Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm von Lindsay, Mark E, Schepers, Dorien, Bolar, Nikhita Ajit, Doyle, Jefferson J, Gallo, Elena, Fert-Bober, Justyna, Kempers, Marlies J E, Fishman, Elliot K, Chen, Yichun, Myers, Loretha, Bjeda, Djahita, Oswald, Gretchen, Elias, Abdallah F, Levy, Howard P, Anderlid, Britt-Marie, Yang, Margaret H, Bongers, Ernie M H F, Timmermans, Janneke, Braverman, Alan C, Canham, Natalie, Mortier, Geert R, Brunner, Han G, Byers, Peter H, Van Eyk, Jennifer, Van Laer, Lut, Dietz, Harry C, Loeys, Bart L

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Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability von Lelieveld, Stefan H, Reijnders, Margot R F, Pfundt, Rolph, Yntema, Helger G, Kamsteeg, Erik-Jan, de Vries, Petra, de Vries, Bert B A, Willemsen, Marjolein H, Kleefstra, Tjitske, Löhner, Katharina, Vreeburg, Maaike, Stevens, Servi J C, van der Burgt, Ineke, Bongers, Ernie M H F, Stegmann, Alexander P A, Rump, Patrick, Rinne, Tuula, Nelen, Marcel R, Veltman, Joris A, Vissers, Lisenka E L M, Brunner, Han G, Gilissen, Christian

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Mutations in the pre-replication complex cause Meier-Gorlin syndrome von Bicknell, Louise S, Bongers, Ernie M H F, Leitch, Andrea, Brown, Stephen, Schoots, Jeroen, Harley, Margaret E, Aftimos, Salim, Al-Aama, Jumana Y, Bober, Michael, Brown, Paul A J, van Bokhoven, Hans, Dean, John, Edrees, Alaa Y, Feingold, Murray, Fryer, Alan, Hoefsloot, Lies H, Kau, Nikolaus, Knoers, Nine V A M, MacKenzie, James, Opitz, John M, Sarda, Pierre, Ross, Alison, Temple, I Karen, Toutain, Annick, Wise, Carol A, Wright, Michael, Jackson, Andrew P

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Diversity enhances carbon storage in tropical forests von Poorter, L, Sande, M. T, Thompson, J, Arets, E. J. M. M, Alarcón, A, Álvarez‐Sánchez, J, Ascarrunz, N, Balvanera, P, Barajas‐Guzmán, G, Boit, A, Bongers, F, Carvalho, F. A, Casanoves, F, Cornejo‐Tenorio, G, Costa, F. R. C, Castilho, C. V, Duivenvoorden, J. F, Dutrieux, L. P, Enquist, B. J, Fernández‐Méndez, F, Finegan, B, Gormley, L. H. L, Healey, J. R, Hoosbeek, M. R, Ibarra‐Manríquez, G, Junqueira, A. B, Levis, C, Licona, J. C, Lisboa, L. S, Magnusson, W. E, Martínez‐Ramos, M, Martínez‐Yrizar, A, Martorano, L. G, Maskell, L. C, Mazzei, L, Meave, J. A, Mora, F, Muñoz, R, Nytch, C, Pansonato, M. P, Parr, T. W, Paz, H, Pérez‐García, E. A, Rentería, L. Y, Rodríguez‐Velazquez, J, Rozendaal, D. M. A, Ruschel, A. R, Sakschewski, B, Salgado‐Negret, B, Schietti, J, Simões, M, Sinclair, F. L, Souza, P. F, Souza, F. C, Stropp, J, Steege, H, Swenson, N. G, Thonicke, K, Toledo, M, Uriarte, M, Hout, P, Walker, P, Zamora, N, Peña‐Claros, M

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Deficiency in origin licensing proteins impairs cilia formation: implications for the aetiology of Meier-Gorlin syndrome von Stiff, Tom, Alagoz, Meryem, Alcantara, Diana, Outwin, Emily, Brunner, Han G, Bongers, Ernie M H F, O'Driscoll, Mark, Jeggo, Penny A

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Cell-based assay for ciliopathy patients to improve accurate diagnosis using ALPACA von Doornbos, Cenna, van Beek, Ronald, Bongers, Ernie M H F, Lugtenberg, Dorien, Klaren, Peter H M, Vissers, Lisenka E L M, Roepman, Ronald, Oud, Machteld M

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Diversity, composition and density of trees and shrubs in agroforestry homegardens in Southern Ethiopia von Abebe, Tesfaye, Sterck, F. J., Wiersum, K. F., Bongers, F.

