The double face of the histone variant H3.3 von Szenker, Emmanuelle, Ray-gallet, Dominique, Almouzni, Geneviève

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A Developmental Requirement for HIRA-Dependent H3.3 Deposition Revealed at Gastrulation in Xenopus von Szenker, Emmanuelle, Lacoste, Nicolas, Almouzni, Geneviève

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A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing von Nabavizadeh, Nasrinsadat, Bressin, Annkatrin, Shboul, Mohammad, Moreno Traspas, Ricardo, Chia, Poh Hui, Bonnard, Carine, Szenker‐Ravi, Emmanuelle, Sarıbaş, Burak, Beillard, Emmanuel, Altunoglu, Umut, Hojati, Zohreh, Drutman, Scott, Freier, Susanne, El‐Khateeb, Mohammad, Fathallah, Rajaa, Casanova, Jean‐Laurent, Soror, Wesam, Arafat, Alaa, Escande‐Beillard, Nathalie, Mayer, Andreas, Reversade, Bruno

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R-spondin signalling is essential for the maintenance and differentiation of mouse nephron progenitors von Vidal, Valerie Pi, Jian-Motamedi, Fariba, Rekima, Samah, Gregoire, Elodie P, Szenker-Ravi, Emmanuelle, Leushacke, Marc, Reversade, Bruno, Chaboissier, Marie-Christine, Schedl, Andreas

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A GLI3 variant leading to polydactyly in heterozygotes and Pallister‐Hall‐like syndrome in a homozygote von Kariminejad, Ariana, Ghaderi‐Sohi, Siavash, Keshavarz, Elham, Hashemi, Seyed Abolghasem, Parsimehr, Elham, Szenker‐Ravi, Emmanuelle, Khatoo, Muznah, Faraji Zonooz, Mehrshid, Reversade, Bruno, Najmabadi, Hossein, Hennekam, Raoul C.

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RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6 von Szenker-Ravi, Emmanuelle, Altunoglu, Umut, Leushacke, Marc, Bosso-Lefèvre, Célia, Khatoo, Muznah, Thi Tran, Hong, Naert, Thomas, Noelanders, Rivka, Hajamohideen, Amin, Beneteau, Claire, de Sousa, Sergio B., Karaman, Birsen, Latypova, Xenia, Başaran, Seher, Yücel, Esra Börklü, Tan, Thong Teck, Vlaminck, Lena, Nayak, Shalini S., Shukla, Anju, Girisha, Katta Mohan, Le Caignec, Cédric, Soshnikova, Natalia, Uyguner, Zehra Oya, Vleminckx, Kris, Barker, Nick, Kayserili, Hülya, Reversade, Bruno

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Novel CYCLIN‐O pathogenic variants in a patient presenting with bronchiectasis secondary to reduced generation of multiple motile cilia von Yap, Kim Hoong, Lim, Albert Yick Hou, Thomas, Biju, Bonnard, Carine, Szenker‐Ravi, Emmanuelle, Chong, Yan Ling, Roy, Sudipto, Reversade, Bruno

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R-SPONDIN2+ mesenchymal cells form the bud tip progenitor niche during human lung development von Hein, Renee F.C., Wu, Joshua H., Holloway, Emily M., Frum, Tristan, Conchola, Ansley S., Tsai, Yu-Hwai, Wu, Angeline, Fine, Alexis S., Miller, Alyssa J., Szenker-Ravi, Emmanuelle, Yan, Kelley S., Kuo, Calvin J., Glass, Ian, Reversade, Bruno, Spence, Jason R.

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HIRA dependent H3.3 deposition is required for transcriptional reprogramming following nuclear transfer to Xenopus oocytes von Jullien, Jerome, Astrand, Carolina, Szenker, Emmanuelle, Garrett, Nigel, Almouzni, Genevieve, Gurdon, John B

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Developmental roles of histone H3 variants and their chaperones von Filipescu, Dan, Szenker, Emmanuelle, Almouzni, Geneviève

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Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6 von Szenker-Ravi, Emmanuelle, Altunoglu, Umut, Leushacke, Marc, Bosso-Lefèvre, Célia, Khatoo, Muznah, Thi Tran, Hong, Naert, Thomas, Noelanders, Rivka, Hajamohideen, Amin, Beneteau, Claire, de Sousa, Sergio B., Karaman, Birsen, Latypova, Xenia, Başaran, Seher, Yücel, Esra Börklü, Tan, Thong Teck, Vlaminck, Lena, Nayak, Shalini S., Shukla, Anju, Girisha, Katta Mohan, Le Caignec, Cédric, Soshnikova, Natalia, Uyguner, Zehra Oya, Vleminckx, Kris, Barker, Nick, Kayserili, Hülya, Reversade, Bruno

