Hala T El-Bassyouni

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 22

Top Venues

Genes

Current issues in molecular biology

Journal of pediatric endocrinology & metabolism : JPEM

Ophthalmic genetics

National Research Centre

Ain Shams University Faculty of Medicine (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Research Centre

Egypt

Prof. of Clinical Genetics :: Clinical Genetics Department

Education History

Ain Shams University Faculty of Medicine

Egypt

PHD :: Pediatrics Department

Cairo University Kasr Alainy Faculty of Medicine

Egypt

MSC :: Paediatrics

Cairo University Kasr Alainy Faculty of Medicine

Egypt

BSC

Publications

Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
May E Zekry, Al-Aliaa M Sallam, Sherihan G Abdel-Hamid, Waheba A Zarouk, Hala T El-Bassyouni, Hala O El-Mesallamy
Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients. Current issues in molecular biology 45 (1) (2023)
May E Zekry, Al-Aliaa M Sallam, Sherihan G Abdel-Hamid, Waheba A Zarouk, Hala T El-Bassyouni, Hala O El-Mesallamy
Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients. Current issues in molecular biology 45 (1) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
May E Zekry, Al-Aliaa M Sallam, Sherihan G Abdel-Hamid, Waheba A Zarouk, Hala T El-Bassyouni, Hala O El-Mesallamy
Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients. Current issues in molecular biology 45 (1) (2023)
May E Zekry, Al-Aliaa M Sallam, Sherihan G Abdel-Hamid, Waheba A Zarouk, Hala T El-Bassyouni, Hala O El-Mesallamy
Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients. Current issues in molecular biology 45 (1) (2023)
May E Zekry, Al-Aliaa M Sallam, Sherihan G Abdel-Hamid, Waheba A Zarouk, Hala T El-Bassyouni, Hala O El-Mesallamy
Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients. Current issues in molecular biology 45 (1) (2023)
May E Zekry, Al-Aliaa M Sallam, Sherihan G Abdel-Hamid, Waheba A Zarouk, Hala T El-Bassyouni, Hala O El-Mesallamy
Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients. Current issues in molecular biology 45 (1) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ola M Eid, Hosam El Zomor, Amal M Mohamed, Hala T El-Bassyouni, Hanan H Afifi, Moatasem El-Ayadi, Sherin H Sadek, Saida A Hammad, Sherine I Salem, Rana Mahrous, Islam M Fadel, Khaled Refaat, Mahmoud A Afifi, Abdallah E Shelil, Othman A O Ziko, Amira A Abdel Azeem, Alaa El-Haddad
Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening RB1 copy number variations in Egyptian patients with retinoblastoma. Ophthalmic genetics (2022)
Eman R Youness, Shaimaa A Hashem, Khaled Hamed, Azzah A Khedr, Eatemad Nabil Abdulhalim, Shimaa Mostafa Kamel, Hala T El-Bassyouni
The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome. Journal of pediatric endocrinology & metabolism : JPEM 36 (2) (2022)
Eman R Youness, Shaimaa A Hashem, Khaled Hamed, Azzah A Khedr, Eatemad Nabil Abdulhalim, Shimaa Mostafa Kamel, Hala T El-Bassyouni
The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome. Journal of pediatric endocrinology & metabolism : JPEM (2022)
Eman R Youness, Shaimaa A Hashem, Khaled Hamed, Azzah A Khedr, Eatemad Nabil Abdulhalim, Shimaa Mostafa Kamel, Hala T El-Bassyouni
The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome. Journal of pediatric endocrinology & metabolism : JPEM 36 (2) (2022)
Eman R Youness, Sherien M El-Daly, Hanaa Reyad Abdallah, Hala T El-Bassyouni, Hisham Megahed, Azzah A Khedr, Marwa Elhady, Walaa Alsharany Abuelhamd
Serum homocysteine, lipid profile and BMI as atherosclerotic risk factors in children with numerical chromosomal aberrations. World journal of pediatrics : WJP 18 (6) (2022)
Khalda Sayed Amr, Hala T El-Bassyouni, Sawsan Abdel Hady, Mostafa I Mostafa, Mennat I Mehrez, Domenico A Coviello, Ghada Y El-Kamah
Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease. Genes 12 (10) (2021)
Miral M Refeat, Taghreed Shalabi, Hala T El-Bassyouni, Mai M Shaker
The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women. Molecular biology reports 48 (5) (2021)
Khalda Amr, Ekram Fateen, Lobna Mansour, Angie Ms Tosson, Maha S Zaki, Ghada Mh Abdel Salam, Ahmed Nabil Mohamed, Hala T El-Bassyouni
Clinical, Biochemical, and Molecular Characterization of Metachromatic Leukodystrophy Among Egyptian Pediatric Patients: Expansion of the ARSA Mutational Spectrum. Journal of molecular neuroscience : MN 71 (5) (2020)
Hala T El-Bassyouni, Nagwa Hassan, Inas Mahfouz, Azza E Abd-Elnaby, Mostafa I Mostafa, Angie M S Tosson
Early Detection and Management of Prader-Willi Syndrome in Egyptian Patients. Journal of pediatric genetics 8 (4) (2019)
Hala T El-Bassyouni, Manal M Thomas, Angie M S Tosson
Mutation in the SLC29A3 Gene in an Egyptian Patient with H Syndrome: A Case Report and Review of Literature. Journal of pediatric genetics 9 (2) (2019)
Ola M Eid, Sawsan Abdel Hady, Ahmed El-Kotoury, Khalda A Said, Karima Rafat, Hala T El-Bassyouni
Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt. Ophthalmic genetics 38 (5) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Hala T El-Bassyouni