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E. Fateen · SciRah

Researcher profile · Semantic Scholar

E. Fateen

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E. Fateen — researcher profile on SciRah

h-index: 10
Works: 58
Citations: 319

Most-cited papers

PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and Microcephaly
M. Zaki, R. Heller, M. Thoenes, G. Nürnberg +11 more
2016Human Mutation44 citations Open access
Semantic Scholar
Outcome of enzyme replacement therapy in children with Gaucher disease: The Egyptian experience
A. S. Khalifa, A. Tantawy, R. Shawky, Eman Monir +3 more
201128 citations Open access
Semantic Scholar
Dyggve–Melchior–Clausen syndrome: clinical, genetic, and radiological study of 15 Egyptian patients from nine unrelated families
M. Aglan, S. Temtamy, E. Fateen, A. Ashour +2 more
2009Journal of Children's Orthopaedics25 citations Open access
Semantic Scholar
Molecular characterization of Egyptian patients with glycogen storage disease type IIIa
Y. Endo, E. Fateen, Yoshiko Aoyama, A. Horinishi +4 more
2005Journal of Human Genetics24 citations
Semantic Scholar
Biochemical diagnosis of mucopolysaccharidoses over 11 years: the Egyptian experience
E. Fateen, Mona M. Ibrahim, A. Gouda, Zienab A. Youssef
201418 citations
Semantic Scholar
Twenty- five years of biochemical diagnosis of Gaucher disease: the Egyptian experience
E. Fateen, Zeinab Y. Abdallah
2019Heliyon17 citations Open access
Semantic Scholar
Glycogen storage disease type III in Egyptian children: a single centre clinico-laboratory study.
H. El-Karaksy, Ghada M. Anwar, M. El-Raziky, E. Mogahed +4 more
2014Arab Journal of Gastroenterology12 citations
Semantic Scholar
Mucopolysaccharidoses diagnosis in the era of enzyme replacement therapy in Egypt
E. Fateen, Zeinab Y. Abdallah, W. Nazim, Mona M. Ibrahim +1 more
2021Heliyon11 citations Open access
Semantic Scholar
Egyptian glycogen storage disease type III – identification of six novel AGL mutations, including a large 1.5 kb deletion and a missense mutation p.L620P with subtype IIId
Y. Endo, E. Fateen, Mortada El Shabrawy, Yoshiko Aoyama +5 more
2009Clinical Chemistry and Laboratory Medicine11 citations Open access
Semantic Scholar
Prenatal diagnosis of mucopolysaccharidoses (MPS): the first Egyptian experience.
A. Nasr, E. Fateen
2004Bratislava Medical Journal11 citations
Semantic Scholar
Fifteen years experience: Egyptian metabolic lab
E. Fateen, A. Gouda, Mona M. Ibrahim, Zeinab Y. Abdallah
201410 citations Open access
Semantic Scholar
Biochemical and mutational analyses of HEXA in a cohort of Egyptian patients with infantile Tay-Sachs disease. Expansion of the mutation spectrum
D. Ibrahim, O. Ali, Hala Nasr, E. Fateen +1 more
2023Orphanet Journal of Rare Diseases9 citations Open access
Semantic Scholar
Profile of plasma free amino acids, carnitine and acylcarnitines, and JAK2v617f mutation as potential metabolic markers in children with type 1 diabetic nephropathy.
Mohammed H. Hassan, Omyma Galal, H. Sakhr, Eman B. Kamaleldeen +3 more
2023Biomedical chromotography8 citations
Semantic Scholar
Identification of Three Novel Homozygous NAGLU Mutations in Egyptian Patients with Sanfilippo Syndrome B
E. A. Mohammed, E. Fateen
2019Meta Gene7 citations
Semantic Scholar
Clinical, Biochemical, and Molecular Characterization of Metachromatic Leukodystrophy Among Egyptian Pediatric Patients: Expansion of the ARSA Mutational Spectrum
K. Amr, E. Fateen, L. Mansour, Angie M. S. Tosson +4 more
2020Journal of Molecular Neuroscience6 citations
Semantic Scholar
A multicenter, open-label, phase III study of Abcertin in Gaucher disease
B. Lee, Ahmed Abdalla, Jin-Ho Choi, A. El-Beshlawy +11 more
2017Medicine6 citations Open access
Semantic Scholar
Novel gene-specific Bayesian Gaussian mixture model to predict the missense variants pathogenicity of Sanfilippo syndrome
Eman E. A. Mohammed, A. Fayez, N. Abdelfattah, E. Fateen
2024Scientific Reports5 citations Open access
Semantic Scholar
