Ghada M H Abdel-Salam

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 17

Top Venues

American journal of medical genetics. Part A

Ophthalmic genetics

Clinical genetics

Neurogenetics

National Research Centre

National Research Centre (PHD)

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

Affiliation History

National Research Centre

Egypt

Professor :: Clinical Genetics Department

Education History

National Research Centre

Egypt

PHD :: Clinical Genetics Department

Publications

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)
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)
Mohamed S Abdel-Hamid, Sahar Sabry, Sherif F Abdel-Ghafar, Sara H El-Dessouky, Ghada M H Abdel-Salam
Fetal brain arrest broadens the spectrum of WDR81-related developmental brain malformations. Neurogenetics 22 (4) (2021)
Silvia Kalantari, Colleen M Carlston, Norah S Alsaleh, Ghada M H Abdel-Salam, Fowzan Sami Alkuraya, Mitsuhiro Kato, Naomichi Matsumoto, Satoko Miyatake, Tatsuya Yamamoto, Lucas Fares-Taie, Jean-Michel Rozet, Nicolas Chassaing, Catherine Vincent-Delorme, Anjeung Kang-Bellin, Kirsty McWalter, Caleb P Bupp, Emily Palen, Monisa D Wagner, Marcello Niceta, Claudia Cesario, Roberta Milone, Julie Kaplan, Erin Wadman, William B Dobyns, Isabel Filges
Expanding the KIF4A-associated phenotype. American journal of medical genetics. Part A 185 (12) (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)
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)
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)
Maha Eid, Ola Eid, Ibrahim Hegazy, Marian Girgis, Amal Mohamed, Ghada M H Abdel-Salam
Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion. Neuropediatrics 51 (1) (2019)
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)
Ghada M H Abdel-Salam, Inas Mazen, Maha Eid, Nour Ewida, Ranad Shaheen, Fowzan Sami Alkuraya
Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar-vermis hypoplasia. American journal of medical genetics. Part A 179 (6) (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)
Mona El-Ruby, Alaa El-Din Fayez, Sara H El-Dessouky, Mona S Aglan, Inas Mazen, Nora Ismail, Hanan H Afifi, Maha M Eid, Mostafa I Mostafa, Mennat I Mehrez, Yasmin Khalil, Maha S Zaki, Khaled R Gaber, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam
Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2. American journal of medical genetics. Part A 176 (5) (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)
Ghada M H Abdel-Salam, Noriko Miyake, Mohamed S Abdel-Hamid, Inas S M Sayed, Mohamed I Gadelhak, Samira I Ismail, Mona S Aglan, Hanan H Afifi, Samia A Temtamy, Naomichi Matsumoto
Phenotypic and molecular insights into PQBP1-related intellectual disability. American journal of medical genetics. Part A 176 (11) (2018)
Ebba Alkhunaizi, Ranad Shaheen, Sanjay Kumar Bharti, Ann M Joseph-George, Karen Chong, Ghada M H Abdel-Salam, Mohammed Alowain, Susan I Blaser, Blake C Papsin, Mohammed Butt, Mais Hashem, Nicole Martin, Ruth Godoy, Robert M Brosh, Fowzan Sami Alkuraya, David Chitayat
Warsaw breakage syndrome: Further clinical and genetic delineation. American journal of medical genetics. Part A 176 (11) (2018)
Ghada M H Abdel-Salam, Mohamed S Abdel-Hamid, Mennat I Mehrez, Ahmad M Kamal, Mohamed B Taher, Hanan H Afifi
Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation. Ophthalmic genetics 39 (2) (2017)
Tamer H A Ammar, Somaia Ismail, Ossama Abd Al-Motaal Mansour, Mostafa M El-Shafey, Ahmed S Doghish, Ahmad M Kamal, Ghada M H Abdel-Salam
Genetic analysis of SOX2 and VSX2 genes in 27 Egyptian families with anophthalmia and microphthalmia. Ophthalmic genetics 38 (5) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ghada M H Abdel-Salam