4× 49 0.9× 24 0.4× 36 0.7× 14 0.3× 15 337
Michel Rolland France 10 45 0.5× 59 1.0× 19 0.4× 35 0.7× 62 1.3× 32 398
Cihangir Akgün Türkiye 13 32 0.3× 42 0.7× 7 0.1× 39 0.7× 45 0.9× 44 382
Sarah King United Kingdom 8 48 0.5× 46 0.8× 44 0.8× 29 0.5× 53 1.1× 17 314
Delnaz Roshandel Canada 15 177 1.9× 116 2.0× 109 2.0× 46 0.9× 169 3.4× 33 549

Countries citing papers authored by Mohammad‐Sadegh Fallah

Since Specialization
Citations

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

Fields of papers citing papers by Mohammad‐Sadegh Fallah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammad‐Sadegh Fallah. 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 Mohammad‐Sadegh Fallah. The network helps show where Mohammad‐Sadegh Fallah may publish in the future.

Co-authorship network of co-authors of Mohammad‐Sadegh Fallah

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammad‐Sadegh Fallah. A scholar is included among the top collaborators of Mohammad‐Sadegh Fallah 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 Mohammad‐Sadegh Fallah. Mohammad‐Sadegh Fallah 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.
Karimipoor, Morteza, et al.. (2024). Mutations in COL6A Gene Family Responsible for Muscular Dystrophies in Three Unrelated Families. PubMed. 28(5). 297–304.
2.
Faranoush, Mohammad, Saba Arshi, Mohammad Nabavi, et al.. (2022). Neonatal Onset of Hemophagocytic Lymphohistiocytosis Due to Prenatal Varicella-Zoster Infection in a Neonate with Griscelli Syndrome Type 2. Iranian Journal of Allergy Asthma and Immunology. 21(4). 488–493. 3 indexed citations
3.
Dehnavi, Ali Zare, Morteza Heidari, Mahmoud Reza Ashrafi, et al.. (2021). ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants. Human Genomics. 15(1). 2 indexed citations
4.
5.
Tran, Thao, Rachel B. Keller, Brecht Guillemyn, et al.. (2021). Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta. SHILAP Revista de lepidopterología. 2(4). 100051–100051. 6 indexed citations
6.
Taheri, Mohammad, et al.. (2021). Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran. Journal of Molecular Neuroscience. 71(11). 2281–2298. 10 indexed citations
7.
Fallah, Mohammad‐Sadegh, et al.. (2019). Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations. Orphanet Journal of Rare Diseases. 14(1). 87–87. 9 indexed citations
8.
Sedaghati-khayat, Bahareh, Maryam Barzin, Mahdi Akbarzadeh, et al.. (2018). Lack of association between FTO gene variations and metabolic healthy obese (MHO) phenotype: Tehran Cardio-metabolic Genetic Study (TCGS). Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity. 25(1). 25–35. 13 indexed citations
9.
Fallah, Mohammad‐Sadegh, Bahareh Sedaghati-khayat, Kamran Guity, et al.. (2017). Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS). JMIR Research Protocols. 6(2). e28–e28. 53 indexed citations
10.
Fallah, Mohammad‐Sadegh, et al.. (2017). Increased Risk of CHD in the Presence of rs7865618 (A allele): Tehran Lipid and Glucose Study.. PubMed. 20(3). 153–157. 7 indexed citations
11.
Fallah, Mohammad‐Sadegh, et al.. (2016). The Relation between Metabolic Syndrome Risk Factors and Genetic Variations of Apolipoprotein V in Relation with Serum Triglyceride and HDL-C Level.. PubMed. 19(1). 46–50. 11 indexed citations
12.
Fallah, Mohammad‐Sadegh, et al.. (2014). Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family withTMC1mutation identified by next-generation sequencing. Acta Oto-Laryngologica. 135(2). 125–129. 8 indexed citations
13.
Khajehkazemi, Razieh, Behnam Sadeghirad, Mohammad Karamouzian, et al.. (2013). The Projection of Burden of Disease in Islamic Republic of Iran to 2025. PLoS ONE. 8(10). e76881–e76881. 20 indexed citations
14.
Fallah, Mohammad‐Sadegh, et al.. (2013). Reporting the presence of three different diseases causingGJB2mutations in a consanguineous deaf family. International Journal of Audiology. 53(2). 128–131. 5 indexed citations
15.
Zarkesh, Maryam, Maryam S. Daneshpour, Mohammad‐Sadegh Fallah, et al.. (2012). Heritability of the metabolic syndrome and its components in the Tehran Lipid and Glucose Study (TLGS). Genetics Research. 94(6). 331–337. 41 indexed citations
16.
Zeinali, Sirous, et al.. (2011). The Occurrence and Contribution of Germline BRCA1/2 Sequence Alterations in Iranian Patients With Breast Cancer. SHILAP Revista de lepidopterología. 1 indexed citations
17.
Fallah, Mohammad‐Sadegh, et al.. (2010). Development of a quantitative real-time PCR assay for detection of unknown α-globin gene deletions. Blood Cells Molecules and Diseases. 45(1). 58–64. 14 indexed citations
18.
Ebrahimi, Ahmad, et al.. (2010). Two Novel Mutations in SCN1A Gene in Iranian Patients with Epilepsy. Archives of Medical Research. 41(3). 207–214. 14 indexed citations
19.
Movahedi, Mohammad, Ali Akbar Haghdoost, Omid Pournik, Behzad Hajarizadeh, & Mohammad‐Sadegh Fallah. (2008). Temporal variations of health indicators in Iran comparing with other Eastern Mediterranean Region countries in the last two decades. Journal of Public Health. 30(4). 499–504. 25 indexed citations
20.
Sharami, Seyedeh Hajar, et al.. (2003). Helicobacter pylori aeropositivity and the incidence of hyperemesis gravidarum.. PubMed. 9(1). CR12–5. 24 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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