Al-Sarraj Y - Search Results

1

Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.

Al-Sarraj Y, Al-Dous E, Taha RZ, Ahram D, Alshaban F, Tolfat M, El-Shanti H, Albagha OME. Al-Sarraj Y, et al. Genes (Basel). 2021 May 18;12(5):761. doi: 10.3390/genes12050761. Genes (Basel). 2021. PMID: 34069769 Free PMC article.

2

Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndrome.

Kambouris M, Maroun RC, Ben-Omran T, Al-Sarraj Y, Errafii K, Ali R, Boulos H, Curmi PA, El-Shanti H. Kambouris M, et al. Orphanet J Rare Dis. 2014 Jun 7;9:80. doi: 10.1186/1750-1172-9-80. Orphanet J Rare Dis. 2014. PMID: 24907849 Free PMC article.

3

T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility.

Ghassibe-Sabbagh M, Haber M, Salloum AK, Al-Sarraj Y, Akle Y, Hirbli K, Romanos J, Mouzaya F, Gauguier D, Platt DE, El-Shanti H, Zalloua PA. Ghassibe-Sabbagh M, et al. Sci Rep. 2014 Dec 8;4:7351. doi: 10.1038/srep07351. Sci Rep. 2014. PMID: 25483131 Free PMC article.

4

Distal trisomy 10q syndrome, report of a patient with duplicated q24.31 - qter, autism spectrum disorder and unusual features.

Al-Sarraj Y, Al-Khair HA, Taha RZ, Khattab N, El Sayed ZH, Elhusein B, El-Shanti H. Al-Sarraj Y, et al. Clin Case Rep. 2014 Oct;2(5):201-5. doi: 10.1002/ccr3.94. Epub 2014 Jul 25. Clin Case Rep. 2014. PMID: 25614812 Free PMC article.

5

Caffeine Impact on Metabolic Syndrome Components Is Modulated by a CYP1A2 Variant.

Platt DE, Ghassibe-Sabbagh M, Salameh P, Salloum AK, Haber M, Mouzaya F, Gauguier D, Al-Sarraj Y, El-Shanti H, Zalloua PA, Abchee AB. Platt DE, et al. Ann Nutr Metab. 2016;68(1):1-11. doi: 10.1159/000441481. Epub 2015 Nov 21. Ann Nutr Metab. 2016. PMID: 26588584

6

Mosaic partial pericentromeric trisomy 8 and maternal uniparental disomy in a male patient with autism spectrum disorder.

Ahram DF, Stambouli D, Syrogianni A, Al-Sarraj Y, Gerou S, El-Shanti H, Kambouris M. Ahram DF, et al. Clin Case Rep. 2016 Oct 21;4(12):1125-1131. doi: 10.1002/ccr3.705. eCollection 2016 Dec. Clin Case Rep. 2016. PMID: 27980747 Free PMC article.

7

Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathy.

Kambouris M, Thevenon J, Soldatos A, Cox A, Stephen J, Ben-Omran T, Al-Sarraj Y, Boulos H, Bone W, Mullikin JC; NISC Comparative Sequencing Program; Masurel-Paulet A, St-Onge J, Dufford Y, Chantegret C, Thauvin-Robinet C, Al-Alami J, Faivre L, Riviere JB, Gahl WA, Bassuk AG, Malicdan MC, El-Shanti H. Kambouris M, et al. Ann Clin Transl Neurol. 2016 Dec 20;4(1):26-35. doi: 10.1002/acn3.372. eCollection 2017 Jan. Ann Clin Transl Neurol. 2016. PMID: 28078312 Free PMC article.

8

Type II diabetes mellitus and hyperhomocysteinemia: a complex interaction.

Platt DE, Hariri E, Salameh P, Merhi M, Sabbah N, Helou M, Mouzaya F, Nemer R, Al-Sarraj Y, El-Shanti H, Abchee AB, Zalloua PA. Platt DE, et al. Diabetol Metab Syndr. 2017 Mar 21;9:19. doi: 10.1186/s13098-017-0218-0. eCollection 2017. Diabetol Metab Syndr. 2017. PMID: 28331553 Free PMC article.

9

A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report.

Ahram DF, Al-Sarraj Y, Taha RZ, Elhag SF, Al-Shaban FA, El-Shanti H, Kambouris M. Ahram DF, et al. Clin Case Rep. 2017 May 12;5(6):1013-1017. doi: 10.1002/ccr3.945. eCollection 2017 Jun. Clin Case Rep. 2017. PMID: 28588858 Free PMC article.

10

Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome.

Hadj-Rabia S, Brideau G, Al-Sarraj Y, Maroun RC, Figueres ML, Leclerc-Mercier S, Olinger E, Baron S, Chaussain C, Nochy D, Taha RZ, Knebelmann B, Joshi V, Curmi PA, Kambouris M, Vargas-Poussou R, Bodemer C, Devuyst O, Houillier P, El-Shanti H. Hadj-Rabia S, et al. Genet Med. 2018 Feb;20(2):190-201. doi: 10.1038/gim.2017.71. Epub 2017 Aug 3. Genet Med. 2018. PMID: 28771254 Free article.

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