Dalia Ghoneim

636 total citations
15 papers, 409 citations indexed

About

Dalia Ghoneim is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Dalia Ghoneim has authored 15 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Oncology and 4 papers in Genetics. Recurrent topics in Dalia Ghoneim's work include Genetic Associations and Epidemiology (3 papers), Pancreatic and Hepatic Oncology Research (3 papers) and RNA and protein synthesis mechanisms (3 papers). Dalia Ghoneim is often cited by papers focused on Genetic Associations and Epidemiology (3 papers), Pancreatic and Hepatic Oncology Research (3 papers) and RNA and protein synthesis mechanisms (3 papers). Dalia Ghoneim collaborates with scholars based in United States, United Kingdom and China. Dalia Ghoneim's co-authors include Alex R. Paciorkowski, Emily Tuttle, William B. Dobyns, Jason R. Myers, Susan L. Christian, Laura A. Jansen, Sonya A. Gunter, Robert W. Marion, Jonathan G.L. Mullins and Laurie E. Seltzer and has published in prestigious journals such as Nucleic Acids Research, Cancer Research and The American Journal of Human Genetics.

In The Last Decade

Dalia Ghoneim

15 papers receiving 407 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dalia Ghoneim United States	10	277	125	59	43	33	15	409
Emily Tuttle United States	7	211 0.8×	113 0.9×	62 1.1×	28 0.7×	32 1.0×	10	314
Kristina Jülich United States	8	475 1.7×	116 0.9×	63 1.1×	30 0.7×	57 1.7×	14	674
Luigina Spaccini Italy	13	208 0.8×	159 1.3×	43 0.7×	10 0.2×	29 0.9×	47	455
Bret L. Bostwick United States	9	225 0.8×	215 1.7×	22 0.4×	18 0.4×	9 0.3×	17	414
Martin Krenn Austria	13	135 0.5×	60 0.5×	24 0.4×	15 0.3×	18 0.5×	36	394
Emmanuelle Ranza Switzerland	12	137 0.5×	103 0.8×	19 0.3×	14 0.3×	30 0.9×	22	295
Jutta Gärtner Germany	14	366 1.3×	109 0.9×	29 0.5×	66 1.5×	14 0.4×	19	650
Chiara Parodi Italy	9	165 0.6×	48 0.4×	39 0.7×	17 0.4×	13 0.4×	25	375
Corinna Friedrich Germany	15	459 1.7×	244 2.0×	24 0.4×	39 0.9×	9 0.3×	25	768
Nobuyoshi Shimizu Japan	11	258 0.9×	81 0.6×	27 0.5×	17 0.4×	8 0.2×	14	376

Countries citing papers authored by Dalia Ghoneim

Since Specialization

Citations

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

Fields of papers citing papers by Dalia Ghoneim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dalia Ghoneim

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

All Works

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15 of 15 papers shown

Zhu, Jingjing, Shuai Liu, Keenan A. Walker, et al.. (2024). Associations between genetically predicted plasma protein levels and Alzheimer’s disease risk: a study using genetic prediction models. Alzheimer s Research & Therapy. 16(1). 8–8. 7 indexed citations

Zhu, Jingjing, Ke Wu, Shuai Liu, et al.. (2024). Proteome-wide association study and functional validation identify novel protein markers for pancreatic ductal adenocarcinoma. GigaScience. 13. 1 indexed citations

Zhong, Hua, Jingjing Zhu, Shuai Liu, et al.. (2023). Identification of blood protein biomarkers associated with prostate cancer risk using genetic prediction models: analysis of over 140,000 subjects. Human Molecular Genetics. 32(22). 3181–3193. 5 indexed citations

Ghoneim, Dalia, et al.. (2021). Abstract 882: Associations of genetically predicted blood protein biomarkers with pancreatic ductal adenocarcinoma risk: A study using comprehensive protein genetic prediction models. Cancer Research. 81(13_Supplement). 882–882. 1 indexed citations

Sun, Yanfa, Dan Zhou, Md Rezanur Rahman, et al.. (2021). A transcriptome-wide association study identifies novel blood-based gene biomarker candidates for Alzheimer’s disease risk. Human Molecular Genetics. 31(2). 289–299. 9 indexed citations

Liu, Duo, Dan Zhou, Yanfa Sun, et al.. (2020). A Transcriptome-Wide Association Study Identifies Candidate Susceptibility Genes for Pancreatic Cancer Risk. Cancer Research. 80(20). 4346–4354. 30 indexed citations

Radwan, Sara M., et al.. (2020). Adipose Tissue–Derived Mesenchymal Stem Cells Protect Against Amiodarone-Induced Lung Injury in Rats. Applied Biochemistry and Biotechnology. 191(3). 1027–1041. 15 indexed citations

Braun, Johannes, Sandra E. Fischer, Zhenjiang Zech Xu, et al.. (2018). Identification of new high affinity targets for Roquin based on structural conservation. Nucleic Acids Research. 46(22). 12109–12125. 18 indexed citations

Ghoneim, Dalia, et al.. (2018). Conservation of location of several specific inhibitory codon pairs in theSaccharomyces sensu stricto yeastsreveals translational selection. Nucleic Acids Research. 47(3). 1164–1177. 8 indexed citations

10.

Sun, Yu, Li Xie, Xiaoyu Zhuo, et al.. (2017). Domestic chickens activate a piRNA defense against avian leukosis virus. eLife. 6. 35 indexed citations

11.

Snow, Chelsi J., Emily Tuttle, Dalia Ghoneim, et al.. (2015). De Novo Mutations in SIK1 Cause a Spectrum of Developmental Epilepsies. The American Journal of Human Genetics. 96(4). 682–690. 43 indexed citations

12.

Paciorkowski, Alex R., Sharon S. McDaniel, Laura A. Jansen, et al.. (2015). Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly. Epilepsia. 56(3). 422–430. 96 indexed citations

13.

Ghoneim, Dalia, Jason R. Myers, Emily Tuttle, & Alex R. Paciorkowski. (2014). Comparison of insertion/deletion calling algorithms on human next-generation sequencing data. BMC Research Notes. 7(1). 864–864. 38 indexed citations

14.

Cushion, Thomas D., Alex R. Paciorkowski, Daniela T. Pilz, et al.. (2014). De Novo Mutations in the Beta-Tubulin Gene TUBB2A Cause Simplified Gyral Patterning and Infantile-Onset Epilepsy. The American Journal of Human Genetics. 94(4). 634–641. 81 indexed citations

15.

Paciorkowski, Alex R., Joshua B. Kelley, Adam Spencer, et al.. (2013). Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation. European Journal of Human Genetics. 22(5). 587–593. 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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