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CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation von Mougou-Zerelli, Soumaya, Thomas, Sophie, Szenker, Emmanuelle, Audollent, Sophie, Elkhartoufi, Nadia, Babarit, Candice, Romano, Stéphane, Salomon, Rémi, Amiel, Jeanne, Esculpavit, Chantal, Gonzales, Marie, Escudier, Estelle, Leheup, Bruno, Loget, Philippe, Odent, Sylvie, Roume, Joëlle, Gérard, Marion, Delezoide, Anne-Lise, Khung, Suonavy, Patrier, Sophie, Cordier, Marie-Pierre, Bouvier, Raymonde, Martinovic, Jéléna, Gubler, Marie-Claire, Boddaert, Nathalie, Munnich, Arnold, Encha-Razavi, Férechté, Valente, Enza Maria, Saad, Ali, Saunier, Sophie, Vekemans, Michel, Attié-Bitach, Tania

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Characterization of a missense variant in COG5 in a Tunisian patient with COG5-CDG syndrome and insights into the effect of non-synonymous variants on COG5 protein von Khabou, Boudour, Sahari, Umar Bin Mohamad, ben Issa, Abir, Bouchaala, Wafa, Szenker-Ravi, Emmanuelle, Yu Jin Ng, Alvin, Bonnard, Carine, Mbarek, Hamdi, Zeyaul, Islam, Fakhfakh, Faiza, Kammoun, Fatma, Reversade, Bruno, Charfi Triki, Chahnez

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Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia von Kariminejad, Ariana, Szenker-Ravi, Emmanuelle, Lekszas, Caroline, Tajsharghi, Homa, Moslemi, Ali-Reza, Naert, Thomas, Tran, Hong Thi, Ahangari, Fatemeh, Rajaei, Minoo, Nasseri, Mojila, Haaf, Thomas, Azad, Afrooz, Superti-Furga, Andrea, Maroofian, Reza, Ghaderi-Sohi, Siavash, Najmabadi, Hossein, Abbaszadegan, Mohammad Reza, Vleminckx, Kris, Nikuei, Pooneh, Reversade, Bruno

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A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion von Chai, Guoliang, Szenker-Ravi, Emmanuelle, Chung, Changuk, Li, Zhen, Wang, Lu, Khatoo, Muznah, Marshall, Trevor, Jiang, Nan, Yang, Xiaoxu, McEvoy-Venneri, Jennifer, Stanley, Valentina, Anzenberg, Paula, Lang, Nhi, Wazny, Vanessa, Yu, Jia, Virshup, David M, Nygaard, Rie, Mancia, Filippo, Merdzanic, Rijad, Toralles, Maria B.P, Pitanga, Paula M.L, Puri, Ratna D, Hernan, Rebecca, Chung, Wendy K, Bertoli-Avella, Aida M, Al-Sannaa, Nouriya, Zaki, Maha S, Willert, Karl, Reversade, Bruno, Gleeson, Joseph G

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Functional analysis of germline VANGL2 variants using rescue assays of vangl2 knockout zebrafish von Derrick, Christopher J, Szenker-Ravi, Emmanuelle, Santos-Ledo, Adrian, Alqahtani, Ahlam, Yusof, Amirah, Eley, Lorraine, Coleman, Alistair H L, Tohari, Sumanty, Ng, Alvin Yu-Jin, Venkatesh, Byrappa, Alharby, Essa, Mansard, Luke, Bonnet-Dupeyron, Marie-Noelle, Roux, Anne-Francoise, Vaché, Christel, Roume, Joëlle, Bouvagnet, Patrice, Almontashiri, Naif A M, Henderson, Deborah J, Reversade, Bruno, Chaudhry, Bill

