Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset

par Gui, Hongsheng, Li, Miaoxin, Sham, Pak C, Cherny, Stacey S
Publié 2011

The Contribution of Genetic Diversity to Subdivide Populations Living in the Silk Road of China

par Zhang, Zhe, Wei, Shuguang, Gui, Hongsheng, Yuan, Zuyi, Li, Shengbin
Publié 2014

Sharing of Genes and Pathways Across Complex Phenotypes: A Multilevel Genome-Wide Analysis

par Gui, Hongsheng, Kwan, Johnny S., Sham, Pak C., Cherny, Stacey S., Li, Miaoxin
Publié dans Genetics (2017)

Genetics of heart rate in heart failure patients (GenHRate)

par Evans, Kaleigh L., Wirtz, Heidi S., Li, Jia, She, Ruicong, Maya, Juan, Gui, Hongsheng, Hamer, Andrew, Depre, Christophe, Lanfear, David E.
Publié dans Hum Genomics (2019)

Plasma Proteomic Profile Predicts Survival in Heart Failure with Reduced Ejection Fraction

par Gui, Hongsheng, She, Ruicong, Luzum, Jasmine, Li, Jia, Bryson, Timothy D., Pinto, Yigal, Sabbah, Hani N., Williams, L. Keoki, Lanfear, David E.
Publié dans Circ Genom Precis Med (2021)

Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis

par Wong, John K.L., Gui, Hongsheng, Kwok, Maxwell, Ng, Ping Wing, Lui, Colin H.T., Baum, Larry, Sham, Pak Chung, Kwan, Patrick, Cherny, Stacey S.
Publié dans Neurol Genet (2018)

Performance of the Meta-Analysis Global Group in Chronic Heart Failure (MAGGIC) Score in African American Patients Compared to Whites

par Radjef, Ryhm, Peterson, Edward L., Michaels, Alexander, Liu, Bin, Gui, Hongsheng, Sabbah, Hani N., Spertus, John A., Williams, L. Keoki, Lanfear, David E.
Publié dans Circ Cardiovasc Qual Outcomes (2019)

Association of Regulatory Genetic Variants for Protein Kinase C α with Mortality and Drug Efficacy in Patients with Heart Failure

par Luzum, Jasmine A., Ting, Christopher, Peterson, Edward L., Gui, Hongsheng, Shugg, Tyler, Williams, L. Keoki, Li, Liang, Sadee, Wolfgang, Wang, Danxin, Lanfear, David E.
Publié dans Cardiovasc Drugs Ther (2019)

Suppression Tumorigenicity 2 (ST2) Turbidimetric Immunoassay Compared to Enzyme-Linked Immunosorbent Assay in Predicting Survival in Heart Failure Patients with Reduced Ejection Fr...

par Aurora, Lindsey, Peterson, Edward, Gui, Hongsheng, Zeld, Nicole, McCord, James, Pinto, Yigal, Cook, Bernard, Sabbah, Hani N., Williams, L. Keoki, Snider, James, Lanfear, David E.
Publié dans Clin Chim Acta (2020)

Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet

par Basil, Paul, Li, Qi, Gui, Hongsheng, Hui, Tomy C. K., Ling, Vicki H. M., Wong, Chloe C. Y., Mill, Jonathan, McAlonan, Grainne M., Sham, Pak-Chung
Publié dans Transl Psychiatry (2018)

Race and Beta‐Blocker Survival Benefit in Patients With Heart Failure: An Investigation of Self‐Reported Race and Proportion of African Genetic Ancestry

par Luzum, Jasmine A., Peterson, Edward, Li, Jia, She, Ruicong, Gui, Hongsheng, Liu, Bin, Spertus, John A., Pinto, Yigal M., Williams, L. Keoki, Sabbah, Hani N., Lanfear, David E.
Publié dans J Am Heart Assoc (2018)

A Genome-Wide Linkage and Association Scan Reveals Novel Loci for Hypertension and Blood Pressure Traits

par Guo, Youling, Tomlinson, Brian, Chu, Tanya, Fang, Yu Jing, Gui, Hongsheng, Tang, Clara S., Yip, Benjamin H., Cherny, Stacey S., Hur, Yoon-Mi, Sham, Pak Chung, Lam, Tai Hing, Thomas, Neil G.
Publié 2012

Correction: A Genome-Wide Linkage and Association Scan Reveals Novel Loci for Hypertension and Blood Pressure Traits

par Guo, Youling, Tomlinson, Brian, Chu, Tanya, Fang, Yu Jing, Gui, Hongsheng, Tang, Clara S., Yip, Benjamin H., Cherny, Stacey S., Hur, Yoon-Mi, Sham, Pak Chung, Lam, Tai Hing, Thomas, Neil G.
Publié 2012

Polygenic Score for Beta-Blocker Survival Benefit in European Ancestry Patients with Reduced Ejection Fraction Heart Failure

par Lanfear, David E., Luzum, Jasmine A., She, Ruicong, Gui, Hongsheng, Donahue, Mark P., O’Connor, Christopher M., Adams, Kirkwood F., Sanders-van Wijk, Sandra, Zeld, Nicole, Maeder, Micha T., Sabbah, Hani N., Kraus, William E., Brunner-LaRocca, Hans-Peter, Li, Jia, Williams, L. Keoki
Publié dans Circ Heart Fail (2020)

