Makia J. Marafie

Safat, KU 13059, Kuwait

Last Updated: 09/26/2026

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Found 14 publications

Insights from the Newborn Screening Program for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency in Kuwait.

Insights from the Newborn Screening Program for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency in Kuwait.

Journal: International journal of neonatal screening
Published: January 24, 2025

Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries.

Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries.

Journal: Familial cancer
Published: May 06, 2020

The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries.

The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries.

Journal: Human mutation
Published: March 26, 2019

Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancer.

Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancer.

Journal: Familial cancer
Published: November 16, 2016

Next-generation sequencing in familial breast cancer patients from Lebanon.

Next-generation sequencing in familial breast cancer patients from Lebanon.

Journal: BMC medical genomics
Published: August 20, 2016

Functionally-focused algorithmic analysis of high resolution microarray-CGH genomic landscapes demonstrates comparable genomic copy number aberrations in MSI and MSS sporadic colorectal cancer.

Functionally-focused algorithmic analysis of high resolution microarray-CGH genomic landscapes demonstrates comparable genomic copy number aberrations in MSI and MSS sporadic colorectal cancer.

Journal: PloS one
Published: July 31, 2016

Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis.

Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis.

Journal: Haematologica
Published: April 20, 2016

Identification of 42 Genes Linked to Stage II Colorectal Cancer Metastatic Relapse.

Identification of 42 Genes Linked to Stage II Colorectal Cancer Metastatic Relapse.

Journal: International journal of molecular sciences
Published: March 09, 2016

The influence of admixture and consanguinity on population genetic diversity in Middle East.

The influence of admixture and consanguinity on population genetic diversity in Middle East.

Journal: Journal of human genetics
Published: July 08, 2014

Gender-associated genomic differences in colorectal cancer: clinical insight from feminization of male cancer cells.

Gender-associated genomic differences in colorectal cancer: clinical insight from feminization of male cancer cells.

Journal: International journal of molecular sciences
Published: May 27, 2014

Raf kinase inhibitory protein role in the molecular subtyping of breast cancer.

Raf kinase inhibitory protein role in the molecular subtyping of breast cancer.

Journal: Journal of cellular biochemistry
Published: September 20, 2013

Human Variome Project country nodes: documenting genetic information within a country.

Human Variome Project country nodes: documenting genetic information within a country.

Journal: Human mutation
Published: March 14, 2012
Showing 1-12 of 14

Last Updated: 09/26/2026