Alghofaili L - Search Results

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Molecular genetics and phenotype/genotype correlation of 5-α reductase deficiency in a highly consanguineous population.

Alswailem MM, Alzahrani OS, Alghofaili L, Qasem E, Almohanaa M, Alsagheir A, Bin Abbas B, Attia NA, Al Shaikh A, Alzahrani AS. Alswailem MM, et al. Among authors: alghofaili l. Endocrine. 2019 Feb;63(2):361-368. doi: 10.1007/s12020-018-1767-1. Epub 2018 Sep 29. Endocrine. 2019. PMID: 30269266

Non-invasive Molecular Detection of Minimal Residual Disease in Papillary Thyroid Cancer Patients.

Almubarak H, Qassem E, Alghofaili L, Alzahrani AS, Karakas B. Almubarak H, et al. Among authors: alghofaili l. Front Oncol. 2020 Jan 10;9:1510. doi: 10.3389/fonc.2019.01510. eCollection 2019. Front Oncol. 2020. PMID: 31998653 Free PMC article.

High prevalence of deleterious BRCA1 and BRCA2 germline mutations in arab breast and ovarian cancer patients.

Alhuqail AJ, Alzahrani A, Almubarak H, Al-Qadheeb S, Alghofaili L, Almoghrabi N, Alhussaini H, Park BH, Colak D, Karakas B. Alhuqail AJ, et al. Among authors: alghofaili l. Breast Cancer Res Treat. 2018 Apr;168(3):695-702. doi: 10.1007/s10549-017-4635-4. Epub 2018 Jan 2. Breast Cancer Res Treat. 2018. PMID: 29297111

Cell-free DNA levels of twins and sibling pairs indicate individuality and possible use as a personalized biomarker.

Alghofaili L, Almubarak H, Gassem K, Islam SS, Coskun S, Kaya N, Karakas B. Alghofaili L, et al. PLoS One. 2019 Oct 10;14(10):e0223470. doi: 10.1371/journal.pone.0223470. eCollection 2019. PLoS One. 2019. PMID: 31600277 Free PMC article.

Methylation of BRCA1 and MGMT genes in white blood cells are transmitted from mothers to daughters.

Al-Moghrabi N, Al-Showimi M, Al-Yousef N, Al-Shahrani B, Karakas B, Alghofaili L, Almubarak H, Madkhali S, Al Humaidan H. Al-Moghrabi N, et al. Among authors: alghofaili l. Clin Epigenetics. 2018 Jul 26;10(1):99. doi: 10.1186/s13148-018-0529-5. Clin Epigenetics. 2018. PMID: 30049288 Free PMC article.

Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses.

Al-Zayed Z, Al-Rijjal RA, Al-Ghofaili L, BinEssa HA, Pant R, Alrabiah A, Al-Hussainan T, Zou M, Meyer BF, Shi Y. Al-Zayed Z, et al. Orphanet J Rare Dis. 2021 Feb 25;16(1):100. doi: 10.1186/s13023-021-01738-z. Orphanet J Rare Dis. 2021. PMID: 33632255 Free PMC article.

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