• 783 Citations
  • 9 h-Index
20112019

Research output per year

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Research Output

  • 783 Citations
  • 9 h-Index
  • 17 Article
  • 1 Comment/debate
  • 1 Review article
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Article
2019

Whole-methylome analysis of circulating monocytes in acute diabetic Charcot foot reveals differentially methylated genes involved in the formation of osteoclasts

Pasquier, J., Spurgeon, M., Bradic, M., Thomas, B., Robay, A., Chidiac, O., DIb, M. J., Turjoman, R., Liberska, A., Staudt, M., Fakhro, K. A., Menzies, R., Jayyousi, A., Zirie, M., Suwaidi, J. A., Malik, R. A., Talal, T., Rafii, A., Mezey, J., Rodriguez-Flores, J. & 2 others, Crystal, R. G. & Khalil, C. A., Feb 2019, In : Epigenomics. 11, 3, p. 281-296 16 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)
2018

A systematic review on the genetics of male infertility in the era of next-generation sequencing

Robay, A., Abbasi, S., Akil, A., El-Bardisi, H., Arafa, M., Crystal, R. & Fakhro, K. A. M. A., 1 Mar 2018, In : Arab Journal of Urology. 16, 1, p. 53-64 12 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)

Differentially expressed circulating microRNAs in the development of acute diabetic Charcot foot

Pasquier, J., Ramachandran, V., Abu-Qaoud, MD. R., Thomas, B., Benurwar, M. J., Chidiac, O., Hoarau, J., Robay, A., Fakhro, K. A. M. A., Menzies, R. A., Jayyousi, A., Zirie, M., Al Suwaidi, J., Malik, R., Talal, T. K., Najafi, H., Tabrizi, A. R. & Abi Khalil, C., 1 Oct 2018, In : Epigenomics. 10, 10, p. 1267-1278 12 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Exome sequencing-based identification of novel type 2 diabetes risk allele loci in the Qatari population

O’Beirne, S. L., Salit, J., Rodriguez-Flores, J. L., Staudt, M. R., Khalil, C. A., Fakhro, K. A., Robay, A., Ramstetter, M. D., Malek, J. A., Zirie, M., Jayyousi, A., Badii, R., Al-Marri, A. A. N., Bener, A., Mahmoud, M., Chiuchiolo, M. J., Al-Shakaki, A., Chidiac, O., Stadler, D., Mezey, J. G. & 1 others, Crystal, R. G., Sep 2018, In : PloS one. 13, 9, e0199837.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Hypertrophic cardiomyopathy-linked variants of cardiac myosin-binding protein C3 display altered molecular properties and actin interaction

Da’as, S. I., Fakhro, K., Thanassoulas, A., Krishnamoorthy, N., Saleh, A., Calver, B. L., Safieh-Garabedian, B., Toft, E., Nounesis, G., Anthony Lai, F. & Nomikos, M., 14 Dec 2018, In : Biochemical Journal. 475, 24, p. 3933-3948 16 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)

Point-of-care whole-exome sequencing of idiopathic male infertility

Fakhro, K. A. M. A., Elbardisi, H., Arafa, M., Robay, A., Rodriguez-Flores, J. L., Al-Shakaki, A., Syed, N., Mezey, J. G., Abi Khalil, C., Malek, J., Al-Ansari, A., Al Said, S. & Crystal, R., 1 Nov 2018, In : Genetics in Medicine. 20, 11, p. 1365-1373 9 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)
14 Citations (Scopus)
2017
8 Citations (Scopus)
2016

Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations

Rodriguez-Flores, J. L., Fakhro, K., Agosto-Perez, F., Ramstetter, M. D., Arbiza, L., Vincent, T. L., Robay, A., Malek, J. A., Suhre, K., Chouchane, L., Badii, R., Al-Marri, A. A. N., Khalil, C. A., Zirie, M., Jayyousi, A., Salit, J., Keinan, A., Clark, A. G., Crystal, R. G. & Mezey, J. G., Feb 2016, In : Genome Research. 26, 2, p. 151-162 12 p.

Research output: Contribution to journalArticle

36 Citations (Scopus)

The Qatar genome: A population-specific tool for precision medicine in the Middle East

Fakhro, K. A. M. A., Staudt, M. R., Ramstetter, M. D., Robay, A., Malek, J., Badii, R., Al-Marri, A. A. N., Abi Khalil, C., Al-Shakaki, A., Chidiac, O., Stadler, D., Zirie, M., Jayyousi, A., Salit, J., Mezey, J. G., Crystal, R. & Rodriguez-Flores, J. L., 30 Jun 2016, In : Human Genome Variation. 3, 16016.

