Niema Ibrahim

3.4k total citations
22 papers, 767 citations indexed

About

Niema Ibrahim is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Niema Ibrahim has authored 22 papers receiving a total of 767 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Niema Ibrahim's work include Genomics and Rare Diseases (5 papers), RNA Research and Splicing (5 papers) and Congenital heart defects research (3 papers). Niema Ibrahim is often cited by papers focused on Genomics and Rare Diseases (5 papers), RNA Research and Splicing (5 papers) and Congenital heart defects research (3 papers). Niema Ibrahim collaborates with scholars based in Saudi Arabia, United States and United Arab Emirates. Niema Ibrahim's co-authors include Fowzan S. Alkuraya, Firdous Abdulwahab, Mais Hashem, Sateesh Maddirevula, Hanan E. Shamseldin, Eissa Faqeih, Hessa S. Alsaif, Serdar Coşkun, Saad S. M. Hassan and Muneera Alshammari and has published in prestigious journals such as Brain, Journal of Allergy and Clinical Immunology and The American Journal of Human Genetics.

In The Last Decade

Niema Ibrahim

22 papers receiving 760 citations

Peers

Countries citing papers authored by Niema Ibrahim

Since Specialization

Citations

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

Fields of papers citing papers by Niema Ibrahim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Niema Ibrahim

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

All Works

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	CNP deficiency causes severe hypomyelinating leukodystrophy in humans	Human Genetics	Lama AlAbdi, Fathiya Al Murshedi et al.	18
2	An exome-first approach to aid in the diagnosis of primary ciliary dyskinesia	Human Genetics	Hanan E. Shamseldin, Muslim M. Alsaadi et al.	16
3	A genomics approach to females with infertility and recurrent pregnancy loss	Human Genetics	Sateesh Maddirevula, Khalid Awartani et al.	58
4	A genomics approach to male infertility	Genetics in Medicine	Naif Alhathal, Sateesh Maddirevula et al.	51
5	Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans	Human Genetics	Hessa S. Alsaif, Khalid Al-Hussein et al.	9
6	Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2	Annals of Clinical and Translational Neurology	Patrick R. Blackburn, Matthew Schultz et al.	5
7	Phenotypic delineation of the retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome	Clinical Genetics	Hisham Alkuraya, Nisha Patel et al.	5
8	NUP214 deficiency causes severe encephalopathy and microcephaly in humans	Human Genetics	Hanan E. Shamseldin, Nawal Makhseed et al.	14
9	Immunodeficiency and EBV-induced lymphoproliferation caused by 4-1BB deficiency	Journal of Allergy and Clinical Immunology	Mohammed F. Alosaimi, Manfred Hoenig et al.	57
10	Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans	The American Journal of Human Genetics	Ranad Shaheen, Nan Jiang et al.	21
11	Congenital glaucoma and CYP1B1: an old story revisited	Human Genetics	Hessa S. Alsaif, Arif O. Khan et al.	23
12	Identification of novel loci for pediatric cholestatic liver disease defined by KIF12, PPM1F, USP53, LSR, and WDR83OS pathogenic variants	Genetics in Medicine	Sateesh Maddirevula, Talal Algoufi et al.	69
13	GWAS signals revisited using human knockouts	Genetics in Medicine	Sateesh Maddirevula, Fatema Alzahrani et al.	3
14	A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder	Brain	Hanan E. Shamseldin, Ali Alasmari et al.	40
15	Increasing the sensitivity of clinical exome sequencing through improved filtration strategy	Genetics in Medicine	Hanan E. Shamseldin, Sateesh Maddirevula et al.	43
16	Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract	Human Genetics	Nisha Patel, Deepti Anand et al.	64
17	GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition	Genome biology	Hanan E. Shamseldin, Ikuo Masuho et al.	28
18	Positional mapping of PRKD1 , NRP1 and PRDM1 as novel candidate disease genes in truncus arteriosus	Journal of Medical Genetics	Ranad Shaheen, Mohammed Hussien Alghamdi et al.	27
19	Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families	Genome Biology	Hanan E. Shamseldin, Maha Tulbah et al.	78
20	Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly	The American Journal of Human Genetics	Jawahir Y. Mohamed, Eissa Faqeih et al.	59

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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