Mohammad Keramatipour

796 total citations
60 papers, 549 citations indexed

About

Mohammad Keramatipour is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Mohammad Keramatipour has authored 60 papers receiving a total of 549 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 19 papers in Genetics and 11 papers in Clinical Biochemistry. Recurrent topics in Mohammad Keramatipour's work include Metabolism and Genetic Disorders (11 papers), Genomics and Rare Diseases (5 papers) and Mitochondrial Function and Pathology (5 papers). Mohammad Keramatipour is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Genomics and Rare Diseases (5 papers) and Mitochondrial Function and Pathology (5 papers). Mohammad Keramatipour collaborates with scholars based in Iran, United Kingdom and United States. Mohammad Keramatipour's co-authors include Saeed Talebi, Fariba Koohdani, Gity Sotoudeh, Mahmoud Djalali, Farzad Shidfar, Ensieh Nasli‐Esfahani, Ehsan Alvandi, Omid Toupchian, Anahita Mansoori and Mohammadreza Eshraghian and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Mohammad Keramatipour

58 papers receiving 535 citations

Peers

Countries citing papers authored by Mohammad Keramatipour

Since Specialization

Citations

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

Fields of papers citing papers by Mohammad Keramatipour

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohammad Keramatipour

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammad Keramatipour. A scholar is included among the top collaborators of Mohammad Keramatipour 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 Keramatipour. Mohammad Keramatipour 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	Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritance 2024 ·Molecular Biology Reports ·(unknown), (unknown), (unknown), Susan Amirsalari, (unknown), Mahmoud Reza Ashrafi, Ali Reza Tavasoli, Mohammad Keramatipour, Morteza Heidari	0
2	Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literature 2023 ·CEN Case Reports ·(unknown), Mahnaz Jamee, John A. Sayer, Simin Sadeghi‐Bojd, (unknown), (unknown), Mohammad Keramatipour, (unknown)	2
3	Integrated genomic sequencing in myeloid blast crisis chronic myeloid leukemia (MBC-CML), identified potentially important findings in the context of leukemogenesis model 2022 ·Scientific Reports ·(unknown), Mohammad Keramatipour, Mohammad Vaezi, Seyed Mohsen Razavi, Kaveh Kavousi, (unknown), (unknown), Marjan Yaghmaie, Bahram Chahardouli, Saeed Talebi, Kazem Mousavizadeh‬	2
4	The importance of CDC27 in cancer: molecular pathology and clinical aspects 2021 ·Cancer Cell International ·(unknown), Mohammad Keramatipour, Saeed Talebi, Kaveh Kavousi, (unknown), (unknown), Kazem Mousavizadeh‬	27
5	Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum 2021 ·Molecular Biology Reports ·(unknown), (unknown), Mohammad Reza Saberi, (unknown), (unknown), (unknown), (unknown), Mohammad Keramatipour	5
6	Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report 2021 ·BMC Pediatrics ·(unknown), (unknown), (unknown), (unknown), Mohammad Keramatipour, (unknown), (unknown)	3
7	Whole Exome Sequencing Reveals a XPNPEP3 Novel Mutation Causing Nephronophthisis in a Pediatric Patient 2020 ·Iranian Biomedical Journal ·(unknown), (unknown), Mohammad Keramatipour, (unknown), (unknown), Hasan Otukesh, Saeed Talebi	7
8	CRB1-Related Leber Congenital Amaurosis: Reporting Novel Pathogenic Variants and a Brief Review on Mutations Spectrum 2019 ·Iranian Biomedical Journal ·Mohammad Reza Saberi, (unknown), (unknown), (unknown), (unknown), (unknown), Hassan Jafari, Mohammad Keramatipour	6
9	Investigation of the association of G-7A and T-138C single nucleotide polymorphisms on the promoter of MGP gene with renal stone 2018 ·Mohammad Keramatipour, (unknown), Mohsen Taghizadeh, Ali Tabibi, (unknown), Babak Javanmard, Behzad Narouie	1
10	Effect of whole exome sequencing in diagnosis of inborn errors of metabolism and neurogenetic disorders: A review articles 2018 ·(unknown), Mohammad Keramatipour	4
11	Multi affected pedigree with congenital microcephaly: WES revealed PNKP gene mutation 2018 ·Brain and Development ·(unknown), (unknown), Saeed Talebi, Mehran Beiraghi Toosi, Mohammad Keramatipour	10
12	First report of Klein-Waardenburg Syndrome in Iran and a novel pathogenic splice site variant in PAX3 gene 2018 ·International Journal of Pediatric Otorhinolaryngology ·Mohammad Reza Saberi, (unknown), (unknown), (unknown), (unknown), Mohammad Keramatipour	6
13	Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes 2017 ·Metabolic Brain Disease ·(unknown), (unknown), (unknown), Saeed Talebi, (unknown), (unknown), (unknown), Jalal Gharesouran, Aria Setoodeh, (unknown), Mohammad Keramatipour	15
14	PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data 2016 ·Kidney Research and Clinical Practice ·(unknown), (unknown), (unknown), Mohsen Ayati, Jamshid Roozbeh, Mohammad Keramatipour	2
15	Docosahexaenoic Acid-Rich Fish Oil Supplementation Improves Body Composition without Influence of the PPARγ Pro12Ala Polymorphism in Patients with Type 2 Diabetes: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial 2015 ·Lifestyle Genomics ·Anahita Mansoori, Gity Sotoudeh, Mahmoud Djalali, Mohammadreza Eshraghian, Mohammad Keramatipour, Ensieh Nasli‐Esfahani, Farzad Shidfar, Ehsan Alvandi, Omid Toupchian, Fariba Koohdani	11
16	Impact of Vitamin A Supplementation on RAR Gene Expression in Multiple Sclerosis Patients 2013 ·Journal of Molecular Neuroscience ·Sama Bitarafan, Mohammad Hossein Harirchian, Mohammad Ali Sahraian, Mohammad Keramatipour, Nahid Beladi Moghadam, Mansoureh Togha, Shahriar Nafissi, Fereydoun Siassi, Mohammad Reza Eshraghian, Niyaz Mohammadzadeh Honarvar, Hastimansooreh Ansar, Saeed Talebi, (unknown)	14
17	Cytokines Genes Polymorphisms and Risk of Multiple Sclerosis 2010 ·The American Journal of the Medical Sciences ·Maryam Izad, (unknown), (unknown), Aliakbar Amirzargar, (unknown), (unknown), Mohammad Keramatipour	13
18	The Relationship between Polymorphisms of Blood Coagulation Factor V Gene and Recurrent Pregnancy Losses 2009 ·Journal of Reproduction & Infertility ·Raheleh Torabi, (unknown), Afsaneh Mohammadzadeh, (unknown), Mohammad Keramatipour, (unknown), Hojjat Zeraati, (unknown)	5
19	Splenomegaly and Modified Erythropoiesis in KLF13–/– Mice 2008 ·Journal of Biological Chemistry ·Adele Gordon, Susan V. Outram, Mohammad Keramatipour, (unknown), William H Colledge, James C. Metcalfe, Ariadne L. Hager‐Theodorides, Tessa Crompton, Paul R. Kemp	31
20	The ACE I allele is associated with increased risk for ruptured intracranial aneurysms 2000 ·Journal of Medical Genetics ·Mohammad Keramatipour, (unknown), (unknown), (unknown), (unknown), (unknown)	42

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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