Differential cross sections, polarisations and proton-gamma angular correlations for 54Fe, 60Ni(p, p) and (p, p′γ) at 10 MeV von Ahmed, M., Lowe, J., Rolph, P.M., Karban, O.

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Elastic scattering of 29 MeV 3He by complex nuclei von Baugh, D.J., Pyle, G.J.B., Rolph, P.M., Scarrott, S.M.

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The elastic scattering of 25MeV α-particles and neutron shell effects in the A = 50 TO A = 93 mass region von England, J.B.A., Baird, S., Newton, D.H., Picazo, T., Pollacco, E.C., Pyle, G.J., Rolph, P.M., Alabau, J., Casal, E., Garcia, A.

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Elastic scattering of polarized deuterons from a polarized proton target von Berovic, N., Blyth, C.O., Clews, C.J., Maughan, R.L., Rolph, P.M.

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The elastic scattering of 9.6 MeV protons and the reformulated optical model von Berovic, N., Rolph, P.M., Scarrott, S.M.

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The elastic scattering of 33 MeV 3He particles from 58,60,62,64Ni, 63,65Cu and 64,66,68Zn von Cage, M.E., Clough, D.L., Cole, A.J., England, J.B.A., Pyle, G.J., Rolph, P.M., Watson, L.H., Worledge, D.H.

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Differential cross sections and polarisations of 9.4 MeV protons elastically scattered by Ni 58, Ni 60 and Co 59 von Greenlees, G.W., Haznedaroglu, U., Robbins, A.B., Rolph, P.M., Rosenblatt, J.

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The Inelastic Scattering of 9.8 mev Protons by Medium Weight Nuclei von Greenlees, G W, Lowe, J, Robbins, A B, Rolph, P M

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A polarized proton target for low energy nuclear scattering experiments von Berovic, N., Clews, C.J., Maughan, R.L., Rolph, P.M.

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Differential cross sections and polarisations of 9.4 MeV protons elastically scattered by Ni58, Ni60 and Co59 von Greenlees, G.W., Haznedaroglu, U., Robbins, A.B., Rolph, P.M., Rosenblatt, J.

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Clinical Significance of De Novo and Inherited Copy-Number Variation von Vulto-van Silfhout, Anneke T., Hehir-Kwa, Jayne Y., van Bon, Bregje W.M., Schuurs-Hoeijmakers, Janneke H.M., Meader, Stephen, Hellebrekers, Claudia J.M., Thoonen, Ilse J.M., de Brouwer, Arjan P.M., Brunner, Han G., Webber, Caleb, Pfundt, Rolph, de Leeuw, Nicole, de Vries, Bert B.A.

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Pathogenic Variants in GPC4 Cause Keipert Syndrome von Amor, David J., Stephenson, Sarah E.M., Mustapha, Mirna, Mensah, Martin A., Ockeloen, Charlotte W., Lee, Wei Shern, Tankard, Rick M., Phelan, Dean G., Shinawi, Marwan, de Brouwer, Arjan P.M., Pfundt, Rolph, Dowling, Cari, Toler, Tomi L., Sutton, V. Reid, Agolini, Emanuele, Rinelli, Martina, Capolino, Rossella, Martinelli, Diego, Zampino, Giuseppe, Dumić, Miroslav, Reardon, William, Shaw-Smith, Charles, Leventer, Richard J., Delatycki, Martin B., Kleefstra, Tjitske, Mundlos, Stefan, Mortier, Geert, Bahlo, Melanie, Allen, Nicola J., Lockhart, Paul J.

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Variants in PUS7 Cause Intellectual Disability with Speech Delay, Microcephaly, Short Stature, and Aggressive Behavior von de Brouwer, Arjan P.M., Abou Jamra, Rami, Körtel, Nadine, Soyris, Clara, Polla, Daniel L., Safra, Modi, Zisso, Avia, Powell, Christopher A., Rebelo-Guiomar, Pedro, Dinges, Nadja, Morin, Violeta, Stock, Michael, Hussain, Mureed, Shahzad, Mohsin, Riazuddin, Saima, Ahmed, Zubair M., Pfundt, Rolph, Schwarz, Franziska, de Boer, Lonneke, Reis, André, Grozeva, Detilina, Raymond, F. Lucy, Riazuddin, Sheikh, Koolen, David A., Minczuk, Michal, Roignant, Jean-Yves, van Bokhoven, Hans, Schwartz, Schraga

