Muhammad Mahajnah

1.3k total citations
55 papers, 831 citations indexed

About

Muhammad Mahajnah is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Muhammad Mahajnah has authored 55 papers receiving a total of 831 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Genetics and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Muhammad Mahajnah's work include Genetics and Neurodevelopmental Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and Genomics and Rare Diseases (5 papers). Muhammad Mahajnah is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and Genomics and Rare Diseases (5 papers). Muhammad Mahajnah collaborates with scholars based in Israel, Germany and United States. Muhammad Mahajnah's co-authors include Rajech Sharkia, Nathanel Zelnik, Christopher A. Walsh, Rachel Straussberg, Lina Basel‐Vanagaite, Abdussalam Azem, Adria Bodell, Danielle Gleason, Anthony D. Hill and Robert Hill and has published in prestigious journals such as Cell, Brain and Neurology.

In The Last Decade

Muhammad Mahajnah

54 papers receiving 814 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Muhammad Mahajnah Israel 16 391 281 126 117 83 55 831
Sunita Venkateswaran Canada 15 333 0.9× 261 0.9× 81 0.6× 73 0.6× 143 1.7× 33 769
Takahito Wada Japan 19 626 1.6× 383 1.4× 166 1.3× 97 0.8× 73 0.9× 77 1.1k
Karine Lascelles United Kingdom 16 295 0.8× 183 0.7× 126 1.0× 136 1.2× 109 1.3× 25 858
Tamar Harel Israel 18 458 1.2× 348 1.2× 111 0.9× 104 0.9× 39 0.5× 66 1.1k
Mercédes Pineda Spain 18 499 1.3× 278 1.0× 82 0.7× 149 1.3× 94 1.1× 29 1.0k
Alexandre Dionne‐Laporte Canada 15 436 1.1× 391 1.4× 68 0.5× 115 1.0× 44 0.5× 32 905
Jean‐Baptiste Rivière Canada 18 591 1.5× 575 2.0× 141 1.1× 145 1.2× 64 0.8× 36 1.2k
Amy Yang United States 14 367 0.9× 414 1.5× 93 0.7× 59 0.5× 43 0.5× 28 841
Milen Velinov United States 19 413 1.1× 476 1.7× 153 1.2× 76 0.6× 68 0.8× 57 1.0k
Vanessa Douet United States 16 272 0.7× 205 0.7× 168 1.3× 81 0.7× 35 0.4× 25 748

Countries citing papers authored by Muhammad Mahajnah

Since Specialization
Citations

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

Fields of papers citing papers by Muhammad Mahajnah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muhammad Mahajnah

This figure shows the co-authorship network connecting the top 25 collaborators of Muhammad Mahajnah. A scholar is included among the top collaborators of Muhammad Mahajnah 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 Muhammad Mahajnah. Muhammad Mahajnah 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.
Paz, Eyal, Sahil Jain, Irit Gottfried, et al.. (2024). Biochemical and neurophysiological effects of deficiency of the mitochondrial import protein TIMM50. eLife. 13. 1 indexed citations
2.
Paz, Eyal, Sahil Jain, Irit Gottfried, et al.. (2024). Biochemical and neurophysiological effects of deficiency of the mitochondrial import protein TIMM50. eLife. 13. 2 indexed citations
3.
Cohen, Rony, et al.. (2023). Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor Cerebri. Brain Sciences. 13(2). 361–361. 1 indexed citations
4.
Genizi, Jacob, Muhammad Mahajnah, Ayelet Halevy, et al.. (2023). High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome. Children. 10(7). 1122–1122. 1 indexed citations
5.
Steinberg, Daniel, I. M. Kustanovich, Sergey Viukov, et al.. (2021). Modeling genetic epileptic encephalopathies using brain organoids. EMBO Molecular Medicine. 13(8). e13610–e13610. 34 indexed citations
6.
Mayer, Anja K., Muhammad Mahajnah, Mervyn G. Thomas, et al.. (2019). Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus. Brain. 142(6). 1528–1534. 25 indexed citations
7.
Sharkia, Rajech, Holger Hengel, Lüdger Schöls, et al.. (2019). A novel biallelic loss‐of‐function mutation in TMCO1 gene confirming and expanding the phenotype spectrum of cerebro‐facio‐thoracic dysplasia. American Journal of Medical Genetics Part A. 179(7). 1338–1345. 8 indexed citations
8.
Sharkia, Rajech, et al.. (2019). Exploration of Risk Factors for Type 2 Diabetes among Arabs in Israel. Annals of Global Health. 85(1). 8 indexed citations
9.
Sharkia, Rajech, et al.. (2018). A new case confirming and expanding the phenotype spectrum of ADAT3-related intellectual disability syndrome. European Journal of Medical Genetics. 62(11). 103549–103549. 18 indexed citations
10.
Watemberg, Nathan, et al.. (2018). Clinical Features at the Time of Diagnosis of Benign Epilepsy With Centrotemporal Spikes Do Not Predict Subsequent Seizures. Pediatric Neurology. 88. 36–39. 6 indexed citations
11.
Sharkia, Rajech, Stavit A. Shalev, Nathan Watemberg, et al.. (2017). Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy. American Journal of Medical Genetics Part A. 173(4). 1051–1055. 9 indexed citations
12.
Kurolap, Alina, Tova Hershkovitz, Adi Mory, et al.. (2016). Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine. The American Journal of Human Genetics. 99(5). 1172–1180. 25 indexed citations
13.
Sharkia, Rajech, Holger Hengel, Lüdger Schöls, et al.. (2016). Parental mosaicism in another case of Dravet syndrome caused by a novel SCN1A deletion: a case report. Journal of Medical Case Reports. 10(1). 67–67. 5 indexed citations
14.
Mahajnah, Muhammad, et al.. (2015). Clinical Characteristics of Autism Spectrum Disorder in Israel: Impact of Ethnic and Social Diversities. BioMed Research International. 2015. 1–7. 17 indexed citations
15.
Sharkia, Rajech, et al.. (2013). Comparative screening of FMF mutations in various communities of the Israeli society. European Journal of Medical Genetics. 56(7). 351–355. 16 indexed citations
16.
Masalha, Rafik, Ella Kordysh, Gershon Alpert, et al.. (2010). The prevalence of Parkinson's disease in an Arab population, Wadi Ara, Israel.. PubMed. 12(1). 32–5. 15 indexed citations
17.
Mochida, Ganeshwaran H., Muhammad Mahajnah, Anthony D. Hill, et al.. (2009). A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly. The American Journal of Human Genetics. 85(6). 897–902. 107 indexed citations
18.
19.
Iancu, Theodore C., et al.. (2007). The Liver in Congenital Disorders of Glycosylation: Ultrastructural Features. Ultrastructural Pathology. 31(3). 189–197. 12 indexed citations
20.
Shahar, Eli, et al.. (2007). Pediatric-Onset Gelastic Seizures: Clinical Data and Outcome. Pediatric Neurology. 37(1). 29–34. 22 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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