AB053. NRG1 rare variant effects in Hirschsprung disease patients

per Gunadi, Budi, Nova, Iskandar, Kristy, Adrianto, Indra
Publicat a Ann Transl Med (2017)

Current Developments in Machine Learning Techniques in Biological Data Mining

per Dumancas, Gerard G, Adrianto, Indra, Bello, Ghalib, Dozmorov, Mikhail
Publicat a Bioinform Biol Insights (2017)

Single-Cell RNA-Seq Analysis Uncovers Distinct Functional Human NKT Cell Sub-Populations in Peripheral Blood

per Zhou, Li, Adrianto, Indra, Wang, Jie, Wu, Xiaojun, Datta, Indrani, Mi, Qing-Sheng
Publicat a Front Cell Dev Biol (2020)

Disease Activity in Lupus Correlates with Expression of the Transcription Factor ARID3a

per Ward, Julie M, Rose, Kira, Montgomery, Courtney, Adrianto, Indra, James, Judith A, Merrill, Joan T, Webb, Carol F
Publicat a Arthritis Rheumatol (2014)

Fine mapping of chromosome 15q25 implicates ZNF592 in neurosarcoidosis patients

per Lareau, Caleb A, Adrianto, Indra, Levin, Albert M, Iannuzzi, Michael C, Rybicki, Benjamin A, Montgomery, Courtney G
Publicat a Ann Clin Transl Neurol (2015)

Genome-Wide Association Scan of Dupuytren's Disease

per Ojwang, Joshua O., Adrianto, Indra, Gray-McGuire, Courtney, Nath, Swapan K., Harley, John B., Rayan, Ghazi M.
Publicat 2010

Role of NOD2 Pathway Genes in Sarcoidosis Cases with Clinical Characteristics of Blau Syndrome

per Bello, Ghalib A., Adrianto, Indra, Dumancas, Gerard G., Levin, Albert M., Iannuzzi, Michael C., Rybicki, Benjamin A., Montgomery, Courtney
Publicat a Am J Respir Crit Care Med (2015)

Extended methods for gene-environment-wide interaction scans in studies of admixed individuals with varying degrees of relationships.

per Chen, Yalei, Adrianto, Indra, Iannuzzi, Michael C., Garman, Lori, Montgomery, Courtney G., Rybicki, Benjamin A., Levin, Albert M., Li, Jia
Publicat a Genet Epidemiol (2019)

Performance of HLA allele prediction methods in African Americans for class II genes HLA-DRB1, −DQB1, and –DPB1

per Levin, Albert M, Adrianto, Indra, Datta, Indrani, Iannuzzi, Michael C, Trudeau, Sheri, McKeigue, Paul, Montgomery, Courtney G, Rybicki, Benjamin A
Publicat 2014

The Genomics of Autoimmune Disease in the Era of Genome-Wide Association Studies and Beyond

per Lessard, Christopher J, Ice, John A, Adrianto, Indra, Wiley, Graham, Kelly, Jennifer A, Gaffney, Patrick M, Montgomery, Courtney G, Moser, Kathy L
Publicat 2011

Genetics of Sjögren’s syndrome in the genome-wide association era

per Ice, John A., Li, He, Adrianto, Indra, Lin, Paul Chee, Kelly, Jennifer A., Montgomery, Courtney G., Lessard, Christopher J., Moser, Kathy L.
Publicat 2012

Association of HLA-DRB1 with Sarcoidosis Susceptibility and Progression in African Americans

per Levin, Albert M., Adrianto, Indra, Datta, Indrani, Iannuzzi, Michael C., Trudeau, Sheri, Li, Jia, Drake, Wonder P., Montgomery, Courtney G., Rybicki, Benjamin A.
Publicat a Am J Respir Cell Mol Biol (2015)

Down-regulation of E protein activity augments an ILC2 differentiation program in the thymus

per Wang, Hong-Cheng, Qian, Liangyue, Zhao, Ying, Mengarreli, Joni, Adrianto, Indra, Montgomery, Courtney G., Urban, Joseph F., Fung, Kar-Ming, Sun, Xiao-Hong
Publicat a J Immunol (2017)

Admixture Fine-Mapping in African Americans Implicates XAF1 as a Possible Sarcoidosis Risk Gene

per Levin, Albert M., Iannuzzi, Michael C., Montgomery, Courtney G., Trudeau, Sheri, Datta, Indrani, Adrianto, Indra, Chitale, Dhananjay A., McKeigue, Paul, Rybicki, Benjamin A.
Publicat 2014

NRG1 variant effects in patients with Hirschsprung disease

per Gunadi, Budi, Nova Yuli Prasetyo, Sethi, Raman, Fauzi, Aditya Rifqi, Kalim, Alvin Santoso, Indrawan, Taufik, Iskandar, Kristy, Makhmudi, Akhmad, Adrianto, Indra, San, Lai Poh
Publicat a BMC Pediatr (2018)

Suppression of ILC2 differentiation from committed T cell precursors by E protein transcription factors

per Qian, Liangyue, Bajana, Sandra, Georgescu, Constantin, Peng, Vincent, Wang, Hong-Cheng, Adrianto, Indra, Colonna, Marco, Alberola-Ila, Jose, Wren, Jonathan D., Sun, Xiao-Hong
Publicat a J Exp Med (2019)

Efficient Generalized Least Squares Method for Mixed Population and Family-based Samples in Genome-wide Association Studies

per Li, Jia, Yang, James, Levin, Albert M., Montgomery, Courtney G., Datta, Indrani, Trudeau, Sheri, Adrianto, Indra, McKeigue, Paul, Iannuzzi, Michael C., Rybicki, Benjamin A.
Publicat 2014

Histone deacetylase 3 controls lung alveolar macrophage development and homeostasis

per Yao, Yi, Liu, Queping, Adrianto, Indra, Wu, Xiaojun, Glassbrook, James, Khalasawi, Namir, Yin, Congcong, Yi, Qijun, Dong, Zheng, Geissmann, Frederic, Zhou, Li, Mi, Qing-Sheng
Publicat a Nat Commun (2020)

Genome-wide association study of ocular sarcoidosis confirms HLA associations and implicates barrier function and autoimmunity in African Americans

per Garman, Lori, Pezant, Nathan, Pastori, Ambra, Savoy, Kathryn A., Li, Chuang, Levin, Albert M., Iannuzzi, Michael C., Rybicki, Benjamin A., Adrianto, Indra, Montgomery, Courtney G.
Publicat a Ocul Immunol Inflamm (2020)

Polygenic Risk Assessment Reveals Pleiotropy between Sarcoidosis and Inflammatory Disorders in the Context of Genetic Ancestry

per Lareau, Caleb A., DeWeese, Colby F., Adrianto, Indra, Lessard, Christopher J., Gaffney, Patrick M., Iannuzzi, Michael C., Rybicki, Benjamin A., Levin, Albert M., Montgomery, Courtney G.
Publicat a Genes Immun (2017)