Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles by Hautakangas, Heidi, Winsvold, Bendik K S, Ruotsalainen, Sanni, Bjornsdottir, Gyda, Harder, Aster V. E, Kogelman, Lisette J. A, Thomas, Laurent, Noordam, Raymond, Benner, Christian, Gormley, Padhraig, Artto, Ville, Banasik, Karina, Bjornsdottir, Anna, Boomsma, Dorret I, Brumpton, Ben Michael, Burgdorf, Kristoffer Sølvsten, Buring, Julie E, Chalmer, Mona Ameri, de Boer, Irene, Dichgans, Martin, Erikstrup, Christian, Färkkilä, Markus, Gabrielsen, Maiken Elvestad, Ghanbari, Mohsen, Hagen, Knut, Häppölä, Paavo, Hottenga, Jouke-Jan, Hrafnsdottir, Maria G, Hveem, Kristian, Johnsen, Marianne Bakke, Kähönen, Mika, Kristoffersen, Espen Saxhaug, Kurth, Tobias, Lehtimäki, Terho, Lighart, Lannie, Magnusson, Sigurdur H, Malik, Rainer, Pedersen, Ole Birger, Pelzer, Nadine, Penninx, Brenda W. J. H, Ran, Caroline, Ridker, Paul M, Rosendaal, Frits Richard, Sigurdardottir, Gudrun R, Skogholt, Anne Heidi, Sveinsson, Olafur A, Thorgeirsson, Thorgeir E, Ullum, Henrik, Zwart, John Anker Henrik

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Clinical Characteristics, Management, and Factors Associated with Poor Visual Prognosis of Acute Retinal Necrosis by Takase, Hiroshi, Goto, Hiroshi, Namba, Kenichi, Mizuki, Nobuhisa, Okada, Annabelle A, Ohguro, Nobuyuki, Sonoda, Koh-Hei, Tomita, Makoto, Keino, Hiroshi, Kezuka, Takeshi, Kubono, Reo, Mizuuchi, Kazuomi, Shibuya, Etsuko, Takahashi, Hiroyuki, Yanai, Ryoji, Mochizuki, Manabu

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Recognition of a bicoid mRNA Localization Signal by a Protein Complex Containing Swallow, Nod, and RNA Binding Proteins by Arn, Eric A., Cha, Byeong J., Theurkauf, William E., Macdonald, Paul M.

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The Yeast tRNA Splicing Endonuclease: A Tetrameric Enzyme with Two Active Site Subunits Homologous to the Archaeal tRNA Endonucleases by Trotta, Christopher R, Miao, Feng, Arn, Eric A, Stevens, Scott W, Ho, Calvin K, Rauhut, Reinhard, Abelson, John N

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Recognition of the bcd mRNA Localization Signal in Drosophila Embryos and Ovaries by Snee, Mark J., Arn, Eric A., Bullock, Simon L., Macdonald, Paul M.

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Distinct neurological disorders with ATP1A3 mutations by Heinzen, Erin L, Dr, Arzimanoglou, Alexis, MD, Brashear, Allison, Prof, Clapcote, Steven J, PhD, Gurrieri, Fiorella, Prof, Goldstein, David B, Prof, Jóhannesson, Sigurður H, Mikati, Mohamad A, Prof, Neville, Brian, Prof, Nicole, Sophie, PhD, Ozelius, Laurie J, PhD, Poulsen, Hanne, PhD, Schyns, Tsveta, PhD, Sweadner, Kathleen J, PhD, van den Maagdenberg, Arn, Prof, Vilsen, Bente, Prof

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Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological Diseases by Poole, Olivia V., Pizzamiglio, Chiara, Murphy, David, Falabella, Micol, Macken, William L., Bugiardini, Enrico, Woodward, Cathy E., Labrum, Robyn, Efthymiou, Stephanie, Salpietro, Vincenzo, Chelban, Viorica, Kaiyrzhanov, Rauan, Maroofian, Reza, Amato, Anthony A., Gregory, Allison, Hayflick, Susan J., Jonvik, Hallgeir, Wood, Nicholas, Houlden, Henry, Vandrovcova, Jana, Hanna, Michael G., Pittman, Alan, Pitceathly, Robert D.S., Alkhawaja, Issam, Banu, Selina, Bonsignore, Maria, Breza, Marianthi, Di Rosa, Gabriella, Heidari, Morteza, Koutsis, Georgios, Maagdenberg, Arn M.J.M., Macaya, Alfons, Münchau, Alexander, Scuderi, Carmela, Zharkinbekova, Nazira

