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 — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Niema Ibrahim Saudi Arabia 17 411 257 110 97 97 22 767
Zeynep Coban‐Akdemir United States 18 544 1.3× 396 1.5× 41 0.4× 66 0.7× 131 1.4× 50 965
Jianhua Xu China 17 313 0.8× 71 0.3× 59 0.5× 46 0.5× 167 1.7× 35 730
Hadia Hijazi Saudi Arabia 11 333 0.8× 226 0.9× 110 1.0× 38 0.4× 20 0.2× 15 579
Jessica K. Booker United States 13 304 0.7× 292 1.1× 54 0.5× 50 0.5× 114 1.2× 25 850
Sylvie Tondeur France 12 491 1.2× 82 0.3× 153 1.4× 51 0.5× 138 1.4× 25 832
Vivien Grant United Kingdom 13 343 0.8× 67 0.3× 86 0.8× 35 0.4× 152 1.6× 19 686
Nicole L. Hoppman United States 14 279 0.7× 279 1.1× 88 0.8× 58 0.6× 31 0.3× 62 704
Arseni Markoff Germany 18 611 1.5× 319 1.2× 60 0.5× 21 0.2× 253 2.6× 49 1.1k
Biola M. Javierre Spain 22 1.3k 3.0× 204 0.8× 48 0.4× 74 0.8× 225 2.3× 32 1.6k
Stephanie Schubert Germany 14 261 0.6× 222 0.9× 40 0.4× 71 0.7× 33 0.3× 32 563

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

20 of 20 papers shown
1.
AlAbdi, Lama, Fathiya Al Murshedi, Anuradha Ganesh, et al.. (2020). CNP deficiency causes severe hypomyelinating leukodystrophy in humans. Human Genetics. 139(5). 615–622. 18 indexed citations
2.
Shamseldin, Hanan E., Muslim M. Alsaadi, Amal Alhashem, et al.. (2020). An exome-first approach to aid in the diagnosis of primary ciliary dyskinesia. Human Genetics. 139(10). 1273–1283. 16 indexed citations
3.
Maddirevula, Sateesh, Khalid Awartani, Serdar Coşkun, et al.. (2020). A genomics approach to females with infertility and recurrent pregnancy loss. Human Genetics. 139(5). 605–613. 58 indexed citations
4.
Alhathal, Naif, Sateesh Maddirevula, Serdar Coşkun, et al.. (2020). A genomics approach to male infertility. Genetics in Medicine. 22(12). 1967–1975. 51 indexed citations
5.
Alsaif, Hessa S., Khalid Al-Hussein, Niema Ibrahim, et al.. (2020). Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans. Human Genetics. 139(4). 513–519. 9 indexed citations
6.
Blackburn, Patrick R., Matthew Schultz, Dong Li, et al.. (2020). Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2. Annals of Clinical and Translational Neurology. 7(6). 1013–1028. 5 indexed citations
7.
Alkuraya, Hisham, Nisha Patel, Niema Ibrahim, et al.. (2019). Phenotypic delineation of the retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome. Clinical Genetics. 97(3). 447–456. 5 indexed citations
8.
Shamseldin, Hanan E., Nawal Makhseed, Niema Ibrahim, et al.. (2019). NUP214 deficiency causes severe encephalopathy and microcephaly in humans. Human Genetics. 138(3). 221–229. 14 indexed citations
9.
Alosaimi, Mohammed F., Manfred Hoenig, Craig D. Platt, et al.. (2019). Immunodeficiency and EBV-induced lymphoproliferation caused by 4-1BB deficiency. Journal of Allergy and Clinical Immunology. 144(2). 574–583.e5. 57 indexed citations
10.
Shaheen, Ranad, Nan Jiang, Fatema Alzahrani, et al.. (2019). Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. The American Journal of Human Genetics. 104(4). 731–737. 21 indexed citations
11.
Alsaif, Hessa S., Arif O. Khan, Nisha Patel, et al.. (2018). Congenital glaucoma and CYP1B1: an old story revisited. Human Genetics. 138(8-9). 1043–1049. 23 indexed citations
12.
Maddirevula, Sateesh, Talal Algoufi, Hessa S. Alsaif, et al.. (2018). Identification of novel loci for pediatric cholestatic liver disease defined by KIF12, PPM1F, USP53, LSR, and WDR83OS pathogenic variants. Genetics in Medicine. 21(5). 1164–1172. 69 indexed citations
13.
Maddirevula, Sateesh, Fatema Alzahrani, Shams Anazi, et al.. (2017). GWAS signals revisited using human knockouts. Genetics in Medicine. 20(1). 64–68. 3 indexed citations
14.
Shamseldin, Hanan E., Ali Alasmari, Mohammed A. Salih, et al.. (2017). A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder. Brain. 140(11). 2806–2813. 40 indexed citations
15.
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
16.
Patel, Nisha, Deepti Anand, Dorota Monies, et al.. (2016). Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract. Human Genetics. 136(2). 205–225. 64 indexed citations
17.
Shamseldin, Hanan E., Ikuo Masuho, Ahmed Alenizi, et al.. (2016). GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition. Genome biology. 17(1). 195–195. 28 indexed citations
18.
Shaheen, Ranad, Mohammed Hussien Alghamdi, Salma M. Wakil, et al.. (2015). Positional mapping of PRKD1 , NRP1 and PRDM1 as novel candidate disease genes in truncus arteriosus. Journal of Medical Genetics. 52(5). 322–329. 27 indexed citations
19.
Shamseldin, Hanan E., Maha Tulbah, Wesam Kurdi, et al.. (2015). Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families. Genome Biology. 16(1). 116–116. 78 indexed citations
20.
Mohamed, Jawahir Y., Eissa Faqeih, Abdulmonem Alsiddiky, et al.. (2013). Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly. The American Journal of Human Genetics. 92(1). 157–161. 59 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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