Effect of inbreeding on intellectual disability revisited by trio sequencing von Kahrizi, Kimia, Hu, Hao, Hosseini, Masoumeh, Kalscheuer, Vera M., Fattahi, Zohreh, Beheshtian, Maryam, Suckow, Vanessa, Mohseni, Marzieh, Lipkowitz, Bettina, Mehvari, Sepideh, Mehrjoo, Zohreh, Akhtarkhavari, Tara, Ghaderi, Zhila, Rahimi, Maryam, Arzhangi, Sanaz, Jamali, Payman, Falahat Chian, Milad, Nikuei, Pooneh, Sabbagh Kermani, Farahnaz, Sadeghinia, Farnaz, Jazayeri, Roshanak, Tonekaboni, S. Hassan, Khoshaeen, Atefeh, Habibi, Haleh, Pourfatemi, Fatemeh, Mojahedi, Faezeh, Khodaie‐Ardakani, Mohammad‐Reza, Najafipour, Reza, Wienker, Thomas F., Najmabadi, Hossein, Ropers, Hans‐Hilger

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GPR30 estrogen receptor agonists induce mechanical hyperalgesia in the rat von Kuhn, Julia, Dina, Olayinka A., Goswami, Chandan, Suckow, Vanessa, Levine, Jon D., Hucho, Tim

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The Opitz Syndrome Gene Product, MID1, Associates with Microtubules von Schweiger, Susann, Foerster, John, Lehmann, Tanja, Suckow, Vanessa, Muller, Yves A., Walter, Gerald, Davies, Theresa, Porter, Helen, van Bokhoven, Hans, Lunt, Peter W., Traub, Peter, Ropers, Hans-Hilger

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Elevated levels of Rad51 recombination protein in tumor cells von RADERSCHALL, Elke, STOUT, Karen, FREIER, Susanne, SUCKOW, Vanessa, SCHWEIGER, Susann, HAAF, Thomas

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Deleterious de novo variants of X‐linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita von Frints, Suzanna G.M., Hennig, Friederike, Colombo, Roberto, Jacquemont, Sebastien, Terhal, Paulien, Zimmerman, Holly H., Hunt, David, Mendelsohn, Bryce A., Kordaß, Ulrike, Webster, Richard, Sinnema, Margje, Abdul‐Rahman, Omar, Suckow, Vanessa, Fernández‐Jaén, Alberto, Roozendaal, Kees, Stevens, Servi J.C., Macville, Merryn V.E., Al‐Nasiry, Salwan, Gassen, Koen, Utzig, Norbert, Koudijs, Suzanne M., McGregor, Lesley, Maas, Saskia M., Baralle, Diana, Dixit, Abhijit, Wieacker, Peter, Lee, Marcus, Lee, Arthur S., Engle, Elizabeth C., Houge, Gunnar, Gradek, Gyri A., Douglas, Andrew G.L., Longman, Cheryl, Joss, Shelagh, Velasco, Danita, Hennekam, Raoul C., Hirata, Hiromi, Kalscheuer, Vera M.

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Novel pathogenic EIF2S3 missense variants causing clinically variable MEHMO syndrome with impaired eIF2γ translational function, and literature review von Kotzaeridou, Urania, Young‐Baird, Sara K., Suckow, Vanessa, Thornburg, Alexis G., Wagner, Matias, Harting, Inga, Christ, Stine, Strom, Tim, Dever, Thomas E., Kalscheuer, Vera M.

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Redefining the MED13L syndrome von Adegbola, Abidemi, Musante, Luciana, Callewaert, Bert, Maciel, Patricia, Hu, Hao, Isidor, Bertrand, Picker-Minh, Sylvie, Le Caignec, Cedric, Delle Chiaie, Barbara, Vanakker, Olivier, Menten, Björn, Dheedene, Annelies, Bockaert, Nele, Roelens, Filip, Decaestecker, Karin, Silva, João, Soares, Gabriela, Lopes, Fátima, Najmabadi, Hossein, Kahrizi, Kimia, Cox, Gerald F, Angus, Steven P, Staropoli, John F, Fischer, Ute, Suckow, Vanessa, Bartsch, Oliver, Chess, Andrew, Ropers, Hans-Hilger, Wienker, Thomas F, Hübner, Christoph, Kaindl, Angela M, Kalscheuer, Vera M

