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Ghazi Alghanim, PhD

Postdoctoral Fellow

Postdoctoral Fellow, Genetics and Bioinformatics

P.O Box 1180, Dasman
Kuwait

Source: Scopus
Calculated based on no. of publications stored in Pure and citations from Scopus

Research activity per year

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12 Citations
2 h-Index
4 Article
1 Comment/debate

5 results

Caveolin-1 variant is associated with the Metabolic syndrome in Kuwaiti children.
Nizam, R., Al Ozairi, E., Goodson, J. M., Melhem, M., Davidsson, L., Mohammad Abdullah Al-kandari, H., Al Madhoun, A., Alghanim, G., Abu-Farha, M., Abubaker, J., Sami Bitar, M., Mohamed Ali Yaseen, H., Arefanian, H., Sriraman, D., Alrefai, F., Tuomilehto, J. & Al-Mulla, F., 2018, In: Frontiers in Genetics. 9
Research output: Contribution to journal › Article › peer-review
Caveolin-1 Variant Is Associated With the Metabolic Syndrome in Kuwaiti Children (vol 9, 689, 2018)
Nizam, R., Al-Ozairi, E., Goodson, J. M., Melhem, M., Davidsson, L., Alkhandari, H., Al Madhoun, A., Shamsah, S., Qaddoumi, M. & Alghanim, G., 2019, In: Frontiers in Genetics. 10
Research output: Contribution to journal › Article › peer-review
Corrigendum: Caveolin-1 Variant Is Associated With the Metabolic Syndrome in Kuwaiti Children: Caveolin-1 variant is associated with the metabolic syndrome in Kuwaiti children (Frontiers in Genetics ( 2018) 9 (689) DOI: 10.3389/fgene.2018.00689)
Nizam, R., Al-Ozairi, E., Goodson, J. M., Melhem, M., Davidsson, L., Alkhandari, H., Al Madhoun, A., Shamsah, S., Qaddoumi, M., Alghanim, G., Alhasawi, N., Abu-Farha, M., Abubaker, J., Shi, P., Hartman, M-L., Tavares, M., Bitar, M., Ali, H., Arefanian, H., Devarajan, S. & 4 others, Al-Refaei, F., Alsmadi, O., Tuomilehto, J. & Al-Mulla, F., 1 Jan 2019, In: Frontiers in Genetics. 10, MAR, p. 221 1 p., 221.
Research output: Contribution to journal › Comment/debate
Higher Levels of ANGPTL5 in the Circulation of Subjects With Obesity and Type 2 Diabetes Are Associated With Insulin Resistance
Alghanim, G., Qaddoumi, M. G., Alhasawi, N., Cherian, P., Al-Khairi, I., Nizam, R., Alkayal, F., Alanbaei, M., Tuomilehto, J., Abubaker, J., Abu-Farha, M. & Al-Mulla, F., 1 Jan 2019, In: Frontiers in Endocrinology. 10, p. 495 1 p., 495.
Research output: Contribution to journal › Article › peer-review
5 Citations (Scopus)
ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait
Behbehani, R., Melhem, M., Alghanim, G., Behbehani, K. & Alsmadi, O., 1 Jan 2014, In: British Journal of Ophthalmology. 98, 6, p. 826-831 6 p.
Research output: Contribution to journal › Article › peer-review

Open Access
7 Citations (Scopus)