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Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates von Szenker-Ravi, Emmanuelle, Ott, Tim, Khatoo, Muznah, Moreau de Bellaing, Anne, Goh, Wei Xuan, Chong, Yan Ling, Beckers, Anja, Kannesan, Darshini, Louvel, Guillaume, Anujan, Priyanka, Ravi, Vydianathan, Bonnard, Carine, Moutton, Sébastien, Schoen, Patric, Fradin, Mélanie, Colin, Estelle, Megarbane, André, Daou, Linda, Chehab, Ghassan, Di Filippo, Sylvie, Rooryck, Caroline, Deleuze, Jean-François, Boland, Anne, Arribard, Nicolas, Eker, Rukiye, Tohari, Sumanty, Ng, Alvin Yu-Jin, Rio, Marlène, Lim, Chun Teck, Eisenhaber, Birgit, Eisenhaber, Frank, Venkatesh, Byrappa, Amiel, Jeanne, Crollius, Hugues Roest, Gordon, Christopher T., Gossler, Achim, Roy, Sudipto, Attie-Bitach, Tania, Blum, Martin, Bouvagnet, Patrice, Reversade, Bruno

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Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations von Chundru, V. Kartik, Zhang, Zhancheng, Walter, Klaudia, Lindsay, Sarah J., Danecek, Petr, Eberhardt, Ruth Y., Gardner, Eugene J., Malawsky, Daniel S., Wigdor, Emilie M., Torene, Rebecca, Retterer, Kyle, Wright, Caroline F., Ólafsdóttir, Hildur, Guillen Sacoto, Maria J., Ayaz, Akif, Akbeyaz, Ismail Hakki, Türkdoğan, Dilşad, Al Balushi, Aaisha Ibrahim, Bertoli-Avella, Aida, Bauer, Peter, Szenker-Ravi, Emmanuelle, Reversade, Bruno, McWalter, Kirsty, Sheridan, Eamonn, Firth, Helen V., Hurles, Matthew E., Samocha, Kaitlin E., Ustach, Vincent D., Martin, Hilary C.

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Next‐generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy von Liu, Hui, Giguet‐Valard, Anna‐Gaëlle, Simonet, Thomas, Szenker‐Ravi, Emmanuelle, Lambert, Laetitia, Vincent‐Delorme, Catherine, Scheidecker, Sophie, Fradin, Mélanie, Morice‐Picard, Fanny, Naudion, Sophie, Ciorna‐Monferrato, Viorica, Colin, Estelle, Fellmann, Florence, Blesson, Sophie, Jouk, Pierre‐Simon, Francannet, Christine, Petit, Florence, Moutton, Sébastien, Lehalle, Daphné, Chassaing, Nicolas, El Zein, Loubna, Bazin, Anne, Bénéteau, Claire, Attié‐Bitach, Tania, Hanu, Sylvie M., Brechard, Marie‐Pierre, Chiesa, Jean, Pasquier, Laurent, Rooryck‐Thambo, Caroline, Van Maldergem, Lionel, Cabrol, Christelle, El Chehadeh, Salima, Vasiljevic, Alexandre, Isidor, Bertrand, Abel, Carine, Thevenon, Julien, Di Filippo, Sylvie, Vigouroux‐Castera, Adeline, Attia, Jocelyne, Quelin, Chloé, Odent, Sylvie, Piard, Juliette, Giuliano, Fabienne, Putoux, Audrey, Khau Van Kien, Philippe, Yardin, Catherine, Touraine, Renaud, Reversade, Bruno, Bouvagnet, Patrice

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Publisher Correction: Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates von Szenker-Ravi, Emmanuelle, Ott, Tim, Khatoo, Muznah, Moreau de Bellaing, Anne, Goh, Wei Xuan, Chong, Yan Ling, Beckers, Anja, Kannesan, Darshini, Louvel, Guillaume, Anujan, Priyanka, Ravi, Vydianathan, Bonnard, Carine, Moutton, Sébastien, Schoen, Patric, Fradin, Mélanie, Colin, Estelle, Megarbane, André, Daou, Linda, Chehab, Ghassan, Di Filippo, Sylvie, Rooryck, Caroline, Deleuze, Jean-François, Boland, Anne, Arribard, Nicolas, Eker, Rukiye, Tohari, Sumanty, Ng, Alvin Yu-Jin, Rio, Marlène, Lim, Chun Teck, Eisenhaber, Birgit, Eisenhaber, Frank, Venkatesh, Byrappa, Amiel, Jeanne, Crollius, Hugues Roest, Gordon, Christopher T., Gossler, Achim, Roy, Sudipto, Attie-Bitach, Tania, Blum, Martin, Bouvagnet, Patrice, Reversade, Bruno

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