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Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients by Panagiotakaki, Eleni, De Grandis, Elisa, Stagnaro, Michela, Heinzen, Erin L, Fons, Carmen, Sisodiya, Sanjay, de Vries, Boukje, Goubau, Christophe, Weckhuysen, Sarah, Kemlink, David, Scheffer, Ingrid, Lesca, Gaëtan, Rabilloud, Muriel, Klich, Amna, Ramirez-Camacho, Alia, Ulate-Campos, Adriana, Campistol, Jaume, Giannotta, Melania, Moutard, Marie-Laure, Doummar, Diane, Hubsch-Bonneaud, Cecile, Jaffer, Fatima, Cross, Helen, Gurrieri, Fiorella, Tiziano, Danilo, Nevsimalova, Sona, Nicole, Sophie, Neville, Brian, van den Maagdenberg, Arn M J M, Mikati, Mohamad, Goldstein, David B, Vavassori, Rosaria, Arzimanoglou, Alexis

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Molecular genetic overlap between migraine and major depressive disorder by Yang, Yuanhao, Zhao, Huiying, Boomsma, Dorret I, Ligthart, Lannie, Belin, Andrea C, Smith, George Davey, Esko, Tonu, Freilinger, Tobias M, Hansen, Thomas Folkmann, Ikram, M Arfan, Kallela, Mikko, Kubisch, Christian, Paraskevi, Christofidou, Strachan, David P, Wessman, Maija, van den Maagdenberg, Arn M J M, Terwindt, Gisela M, Nyholt, Dale R

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PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation by Chelban, Viorica, Wilson, Matthew P., Warman Chardon, Jodi, Vandrovcova, Jana, Zamba‐Papanicolaou, Eleni, Pope, Simon, Conte, Maria R., Abis, Giancarlo, Liu, Yo‐Tsen, Tribollet, Eloise, Haridy, Nourelhoda A., Botía, Juan A., Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Kernohan, Kristin D., Eaton, Alison, Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M., Foiani, Martha, Zetterberg, Henrik, Heales, Simon J. R., Rothman, James E., Clayton, Peter T., Houlden, Henry, Kriouile, Yamna, Aguennouz, Mhammed, Groppa, Stanislav, Marinova Karashova, Blagovesta, Van Maldergem, Lionel, Nachbauer, Wolfgang, Boesch, Sylvia, Arning, Larissa, Timmann, Dagmar, Cormand, Bru, Pérez‐Dueñas, Belen, Di Rosa, Gabriella, Goraya, Jatinder S., Sultan, Tipu, Mine, Jun, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Pineda‐Marfa, Mercedes, Ferrari, Michel D., van den Maagdenberg, Arn M J M, Verrotti, Alberto, Marseglia, Giangluigi, García‐Silva, Mayte, Ruiz, Alfons Macaya, Garavaglia, Barbara, Borgione, Eugenia, Portaro, Simona, Boles, Richard, Giunti, Paola, Chelban, Viorica, Salpietro, Vincenzo, Efthymiou, Stephanie, Kullmann, Dimitri, Kaiyrzhanov, Rauan, Sullivan, Roisin, Khan, Alaa Matooq, Yau, Wai Yan, Papanicolaou, Eleni Zamba, Maqbool, Shazia, Rana, Nuzhat Noureen, Atawneh, Osama, Shaikh, Farooq, Koutsis, George, Breza, Marianthi, Mangano, Salvatore, Scuderi, Carmela, Borgione, Eugenia, Stojkovic, Tanya, Torti, Erin, Zollo, Massimi, Dauvilliers, Yves A., Rizig, Mie, Okubadejo, Njideka U., Ojo, Oluwadamilola O., Wahab, Kolawole, Bello, Abiodun H., Obiabo, Yahaya, Nwazor, Ernest, Iyagba, Alagoma, Taiwo, Lolade, Komolafe, Morenikeji, Oguntunde, Olapeju, Senkevich, Konstantin, Haridy, Nourelhoda, Shashkin, Chingiz, Zharkynbekova, Nazira, Koneyev, Kairgali, Isrofilov, Maksud, Khachatryan, Samson, Silvestri, Gabriella, Bourinaris, Thomas, Fidani, Liana

