Complaints against scientology doctors von Retief, L, Neveling, H, Bredell, C

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Test of the Brink-Axel Hypothesis for the Pygmy Dipole Resonance von Martin, D, von Neumann-Cosel, P, Tamii, A, Aoi, N, Bassauer, S, Bertulani, C A, Carter, J, Donaldson, L, Fujita, H, Fujita, Y, Hashimoto, T, Hatanaka, K, Ito, T, Krugmann, A, Liu, B, Maeda, Y, Miki, K, Neveling, R, Pietralla, N, Poltoratska, I, Ponomarev, V Yu, Richter, A, Shima, T, Yamamoto, T, Zweidinger, M

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Ethylene Tetramerization:  A New Route to Produce 1-Octene in Exceptionally High Selectivities von Bollmann, Annette, Blann, Kevin, Dixon, John T, Hess, Fiona M, Killian, Esna, Maumela, Hulisani, McGuinness, David S, Morgan, David H, Neveling, Arno, Otto, Stefanus, Overett, Matthew, Slawin, Alexandra M. Z, Wasserscheid, Peter, Kuhlmann, Sven

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Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy von Neveling, Kornelia, Martinez-Carrera, Lilian A., Hölker, Irmgard, Heister, Angelien, Verrips, Aad, Hosseini-Barkooie, Seyyed Mohsen, Gilissen, Christian, Vermeer, Sascha, Pennings, Maartje, Meijer, Rowdy, te Riele, Margot, Frijns, Catharina J.M., Suchowersky, Oksana, MacLaren, Linda, Rudnik-Schöneborn, Sabine, Sinke, Richard J., Zerres, Klaus, Lowry, R. Brian, Lemmink, Henny H., Garbes, Lutz, Veltman, Joris A., Schelhaas, Helenius J., Scheffer, Hans, Wirth, Brunhilde

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Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease von Khan, Mubeen, Cornelis, Stéphanie S., Khan, Muhammad Imran, Elmelik, Duaa, Manders, Eline, Bakker, Sem, Derks, Ronny, Neveling, Kornelia, Vorst, Maartje, Gilissen, Christian, Meunier, Isabelle, Defoort, Sabine, Puech, Bernard, Devos, Aurore, Schulz, Heidi L., Stöhr, Heidi, Grassmann, Felix, Weber, Bernhard H. F., Dhaenens, Claire‐Marie, Cremers, Frans P. M.

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The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia von Levran, Orna, Milton, Kelly L, Henry, Rashida T, Neveling, Kornelia, Ott, Jurg, Attwooll, Claire, Rio, Paula, Schindler, Detlev, Petrini, John, Batish, Sat Dev, Auerbach, Arleen D, Velleuer, Eunike, Kalb, Reinhard, Barral, Sandra, Hanenberg, Helmut

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Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability von Kleefstra, Tjitske, Kramer, Jamie M., Neveling, Kornelia, Willemsen, Marjolein H., Koemans, Tom S., Vissers, Lisenka E.L.M., Wissink-Lindhout, Willemijn, Fenckova, Michaela, van den Akker, Willem M.R., Kasri, Nael Nadif, Nillesen, Willy M., Prescott, Trine, Clark, Robin D., Devriendt, Koenraad, van Reeuwijk, Jeroen, de Brouwer, Arjan P.M., Gilissen, Christian, Zhou, Huiqing, Brunner, Han G., Veltman, Joris A., Schenck, Annette, van Bokhoven, Hans

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Nonquenched Isoscalar Spin-M1 Excitations in sd-Shell Nuclei von Matsubara, H, Tamii, A, Nakada, H, Adachi, T, Carter, J, Dozono, M, Fujita, H, Fujita, K, Fujita, Y, Hatanaka, K, Horiuchi, W, Itoh, M, Kawabata, T, Kuroita, S, Maeda, Y, Navrátil, P, von Neumann-Cosel, P, Neveling, R, Okamura, H, Popescu, L, Poltoratska, I, Richter, A, Rubio, B, Sakaguchi, H, Sakaguchi, S, Sakemi, Y, Sasamoto, Y, Shimbara, Y, Shimizu, Y, Smit, F D, Suda, K, Tameshige, Y, Tokieda, H, Yamada, Y, Yosoi, M, Zenihiro, J

