Eissa Faqeih

7.7k citations

80 papers · 2.2k · h-index 28

Impact in

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Genetics top 2%
- Connective tissue disorders research
- Genetic and Kidney Cyst Diseases
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders

Papers in

Molecular Biology 51
- Mitochondrial Function and Pathology 10
- RNA modifications and cancer 7
- Epigenetics and DNA Methylation 5
Genetics 34
- Genomics and Rare Diseases 10
- Genetic and Kidney Cyst Diseases 9
- Connective tissue disorders research 9
- Genetics and Neurodevelopmental Disorders 8

Co-authors: Fowzan S. Alkuraya (39 shared papers)Ranad Shaheen (16 shared papers)Shinu Ansari (5 shared papers)Muneera Alshammari (6 shared papers)Hanan E. Shamseldin (7 shared papers)Mohammed Al‐Owain (11 shared papers)Ali Alasmari (15 shared papers)Niema Ibrahim (4 shared papers)
Journals: The American Journal of Human Genetics (10 papers)Clinical Genetics (5 papers)Human Genetics (3 papers)Human Mutation (3 papers)Journal of Medical Genetics (3 papers)
Partner nations: Saudi Arabia United States United Kingdom

In The Last Decade

Eissa Faqeih

78 papers receiving 2.2k citations

Peers

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-authors

The 25 scholars most cited alongside Eissa Faqeih, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eissa Faqeih Line = papers co-authored together Eissa Faqeih links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 80 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Genomic analysis of primordial dwarfism reveals novel disease genes Genome Research ·Ranad Shaheen, Eissa Faqeih, Shinu Ansari, Ghada M. H. Abdel‐Salam, Zuhair N. Al‐Hassnan, Tarfa Alshidi, Rana Alomar, Sameera Sogaty, Fowzan S. Alkuraya	2014	125
2	Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome The American Journal of Human Genetics ·Patrick R. Blackburn, Xu Zhi, Kathleen E. Tumelty, Rose Zhao, William J. Monis, Kimberly G. Harris, Jennifer Gass, Margot A. Cousin, Nicole J. Boczek, Mario Mitkov, Mark A. Cappel, Clair A. Francomano, Joseph E. Parisi, Eric W. Klee, Eissa Faqeih, Fowzan S. Alkuraya, Matthew D. Layne, Nazli B. McDonnell, Paldeep S. Atwal	2018	118
3	A homozygous truncating mutation in PUS3 expands the role of tRNA modification in normal cognition Human Genetics ·Ranad Shaheen, Lu Han, Eissa Faqeih, Nour Ewida, Eman Alobeid, Eric M. Phizicky, Fowzan S. Alkuraya	2016	114
4	Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation Journal of Medical Genetics ·Ranad Shaheen, Anas M. Alazami, Muneera Alshammari, Eissa Faqeih, Nadia Alhashmi, Noon Mousa, Aisha Al-Sinani, Shinu Ansari, Fatema Alzahrani, Mohammed Al‐Owain, Zayed Al‐Zayed, Fowzan S. Alkuraya	2012	110
5	Recessive Mutations in DOCK6, Encoding the Guanidine Nucleotide Exchange Factor DOCK6, Lead to Abnormal Actin Cytoskeleton Organization and Adams-Oliver Syndrome The American Journal of Human Genetics ·Ranad Shaheen, Eissa Faqeih, Asma Sunker, Heba Morsy, Tarfa Al‐Sheddi, Hanan E. Shamseldin, Nouran Adly, (unknown), Fowzan S. Alkuraya	2011	97
6	Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome The American Journal of Human Genetics ·Ranad Shaheen, Mona Aglan, Kim M. Keppler‐Noreuil, Eissa Faqeih, Shinu Ansari, Kim Horton, Adel M. Ashour, Maha S. Zaki, Fatema Alzahrani, Anna M. Cueto‐González, Ghada M. H. Abdel‐Salam, Samia A. Temtamy, Fowzan S. Alkuraya	2013	87
7	Neu-Laxova Syndrome, an Inborn Error of Serine Metabolism, Is Caused by Mutations in PHGDH The American Journal of Human Genetics ·Ranad Shaheen, Zuhair Rahbeeni, Amal Alhashem, Eissa Faqeih, Qi Zhao, Yong Xiong, Agaadir Almoisheer, Sarah M. Al-Qattan, Halima A. Almadani, Noufa Alonazi, Badi Shoaib Albaqawi, Mohammad A. M. Saleh, Fowzan S. Alkuraya	2014	65
8	Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract Human Genetics ·Nisha Patel, Deepti Anand, Dorota Monies, Sateesh Maddirevula, Arif O. Khan, Talal Algoufi, Mohammed Al‐Owain, Eissa Faqeih, Muneera Alshammari, Ahmed Qudair, Hadeel Alsharif, Fatimah Aljubran, Hessa S. Alsaif, Niema Ibrahim, Firdous Abdulwahab, (unknown), Haifa Alsedairy, Mohammed A. Aldahmesh, Salil A. Lachke, Fowzan S. Alkuraya	2016	64
9	POC1A Truncation Mutation Causes a Ciliopathy in Humans Characterized by Primordial Dwarfism The American Journal of Human Genetics ·Ranad Shaheen, Eissa Faqeih, Hanan E. Shamseldin, Ramil R. Noche, Asma Sunker, Muneera Alshammari, Tarfa Al‐Sheddi, Nouran Adly, Mohammed S. Al-Dosari, Sean G. Megason, Muneera Al-Husain, Futwan Al‐Mohanna, Fowzan S. Alkuraya	2012	64
