Powerful testing via hierarchical linkage disequilibrium in haplotype association studies

por Balliu, Brunilda, Houwing‐Duistermaat, Jeanine J., Böhringer, Stefan
Publicado 2019

Classification and Visualization Based on Derived Image Features: Application to Genetic Syndromes

por Balliu, Brunilda, Würtz, Rolf P., Horsthemke, Bernhard, Wieczorek, Dagmar, Böhringer, Stefan
Publicado 2014

Evaluating supervised and unsupervised background noise correction in human gut microbiome data

por Briscoe, Leah, Balliu, Brunilda, Sankararaman, Sriram, Halperin, Eran, Garud, Nandita R.
Publicado 2022

Distinctive facial features in idiopathic Moyamoya disease in Caucasians: a first systematic analysis

por Kraemer, Markus, Huynh, Quoc Bao, Wieczorek, Dagmar, Balliu, Brunilda, Mikat, Barbara, Boehringer, Stefan
Publicado 2018

Combining information from linkage and association mapping for next-generation sequencing longitudinal family data

por Balliu, Brunilda, Uh, Hae-Won, Tsonaka, Roula, Boehringer, Stefan, Helmer, Quinta, Houwing-Duistermaat, Jeanine J
Publicado 2014

Gene coexpression network analysis for family studies based on a meta-analytic approach

por Tissier, Renaud, Uh, Hae-Won, van den Akker, Erik, Balliu, Brunilda, Tsonaka, Spyridoula, Houwing-Duistermaat, Jeanine
Publicado 2016

Multi-context genetic modeling of transcriptional regulation resolves novel disease loci

por Thompson, Mike, Gordon, Mary Grace, Lu, Andrew, Tandon, Anchit, Halperin, Eran, Gusev, Alexander, Ye, Chun Jimmie, Balliu, Brunilda, Zaitlen, Noah
Publicado 2022

Association of image‐defined risk factors with clinical features, histopathology, and outcomes in neuroblastoma

por Temple, William C., Vo, Kieuhoa T., Matthay, Katherine K., Balliu, Brunilda, Coleman, Christina, Michlitsch, Jennifer, Phelps, Andrew, Behr, Spencer, Zapala, Matthew A.
Publicado 2020

Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms

por Liu, Boxiang, Calton, Melissa A., Abell, Nathan S., Benchorin, Gillie, Gloudemans, Michael J., Chen, Ming, Hu, Jane, Li, Xin, Balliu, Brunilda, Bok, Dean, Montgomery, Stephen B., Vollrath, Douglas
Publicado 2019

Integration of genetic colocalizations with physiological and pharmacological perturbations identifies cardiometabolic disease genes

por Gloudemans, Michael J., Balliu, Brunilda, Nachun, Daniel, Schnurr, Theresia M., Durrant, Matthew G., Ingelsson, Erik, Wabitsch, Martin, Quertermous, Thomas, Montgomery, Stephen B., Knowles, Joshua W., Carcamo-Orive, Ivan
Publicado 2022

Increased body mass index is linked to systemic inflammation through altered chromatin co-accessibility in human preadipocytes

por Garske, Kristina M., Kar, Asha, Comenho, Caroline, Balliu, Brunilda, Pan, David Z., Bhagat, Yash V., Rosenberg, Gregory, Koka, Amogha, Das, Sankha Subhra, Miao, Zong, Sinsheimer, Janet S., Kaprio, Jaakko, Pietiläinen, Kirsi H., Pajukanta, Päivi
Publicado 2023

RNA-seq data science: From raw data to effective interpretation

por Deshpande, Dhrithi, Chhugani, Karishma, Chang, Yutong, Karlsberg, Aaron, Loeffler, Caitlin, Zhang, Jinyang, Muszyńska, Agata, Munteanu, Viorel, Yang, Harry, Rotman, Jeremy, Tao, Laura, Balliu, Brunilda, Tseng, Elizabeth, Eskin, Eleazar, Zhao, Fangqing, Mohammadi, Pejman, P. Łabaj, Paweł, Mangul, Serghei
Publicado 2023

Technology dictates algorithms: recent developments in read alignment

por Alser, Mohammed, Rotman, Jeremy, Deshpande, Dhrithi, Taraszka, Kodi, Shi, Huwenbo, Baykal, Pelin Icer, Yang, Harry Taegyun, Xue, Victor, Knyazev, Sergey, Singer, Benjamin D., Balliu, Brunilda, Koslicki, David, Skums, Pavel, Zelikovsky, Alex, Alkan, Can, Mutlu, Onur, Mangul, Serghei
Publicado 2021