Egyptian Gaucher disease type 3 patients: a large cohort study spanning two decades
A. El-Beshlawy, Khaled Abdel-Azim, A. Abdel-Salam, Yasmeen M. M. Selim +4 more
2023Journal of Rare Diseases5 citations Open access
Semantic Scholar
Biochemical diagnosis of Sanfilippo disorder types A and B
Soha S. Nosier, Seham M. S. El Nakeeb, Mona M. Ibrahim, M. El-Gammal +1 more
2023Journal of Genetic Engineering and Biotechnology5 citations Open access
Semantic Scholar
Quaternary diagnostics scheme for mucolipidosis II and detection of novel mutation in GNPTAB gene
M. Essawi, E. Fateen, H. Atia, Noura R. Eissa +4 more
2021Journal of Genetic Engineering and Biotechnology5 citations Open access
Semantic Scholar
Prenatal genetic testing, counseling and follow-up of 33 Egyptian pregnant females with history of mucopolysaccharidoses
K. Gaber, Mona M. Ibrahim, Mona K. Farag, Zeinab Y. Abdallah +2 more
20155 citations Open access
Semantic Scholar
Diagnosis and management of galactosemia: an Egyptian experience.
E. Fateen, S. El-Shafei, H. el-Karaksy, M. Mahmoud +3 more
2004Bratislava Medical Journal5 citations
Semantic Scholar
Molecular study of Pompe disease in Egyptian infants
M. Essawi, N. Elbagoury, E. Ashaat, Wessam E. Sharaf-Eldin +1 more
2021Egyptian Journal of Medical Human Genetics4 citations Open access
Semantic Scholar
Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease
E. Fateen, H. Fathy, A. A. Abd El-Fattah, H. Soliman +2 more
20194 citations
Semantic Scholar
Disorders associated with abnormal acylcarnitine profile among high risk Egyptian children
H. El-Mesellamy, A. Gouda, E. Fateen, S. Zaki
2014Bratislava Medical Journal4 citations Open access
Semantic Scholar
Mutational Analysis of the α-L-Iduronidase Gene in Three Egyptian Families: Identification of Three Novel Mutations and Five Novel Polymorphisms
K. Amr, Ahmed Katoury, M. Abdel-Hamid, R. Bassiouni +2 more
2009Genetic Testing and Molecular Biomarkers4 citations
Semantic Scholar
Diagnosis and management of patients with Gaucher disease: an Egyptian expert opinion
Amal El-Beshlawy, A. Tantawy, R. Shawky, S. Elsayed +15 more
2024Egyptian Journal of Medical Human Genetics3 citations Open access
Semantic Scholar
CLN genes mutational analysis in a sample of Egyptian patients
Miral M. Refeat, S. Zaki, A. Gouda, A. Radwan +1 more
20193 citations
Semantic Scholar
Differential diagnosis of mucopolysaccharidosis and oligosaccharidosis of a sample of Egyptian children
E. Fateen, M. Ismail, N. A. El-Boghdady, M. Aglan +2 more
2018Bulletin of Faculty of Pharmacy, Cairo University3 citations Open access
Semantic Scholar
Four novel mutations in the N-acetylgalactosamine-6-sulfate sulfatase gene among Egyptian patients with Morquio A disease.
E. Fateen, Hanan Abd El Mawgoud, Noura R. Eissa, Mona M. Ibrahim +2 more
2017Gene3 citations
Semantic Scholar
Clinical, biochemical, and molecular characteristics of Sanfilippo a syndrome (MPS IIIA) in a cohort of Egyptian patients
E. Fateen, Soha S. Nosier, Nahla N. Abdel Aziz, A. Radwan +1 more
2025Orphanet Journal of Rare Diseases2 citations Open access
Semantic Scholar
Mass spectrometry for screening of metabolic disorders: 9-year biochemical genetics experience
W. Nazim, E. Fateen, A. Gouda, A. Radwan +2 more
2023Journal of The Arab Society for Medical Research2 citations Open access
Semantic Scholar
Biochemical Diagnosis of Peroxisomal Disorders by GC/MS: Egyptian Patients with X-linked Adrenoleukodystrophy
E. Fateen, A. Gouda, Mona M. Ibrahim
20132 citations Open access
Semantic Scholar
Prenatal diagnosis of perplexing cases of lipidoses.
A. L. Aboul Nasr, E. Fateen
2008Bratislava Medical Journal2 citations
Semantic Scholar
Relative Frequency of Metachromatic Leukodystrophy in Egypt: A Reference Laboratory Report.
E. Fateen, Zeinab Y. Abdallah
2024Frontiers in Bioscience1 citations Open access
Semantic Scholar
N- and O-glycan analysis for the detection of glycosylation disorders
A. Gouda, A. Elbaz, T. Dupré, O. Ali +2 more
