EnsembleCNV: an ensemble machine learning algorithm to identify and genotype copy number variation using SNP array data

por Zhang, Zhongyang, Cheng, Haoxiang, Hong, Xiumei, Di Narzo, Antonio F, Franzen, Oscar, Peng, Shouneng, Ruusalepp, Arno, Kovacic, Jason C, Bjorkegren, Johan L M, Wang, Xiaobin, Hao, Ke
Publicado 2019

High-Throughput Characterization of Blood Serum Proteomics of IBD Patients with Respect to Aging and Genetic Factors

por Di Narzo, Antonio F., Telesco, Shannon E., Brodmerkel, Carrie, Argmann, Carmen, Peters, Lauren A., Li, Katherine, Kidd, Brian, Dudley, Joel, Cho, Judy, Schadt, Eric E., Kasarskis, Andrew, Dobrin, Radu, Hao, Ke
Publicado 2017

Genetic regulation of the placental transcriptome underlies birth weight and risk of childhood obesity

por Peng, Shouneng, Deyssenroth, Maya A., Di Narzo, Antonio F., Cheng, Haoxiang, Zhang, Zhongyang, Lambertini, Luca, Ruusalepp, Arno, Kovacic, Jason C., Bjorkegren, Johan L. M., Marsit, Carmen J., Chen, Jia, Hao, Ke
Publicado 2018

High-Throughput Identification of the Plasma Proteomic Signature of Inflammatory Bowel Disease

por Di Narzo, Antonio F, Brodmerkel, Carrie, Telesco, Shannon E, Argmann, Carmen, Peters, Lauren A, Li, Katherine, Kidd, Brian, Dudley, Joel, Cho, Judy, Schadt, Eric E, Kasarskis, Andrew, Dobrin, Radu, Hao, Ke
Publicado 2019

Pericytes impair capillary blood flow and motor function after chronic spinal cord injury

por Li, Yaqing, Lucas-Osma, Ana M., Black, Sophie, Bandet, Mischa V., Stephens, Marilee J., Vavrek, Romana, Sanelli, Leo, Fenrich, Keith K., Di Narzo, Antonio F., Dracheva, Stella, Winship, Ian R., Fouad, Karim, Bennett, David J.
Publicado 2017

Blood and Intestine eQTLs from an Anti-TNF-Resistant Crohn's Disease Cohort Inform IBD Genetic Association Loci

por Di Narzo, Antonio F, Peters, Lauren A, Argmann, Carmen, Stojmirovic, Aleksandar, Perrigoue, Jacqueline, Li, Katherine, Telesco, Shannon, Kidd, Brian, Walker, Jennifer, Dudley, Joel, Cho, Judy, Schadt, Eric E, Kasarskis, Andrew, Curran, Mark, Dobrin, Radu, Hao, Ke
Publicado 2016

The HDAC9-associated risk locus promotes coronary artery disease by governing TWIST1

por Ma, Lijiang, Bryce, Nicole S., Turner, Adam W., Di Narzo, Antonio F., Rahman, Karishma, Xu, Yang, Ermel, Raili, Sukhavasi, Katyayani, d’Escamard, Valentina, Chandel, Nirupama, V’Gangula, Bhargavi, Wolhuter, Kathryn, Kadian-Dodov, Daniella, Franzen, Oscar, Ruusalepp, Arno, Hao, Ke, Miller, Clint L., Björkegren, Johan L. M., Kovacic, Jason C.
Publicado 2022

Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia

por Georges, Adrien, Albuisson, Juliette, Berrandou, Takiy, Dupré, Délia, Lorthioir, Aurélien, D’Escamard, Valentina, Di Narzo, Antonio F, Kadian-Dodov, Daniella, Olin, Jeffrey W, Warchol-Celinska, Ewa, Prejbisz, Aleksander, Januszewicz, Andrzej, Bruneval, Patrick, Baranowska, Anna A, Webb, Tom R, Hamby, Stephen E, Samani, Nilesh J, Adlam, David, Fendrikova-Mahlay, Natalia, Hazen, Stanley, Wang, Yu, Yang, Min-Lee, Hunker, Kristina, Combaret, Nicolas, Motreff, Pascal, Chédid, Antoine, Fiquet, Béatrice, Plouin, Pierre-François, Mousseaux, Elie, Azarine, Arshid, Amar, Laurence, Azizi, Michel, Gornik, Heather L, Ganesh, Santhi K, Kovacic, Jason C, Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Publicado 2020