Author

Ibrahim Al Abdulkareem

Observed names: I Al Abdulkareem, I. Al Abdulkareem, Ibrahim Abdulkareem, Ibrahim Al AbdulKareem, Ibrahim Al Abdulkareem, Ibrahim B. Al Abdulkareem

Observed institutions: Princess Nourah bint Abdulrahman University, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, King Abdullah International Medical Research Center, National Guard Health Affairs

OpenAlex ID: A5111928043

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

2012 · Christelle Tesson, Magdalena Nawara, et al. · The American Journal of Human Genetics · 210

Monomeric C-reactive protein and Notch-3 co-operatively increase angiogenesis through PI3K signalling pathway

2014 · Emhamed Boras, Mark Slevin, et al. · Cytokine · 106

HLA ‐A, ‐B, ‐C, ‐ DRB1 and ‐ DQB1 allele and haplotype frequencies in Saudis using next generation sequencing technique

2013 · A. H. Hajeer, M. A. Al Balwi, et al. · Tissue Antigens · 43

A novel mutation in the SHH long‐range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency

2012 · Mohammad M. Al‐Qattan, Ibrahim Al Abdulkareem, et al. · American Journal of Medical Genetics Part A · 40

A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra‐amelia in two Saudi families

2011 · Wafaa Eyaid, Mohammad M. Al‐Qattan, et al. · American Journal of Medical Genetics Part A · 35

Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3

2013 · Ahmed Al-Qahtani, Hanif G Khalak, et al. · Journal of Medical Genetics · 27

Spinal muscular atrophy carrier frequency in Saudi Arabia

2022 · Mohammed Al Jumah, Saad Al Rajeh, et al. · Molecular Genetics & Genomic Medicine · 19

Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease

2012 · M Al Jumah, M Al Balwi, et al. · Multiple Sclerosis Journal · 10

Differential Gene Expression in Peripheral White Blood Cells with Permissive Underfeeding and Standard Feeding in Critically Ill Patients: A Descriptive Sub-study of the PermiT Randomized Controlled Trial

2018 · Yaseen M. Arabi, Mohammed Al-Balwi, et al. · Scientific Reports · 5

Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report

2009 · Mohammed Al Balwi, Sulaiman Al Ajaji, et al. · Cases Journal · 3

How does Arab genome different from other genomes?

2014 · Ibrahim Abdulkareem · BMC Genomics

PRF1 gene mutation in a Saudi patient with haemophagocytic lymphohistiocytosis

2010 · M. A. Al Balwi, T. Al Harbi, et al. · British Journal of Biomedical Science

Works count: 12

Citation count: 498

H-index: 8

I10-index: 8