Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population.

Autor: Yousri NA; Genetic Medicine, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar. nay2005@qatar-med.cornell.edu.; Computer and Systems Engineering, Alexandria University, Alexandria, Egypt. nay2005@qatar-med.cornell.edu., Fakhro KA; Genetic Medicine, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar. kfakhro@sidra.org.; Sidra Medical Research Center, Department of Human Genetics, PO Box 26999, Doha, Qatar. kfakhro@sidra.org., Robay A; Genetic Medicine, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Rodriguez-Flores JL; Genetic Medicine, Weill Cornell Medicine, New York, NY, 10065, USA., Mohney RP; Metabolon Inc, Durham, NC, 27560, USA., Zeriri H; Genetic Medicine, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Odeh T; Genetic Medicine, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Kader SA; Physiology and Biophysics, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Aldous EK; Genomics Core, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Thareja G; Physiology and Biophysics, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Kumar M; Physiology and Biophysics, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Al-Shakaki A; Genetic Medicine, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Chidiac OM; Genetic Medicine, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Mohamoud YA; Genomics Core, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Mezey JG; Genetic Medicine, Weill Cornell Medicine, New York, NY, 10065, USA., Malek JA; Genetic Medicine, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar.; Genomics Core, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar., Crystal RG; Genetic Medicine, Weill Cornell Medicine, New York, NY, 10065, USA., Suhre K; Physiology and Biophysics, Weill Cornell Medicine-Qatar, PO Box 24144, Doha, Qatar. karsten@suhre.fr.

Publikováno v: Nature communications [Nat Commun] 2018 Jan 23; Vol. 9 (1), pp. 333. Date of Electronic Publication: 2018 Jan 23.

Integrated epigenome, whole genome sequence and metabolome analyses identify novel multi-omics pathways in type 2 diabetes: a Middle Eastern study.

Autor: Yousri, Noha A.^1,2,3 (AUTHOR) nyousri@hbku.edu.qa, Albagha, Omar M. E.² (AUTHOR), Hunt, Steven C.¹ (AUTHOR)

Publikováno v: BMC Medicine. 9/8/2023, Vol. 21 Issue 1, p1-20. 20p.

Unraveling the functional role of the orphan solute carrier, SLC22A24 in the transport of steroid conjugates through metabolomic and genome-wide association studies.

Autor: Yee, Sook Wah¹, Stecula, Adrian¹, Chien, Huan-Chieh¹, Zou, Ling¹, Feofanova, Elena V.², van Borselen, Marjolein¹, Cheung, Kit Wun Kathy¹ kathy.giacomini@ucsf.edu, Yousri, Noha A.^3,4, Suhre, Karsten⁵, Kinchen, Jason M.⁶, Boerwinkle, Eric^2,7, Irannejad, Roshanak⁸, Yu, Bing², Giacomini, Kathleen M.^1,9

Publikováno v: PLoS Genetics. 9/25/2019, Vol. 15 Issue 9, p1-38. 38p.

Crosstalk between Host Genome and Metabolome among People with HIV in South Africa.

Autor: Liu, Chang, Wang, Zicheng, Hui, Qin, Chiang, Yiyun, Chen, Junyu, Brijkumar, Jaysingh, Edwards, Johnathan A., Ordonez, Claudia E., Dudgeon, Mathew R., Sunpath, Henry, Pillay, Selvan, Moodley, Pravi, Kuritzkes, Daniel R., Moosa, Mohamed Y. S., Jones, Dean P., Marconi, Vincent C., Sun, Yan V.

Publikováno v: Metabolites (2218-1989); Jul2022, Vol. 12 Issue 7, pN.PAG-N.PAG, 15p

Systems Genetics for Mechanistic Discovery in Heart Diseases.

Autor: Rau, Christoph D., Lusis, Aldons J., Wang, Yibin

Publikováno v: Circulation Research; 6/5/2020, Vol. 126 Issue 12, p1795-1815, 21p