10	A TCTN2 mutation defines a novel Meckel Gruber syndrome locus Human Mutation ·Ranad Shaheen, Eissa Faqeih, Mohammed Zain Seidahmed, Asma Sunker, Faten Ezzat Alali, AlQahtani Khadijah, Fowzan S. Alkuraya	2011	60
11	Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly The American Journal of Human Genetics ·Jawahir Y. Mohamed, Eissa Faqeih, Abdulmonem Alsiddiky, Muneera Alshammari, Niema Ibrahim, Fowzan S. Alkuraya	2013	59
12	Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans American Journal of Medical Genetics Part A ·Ranad Shaheen, Mohammed Al‐Owain, Eissa Faqeih, Nadia Alhashmi, Ali Awaji, Zayed Al‐Zayed, Fowzan S. Alkuraya	2011	57
13	Biallelic Mutations in FUT8 Cause a Congenital Disorder of Glycosylation with Defective Fucosylation The American Journal of Human Genetics ·Bobby G. Ng, Gege Xu, Nandini Chandy, Joan Steyermark, Deepali N. Shinde, Kelly Radtke, Kimiyo Raymond, Carlito B. Lebrilla, Ali Alasmari, Sharon F. Suchy, Zöe Powis, Eissa Faqeih, Susan A. Berry, David F. Kronn, Hudson H. Freeze	2018	53
14	A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies Human Molecular Genetics ·Ranad Shaheen, Miriam Schmidts, Eissa Faqeih, Amal Hashem, Ekkehart Lausch, Isabel Holder, Andrea Superti‐Furga, Hannah M. Mitchison, Agaadir Almoisheer, Rana Alamro, Tarfa Alshiddi, Fatma Alzahrani, Philip L. Beales, Fowzan S. Alkuraya	2014	53
15	A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B Journal of Medical Genetics ·Anas M. Alazami, Amal Y. Kentab, Eissa Faqeih, Jawahir Y. Mohamed, Hisham Alkhalidi, Hadia Hijazi, Fowzan S. Alkuraya	2015	52
16	DALRD3 encodes a protein mutated in epileptic encephalopathy that targets arginine tRNAs for 3-methylcytosine modification Nature Communications ·Jenna M. Lentini, Hessa S. Alsaif, Eissa Faqeih, Fowzan S. Alkuraya, Dragony Fu	2020	47
17	Increasing the sensitivity of clinical exome sequencing through improved filtration strategy Genetics in Medicine ·Hanan E. Shamseldin, Sateesh Maddirevula, Eissa Faqeih, Niema Ibrahim, (unknown), Ranad Shaheen, Fowzan S. Alkuraya	2016	44
18	Genomic analysis of Meckel–Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes European Journal of Human Genetics ·Ranad Shaheen, Eissa Faqeih, Muneera Alshammari, Abdulrahman Swaid, Lihadh Al‐Gazali, Elham Al Mardawi, Shinu Ansari, Sameera Sogaty, Mohammed Zain Seidahmed, Muhammed Al-Motairi, Chantal Farra, Wesam Kurdi, Shatha Alrasheed, Fowzan S. Alkuraya	2012	43
19	A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder Brain ·Hanan E. Shamseldin, Ali Alasmari, Mohammed A. Salih, Manar Samman, (unknown), Tarfa Alshidi, Niema Ibrahim, (unknown), Eissa Faqeih, Futwan Al‐Mohanna, Fowzan S. Alkuraya	2017	42
20	Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia The American Journal of Human Genetics ·Céline Huber, Eissa Faqeih, Deborah Bartholdi, Christine Bôle‐Feysot, Zvi Borochowitz, Denise P. Cavalcanti, Amandine Frigo, Patrick Nitschké, J. Roume, Heloísa G. dos Santos, Stavit Shalev, Andrea Superti‐Furga, Anne‐Lise Delezoide, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire	2012	41

About Eissa Faqeih

Eissa Faqeih is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Surgery, having authored 80 papers that have together received 2.2k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (16 papers), Genomics and Rare Diseases (10 papers), Mitochondrial Function and Pathology (10 papers), Genetic and Kidney Cyst Diseases (9 papers), Connective tissue disorders research (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), RNA modifications and cancer (7 papers) and Epigenetics and DNA Methylation (5 papers). The work is most often cited by research in Clinical Biochemistry (207 citations), Genetics (863 citations), Molecular Biology (1.3k citations), Cell Biology (228 citations) and Rheumatology (146 citations). Eissa Faqeih has collaborated with scholars based in Saudi Arabia, United States and United Kingdom. Frequent co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Shinu Ansari, Muneera Alshammari, Hanan E. Shamseldin, Mohammed Al‐Owain, Ali Alasmari, Niema Ibrahim, Zuhair N. Al‐Hassnan and Ghada M. H. Abdel‐Salam. Their work appears in journals such as The American Journal of Human Genetics, Clinical Genetics, Human Genetics, Human Mutation and Journal of Medical Genetics.

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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Eissa Faqeih

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About Eissa Faqeih

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