Mohamed S Abdel-Hamid (Mohamed Abdel-Hamid)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 24

Top Topics

Ejection Fraction

Congenital Heart Disease

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

Clinical genetics

Molecular genetics and genomics : MGG

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA

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

Publications

Nour Elkhateeb, Mahmoud Y Issa, Hasnaa M Elbendary, Walaa Elnaggar, Areef Ramadan, Karima Rafat, Mona Kamel, Sherif F Abdel-Ghafar, Fawzia Amer, Hebatallah M Hassaan, Roberta Trunzo, Catarina Pereira, Mohamed S Abdel-Hamid, Felice D'Arco, Peter Bauer, Aida Maria Bertoli-Avella, Marian Girgis, Joseph G Gleeson, Maha Saad Zaki, Laila Selim
The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children. Clinical genetics 105 (5) (2024)
Nour Elkhateeb, Mahmoud Y Issa, Hasnaa M Elbendary, Walaa Elnaggar, Areef Ramadan, Karima Rafat, Mona Kamel, Sherif F Abdel-Ghafar, Fawzia Amer, Hebatallah M Hassaan, Roberta Trunzo, Catarina Pereira, Mohamed S Abdel-Hamid, Felice D'Arco, Peter Bauer, Aida Maria Bertoli-Avella, Marian Girgis, Joseph G Gleeson, Maha Saad Zaki, Laila Selim
The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children. Clinical genetics (2024)
Nour Elkhateeb, Mahmoud Y Issa, Hasnaa M Elbendary, Walaa Elnaggar, Areef Ramadan, Karima Rafat, Mona Kamel, Sherif F Abdel-Ghafar, Fawzia Amer, Hebatallah M Hassaan, Roberta Trunzo, Catarina Pereira, Mohamed S Abdel-Hamid, Felice D'Arco, Peter Bauer, Aida Maria Bertoli-Avella, Marian Girgis, Joseph G Gleeson, Maha Saad Zaki, Laila Selim
The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children. Clinical genetics 105 (5) (2024)
Nour Elkhateeb, Mahmoud Y Issa, Hasnaa M Elbendary, Walaa Elnaggar, Areef Ramadan, Karima Rafat, Mona Kamel, Sherif F Abdel-Ghafar, Fawzia Amer, Hebatallah M Hassaan, Roberta Trunzo, Catarina Pereira, Mohamed S Abdel-Hamid, Felice D'Arco, Peter Bauer, Aida Maria Bertoli-Avella, Marian Girgis, Joseph G Gleeson, Maha Saad Zaki, Laila Selim
The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children. Clinical genetics 105 (5) (2024)
Mahmoud Y Issa, Mona A Hafez, Samir M Mounir, Sherif F Abdel Ghafar, Maha Saad Zaki, Mohamed S Abdel-Hamid
Refining the phenotypic spectrum of CCDC88A-related PEHO-like syndrome. American journal of medical genetics. Part A (2023)
Inas H Mazen, Mona A El-Gammal, Aya A Elaidy, Ghada M Anwar, Engy A Ashaat, Sherif F Abdel-Ghafar, Mohamed S Abdel-Hamid
Congenital leptin and leptin receptor deficiencies in nine new families: identification of six novel variants and review of literature. Molecular genetics and genomics : MGG (2023)
Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam, Sherif F Abdel-Ghafar, Maha Saad Zaki
Delineating the phenotype of PNPLA8-related mitochondriopathies. Clinical genetics (2023)
Rasha Moheb Elhossini, Inas S M Sayed, Usama Saad Hellal, Sarah A M Mahmoud, Mona S Aglan, Nehal F Hassib, Mohamed S Abdel-Hamid
A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management. American journal of medical genetics. Part A (2023)
Ghada M H Abdel-Salam, Mohamed S Abdel-Hamid
A founder PPIL1 variant underlies a recognizable form of microlissencephaly with pontocerebellar hypoplasia. Clinical genetics (2023)
Ghada A Otaify, Rasha Moheb Elhossini, Sherif F Abdel-Ghafar, Inas S M Sayed, Ghada M H Abdel-Salam, Mona S Aglan, Mohamed S Abdel-Hamid
CHST3-related skeletal dysplasia in 14 patients: Identification of 8 novel variants and further expansion of the phenotypic spectrum. American journal of medical genetics. Part A (2023)
Maha Saad Zaki, Wessam E Sharaf-Eldin, Karima Rafat, Hasnaa M Elbendary, Mona Kamel, Nour Elkhateeb, Mahmoud M Noureldeen, Mohamed A Abdeltawab, Abdelrahim A Sadek, Mona L Essawi, Tracy Lau, David Murphy, Mohamed S Abdel-Hamid, Henry Holuden, Mahmoud Y Issa, Joseph G Gleeson
