Curating Genetic Associations With Rheumatologic Autoimmune Diseases to Improve Patient Outcomes von Bridges, S. Louis, Shapira, Rachel, Aksentijevich, Ivona, Mack, Steven J., Merriman, Tony R., Klein, Clarissa J., Bowen, B. Monica, Klein, Teri E., Ainsworth, Hannah C., Langefeld, Carl D., Jesus, Adriana A., Deuitch, Natalie T., Ombrello, Michael J., Fernandez‐Ruiz, Ruth, Fernández‐Viña, Marcelo, Keseler, Ingrid M., Wright, Matt W., Lakhanpal, Amit, Laufer, Vincent A., Varga, John, Martin, Javier, Okada, Yukinori, Plon, Sharon E., Reveille, John D., Tsokos, George C.

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Integrating Pharmacogenomics into the Broader Construct of Genomic Medicine: Efforts by the ClinGen Pharmacogenomics Working Group (PGxWG) von Gong, Li, Klein, Clarissa J, Caudle, Kelly E, Moyer, Ann M, Scott, Stuart A, Whirl-Carrillo, Michelle, Klein, Teri E

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Prominin‐1 controls stem cell activation by orchestrating ciliary dynamics von Singer, Donald, Thamm, Kristina, Zhuang, Heng, Karbanová, Jana, Gao, Yan, Walker, Jemma Victoria, Jin, Heng, Wu, Xiangnan, Coveney, Clarissa R, Marangoni, Pauline, Lu, Dongmei, Grayson, Portia Rebecca Clare, Gulsen, Tulay, Liu, Karen J, Ardu, Stefano, Wann, Angus KT, Luo, Shouqing, Zambon, Alexander C, Jetten, Anton M, Tredwin, Christopher, Klein, Ophir D, Attanasio, Massimo, Carmeliet, Peter, Huttner, Wieland B, Corbeil, Denis, Hu, Bing

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Systemic Polyarteritis Nodosa in the Young: A Single‐Center Experience Over Thirty‐Two Years von Eleftheriou, Despina, Dillon, Michael J., Tullus, Kjell, Marks, Stephen D., Pilkington, Clarissa A., Roebuck, Derek J., Klein, Nigel J., Brogan, Paul A.

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International Multicenter Analysis of Brain Structure Across Clinical Stages of Parkinson's Disease von Laansma, Max A., Bright, Joanna K., Al‐Bachari, Sarah, Anderson, Tim J., Ard, Tyler, Assogna, Francesca, Baquero, Katherine A., Berendse, Henk W., Blair, Jamie, Cendes, Fernando, Dalrymple‐Alford, John C., Bie, Rob M.A., Debove, Ines, Dirkx, Michiel F., Druzgal, Jason, Emsley, Hedley C.A., Garraux, Gäetan, Guimarães, Rachel P., Gutman, Boris A., Helmich, Rick C., Klein, Johannes C., Mackay, Clare E., McMillan, Corey T., Melzer, Tracy R., Parkes, Laura M., Piras, Fabrizio, Pitcher, Toni L., Poston, Kathleen L., Rango, Mario, Ribeiro, Letícia F., Rocha, Cristiane S., Rummel, Christian, Santos, Lucas S.R., Schmidt, Reinhold, Schwingenschuh, Petra, Spalletta, Gianfranco, Squarcina, Letizia, Heuvel, Odile A., Vriend, Chris, Wang, Jiun‐Jie, Weintraub, Daniel, Wiest, Roland, Yasuda, Clarissa L., Jahanshad, Neda, Thompson, Paul M., Werf, Ysbrand D.

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Biologic therapy in primary systemic vasculitis of the young von Eleftheriou, Despina, Melo, Marianna, Marks, Stephen D., Tullus, Kjell, Sills, John, Cleary, Gavin, Dolezalova, Pavla, Ozen, Seza, Pilkington, Clarissa, Woo, Pat, Klein, Nigel, Dillon, Michael J., Brogan, Paul A.

