Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project von Bourinaris, Thomas, Smedley, Damian, Cipriani, Valentina, Sheikh, Isabella, Athanasiou-Fragkouli, Alkyoni, Chinnery, Patrick, Morris, Huw, Real, Raquel, Harrison, Victoria, Reid, Evan, Wood, Nicholas, Vandrovcova, Jana, Houlden, Henry, Tucci, Arianna

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Expanding the Spectrum of AP5Z1‐Related Hereditary Spastic Paraplegia (HSP‐SPG48): A Multicenter Study on a Rare Disease von Breza, Marianthi, Hirst, Jennifer, Chelban, Viorica, Banneau, Guillaume, Tissier, Laurène, Kol, Bophara, Bourinaris, Thomas, Said, Samia A., Péréon, Yann, Heinzmann, Anna, Debs, Rabab, Juntas‐Morales, Raul, Martinez, Victoria G., Camdessanche, Jean P., Scherer‐Gagou, Clarisse, Zola, Jean‐Médard, Athanasiou‐Fragkouli, Alkyoni, Efthymiou, Stephanie, Vavougios, George, Velonakis, Georgios, Stamelou, Maria, Tzartos, John, Potagas, Constantin, Zambelis, Thomas, Mariotti, Caterina, Blackstone, Craig, Vandrovcova, Jana, Mavridis, Theodoros, Kartanou, Chrisoula, Stefanis, Leonidas, Wood, Nicholas, Karadima, Georgia, LeGuern, Eric, Koutsis, Georgios, Houlden, Henry, Stevanin, Giovanni

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The value of real world evidence: The case of medical cannabis von Schlag, Anne Katrin, Zafar, Rayyan R., Lynskey, Michael T., Athanasiou-Fragkouli, Alkyoni, Phillips, Lawrence D., Nutt, David J.

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Correction to: DRPLA: understanding the natural history and developing biomarkers to accelerate therapeutic trials in a globally rare repeat expansion disorder von Chaudhry, Aiysha, Athanasiou-Fragkouli, Alkyoni, Garcia-Moreno, Hector, Abadias, Silvia Prades, Greenfield, Julie, Shiloh-Malawsky, Yael, Giunti, Paola, Houlden, Henry

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Medicinal cannabis for treating post-traumatic stress disorder and comorbid depression: real-world evidence von Lynskey, Michael T., Athanasiou-Fragkouli, Alkyoni, Thurgur, Hannah, Schlag, Anne Katrin, Nutt, David J.

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Characteristics of People Seeking Prescribed Cannabinoids for the Treatment of Chronic Pain: Evidence From Project Twenty 21 von Schlag, Anne Katrin, Lynskey, Michael, Fayaz, Alan, Athanasiou-Fragkouli, Alkyoni, Brandner, Brigitta, Haja, Barbara, Iveson, Elizabeth, Nutt, David J

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Prescribed Medical Cannabis Use Among Older Individuals: Patient Characteristics and Improvements in Well-Being: Findings from T21 von Lynskey, Michael T., Thurgur, Hannah, Athanasiou-Fragkouli, Alkyoni, Schlag, Anne K., Nutt, David J.

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Molecular basis of FAAH-OUT-associated human pain insensitivity von Mikaeili, Hajar, Habib, Abdella M, Yeung, Charlix Wai-Lok, Santana-Varela, Sonia, Luiz, Ana P, Panteleeva, Kseniia, Zuberi, Sana, Athanasiou-Fragkouli, Alkyoni, Houlden, Henry, Wood, John N, Okorokov, Andrei L, Cox, James J

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Negative screening for 12 rare LRRK2 pathogenic variants in a cohort of Nigerians with Parkinson's disease von Rizig, Mie, Ojo, Oluwadamilola O., Athanasiou-Fragkouli, Alkyoni, Agabi, Osigwe P., Oshinaike, Olajumoke O., Houlden, Henry, Okubadejo, Njideka U.

