Al-Aama JY - Search Results

1

Prevalence and characteristics of non-syndromic orofacial clefts and the influence of consanguinity.

Alamoudi NM, Sabbagh HJ, Innes NP, El Derwi D, Hanno AZ, Al-Aama JY, Habiballah AH, Mossey PA. Alamoudi NM, et al. J Clin Pediatr Dent. 2014 Spring;38(3):241-6. doi: 10.17796/jcpd.38.3.bm4m2158v17p2535. J Clin Pediatr Dent. 2014. PMID: 25095319 Free article.

2

Pattern of infant feeding at a University Hospital in Western Saudi Arabia.

Fida NM, Al-Aama JY. Fida NM, et al. Saudi Med J. 2003 Jul;24(7):725-9. Saudi Med J. 2003. PMID: 12883602

3

Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot.

Alrayes N, Mallah BA, Issa NM, Banaganapalli B, Ahmad Shaik N, Nasser KK, Alshehri BA, Bhuiyan ZA, Bdier AY, Al-Aama JY. Alrayes N, et al. Among authors: al aama jy. Gene. 2023 Jan 30;851:146909. doi: 10.1016/j.gene.2022.146909. Epub 2022 Sep 23. Gene. 2023. PMID: 36162527

4

Discordance Between Germline and Blood Mosaicism in Calmodulinopathy.

Bhuiyan ZA, Bdier A, Al-Aama JY, Abramova T, George AL Jr. Bhuiyan ZA, et al. Among authors: al aama jy. Circ Genom Precis Med. 2022 Aug;15(4):e003695. doi: 10.1161/CIRCGEN.121.003695. Epub 2022 May 11. Circ Genom Precis Med. 2022. PMID: 35543700 No abstract available.

5

Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease.

Mansour H, Banaganapalli B, Nasser KK, Al-Aama JY, Shaik NA, Saadah OI, Elango R. Mansour H, et al. Among authors: al aama jy. Front Pediatr. 2022 Feb 14;10:837957. doi: 10.3389/fped.2022.837957. eCollection 2022. Front Pediatr. 2022. PMID: 35237542 Free PMC article.

6

Exploring the role of Islam on the lived experience of patients with Long QT Syndrome in Saudi Arabia.

Bakur KH, Al-Aama JY, Alhassnan ZN, Brooks H, Clancy T, Manea W, Takroni SA, Ulph F. Bakur KH, et al. Among authors: al aama jy. J Genet Couns. 2022 Aug;31(4):922-936. doi: 10.1002/jgc4.1562. Epub 2022 Feb 22. J Genet Couns. 2022. PMID: 35194886

7

Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects.

Alsafwani RS, Nasser KK, Shinawi T, Banaganapalli B, ElSokary HA, Zaher ZF, Shaik NA, Abdelmohsen G, Al-Aama JY, Shapiro AJ, O Al-Radi O, Elango R, Alahmadi T. Alsafwani RS, et al. Among authors: al aama jy. Front Med (Lausanne). 2021 Sep 13;8:724826. doi: 10.3389/fmed.2021.724826. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34589502 Free PMC article.

8

Saudi Familial Hypercholesterolemia Patients With Rare LDLR Stop Gain Variant Showed Variable Clinical Phenotype and Resistance to Multiple Drug Regimen.

Awan ZA, Rashidi OM, Al-Shehri BA, Jamil K, Elango R, Al-Aama JY, Hegele RA, Banaganapalli B, Shaik NA. Awan ZA, et al. Among authors: al aama jy. Front Med (Lausanne). 2021 Jun 25;8:694668. doi: 10.3389/fmed.2021.694668. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34249980 Free PMC article.

9

TagSNP approach for HLA risk allele genotyping of Saudi celiac disease patients: effectiveness and pitfalls.

Baaqeel RH, Banaganapalli B, Al Mahdi HB, Salama MA, Alhussaini BH, Alaifan MA, Bin-Taleb Y, Shaik NA, Al-Aama JY, Elango R, Saadah OI. Baaqeel RH, et al. Among authors: al aama jy. Biosci Rep. 2021 Jun 25;41(6):BSR20210509. doi: 10.1042/BSR20210509. Biosci Rep. 2021. PMID: 34042155 Free PMC article.

10

Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families.

Saadah OI, Banaganapalli B, Kamal NM, Sahly AN, Alsufyani HA, Mohammed A, Ahmad A, Nasser KK, Al-Aama JY, Shaik NA, Elango R. Saadah OI, et al. Among authors: al aama jy. Front Pediatr. 2021 Apr 26;9:652011. doi: 10.3389/fped.2021.652011. eCollection 2021. Front Pediatr. 2021. PMID: 33981653 Free PMC article.

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