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A worldwide study of white matter microstructural alterations in people living with Parkinson’s disease von Owens-Walton, Conor, Nir, Talia M., Al-Bachari, Sarah, Ambrogi, Sonia, Anderson, Tim J., Aventurato, Ítalo Karmann, Cendes, Fernando, Chen, Yao-Liang, Ciullo, Valentina, Cook, Phil, Dalrymple-Alford, John C., Dirkx, Michiel F., Druzgal, Jason, Emsley, Hedley C. A., Guimarães, Rachel, Haroon, Hamied A., Helmich, Rick C., Hu, Michele T., Johansson, Martin E., Kim, Ho Bin, Klein, Johannes C., Laansma, Max, Lawrence, Katherine E., Lochner, Christine, Mackay, Clare, McMillan, Corey T., Melzer, Tracy R., Nabulsi, Leila, Newman, Ben, Opriessnig, Peter, Parkes, Laura M., Pellicano, Clelia, Piras, Fabrizio, Piras, Federica, Pirpamer, Lukas, Pitcher, Toni L., Poston, Kathleen L., Roos, Annerine, Silva, Lucas Scárdua, Schmidt, Reinhold, Schwingenschuh, Petra, Shahid-Besanti, Marian, Spalletta, Gianfranco, Stein, Dan J., Thomopoulos, Sophia I., Tosun, Duygu, Tsai, Chih-Chien, van den Heuvel, Odile A., van Heese, Eva, Vecchio, Daniela, Villalón-Reina, Julio E., Vriend, Chris, Wang, Jiun-Jie, Wu, Yih-Ru, Yasuda, Clarissa Lin, Thompson, Paul M., Jahanshad, Neda, van der Werf, Ysbrand

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Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy von Park, Joohyun, Tucci, Arianna, Cipriani, Valentina, Demidov, German, Rocca, Clarissa, Senderek, Jan, Butryn, Michaela, Velic, Ana, Lam, Tanya, Galanaki, Evangelia, Cali, Elisa, Vestito, Letizia, Maroofian, Reza, Deininger, Natalie, Rautenberg, Maren, Admard, Jakob, Hahn, Gesa-Astrid, Bartels, Claudius, van Os, Nienke J.H., Horvath, Rita, Chinnery, Patrick F., Tiet, May Yung, Hewamadduma, Channa, Hadjivassiliou, Marios, Downes, Susan M., Németh, Andrea H., Tofaris, George K., Wood, Nicholas W., Hayer, Stefanie N., Bender, Friedemann, Menden, Benita, Cordts, Isabell, Klein, Katrin, Nguyen, Huu Phuc, Krauss, Joachim K., Blahak, Christian, Strom, Tim M., Sturm, Marc, van de Warrenburg, Bart, Lerche, Holger, Maček, Boris, Synofzik, Matthis, Ossowski, Stephan, Timmann, Dagmar, Wolf, Marc E., Smedley, Damian, Riess, Olaf, Schöls, Ludger, Houlden, Henry, Haack, Tobias B., Hengel, Holger

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A worldwide study of subcortical shape as a marker for clinical staging in Parkinson’s disease von Laansma, Max A., Zhao, Yuji, van Heese, Eva M., Bright, Joanna K., Owens-Walton, Conor, Al-Bachari, Sarah, Anderson, Tim J., Assogna, Francesca, van Balkom, Tim D., Berendse, Henk W., Cendes, Fernando, Dalrymple-Alford, John C., Debove, Ines, Dirkx, Michiel F., Druzgal, Jason, Emsley, Hedley C. A., Fouche, Jean-Paul, Garraux, Gaëtan, Guimarães, Rachel P., Helmich, Rick C., Hu, Michele, van den Heuvel, Odile A., Isaev, Dmitry, Kim, Ho-Bin, Klein, Johannes C., Lochner, Christine, McMillan, Corey T., Melzer, Tracy R., Newman, Benjamin, Parkes, Laura M., Pellicano, Clelia, Piras, Fabrizio, Pitcher, Toni L., Poston, Kathleen L., Rango, Mario, Ribeiro, Leticia F., Rocha, Cristiane S., Rummel, Christian, Santos, Lucas S. R., Schmidt, Reinhold, Schwingenschuh, Petra, Squarcina, Letizia, Stein, Dan J., Vecchio, Daniela, Vriend, Chris, Wang, Jiunjie, Weintraub, Daniel, Wiest, Roland, Yasuda, Clarissa L., Jahanshad, Neda, Thompson, Paul M., van der Werf, Ysbrand D., Gutman, Boris A.

