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Owolabi, Mayowa O, Leonardi, Matilde, Bassetti, Claudio, Jaarsma, Joke, Hawrot, Tadeusz, Makanjuola, Akintomiwa I, Dhamija, Rajinder K, Feng, Wuwei, Straub, Volker, Camaradou, Jennifer et al (show 55 more authors) , Dodick, David W, Sunna, Rosita, Menon, Bindu, Wright, Claire, Lynch, Chris, Chadha, Antonella Santuccione, Ferretti, Maria Teresa, De, Anna, Catsman-Berrevoets, Coriene E, Gichu, Muthoni, Tassorelli, Cristina, Oliver, David, Paulus, Walter, Mohammed, Ramla K, Charway-Felli, Augustina, Rostasy, Kevin, Feigin, Valery, Craven, Audrey, Cunningham, Elizabeth, Galvin, Orla, Perry, Alexandra Heumber, Fink, Ericka L, Baneke, Peer, Helme, Anne, Laurson-Doube, Joanna, Medina, Marco T, Roa, Juan David, Hogl, Birgit, O'Bryan, Allan, Trenkwalder, Claudia, Wilmshurst, Jo, Akinyemi, Rufus O, Yaria, Joseph O, Good, David C, Hoemberg, Volker, Boon, Paul, Wiebe, Samuel, Cross, J Helen, Haas, Magali, Jabalpurwala, Inez, Mojasevic, Marijeta, DiLuca, Monica, Barbarino, Paola, Clarke, Stephanie, Zuberi, Sameer M, Olowoyo, Paul, Owolabi, Ayomide, Oyesiku, Nelson, Maly-Sundgren, Pia C, Norrving, Bo, Soekadar, Surjo R, van Doorn, Pieter A, Lewis, Richard, Solomon, Tom ORCID: 0000-0001-7266-6547 and Servadei, Franco (2023) Global synergistic actions to improve brain health for human development. NATURE REVIEWS NEUROLOGY, 19 (6). pp. 371-383.

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Tilch, Erik, Schormair, Barbara, Zhao, Chen, Salminen, Aaro V, Nikolic, Ana Antic, Holzknecht, Evi, Hoegl, Birgit, Poewe, Werner, Bachmann, Cornelius G, Paulus, Walter et al (show 12 more authors) , Trenkwalder, Claudia, Oertel, Wolfgang H, Hornyak, Magdolna, Fietze, Ingo, Berger, Klaus, Lichtner, Peter, Gieger, Christian, Peters, Annette, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hoischen, Alexander, Winkelmann, Juliane and Oexle, Konrad (2020) Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. ANNALS OF NEUROLOGY, 87 (2). pp. 184-193.

Heide, Ev-Christin, Puk, Oliver, Biskup, Saskia, Krahn, Arne, Rauf, Erik, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, Paulus, Walter and Focke, Niels K (2021) A novel likely pathogenic heterozygous <i>HECW2</i> missense variant in a family with variable expressivity of neurodevelopmental delay, hypotonia, and epileptiform EEG patterns. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 185 (12). pp. 3838-3843.