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A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia von Breza, Marianthi, Bourinaris, Thomas, Efthymiou, Stephanie, Maroofian, Reza, Athanasiou-Fragkouli, Alkyoni, Tzartos, John, Velonakis, Georgios, Karavasilis, Efstratios, Angelopoulou, Georgia, Kasselimis, Dimitrios, Potagas, Constantin, Stefanis, Leonidas, Karadima, Georgia, Koutsis, Georgios, Houlden, Henry

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Characteristics of and 3-month health outcomes for people seeking treatment with prescribed cannabis: Real-world evidence from Project Twenty21 von Lynskey, Michael T, Schlag, Anne K, Athanasiou-Fragkouli, Alkyoni, Badcock, David, Nutt, David J

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Medicinal cannabis for pain: Real-world data on three-month changes in symptoms and quality of life von O’Brien, Kylie, Beilby, Justin, Frans, Michelle, Lynskey, Michael, Barnes, Michael, Jayasuriya, Mihindu, Athanasiou-Fragkouli, Alkyoni, Blair, Philip, Nutt, David

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Preliminary findings from project Twenty21 Australia: An observational study of patients prescribed medicinal Cannabis for chronic pain, anxiety, posttraumatic stress disorder and... von O’Brien, Kylie, Beilby, Justin, Frans, Michelle, Lynskey, Michael, Barnes, Michael, Jayasuriya, Mihindu, Athanasiou-Fragkouli, Alkyoni, Blair, Philip, Nutt, David

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LRRK2 mutations in Parkinson's disease patients from Central Europe: A case control study von Skorvanek, Matej, Rizig, Mie, Athanasiou-Fragkouli, Alkyoni, Necpal, Jan, Straka, Igor, Tamas, Gertrud, Kurca, Egon, Mosejova, Alexandra, Han, Vladimir, Lorincova, Tatiana, Ostrozovicova, Miriam, Liesenerova, Simona, Levicka, Petra, Fajcikova, Lucia, Minar, Michal, Valkovic, Peter, Mákos, Orsolya, Kelemen, Andrea, Grofik, Milan, Cibulka, Michal, Jama, Fatumah, Houlden, Henry, Sendekova, Daniela, Cobejova, Jana, Cobej, Martin, Sukovska, Viktoria, Pálvölgyi, Károlyné, Kovacs, Norbert, Pintér, David, Ruzicka, Evzen, Holly, Petr, Dusek, Petr, Starkova, Irena, Brdkova, Jana, Smilowska, Katarzyna, Falup-Pecurariu, Cristian, Diaconu, Stefania, Klivenyi, Peter, Balaz, Marek

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Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification von Schottlaender, Lucia V, Abeti, Rosella, Jaunmuktane, Zane, Macmillan, Carol, Chelban, Viorica, O'Callaghan, Benjamin, McKinley, John, Maroofian, Reza, Efthymiou, Stepanie, Athanasiou Fragkouli, Alkyoni, Forbes, Raeburn, Soutar, Marc P.M, Livingston, John H, Kalmar, Bernadett, Swayne, Orlando, Hotton, Gary, SYNAPS Study Group, Pittman, Alan, Mendes de Oliveira, João Ricardo, de Grandis, Maria, Richard Loendt, Angela, Launchbury, Francesca, Althonayan, Juri, McDonnell, Gavin, Carr, Aisling S, Khan, Suliman, Beetz, Christian, Bisgin, Atil, Tug Bozdogan, Sevcan, Begtrup, Amber, Torti, Erin, Greensmith, Linda, Giunti, Paola, Morrison, Patrick J, Brandner, Sebastian, Aurrand Lions, Michael, Houlden, Henry, Cormand Rifà, Bru

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Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes von Cortese, Andrea, Zhu, Yi, Rebelo, Adriana P., Negri, Sara, Courel, Steve, Abreu, Lisa, Bacon, Chelsea J., Bai, Yunhong, Bis-Brewer, Dana M., Bugiardini, Enrico, Buglo, Elena, Danzi, Matt C., Feely, Shawna M. E., Athanasiou-Fragkouli, Alkyoni, Haridy, Nourelhoda A., Isasi, Rosario, Khan, Alaa, Laurà, Matilde, Magri, Stefania, Pipis, Menelaos, Pisciotta, Chiara, Powell, Eric, Rossor, Alexander M., Saveri, Paola, Sowden, Janet E., Tozza, Stefano, Vandrovcova, Jana, Dallman, Julia, Grignani, Elena, Marchioni, Enrico, Scherer, Steven S., Tang, Beisha, Lin, Zhiqiang, Al-Ajmi, Abdullah, Schüle, Rebecca, Synofzik, Matthis, Maisonobe, Thierry, Stojkovic, Tanya, Auer-Grumbach, Michaela, Abdelhamed, Mohamed A., Hamed, Sherifa A., Zhang, Ruxu, Manganelli, Fiore, Santoro, Lucio, Taroni, Franco, Pareyson, Davide, Houlden, Henry, Herrmann, David N., Reilly, Mary M., Shy, Michael E., Zhai, R. Grace, Zuchner, Stephan