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Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination by Efthymiou, Stephanie, Salpietro, Vincenzo, Malintan, Nancy, Poncelet, Mallory, Kriouile, Yamna, Fortuna, Sara, De Zorzi, Rita, Payne, Katelyn, Henderson, Lindsay B, Cortese, Andrea, Maddirevula, Sateesh, Alhashmi, Nadia, Wiethoff, Sarah, Ryten, Mina, Botia, Juan A, Provitera, Vincenzo, Schuelke, Markus, Vandrovcova, Jana, Walsh, Laurence, Torti, Erin, Iodice, Valeria, Najafi, Maryam, Karimiani, Ehsan Ghayoor, Maroofian, Reza, Siquier-Pernet, Karine, Boddaert, Nathalie, De Lonlay, Pascale, Cantagrel, Vincent, Aguennouz, Mhammed, El Khorassani, Mohamed, Schmidts, Miriam, Alkuraya, Fowzan S, Edvardson, Simon, Nolano, Maria, Devaux, Jérôme, Houlden, Henry

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A causal effects of gut microbiota in the development of migraine by He, Qiang, Wang, Wenjing, Xiong, Yang, Tao, Chuanyuan, Ma, Lu, Ma, Junpeng, You, Chao

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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families by Gormley, Padhraig, Kurki, Mitja I., Hiekkala, Marjo Eveliina, Häppölä, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli, Hämäläinen, Eija, Vepsäläinen, Salli, Havanka, Hannele, Harno, Hanna, Ilmavirta, Matti, Sumelahti, Marja-Liisa, Sillanpää, Matti, Metsähonkala, Liisa, Koskinen, Seppo, Raitakari, Olli, Jousilahti, Pekka, Anttila, Verneri, Salomaa, Veikko, Artto, Ville, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K., Elson, Sarah L., Furlotte, Nicholas A., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McCreight, Jennifer C., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Vacic, Vladimir, Wilson, Catherine H., Anttila, Verneri, Artto, Ville, Belin, Andrea Carmine, Børte, Sigrid, Cherkas, Lynn, Christensen, Anne Francke, Cuenca-Leon, Ester, Dichgans, Martin, van Duijn, Cornelia, Esko, Tonu, Esserlind, Ann-Louise, Frants, Rune R., Freilinger, Tobias, Furlotte, Nick, Gormley, Padhraig, Hansen, Thomas Folkmann, Hiekkala, Marjo, Ikram, M Arfan, Ingason, Andres, Kajanne, Risto, Kallela, Mikko, Kaprio, Jaakko, Kaunisto, Mari, Kubisch, Christian, Kurth, Tobias, Launer, Lenore, Lehtimaki, Terho, Lessel, Davor, Ligthart, Lannie, Litterman, Nadia, van den Maagdenberg, Arn, Macaya, Alfons, Malik, Rainer, Muller-Myhsok, Bertram, Neale, Benjamin M., Northover, Carrie, Palta, Priit, Pedersen, Nancy, Posthuma, Danielle, Pressman, Alice, Quaye, Lydia, Raitakari, Olli, Schürks, Markus, Sintas, Celia, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Strachan, David, Terwindt, Gisela, Vila-Pueyo, Marta, Winsvold, Bendik S., Wrenthal, William, Daly, Mark J., Neale, Benjamin M., Ripatti, Samuli, Kallela, Mikko, Wessman, Maija, Palotie, Aarno

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Causal relationships between migraine and microstructural white matter: a Mendelian randomization study by Zhao, Lei, Zhao, Wenhui, Cao, Jin, Tu, Yiheng