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

par Luzón-Toro, Berta, Gui, Hongsheng, Ruiz-Ferrer, Macarena, Sze-Man Tang, Clara, Fernández, Raquel M., Sham, Pak-Chung, Torroglosa, Ana, Kwong-Hang Tam, Paul, Espino-Paisán, Laura, Cherny, Stacey S., Bleda, Marta, Enguix-Riego, María del Valle, Dopazo, Joaquín, Antiñolo, Guillermo, García-Barceló, María-Mercé, Borrego, Salud
Publié dans Sci Rep (2015)

Integrative approach identifies corticosteroid response variant in diverse populations with asthma

par Levin, Albert M., Gui, Hongsheng, Hernandez-Pacheco, Natalia, Yang, Mao, Xiao, Shujie, Yang, James J., Hochstadt, Samantha, Barczak, Andrea J., Eckalbar, Walter L., Rynkowski, Dean, Samedy, Lesly-Anne, Kwok, Pui-Yan, Pino-Yanes, Maria, Erle, David J., Lanfear, David E., Burchard, Esteban G., Williams, L. Keoki
Publié dans J Allergy Clin Immunol (2018)

Asthma and its relationship to mitochondrial copy number: Results from the Asthma Translational Genomics Collaborative (ATGC) of the Trans-Omics for Precision Medicine (TOPMed) pro...

par Cocco, Maxwell P., White, Evan, Xiao, Shujie, Hu, Donglei, Mak, Angel, Sleiman, Patrick, Yang, Mao, Bobbitt, Kevin R., Gui, Hongsheng, Levin, Albert M., Hochstadt, Samantha, Whitehouse, Kyle, Rynkowski, Dean, Barczak, Andrea J., Abecasis, Gonçalo, Blackwell, Thomas W., Kang, Hyun Min, Nickerson, Deborah A., Germer, Soren, Ding, Jun, Lanfear, David E., Gilliland, Frank, Gauderman, W. James, Kumar, Rajesh, Erle, David J., Martinez, Fernando, Hakonarson, Hakon, Burchard, Esteban G., Williams, L. Keoki
Publié dans PLoS One (2020)

Mapping the 17q12–21.1 Locus for Variants Associated with Early-Onset Asthma in African Americans

par Gui, Hongsheng, Levin, Albert M., Hu, Donglei, Sleiman, Patrick, Xiao, Shujie, Mak, Angel C. Y., Yang, Mao, Barczak, Andrea J., Huntsman, Scott, Eng, Celeste, Hochstadt, Samantha, Zhang, Ellen, Whitehouse, Kyle, Simons, Samantha, Cabral, Whitney, Takriti, Sami, Abecasis, Gonçalo, Blackwell, Thomas W., Kang, Hyun Min, Nickerson, Deborah A., Germer, Soren, Lanfear, David E., Gilliland, Frank, Gauderman, W. James, Kumar, Rajesh, Erle, David J., Martinez, Fernando D., Hakonarson, Hakon, Burchard, Esteban G., Williams, L. Keoki
Publié dans Am J Respir Crit Care Med (2021)

Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

par Kachroo, Priyadarshini, Hecker, Julian, Chawes, Bo L., Ahluwalia, Tarunveer S., Cho, Michael H., Qiao, Dandi, Kelly, Rachel S., Chu, Su H., Virkud, Yamini V., Huang, Mengna, Barnes, Kathleen C., Burchard, Esteban G., Eng, Celeste, Hu, Donglei, Celedón, Juan C., Daya, Michelle, Levin, Albert M., Gui, Hongsheng, Williams, L. Keoki, Forno, Erick, Mak, Angel C.Y., Avila, Lydiana, Soto-Quiros, Manuel E., Cloutier, Michelle M., Acosta-Pérez, Edna, Canino, Glorisa, Bønnelykke, Klaus, Bisgaard, Hans, Raby, Benjamin A., Lange, Christoph, Weiss, Scott T., Lasky-Su, Jessica A.
Publié dans Chest (2019)

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease

par Tang, Clara Sze-man, Gui, Hongsheng, Kapoor, Ashish, Kim, Jeong-Hyun, Luzón-Toro, Berta, Pelet, Anna, Burzynski, Grzegorz, Lantieri, Francesca, So, Man-ting, Berrios, Courtney, Shin, Hyoung Doo, Fernández, Raquel M., Le, Thuy-Linh, Verheij, Joke B.G.M., Matera, Ivana, Cherny, Stacey S., Nandakumar, Priyanka, Cheong, Hyun Sub, Antiñolo, Guillermo, Amiel, Jeanne, Seo, Jeong-Meen, Kim, Dae-Yeon, Oh, Jung-Tak, Lyonnet, Stanislas, Borrego, Salud, Ceccherini, Isabella, Hofstra, Robert M.W., Chakravarti, Aravinda, Kim, Hyun-Young, Sham, Pak Chung, Tam, Paul K.H., Garcia-Barceló, Maria-Mercè
Publié dans Hum Mol Genet (2016)