Niema Ibrahim

3.4k citations

22 papers · 767 indexed · h-index 17

Genetics top 10%
- Genomics and Rare Diseases 5
Reproductive Medicine top 10%
Molecular Biology
- RNA Research and Splicing 5
- Congenital heart defects research 3
- RNA modifications and cancer 3
- Mitochondrial Function and Pathology 2
- RNA regulation and disease 2
- Renal and related cancers 2
Ophthalmology top 10%
Immunology
Clinical Biochemistry
- Metabolism and Genetic Disorders 2

Co-authors: Fowzan S. Alkuraya Firdous Abdulwahab Mais Hashem Sateesh Maddirevula Hanan E. Shamseldin Eissa Faqeih Hessa S. Alsaif Serdar Coşkun
Cited by: Genetics Reproductive Medicine Molecular Biology
Journals: Brain (1 paper)Journal of Allergy and Clinical Immunology (1 paper)The American Journal of Human Genetics (3 papers)
Partner nations: Saudi Arabia United States United Arab Emirates

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

The 25 scholars most cited alongside Niema Ibrahim, 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 Niema Ibrahim Line = papers co-authored together Niema Ibrahim links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	CNP deficiency causes severe hypomyelinating leukodystrophy in humans Human Genetics ·Lama AlAbdi,Fathiya Al Murshedi,Alaa Elmanzalawy,Asila Al Habsi,Rana Helaby,Anuradha Ganesh,Niema Ibrahim,Nisha Patel,Fowzan S. Alkuraya	2020	18
2	An exome-first approach to aid in the diagnosis of primary ciliary dyskinesia Human Genetics ·Hanan E. Shamseldin,Ibrahim Mogarri,Mansour Alqwaiee,Adel S. Alharbi,Khaled Baqais,Muslim M. Alsaadi,Talal Alanzi,Amal Alhashem,Afaf Al Saghier,Waleed S. Ameen,Niema Ibrahim,Jason Yang,Firdous Abdulwahab,Mais Hashem,Raghu R. Chivukula,Fowzan S. Alkuraya	2020	16
3	A genomics approach to females with infertility and recurrent pregnancy loss Human Genetics ·Sateesh Maddirevula,Khalid Awartani,Serdar Coşkun,Latifa F. AlNaim,Niema Ibrahim,Firdous Abdulwahab,Mais Hashem,Saad S. M. Hassan,Fowzan S. Alkuraya	2020	58
4	A genomics approach to male infertility Genetics in Medicine ·Naif Alhathal,Sateesh Maddirevula,Serdar Coşkun,Hamed Alali,Mirna Assoum,T.J. Morris,Hesham A. Deek,Soha A. Hamed,Shaheed Alsuhaibani,Abdulmalik Mirdawi,Nour Ewida,Mashael Alqahtani,Niema Ibrahim,Firdous Abdulwahab,Waleed Altaweel,Majed Dasouki,Abdullah M. Assiri,Wafa Qabbaj,Fowzan S. Alkuraya	2020	51
5	Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans Human Genetics ·Mohammed Zain Seidahmed,Adila Al‐Kindi,Hessa S. Alsaif,Abeer M. Miqdad,Nasser Alabbad,Abdallah Alfifi,Omer Bashir Abdelbasit,Khalid Al-Hussein,Abdulmohsen Alsamadi,Niema Ibrahim,Amna Al‐Futaisi,Almundher Al‐Maawali,Fowzan S. Alkuraya	2020	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,Carrie A. Lahner,Dong Li,Elizabeth Bhoj,Laura J. Fisher,Deborah L. Renaud,Amy Kenney,Niema Ibrahim,Mais Hashem,Mohammed Zain Seidahmed,Linda Hasadsri,Samantha A. Schrier Vergano,Fowzan S. Alkuraya,Brendan C. Lanpher	2020	5
7	Phenotypic delineation of the retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome Clinical Genetics ·Hisham Alkuraya,Nisha Patel,Niema Ibrahim,Bandar Al‐Ghamdi,Sulaiman M. Alsulaiman,Sawsan R. Nowilaty,Emad B. Abboud,Ramadan Alturki,Abdullah S. Al-Kharashi,Wafaa Eyaid,Zainab Al Masseri,Hamad Alzaidan,Mohammed D. Alotaibi,Ahmed M. Abu El‐Asrar,Bandar Alamro,Rana Helaby,Amani Elshaer,Naif A. M. Almontashiri,Abdulrahman Al‐Hussaini,Fowzan S. Alkuraya	2019	5
8	NUP214 deficiency causes severe encephalopathy and microcephaly in humans Human Genetics ·Hanan E. Shamseldin,Nawal Makhseed,Niema Ibrahim,Tarfa Al‐Sheddi,Eman Alobeid,Firdous Abdulwahab,Fowzan S. Alkuraya	2019	14