Research output: Contribution to journalArticle

Open Access
28 Citations (Scopus)
8 Citations (Scopus)

Type 2 diabetes risk allele loci in the Qatari population

O'Beirne, S. L., Salit, J., Rodriguez-Flores, J. L., Staudt, M. R., Abi Khalil, C., Fakhro, K. A. M. A., Robay, A., Ramstetter, M. D., Al Azwani, I., Malek, J., Zirie, M., Jayyousi, A., Badii, R., Al-Nabet Al-marri, A., Chiuchiolo, M. J., Al-Shakaki, A., Chidiac, O., Gharbiah, M., Bener, A., Stadler, D. & 3 others, Hackett, N. R., Mezey, J. G. & Crystal, R., 1 Jul 2016, In : PLoS One. 11, 7, e0156834.

Research output: Contribution to journalArticle

10 Citations (Scopus)
2015

Copy number variations in the genome of the Qatari population

Fakhro, K. A., Yousri, N. A., Rodriguez-Flores, J. L., Robay, A., Staudt, M. R., Agosto-Perez, F., Salit, J., Malek, J. A., Suhre, K., Jayyousi, A., Zirie, M., Stadler, D., Mezey, J. G. & Crystal, R. G., 22 Oct 2015, In : BMC genomics. 16, 1, 834.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Role of SLMAP genetic variants in susceptibility of diabetes and diabetic retinopathy in Qatari population

Upadhyay, R., Robay, A., Fakhro, K. A. M. A., Khalil, A. A., Zirie, M., Jayyousi, A., El-Shafei, M., Kiss, S., D'Amico, D. J., Salit, J., Staudt, M. R., O'Beirne, S. L., Chen, X., Tuana, B., Crystal, R. & Ding, H., 15 Feb 2015, In : Journal of Translational Medicine. 13, 1, 61.

Research output: Contribution to journalArticle

6 Citations (Scopus)
2014

Exome Sequencing Identifies Potential Risk Variants for Mendelian Disorders at High Prevalence in Qatar

Rodriguez-Flores, J. L., Fakhro, K., Hackett, N. R., Salit, J., Fuller, J., Agosto-Perez, F., Gharbiah, M., Malek, J. A., Zirie, M., Jayyousi, A., Badii, R., Al-Nabet Al-Marri, A., Chouchane, L., Stadler, D. J., Mezey, J. G. & Crystal, R. G., 1 Jan 2014, In : Human mutation. 35, 1, p. 105-116 12 p.

Research output: Contribution to journalArticle

29 Citations (Scopus)
2013

De novo mutations in histone-modifying genes in congenital heart disease

Zaidi, S., Choi, M., Wakimoto, H., Ma, L., Jiang, J., Overton, J. D., Romano-Adesman, A., Bjornson, R. D., Breitbart, R. E., Brown, K. K., Carriero, N. J., Cheung, Y. H., Deanfield, J., Depalma, S., Fakhro, K. A., Glessner, J., Hakonarson, H., Italia, M. J., Kaltman, J. R., Kaski, J. & 30 others, Kim, R., Kline, J. K., Lee, T., Leipzig, J., Lopez, A., Mane, S. M., Mitchell, L. E., Newburger, J. W., Parfenov, M., Pe'Er, I., Porter, G., Roberts, A. E., Sachidanandam, R., Sanders, S. J., Seiden, H. S., State, M. W., Subramanian, S., Tikhonova, I. R., Wang, W., Warburton, D., White, P. S., Williams, I. A., Zhao, H., Seidman, J. G., Brueckner, M., Chung, W. K., Gelb, B. D., Goldmuntz, E., Seidman, C. E. & Lifton, R. P., 14 May 2013, In : Nature. 498, 7453, p. 220-223 4 p.

Research output: Contribution to journalArticle

460 Citations (Scopus)
2011

Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Fakhro, K. A., Choi, M., Ware, S. M., Belmont, J. W., Towbin, J. A., Lifton, R. P., Khokha, M. K. & Brueckner, M., 15 Feb 2011, In : Proceedings of the National Academy of Sciences of the United States of America. 108, 7, p. 2915-2920 6 p.

Research output: Contribution to journalArticle

142 Citations (Scopus)