Update of variants identified in the pancreatic β‐cell KATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes von De Franco, Elisa, Saint‐Martin, Cécile, Brusgaard, Klaus, Knight Johnson, Amy E., Aguilar‐Bryan, Lydia, Bowman, Pamela, Arnoux, Jean‐Baptiste, Larsen, Annette Rønholt, May, Sanyoura, Greeley, Siri Atma W., Calzada‐León, Raúl, Harman, Bradley, Houghton, Jayne A. L., Nishimura‐Meguro, Elisa, Laver, Thomas W., Ellard, Sian, Gaudio, Daniela, Christesen, Henrik Thybo, Bellanné‐Chantelot, Christine, Flanagan, Sarah E.

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Monogenic Diabetes in Children and Adolescents: Recognition and Treatment Options von Sanyoura, May, Philipson, Louis H., Naylor, Rochelle

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Update of variants identified in the pancreatic beta-cell K-ATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes von De Franco, Elisa, Saint-Martin, Cecile, Brusgaard, Klaus, Knight Johnson, Amy E., Aguilar-Bryan, Lydia, Bowman, Pamela, Arnoux, Jean-Baptiste, Larsen, Annette Ronholt, May, Sanyoura, Greeley, Siri Atma W., Calzada-Leon, Raul, Harman, Bradley, Houghton, Jayne A. L., Nishimura-Meguro, Elisa, Laver, Thomas W., Ellard, Sian, del Gaudio, Daniela, Christesen, Henrik Thybo, Bellanne-Chantelot, Christine, Flanagan, Sarah E.

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α Cell Function and Gene Expression Are Compromised in Type 1 Diabetes von Brissova, Marcela, Haliyur, Rachana, Saunders, Diane, Shrestha, Shristi, Dai, Chunhua, Blodgett, David M., Bottino, Rita, Campbell-Thompson, Martha, Aramandla, Radhika, Poffenberger, Gregory, Lindner, Jill, Pan, Fong Cheng, von Herrath, Matthias G., Greiner, Dale L., Shultz, Leonard D., Sanyoura, May, Philipson, Louis H., Atkinson, Mark, Harlan, David M., Levy, Shawn E., Prasad, Nripesh, Stein, Roland, Powers, Alvin C.

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Diabetes Presentation in Infancy: High Risk of Diabetic Ketoacidosis von Letourneau, Lisa R, Carmody, David, Wroblewski, Kristen, Denson, Anna M, Sanyoura, May, Naylor, Rochelle N, Philipson, Louis H, Greeley, Siri Atma W

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P242: Tissue specific pathogenic NIPBL variant causing Cornelia de Lange syndrome: A call to clinicians von Mehta, Lakshmi, Begun, Yakira, Sanyoura, May, Stanley, Christine

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Management and pregnancy outcomes of women with GCK-MODY enrolled in the US Monogenic Diabetes Registry von Dickens, Laura T., Letourneau, Lisa R., Sanyoura, May, Greeley, Siri Atma W., Philipson, Louis H., Naylor, Rochelle N.

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Pancreatic Histopathology of Human Monogenic Diabetes Due to Causal Variants in KCNJ11, HNF1A, GATA6, and LMNA von Sanyoura, May, Jacobsen, Laura, Carmody, David, del Gaudio, Daniela, Alkorta-Aranburu, Gorka, Arndt, Kelly, Hu, Ying, Kobiernicki, Frances, Kusmartseva, Irina, Atkinson, Mark A, Philipson, Louis H, Schatz, Desmond, Campbell-Thompson, Martha, Greeley, Siri Atma W

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GCK-MODY in the US Monogenic Diabetes Registry: Description of 27 unpublished variants von Sanyoura, May, Letourneau, Lisa, Knight Johnson, Amy E., del Gaudio, Daniela, Greeley, Siri Atma W., Philipson, Louis H., Naylor, Rochelle N.

