Modelling land-use effects of future urbanization using cellular automata: An Eastern Danish case von Fuglsang, Morten, Münier, Bernd, Hansen, Henning Sten

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Wildlife vulnerability and risk maps for combined pollutants von Lahr, Joost, Münier, Bernd, De Lange, Hendrika J., Faber, Jack F., Sørensen, Peter Borgen

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Conscious worst case definition for risk assessment, part II: a methodological case study for pesticide risk assessment von Sørensen, Peter B, Giralt, Francesc, Rallo, Robert, Espinosa, Gabriela, Münier, Bernd, Gyldenkaerne, Steen, Thomsen, Marianne

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Accessibility Analysis and Modelling in Public Transport Networks – A Raster Based Approach von Fuglsang, Morten, Hansen, Henning Sten, Münier, Bernd

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Mapping Transport Sensitive Areas at EU Level: The ASSET Project von Enei, Riccardo, Münier, Bernd, Ricci, Andrea, Fuglsang, Morten

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Wildlife vulnerability and risk maps for combined pollutants: Cumulative Stressors - Risk assessment of mixtures of chemicals and combinations of chemicals and natural stressors von LAHR, Joost, MÜNIER, Bernd, DE LANGE, Hendrika J, FABER, Jack F, BORGEN SØRENSEN, Peter

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Conscious worst case definition for risk assessment, part II A methodological case study for pesticide risk assessment: Cumulative Stressors - Risk assessment of mixtures of chemic... von SORENSEN, Peter B, GIRALT, Francesc, RALLO, Robert, ESPINOSA, Gabriela, MÜNIER, Bernd, GYLDENKAERNE, Steen, THOMSEN, Marianne

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Conscious worst case definition for risk assessment, part II von Sørensen, Peter B., Giralt, Francesc, Rallo, Robert, Espinosa, Gabriela, Münier, Bernd, Gyldenkærne, Steen, Thomsen, Marianne

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Prediction of Habitat Quality Using Ordination and Neural Networks von Ejrnæs, Rasmus, Aude, Erik, Nygaard, Bettina, Münier, Bernd

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A biotope landscape model for prediction of semi-natural vegetation in Denmark von Münier, Bernd, Nygaard, B, Ejrnæs, R, Bruun, H.G

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A spatial assessment of ecosystem services in Europe: methods, case studies and policy analysis: phase 2, synthesis report von Maes, Joachim, Hauck, Jennifer, Termansen, Mette, Paracchini, Maria Luisa, Ratamäki, Outi, Perez-Soba, Marta, Kopperoinen, Leena, Rankinen, Katri, Schägner, Jan Philipp, Henrys, Peter, Cisowska, Iwona, Zandersen, Marianne, Jax, Kurt, La Notte, Alessandra, Leikola, Niko, Pouta, Eija, Smart, Simon, Hasler, Berit, Lankia, Tuija, Estrup Andersen, Hans, Lavalle, Carlo, Vermaas, Tommer, Hussen Alemu, Mohammed, Scholefield, Paul, Batista, Filipe, Pywell, Richard, Hutchins, Mike, Blemmer, Morten, Fonnesbech-Wulff, Anders, Vanbergen, Adam J, Münier, Bernd, Baranzelli, Claudia, Roy, David, Thieu, Vincent, Zulian, Grazia, Kuussaari, Mikko, Thodsen, Hans, Alanen, Eeva-Liisa, Egoh, Benis, Borgen Sørensen, Peter, Braat, Leon, Bidoglio, Giovanni

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Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F‐mediated inherited retinal disorders von Zeitz, Christina, Michiels, Christelle, Neuillé, Marion, Friedburg, Christoph, Condroyer, Christel, Boyard, Fiona, Antonio, Aline, Bouzidi, Nassima, Milicevic, Diana, Veaux, Robin, Tourville, Aurore, Zoumba, Axelle, Seneina, Imene, Foussard, Marine, Andrieu, Camille, N. Preising, Markus, Blanchard, Steven, Saraiva, Jean‐Paul, Mesrob, Lilia, Le Floch, Edith, Jubin, Claire, Meyer, Vincent, Blanché, Hélène, Boland, Anne, Deleuze, Jean‐François, Sharon, Dror, Drumare, Isabelle, Defoort‐Dhellemmes, Sabine, Baere, Elfride, Leroy, Bart P., Zanlonghi, Xavier, Casteels, Ingele, Ravel, Thomy J., Balikova, Irina, Koenekoop, Rob K., Laffargue, Fanny, McLean, Rebecca, Gottlob, Irene, Bonneau, Dominique, Schorderet, Daniel F., L. Munier, Francis, McKibbin, Martin, Prescott, Katrina, Pelletier, Valerie, Dollfus, Hélène, Perdomo‐Trujillo, Yaumara, Faure, Céline, Reiff, Charlotte, Wissinger, Bernd, Meunier, Isabelle, Kohl, Susanne, Banin, Eyal, Zrenner, Eberhart, Jurklies, Bernhard, Lorenz, Birgit, Sahel, José‐Alain, Audo, Isabelle

