Engy A Ashaat

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Venues

Molecular neurobiology

American journal of medical genetics. Part A

Molecular genetics & genomic medicine

BMC genomics

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

Publications

Engy A Ashaat, Nora N Esmaiel, Sonia A El-Saiedi, Neveen A Ashaat, Dalia Farouk Hussen, Abeer Ramadan, Mohamed Ahmed Al Kersh, Nirvana S AbdelHakim, Ibrahim Said, Ammal M Metwally, Alaaeldin Fayez
Biallelic TYR and TKFC variants in Egyptian patients with OCA1 and new expanded TKFC features. BMC genomics 25 (1) (2024)
Engy A Ashaat, Hoda A Ahmed, Nesma M Elaraby, Alaaeldin Fayez, Ammal M Metwally, Mona K Mekkawy, Dalia Farouk Hussen, Neveen A Ashaat, Rasha M Elhossini, Heba Ahmed ElAwady, Randa H A Abdelgawad, Mona El Gammal, Mohamed Ahmed Al Kersh, Dina Amin Saleh
The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy. Molecular neurobiology 61 (8) (2023)
Engy A Ashaat, Hoda A Ahmed, Nesma M Elaraby, Alaaeldin Fayez, Ammal M Metwally, Mona K Mekkawy, Dalia Farouk Hussen, Neveen A Ashaat, Rasha M Elhossini, Heba Ahmed ElAwady, Randa H A Abdelgawad, Mona El Gammal, Mohamed Ahmed Al Kersh, Dina Amin Saleh
The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy. Molecular neurobiology (2023)
Engy A Ashaat, Hoda A Ahmed, Nesma M Elaraby, Alaaeldin Fayez, Ammal M Metwally, Mona K Mekkawy, Dalia Farouk Hussen, Neveen A Ashaat, Rasha M Elhossini, Heba Ahmed ElAwady, Randa H A Abdelgawad, Mona El Gammal, Mohamed Ahmed Al Kersh, Dina Amin Saleh
The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy. Molecular neurobiology 61 (8) (2023)
Engy A Ashaat, Hoda A Ahmed, Nesma M Elaraby, Alaaeldin Fayez, Ammal M Metwally, Mona K Mekkawy, Dalia Farouk Hussen, Neveen A Ashaat, Rasha M Elhossini, Heba Ahmed ElAwady, Randa H A Abdelgawad, Mona El Gammal, Mohamed Ahmed Al Kersh, Dina Amin Saleh
The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy. Molecular neurobiology 61 (8) (2023)
Mona K Mekkawy, Alaa K Kamel, Manal M Thomas, Engy A Ashaat, Maha S Zaki, Ola M Eid, Samira Ismail, Saida A Hammad, Hisham Megahed, Heba Ahmed El-Awady, Khaled M Refaat, Shymaa Hussien, Nivine Helmy, Sally G Abd Allah, Amal M Mohamed, Mona O El Ruby
Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature. Molecular genetics & genomic medicine 9 (2) (2020)
Maha Saad Zaki, Ghada A Otaify, Samira Ismail, Mahmoud Y Issa, Mona O El-Ruby, Abdelrahim A Sadek, Engy A Ashaat, Sonia A El Saeidi, Mona S Aglan, Samia Temtamy, Mohamed S Abdel-Hamid
Blepharophimosis-ptosis-intellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum. American journal of medical genetics. Part A 182 (12) (2020)
Paul S Kruszka, Yonit A Addissie, Cedrik Tekendo-Ngongang, Kelly L Jones, Sarah K Savage, Neerja Gupta, Nirmala D Sirisena, Vajira H W Dissanayake, C Sampath Paththinige, Teresa Aravena, Sheela Nampoothiri, Dhanya Yesodharan, Katta Mohan Girisha, Siddaramappa Jagdish Patil, Saumya Shekhar Jamuar, Jasmine Chew-Yin Goh, Agustini Utari, Nydia Sihombing, Rupesh Mishra, Neer Shoba Chitrakar, Brenda C Iriele, Ezana Lulseged, Andre Megarbane, Annette Uwineza, Elizabeth Eberechi Oyenusi, Oluwarotimi Bolaji Olopade, Olufemi Adetola Fasanmade, Milagros M Duenas-Roque, Meow-Keong Thong, Joanna Y L Tung, Gary T K Mok, Nicole Fleischer, Godfrey M Rwegerera, María Beatriz de Herreros, Johnathan Watts, Karen Fieggen, Victoria Huckstadt, Angélica Moresco, María Gabriela Obregon, Dalia Farouk Hussen, Neveen A Ashaat, Engy A Ashaat, Brian H Y Chung, Eben Badoe, Sultana M H Faradz, Mona O El Ruby, Vorasuk Shotelersuk, Ambroise Wonkam, Ekanem Nsikak Ekure, Shubha Rao Phadke, Antonio Richieri-Costa, Maximilian Muenke
Turner syndrome in diverse populations. American journal of medical genetics. Part A 182 (2) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Engy A Ashaat