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Diagnostic exome sequencing in 266 Dutch patients with visual impairment von Haer-Wigman, Lonneke, van Zelst-Stams, Wendy Ag, Pfundt, Rolph, van den Born, L Ingeborgh, Klaver, Caroline Cw, Verheij, Joke Bgm, Hoyng, Carel B, Breuning, Martijn H, Boon, Camiel Jf, Kievit, Anneke J, Verhoeven, Virginie Jm, Pott, Jan Wr, Sallevelt, Suzanne Ceh, van Hagen, Johanna M, Plomp, Astrid S, Kroes, Hester Y, Lelieveld, Stefan H, Hehir-Kwa, Jayne Y, Castelein, Steven, Nelen, Marcel, Scheffer, Hans, Lugtenberg, Dorien, Cremers, Frans Pm, Hoefsloot, Lies, Yntema, Helger G

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Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome von Willemsen, Marjolein H, Fernandez, Bridget A, Bacino, Carlos A, Gerkes, Erica, de Brouwer, Arjan PM, Pfundt, Rolph, Sikkema-Raddatz, Birgit, Scherer, Stephen W, Marshall, Christian R, Potocki, Lorraine, van Bokhoven, Hans, Kleefstra, Tjitske

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The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands von Zazo Seco, Celia, Wesdorp, Mieke, Feenstra, Ilse, Pfundt, Rolph, Hehir-Kwa, Jayne Y, Lelieveld, Stefan H, Castelein, Steven, Gilissen, Christian, de Wijs, Ilse J, Admiraal, Ronald Jc, Pennings, Ronald Je, Kunst, Henricus Pm, van de Kamp, Jiddeke M, Tamminga, Saskia, Houweling, Arjan C, Plomp, Astrid S, Maas, Saskia M, de Koning Gans, Pia Am, Kant, Sarina G, de Geus, Christa M, Frints, Suzanna Gm, Vanhoutte, Els K, van Dooren, Marieke F, van den Boogaard, Marie-José H, Scheffer, Hans, Nelen, Marcel, Kremer, Hannie, Hoefsloot, Lies, Schraders, Margit, Yntema, Helger G

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NR2F1 Mutations Cause Optic Atrophy with Intellectual Disability von Bosch, Daniëlle G.M., Boonstra, F. Nienke, Gonzaga-Jauregui, Claudia, Xu, Mafei, de Ligt, Joep, Jhangiani, Shalini, Wiszniewski, Wojciech, Muzny, Donna M., Yntema, Helger G., Pfundt, Rolph, Vissers, Lisenka E.L.M., Spruijt, Liesbeth, Blokland, Ellen A.W., Chen, Chun-An, Lewis, Richard A., Tsai, Sophia Y., Gibbs, Richard A., Tsai, Ming-Jer, Lupski, James R., Zoghbi, Huda Y., Cremers, Frans P.M., de Vries, Bert B.A., Schaaf, Christian P.

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De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalus von Nabais Sá, Maria J, Olson, Alexandra N, Yoon, Grace, Nimmo, Graeme A M, Gomez, Christopher M, Willemsen, Michèl A, Millan, Francisca, Schneider, Alexandra, Pfundt, Rolph, de Brouwer, Arjan P M, Dinman, Jonathan D, de Vries, Bert B A

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Novel genetic causes for cerebral visual impairment von Bosch, Daniëlle GM, Boonstra, F Nienke, de Leeuw, Nicole, Pfundt, Rolph, Nillesen, Willy M, de Ligt, Joep, Gilissen, Christian, Jhangiani, Shalini, Lupski, James R, Cremers, Frans PM, de Vries, Bert BA

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Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability von Willemsen, Marjolein H, Vallès, Astrid, Kirkels, Laurens A M H, Mastebroek, Mathilde, Olde Loohuis, Nikkie, Kos, Aron, Wissink-Lindhout, Willemijn M, de Brouwer, Arjan P M, Nillesen, Willy M, Pfundt, Rolph, Holder-Espinasse, Muriel, Vallée, Louis, Andrieux, Joris, Coppens-Hofman, Marjolein C, Rensen, Hanneke, Hamel, Ben C J, van Bokhoven, Hans, Aschrafi, Armaz, Kleefstra, Tjitske

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