Fine-scale population structure and demographic history of British Pakistanis by 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 by 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 by 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 by 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 by Small, Neil, Kelly, Brian, Malawsky, Daniel S., Lodh, Rajib, Oddie, Sam, Wright, John

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Examining the role of common variants in rare neurodevelopmental conditions by Huang, Qin Qin, Wigdor, Emilie M., Malawsky, Daniel S., Campbell, Patrick, Samocha, Kaitlin E., Chundru, V. Kartik, Danecek, Petr, Lindsay, Sarah, Marchant, Thomas, Koko, Mahmoud, Amanat, Sana, Bonfanti, Davide, Sheridan, Eamonn, Radford, Elizabeth J., Barrett, Jeffrey C., Wright, Caroline F., Firth, Helen V., Warrier, Varun, Strudwick Young, Alexander, Hurles, Matthew E., Martin, Hilary C.

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Genetic architecture of routinely acquired blood tests in a British South Asian cohort by 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 by 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 by 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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Altered IL-6 signalling and risk of tuberculosis: a multi-ancestry mendelian randomisation study by Hamilton, Fergus, Schurz, Haiko, Yates, Tom A, Gilchrist, James J, Möller, Marlo, Naranbhai, Vivek, Ghazal, Peter, Timpson, Nicholas J, Akhtar, Shaheen, Anwar, Mohammad, Asgar, Omar, Ashraf, Samina, Bidi, Saeed, Breen, Gerome, Chung, Raymond, Collier, David, Curtis, Charles J, Chaudhary, Shabana, Colligan, Grainne, Deloukas, Panos, Durham, Ceri, Durrani, Faiza, Eto, Fabiola, Finer, Sarah, Gafton, Joseph, Angel, Ana, Griffiths, Chris, Harvey, Joanne, Heng, Teng, Huang, Qin Qin, Hurles, Matt, Hunt, Karen A, Hussain, Shapna, Islam, Kamrul, Iyer, Vivek, Jacobs, Benjamin M, Kalantzis, Georgios, Khan, Ahsan, Lavery, Cath, Lee, Sang Hyuck, MacArthur, Daniel, Malik, Sidra, Malawsky, Daniel, Martin, Hilary, Mason, Dan, Mazid, Mohammed Bodrul, McDermott, John, Morton, Caroline, Newman, Bill, Owor, Elizabeth, Qureshi, Asma, Ramachandrappa, Shwetha, Raza, Mehru, Russell, Jessry, Safa, Nishat, Samuel, Miriam, Siddiqui, Moneeza, Simpson, Michael, Spreckley, Marie, Stow, Daniel, Taylor, Michael, Trembath, Richard C, Tricker, Karen, van Heel, David A, Walter, Klaudia, Winckley, Caroline, Wood, Suzanne, Wright, John, Zengeya, Ishevanhu, Zöllner, Julia, Schurz, Haiko, Naranbhai, Vivek, Yates, Tom A, Gilchrist, James J, Parks, Tom, Möller, Marlo, Hoal, Eileen G, Morris, Andrew P, Hill, Adrian V S, van Crevel, Reinout, van Laarhoven, Arjan, Ottenhoff, Tom H M, Metspalu, Andres, Ellis, Magda, Thye, Thorsten, Mahasirimongkol, Surakameth, Pasomsub, Ekawat, Tokunaga, Katsushi, Omae, Yosuke, Yanai, Hideki, Mushiroda, Taisei, Kubo, Michiaki, Takahashi, Atsushi, Kamatani, Yoichiro, Alisjahbana, Bachti, Liu, Wei, Sheng, A-dong, Yang, Yurong, Parks, Tom, Pollara, Gabriele

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Polygenic risk score prediction of multiple sclerosis in individuals of South Asian ancestry by 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 by 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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Add‐on cannabidiol in patients with Dravet syndrome: Results of a long‐term open‐label extension trial by 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 by 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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OLIG2 is a determinant for the relapse of MYC-amplified medulloblastoma by 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 by 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 by Pauneto, Coral Alicea, Hwang, Duhyeong, Malawsky, Daniel, Kim, Kyoungtea, Park, Christopher, Sokolsky, Marina, Gershon, Timothy

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Cryptic developmental events determine medulloblastoma radiosensitivity and cellular heterogeneity without altering transcriptomic profile by Malawsky, Daniel Shiloh, Weir, Seth J., Ocasio, Jennifer Karin, Babcock, Benjamin, Dismuke, Taylor, Cleveland, Abigail H., Donson, Andrew M., Vibhakar, Rajeev, Wilhelmsen, Kirk, Gershon, Timothy R.

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Author Correction: scRNA-seq in medulloblastoma shows cellular heterogeneity and lineage expansion support resistance to SHH inhibitor therapy by 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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Chronic AMPK inactivation slows SHH medulloblastoma progression by inhibiting mTORC1 signaling and depleting tumor stem cells by Malawsky, Daniel Shiloh, Dismuke, Taylor, Liu, Hedi, Castellino, Ethan, Brenman, Jay, Dasgupta, Biplab, Tikunov, Andrey, Gershon, Timothy R.

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