2021Egyptian Journal of Medical Human Genetics1 citations Open access
Semantic Scholar
Enzyme based diagnosis of type 1 and 2 neuronal ceroid lipofuscinoses
A. Radwan, E. Fateen, A. Gouda, M. Zaki +1 more
20211 citations Open access
Semantic Scholar
Largest Cohort Study of Gaucher Disease Type 3 from a Single Center in Egypt Spanning Two Decades
A. El-Beshlawy, K. Eid, A. Abdel-Salam, F. Mohamed +4 more
20201 citations
Semantic Scholar
Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder
M. Essawi, Nagham M El-Bagoury, Ola M. Sayed, M. Aglan +3 more
20181 citations
Semantic Scholar
Biochemical study of glycogen storage disease type II (Pompe disease) in Egyptian infants
E. Fateen, H. Hamza, D. Abo-elmatty, A. Gouda +4 more
20171 citations
Semantic Scholar
Mutational analysis of a cohort of Egyptian patients with Gaucher disease
E. Fateen, H. Fathy, Dina M. Aboul Maaty, N. Kamel +1 more
20171 citations
Semantic Scholar
Effect of diode laser on antioxidant enzymes of salivary glands in diabetic rats
Hoda A. El-Sadek, Sahar M.A. El-Hadidi, E. Aboul-Ezz, E. Fateen +3 more
20171 citations
Semantic Scholar
Clinical spectrum associated with some structural cerebellar abnormalities.
G. Abdel-Salam, Marwa I Shahab, A. Galal, A. Abdelkader +1 more
2006Neurosciences1 citations
Semantic Scholar
Management of mucopolysaccharidosis type I using enzyme replacement therapy: Egyptian experience
E. Fateen, S. el-Sahrigy, Mona M. Ibrahim, R. Elhossini +8 more
2025Egyptian Journal of Medical Human Genetics0 citations Open access
Semantic Scholar
Clinical versus Genetic Diagnosis of Cystic Fibrosis in High Risk Egyptian Children
Eman Rateb Abd Al-Monaem, D. Soliman, Waleed E. Abdulghany, H. El-Bassyouni +3 more
2024Benha Journal of Applied Sciences0 citations
Semantic Scholar
Expanding the genetic spectrum of Mucolipidosis in Egyptian patients: Recurrent and novel GNPTAB and GNPTG genes variants
Noura R. Eissa, M. Essawi, G. Abdel-Salam, H. Hassan +2 more
2022Middle East Journal of Medical Genetics0 citations Open access
Semantic Scholar
Biochemical evaluations at two time points in 15 patients with nephropathic cystinosis under cysteamine treatment
Zeinab Y. Abdallah, Soha S. Nosier, Neveen A. Soliman, E. Fateen
20210 citations
Semantic Scholar
Variants in the NPC1 Gene in Egyptian Patients with Niemann-Pick Type C
M. Essawi, Asmaa F. Abdel-aleem, M. Badawy, M. Zaki +3 more
20200 citations Open access
Semantic Scholar
A rare NAGLU mutation in an Egyptian family with Sanfilippo B syndrome
Eman E. A. Mohammed, E. Fateen
20190 citations
Semantic Scholar
Prenatal counseling and diagnosis of Gaucher disease in Egypt: an 18-year experience
A. Aboulnasr, E. Fateen
20190 citations
Semantic Scholar

Frequent co-authors

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Mona M. Ibrahim×12
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Mona M. Ibrahim — researcher profile on SciRah
A. Gouda×10
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A. Gouda — researcher profile on SciRah
A. Radwan×7
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A. Radwan — researcher profile on SciRah
M. Essawi×7
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M. Essawi — researcher profile on SciRah

Zeinab Y. Abdallah

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M. Aglan — researcher profile on SciRah

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M. Zaki — researcher profile on SciRah

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S. Temtamy — researcher profile on SciRah

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O. Ali — researcher profile on SciRah

A. El-Beshlawy×3

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A. El-Beshlawy — researcher profile on SciRah

Eman E. A. Mohammed×3

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Eman E. A. Mohammed — researcher profile on SciRah

Soha S. Nosier×3

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Soha S. Nosier — researcher profile on SciRah