Fine-scale population structure and demographic history of British Pakistanis von Arciero, Elena, Dogra, Sufyan A., Malawsky, Daniel S., Mezzavilla, Massimo, Tsismentzoglou, Theofanis, Huang, Qin Qin, Hunt, Karen A., Mason, Dan, Sharif, Saghira Malik, van Heel, David A., Sheridan, Eamonn, Wright, John, Small, Neil, Carmi, Shai, Iles, Mark M., Martin, Hilary C.

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Mortality, morbidity and educational outcomes in children of consanguineous parents in the Born in Bradford cohort von Small, Neil, Kelly, Brian, Malawsky, Daniel S, Lodh, Rajib, Oddie, Sam, Wright, John

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Neoplastic and immune single-cell transcriptomics define subgroup-specific intra-tumoral heterogeneity of childhood medulloblastoma von Riemondy, Kent A, Venkataraman, Sujatha, Willard, Nicholas, Nellan, Anandani, Sanford, Bridget, Griesinger, Andrea M, Amani, Vladimir, Mitra, Siddhartha, Hankinson, Todd C, Handler, Michael H, Sill, Martin, Ocasio, Jennifer, Weir, Seth J, Malawsky, Daniel S, Gershon, Timothy R, Garancher, Alexandra, Wechsler-Reya, Robert J, Hesselberth, Jay R, Foreman, Nicholas K, Donson, Andrew M, Vibhakar, Rajeev

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Influence of autozygosity on common disease risk across the phenotypic spectrum von Malawsky, Daniel S., van Walree, Eva, Jacobs, Benjamin M., Heng, Teng Hiang, Huang, Qin Qin, Sabir, Ataf H., Rahman, Saadia, Sharif, Saghira Malik, Khan, Ahsan, Mirkov, Maša Umićević, Kuwahara, Hiroyuki, Gao, Xin, Alkuraya, Fowzan S., Posthuma, Danielle, Newman, William G., Griffiths, Christopher J., Mathur, Rohini, van Heel, David A., Finer, Sarah, O’Connell, Jared, Martin, Hilary C.

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Mortality, morbidity and educational outcomes in children of consanguineous parents in the Born in Bradford cohort von Small, Neil, Kelly, Brian, Malawsky, Daniel S., Lodh, Rajib, Oddie, Sam, Wright, John

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Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations von Chundru, V. Kartik, Zhang, Zhancheng, Walter, Klaudia, Lindsay, Sarah J., Danecek, Petr, Eberhardt, Ruth Y., Gardner, Eugene J., Malawsky, Daniel S., Wigdor, Emilie M., Torene, Rebecca, Retterer, Kyle, Wright, Caroline F., Ólafsdóttir, Hildur, Guillen Sacoto, Maria J., Ayaz, Akif, Akbeyaz, Ismail Hakki, Türkdoğan, Dilşad, Al Balushi, Aaisha Ibrahim, Bertoli-Avella, Aida, Bauer, Peter, Szenker-Ravi, Emmanuelle, Reversade, Bruno, McWalter, Kirsty, Sheridan, Eamonn, Firth, Helen V., Hurles, Matthew E., Samocha, Kaitlin E., Ustach, Vincent D., Martin, Hilary C.

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Genetic architecture of routinely acquired blood tests in a British South Asian cohort von Jacobs, Benjamin M., Stow, Daniel, Hodgson, Sam, Zöllner, Julia, Samuel, Miriam, Kanoni, Stavroula, Bidi, Saeed, Walter, Klaudia, Langenberg, Claudia, Dobson, Ruth, Finer, Sarah, Morton, Caroline, Siddiqui, Moneeza K., Martin, Hilary C., Pietzner, Maik, Mathur, Rohini, van Heel, David A.

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Rare variant contribution to cholestatic liver disease in a South Asian population in the United Kingdom von Zöllner, Julia, Finer, Sarah, Linton, Kenneth J., van Heel, David A., Williamson, Catherine, Dixon, Peter H.

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Exome sequencing of UK birth cohorts von Koko, Mahmoud, Fabian, Laurie, Popov, Iaroslav, Eberhardt, Ruth Y., Zakharov, Gennadii, Huang, Qin Qin, Wade, Emma E., Azad, Rafaq, Danecek, Petr, Ho, Karen, Hough, Amy, Huang, Wei, Lindsay, Sarah J., Malawsky, Daniel S., Bonfanti, Davide, Mason, Dan, Plowman, Deborah, Quail, Michael A., Ring, Susan M., Shireby, Gemma, Widaa, Sara, Fitzsimons, Emla, Iyer, Vivek, Bann, David, Timpson, Nicholas J., Wright, John, Hurles, Matthew E., Martin, Hilary C.