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Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness von ZEITZ, Christina, KLOECKENER-GRUISSEM, Barbara, MUNIER, Francis L, BERGER, Wolfgang, FORSTER, Ursula, KOHL, Susanne, MAGYAR, Istvan, WISSINGER, Bernd, MATYAS, Gabor, BORRUAT, Francois-Xavier, SCHORDERET, Daniel F, ZRENNER, Eberhart

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TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Kohl, Susanne, Leroy, Bart P., Munier, Francis L., Guillonneau, Xavier, Mohand-Saïd, Saddek, Bujakowska, Kinga, Nandrot, Emeline F., Lorenz, Birgit, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Bernd, Antje, Antonio, Aline, Moskova-Doumanova, Veselina, Lancelot, Marie-Elise, Poloschek, Charlotte M., Drumare, Isabelle, Defoort-Dhellemmes, Sabine, Wissinger, Bernd, Léveillard, Thierry, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Berger, Wolfgang, Jacobson, Samuel G., Zrenner, Eberhart, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M., Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D., Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P., Munier, Francis L., Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G., Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W., Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia von KOHL, Susanne, VARSANYI, Balazs, JURKLIES, Bernhard, FARKAS, Agnes, ANDREASSON, Sten, WELEBER, Richard G, JACOBSON, Samuel G, RUDOLPH, Günther, CASTELLAN, Claudio, DOLLFUS, Helene, LEGIUS, Eric, ANASTASI, Mario, ANTUNES, Gesine Abadin, BITOUN, Pierre, LEV, Dorit, SIEVING, Paul A, MUNIER, Francis L, ZRENNER, Eberhart, SHARPE, Lindsay T, CREMERS, Frans P. M, WISSINGER, Bernd, BAUMANN, Britta, HOYNG, Carel B, JÄGLE, Herbert, ROSENBERG, Thomas, KELLNER, Ulrich, LORENZ, Birgit, SALATI, Roberto

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Genotyping Microarray for CSNB-Associated Genes von Zeitz, Christina, Labs, Stephan, Lorenz, Birgit, Forster, Ursula, Uksti, Janne, Kroes, Hester Y, De Baere, Elfride, Leroy, Bart P, Cremers, Frans P. M, Wittmer, Mariana, van Genderen, Maria M, Sahel, Jose-Alain, Audo, Isabelle, Poloschek, Charlotte M, Mohand-Said, Saddek, Fleischhauer, Johannes C, Huffmeier, Ulrike, Moskova-Doumanova, Veselina, Levin, Alex V, Hamel, Christian P, Leifert, Dorothee, Munier, Francis L, Schorderet, Daniel F, Zrenner, Eberhart, Friedburg, Christoph, Wissinger, Bernd, Kohl, Susanne, Berger, Wolfgang

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Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders von Zeitz, Christina, Michiels, Christelle, Neuille, Marion, Friedburg, Christoph, Condroyer, Christel, Boyard, Fiona, Antonio, Aline, Bouzidi, Nassima, Milicevic, Diana, Veaux, Robin, Tourville, Aurore, Zoumba, Axelle, Seneina, Imene, Foussard, Marine, Andrieu, Camille, Preising, Markus N, Blanchard, Steven, Saraiva, Jean-Paul, Mesrob, Lilia, Le Floch, Edith, Jubin, Claire, Meyer, Vincent, Blanche, Helene, Boland, Anne, Deleuze, Jean-Francois, Sharon, Dror, Drumare, Isabelle, Defoort-Dhellemmes, Sabine, De Baere, Elfride, Leroy, Bart P, Zanlonghi, Xavier, Casteels, Ingele, de Ravel, Thorny J, Balikova, Irina, Koenekoop, Rob K, Laffargue, Fanny, McLean, Rebecca, Gottlob, Irene, Bonneau, Dominique, Schorderet, Daniel F, Munier, Francis L, McKibbin, Martin, Prescott, Katrina, Pelletier, Valerie, Dollfus, Helene, Perdomo-Trujillo, Yaumara, Faure, Celine, Reiff, Charlotte, Wissinger, Bernd, Meunier, Isabelle, Kohl, Susanne, Banin, Eyal, Zrenner, Eberhart, Jurklies, Bernhard, Lorenz, Birgit, Sahel, Jose-Alain, Audo, Isabelle

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Modelling the alteration gel composition of simplified borosilicate glasses by precipitation of an ideal solid solution in equilibrium with the leachant von Munier, I., Crovisier, J.-L., Grambow, B., Fritz, B., Clément, A.

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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M., Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D., Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P., Munier, Francis L., Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G., Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W., Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

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