Masoud Garshasbi

5.1k total citations
127 papers, 2.4k citations indexed

About

Masoud Garshasbi is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Masoud Garshasbi has authored 127 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Molecular Biology, 44 papers in Genetics and 12 papers in Rheumatology. Recurrent topics in Masoud Garshasbi's work include Genetics and Neurodevelopmental Disorders (23 papers), Genomics and Rare Diseases (21 papers) and Mitochondrial Function and Pathology (13 papers). Masoud Garshasbi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (23 papers), Genomics and Rare Diseases (21 papers) and Mitochondrial Function and Pathology (13 papers). Masoud Garshasbi collaborates with scholars based in Iran, Germany and United States. Masoud Garshasbi's co-authors include Andreas W. Kuß, Andreas Tzschach, Hossein Najmabadi, Kimia Kahrizi, Mahdi Mahmoudi, Ahmadreza Jamshidi, Ehsan Razmara, Jafar Karami, Hans‐Hilger Ropers and Hans Hilger Ropers and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Masoud Garshasbi

121 papers receiving 2.4k citations

Peers

Countries citing papers authored by Masoud Garshasbi

Since Specialization

Citations

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

Fields of papers citing papers by Masoud Garshasbi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masoud Garshasbi

This figure shows the co-authorship network connecting the top 25 collaborators of Masoud Garshasbi. A scholar is included among the top collaborators of Masoud Garshasbi 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 Masoud Garshasbi. Masoud Garshasbi 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	Genetic Heterogeneity of Autism Spectrum Disorder: Identification of Five Novel Mutations (RIMS2, FOXG1, AUTS2, ZCCHC17, and SPTBN5) in Iranian Families via Whole-Exome and Whole-Genome Sequencing 2025 ·Biochemical Genetics ·(unknown), (unknown), Ali Sharifi‐Zarchi, Saghar Ghasemi Firouzabadi, Farkhondeh Behjati, Masoud Garshasbi	1
2	Homozygous TREM2 c.549del; p.(Leu184Serfs5) variant causing Nasu‐Hakola disease in three siblings in a consanguineous Iraqi family: Case report and review of literature 2024 ·Molecular Genetics & Genomic Medicine* ·(unknown), (unknown), Mehmet Özaslan, (unknown), Morteza Heidari, Masoud Garshasbi	1
3	Novel homozygous frameshift variant in the ATCAY gene in an Iranian patient with Cayman cerebellar ataxia; expanding the neuroimaging and clinical features: a case report 2023 ·BMC Medical Genomics ·(unknown), Mahmoud Reza Ashrafi, (unknown), Morteza Heidari, Masoud Garshasbi	1
4	Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers 2023 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), (unknown), (unknown), (unknown), Javad Behroozi, (unknown), (unknown), Masoud Garshasbi	1
5	Cell-free fetal DNA (cffDNA) extraction from whole blood by using a fully automatic centrifugal microfluidic device based on displacement of magnetic silica beads 2023 ·Talanta ·(unknown), Maryam Saadatmand, Masoud Garshasbi	20
6	Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literature 2023 ·Irish Journal of Medical Science (1971 -) ·(unknown), (unknown), (unknown), (unknown), (unknown), Mahmoud Reza Ashrafi, Morteza Heidari, (unknown), Masoud Garshasbi, Ali Reza Tavasoli	1
7	Pathogenic DST sequence variants result in either epidermolysis bullosa simplex (EBS) or hereditary sensory and autonomic neuropathy type 6 (HSAN‐VI) 2022 ·Experimental Dermatology ·(unknown), (unknown), Masoud Garshasbi, (unknown), Leila Youssefian, Hassan Vahidnezhad, Jouni Uitto	9
8	ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants 2021 ·Human Genomics ·Ali Zare Dehnavi, (unknown), (unknown), Morteza Heidari, Mahmoud Reza Ashrafi, (unknown), (unknown), Mohammad‐Sadegh Fallah, (unknown), (unknown), Masoud Garshasbi, Ali Reza Tavasoli	2
9	A novel homozygous missense variant in the NAXE gene in an Iranian family with progressive encephalopathy with brain edema and leukoencephalopathy 2021 ·Acta Neurologica Belgica ·(unknown), Morteza Heidari, Mahmoud Reza Ashrafi, Nejat Mahdieh, Masoud Garshasbi	15
10	A novel metabolic disorder in the degradation pathway of endogenous methanol due to a mutation in the gene of alcohol dehydrogenase 2021 ·Clinical Biochemistry ·Maryam Razzaghy‐Azar, Mitra Nourbakhsh, (unknown), Mona Nourbakhsh, Saeed Talebi, Ali Sharifi‐Zarchi, (unknown), Masoud Garshasbi	3
11	A novel deletion variant in CLN3 with highly variable expressivity is responsible for juvenile neuronal ceroid lipofuscinoses 2021 ·Acta Neurologica Belgica ·(unknown), Ehsan Razmara, Mehmet Özaslan, (unknown), (unknown), Ali Reza Tavasoli, Masoud Garshasbi	5
12	Identification of a novel missense c.386G > A variant in a boy with the POMGNT1-related muscular dystrophy-dystroglycanopathy 2020 ·Acta Neurologica Belgica ·(unknown), (unknown), Nejat Mahdieh, (unknown), Morteza Heidari, Masoud Garshasbi	9
13	S3440P Substitution in C-Terminal Region of Human Reelin Dramatically Impairs Secretion of Reelin from HEK 293T cells 2019 ·Cellular and Molecular Biology ·(unknown), Ehsan Razmara, Amirreza Bitaraf, Mahdi Mahmoudi, Masoud Garshasbi	8
14	Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature review 2019 ·Acta Neurologica Belgica ·Parastoo Rostami, (unknown), Mahmoud Reza Ashrafi, Houman Alizadeh, Masoud Garshasbi, Ali Reza Tavasoli	14
15	miR-31 and miR-145 as Potential Non-Invasive Regulatory\nBiomarkers in Patients with Endometriosis 2018 ·SHILAP Revista de lepidopterología ·(unknown), Mehrdad Noruzinia, Masoud Garshasbi, (unknown)	24
16	Association Study of an AFF1 Gene Polymorphism (rs340630) with Iranian Systemic Lupus Erythematosus Patients. 2017 ·PubMed ·(unknown), Masoud Garshasbi, (unknown), (unknown), (unknown), M. Akbarian, Maryam Mahmoudi	4
17	Pharmacogenetics and Personalized Medicine in Pancreatic Cancer. 2017 ·PubMed ·(unknown), (unknown), (unknown), (unknown), Masoud Garshasbi	3
18	Identification of Novel Mutation in EIF2AK3 Gene as a Causal Variant in a Family With Rare Disease 2017 ·Journal of Medical Cases ·(unknown), Masoud Garshasbi	1
19	Prevalence of Methylenetetrahydrofolate Reductase C677T Polymorphism in women with Polycystic Ovary Syndrome in southeast of Iran. 2015 ·Europe PMC (PubMed Central) ·Anoosh Naghavi, Hossein Mozdarani, Masoud Garshasbi, Minoo Yaghmaei	6
20	A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation 2007 ·The American Journal of Human Genetics ·Mohammad Mahdi Motazacker, Benjamin R. Rost, Tim Hucho, Masoud Garshasbi, Kimia Kahrizi, Reinhard Ullmann, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, (unknown), Chandan Goswami, Andreas Tzschach, Lars Riff Jensen, Dietmar Schmitz, Hans Hilger Ropers, Hossein Najmabadi, Andreas W. Kuß	112

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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