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Polygenic risk score prediction of multiple sclerosis in individuals of South Asian ancestry von Breedon, Joshua R, Marshall, Charles R, Giovannoni, Gavin, van Heel, David A, Dobson, Ruth, Jacobs, Benjamin M

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PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry von Burley, Kate, Fitzgibbon, Lucy, van Heel, David, Akhtar, Shaheen, Anwar, Mohammad, Arciero, Elena, Asgar, Omar, Ashraf, Samina, Breen, Gerome, Chung, Raymond, Curtis, Charles J., Chaudhary, Shabana, Chowdhury, Maharun, Colligan, Grainne, Deloukas, Panos, Durham, Ceri, Durrani, Faiza, Eto, Fabiola, Finer, Sarah, Garcia, Ana Angel, Griffiths, Chris, Harvey, Joanne, Heng, Teng, Huang, Qin Qin, Hurles, Matt, Hunt, Karen A., Hussain, Shapna, Islam, Kamrul, Jacobs, Ben, Khan, Ahsan, Khan, Amara, Lavery, Cath, Lee, Sang Hyuck, Lerner, Robin, MacArthur, Daniel, Malawsky, Daniel, Martin, Hilary, Mason, Dan, Mazid, Mohammed Bodrul, McDermott, John, McSweeney, Sanam, Miah, Shefa, Munir, Sabrina, Newman, Bill, Owor, Elizabeth, Qureshi, Asma, Rahman, Samiha, Safa, Nishat, Solly, John, Tahmasebi, Farah, Trembath, Richard C., Tricker, Karen, Uddin, Nasir, van Heel, David A., Winckley, Caroline, Wright, John, Vuckovic, Dragana, Mumford, Andrew D.

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Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations von Chundru, V Kartik, Zhang, Zhancheng, Walter, Klaudia, Lindsay, Sarah J, Danecek, Petr, Eberhardt, Ruth Y, Gardner, Eugene J, Malawsky, Daniel S, Wigdor, Emilie M, Torene, Rebecca, Retterer, Kyle, Wright, Caroline F, Ólafsdóttir, Hildur, Guillen Sacoto, Maria J, Ayaz, Akif, Akbeyaz, Ismail Hakki, Türkdoğan, Dilşad, Al Balushi, Aaisha Ibrahim, Bertoli-Avella, Aida, Bauer, Peter, Szenker-Ravi, Emmanuelle, Reversade, Bruno, McWalter, Kirsty, Sheridan, Eamonn, Firth, Helen V, Hurles, Matthew E, Samocha, Kaitlin E, Ustach, Vincent D, Martin, Hilary C

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Preventing recurrence in Sonic Hedgehog Subgroup Medulloblastoma using the OLIG2 inhibitor CT-179 von Li, Y, Lim, C, Dismuke, T, Malawsky, DS, Oasa, S, Bruce, ZC, Offenhäuser, C, Baumgartner, U, D'Souza, RCJ, Edwards, SL, French, JD, Ock, LSH, Nair, S, Sivakumaran, H, Harris, L, Tikunov, AP, Hwang, D, Del Mar Alicea Pauneto, C, Maybury, M, Hassall, T, Wainwright, B, Kesari, S, Stein, G, Piper, M, Johns, TG, Sokolsky-Papkov, M, Terenius, L, Vukojević, V, Gershon, TR, Day, BW

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Add‐on cannabidiol in patients with Dravet syndrome: Results of a long‐term open‐label extension trial von Scheffer, Ingrid E., Halford, Jonathan J., Miller, Ian, Nabbout, Rima, Sanchez‐Carpintero, Rocio, Shiloh‐Malawsky, Yael, Wong, Matthew, Zolnowska, Marta, Checketts, Daniel, Dunayevich, Eduardo, Devinsky, Orrin

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scRNA-seq in medulloblastoma shows cellular heterogeneity and lineage expansion support resistance to SHH inhibitor therapy von Ocasio, Jennifer Karin, Babcock, Benjamin, Malawsky, Daniel, Weir, Seth J., Loo, Lipin, Simon, Jeremy M., Zylka, Mark J., Hwang, Duhyeong, Dismuke, Taylor, Sokolsky, Marina, Rosen, Elias P., Vibhakar, Rajeev, Zhang, Jiao, Saulnier, Olivier, Vladoiu, Maria, El-Hamamy, Ibrahim, Stein, Lincoln D., Taylor, Michael D., Smith, Kyle S., Northcott, Paul A., Colaneri, Alejandro, Wilhelmsen, Kirk, Gershon, Timothy R.

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scRNA-seq for Microcephaly Research [IV]: Dirichlet Regression for Single-Cell Population Differences von Malawsky, Daniel, Gershon, Timothy R.

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OLIG2 is a determinant for the relapse of MYC-amplified medulloblastoma von Xu, Zhenhua, Murad, Najiba, Malawsky, Daniel Shiloh, Tao, Ran, Rivero-Hinojosa, Samuel, Holdhof, Dörthe, Schuller, Ulrich, Zhang, Peng, Lazarski, Christopher A, Rood, Brian R, Packer, Roger, Gershon, Timothy R, Pei, Yanxin

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EMBR-15. PRC2 COMPLEX ENFORCES NEURONAL LINEAGE AND SUPPRESSES TUMOR GROWTH IN SHH MEDULLOBLASTOMA von Cleveland, Abigail, Malawsky, Daniel, Churiwal, Mehal, Gershon, Timothy

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IMMU-14. WAKING THE SLEEPING GIANT: TLR7/8 AGONIST TREATMENT STIMULATES TUMOR-ASSOCIATED MYELOID CELLS FOR MEDULLOBLASTOMA IMMUNOTHERAPY von Pauneto, Coral Alicea, Hwang, Duhyeong, Malawsky, Daniel, Kim, Kyoungtea, Park, Christopher, Sokolsky, Marina, Gershon, Timothy

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scRNA-seq for Microcephaly Research [III]: Computational Analysis of scRNA-seq Data von Babcock, Benjamin, Malawsky, Daniel

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