Current Developments in Detection of Identity-by-Descent Methods and Applications

por Sticca, Evan L., Belbin, Gillian M., Gignoux, Christopher R.
Publicado 2021

Rapid detection of identity-by-descent tracts for mega-scale datasets

por Shemirani, Ruhollah, Belbin, Gillian M., Avery, Christy L., Kenny, Eimear E., Gignoux, Christopher R., Ambite, José Luis
Publicado 2021

The role of country of birth, and genetic and self-identified ancestry, in obesity susceptibility among African and Hispanic Americans

por Vishnu, Abhishek, Belbin, Gillian M, Wojcik, Genevieve L, Bottinger, Erwin P, Gignoux, Christopher R, Kenny, Eimear E, Loos, Ruth J F
Publicado 2019

Selecting Clustering Algorithms for Identity-By-Descent Mapping

por Shemirani, Ruhollah, Belbin, Gillian M, Burghardt, Keith, Lerman, Kristina, Avery, Christy L, Kenny, Eimear E, Gignoux, Christopher R, Ambite, José Luis
Publicado 2023

Genome-wide analysis indicates association between heterozygote advantage and healthy aging in humans

por Xu, Ke, Kosoy, Roman, Shameer, Khader, Kumar, Sudhir, Liu, Li, Readhead, Ben, Belbin, Gillian M., Lee, Hao-Chih, Chen, Rong, Dudley, Joel T.
Publicado 2019

Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry

por Wenric, Stephane, Jeff, Janina M., Joseph, Thomas, Yee, Muh-Ching, Belbin, Gillian M., Owusu Obeng, Aniwaa, Ellis, Stephen B., Bottinger, Erwin P., Gottesman, Omri, Levin, Matthew A., Kenny, Eimear E.
Publicado 2020

Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank

por Abul-Husn, Noura S., Soper, Emily R., Odgis, Jacqueline A., Cullina, Sinead, Bobo, Dean, Moscati, Arden, Rodriguez, Jessica E., Loos, Ruth J. F., Cho, Judy H., Belbin, Gillian M., Suckiel, Sabrina A., Kenny, Eimear E.
Publicado 2019

Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35

por Cullina, Sinead, Wojcik, Genevieve L., Shemirani, Ruhollah, Klarin, Derek, Gorman, Bryan R., Sorokin, Elena P., Gignoux, Christopher R., Belbin, Gillian M., Pyarajan, Saiju, Asgari, Samira, Tsao, Philip S., Damrauer, Scott M., Abul-Husn, Noura S., Kenny, Eimear E.
Publicado 2023

Implementing genomic screening in diverse populations

por Abul-Husn, Noura S., Soper, Emily R., Braganza, Giovanna T., Rodriguez, Jessica E., Zeid, Natasha, Cullina, Sinead, Bobo, Dean, Moscati, Arden, Merkelson, Amanda, Loos, Ruth J. F., Cho, Judy H., Belbin, Gillian M., Suckiel, Sabrina A., Kenny, Eimear E.
Publicado 2021

Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits

por Glicksberg, Benjamin S., Amadori, Letizia, Akers, Nicholas K., Sukhavasi, Katyayani, Franzén, Oscar, Li, Li, Belbin, Gillian M., Akers, Kristin L., Shameer, Khader, Badgeley, Marcus A., Johnson, Kipp W., Readhead, Ben, Darrow, Bruce J., Kenny, Eimear E., Betsholtz, Christer, Ermel, Raili, Skogsberg, Josefin, Ruusalepp, Arno, Schadt, Eric E., Dudley, Joel T., Ren, Hongxia, Kovacic, Jason C., Giannarelli, Chiara, Li, Shuyu D., Björkegren, Johan L. M., Chen, Rong
Publicado 2019

Correction to: Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits

por Glicksberg, Benjamin S., Amadori, Letizia, Akers, Nicholas K., Sukhavasi, Katyayani, Franzén, Oscar, Li, Li, Belbin, Gillian M., Ayers, Kristin L., Shameer, Khader, Badgeley, Marcus A., Johnson, Kipp W., Readhead, Ben, Darrow, Bruce J., Kenny, Eimear E., Betsholtz, Christer, Ermel, Raili, Skogsberg, Josefin, Ruusalepp, Arno, Schadt, Eric E., Dudley, Joel T., Ren, Hongxia, Kovacic, Jason C., Giannarelli, Chiara, Li, Shuyu D., Björkegren, Johan L. M., Chen, Rong
Publicado 2019

An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease

por Cohain, Ariella T., Barrington, William T., Jordan, Daniel M., Beckmann, Noam D., Argmann, Carmen A., Houten, Sander M., Charney, Alexander W., Ermel, Raili, Sukhavasi, Katyayani, Franzen, Oscar, Koplev, Simon, Whatling, Carl, Belbin, Gillian M., Yang, Jialiang, Hao, Ke, Kenny, Eimear E., Tu, Zhidong, Zhu, Jun, Gan, Li-Ming, Do, Ron, Giannarelli, Chiara, Kovacic, Jason C., Ruusalepp, Arno, Lusis, Aldons J., Bjorkegren, Johan L. M., Schadt, Eric E.
Publicado 2021

Multiscale causal networks identify VGF as a key regulator of Alzheimer’s disease

por Beckmann, Noam D., Lin, Wei-Jye, Wang, Minghui, Cohain, Ariella T., Charney, Alexander W., Wang, Pei, Ma, Weiping, Wang, Ying-Chih, Jiang, Cheng, Audrain, Mickael, Comella, Phillip H., Fakira, Amanda K., Hariharan, Siddharth P., Belbin, Gillian M., Girdhar, Kiran, Levey, Allan I., Seyfried, Nicholas T., Dammer, Eric B., Duong, Duc, Lah, James J., Haure-Mirande, Jean-Vianney, Shackleton, Ben, Fanutza, Tomas, Blitzer, Robert, Kenny, Eimear, Zhu, Jun, Haroutunian, Vahram, Katsel, Pavel, Gandy, Sam, Tu, Zhidong, Ehrlich, Michelle E., Zhang, Bin, Salton, Stephen R., Schadt, Eric E.
Publicado 2020

Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations

por Bonnemaijer, Pieter W. M., Iglesias, Adriana I., Nadkarni, Girish N., Sanyiwa, Anna J., Hassan, Hassan G., Cook, Colin, Simcoe, Mark, Taylor, Kent D., Schurmann, Claudia, Belbin, Gillian M., Kenny, Eimear E., Bottinger, Erwin P., van de Laar, Suzanne, Wiliams, Susan E. I., Akafo, Stephen K., Ashaye, Adeyinka O., Zangwill, Linda M., Girkin, Christopher A., Ng, Maggie C. Y., Rotter, Jerome I., Weinreb, Robert N., Li, Zheng, Allingham, R. Rand, Nag, Abhishek, Hysi, Pirro G., Meester-Smoor, Magda A., Wiggs, Janey L, Hauser, Michael A., Hammond, Christopher J., Lemij, Hans G., Loos, Ruth J. F., van Duijn, Cornelia M., Thiadens, Alberta A. H. J., Klaver, Caroline C. W.
Publicado 2018