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Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits by Rafnar, Thorunn, Gunnarsson, Bjarni, Stefansson, Olafur A., Sulem, Patrick, Ingason, Andres, Frigge, Michael L., Stefansdottir, Lilja, Sigurdsson, Jon K., Tragante, Vinicius, Steinthorsdottir, Valgerdur, Styrkarsdottir, Unnur, Stacey, Simon N., Gudmundsson, Julius, Arnadottir, Gudny A., Oddsson, Asmundur, Zink, Florian, Halldorsson, Gisli, Sveinbjornsson, Gardar, Kristjansson, Ragnar P., Davidsson, Olafur B., Salvarsdottir, Anna, Thoroddsen, Asgeir, Helgadottir, Elisabet A., Kristjansdottir, Katrin, Ingthorsson, Orri, Gudmundsson, Valur, Geirsson, Reynir T., Arnadottir, Ragnheidur, Gudbjartsson, Daniel F., Masson, Gisli, Asselbergs, Folkert W., Jonasson, Jon G., Olafsson, Karl, Thorsteinsdottir, Unnur, Halldorsson, Bjarni V., Thorleifsson, Gudmar, Stefansson, Kari

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Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder by Aughey, Gabriel N, Cali, Elisa, Maroofian, Reza, Zaki, Maha S, Pagnamenta, Alistair T, Ali, Zafar, Abdulllah, Uzma, Rahman, Fatima, Menzies, Lara, Shafique, Anum, Suri, Mohnish, Roze, Emmanuel, Aguennouz, Mohammed, Ghizlane, Zouiri, Saadi, Saadia Maryam, Fatima, Ambrin, Cheema, Huma Arshad, Anjum, Muhammad Nadeem, Morel, Godelieve, Robin, Stephanie, McFarland, Robert, Altunoglu, Umut, Kraus, Verena, Shoukier, Moneef, Murphy, David, Flemming, Kristina, Yttervik, Hilde, Rhouda, Hajar, Lesca, Gaetan, Chatron, Nicolas, Rossi, Massimiliano, Murtaza, Bibi Nazia, Ur Rehman, Mujaddad, Lord, Jenny, Giacopuzzi, Edoardo, Hayat, Azam, Siraj, Muhammad, Badv, Reza Shervin, Seo, Go Hun, Beetz, Christian, Kayserili, Hülya, Krioulie, Yamna, Chung, Wendy K, Naz, Sadaf, Maqbool, Shazia, Chandler, Kate, Kershaw, Christopher, Wright, Thomas, Banka, Siddharth, Gleeson, Joseph G, Taylor, Jenny C, Efthymiou, Stephanie, Baig, Shahid Mahmood, Severino, Mariasavina, Jepson, James E C, Houlden, Henry

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Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults by Panagiotakaki, Eleni, Gobbi, Giuseppe, Neville, Brian, Ebinger, Friedrich, Campistol, Jaume, Nevšímalová, Soňa, Laan, Laura, Casaer, Paul, Spiel, Georg, Giannotta, Melania, Fons, Carmen, Ninan, Miriam, Sange, Guenter, Schyns, Tsveta, Vavassori, Rosaria, Poncelin, Dominique, Arzimanoglou, Alexis

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Motors Driving mRNA Localization: New Insights from In Vivo Imaging by Arn, Eric A, Macdonald, Paul M

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Feasibility of early infant diagnosis of HIV in resource-limited settings: the ANRS 12140-PEDIACAM study in Cameroon by Tejiokem, Mathurin C, Faye, Albert, Penda, Ida C, Guemkam, Georgette, Ateba Ndongo, Francis, Chewa, Gisèle, Rekacewicz, Claire, Rousset, Dominique, Kfutwah, Anfumbom, Boisier, Pascal, Warszawski, Josiane

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Migraine, chronic kidney disease and kidney function: observational and genetic analyses by Zhang, Wenqiang, Zhang, Li, Yang, Luo, Xiao, Chenghan, Wu, Xueyao, Yan, Peijing, Cui, Huijie, Yang, Chao, Zhu, Jingwei, Wu, Xuan, Tang, Mingshuang, Wang, Yutong, Chen, Lin, Liu, Yunjie, Zou, Yanqiu, Zhang, Ling, Yang, Chunxia, Yao, Yuqin, Li, Jiayuan, Liu, Zhenmi, Zhang, Ben, Jiang, Xia

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