Motasem Melhem - Search Results

Year	Number of Results
2012	1
2013	2
2014	4
2016	2
2017	3
2018	2
2019	5
2020	6
2021	4
2022	2
2023	3
2024	0

1

Ceramide kinase regulates TNF-α-induced immune responses in human monocytic cells.

Al-Rashed F, Ahmad Z, Snider AJ, Thomas R, Kochumon S, Melhem M, Sindhu S, Obeid LM, Al-Mulla F, Hannun YA, Ahmad R. Al-Rashed F, et al. Among authors: melhem m. Sci Rep. 2021 Apr 15;11(1):8259. doi: 10.1038/s41598-021-87795-7. Sci Rep. 2021. PMID: 33859296 Free PMC article.

2

Identification of Maturity-Onset-Diabetes of the Young (MODY) mutations in a country where diabetes is endemic.

Al-Kandari H, Al-Abdulrazzaq D, Davidsson L, Nizam R, Jacob S, Melhem M, John SE, Al-Mulla F. Al-Kandari H, et al. Among authors: melhem m. Sci Rep. 2021 Aug 9;11(1):16060. doi: 10.1038/s41598-021-95552-z. Sci Rep. 2021. PMID: 34373539 Free PMC article.

3

GALNT2 rs4846914 SNP Is Associated with Obesity, Atherogenic Lipid Traits, and ANGPTL3 Plasma Level.

Qaddoumi M, Hebbar P, Abu-Farha M, Al Somaly A, Melhem M, Al-Kayal F, AlKhairi I, Cherian P, Alanbaei M, Al-Mulla F, Abubaker J, Thanaraj TA. Qaddoumi M, et al. Among authors: melhem m. Genes (Basel). 2022 Jul 4;13(7):1201. doi: 10.3390/genes13071201. Genes (Basel). 2022. PMID: 35885984 Free PMC article.

4

Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literature.

Antony D, Nampoory N, Bacchelli C, Melhem M, Wu K, James CT, Beales PL, Hubank M, Thomas D, Mashankar A, Behbehani K, Schmidts M, Alsmadi O. Antony D, et al. Among authors: melhem m. Eur J Med Genet. 2017 Dec;60(12):658-666. doi: 10.1016/j.ejmg.2017.08.019. Epub 2017 Sep 12. Eur J Med Genet. 2017. PMID: 28870638 Review.

5

Neutral sphingomyelinase 2 regulates inflammatory responses in monocytes/macrophages induced by TNF-α.

Al-Rashed F, Ahmad Z, Thomas R, Melhem M, Snider AJ, Obeid LM, Al-Mulla F, Hannun YA, Ahmad R. Al-Rashed F, et al. Among authors: melhem m. Sci Rep. 2020 Oct 8;10(1):16802. doi: 10.1038/s41598-020-73912-5. Sci Rep. 2020. PMID: 33033337 Free PMC article.

6

The miR-668 binding site variant rs1046322 on WFS1 is associated with obesity in Southeast Asians.

Hammad MM, Abu-Farha M, Hebbar P, Anoop E, Chandy B, Melhem M, Channanath A, Al-Mulla F, Thanaraj TA, Abubaker J. Hammad MM, et al. Among authors: melhem m. Front Endocrinol (Lausanne). 2023 Oct 4;14:1185956. doi: 10.3389/fendo.2023.1185956. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37859980 Free PMC article.

7

Increased Expression of Meteorin-Like Hormone in Type 2 Diabetes and Obesity and Its Association with Irisin.

AlKhairi I, Cherian P, Abu-Farha M, Madhoun AA, Nizam R, Melhem M, Jamal M, Al-Sabah S, Ali H, Tuomilehto J, Al-Mulla F, Abubaker J. AlKhairi I, et al. Among authors: melhem m. Cells. 2019 Oct 19;8(10):1283. doi: 10.3390/cells8101283. Cells. 2019. PMID: 31635130 Free PMC article.

8

Single nucleotide polymorphisms in vitamin D binding protein and 25-hydroxylase genes affect vitamin D levels in adolescents of Arab ethnicity in Kuwait.

Rahman A, Abu-Farha M, Channanath A, Hammad MM, Anoop E, Chandy B, Melhem M, Al-Mulla F, Thanaraj TA, Abubaker J. Rahman A, et al. Among authors: melhem m. Front Endocrinol (Lausanne). 2023 Oct 20;14:1257051. doi: 10.3389/fendo.2023.1257051. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37929021 Free PMC article.

9

ONECUT1 variants beyond type 1 and type 2 diabetes: exploring clinical diversity and epigenetic associations in Arab cohorts.

Dashti M, Nizam R, John SE, Melhem M, Channanath A, Alkandari H, Thanaraj TA, Al-Mulla F. Dashti M, et al. Among authors: melhem m. Front Genet. 2023 Oct 24;14:1254833. doi: 10.3389/fgene.2023.1254833. eCollection 2023. Front Genet. 2023. PMID: 37941991 Free PMC article.

10

Mitochondrial DNA D-loop sequencing reveals obesity variants in an Arab population.

Eaaswarkhanth M, Melhem M, Sharma P, Nizam R, Al Madhoun A, Chaubey G, Alsmadi O, AlOzairi E, Al-Mulla F. Eaaswarkhanth M, et al. Among authors: melhem m. Appl Clin Genet. 2019 May 24;12:63-70. doi: 10.2147/TACG.S198593. eCollection 2019. Appl Clin Genet. 2019. PMID: 31213875 Free PMC article.

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