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Damping of the isovector giant dipole resonance in 40,48Ca von Carter, J., Donaldson, L.M., Fujita, H., Fujita, Y., Jingo, M., Kureba, C.O., Latif, M.B., Litvinova, E., Nemulodi, F., von Neumann-Cosel, P., Neveling, R., Papakonstantinou, P., Papka, P., Pellegri, L., Ponomarev, V.Yu, Richter, A., Roth, R., Sideras-Haddad, E., Smit, F.D., Swartz, J.A., Tamii, A., Trippel, R., Usman, I.T., Wibowo, H.

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Mutations in the Mevalonate Kinase ( MVK ) Gene Cause Nonsyndromic Retinitis Pigmentosa von Siemiatkowska, Anna M., PhD, van den Born, L. Ingeborgh, MD, PhD, van Hagen, P. Martin, MD, PhD, Stoffels, Monique, MSc, Neveling, Kornelia, PhD, Henkes, Arjen, BSc, Kipping-Geertsema, Mieke, BSc, Hoefsloot, Lies H., PhD, Hoyng, Carel B., MD, PhD, Simon, Anna, MD, PhD, den Hollander, Anneke I., PhD, Cremers, Frans P.M., PhD, Collin, Rob W.J., PhD

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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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Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant von Smits, Jeroen J., de Bruijn, Suzanne E., Lanting, Cornelis P., Oostrik, Jaap, O’Gorman, Luke, Mantere, Tuomo, Cremers, Frans P. M., Roosing, Susanne, Yntema, Helger G., de Vrieze, Erik, Derks, Ronny, Hoischen, Alexander, Pegge, Sjoert A. H., Neveling, Kornelia, Pennings, Ronald J. E., Kremer, Hannie

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Complete Electric Dipole Response and the Neutron Skin in Pb 208 von Tamii, A., Poltoratska, I., von Neumann-Cosel, P., Fujita, Y., Adachi, T., Bertulani, C. A., Carter, J., Dozono, M., Fujita, H., Fujita, K., Hatanaka, K., Ishikawa, D., Itoh, M., Kawabata, T., Kalmykov, Y., Krumbholz, A. M., Litvinova, E., Matsubara, H., Nakanishi, K., Neveling, R., Okamura, H., Ong, H. J., Özel-Tashenov, B., Ponomarev, V. Yu, Richter, A., Rubio, B., Sakaguchi, H., Sakemi, Y., Sasamoto, Y., Shimbara, Y., Shimizu, Y., Smit, F. D., Suzuki, T., Tameshige, Y., Wambach, J., Yamada, R., Yosoi, M., Zenihiro, J.

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Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant von Smits, Jeroen J., de Bruijn, Suzanne E., Lanting, Cornelis P., Oostrik, Jaap, O’Gorman, Luke, Mantere, Tuomo, Cremers, Frans P. M., Roosing, Susanne, Yntema, Helger G., de Vrieze, Erik, Derks, Ronny, Hoischen, Alexander, Pegge, Sjoert A. H., Neveling, Kornelia, Pennings, Ronald J. E., Kremer, Hannie

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Long-Read Sequencing Identifies Novel Pathogenic Intronic Variants in Gitelman Syndrome von Viering, Daan H H M, Hureaux, Marguerite, Neveling, Kornelia, Latta, Femke, Kwint, Michael, Blanchard, Anne, Konrad, Martin, Bindels, René J M, Schlingmann, Karl-Peter, Vargas-Poussou, Rosa, de Baaij, Jeroen H F

