2023 in the European Journal of Human Genetics von McNeill, Alisdair

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Happy 30th birthday to the European Journal of Human Genetics von McNeill, Alisdair

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A new impact factor for European Journal of Human Genetics von McNeill, Alisdair

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2022: the year that was in the European Journal of Human Genetics von McNeill, Alisdair

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Correction: 2021 at European Journal of Human Genetics: the year in review von McNeill, Alisdair

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2021 at European Journal of Human Genetics: the year in review von McNeill, Alisdair

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The European Journal of Human Genetics is turning 30: a selection of major cancer genetics papers published by the Journal von Benusiglio, Patrick R

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European Journal of Human Genetics von De Lobel, Lizzy, Thijs, L, Kouznetsova, T, Staessens, J, Van Steen, Kristel

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Pharmacogenomics, a novel section in the European Journal of Human Genetics von Guchelaar, Henk-Jan

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European Journal of Human Genetics von Mahachie John, Jestinah, Van Lishout, François, Van Steen, Kristel

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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2) von de Boer, Elke, Ockeloen, Charlotte W., Matalonga, Leslie, Horvath, Rita, Cohen, Enzo, Nelson, Isabelle, Rodenburg, Richard J., Coenen, Marieke J. H., Janssen, Mirian, Henssen, Dylan, Gilissen, Christian, Steyaert, Wouter, Paramonov, Ida, Trimouille, Aurelien, Kleefstra, Tjitske, Verloes, Alain, Vissers, Lisenka E. L. M.

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European Journal of Human Genetics von De Lobel, L, Geurts, Pierre, Baele, G, Castro-Giner, F, Kogevinas, M, Van Steen, Kristel

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European Journal of Human Genetics von Ripatti, Samuli, Becker, Tim, Bickeboller, Heike, Dominicus, Annica, Fischer, Christine, Humphreys, Keith, Jonasdottir, Gudrun, Moreau, Yves, Olsson, Marita, Ploner, Alexander, Sheehan, Nuala, Van Steen, Kristel, Baur, Max, van Duijn, Cornelia, Palmgren, Juni

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European Journal of Human Genetics von Hilton, Emma, Johnston, Jennifer, Whalen, Sandra, Okamoto, Nobuhiko, Hatsukawa, Yoshikazu, Nishio, Juntaro, Kohara, Hiroshi, Hirano, Yoshiko, Mizuno, Seiji, Torii, Chiharu, Kosaki, Kenjiro, Manouvrier, Sylvie, Boute, Odile, Perveen, Rahat, Law, Caroline, Moore, Anthony, Fitzpatrick, David, Lemke, Johannes, Fellmann, Florence, Debray, François-Guillaume, Dastot-Le-Moal, Florence, Gerard, Marion, Martin, Josiane, Bitoun, Pierre, Goossens, Michel, Verloes, Alain, Schinzel, Albert, Bartholdi, Deborah, Bardakjian, Tanya, Hay, Beverly, Jenny, Kim, Johnston, Kathreen, Lyons, Michael, Belmont, John W, Biesecker, Leslie G, Giurgea, Irina, Black, Graeme

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European Journal of Human Genetics von heath, sc, gut, ivo, brennan, p, mckay, jd, bencko, v, fabianova, e, foretova, l, Georges, Michel, janout, v, kabesch, m, krokan, he, elvestad, mb, lissowska, j, mates, d, rudnai, p, skorpen, f, schreiber, s, soria, jm, syvänen, ac, meneton, p, herçberg, s, galan, p, szeszenia-dabrowska, n, zaridze, d, génin, e, CARDON, Wesley, Lathrop, Mark

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Erratum: Clinical utility gene card for: Glanzmann thrombasthenia von Fiore, Mathieu, Nurden, Alan T, Nurden, Paquita, Seligsohn, Uri

