Tawfeg Ben‐Omran

4.9k citations

62 papers · 1.4k indexed · h-index 25

Co-authors: Noora Shahbeck Georg F. Hoffmann Johannes Häberle Rehab Ali Mariam Al‐Mureikhi Khalid Ibrahim Mahmoud F. Elsaid Nader Al‐Dewik
Topics: Metabolism and Genetic Disorders (13 papers)Folate and B Vitamins Research (13 papers)Genomics and Rare Diseases (11 papers)
Cited by: Clinical Biochemistry Biochemistry Rheumatology
Journals: Journal of Clinical InvestigationSHILAP Revista de lepidopterologíaBlood
Partner nations: Qatar United States Germany

In The Last Decade

Tawfeg Ben‐Omran

58 papers receiving 1.4k citations

Peers

Countries citing papers authored by Tawfeg Ben‐Omran

Since Specialization

Citations

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

Fields of papers citing papers by Tawfeg Ben‐Omran

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tawfeg Ben‐Omran. 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 Tawfeg Ben‐Omran. The network helps show where Tawfeg Ben‐Omran may publish in the future.

Co-authorship network of co-authors of Tawfeg Ben‐Omran

This figure shows the co-authorship network connecting the top 25 collaborators of Tawfeg Ben‐Omran. A scholar is included among the top collaborators of Tawfeg Ben‐Omran 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 Tawfeg Ben‐Omran. Tawfeg Ben‐Omran 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