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MID1 , mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation von Schweiger, Susann, Trockenbacher, Alexander, Suckow, Vanessa, Foerster, John, Winter, Jennifer, Krauß, Sybille, Ropers, Hans-Hilger, Schneider, Rainer

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Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutations von Hu, Hao, Suckow, Vanessa, Musante, Luciana, Roggenkamp, Viola, Kraemer, Nadine, Ropers, Hans-Hilger, Hübner, Christoph, Wienker, Thomas F, Kaindl, Angela M

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Ca++/CaMKII switches nociceptor-sensitizing stimuli into desensitizing stimuli von Hucho, Tim, Suckow, Vanessa, Joseph, Elizabeth K., Kuhn, Julia, Schmoranzer, Jan, Dina, Olayinka A., Chen, Xiaojie, Karst, Matthias, Bernateck, Michael, Levine, Jon D., Ropers, Hans-Hilger

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ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation von Alber, Michael, Kalscheuer, Vera M, Marco, Elysa, Sherr, Elliott, Lesca, Gaetan, Till, Marianne, Gradek, Gyri, Wiesener, Antje, Korenke, Christoph, Mercier, Sandra, Becker, Felicitas, Yamamoto, Toshiyuki, Scherer, Stephen W, Marshall, Christian R, Walker, Susan, Dutta, Usha R, Dalal, Ashwin B, Suckow, Vanessa, Jamali, Payman, Kahrizi, Kimia, Najmabadi, Hossein, Minassian, Berge A

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NYX (Nyctalopin on Chromosome X), the Gene Mutated in Congenital Stationary Night Blindness, Encodes a Cell Surface Protein von Zeitz, Christina, Scherthan, Harry, Freier, Susanne, Feil, Silke, Suckow, Vanessa, Schweiger, Susann, Berger, Wolfgang

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Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations von So, Joyce, Suckow, Vanessa, Kijas, Zofia, Kalscheuer, Vera, Moser, Bettina, Winter, Jennifer, Baars, Marieke, Firth, Helen, Lunt, Peter, Hamel, Ben, Meinecke, Peter, Moraine, Claude, Odent, Sylvie, Schinzel, Albert, van der Smagt, J.J., Devriendt, Koen, Albrecht, Beate, Gillessen-Kaesbach, Gabriele, van der Burgt, Ineke, Petrij, Fred, Faivre, Laurence, McGaughran, Julie, McKenzie, Fiona, Opitz, John M., Cox, Timothy, Schweiger, Susann

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Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing von WINTER, Jennifer, LEHMANN, Tanja, SCHNEIDER, Rainer, SCHWEIGER, Susann, KRAUSS, Sybille, TROCKENBACHER, Alexander, KIJAS, Zofia, FOERSTER, John, SUCKOW, Vanessa, YASPO, Marie-Laure, KULOZIK, Andreas, KALSCHEUER, Vera

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Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations von So, Joyce, Suckow, Vanessa, Kijas, Zofia, Schinzel, Albert

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Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome von WINTER, Jennifer, LEHMANN, Tanja, ROPERS, Hans-Hilger, SCHWEIGER, Susann, SUCKOW, Vanessa, KIJAS, Zofia, KULOZIK, Andreas, KALSCHEUER, Vera, HAMEL, Ben, DEVRIENDT, Koen, OPITZ, John, LENZNER, Steffen

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NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein von Zeitz, Christina, Scherthan, Harry, Freier, Susanne, Feil, Silke, Suckow, Vanessa, Schweiger, Susann, Berger, Wolfgang

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A rapid and inexpensive method for large-scale DNA sequencing of regions with large amounts of repetitive elements von Suckow, Vanessa, Fartmann, Berthold, Todt, Tilman, van der Maarel, Silvere M., Foerster, John, Schweiger, Susann

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Means for use in treating diseases correlated with or caused by non-physiological levels of microtubule-associated PP2Ac von TROCKENBACHER ALEXANDER, KRAUSS SYBILLE, SUCKOW VANESSA, ROPERS HANS-HILGER, WINTER JENNIFER, SCHNEIDER RAINER, SCHWEIGER SUSANN, FOERSTER JOHN

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Means for use in treating diseases correlated with or caused by non-physiological levels of microtubule-associated PP2Ac von Schweiger, Susann, Ropers, Hans-Hilger, Winter, Jennifer, Krauss, Sybille, Suckow, Vanessa, Schneider, Rainer, Trockenbacher, Alexander, Foerster, John

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