Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score von Onengut-Gumuscu, Suna, Chen, Wei-Min, Robertson, Catherine C, Bonnie, Jessica K, Farber, Emily, Zhu, Zhennan, Oksenberg, Jorge R, Brant, Steven R, Bridges, Jr, S Louis, Edberg, Jeffrey C, Kimberly, Robert P, Gregersen, Peter K, Rewers, Marian J, Steck, Andrea K, Black, Mary H, Dabelea, Dana, Pihoker, Catherine, Atkinson, Mark A, Wagenknecht, Lynne E, Divers, Jasmin, Bell, Ronny A, Erlich, Henry A, Concannon, Patrick, Rich, Stephen S

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Childhood body size directly increases type 1 diabetes risk based on a lifecourse Mendelian randomization approach von Richardson, Tom G., Crouch, Daniel J. M., Power, Grace M., Morales-Berstein, Fernanda, Hazelwood, Emma, Fang, Si, Cho, Yoonsu, Inshaw, Jamie R. J., Robertson, Catherine C., Sidore, Carlo, Cucca, Francesco, Rich, Steven S., Todd, John A., Davey Smith, George

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Untangling the genetics of beta cell dysfunction and death in type 1 diabetes von Robertson, Catherine C., Elgamal, Ruth M., Henry-Kanarek, Belle A., Arvan, Peter, Chen, Shuibing, Dhawan, Sangeeta, Eizirik, Decio L., Kaddis, John S., Vahedi, Golnaz, Parker, Stephen C.J., Gaulton, Kyle J., Soleimanpour, Scott A.

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Genetics of type 1 diabetes von .Robertson, Catherine C, Rich, Stephen S

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Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes von Robertson, Catherine C., Inshaw, Jamie R. J., Onengut-Gumuscu, Suna, Chen, Wei-Min, Santa Cruz, David Flores, Yang, Hanzhi, Cutler, Antony J., Crouch, Daniel J. M., Farber, Emily, Bridges, S. Louis, Edberg, Jeffrey C., Kimberly, Robert P., Buckner, Jane H., Deloukas, Panos, Divers, Jasmin, Dabelea, Dana, Lawrence, Jean M., Marcovina, Santica, Shah, Amy S., Greenbaum, Carla J., Atkinson, Mark A., Gregersen, Peter K., Oksenberg, Jorge R., Pociot, Flemming, Rewers, Marian J., Steck, Andrea K., Dunger, David B., Wicker, Linda S., Concannon, Patrick, Todd, John A., Rich, Stephen S.

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A multi-ancestry genome-wide association study in type 1 diabetes von Michalek, Dominika A, Tern, Courtney, Zhou, Wei, Robertson, Catherine C, Farber, Emily, Campolieto, Paul, Chen, Wei-Min, Onengut-Gumuscu, Suna, Rich, Stephen S

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Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects von Sampson, Matthew G, Robertson, Catherine C, Martini, Sebastian, Mariani, Laura H, Lemley, Kevin V, Gillies, Christopher E, Otto, Edgar A, Kopp, Jeffrey B, Randolph, Anne, Vega-Warner, Virginia, Eichinger, Felix, Nair, Viji, Gipson, Debbie S, Cattran, Daniel C, Johnstone, Duncan B, O'Toole, John F, Bagnasco, Serena M, Song, Peter X, Barisoni, Laura, Troost, Jonathan P, Kretzler, Matthias, Sedor, John R

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Human vascularized macrophage-islet organoids to model immune-mediated pancreatic β cell pyroptosis upon viral infection von Yang, Liuliu, Han, Yuling, Zhang, Tuo, Dong, Xue, Ge, Jian, Roy, Aadita, Zhu, Jiajun, Lu, Tiankun, Jeya Vandana, J., de Silva, Neranjan, Robertson, Catherine C., Xiang, Jenny Z., Pan, Chendong, Sun, Yanjie, Que, Jianwen, Evans, Todd, Liu, Chengyang, Wang, Wei, Naji, Ali, Parker, Stephen C.J., Schwartz, Robert E., Chen, Shuibing

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Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 h von Grenko, Caleb M., Taylor, Henry J., Bonnycastle, Lori L., Xue, Dongxiang, Lee, Brian N., Weiss, Zoe, Yan, Tingfen, Swift, Amy J., Mansell, Erin C., Lee, Angela, Robertson, Catherine C., Narisu, Narisu, Erdos, Michael R., Chen, Shuibing, Collins, Francis S., Taylor, D. Leland

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112-OR: Integrative Analysis of Chromatin Accessibility and Genetic Risk in T1D Patients and Controls von ROBERTSON, CATHERINE C., CHEN, WEI-MIN, ONENGUT-GUMUSCU, SUNA, CONCANNON, PATRICK J., RICH, STEPHEN S.

