Eissa Faqeih

7.6k total citations
80 papers, 2.2k citations indexed

About

Eissa Faqeih is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Eissa Faqeih has authored 80 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 35 papers in Genetics and 17 papers in Clinical Biochemistry. Recurrent topics in Eissa Faqeih's work include Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (14 papers) and Genomics and Rare Diseases (10 papers). Eissa Faqeih is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (14 papers) and Genomics and Rare Diseases (10 papers). Eissa Faqeih collaborates with scholars based in Saudi Arabia, United States and Egypt. Eissa Faqeih's co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Shinu Ansari, Muneera Alshammari, Hanan E. Shamseldin, Mais Hashem, Mohammed Al‐Owain, Ali Alasmari, Niema Ibrahim and Zuhair N. Al‐Hassnan and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Eissa Faqeih

77 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eissa Faqeih Saudi Arabia 28 1.5k 920 238 222 181 80 2.2k
Małgorzata Krajewska‐Walasek Poland 23 1.4k 0.9× 1.0k 1.1× 149 0.6× 185 0.8× 67 0.4× 110 2.2k
Mohammed Al‐Owain Saudi Arabia 25 1.1k 0.8× 595 0.6× 128 0.5× 267 1.2× 350 1.9× 87 2.0k
Mordechai Shohat Israel 26 1.7k 1.1× 540 0.6× 154 0.6× 331 1.5× 79 0.4× 83 2.9k
Susana Balcells Spain 26 1.2k 0.8× 467 0.5× 228 1.0× 73 0.3× 297 1.6× 105 2.0k
Hanan E. Shamseldin Saudi Arabia 24 981 0.7× 590 0.6× 182 0.8× 159 0.7× 46 0.3× 55 1.5k
Tony Roscioli Australia 24 877 0.6× 769 0.8× 106 0.4× 88 0.4× 81 0.4× 85 1.7k
H.J.M. Smeets Netherlands 30 1.5k 1.0× 501 0.5× 100 0.4× 301 1.4× 36 0.2× 63 2.4k
Anas M. Alazami Saudi Arabia 22 857 0.6× 584 0.6× 100 0.4× 52 0.2× 129 0.7× 55 1.5k
Juha Saharinen Finland 25 1.9k 1.3× 717 0.8× 267 1.1× 98 0.4× 116 0.6× 34 3.0k
Satomi Mitsuhashi Japan 28 1.8k 1.3× 454 0.5× 299 1.3× 94 0.4× 90 0.5× 99 2.4k

Countries citing papers authored by Eissa Faqeih

Since Specialization
Citations

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

Fields of papers citing papers by Eissa Faqeih

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eissa Faqeih

This figure shows the co-authorship network connecting the top 25 collaborators of Eissa Faqeih. A scholar is included among the top collaborators of Eissa Faqeih 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 Eissa Faqeih. Eissa Faqeih 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.
Peer‐Zada, Abdul Ali, et al.. (2024). Incidence of Inborn Errors of Metabolism and Endocrine Disorders Among 40965 Newborn Infants at Riyadh Second Health Cluster of the Ministry of Health Saudi Arabia. International Journal of Neonatal Screening. 10(4). 72–72. 1 indexed citations
2.
Altassan, Ruqaiah, Riyadh Alokaili, Khalid Alhasan, et al.. (2022). Further delineation of GEMIN4 related neurodevelopmental disorder with microcephaly, cataract, and renal abnormalities syndrome. American Journal of Medical Genetics Part A. 188(10). 2932–2940. 1 indexed citations
3.
Alsaif, Hessa S., Eissa Faqeih, Magalie Barth, et al.. (2021). ZNF668 deficiency causes a recognizable disorder of DNA damage repair. Human Genetics. 140(9). 1395–1401. 1 indexed citations
4.
Olinger, Eric, Issa Al Salmi, Elisa Molinari, et al.. (2021). A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families. Human Mutation. 42(10). 1221–1228. 9 indexed citations
5.
Shamsi, Monis Bilal, Mohamed Saleh, Roy W A Peake, et al.. (2021). Clinical characterization and further confirmation of the autosomal recessive SLC12A2 disease. Journal of Human Genetics. 66(7). 689–695. 9 indexed citations
6.
Lentini, Jenna M., Hessa S. Alsaif, Eissa Faqeih, Fowzan S. Alkuraya, & Dragony Fu. (2020). DALRD3 encodes a protein mutated in epileptic encephalopathy that targets arginine tRNAs for 3-methylcytosine modification. Nature Communications. 11(1). 2510–2510. 47 indexed citations
7.
Almannai, Mohammed, Eissa Faqeih, Ali Alasmari, et al.. (2020). Further delineation of METTL23‐associated intellectual disability. American Journal of Medical Genetics Part A. 182(4). 785–791. 7 indexed citations
8.
Faqeih, Eissa, et al.. (2018). Phenotypic characterization of KCTD3‐related developmental epileptic encephalopathy. Clinical Genetics. 93(5). 1081–1086. 13 indexed citations
9.
Almannai, Mohammed, Ali Alasmari, Eissa Faqeih, et al.. (2018). Expanding the phenotype of SLC25A42‐associated mitochondrial encephalomyopathy. Clinical Genetics. 93(5). 1097–1102. 24 indexed citations
10.
Ramadan, Wafaa S., Nisha Patel, Shamsa Anazi, et al.. (2018). Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy. Journal of Neurology and Neuroscience. 4 indexed citations
11.
Patel, Nisha, Shams Anazi, Amal Y. Kentab, et al.. (2017). Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy. Clinical Genetics. 92(3). 327–331. 38 indexed citations
12.
Alhashem, Amal, Eissa Faqeih, Majid Alfadhel, et al.. (2017). Congenital disorders of glycosylation: The Saudi experience. American Journal of Medical Genetics Part A. 173(10). 2614–2621. 29 indexed citations
13.
Shamseldin, Hanan E., Shams Anazi, Salma M. Wakil, et al.. (2016). Novel copy number variants and major limb reduction malformation: Report of three cases. American Journal of Medical Genetics Part A. 170(5). 1245–1250. 8 indexed citations
14.
Shamseldin, Hanan E., Sateesh Maddirevula, Eissa Faqeih, et al.. (2016). Increasing the sensitivity of clinical exome sequencing through improved filtration strategy. Genetics in Medicine. 19(5). 593–598. 43 indexed citations
15.
Barakeh, Duna, Eissa Faqeih, Shams Anazi, et al.. (2015). The many faces of KIF7. Human Genome Variation. 2(1). 15006–15006. 14 indexed citations
16.
Faqeih, Eissa, et al.. (2015). Novel STAMBP mutation and additional findings in an Arabic family. American Journal of Medical Genetics Part A. 167(4). 805–809. 11 indexed citations
17.
Shaheen, Ranad, Mona Aglan, Kim M. Keppler‐Noreuil, et al.. (2013). Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome. The American Journal of Human Genetics. 92(4). 598–604. 86 indexed citations
18.
Shaheen, Ranad, Anas M. Alazami, Muneera Alshammari, et al.. (2012). Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation. Journal of Medical Genetics. 49(10). 630–635. 108 indexed citations
19.
Shaheen, Ranad, Eissa Faqeih, Muneera Alshammari, et al.. (2012). Genomic analysis of Meckel–Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes. European Journal of Human Genetics. 21(7). 762–768. 42 indexed citations
20.
Huber, Céline, Eissa Faqeih, Deborah Bartholdi, et al.. (2012). Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia. The American Journal of Human Genetics. 92(1). 144–149. 41 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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