El Hajj Chehadeh S - Search Results

1

Whole-Exome Sequencing in Family Trios Reveals De Novo Mutations Associated with Type 1 Diabetes Mellitus.

Mousa M, Albarguthi S, Albreiki M, Farooq Z, Sajid S, El Hajj Chehadeh S, ElBait GD, Tay G, Deeb AA, Alsafar H. Mousa M, et al. Among authors: el hajj chehadeh s. Biology (Basel). 2023 Mar 7;12(3):413. doi: 10.3390/biology12030413. Biology (Basel). 2023. PMID: 36979105 Free PMC article.

2

Genetic Variants and Their Associations to Type 2 Diabetes Mellitus Complications in the United Arab Emirates.

ElHajj Chehadeh S, Sayed NS, Abdelsamad HS, Almahmeed W, Khandoker AH, Jelinek HF, Alsafar HS. ElHajj Chehadeh S, et al. Front Endocrinol (Lausanne). 2022 Jan 6;12:751885. doi: 10.3389/fendo.2021.751885. eCollection 2021. Front Endocrinol (Lausanne). 2022. PMID: 35069435 Free PMC article.

3

Association between type 2 diabetes mellitus & TCF7L2 gene variants in the Emirati population: Genetics of diabetes in the United Arab Emirates.

Khan SM, El Karte N, El Hajj Chehadeh S, Hassoun A, Afandi B, Tay GK, Alsafar H. Khan SM, et al. Among authors: el hajj chehadeh s. Am J Hum Biol. 2021 Jan;33(1):e23434. doi: 10.1002/ajhb.23434. Epub 2020 May 23. Am J Hum Biol. 2021. PMID: 32445548

4

Implication of genetic variants in overweight and obesity susceptibility among the young Arab population of the United Arab Emirates.

El Hajj Chehadeh S, Osman W, Nazar S, Jerman L, Alghafri A, Sajwani A, Alawlaqi M, AlObeidli M, Jelinek HF, AlAnouti F, Khalaf K, Alsafar H. El Hajj Chehadeh S, et al. Gene. 2020 May 20;739:144509. doi: 10.1016/j.gene.2020.144509. Epub 2020 Feb 25. Gene. 2020. PMID: 32109558

5

Establishing a genetic link between FTO and VDR gene polymorphisms and obesity in the Emirati population.

Khan SM, El Hajj Chehadeh S, Abdulrahman M, Osman W, Al Safar H. Khan SM, et al. Among authors: el hajj chehadeh s. BMC Med Genet. 2018 Jan 17;19(1):11. doi: 10.1186/s12881-018-0522-z. BMC Med Genet. 2018. PMID: 29343214 Free PMC article.

6

Relationship between MTHFR C677T and A1298C gene polymorphisms and complications of type 2 diabetes mellitus in an Emirati population.

El Hajj Chehadeh SW, Jelinek HF, Al Mahmeed WA, Tay GK, Odama UO, Elghazali GE, Al Safar HS. El Hajj Chehadeh SW, et al. Meta Gene. 2016 Apr 17;9:70-5. doi: 10.1016/j.mgene.2016.04.002. eCollection 2016 Sep. Meta Gene. 2016. PMID: 27222819 Free PMC article.

7

Folate- and vitamin B12-deficient diet during gestation and lactation alters cerebellar synapsin expression via impaired influence of estrogen nuclear receptor α.

Pourié G, Martin N, Bossenmeyer-Pourié C, Akchiche N, Guéant-Rodriguez RM, Geoffroy A, Jeannesson E, El Hajj Chehadeh S, Mimoun K, Brachet P, Koziel V, Alberto JM, Helle D, Debard R, Leininger B, Daval JL, Guéant JL. Pourié G, et al. Among authors: el hajj chehadeh s. FASEB J. 2015 Sep;29(9):3713-25. doi: 10.1096/fj.14-264267. Epub 2015 May 27. FASEB J. 2015. PMID: 26018677

8

Early methyl donor deficiency alters cAMP signaling pathway and neurosteroidogenesis in the cerebellum of female rat pups.

El Hajj Chehadeh S, Dreumont N, Willekens J, Canabady-Rochelle L, Jeannesson E, Alberto JM, Daval JL, Guéant JL, Leininger-Muller B. El Hajj Chehadeh S, et al. Am J Physiol Endocrinol Metab. 2014 Dec 1;307(11):E1009-19. doi: 10.1152/ajpendo.00364.2014. Epub 2014 Oct 7. Am J Physiol Endocrinol Metab. 2014. PMID: 25294213 Free PMC article.

9

Gestational methyl donor deficiency alters key proteins involved in neurosteroidogenesis in the olfactory bulbs of newborn female rats and is associated with impaired olfactory performance.

El Hajj Chehadeh S, Pourié G, Martin N, Alberto JM, Daval JL, Guéant JL, Leininger-Muller B. El Hajj Chehadeh S, et al. Br J Nutr. 2014 Mar 28;111(6):1021-31. doi: 10.1017/S0007114513003553. Epub 2013 Nov 12. Br J Nutr. 2014. PMID: 24229781

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