Whole Genome Sequencing of Coronary Heart Disease in a Middle Eastern Cohort Validates Polygenic Risk Scores, Replicates Known Loci, and Suggests New Loci

Mohamad Saad; Khalid Kunji; Ehsan Ullah; Ayman El Menyar; Iftikhar J. Kullo; Jassim Al Suwaidi

Whole Genome Sequencing of Coronary Heart Disease in a Middle Eastern Cohort Validates Polygenic Risk Scores, Replicates Known Loci, and Suggests New Loci

Mohamad Saad
, Khalid Kunji
, Ehsan Ullah
, Ayman El Menyar
, Iftikhar J. Kullo
, Jassim Al Suwaidi

Qatar Computing Research Institute

Research output: Contribution to journal › Meeting Abstract › peer-review

Original language	English
Pages (from-to)	786-787
Number of pages	2
Journal	Genetic Epidemiology
Volume	45
Issue number	7
Publication status	Published - Oct 2021

Cite this

@article{25d65a6b91e64f67ab923f15c2355462,

title = "Whole Genome Sequencing of Coronary Heart Disease in a Middle Eastern Cohort Validates Polygenic Risk Scores, Replicates Known Loci, and Suggests New Loci",

author = "Mohamad Saad and Khalid Kunji and Ehsan Ullah and \{El Menyar\}, Ayman and Kullo, \{Iftikhar J.\} and \{Al Suwaidi\}, Jassim",

year = "2021",

month = oct,

language = "English",

volume = "45",

pages = "786--787",

journal = "Genetic Epidemiology",

issn = "0741-0395",

publisher = "Wiley-Liss Inc.",

number = "7",

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TY - JOUR

T1 - Whole Genome Sequencing of Coronary Heart Disease in a Middle Eastern Cohort Validates Polygenic Risk Scores, Replicates Known Loci, and Suggests New Loci

AU - Saad, Mohamad

AU - Kunji, Khalid

AU - Ullah, Ehsan

AU - El Menyar, Ayman

AU - Kullo, Iftikhar J.

AU - Al Suwaidi, Jassim

PY - 2021/10

Y1 - 2021/10

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=hbku_researchportal&SrcAuth=WosAPI&KeyUT=WOS:000694656700111&DestLinkType=FullRecord&DestApp=WOS_CPL

M3 - Meeting Abstract

SN - 0741-0395

VL - 45

SP - 786

EP - 787

JO - Genetic Epidemiology

JF - Genetic Epidemiology

IS - 7

ER -

Whole Genome Sequencing of Coronary Heart Disease in a Middle Eastern Cohort Validates Polygenic Risk Scores, Replicates Known Loci, and Suggests New Loci

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