Clinical and molecular spectrum of a large Egyptian cohort with ALS2-related disorders of infantile-onset of clinical continuum IAHSP/JPLS. Clinical genetics (2023)
Ghada A Otaify, Mohamed S Abdel-Hamid, Nehal F Hassib, Rasha Moheb Elhossini, Sherif F Abdel-Ghafar, Mona S Aglan
Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum. American journal of medical genetics. Part A 188 (6) (2022)
Mohamed S Abdel-Hamid, Rasha M Elhossini, Ghada A Otaify, Sherif F Abdel-Ghafar, Mona S Aglan
Osteoporosis-pseudoglioma syndrome in four new patients: identification of two novel LRP5 variants and insights on patients' management using bisphosphonates therapy. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 33 (7) (2022)
Manal M Thomas, Heba Mostafa Ahmed, Sara H El-Dessouky, Abeer Ramadan, Osama Ezzat Botrous, Mohamed S Abdel-Hamid
Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect. Molecular genetics and genomics : MGG 297 (3) (2022)
Mohamed S Abdel-Hamid, Sherif F Abdel-Ghafar, Suzan R Ismail, Lubna M Desouky, Mahmoud Y Issa, Laila K Effat, Maha Saad Zaki
Micro and Martsolf syndromes in 34 new patients: Refining the phenotypic spectrum and further molecular insights. Clinical genetics 98 (5) (2021)
Ghada M H Abdel-Salam, Ruizhi Duan, Mohamed S Abdel-Hamid, Inas S M Sayed, Shalini N Jhangiani, Ziad Khan, Haowei Du, Richard A Gibbs, Jennifer E Posey, Dana Marafi, James R. Lupski
Expanding the phenotypic and allelic spectrum of SMG8: Clinical observations reveal overlap with SMG9-associated disease trait. American journal of medical genetics. Part A (2021)
Inas Mazen, Mona Mekkawy, Alaa Kamel, Mona Essawi, Heba Amin Hassan, Mohamed S Abdel-Hamid, Khalda Sayed Amr, Hala Soliman, Mona El-Ruby, Ahmed Torky, Mona El Gammal, Aya Elaidy, Anu Bashamboo, Kenneth McElreavey
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development. American journal of medical genetics. Part A 185 (6) (2021)
Ghada M H Abdel-Salam, Inas S M Sayed, Hanan H Afifi, Sherif F Abdel-Ghafar, Maha R Abouzaid, Samira I Ismail, Mona S Aglan, Mahmoud Y Issa, Hala T El-Bassyouni, Ghada El-Kamah, Laila K Effat, Maha Eid, Maha S Zaki, Samia A Temtamy, Mohamed S Abdel-Hamid
Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation. American journal of medical genetics. Part A 182 (6) (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)
Inas S M Sayed, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam
KBG syndrome in two patients from Egypt. American journal of medical genetics. Part A 182 (6) (2020)
Iman G Mahmoud, Mohamed A Elmonem, Maha Saad Zaki, Areef Ramadan, Nihal M Al-Menabawy, Aya El-Gamal, Lobna Mansour, Mahmoud Y Issa, Mohamed S Abdel-Hamid, Sawsan Abdel-Hady, Iman Khalifa, Ahmed Ibrahim, Alexander Solyom, Arndt Rolfs, Laila Selim
ASAH1-related disorders: Description of 15 novel pediatric patients and expansion of the clinical phenotype. Clinical genetics 98 (6) (2020)
Mohamed S Abdel-Hamid, Sara H El-Dessouky, Mohamed I Ateya, Hassan M Gaafar, Ghada M H Abdel-Salam
Phenotypic spectrum of NDE1-related disorders: from microlissencephaly to microhydranencephaly. American journal of medical genetics. Part A 179 (3) (2019)
Hanan H Afifi, Mohamed S Abdel-Hamid, Mennat I Mehrez, Ghada El-Kamah, Ghada M H Abdel-Salam
Lenz-Majewski syndrome in a patient from Egypt. American journal of medical genetics. Part A 179 (10) (2019)
Mohamed S Abdel-Hamid, Samira Ismail, Maha S Zaki, Ghada M H Abdel-Salam, Ghada A Otaify, Mahmoud Y Issa, Mohamed Abdel-Kader, Marian Girgis, Eman Aboul-Ezz, Inas Mazen, Mona S Aglan, Samia A Temtamy
GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion. American journal of medical genetics. Part A 179 (2) (2018)