A. Al-Kindi

Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits

A. Al-Futaisi, K. Al-Thihli, F. Zadjali, 2018, Clinical genetics.

Valve Replacement for Massive Hemoptysis in Mitral Stenosis: An Uncommon Course in Modern Practice

B. Jayakrishnan, Suresh Chengode, Hatim Al-Lawati, 2021, Cureus.

A novel POC1A variant in an alternatively spliced exon causes classic SOFT syndrome: clinical presentation of seven patients

A. Rolfs, C. Beetz, L. Abbasi-Moheb, 2019, Journal of Human Genetics.

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families

A. Al-Asmi, Z. Bruwer, F. Zadjali, 2022, Scientific Reports.

The phenotypic spectrum of baraitser-winter syndrome: a new case and review of literature.

A. Ganesh, R. Jain, S. Raeburn, 2005, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

A novel mutation in DDR2 causing spondylo-meta-epiphyseal dysplasia with short limbs and abnormal calcifications (SMED-SL) results in defective intra-cellular trafficking

L. Al-Gazali, A. Ganesh, B. Ali, 2014, BMC Medical Genetics.

Pulmonary infarction mimicking a lung mass: a case report

B. Jayakrishnan, Jojy George, Rashid Al-Sukaiti, 2021, The Pan African Medical Journal.

Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly

S. Banka, K. Girisha, A. Shukla, 2023, Human Genetics.

Lung cancer screening in the gulf: Rationale and recommendations

B. Jayakrishnan, S. Bennji, Z. Al-Hashami, 2022, Annals of thoracic medicine.

Cheerios sign: A rare sign on chest computed tomography

B. Jayakrishnan, S. Bennji, A. Al-Kindi, 2022, African journal of thoracic and critical care medicine.

A novel POC1A variant in an alternatively spliced exon causes classic SOFT syndrome: clinical presentation of seven patients

P. Bauer, A. Rolfs, C. Beetz, 2019, Journal of Human Genetics.