Sequence and analysis of a whole genome from Kuwaiti population subgroup of Persian ancestry

著者: Thareja, Gaurav, John, Sumi Elsa, Hebbar, Prashantha, Behbehani, Kazem, Thanaraj, Thangavel Alphonse, Alsmadi, Osama
出版年 BMC Genomics (2015)

Kuwaiti population subgroup of nomadic Bedouin ancestry—Whole genome sequence and analysis

著者: John, Sumi Elsa, Thareja, Gaurav, Hebbar, Prashantha, Behbehani, Kazem, Thanaraj, Thangavel Alphonse, Alsmadi, Osama
出版年 Genom Data (2014)

Genotyping-by-sequencing identifies date palm clone preference in agronomics of the State of Qatar

著者: Thareja, Gaurav, Mathew, Sweety, Mathew, Lisa S., Mohamoud, Yasmin Ali, Suhre, Karsten, Malek, Joel A.
出版年 PLoS One (2018)

Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits

著者: Thareja, Gaurav, Al-Sarraj, Yasser, Belkadi, Aziz, Almotawa, Maryam, Suhre, Karsten, Albagha, Omar M. E.
出版年 Nat Commun (2021)

Genome at Juncture of Early Human Migration: A Systematic Analysis of Two Whole Genomes and Thirteen Exomes from Kuwaiti Population Subgroup of Inferred Saudi Arabian Tribe Ancestr...

著者: Alsmadi, Osama, John, Sumi E., Thareja, Gaurav, Hebbar, Prashantha, Antony, Dinu, Behbehani, Kazem, Thanaraj, Thangavel Alphonse
出版事項 2014

Identification of genetic variants controlling RNA editing and their effect on RNA structure stabilization

著者: Belkadi, Aziz, Thareja, Gaurav, Halama, Anna, Mahmoud, Yasmin, Jones, Danielle, Agnew, Sam, Malek, Joel, Suhre, Karsten
出版年 Eur J Hum Genet (2020)

Genetic Substructure of Kuwaiti Population Reveals Migration History

著者: Alsmadi, Osama, Thareja, Gaurav, Alkayal, Fadi, Rajagopalan, Ramakrishnan, John, Sumi Elsa, Hebbar, Prashantha, Behbehani, Kazem, Thanaraj, Thangavel Alphonse
出版事項 2013

Response to Leptin and Nitric Oxide in Blood Pressure Regulation in Humans

著者: Alsmadi, Osama, Melhem, Motasem, Hebbar, Prashantha, Channanath, Arshad, Thareja, Gaurav, John, Sumi E., Alkayal, Fadi, Behbehani, Kazem, Thanaraj, Thangavel Alphonse
出版年 Am J Hypertens (2014)

Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida

著者: Wolujewicz, Paul, Aguiar-Pulido, Vanessa, AbdelAleem, Alice, Nair, Vidya, Thareja, Gaurav, Suhre, Karsten, Shaw, Gary M., Finnell, Richard H., Elemento, Olivier, Ross, M. Elizabeth
出版年 Genet Med (2021)

Single Nucleotide Variant Counts Computed from RNA Sequencing and Cellular Traffic into Human Kidney Allografts

著者: Thareja, Gaurav, Yang, Hua, Hayat, Shahina, Mueller, Franco B., Lee, John R., Lubetzky, Michelle, Dadhania, Darshana M., Belkadi, Aziz, Seshan, Surya V., Suhre, Karsten, Suthanthiran, Manikkam, Muthukumar, Thangamani
出版年 Am J Transplant (2018)

Deep sequencing of DNA from urine of kidney allograft recipients to estimate donor/recipient-specific DNA fractions

著者: Belkadi, Aziz, Thareja, Gaurav, Dadhania, Darshana, Lee, John R., Muthukumar, Thangamani, Snopkowski, Catherine, Li, Carol, Halama, Anna, Abdelkader, Sara, Abdulla, Silvana, Mahmoud, Yasmin, Malek, Joel, Suthanthiran, Manikkam, Suhre, Karsten
出版年 PLoS One (2021)

