Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs von Schulz, Heidi L, Grassmann, Felix, Kellner, Ulrich, Spital, Georg, Rüther, Klaus, Jägle, Herbert, Hufendiek, Karsten, Rating, Philipp, Huchzermeyer, Cord, Baier, Maria J, Weber, Bernhard H F, Stöhr, Heidi

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TMEM16B, A Novel Protein with Calcium-Dependent Chloride Channel Activity, Associates with a Presynaptic Protein Complex in Photoreceptor Terminals von Stohr, Heidi, Heisig, Julia B, Benz, Peter M, Schoberl, Simon, Milenkovic, Vladimir M, Strauss, Olaf, Aartsen, Wendy M, Wijnholds, Jan, Weber, Bernhard H. F, Schulz, Heidi L

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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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Mutation-Dependent Pathomechanisms Determine the Phenotype in the Bestrophinopathies von Nachtigal, Anna-Lena, Milenkovic, Andrea, Brandl, Caroline, Schulz, Heidi L, Duerr, Lisa M J, Lang, Gabriele E, Reiff, Charlotte, Herrmann, Philipp, Kellner, Ulrich, Weber, Bernhard H F

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Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions von Brandl, Caroline, Schulz, Heidi L, Charbel Issa, Peter, Birtel, Johannes, Bergholz, Richard, Lange, Clemens, Dahlke, Claudia, Zobor, Ditta, Weber, Bernhard H F, Stöhr, Heidi

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Clinical, neuroradiological and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder von Accogli, Andrea, Lin, Sheng-Jia, Severino, Mariasavina, Kim, Sung-Hoon, Huang, Kevin, Rocca, Clarissa, Landsverk, Megan, Zaki, Maha, Al-Maawali, Almundher, srinivasan, Varunvenkat M., Al-Thihli, Khalid, Schaefer, G. Bradly, Davis, Monica, Tonduti, Davide, Doneda, Chiara, Marten, Lara M., Mühlhausen, Chris, Gomez, Maria, Lamantea, Eleonora, Mena, Rafael, Nizon, Mathilde, Procaccio, Vincent, Begtrup, Amber, Telegrafi, Aida, Cui, Hong, Schulz, Heidi L., Mohr, Julia, Biskup, Saskia, Loos, Mariana Amina, Aráoz, Hilda Verónica, Salpietro, Vincenzo, Keppen, Laura Davis, Chitre, Manali, Petree, Cassidy, Raymond, Lucy, Vogt, Julie, Swayer, Lindsey B., Basinger, Alice A., Pedersen, Signe Vandal, Pearson, Toni S., Grange, Dorothy K., Lingapp, Lokesh, McDunnah, Paige, Horvath, Rita, Cogne, Benjamin, Isidor, Bertrand, Hahn, Andreas, Gripp, Karen, Jafarnejad, Seyed Mehdi, Ostergaard, Elsebet, Prada, Carlos E., Ghezzi, Daniele, Gowda, Vykuntaraju K., Taylor, Robert W., Sonenberg, Nahum, Houlden, Henry, Sissler, Marie, Varshney, Gaurav K., Maroofian, Reza

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Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development D... von Ghasemi, Mohammad-Reza, Fateh, Sahand Tehrani, Ben-Mahmoud, Afif, Gupta, Vijay, Stühn, Lara G, Lesca, Gaetan, Chatron, Nicolas, Platzer, Konrad, Edery, Patrick, Sadeghi, Hossein, Isidor, Bertrand, Cogné, Benjamin, Schulz, Heidi L, Krauspe-Stübecke, Ilona, Periyasamy, Radhakrishnan, Nampoothiri, Sheela, Mirfakhraie, Reza, Alijanpour, Sahar, Syrbe, Steffen, Pfeifer, Ulrich, Spranger, Stephanie, Grundmann-Hauser, Kathrin, Haack, Tobias B, Papadopoulou, Maria T, da Silva Gonçalves, Tayrine, Panagiotakaki, Eleni, Arzimanoglou, Alexis, Tonekaboni, Seyed Hassan, Rossi, Massimiliano, Korenke, G Christoph, Lacassie, Yves, Jang, Mi-Hyeon, Layman, Lawrence C, Miryounesi, Mohammad, Kim, Hyung-Goo

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Meta-analysis of genome scans of age-related macular degeneration von Fisher, Sheila A., Abecasis, Goncalo R., Yashar, Beverly M., Zareparsi, Sepideh, Swaroop, Anand, Iyengar, Sudha K., Klein, Barbara E.K., Klein, Ronald, Lee, Kristine E., Majewski, Jacek, Schultz, Dennis W., Klein, Michael L., Seddon, Johanna M., Santangelo, Susan L., Weeks, Daniel E., Conley, Yvette P., Mah, Tammy S., Schmidt, Silke, Haines, Jonathan L., Pericak-Vance, Margaret A., Gorin, Michael B., Schulz, Heidi L., Pardi, Fabio, Lewis, Cathryn M., Weber, Bernhard H.F.