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Drought responses, phenotypic plasticity and survival of Mediterranean species in two different microclimatic sites von Bongers, F J, Olmo, M, Lopez-Iglesias, B, Anten, N P R, Villar, R

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C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome von Arts, Heleen H, Bongers, Ernie M H F, Mans, Dorus A, van Beersum, Sylvia E C, Oud, Machteld M, Bolat, Emine, Spruijt, Liesbeth, Cornelissen, Elisabeth A M, Schuurs-Hoeijmakers, Janneke H M, de Leeuw, Nicole, Cormier-Daire, Valérie, Brunner, Han G, Knoers, Nine V A M, Roepman, Ronald

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The potential of secondary forests von Bongers, F., Chazdon, R., Poorter, L., Peña-Claros, M.

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Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome von Koolen, David A, Kramer, Jamie M, Neveling, Kornelia, Nillesen, Willy M, Moore-Barton, Heather L, Elmslie, Frances V, Toutain, Annick, Amiel, Jeanne, Malan, Valérie, Tsai, Anne Chun-Hui, Cheung, Sau Wai, Gilissen, Christian, Verwiel, Eugene T P, Martens, Sarah, Feuth, Ton, Bongers, Ernie M H F, de Vries, Petra, Scheffer, Hans, Vissers, Lisenka E L M, de Brouwer, Arjan P M, Brunner, Han G, Veltman, Joris A, Schenck, Annette, Yntema, Helger G, de Vries, Bert B A

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TBX4 mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial hypertension von Kerstjens-Frederikse, Wilhelmina S, Bongers, Ernie M H F, Roofthooft, Marcus T R, Leter, Edward M, Douwes, J Menno, Van Dijk, Arie, Vonk-Noordegraaf, Anton, Dijk-Bos, Krista K, Hoefsloot, Lies H, Hoendermis, Elke S, Gille, Johan J P, Sikkema-Raddatz, Birgit, Hofstra, Robert M W, Berger, Rolf M F

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Spatial and temporal variation in crop diversity in agroforestry homegardens of southern Ethiopia von Abebe, Tesfaye, Wiersum, K. F, Bongers, F

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Wnt5a Deficiency Leads to Anomalies in Ureteric Tree Development, Tubular Epithelial Cell Organization and Basement Membrane Integrity Pointing to a Role in Kidney Collecting Duct... von Pietilä, Ilkka, Prunskaite-Hyyryläinen, Renata, Kaisto, Susanna, Tika, Elisavet, van Eerde, Albertien M, Salo, Antti M, Garma, Leonardo, Miinalainen, Ilkka, Feitz, Wout F, Bongers, Ernie M H F, Juffer, André, Knoers, Nine V A M, Renkema, Kirsten Y, Myllyharju, Johanna, Vainio, Seppo J

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Early Development of Hyperparathyroidism Due to Loss of PTH Transcriptional Repression in Patients With HNF1β Mutations? von Ferrè, Silvia, Bongers, Ernie M. H. F, Sonneveld, Ramon, Cornelissen, Elisabeth A. M, van der Vlag, Johan, van Boekel, Gerben A. J, Wetzels, Jack F. M, Hoenderop, Joost G. J, Bindels, René J. M, Nijenhuis, Tom

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Manage or convert Boswellia woodlands? Can frankincense production payoff? von Dejene, T., Lemenih, M., Bongers, F.

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Cellular ciliary phenotyping indicates pathogenicity of novel variants in IFT140 and confirms a Mainzer-Saldino syndrome diagnosis von Oud, Machteld M, Latour, Brooke L, Bakey, Zeineb, Letteboer, Stef J, Lugtenberg, Dorien, Wu, Ka Man, Cornelissen, Elisabeth A M, Yntema, Helger G, Schmidts, Miriam, Roepman, Ronald, Bongers, Ernie M H F

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Identical IFT140 Variants Cause Variable Skeletal Ciliopathy Phenotypes—Challenges for the Accurate Diagnosis von Walczak-Sztulpa, Joanna, Wawrocka, Anna, Doornbos, Cenna, van Beek, Ronald, Sowińska-Seidler, Anna, Jamsheer, Aleksander, Bukowska-Olech, Ewelina, Latos-Bieleńska, Anna, Grenda, Ryszard, Bongers, Ernie M. H. F., Schmidts, Miriam, Obersztyn, Ewa, Krawczyński, Maciej R., Oud, Machteld M.

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Genetic diversity and differentiation of the frankincense tree (Boswellia papyrifera (Del.) Hochst) across Ethiopia and implications for its conservation von Addisalem, A.B., Bongers, F., Kassahun, T., Smulders, M.J.M.

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Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy von Stokman, Marijn F., van der Zwaag, Bert, van de Kar, Nicole C. A. J., van Haelst, Mieke M., van Eerde, Albertien M., van der Heijden, Joost W., Kroes, Hester Y., Ippel, Elly, Schulp, Annelien J. A., van Gassen, Koen L., van Rooij, Iris A. L. M., Giles, Rachel H., Beales, Philip L., Roepman, Ronald, Arts, Heleen H., Bongers, Ernie M. H. F., Renkema, Kirsten Y., Knoers, Nine V. A. M., van Reeuwijk, Jeroen, Lilien, Marc R.

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