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

著者: Yousri, Noha A., Fakhro, Khalid A., Robay, Amal, Rodriguez-Flores, Juan L., Mohney, Robert P., Zeriri, Hassina, Odeh, Tala, Kader, Sara Abdul, Aldous, Eman K., Thareja, Gaurav, Kumar, Manish, Al-Shakaki, Alya, Chidiac, Omar M., Mohamoud, Yasmin A., Mezey, Jason G., Malek, Joel A., Crystal, Ronald G., Suhre, Karsten
出版年 Nat Commun (2018)

Epigenetics meets proteomics in an epigenome-wide association study with circulating blood plasma protein traits

著者: Zaghlool, Shaza B., Kühnel, Brigitte, Elhadad, Mohamed A., Kader, Sara, Halama, Anna, Thareja, Gaurav, Engelke, Rudolf, Sarwath, Hina, Al-Dous, Eman K., Mohamoud, Yasmin A., Meitinger, Thomas, Wilson, Rory, Strauch, Konstantin, Peters, Annette, Mook-Kanamori, Dennis O., Graumann, Johannes, Malek, Joel A., Gieger, Christian, Waldenberger, Melanie, Suhre, Karsten
出版年 Nat Commun (2020)

Connecting genetic risk to disease end points through the human blood plasma proteome

著者: Suhre, Karsten, Arnold, Matthias, Bhagwat, Aditya Mukund, Cotton, Richard J., Engelke, Rudolf, Raffler, Johannes, Sarwath, Hina, Thareja, Gaurav, Wahl, Annika, DeLisle, Robert Kirk, Gold, Larry, Pezer, Marija, Lauc, Gordan, El-Din Selim, Mohammed A., Mook-Kanamori, Dennis O., Al-Dous, Eman K., Mohamoud, Yasmin A., Malek, Joel, Strauch, Konstantin, Grallert, Harald, Peters, Annette, Kastenmüller, Gabi, Gieger, Christian, Graumann, Johannes
出版年 Nat Commun (2017)

Erratum: Connecting genetic risk to disease end points through the human blood plasma proteome

著者: Suhre, Karsten, Arnold, Matthias, Bhagwat, Aditya Mukund, Cotton, Richard J., Engelke, Rudolf, Raffler, Johannes, Sarwath, Hina, Thareja, Gaurav, Wahl, Annika, DeLisle, Robert Kirk, Gold, Larry, Pezer, Marija, Lauc, Gordan, El-Din Selim, Mohammed A., Mook-Kanamori, Dennis O., Al-Dous, Eman K., Mohamoud, Yasmin A., Malek, Joel, Strauch, Konstantin, Grallert, Harald, Peters, Annette, Kastenmüller, Gabi, Gieger, Christian, Graumann, Johannes
出版年 Nat Commun (2017)

Defining the genetic control of human blood plasma N-glycome using genome-wide association study

著者: Sharapov, Sodbo Zh, Tsepilov, Yakov A, Klaric, Lucija, Mangino, Massimo, Thareja, Gaurav, Shadrina, Alexandra S, Simurina, Mirna, Dagostino, Concetta, Dmitrieva, Julia, Vilaj, Marija, Vuckovic, Frano, Pavic, Tamara, Stambuk, Jerko, Trbojevic-Akmacic, Irena, Kristic, Jasminka, Simunovic, Jelena, Momcilovic, Ana, Campbell, Harry, Doherty, Margaret, Dunlop, Malcolm G, Farrington, Susan M, Pucic-Bakovic, Maja, Gieger, Christian, Allegri, Massimo, Louis, Edouard, Georges, Michel, Suhre, Karsten, Spector, Tim, Williams, Frances M K, Lauc, Gordan, Aulchenko, Yurii S
出版年 Hum Mol Genet (2019)