Genetic regulation of gene expression and splicing during a 10-year period of human aging

por Balliu, Brunilda, Durrant, Matthew, Goede, Olivia de, Abell, Nathan, Li, Xin, Liu, Boxiang, Gloudemans, Michael J., Cook, Naomi L., Smith, Kevin S., Knowles, David A., Pala, Mauro, Cucca, Francesco, Schlessinger, David, Jaiswal, Siddhartha, Sabatti, Chiara, Lind, Lars, Ingelsson, Erik, Montgomery, Stephen B.
Publicado 2019

A machine learning algorithm to increase COVID-19 inpatient diagnostic capacity

por Goodman-Meza, David, Rudas, Akos, Chiang, Jeffrey N., Adamson, Paul C., Ebinger, Joseph, Sun, Nancy, Botting, Patrick, Fulcher, Jennifer A., Saab, Faysal G., Brook, Rachel, Eskin, Eleazar, An, Ulzee, Kordi, Misagh, Jew, Brandon, Balliu, Brunilda, Chen, Zeyuan, Hill, Brian L., Rahmani, Elior, Halperin, Eran, Manuel, Vladimir
Publicado 2020

Impact of the X Chromosome and sex on regulatory variation

por Kukurba, Kimberly R., Parsana, Princy, Balliu, Brunilda, Smith, Kevin S., Zappala, Zachary, Knowles, David A., Favé, Marie-Julie, Davis, Joe R., Li, Xin, Zhu, Xiaowei, Potash, James B., Weissman, Myrna M., Shi, Jianxin, Kundaje, Anshul, Levinson, Douglas F., Awadalla, Philip, Mostafavi, Sara, Battle, Alexis, Montgomery, Stephen B.
Publicado 2016

Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTEx

por Gay, Nicole R., Gloudemans, Michael, Antonio, Margaret L., Abell, Nathan S., Balliu, Brunilda, Park, YoSon, Martin, Alicia R., Musharoff, Shaila, Rao, Abhiram S., Aguet, François, Barbeira, Alvaro N., Bonazzola, Rodrigo, Hormozdiari, Farhad, Ardlie, Kristin G., Brown, Christopher D., Im, Hae Kyung, Lappalainen, Tuuli, Wen, Xiaoquan, Montgomery, Stephen B.
Publicado 2020

Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

por Johnson, Ruth, Ding, Yi, Venkateswaran, Vidhya, Bhattacharya, Arjun, Boulier, Kristin, Chiu, Alec, Knyazev, Sergey, Schwarz, Tommer, Freund, Malika, Zhan, Lingyu, Burch, Kathryn S., Caggiano, Christa, Hill, Brian, Rakocz, Nadav, Balliu, Brunilda, Denny, Christopher T., Sul, Jae Hoon, Zaitlen, Noah, Arboleda, Valerie A., Halperin, Eran, Sankararaman, Sriram, Butte, Manish J., Lajonchere, Clara, Geschwind, Daniel H., Pasaniuc, Bogdan
Publicado 2022

Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

por Johnson, Ruth, Ding, Yi, Venkateswaran, Vidhya, Bhattacharya, Arjun, Boulier, Kristin, Chiu, Alec, Knyazev, Sergey, Schwarz, Tommer, Freund, Malika, Zhan, Lingyu, Burch, Kathryn S., Caggiano, Christa, Hill, Brian, Rakocz, Nadav, Balliu, Brunilda, Denny, Christopher T., Sul, Jae Hoon, Zaitlen, Noah, Arboleda, Valerie A., Halperin, Eran, Sankararaman, Sriram, Butte, Manish J., Lajonchere, Clara, Geschwind, Daniel H., Pasaniuc, Bogdan
Publicado 2022

Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts

por Frésard, Laure, Smail, Craig, Ferraro, Nicole M., Teran, Nicole A., Li, Xin, Smith, Kevin S., Bonner, Devon, Kernohan, Kristin D., Marwaha, Shruti, Zappala, Zachary, Balliu, Brunilda, Davis, Joe R., Liu, Boxiang, Prybol, Cameron J., Kohler, Jennefer N., Zastrow, Diane B., Reuter, Chloe M., Fisk, Dianna G., Grove, Megan E., Davidson, Jean M., Hartley, Taila, Joshi, Ruchi, Strober, Benjamin J., Utiramerur, Sowmithri, Lind, Lars, Ingelsson, Erik, Battle, Alexis, Bejerano, Gill, Bernstein, Jonathan A., Ashley, Euan A., Boycott, Kym M., Merker, Jason D., Wheeler, Matthew T., Montgomery, Stephen B.
Publicado 2019