Maryam Abiri

486 total citations
28 papers, 313 citations indexed

About

Maryam Abiri is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Maryam Abiri has authored 28 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Clinical Biochemistry. Recurrent topics in Maryam Abiri's work include Metabolism and Genetic Disorders (7 papers), Skin and Cellular Biology Research (4 papers) and Biochemical and Molecular Research (4 papers). Maryam Abiri is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Skin and Cellular Biology Research (4 papers) and Biochemical and Molecular Research (4 papers). Maryam Abiri collaborates with scholars based in Iran, United States and Italy. Maryam Abiri's co-authors include Sirous Zeinali, Leila Youssefian, Hassan Vahidnezhad, Jouni Uitto, Amir Hossein Saeidian, Paolo Fortina, Sirous Zeinali, Soheila Sotoudeh, Razieh Karamzadeh and Adam Ertel and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Journal of Investigative Dermatology.

In The Last Decade

Maryam Abiri

26 papers receiving 310 citations

Peers

Countries citing papers authored by Maryam Abiri

Since Specialization

Citations

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

Fields of papers citing papers by Maryam Abiri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maryam Abiri

This figure shows the co-authorship network connecting the top 25 collaborators of Maryam Abiri. A scholar is included among the top collaborators of Maryam Abiri 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 Maryam Abiri. Maryam Abiri 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	Comprehensive microarray analysis of severe preeclampsia placenta to identify differentially expressed genes, biological pathways, hub genes, and their related non-coding RNAs 2024 ·Placenta ·(unknown), (unknown), (unknown), Maryam Abiri	1
2	The emerging roles of lncRNAs as a novel player in the pathogenesis of preeclampsia 2023 ·Gene Reports ·(unknown), Maryam Eghbali‐Babadi, (unknown), (unknown), (unknown), (unknown), Maryam Abiri	2
3	First report of a patient with homozygous hemoglobin Ernz: Evidence to support a non-pathogenic variant 2023 ·Blood Cells Molecules and Diseases ·(unknown), Maryam Abiri, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Sirous Zeinali	1
4	Comprehensive transcriptome mining identified the gene expression signature and differentially regulated pathways of the late-onset preeclampsia 2021 ·Pregnancy Hypertension ·(unknown), (unknown), (unknown), (unknown), Maryam Abiri	8
5	Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran 2021 ·Journal of Molecular Neuroscience ·(unknown), Mohammad Taheri, Mohammad‐Sadegh Fallah, Maryam Abiri, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Mehrdad Hashemi, (unknown), Sirous Zeinali	10
6	Hints From the Cellular Functions to the Practical Outlook of Circular RNAs 2021 ·Frontiers in Genetics ·(unknown), (unknown), Maryam Abiri	8
7	Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi−Bickel Syndrome 2021 ·Frontiers in Genetics ·(unknown), (unknown), Shadab Salehpour, Maryam Abiri, (unknown), Saeed Talebi, Nasrin Alipour Olyaei, Vahid Reza Yassaee, Mohammad Hossein Modarressi	7
8	Genetic Assessment of Mucopolysaccharidosis Type IV and the First Pathological Mutation of c.313A>G in the Iranian Population 2020 ·SHILAP Revista de lepidopterología ·(unknown), Mehrdad Hashemi, Ahmad Majd, Maryam Abiri, Sirous Zeinali	0
9	Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b) 2020 ·Orphanet Journal of Rare Diseases ·(unknown), Maryam Abiri, Saeed Talebi, Zahra Noroozi, (unknown), Parastoo Rostami, (unknown), Mehri Najafi, (unknown), Ali Rabbani, Mohammad Hossein Modarressi	5
10	Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations 2019 ·Metabolic Brain Disease ·Maryam Abiri, (unknown), (unknown), Razieh Karamzadeh, (unknown), (unknown), Sirous Zeinali	11
11	Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases 2019 ·Scientific Reports ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Maryam Abiri, Sirous Zeinali	8
12	Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations 2019 ·Orphanet Journal of Rare Diseases ·(unknown), Mohammad‐Sadegh Fallah, (unknown), (unknown), (unknown), (unknown), (unknown), Zivar Salehi, Maryam Abiri, Sirous Zeinali	9
13	Genetic testing of Mucopolysaccharidoses disease using multiplex PCR- based panels of STR markers: in silico analysis of novel mutations 2019 ·Metabolic Brain Disease ·(unknown), Mehrdad Hashemi, Ahmad Majd, Maryam Abiri, Sirous Zeinali	4
14	Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort 2018 ·Metabolic Brain Disease ·(unknown), (unknown), (unknown), Aria Setoodeh, Maryam Razzaghy‐Azar, (unknown), (unknown), (unknown), Mehrdad Hashemi, Maryam Abiri, Sirous Zeinali	8
15	Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications 2017 ·Journal of Investigative Dermatology ·Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Andrew Touati, Soheila Sotoudeh, Maryam Abiri, (unknown), Nessa Aghazadeh, Hamidreza Mahmoudi, (unknown), (unknown), (unknown), (unknown), Sirous Zeinali, Paolo Fortina, Jouni Uitto	27
16	Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy 2017 ·Matrix Biology ·Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Hamidreza Mahmoudi, Andrew Touati, Maryam Abiri, Abdol‐Mohammad Kajbafzadeh, Sophia Aristodemou, Lu Liu, John A. McGrath, Adam Ertel, Eric Londin, Ariana Kariminejad, Sirous Zeinali, Paolo Fortina, Jouni Uitto	37
17	Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysis 2016 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Maryam Abiri, Razieh Karamzadeh, Morteza Karimipoor, (unknown), (unknown), (unknown), (unknown), Aria Setoodeh, Mohammad Reza Noori–Daloii, Sirous Zeinali	12
18	Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity 2016 ·Journal of Investigative Dermatology ·Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Sirous Zeinali, Parvin Mansouri, Soheila Sotoudeh, (unknown), Javad Mohammadi‐Asl, Razieh Karamzadeh, Maryam Abiri, Kevin McCormick, Paolo Fortina, Jouni Uitto	27
19	In silico analysis of novel mutations in maple syrup urine disease patients from Iran 2016 ·Metabolic Brain Disease ·Maryam Abiri, Razieh Karamzadeh, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Mohammad Reza Noori–Daloii, Morteza Karimipoor, Sirous Zeinali	15
20	Molecular Characterization of QDPR Gene in Iranian Families with BH4 Deficiency: Reporting Novel and Recurrent Mutations 2015 ·JIMD Reports ·(unknown), Maryam Abiri, Shadab Salehpour, (unknown), (unknown), (unknown), Shohreh Khatami, (unknown), Aria Setoodeh, (unknown), (unknown), Sirous Zeinali	8

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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