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FOXP3 mutations causing early‐onset insulin‐requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked syndrome von Hwang, Jessica L, Park, Soo‐Young, Ye, Honggang, Sanyoura, May, Pastore, Ashley N, Carmody, David, del Gaudio, Daniela, Wilson, Janna F, Hanis, Craig L, Liu, Xiaoming, Atzmon, Gil, Glaser, Benjamin, Philipson, Louis H, Greeley, Siri Atma W

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P453: Diagnostic yield of copy number variants by exome sequencing vs chromosomal microarray von Douglas, Ganka, Meck, Jeanne, Dyer, Lindsay Havens, Brandon, Rhonda, Dyer, Lisa, Ferri, Patricia Fernandez, Liao, Mingjuan, Liu, Shuxi, Matyakhina, Ludmila, Rajcan-Separovic, Evica, Sack, Laura, Sanyoura, May, Wang, Wei, Kruszka, Paul

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WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon von Zalloua, Pierre A., Azar, Sami T., Delépine, Marc, Makhoul, Nadine J., Blanc, Hervé, Sanyoura, May, Lavergne, Anne, Stankov, Karmen, Lemainque, Arnaud, Baz, Patrick, Julier, Cécile

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Geographical Structure of the Y‐chromosomal Genetic Landscape of the Levant: A coastal‐inland contrast von El‐Sibai, Mirvat, Platt, Daniel E., Haber, Marc, Xue, Yali, Youhanna, Sonia C., Wells, R. Spencer, Izaabel, Hassan, Sanyoura, May F., Harmanani, Haidar, Bonab, Maziar Ashrafian, Behbehani, Jaafar, Hashwa, Fuad, Tyler‐Smith, Chris, Zalloua, Pierre A.

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Human islets expressing HNF1A variant have defective β cell transcriptional regulatory networks von Haliyur, Rachana, Tong, Xin, Sanyoura, May, Shrestha, Shristi, Lindner, Jill, Saunders, Diane C, Aramandla, Radhika, Poffenberger, Greg, Redick, Sambra D, Bottino, Rita, Prasad, Nripesh, Levy, Shawn E, Blind, Raymond D, Harlan, David M, Philipson, Louis H, Stein, Roland W, Brissova, Marcela, Powers, Alvin C

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Novel compound heterozygous LRBA deletions in a 6-month-old with neonatal diabetes von Sanyoura, May, Lundgrin, Erika L., Subramanian, Hari Prasanna, Yu, Min, Sodadasi, Priscilla, Greeley, Siri Atma W., MacLeish, Sarah, del Gaudio, Daniela

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De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis von Timberlake, Andrew T., McGee, Stephen, Allington, Garrett, Kiziltug, Emre, Wolfe, Erin M., Stiegler, Amy L., Boggon, Titus J., Sanyoura, May, Morrow, Michelle, Wenger, Tara L., Fernandes, Erica M., Caluseriu, Oana, Persing, John A., Jin, Sheng Chih, Lifton, Richard P., Kahle, Kristopher T., Kruszka, Paul

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A Non-Coding Disease Modifier of Pancreatic Agenesis Identified by Genetic Correction in a Patient-Derived iPSC Line von Kishore, Siddharth, De Franco, Elisa, Cardenas-Diaz, Fabian L., Letourneau-Freiberg, Lisa R., Sanyoura, May, Osorio-Quintero, Catherine, French, Deborah L., Greeley, Siri Atma W., Hattersley, Andrew T., Gadue, Paul

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Identifying Patients with GDM at Risk for GCK-MODY von DICKENS, LAURA T., LETOURNEAU, LISA R., SANYOURA, MAY, PHILIPSON, LOUIS H., GREELEY, SIRI ATMA W., NAYLOR, ROCHELLE N.

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Insulin Treatment and Clinical Outcomes in 67 Participants with Infancy-Onset Diabetes von LETOURNEAU, LISA R., CARMODY, DAVID, DENSON, ANNA M., SANYOURA, MAY, NAYLOR, ROCHELLE N., PHILIPSON, LOUIS H., GREELEY, SIRI ATMA W.

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Novel variants in the SOX11 gene: clinical description of seven new patients von Schincariol-Manhe, Beatriz, Campagnolo, Érica, Spineli-Silva, Samira, de Leeuw, Nicole, Correia-Costa, Gabriela Roldão, Pessoa, André, de Souza, Carolina Fischinger Moura, Stevens, Cathy, Javaher, Poupak, Scallet, Helena Fabbri, Mohr, Julia, Biskup, Saskia, Herkert, Johanna C., Pfundt, Rolph, Mehta, Lakshmi, Rekab, Aisha, Elloumi, Houda Zghal, Sanyoura, May, Maciel-Guerra, Andréa Trevas, Gil-da-Silva-Lopes, Vera Lúcia, dos Santos, Ana Mondadori, Vieira, Társis Paiva

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