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Ola Ali Khalifa
Observed names:
Ola A Khalifa,
Ola A. Khalifa,
Ola Khalifa,
Ola khalifa
Institution:
Ain Shams University
Observed institutions:
Ain Shams University,
Suez Canal University,
Alfaisal University,
Cairo University,
King Faisal Specialist Hospital & Research Centre,
Ain Shams University Hospital
show all 6
OpenAlex ID:
A5113790008
Molecular autopsy in maternal–fetal medicine
2017
·
Hanan E. Shamseldin
, Wesam Kurdi
, et al.
·
Genetics in Medicine
·
131
PDF
Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families
2015
·
Hanan E. Shamseldin
, Maha Tulbah
, et al.
·
Genome biology
·
114
PDF
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue
2016
·
Anas M. Alazami
, Sarah M. Al-Qattan
, et al.
·
Human Genetics
·
112
Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature
2015
·
Ola Khalifa
, Zahra Al-Sahlawi
, et al.
·
European Journal of Medical Genetics
·
53
Genotype–phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants
2017
·
Osama K. Zaki
, George Priya Doss C
, et al.
·
Human Molecular Genetics
·
39
PDF
KDF1, encoding keratinocyte differentiation factor 1, is mutated in a multigenerational family with ectodermal dysplasia
2016
·
Hanan E. Shamseldin
, Ola Khalifa
, et al.
·
Human Genetics
·
34
Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype
2017
·
Ruqaiah Altassan
, Haya Al Saud
, et al.
·
American Journal of Medical Genetics Part A
·
27
Genotype–phenotype correlation of 33 patients with maple syrup urine disease
2020
·
Ola A. Khalifa
, Faiqa Imtiaz
, et al.
·
American Journal of Medical Genetics Part A
·
18
Clinical, biochemical, neuroradiological and molecular characterization of Egyptian patients with glutaric acidemia type 1
2019
·
Hatem Zayed
, Hamed El Khayat
, et al.
·
Metabolic Brain Disease
·
17
PDF
A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene: Figure 1
2012
·
Ola Khalifa
, Faiqa Imtiaz
, et al.
·
Journal of Medical Genetics
·
17
Oral–facial–digital syndrome type 1
2011
·
Ola Khalifa
, Zuhair Rahbeeni
, et al.
·
Clinical Dysmorphology
·
16
The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patients
2018
·
Zuhair N. Al-Hassnan
, Ola A. Khalifa
, et al.
·
Molecular Genetics and Metabolism Reports
·
14
PDF
Novel mutations in TGM 1 and ABCA 12 cause autosomal recessive congenital ichthyosis in five Saudi families
2016
·
Salma M. Wakil
, Yousef Binamer
, et al.
·
International Journal of Dermatology
·
10
Dyggve–Melchior–Clausen syndrome: novel splice mutation with atlanto-axial subluxation
2010
·
Ola Khalifa
, Faiqa Imtiaz
, et al.
·
European Journal of Pediatrics
·
9
Terminal 4q deletion and 8q duplication in a patient with CHARGE-like features
2010
·
Ola A. Khalifa
, Claudia U. Walter
, et al.
·
European Journal of Medical Genetics
·
8
Optic neuropathy in classical methylmalonic acidemia
2019
·
Mohammed AlOwain
, Ola Ali Khalifa
, et al.
·
Ophthalmic Genetics
·
7
A case of de Barsy syndrome with a severe eye phenotype
2012
·
Mohammed Al‐Owain
, Shamsa Alanazi
, et al.
·
American Journal of Medical Genetics Part A
·
7
The effects of a self-learning package on mothers' knowledge and practices towards caring for their children with phenylketonuria
2023
·
Amira Khalil
, Eman Amin
, et al.
·
Journal of Medicine and Life
·
3
PDF
Alterations in the metabolic signature of full-term infants of diabetic mothers
2024
·
Hesham A. Awad
, Ghada I. Gad
, et al.
·
Egyptian Journal of Medical Human Genetics
·
2
PDF
Efficacy of peritoneal dialysis on encephalopathic patient with Citrullinemia type I
2021
·
Radwa Gamal
, Ola A Khalifa
·
QJM
·
1
A New Patient of Chanarin Dorfman Syndrome in Egypt
2019
·
Zeinab el kabbany
, Ola khalifa
, et al.
·
Archives of Clinical and Medical Case Reports
·
1
Evaluation of a Mental imagery Therapy for Autism application for language improvement in children with autism spectrum disorder
2026
·
Mohamed Abd El-Adl El-Sawy
, Ola Ali Khalifa
, et al.
·
International Journal of Developmental Disabilities
Inherited metabolic diseases mimicking hereditary spastic paraplegia: a cohort of ten Egyptian patients
2026
·
Ola A. Khalifa
, Tarek M. Youssef
, et al.
·
Frontiers in Genetics
PDF
ICAM-1, BDNF, and Neurobehavioral Profiles in Maple Syrup Urine Disease: Exploring Potential Biomarker Links
2026
·
Solaf M. Elsayed
, Heba Hassan Elsedfy
, et al.
·
Research Square
PDF
Profile of children with Faltering Growth in a tertiary hospital
2026
·
Ola Ali Khalifa
, Saif Ibrahim AlSalali
, et al.
·
QJM
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Works count:
34
Citation count:
640
H-index:
12
I10-index:
13
Year
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