Hussein Sheikh Ali Mohamoud[Author] - Search Results

Year	Number of Results
2011	1
2014	2
2015	4
2016	4
2017	1
2018	1
2019	1
2024	0

1

A mutation in the major autophagy gene, WIPI2, associated with global developmental abnormalities.

Jelani M, Dooley HC, Gubas A, Mohamoud HSA, Khan MTM, Ali Z, Kang C, Rahim F, Jan A, Vadgama N, Khan MI, Al-Aama JY, Khan A, Tooze SA, Nasir J. Jelani M, et al. Among authors: mohamoud hsa. Brain. 2019 May 1;142(5):1242-1254. doi: 10.1093/brain/awz075. Brain. 2019. PMID: 30968111 Free PMC article.

2

Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH).

Bibi F, Ali I, Naseer MI, Ali Mohamoud HS, Yasir M, Alvi SA, Jiman-Fatani AA, Sawan A, Azhar EI. Bibi F, et al. Among authors: ali mohamoud hs. PLoS One. 2018 Sep 13;13(9):e0202576. doi: 10.1371/journal.pone.0202576. eCollection 2018. PLoS One. 2018. PMID: 30212456 Free PMC article.

3

From genes to health - challenges and opportunities.

Manwar Hussain MR, Khan A, Ali Mohamoud HS. Manwar Hussain MR, et al. Among authors: ali mohamoud hs. Front Pediatr. 2014 Mar 3;2:12. doi: 10.3389/fped.2014.00012. eCollection 2014. Front Pediatr. 2014. PMID: 24624370 Free PMC article. Review.

4

Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.

Yang C, Xu Y, Yu M, Lee D, Alharti S, Hellen N, Ahmad Shaik N, Banaganapalli B, Sheikh Ali Mohamoud H, Elango R, Przyborski S, Tenin G, Williams S, O'Sullivan J, Al-Radi OO, Atta J, Harding SE, Keavney B, Lako M, Armstrong L. Yang C, et al. Among authors: sheikh ali mohamoud h. Hum Mol Genet. 2017 Aug 15;26(16):3031-3045. doi: 10.1093/hmg/ddx140. Hum Mol Genet. 2017. PMID: 28521042 Free PMC article.

5

Truncating mutation in intracellular phospholipase A₁ gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54).

Alrayes N, Mohamoud HS, Jelani M, Ahmad S, Vadgama N, Bakur K, Simpson M, Al-Aama JY, Nasir J. Alrayes N, et al. Among authors: mohamoud hs. BMC Res Notes. 2015 Jun 27;8:271. doi: 10.1186/s13104-015-1227-4. BMC Res Notes. 2015. PMID: 26113134 Free PMC article.

6

A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family.

Jelani M, Kang C, Mohamoud HS, Al-Rehaili R, Almramhi MM, Serafi R, Yang H, Al-Aama JY, Naeem M, Alkhiary YM. Jelani M, et al. Among authors: mohamoud hs. Arch Oral Biol. 2016 Jul;67:28-33. doi: 10.1016/j.archoralbio.2016.03.012. Epub 2016 Mar 23. Arch Oral Biol. 2016. PMID: 27019138

7

Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3.

Ahmed S, Jelani M, Alrayes N, Mohamoud HS, Almramhi MM, Anshasi W, Ahmed NA, Wang J, Nasir J, Al-Aama JY. Ahmed S, et al. Among authors: mohamoud hs. J Neurol Sci. 2015;353(1-2):149-54. doi: 10.1016/j.jns.2015.04.038. Epub 2015 May 1. J Neurol Sci. 2015. PMID: 25956234

8

Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon-Lefevre syndrome in a Saudi family.

Alkhiary YM, Jelani M, Almramhi MM, Mohamoud HS, Al-Rehaili R, Al-Zahrani HS, Serafi R, Yang H, Al-Aama JY. Alkhiary YM, et al. Among authors: mohamoud hs. Saudi J Biol Sci. 2016 Sep;23(5):571-6. doi: 10.1016/j.sjbs.2015.06.007. Epub 2015 Jun 16. Saudi J Biol Sci. 2016. PMID: 27579005 Free PMC article.

9

First comprehensive in silico analysis of the functional and structural consequences of SNPs in human GalNAc-T1 gene.

Mohamoud HS, Hussain MR, El-Harouni AA, Shaik NA, Qasmi ZU, Merican AF, Baig M, Anwar Y, Asfour H, Bondagji N, Al-Aama JY. Mohamoud HS, et al. Comput Math Methods Med. 2014;2014:904052. doi: 10.1155/2014/904052. Epub 2014 Mar 4. Comput Math Methods Med. 2014. PMID: 24723968 Free PMC article.

10

Novel nonsense mutation in the PTRF gene underlies congenital generalized lipodystrophy in a consanguineous Saudi family.

Jelani M, Ahmed S, Almramhi MM, Mohamoud HS, Bakur K, Anshasi W, Wang J, Al-Aama JY. Jelani M, et al. Among authors: mohamoud hs. Eur J Med Genet. 2015 Apr;58(4):216-21. doi: 10.1016/j.ejmg.2015.02.002. Epub 2015 Feb 23. Eur J Med Genet. 2015. PMID: 25721873

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