COVID-19-Associated Glomerular Disease von Shetty, Aneesha A, Tawhari, Ibrahim, Safar-Boueri, Luisa, Seif, Nay, Alahmadi, Ameen, Gargiulo, Richard, Aggarwal, Vikram, Usman, Irtaza, Kisselev, Sergey, Gharavi, Ali G, Kanwar, Yahspal, Quaggin, Susan E

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Genetic basis of human congenital anomalies of the kidney and urinary tract von Sanna-Cherchi, Simone, Westland, Rik, Ghiggeri, Gian Marco, Gharavi, Ali G

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Pathogenesis of Immunoglobulin A Nephropathy: Recent Insight from Genetic Studies von Kiryluk, Krzysztof, Novak, Jan, Gharavi, Ali G

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Predicting progression of IgA nephropathy: new clinical progression risk score von Xie, Jingyuan, Kiryluk, Krzysztof, Wang, Weiming, Wang, Zhaohui, Guo, Shanmai, Shen, Pingyan, Ren, Hong, Pan, Xiaoxia, Chen, Xiaonong, Zhang, Wen, Li, Xiao, Shi, Hao, Li, Yifu, Gharavi, Ali G, Chen, Nan

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Deep Phenotyping on Electronic Health Records Facilitates Genetic Diagnosis by Clinical Exomes von Son, Jung Hoon, Xie, Gangcai, Yuan, Chi, Ena, Lyudmila, Li, Ziran, Goldstein, Andrew, Huang, Lulin, Wang, Liwei, Shen, Feichen, Liu, Hongfang, Mehl, Karla, Groopman, Emily E., Marasa, Maddalena, Kiryluk, Krzysztof, Gharavi, Ali G., Chung, Wendy K., Hripcsak, George, Friedman, Carol, Weng, Chunhua, Wang, Kai

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Polygenic risk alters the penetrance of monogenic kidney disease von Khan, Atlas, Shang, Ning, Nestor, Jordan G., Weng, Chunhua, Hripcsak, George, Harris, Peter C., Gharavi, Ali G., Kiryluk, Krzysztof

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A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases von Yanagawa, Hiroyuki, Suzuki, Hitoshi, Suzuki, Yusuke, Kiryluk, Krzysztof, Gharavi, Ali G, Matsuoka, Kiyoshi, Makita, Yuko, Julian, Bruce A, Novak, Jan, Tomino, Yasuhiko

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GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway von Kiryluk, Krzysztof, Li, Yifu, Moldoveanu, Zina, Suzuki, Hitoshi, Reily, Colin, Hou, Ping, Xie, Jingyuan, Mladkova, Nikol, Prakash, Sindhuri, Fischman, Clara, Shapiro, Samantha, LeDesma, Robert A, Bradbury, Drew, Ionita-Laza, Iuliana, Eitner, Frank, Rauen, Thomas, Maillard, Nicolas, Berthoux, Francois, Floege, Jürgen, Chen, Nan, Zhang, Hong, Scolari, Francesco, Wyatt, Robert J, Julian, Bruce A, Gharavi, Ali G, Novak, Jan

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Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch–Schönlein purpura nephritis von Kiryluk, Krzysztof, Moldoveanu, Zina, Sanders, John T., Eison, T. Matthew, Suzuki, Hitoshi, Julian, Bruce A., Novak, Jan, Gharavi, Ali G., Wyatt, Robert J.

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Experimental evidence of pathogenic role of IgG autoantibodies in IgA nephropathy von Moldoveanu, Zina, Suzuki, Hitoshi, Reily, Colin, Satake, Kenji, Novak, Lea, Xu, Nuo, Huang, Zhi-Qiang, Knoppova, Barbora, Khan, Atlas, Hall, Stacy, Yanagawa, Hiroyuki, Brown, Rhubell, Winstead, Colleen J., O'Quinn, Darrell B., Weinmann, Amy, Gharavi, Ali G., Kiryluk, Krzysztof, Julian, Bruce A., Weaver, Casey T., Suzuki, Yusuke, Novak, Jan

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IgA nephropathy: molecular mechanisms of the disease von Mestecky, Jiri, Raska, Milan, Julian, Bruce A, Gharavi, Ali G, Renfrow, Matthew B, Moldoveanu, Zina, Novak, Lea, Matousovic, Karel, Novak, Jan

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Aberrant IgA1 Glycosylation Is Inherited in Familial and Sporadic IgA Nephropathy von GHARAVI, Ali G, MOLDOVEANU, Zina, WYATT, Robert J, BARKER, Catherine V, WOODFORD, Susan Y, LIFTON, Richard P, MESTECKY, Jiri, NOVAK, Jan, JULIAN, Bruce A

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Phenotypic Expansion of DGKE-Associated Diseases von WESTLAND, Rik, BODRIA, Monica, SANNA-CHERCHI, Simone, CARREA, Alba, LATA, Sneh, SCOLARI, Francesco, FREMEAUX-BACCHI, Veronique, D'AGATI, Vivette D, LIFTON, Richard P, GHARAVI, Ali G, GHIGGERI, Gian Marco

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The diagnostic yield of exome sequencing in liver diseases from a curated gene panel von Kong, Xiao-Fei, Bogyo, Kelsie, Kapoor, Sheena, Shea, Patrick R., Groopman, Emily E., Thomas-Wilson, Amanda, Cocchi, Enrico, Milo Rasouly, Hila, Zheng, Beishi, Sun, Siming, Zhang, Junying, Martinez, Mercedes, Vittorio, Jennifer M., Dove, Lorna M., Marasa, Maddalena, Wang, Timothy C., Verna, Elizabeth C., Worman, Howard J., Gharavi, Ali G., Goldstein, David B., Wattacheril, Julia

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Leukemia Inhibitory Factor Signaling Enhances Production of Galactose-Deficient IgA1 in IgA Nephropathy von Yamada, Koshi, Huang, Zhi qiang, Raska, Milan, Reily, Colin, Anderson, Joshua C., Suzuki, Hitoshi, Kiryluk, Krzysztof, Gharavi, Ali G., Julian, Bruce A., Willey, Christopher D., Novak, Jan

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Clinical Genetic Screening in Adult Patients with Kidney Disease von Cocchi, Enrico, Nestor, Jordan Gabriela, Gharavi, Ali G

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Medical Records-Based Genetic Studies of the Complement System von Khan, Atlas, Shang, Ning, Petukhova, Lynn, Zhang, Jun, Shen, Yufeng, Hebbring, Scott J, Moncrieffe, Halima, Kottyan, Leah C, Namjou-Khales, Bahram, Knevel, Rachel, Raychaudhuri, Soumya, Karlson, Elizabeth W, Harley, John B, Stanaway, Ian B, Crosslin, David, Denny, Joshua C, Elkind, Mitchell S V, Gharavi, Ali G, Hripcsak, George, Weng, Chunhua, Kiryluk, Krzysztof

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HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort von Thomas, Rosemary, Sanna-Cherchi, Simone, Warady, Bradley A., Furth, Susan L., Kaskel, Frederick J., Gharavi, Ali G.

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Emerging Genetic Insight into ATIN von Khan, Atlas, Gharavi, Ali G

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Genetic testing for kidney disease of unknown etiology von Hays, Thomas, Groopman, Emily E., Gharavi, Ali G.

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