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Neuronal intranuclear inclusion disease is genetically heterogeneous von Chen, Zhongbo, Yan Yau, Wai, Jaunmuktane, Zane, Tucci, Arianna, Sivakumar, Prasanth, Gagliano Taliun, Sarah A., Turner, Chris, Efthymiou, Stephanie, Ibáñez, Kristina, Sullivan, Roisin, Bibi, Farah, Athanasiou‐Fragkouli, Alkyoni, Bourinaris, Thomas, Zhang, David, Revesz, Tamas, Lashley, Tammaryn, DeTure, Michael, Dickson, Dennis W., Josephs, Keith A., Gelpi, Ellen, Kovacs, Gabor G., Halliday, Glenda, Rowe, Dominic B., Blair, Ian, Tienari, Pentti J., Suomalainen, Anu, Fox, Nick C., Wood, Nicholas W., Lees, Andrew J., Haltia, Matti J., Hardy, John, Ryten, Mina, Vandrovcova, Jana, Houlden, Henry

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Molecular basis of FAAH-OUT-associated human pain insensitivity von Mikaeili, Hajar, Habib, Abdella M, Yeung, Charlix Wai-Lok, Santana-Varela, Sonia, Luiz, Ana P, Panteleeva, Kseniia, Zuberi, Sana, Athanasiou-Fragkouli, Alkyoni, Houlden, Henry, Wood, John N, Okorokov, Andrei L, Cox, James J

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TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease von Van Haute, Lindsey, O'Connor, Emily, Díaz-Maldonado, Héctor, Munro, Benjamin, Polavarapu, Kiran, Hock, Daniella H, Arunachal, Gautham, Athanasiou-Fragkouli, Alkyoni, Bardhan, Mainak, Barth, Magalie, Bonneau, Dominique, Brunetti-Pierri, Nicola, Cappuccio, Gerarda, Caruana, Nikeisha J, Dominik, Natalia, Goel, Himanshu, Helman, Guy, Houlden, Henry, Lenaers, Guy, Mention, Karine, Murphy, David, Nandeesh, Bevinahalli, Olimpio, Catarina, Powell, Christopher A, Preethish-Kumar, Veeramani, Procaccio, Vincent, Rius, Rocio, Rebelo-Guiomar, Pedro, Simons, Cas, Vengalil, Seena, Zaki, Maha S, Ziegler, Alban, Thorburn, David R, Stroud, David A, Maroofian, Reza, Christodoulou, John, Gustafsson, Claes, Nalini, Atchayaram, Lochmüller, Hanns, Minczuk, Michal, Horvath, Rita

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TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease von Van Haute, Lindsey, O’Connor, Emily, Díaz-Maldonado, Héctor, Munro, Benjamin, Polavarapu, Kiran, Hock, Daniella H, Arunachal, Gautham, Athanasiou-Fragkouli, Alkyoni, Bardhan, Mainak, Barth, Magalie, Bonneau, Dominique, Brunetti-Pierri, Nicola, Cappuccio, Gerarda, Caruana, Nikeisha J, Dominik, Natalia, Goel, Himanshu, Helman, Guy, Houlden, Henry, Lenaers, Guy, Mention, Karine, Murphy, David, Nandeesh, Bevinahalli, Olimpio, Catarina, Powell, Christopher A, Preethish-Kumar, Veeramani, Procaccio, Vincent, Rius, Rocio, Rebelo-Guiomar, Pedro, Simons, Cas, Vengalil, Seena, Zaki, Maha S, Ziegler, Alban, Thorburn, David R, Stroud, David A, Maroofian, Reza, Christodoulou, John, Gustafsson, Claes, Nalini, Atchayaram, Lochmüller, Hanns, Minczuk, Michal, Horvath, Rita

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