• 159 Citations
  • 7 h-Index
20132019
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Fingerprint Dive into the research topics where Yaser Al-Sarraj is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 8 Similar Profiles
Type 2 Diabetes Mellitus Medicine & Life Sciences
Mutation Medicine & Life Sciences
Selenium Medicine & Life Sciences
Oxidative Stress Medicine & Life Sciences
Parturition Medicine & Life Sciences
Immunological Synapses Medicine & Life Sciences
Platelet-Derived Growth Factor beta Receptor Medicine & Life Sciences
Prediabetic State Medicine & Life Sciences

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Research Output 2013 2019

  • 159 Citations
  • 7 h-Index
  • 12 Article
  • 1 Comment/debate

CD56 expression in breast cancer induces sensitivity to natural killer-mediated cytotoxicity by enhancing the formation of cytotoxic immunological synapse

Taouk, G., Hussein, O., Zekak, M., Abouelghar, A., Al-Sarraj, Y., Mohamed, E. & Doldur, M., 1 Dec 2019, In : Scientific reports. 9, 1, 8756.

Research output: Contribution to journalArticle

Open Access
Immunological Synapses
Breast Neoplasms
Natural Killer Cells
Biomarkers
Cell Line
11 Citations (Scopus)

Multiplex epithelium dysfunction due to CLDN10 mutation: The HELIX syndrome

Hadj-Rabia, S., Brideau, G., Al-Sarraj, Y., Maroun, R. C., Figueres, M. L., Leclerc-Mercier, S., Olinger, E., Baron, S., Chaussain, C., Nochy, D., Taha, R., Knebelmann, B., Joshi, V., Curmi, P. A., Kambouris, M., Vargas-Poussou, R., Bodemer, C., Devuyst, O., Houillier, P. & El-Shanti, H., 1 Feb 2018, In : Genetics in Medicine. 20, 2, p. 190-201 12 p.

Research output: Contribution to journalArticle

Hypohidrosis
Ichthyosis
Xerostomia
Epithelium
Kidney
7 Citations (Scopus)

Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathy

NISC Comparative Sequencing Program, 1 Jan 2017, In : Annals of Clinical and Translational Neurology. 4, 1, p. 26-35 10 p.

Research output: Contribution to journalArticle

Neuromuscular Diseases
Brain Diseases
Autistic Disorder
Voltage-Gated Sodium Channels
Infantile Spasms
4 Citations (Scopus)

Heterozygous PDGFRB mutation in a three-generation family with autosomal dominant infantile myofibromatosis

Lepelletier, C., Al-Sarraj, Y., Bodemer, C., Shaath, H., Fraitag, S., Kambouris, M., Hamel-Teillac, D., El-Shanti, H. & Hadj-Rabia, S., 1 Jan 2017, In : Acta Dermato-Venereologica. 97, 7, p. 858-859 2 p.

Research output: Contribution to journalComment/debate

Platelet-Derived Growth Factor beta Receptor
Mutation
Congenital Generalized Fibromatosis
4 Citations (Scopus)

Type II diabetes mellitus and hyperhomocysteinemia: a complex interaction

Platt, D. E., Hariri, E., Salameh, P., Merhi, M., Sabbah, N., Helou, M., Mouzaya, F., Nemer, R., Al-Sarraj, Y., El-Shanti, H., Abchee, A. B. & Zalloua, P. A., 21 Mar 2017, In : Diabetology and Metabolic Syndrome. 9, 1, p. 1-7 7 p.

Research output: Contribution to journalArticle

Hyperhomocysteinemia
Homocysteine
Type 2 Diabetes Mellitus
Population
Hypertension