Ayman W. El‐Hattab

6.3k citations

103 papers · 3.8k indexed · 1 hit paper · h-index 33

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders 48
Biochemistry top 2%
- Amino Acid Enzymes and Metabolism 11
Molecular Biology top 2%
- Mitochondrial Function and Pathology 46
- ATP Synthase and ATPases Research 17
Genetics top 5%
- Genetics and Neurodevelopmental Disorders 18
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 15
Physiology top 5%
- Nitric Oxide and Endothelin Effects 9

Co-authors: Fernando Scaglia Mohammed Almannai William J. Craigen Pilar Magoulas Jeremy Jones Adekunle M. Adesina Lisa Emrick Jehan Suleiman
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: SHILAP Revista de lepidopterología (2 papers)PLoS ONE (1 paper)Journal of the American Society of Nephrology (1 paper)
Partner nations: United Arab Emirates United States Saudi Arabia

In The Last Decade

Ayman W. El‐Hattab

102 papers receiving 3.7k citations

Hit Papers

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Peers

Countries citing papers authored by Ayman W. El‐Hattab

Since Specialization

Citations

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

Fields of papers citing papers by Ayman W. El‐Hattab

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ayman W. El‐Hattab. 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 Ayman W. El‐Hattab. The network helps show where Ayman W. El‐Hattab may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Ayman W. El‐Hattab, 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 Ayman W. El‐Hattab Line = papers co-authored together Ayman W. El‐Hattab links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Enhancing Equitable Access to Rare Disease Diagnosis and Treatment around the World: A Review of Evidence, Policies, and Challenges International Journal of Environmental Research and Public Health ·Takeya Adachi,Ayman W. El‐Hattab,Ritu Jain,Katya A. Nogales Crespo,Camila I. Quirland Lazo,Maurizio Scarpa,Marshall Summar,Duangrurdee Wattanasirichaigoon	2023	71
2	Disorders of histone methylation: Molecular basis and clinical syndromes Clinical Genetics ·Mode Al Ojaimi,Bashar J. Banimortada,Amna Othman,Korbinian M. Riedhammer,Mohammed Almannai,Ayman W. El‐Hattab	2022	16
3	A homozygous frame‐shift variant in PROSER1 is associated with developmental delay, hypotonia, genitourinary malformations, and distinctive facial features Clinical Genetics ·Azza Salah,Mohammed Almannai,Mode Al Ojaimi,Mandy Radefeldt,Nishtha Gulati,Maria Iqbal,Salem Alawbathani,Ruslan Al‐Ali,Christian Beetz,Ayman W. El‐Hattab	2022	5
4	Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy American Journal of Medical Genetics Part A ·Shuk Ching Chong,Ye Cao,Eva Fung,Soledad Kleppe,Karen W. Gripp,Jozef Hertecant,Ayman W. El‐Hattab,Jehan Suleiman,Gary Clark,Gretchen Von Allmen,Olga Rodziyevska,Richard A. Lewis,Jill A. Rosenfeld,Jie Dong,(unknown),Xia Wang,Marcus J. Miller,Weimin Bi,Pengfei Liu,Fernando Scaglia	2022	2
5	The int22h1/int22h2-Mediated Xq28 Duplication Syndrome: An Intersection between Neurodevelopment, Immunology, and Cancer Genes ·Rami A. Ballout,Ayman W. El‐Hattab	2021	3
6	Biallelic Pathogenic GFRA1 Variants Cause Autosomal Recessive Bilateral Renal Agenesis Journal of the American Society of Nephrology ·Veronica Arora,Suliman Khan,Ayman W. El‐Hattab,Ratna Dua Puri,María Eugenia Rocha,Rijad Merdzanic,Omid Paknia,Christian Beetz,Arndt Rolfs,Aida M. Bertoli‐Avella,Peter Bauer,Ishwar C. Verma	2020	12
7	Clinical trials in mitochondrial disorders, an update Molecular Genetics and Metabolism ·Mohammed Almannai,Ayman W. El‐Hattab,M. Nadir Ali,Claudia Soler‐Alfonso,Fernando Scaglia	2020	50