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A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD) von Grassmann, Felix, Friedrich, Ulrike, Fauser, Sascha, Schick, Tina, Milenkovic, Andrea, Schulz, Heidi L., von Strachwitz, Claudia N., Bettecken, Thomas, Lichtner, Peter, Meitinger, Thomas, Arend, Nicole, Wolf, Armin, Haritoglou, Christos, Rudolph, Guenther, Chakravarthy, Usha, Silvestri, Giuliana, McKay, Gareth J., Freitag-Wolf, Sandra, Krawczak, Michael, Smith, R. Theodore, Merriam, John C., Merriam, Joanna E., Allikmets, Rando, Heid, Iris M., Weber, Bernhard H. F.

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The Retinome - defining a reference transcriptome of the adult mammalian retina/retinal pigment epithelium von Schulz, Heidi L, Goetz, Thomas, Kaschkoetoe, Juergen, Weber, Bernhard H F

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Characterization of three novel isoforms of the metabotrobic glutamate receptor 7 (GRM7) von Schulz, Heidi L., Stohr, Heidi, Weber, Bernhard H.F.

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Antineoplastic agent workplace contamination study: the Alberta Cancer Board Pharmacy perspective von Schulz, Heidi, Bigelow, Susan, Dobish, Roxanne, Chambers, Carole R

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Genomic structure and assessment of the retinally expressed RFamide-related peptide gene in dominant cystoid macular dystrophy von Schulz, Heidi L, Stoehr, Heidi, White, Karen, van Driel, Marc A, Hoyng, Carel B, Cremers, Frans, Weber, Bernhard H F

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Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomes von Mah, Nancy, Stoehr, Heidi, Schulz, Heidi L, White, Karen, Weber, Bernhard H.F

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Antineoplastic agent workplace contamination study: the Alberta Cancer Board Pharmacy perspective Phase III von Bigelow, Susan, Schulz, Heidi, Dobish, Roxanne, Chambers, Carole R

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Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder von Accogli, Andrea, Lin, Sheng-Jia, Severino, Mariasavina, Kim, Sung-Hoon, Huang, Kevin, Rocca, Clarissa, Landsverk, Megan, Zaki, Maha, Al-Maawali, Almundher, Srinivasan, Varunvenkat M, Al-Thihli, Khalid, Schaefer, G Bradly, Davis, Monica, Tonduti, Davide, Doneda, Chiara, Marten, Lara M, Mühlhausen, Chris, Gomez, Maria, Lamantea, Eleonora, Mena, Rafael, Nizon, Mathilde, Procaccio, Vincent, Begtrup, Amber, Telegrafi, Aida, Cui, Hong, Schulz, Heidi L, Mohr, Julia, Biskup, Saskia, Loos, Mariana Amina, Aráoz, Hilda Verónica, Salpietro, Vincenzo, Keppen, Laura Davis, Chitre, Manali, Petree, Cassidy, Raymond, Lucy, Vogt, Julie, Swayer, Lindsey B, Basinger, Alice A, Pedersen, Signe Vandal, Pearson, Toni S, Grange, Dorothy K, Lingapp, Lokesh, McDunnah, Paige, Horvath, Rita, Cogne, Benjamin, Isidor, Bertrand, Hahn, Andreas, Gripp, Karen, Jafarnejad, Seyed Mehdi, Ostergaard, Elsebet, Prada, Carlos E, Ghezzi, Daniele, Gowda, Vykuntaraju K, Taylor, Robert W, Sonenberg, Nahum, Houlden, Henry, Sissler, Marie, Varshney, Gaurav K, Maroofian, Reza

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Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions von Brandl, Caroline, Schulz, Heidi L, Issa, Peter Charbel, Birtel, Johannes, Bergholz, Richard, Lange, Clemens, Dahlke, Claudia, Zobor, Ditta, Weber, Bernhard H. F, Stöhr, Heidi

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Digitale Feedbacksysteme und Mitarbeit von Schülern im Unterricht von Kreuzkam, Stephan, Crusade, Stephan

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The State of Vaccine Confidence 2016: Global Insights Through a 67-Country Survey von Larson, Heidi J., de Figueiredo, Alexandre, Xiahong, Zhao, Schulz, William S., Verger, Pierre, Johnston, Iain G., Cook, Alex R., Jones, Nick S.

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Measuring trust in vaccination: A systematic review von Larson, Heidi J., Clarke, Richard M., Jarrett, Caitlin, Eckersberger, Elisabeth, Levine, Zachary, Schulz, Will S., Paterson, Pauline

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