#	Work	Indexed citations
1	Real-world experience with gene therapy in Duchenne muscular dystrophy center readiness and patients safety: report from Qatar 2025 ·Gene Therapy ·Muhammad Osman,Khalid Ibrahim,(unknown),(unknown),Ikram U. Haque,Nawal Al‐Hamad,Tawfeg Ben‐Omran	0
2	The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar 2024 ·Scientific Reports ·(unknown),(unknown),Nader Al‐Dewik,Houssein Khodjet‐El‐Khil,(unknown),Nazmul Islam,Tawfeg Ben‐Omran,Mashael Al‐Shafai	2
3	Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review 2023 ·European Journal of Pediatrics ·(unknown),(unknown),Malak Alghamdi,Khalid Hundallah,Jehan Suleiman,Tawfeg Ben‐Omran,Majid Alfadhel,Mohammed Almannai,(unknown),Brahim Tabarki	0
4	Li-Fraumeni Syndrome: The Two Faces of a Coin in Myeloid Malignancies 2023 ·Blood ·(unknown),(unknown),Tawfeg Ben‐Omran,(unknown),(unknown)	0
5	Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum Stress 2021 ·Diabetes ·Hossam Montaser,Kashyap Patel,Diego Balboa,Hazem Ibrahim,Väinö Lithovius,Anna Näätänen,Vikash Chandra,Korcan Demir,Sezer Acar,Tawfeg Ben‐Omran,Kevin Colclough,Jonathan M. Locke,Matthew N. Wakeling,Maria Lindahl,Andrew T. Hattersley,Jonna Saarimäki‐Vire,Timo Otonkoski	46
6	Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability 2020 ·Journal of Medical Genetics ·(unknown),(unknown),Maha S. Zaki,Katherine Johnson,(unknown),(unknown),(unknown),Jennifer McEvoy‐Venneri,Valentina Stanley,Sangmoon Lee,(unknown),Tawfeg Ben‐Omran,Joseph G. Gleeson,Sadaf Naz,Ashleigh E. Schaffer	5
7	Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience 2019 ·American Journal of Medical Genetics Part A ·Nader Al‐Dewik,(unknown),Mariam Al‐Mureikhi,Rehab Ali,(unknown),Laila Mahmoud,Noora Shahbeck,(unknown),Mariam AlMulla,(unknown),(unknown),(unknown),Gabriele Richard,Jane Juusola,Benjamin D. Solomon,Fowzan S. Alkuraya,Tawfeg Ben‐Omran	32
8	In silico and in vivo models for Qatari-specific classical homocystinuria as basis for development of novel therapies 2018 ·Human Mutation ·(unknown),Navaneethakrishnan Krishnamoorthy,Nader Al‐Dewik,Hatem Zayed,Nura A. Mohamed,(unknown),Sapna Gupta,Johannes Häberle,Beat Thöny,Henk J. Blom,Warren D. Kruger,Tawfeg Ben‐Omran,Gheyath K. Nasrallah	13
9	Biallelic mutations in DNA ligase 1 underlie a spectrum of immune deficiencies 2018 ·Journal of Clinical Investigation ·Patrick Maffucci,Jose Chavez,(unknown),Patrick O’Brien,Jordan K. Abbott,Paul R. Reynolds,Austen Worth,Luigi D. Notarangelo,Kerstin Felgentreff,Patricia Cortés,Bertrand Boisson,Lin Radigan,Aurélie Cobat,Chitra Dinakar,Mohammad Ehlayel,Tawfeg Ben‐Omran,Erwin W. Gelfand,Jean‐Laurent Casanova,Charlotte Cunningham‐Rundles	29
10	Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy 2017 ·European Journal of Medical Genetics ·Shenela Lakhani,Ryan N. Doan,Mariam Al‐Mureikhi,Jennifer N. Partlow,(unknown),Mahmoud F. Elsaid,Nada Alaaraj,A. James Barkovich,Christopher A. Walsh,Tawfeg Ben‐Omran	21
11	Newborn screening for remethylation disorders and vitamin B12 deficiency-evaluation of new strategies in cohorts from Qatar and Germany 2017 ·World Journal of Pediatrics ·Gwendolyn Gramer,Ghassan Abdoh,Tawfeg Ben‐Omran,Noora Shahbeck,Rehab Ali,Laila Mahmoud,Junmin Fang‐Hoffmann,Georg F. Hoffmann,Hilal Al Rifai,Jürgen G. Okun	18
12	W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report 2016 ·BMC Medical Genetics ·(unknown),Mahmoud F. Elsaid,Rehab Ali,(unknown),Tawfeg Ben‐Omran	21
13	Secondary NAD⁺ deficiency in the inherited defect of glutamine synthetase 2015 ·Journal of Inherited Metabolic Disease ·Liyan Hu,Khalid Ibrahim,Martin Stucki,Michele Frapolli,Noora Shahbeck,Farrukh A. Chaudhry,Boris Görg,Dieter Häussinger,William Todd Penberthy,Tawfeg Ben‐Omran,Johannes Häberle	17
14	Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndrome 2014 ·Orphanet Journal of Rare Diseases ·Marios Kambouris,Rachid C. Maroun,Tawfeg Ben‐Omran,Yasser Al‐Sarraj,(unknown),Rehab Ali,(unknown),Patrick A. Curmi,Hatem El‐Shanti	16
15	Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia 2013 ·The American Journal of Human Genetics ·Naiara Akizu,(unknown),Tawfeg Ben‐Omran,Lailá Bastaki,Asma Al-Tawari,Maha S. Zaki,Roshan Koul,Emily Spencer,Rasim Özgür Rosti,Eric Scott,Elizabeth Nickerson,Stacey Gabriel,(unknown),Li Jiang,Matthew A. Deardorff,Laura K. Conlin,Margaret A. Horton,Elaine H. Zackai,Elliott H. Sherr,Joseph G. Gleeson	19
16	Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome 2010 ·The American Journal of Human Genetics ·Natascia Anastasio,Tawfeg Ben‐Omran,Ahmad S. Teebi,Kevin Ha,Emilie Lalonde,Rehab Ali,Mariam Al‐Mureikhi,Vazken M. Der Kaloustian,Junhui Liu,David S. Rosenblatt,Jacek Majewski,Loydie A. Jerome‐Majewska	45
17	Newborn Population Screening for Classic Homocystinuria by Determination of Total Homocysteine from Guthrie Cards 2009 ·The Journal of Pediatrics ·Hongying Gan‐Schreier,(unknown),Junmin Fang‐Hoffmann,(unknown),Ghassan Abdoh,Tawfeg Ben‐Omran,(unknown),Abdülbari Bener,Hilal Al Rifai,Abdul Latif Al Khal,Martin Lindner,Johannes Zschocke,Georg F. Hoffmann	73
18	Hyperinsulinism–hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype–phenotype correlations 2009 ·European Journal of Endocrinology ·Ritika R. Kapoor,Sarah E. Flanagan,(unknown),Anupam Chakrapani,B. Chadefaux,Tawfeg Ben‐Omran,Indraneel Banerjee,Julian Hamilton‐Shield,Sian Ellard,Khalid Hussain	76
19	Molecular neonatal screening for homocystinuria in the Qatari population 2009 ·Human Mutation ·Johannes Zschocke,(unknown),Hongying Gan‐Schreier,Christine Fischer,Junmin Fang‐Hoffmann,(unknown),Ghassan Abdoh,Tawfeg Ben‐Omran,(unknown),Martin Lindner,Hilal Al Rifai,Abdul Latif Al Khal,Georg F. Hoffmann	32
20	Autosomal Recessive Inheritance of GLUT1 Deficiency Syndrome 2009 ·Neuropediatrics ·Jörg Klepper,Hans Scheffer,Mahmoud F. Elsaid,Erik-Jan Kamsteeg,(unknown),Tawfeg Ben‐Omran	46

About Tawfeg Ben‐Omran

Tawfeg Ben‐Omran is a scholar working on Clinical Biochemistry, Rheumatology and Biochemistry, having authored 62 papers that have together received 1.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (13 papers), Folate and B Vitamins Research (13 papers) and Genomics and Rare Diseases (11 papers). The work is most often cited by research in Clinical Biochemistry (334 citations), Biochemistry (141 citations) and Rheumatology (231 citations). Tawfeg Ben‐Omran has collaborated with scholars based in Qatar, United States and Germany. Frequent co-authors include Noora Shahbeck, Georg F. Hoffmann, Johannes Häberle, Rehab Ali, Mariam Al‐Mureikhi, Khalid Ibrahim, Mahmoud F. Elsaid, Nader Al‐Dewik, Ghassan Abdoh and Junmin Fang‐Hoffmann. Their work appears in journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Blood.

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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