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Deformation dependence of the isovector giant dipole resonance: The neodymium isotopic chain revisited von Donaldson, L.M., Bertulani, C.A., Carter, J., Nesterenko, V.O., von Neumann-Cosel, P., Neveling, R., Ponomarev, V.Yu, Reinhard, P.-G., Usman, I.T., Adsley, P., Brummer, J.W., Buthelezi, E.Z., Cooper, G.R.J., Fearick, R.W., Förtsch, S.V., Fujita, H., Fujita, Y., Jingo, M., Kleinig, W., Kureba, C.O., Kvasil, J., Latif, M., Li, K.C.W., Mira, J.P., Nemulodi, F., Papka, P., Pellegri, L., Pietralla, N., Richter, A., Sideras-Haddad, E., Smit, F.D., Steyn, G.F., Swartz, J.A., Tamii, A.

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Development of (p,p′γ) detection capabilities at iThemba LABS through the study of low-lying E1 strength in 58Ni von Molaeng, R E, Donaldson, L M, Pellegri, L, Usman, I T, Bahini, A, Brümmer, J W, Jivan, H, Jones, P, Jongile, S, Li, K C W, Neveling, R, Smit, F D, Steyn, G F

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Disruption of the Basal Body Protein POC1B Results in Autosomal-Recessive Cone-Rod Dystrophy von Roosing, Susanne, Lamers, Ideke J.C., de Vrieze, Erik, van den Born, L. Ingeborgh, Lambertus, Stanley, Arts, Heleen H., Boldt, Karsten, de Baere, Elfride, Klaver, Caroline C.W., Coppieters, Frauke, Koolen, David A., Lugtenberg, Dorien, Neveling, Kornelia, van Reeuwijk, Jeroen, Ueffing, Marius, van Beersum, Sylvia E.C., Zonneveld-Vrieling, Marijke N., Peters, Theo A., Hoyng, Carel B., Kremer, Hannie, Hetterschijt, Lisette, Letteboer, Stef J.F., van Wijk, Erwin, Roepman, Ronald, den Hollander, Anneke I., Cremers, Frans P.M.

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Investigating the pygmy dipole resonance in 96Mo using the (p,d) reaction von Khumalo, T C, Pellegri, L, Wiedeking, M, Cappuzzello, F, Cavallaro, M, Carbone, D, Spatafora, A, Adsley, P, Agodi, C, Brischetto, G, Calabrese, S, Ciraldo, I, Isaak, J, Jivan, H, Jongile, S, La Fauci, L, Lanza, E G, Malatji, K L, Netshiya, A A, Neveling, R, Sgouros, O, Sideras-Haddad, E, Soukeras, V, Torresi, D

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Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype von Grolleman, Judith E., de Voer, Richarda M., Elsayed, Fadwa A., Nielsen, Maartje, Weren, Robbert D.A., Palles, Claire, Ligtenberg, Marjolijn J.L., Vos, Janet R., ten Broeke, Sanne W., de Miranda, Noel F.C.C., Kuiper, Renske A., Kamping, Eveline J., Jansen, Erik A.M., Vink-Börger, M. Elisa, Popp, Isabell, Lang, Alois, Spier, Isabel, Hüneburg, Robert, James, Paul A., Li, Na, Staninova, Marija, Lindsay, Helen, Cockburn, David, Spasic-Boskovic, Olivera, Clendenning, Mark, Sweet, Kevin, Capellá, Gabriel, Sjursen, Wenche, Høberg-Vetti, Hildegunn, Jongmans, Marjolijn C., Neveling, Kornelia, Geurts van Kessel, Ad, Morreau, Hans, Hes, Frederik J., Sijmons, Rolf H., Schackert, Hans K., Ruiz-Ponte, Clara, Dymerska, Dagmara, Lubinski, Jan, Rivera, Barbara, Foulkes, William D., Tomlinson, Ian P., Valle, Laura, Buchanan, Daniel. D., Kenwrick, Sue, Adlard, Julian, Dimovski, Aleksandar J., Campbell, Ian G., Aretz, Stefan, Schindler, Detlev, van Wezel, Tom, Hoogerbrugge, Nicoline, Kuiper, Roland P.

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