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Prominin-1 controls stem cell activation by orchestrating ciliary dynamics von Singer, Donald, Thamm, Kristina, Zhuang, Heng, Karbanova, Jana, Gao, Yan, Walker, Jemma Victoria, Jin, Heng, Wu, Xiangnan, Coveney, Clarissa R, Marangoni, Pauline, Lu, Dongmei, Grayson, Portia Rebecca Clare, Gulsen, Tulay, Liu, Karen J, Ardu, Stefano, Vvann, Angus K.T, Luo, Shouqing, Zambon, Alexander C, Jetten, Anton M, Tredwin, Christopher, Klein, Ophir D, Attanasio, Massimo, Carmeliet, Peter, Huttner, Wieland B, Corbeii, Denis, Hu, Bing

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TV‐L1 Ordinal Logistic Regression Reveals New Morphometric Patterns Related to Parkinsonian Symptom Severity: An ENIGMA‐PD study von Zhao, Yuji, van Heese, Eva, Laansma, Max A., Al‐Bachari, Sarah, Anderson, Tim, Assogna, Francesca, Berendse, Henk W., Bright, Joanna, Cendes, Fernando, Dalrymple‐Alford, John, Debove, Ines, Dirkx, Michiel, Druzgal, T. Jason, Emsley, Hedley, Fouche, JP, Garraux, Gaëtan, Guimarães, Rachel, Helmich, Rick, Jahanshad, Neda, Kim, Ho Bin, Klein, Johannes C, Lochner, Christine, Mackay, Clare, McMillan, Corey T, Melzer, Tracy R, Newman, Benjamin T, Owens‐Walton, Conor, Parkes, Laura, Piras, Fabrizio, Pitcher, Toni, Poston, Kathleen L, Rango, Mario, Ribeiro, Leticia Franchescheti, Rocha, Cristiane, Roos, Annerine, Rummel, Christian, Santos, Lucas, Schmidt, Reinhold, Spalletta, Gianfranco, Squarcina, Letizia, Schwingenschuh, Petra, Vecchio, Daniela, Vriend, Chris, Wang, Jiun‐Jie, Weintraub, Daniel, Wiest, Roland, Yasuda, Clarissa, Thompson, Paul M, van der Werf, Ysbrand D., Gutman, Boris A

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Up or down? Limpet orientation on steeply sloped substrata von Fraser, CML, Coleman, RA, Klein, JC

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Learning Interpretable Regularized Ordinal Models from 3D Mesh Data for Neurodegenerative Disease Staging von Zhao, Yuji, Laansma, Max A., van Heese, Eva M., Owens-Walton, Conor, Parkes, Laura M., Debove, Ines, Rummel, Christian, Wiest, Roland, Cendes, Fernando, Guimaraes, Rachel, Yasuda, Clarissa Lin, Wang, Jiun-Jie, Anderson, Tim J., Dalrymple-Alford, John C., Melzer, Tracy R., Pitcher, Toni L., Schmidt, Reinhold, Schwingenschuh, Petra, Garraux, Gäetan, Rango, Mario, Squarcina, Letizia, Al-Bachari, Sarah, Emsley, Hedley C. A., Klein, Johannes C., Mackay, Clare E., Dirkx, Michiel F., Helmich, Rick, Assogna, Francesca, Piras, Fabrizio, Bright, Joanna K., Spalletta, Gianfranco, Poston, Kathleen, Lochner, Christine, McMillan, Corey T., Weintraub, Daniel, Druzgal, Jason, Newman, Benjamin, Van Den Heuvel, Odile A., Jahanshad, Neda, Thompson, Paul M., van der Werf, Ysbrand D., Gutman, Boris

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Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy von Park, Joohyun, Tucci, Arianna, Cipriani, Valentina, Demidov, German, Rocca, Clarissa, Senderek, Jan, Butryn, Michaela, Velic, Ana, Lam, Tanya, Galanaki, Evangelia, Cali, Elisa, Vestito, Letizia, Maroofian, Reza, Deininger, Natalie, Rautenberg, Maren, Admard, Jakob, Hahn, Gesa-Astrid, Bartels, Claudius, van Os, Nienke JH, Horvath, Rita, Chinnery, Patrick F, Tiet, May Yung, Hewamadduma, Channa, Hadjivassiliou, Marios, Tofaris, George K, Genomics England Research Consortium, Wood, Nicholas W, Hayer, Stefanie N, Bender, Friedemann, Menden, Benita, Cordts, Isabell, Klein, Katrin, Nguyen, Huu Phuc, Krauss, Joachim K, Blahak, Christian, Strom, Tim M, Sturm, Marc, van de Warrenburg, Bart, Lerche, Holger, Maček, Boris, Synofzik, Matthis, Ossowski, Stephan, Timmann, Dagmar, Wolf, Marc E, Smedley, Damian, Riess, Olaf, Schöls, Ludger, Houlden, Henry, Haack, Tobias B, Hengel, Holger

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