Ammar Zaghlool

1.9k total citations
13 papers, 801 citations indexed

About

Ammar Zaghlool is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Ammar Zaghlool has authored 13 papers receiving a total of 801 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Cancer Research and 3 papers in Genetics. Recurrent topics in Ammar Zaghlool's work include Cancer-related molecular mechanisms research (6 papers), RNA modifications and cancer (5 papers) and RNA Research and Splicing (5 papers). Ammar Zaghlool is often cited by papers focused on Cancer-related molecular mechanisms research (6 papers), RNA modifications and cancer (5 papers) and RNA Research and Splicing (5 papers). Ammar Zaghlool collaborates with scholars based in Sweden, United States and Poland. Ammar Zaghlool's co-authors include Lars Feuk, Jonatan Halvardson, Adam Ameur, Lucia Cavelier, Anna Wetterbom, Ulf Gyllensten, Jan P. Dumanski, Lars A. Forsberg, Hanna Davies and Johanna Sandgren and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Scientific Reports.

In The Last Decade

Ammar Zaghlool

13 papers receiving 797 citations

Peers

Ammar Zaghlool

GENET

IMMUN

Emilie Falconnet Switzerland

Hiroki Ura Japan

Pamela Magini Italy

Helene Kretzmer Germany

Simon Rose Italy

Duen-Mei Wang China

Tatsuaki Kurosaki United States

Merav Hecht Israel

Karin Segers Belgium

Phuc‐Loi Luu Australia

Emilie Falconnet Switzerland

Ammar Zaghlool

409 ×0.7

251 ×1.0

GENET

161 ×0.8

43 ×0.8

IMMUN

32 ×0.6

Citations per year, relative to Ammar Zaghlool Ammar Zaghlool (= 1×) peers Emilie Falconnet

Countries citing papers authored by Ammar Zaghlool

Since Specialization

Citations

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

Fields of papers citing papers by Ammar Zaghlool

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ammar Zaghlool

This figure shows the co-authorship network connecting the top 25 collaborators of Ammar Zaghlool. A scholar is included among the top collaborators of Ammar Zaghlool 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 Ammar Zaghlool. Ammar Zaghlool is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Chavkin, Nicholas W., Jonatan Halvardson, Mark C. Thel, et al.. (2025). Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis. Communications Medicine. 5(1). 246–246. 1 indexed citations

Mattisson, Jonas, Jonatan Halvardson, Hanna Davies, et al.. (2024). Loss of chromosome Y in regulatory T cells. BMC Genomics. 25(1). 243–243. 15 indexed citations

Zaghlool, Ammar, Adnan Niazi, Åsa K. Björklund, et al.. (2021). Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts. Scientific Reports. 11(1). 4076–4076. 34 indexed citations

Ahmad, Tauseef, Ammar Zaghlool, Jonatan Halvardson, et al.. (2019). Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early Development. Frontiers in Genetics. 10. 891–891. 12 indexed citations

Zaghlool, Ammar, Adam Ameur, Chenglin Wu, et al.. (2018). Expression profiling and in situ screening of circular RNAs in human tissues. Scientific Reports. 8(1). 16953–16953. 21 indexed citations

Zhao, Jin, Jonatan Halvardson, Cecilia Zander, et al.. (2017). Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(1). 10–20. 32 indexed citations

Halvardson, Jonatan, Jin Zhao, Ammar Zaghlool, et al.. (2016). Mutations in HECW2 are associated with intellectual disability and epilepsy. Journal of Medical Genetics. 53(10). 697–704. 48 indexed citations

Zaghlool, Ammar, Jonatan Halvardson, Jin Zhao, et al.. (2016). A Role for the Chromatin‐Remodeling FactorBAZ1Ain Neurodevelopment. Human Mutation. 37(9). 964–975. 31 indexed citations

Zaghlool, Ammar, Adam Ameur, Lucia Cavelier, & Lars Feuk. (2014). Splicing in the Human Brain. International review of neurobiology. 116. 95–125. 15 indexed citations

10.

Forsberg, Lars A., Chiara Rasi, Hanna Davies, et al.. (2014). Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer. Nature Genetics. 46(6). 624–628. 287 indexed citations

11.

Zaghlool, Ammar, Adam Ameur, Jonatan Halvardson, et al.. (2013). Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues. BMC Biotechnology. 13(1). 99–99. 40 indexed citations

12.

Halvardson, Jonatan, Ammar Zaghlool, & Lars Feuk. (2012). Exome RNA sequencing reveals rare and novel alternative transcripts. Nucleic Acids Research. 41(1). e6–e6. 37 indexed citations

13.

Ameur, Adam, Ammar Zaghlool, Jonatan Halvardson, et al.. (2011). Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain. Nature Structural & Molecular Biology. 18(12). 1435–1440. 228 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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