9	Immunodeficiency and EBV-induced lymphoproliferation caused by 4-1BB deficiency Journal of Allergy and Clinical Immunology ·Mohammed F. Alosaimi,Manfred Hoenig,Faris Jaber,Craig D. Platt,Jennifer Jones,Jacqueline G. Wallace,Klaus‐Michael Debatin,Ansgar Schulz,E. Jacobsen,Peter Möller,Hanan E. Shamseldin,Ferdous Abdulwahab,Niema Ibrahim,Hosam Alardati,Faisal ALMuhizi,Ibraheem Abosoudah,Talal A. Basha,Janet Chou,Fowzan S. Alkuraya,Raif S. Geha	2019	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,Fatema Alzahrani,Nour Ewida,Tarfa Al‐Sheddi,Eman Alobeid,Damir Musaev,Valentina Stanley,Mais Hashem,Niema Ibrahim,Firdous Abdulwahab,Abduljabbar Alshenqiti,Fatma Müjgan Sönmez,Nadia Saqati,Hamad Alzaidan,Mohammad M. Al‐Qattan,Futwan Al‐Mohanna,Joseph G. Gleeson,Fowzan S. Alkuraya	2019	21
11	Congenital glaucoma and CYP1B1: an old story revisited Human Genetics ·Hessa S. Alsaif,Arif O. Khan,Nisha Patel,Hisham Alkuraya,Mais Hashem,Firdous Abdulwahab,Niema Ibrahim,Mohammed A. Aldahmesh,Fowzan S. Alkuraya	2018	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,Hamoud Alhebbi,Awad Alqahtani,Talal Algoufi,Hessa S. Alsaif,Niema Ibrahim,Firdous Abdulwahab,Mohammed Barr,Hamad Alzaidan,Ali Almehaideb,Omai AlSasi,Amal Alhashem,Hussa Al Hussaini,Sami Wali,Fowzan S. Alkuraya	2018	69
13	GWAS signals revisited using human knockouts Genetics in Medicine ·Sateesh Maddirevula,Fatema Alzahrani,Shams Anazi,Mariam Al‐Mureikhi,Tawfeg Ben‐Omran,Ghada M. H. Abdel‐Salam,Mais Hashem,Niema Ibrahim,Firdous Abdulwahab,Neama Meriki,Fahad A. Bashiri,Meow‐Keong Thong,Premala Muthukumarasamy,Rifhan Azwani Mazlan,Ranad Shaheen,Fowzan S. Alkuraya	2017	3
14	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,Shahzad I. Mian,Tarfa Alshidi,Niema Ibrahim,Mais Hashem,Eissa Faqeih,Futwan Al‐Mohanna,Fowzan S. Alkuraya	2017	40
15	Increasing the sensitivity of clinical exome sequencing through improved filtration strategy Genetics in Medicine ·Hanan E. Shamseldin,Sateesh Maddirevula,Eissa Faqeih,Niema Ibrahim,Mais Hashem,Ranad Shaheen,Fowzan S. Alkuraya	2016	43
16	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,Mais Hashem,Haifa Alsedairy,Mohammed A. Aldahmesh,Salil A. Lachke,Fowzan S. Alkuraya	2016	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,Ahmed Alenizi,Suad Alyamani,Dipak N. Patil,Niema Ibrahim,Kirill A. Martemyanov,Fowzan S. Alkuraya	2016	28
18	Positional mapping of PRKD1 , NRP1 and PRDM1 as novel candidate disease genes in truncus arteriosus Journal of Medical Genetics ·Ranad Shaheen,Amal Al Hashem,Mohammed Hussien Alghamdi,Mohammed Zain Seidahmad,Salma M. Wakil,Khalid Dagriri,Bernard Keavney,Judith Goodship,Saad Alyousif,Fahad Alhabshan,Khalid Al-Hussein,Agaadir Almoisheer,Niema Ibrahim,Fowzan S. Alkuraya	2015	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,Wesam Kurdi,Maha Nemer,Nada Alsahan,Elham Al Mardawi,Ola Khalifa,Amal Hashem,Ahmed M Kurdi,Zainab Babay,Dalal Bubshait,Niema Ibrahim,Firdous Abdulwahab,Zuhair Rahbeeni,Mais Hashem,Fowzan S. Alkuraya	2015	78
20	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

About Niema Ibrahim

Niema Ibrahim is a scholar working on Clinical Biochemistry, Genetics and Ophthalmology, having authored 22 papers that have together received 767 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), RNA Research and Splicing (5 papers), Congenital heart defects research (3 papers), RNA modifications and cancer (3 papers), Mitochondrial Function and Pathology (2 papers), RNA regulation and disease (2 papers), Metabolism and Genetic Disorders (2 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Genetics (257 citations), Reproductive Medicine (57 citations) and Molecular Biology (411 citations). Niema Ibrahim has collaborated with scholars based in Saudi Arabia, United States and United Arab Emirates. Frequent 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. Their work appears in journals such as Brain, Journal of Allergy and Clinical Immunology and The American Journal of Human 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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