8	VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features Clinical Genetics ·Christian Beetz,Najim Ameziane,Ameni Kdissa,Vasiliki Karageorgou,Peter Bauer,Jehan Suleiman,V. Reid Sutton,Ayman W. El‐Hattab	2019	4
9	Homozygous loss‐of‐function variants of TASP1 , a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies Human Mutation ·Jehan Suleiman,Korbinian M. Riedhammer,Timothy Jicinsky,Melinda Mundt,Laurie Werner,Mirjana Gušić,Anna Lena Burgemeister,Hessa S. Alsaif,Maha Abdulrahim,Nabil Moghrabi,Manal Nicolas‐Jilwan,Moeenaldeen AlSayed,Weimin Bi,Srirangan Sampath,Fowzan S. Alkuraya,Ayman W. El‐Hattab	2019	9
10	LOXL3 novel mutation causing a rare form of autosomal recessive Stickler syndrome Clinical Genetics ·Tin K. Chan,Mohammed K. Alkaabi,Ahmed Mohammed Elbarky,Ayman W. El‐Hattab	2018	18
11	WDR45B‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome Clinical Genetics ·Jehan Suleiman,Diane Allingham‐Hawkins,Mais Hashem,Hanan E. Shamseldin,Fowzan S. Alkuraya,Ayman W. El‐Hattab	2017	30
12	Inborn Errors of Metabolism with Seizures Pediatric Clinics of North America ·Mohammed Almannai,Ayman W. El‐Hattab	2017	13
13	Systemic Primary Carnitine Deficiency Ayman W. El‐Hattab	2016	6
14	Mitochondrial Cardiomyopathies Frontiers in Cardiovascular Medicine ·Ayman W. El‐Hattab,Fernando Scaglia	2016	130
15	Xq28 Duplication Syndrome, Int22h1/Int22h2 Mediated Ayman W. El‐Hattab,Christian P. Schaaf,Sau Wai Cheung	2016	4
16	N-acetylglutamate synthase deficiency: Novel mutation associated with neonatal presentation and literature review of molecular and phenotypic spectra Molecular Genetics and Metabolism Reports ·Eiman H. Al Kaabi,Ayman W. El‐Hattab	2016	13
17	Systemic primary carnitine deficiency: an overview of clinical manifestations, diagnosis, and management Orphanet Journal of Rare Diseases ·Pilar Magoulas,Ayman W. El‐Hattab	2012	159
18	Diffuse reticuloendothelial system involvement in type IV glycogen storage disease with a novel GBE1 mutation: a case report and review Human Pathology ·Pilar Magoulas,Ayman W. El‐Hattab,Angshumoy Roy,Deeksha Bali,Milton J. Finegold,William J. Craigen	2012	21
19	Citrulline and arginine utility in treating nitric oxide deficiency in mitochondrial disorders Molecular Genetics and Metabolism ·Ayman W. El‐Hattab,Lisa Emrick,William J. Craigen,Fernando Scaglia	2012	82
20	Deletion and duplication of 15q24: Molecular mechanisms and potential modification by additional copy number variants Genetics in Medicine ·Ayman W. El‐Hattab,Feng Zhang,Rolanda Maxim,Katherine Christensen,Jewell C. Ward,Stacy J. Hines‐Dowell,Fernando Scaglia,James R. Lupski,Sau Wai Cheung	2010	27

About Ayman W. El‐Hattab

Ayman W. El‐Hattab is a scholar working on Clinical Biochemistry, Biochemistry and Genetics, having authored 103 papers that have together received 3.8k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (48 papers), Mitochondrial Function and Pathology (46 papers), Genetics and Neurodevelopmental Disorders (18 papers), ATP Synthase and ATPases Research (17 papers), Genomics and Rare Diseases (16 papers), Genomic variations and chromosomal abnormalities (15 papers), Amino Acid Enzymes and Metabolism (11 papers) and Nitric Oxide and Endothelin Effects (9 papers). The work is most often cited by research in Clinical Biochemistry (1.5k citations), Biochemistry (279 citations) and Molecular Biology (2.6k citations). Ayman W. El‐Hattab has collaborated with scholars based in United Arab Emirates, United States and Saudi Arabia. Frequent co-authors include Fernando Scaglia, Mohammed Almannai, William J. Craigen, Pilar Magoulas, Jeremy Jones, Adekunle M. Adesina, Lisa Emrick, William J. Craigen, Jehan Suleiman and Lee‐Jun C. Wong. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Journal of the American Society of Nephrology.

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