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Using Population Genetics to Interrogate the Monogenic Nephrotic Syndrome Diagnosis in a Case Cohort von Sampson, Matthew G, Gillies, Christopher E, Robertson, Catherine C, Crawford, Brendan, Vega-Warner, Virginia, Otto, Edgar A, Kretzler, Matthias, Kang, Hyun Min

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APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE)... von Ng, Derek K, Robertson, Catherine C, Woroniecki, Robert P, Limou, Sophie, Gillies, Christopher E, Reidy, Kimberly J, Winkler, Cheryl A, Hingorani, Sangeeta, Gibson, Keisha L, Hjorten, Rebecca, Sethna, Christine B, Kopp, Jeffrey B, Moxey-Mims, Marva, Furth, Susan L, Warady, Bradley A, Kretzler, Matthias, Sedor, John R, Kaskel, Frederick J, Sampson, Matthew G

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An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts von Robertson, Catherine C, Gillies, Christopher E, Putler, Rosemary K B, Ng, Derek, Reidy, Kimberly J, Crawford, Brendan, Sampson, Matthew G

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PRF1 mutation alters immune system activation, inflammation, and risk of autoimmunity von Sidore, Carlo, Orrù, Valeria, Cocco, Eleonora, Steri, Maristella, Inshaw, Jamie RJ, Pitzalis, Maristella, Mulas, Antonella, McGurnaghan, Stuart, Frau, Jessica, Porcu, Eleonora, Busonero, Fabio, Dei, Mariano, Lai, Sandra, Sole, Gabriella, Virdis, Francesca, Serra, Valentina, Poddie, Fausto, Delitala, Alessandro, Marongiu, Michele, Deidda, Francesca, Pala, Mauro, Floris, Matteo, Masala, Marco, Onengut-Gumuscu, Suna, Robertson, Catherine C, Leoni, Lidia, Frongia, Annapaola, Ricciardi, Maria Rossella, Chessa, Margherita, Olla, Nazario, Lovicu, Mario, Loizedda, Annalisa, Maschio, Andrea, Mereu, Luisa, Ferrigno, Paola, Curreli, Nicolo, Balaci, Lenuta, Loi, Francesco, Ferreli, Liana AP, Pilia, Maria Grazia, Pani, Antonello, Marrosu, Maria Giovanna, Abecasis, Goncalo R, Rich, Stephen S, Colhoun, Helen, Todd, John A, Schlessinger, David, Fiorillo, Edoardo, Cucca, Francesco, Zoledziewska, Magdalena

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GeneVetter: a web tool for quantitative monogenic assessment of rare diseases von Gillies, Christopher E, Robertson, Catherine C, Sampson, Matthew G, Kang, Hyun Min

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Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability von Crawford, Brendan D., Gillies, Christopher E., Robertson, Catherine C., Kretzler, Matthias, Otto, Edgar, Vega-Wagner, Virginia, Sampson, Matthew G.

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tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine von Gillies, Christopher E, Otto, Edgar A, Vega-Warner, Virginia, Robertson, Catherine C, Sanna-Cherchi, Simone, Gharavi, Ali, Crawford, Brendan, Bhimma, Rajendra, Winkler, Cheryl, Kang, Hyun Min, Sampson, Matthew G

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Erratum to: Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability von Crawford, Brendan D., Gillies, Christopher E., Robertson, Catherine C., Kretzler, Matthias, Otto, Edgar A., Vega-Warner, Virginia, Sampson, Matthew G.

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Analysis of Glucocorticoid-Related Genes Reveal CCHCR1 as a New Candidate Gene for Type 2 Diabetes von Brenner, Laura N, Mercader, Josep M, Robertson, Catherine C, Cole, Joanne, Chen, Ling, Jacobs, Suzanne B R, Rich, Stephen S, Florez, Jose C

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Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow-Up Studies von Crouch, Daniel J M, Inshaw, Jamie R J, Robertson, Catherine C, Ng, Esther, Zhang, Jia-Yuan, Chen, Wei-Min, Onengut-Gumuscu, Suna, Cutler, Antony J, Sidore, Carlo, Cucca, Francesco, Pociot, Flemming, Concannon, Patrick, Rich, Stephen S, Todd, John A

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