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Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples (European Journal of Human Genetics, (2023), 10.1038/s41431-023-01478-7) von Wijngaard, R, Demidov, G, O’Gorman, L, Corominas-Galbany, J, Yaldiz, B, Steyaert, W, de Boer, E, Vissers, LELM, Kamsteeg, EJ, Pfundt, R, Swinkels, H, den Ouden, A, te Paske, IBAW, de Voer, RM, Faivre, L, Denommé-Pichon, AS, Duffourd, Y, Vitobello, A, Chevarin, M, Straub, V, Töpf, A, van der Kooi, AJ, Magrinelli, F, Rocca, C, Hanna, MG, Vandrovcova, J, Ossowski, S, Laurie, S, Gilissen, C

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Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1) von Layo-Carris, Dana E, Lubin, Emily E, Sangree, Annabel K, Clark, Kelly J, Durham, Emily L, Gonzalez, Elizabeth M, Smith, Sarina, Angireddy, Rajesh, Wang, Xiao Min, Weiss, Erin, Toutain, Annick, Mendoza-Londono, Roberto, Dupuis, Lucie, Damseh, Nadirah, Velasco, Danita, Valenzuela, Irene, Codina-Solà, Marta, Ziats, Catherine, Have, Jaclyn, Clarkson, Katie, Steel, Dora, Kurian, Manju, Barwick, Katy, Carrasco, Diana, Dagli, Aditi I, Nowaczyk, M. J.M, Hančárová, Miroslava, Bendová, Šárka, Prchalova, Darina, Sedláček, Zdeněk, Baxová, Alica, Nowak, Catherine Bearce, Douglas, Jessica, Chung, Wendy K, Longo, Nicola, Platzer, Konrad, Klöckner, Chiara, Averdunk, Luisa, Wieczorek, Dagmar, Krey, Ilona, Zweier, Christiane, Reis, Andre, Balci, Tugce, Simon, Marleen, Kroes, Hester Y, Wiesener, Antje, Vasileiou, Georgia, Marinakis, Nikolaos M, Veltra, Danai, Sofocleous, Christalena, Kosma, Konstantina, Synodinos, Joanne Traeger, Voudris, Konstantinos A, Vuillaume, Marie Laure, Gueguen, Paul, Derive, Nicolas, Colin, Estelle, Battault, Clarisse, Au, Billie, Delatycki, Martin, Wallis, Mathew, Gallacher, Lyndon, Majdoub, Fatma, Smal, Noor, Weckhuysen, Sarah, Schoonjans, An Sofie, Kooy, R. Frank, Meuwissen, Marije, Cocanougher, Benjamin T, Taylor, Kathryn, Pizoli, Carolyn E, McDonald, Marie T, James, Philip, Roeder, Elizabeth R, Littlejohn, Rebecca, Borja, Nicholas A, Thorson, Willa, King, Kristine, Stoeva, Radka, Suerink, Manon, Nibbeling, Esther, Baskin, Stephanie, Guyader, Gwenaël L.E, Kaplan, Julie, Muss, Candace, Carere, Deanna Alexis, Bhoj, Elizabeth J.K, Bryant, Laura M

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Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1) von Savige, Judy, Storey, Helen, Watson, Elizabeth, Hertz, Jens Michael, Deltas, Constantinos, Renieri, Alessandra, Mari, Francesca, Hilbert, Pascale, Plevova, Pavlina, Byers, Peter, Cerkauskaite, Agne, Gregory, Martin, Cerkauskiene, Rimante, Ljubanovic, Danica Galesic, Becherucci, Francesca, Errichiello, Carmela, Massella, Laura, Aiello, Valeria, Lennon, Rachel, Hopkinson, Louise, Koziell, Ania, Lungu, Adrian, Rothe, Hansjorg Martin, Hoefele, Julia, Zacchia, Miriam, Martic, Tamara Nikuseva, Gupta, Asheeta, van Eerde, Albertien, Gear, Susie, Landini, Samuela, Palazzo, Viviana, al-Rabadi, Laith, Claes, Kathleen, Corveleyn, Anniek, Van Hoof, Evelien, van Geel, Micheel, Williams, Maggie, Ashton, Emma, Belge, Hendica, Ars, Elisabeth, Bierzynska, Agnieszka, Gangemi, Concetta, Lipska-Ziętkiewicz, Beata S

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The Second Year of the European Journal of Human Genetics von Romeo, Giovanni, de la Chapelle, Albert, Monaco, Tony

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