Associations between pathogen-specific cases of subclinical mastitis and milk yield, quality, protein composition, and cheese-making traits in dairy cows von Bobbo, T., Ruegg, P.L., Stocco, G., Fiore, E., Gianesella, M., Morgante, M., Pasotto, D., Bittante, G., Cecchinato, A.

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Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles von Nolin, Sarah L., Glicksman, Anne, Tortora, Nicole, Allen, Emily, Macpherson, James, Mila, Montserrat, Vianna‐Morgante, Angela M., Sherman, Stephanie L., Dobkin, Carl, Latham, Gary J., Hadd, Andrew G.

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A new version of the grapevine reference genome assembly (12X.v2) and of its annotation (VCost.v3) von Canaguier, A., Grimplet, J., Di Gaspero, G., Scalabrin, S., Duchêne, E., Choisne, N., Mohellibi, N., Guichard, C., Rombauts, S., Le Clainche, I., Bérard, A., Chauveau, A., Bounon, R., Rustenholz, C., Morgante, M., Le Paslier, M.-C., Brunel, D., Adam-Blondon, A.-F.

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Mutations in the Intellectual Disability Gene Ube2a Cause Neuronal Dysfunction and Impair Parkin-Dependent Mitophagy von Haddad, Dominik M., Vilain, Sven, Vos, Melissa, Esposito, Giovanni, Matta, Samer, Kalscheuer, Vera M., Craessaerts, Katleen, Leyssen, Maarten, Nascimento, Rafaella M.P., Vianna-Morgante, Angela M., De Strooper, Bart, Van Esch, Hilde, Morais, Vanessa A., Verstreken, Patrik

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Variation in blood serum proteins and association with somatic cell count in dairy cattle from multi-breed herds von Bobbo, T., Fiore, E., Gianesella, M., Morgante, M., Gallo, L., Ruegg, P. L., Bittante, G., Cecchinato, A.

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FMR1 premutation in children with autism spectrum disorders: Should additional diagnostic tests be performed? von Girardi, Ana Cristina De Sanctis, Opstal Takahashi, Vanessa Naomi, Vadasz, Estevão, Costa, Claudia Ismania Samogi, Zachi, Elaine Cristina, Vianna‐Morgante, Angela M., Passos‐Bueno, Maria Rita

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Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing von Villela, Darine, Barros, Juliana Sobral, da Costa, Silvia Souza, Aguiar, Talita F. M., Campagnari, Francine, Vianna‐Morgante, Angela M., Krepischi, Ana C. V., Rosenberg, Carla

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Short communication: Association between udder health status and blood serum proteins in dairy cows von Bobbo, T., Ruegg, P.L., Fiore, E., Gianesella, M., Morgante, M., Pasotto, D., Gallo, L., Bittante, G., Cecchinato, A.

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Sustainable bioenergy for climate mitigation: developing drought-tolerant trees and grasses von Taylor, G, Donnison, I S, Murphy-Bokern, D, Morgante, M, Bogeat-Triboulot, M-B, Bhalerao, R, Hertzberg, M, Polle, A, Harfouche, A, Alasia, F, Petoussi, V, Trebbi, D, Schwarz, K, Keurentjes, J J B, Centritto, M, Genty, B, Flexas, J, Grill, E, Salvi, S, Davies, W J

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Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents von Rosenberg, C, Knijnenburg, J, Bakker, E, Vianna-Morgante, A M, Sloos, W, Otto, P A, Kriek, M, Hansson, K, Krepischi-Santos, A C V, Fiegler, H, Carter, N P, Bijlsma, E K, van Haeringen, A, Szuhai, K, Tanke, H J

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Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses von Villela, Darine, Mazzonetto, Patricia C., Migliavacca, Michele P., Perrone, Eduardo, Guida, Gustavo, Milanezi, Maria Fernanda G., Jorge, Alexander A. L., Ribeiro‐Bicudo, Lucilene A., Kok, Fernando, Campagnari, Francine, Rosso‐Giuliani, Liane, Costa, Silvia Souza, Vianna‐Morgante, Angela M., Pearson, Peter L., Krepischi, Ana C. V., Rosenberg, Carla

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Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation von Ullmann, Reinhard, Turner, Gillian, Kirchhoff, Maria, Chen, Wei, Tonge, Bruce, Rosenberg, Carla, Field, Michael, Vianna‐Morgante, Angela M., Christie, Louise, Krepischi‐Santos, Ana C., Banna, Lynn, Brereton, Avril V., Hill, Alyssa, Bisgaard, Anne‐Marie, Müller, Ines, Hultschig, Claus, Erdogan, Fikret, Wieczorek, Georg, Ropers, H. Hilger

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Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil von Krepischi, Ana C. V., Villela, Darine, da Costa, Silvia Souza, Mazzonetto, Patricia C., Schauren, Juliana, Migliavacca, Michele P., Milanezi, Fernanda, Santos, Juliana G., Guida, Gustavo, Guarischi-Sousa, Rodrigo, Campana, Gustavo, Kok, Fernando, Schlesinger, David, Kitajima, Joao Paulo, Campagnari, Francine, Bertola, Debora R., Vianna-Morgante, Angela M., Pearson, Peter L., Rosenberg, Carla

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Clinical and molecular delineation of the 17q21.31 microdeletion syndrome von Koolen, D A, Sharp, A J, Hurst, J A, Firth, H V, Knight, S J L, Goldenberg, A, Saugier-Veber, P, Pfundt, R, Vissers, L E L M, Destrée, A, Grisart, B, Rooms, L, Van der Aa, N, Field, M, Hackett, A, Bell, K, Nowaczyk, M J M, Mancini, G M S, Poddighe, P J, Schwartz, C E, Rossi, E, De Gregori, M, Antonacci-Fulton, L L, McLellan, M D, Garrett, J M, Wiechert, M A, Miner, T L, Crosby, S, Ciccone, R, Willatt, L, Rauch, A, Zenker, M, Aradhya, S, Manning, M A, Strom, T M, Wagenstaller, J, Krepischi-Santos, A C, Vianna-Morgante, A M, Rosenberg, C, Price, S M, Stewart, H, Shaw-Smith, C, Brunner, H G, Wilkie, A O M, Veltman, J A, Zuffardi, O, Eichler, E E, de Vries, B B A

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Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes von Carvalho, Claudia M.B., Vasanth, Shivakumar, Shinawi, Marwan, Russell, Chad, Ramocki, Melissa B., Brown, Chester W., Graakjaer, Jesper, Skytte, Anne-Bine, Vianna-Morgante, Angela M., Krepischi, Ana C.V., Patel, Gayle S., Immken, LaDonna, Aleck, Kyrieckos, Lim, Cynthia, Cheung, Sau Wai, Rosenberg, Carla, Katsanis, Nicholas, Lupski, James R.

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Abundance, distribution, and transcriptional activity of repetitive elements in the maize genome von Meyers, B C, Tingey, S V, Morgante, M

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New resources for genetic studies in Populus nigra: genome-wide SNP discovery and development of a 12k Infinium array von Faivre-Rampant, P., Zaina, G., Jorge, V., Giacomello, S., Segura, V., Scalabrin, S., Guérin, V., De Paoli, E., Aluome, C., Viger, M., Cattonaro, F., Payne, A., PaulStephenRaj, P., Le Paslier, M. C., Berard, A., Allwright, M. R., Villar, M., Taylor, G., Bastien, C., Morgante, M.

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A Simple Sequence Repeat-Based Linkage Map of Barley von Ramsay, L, Macaulay, M, degli Ivanissevich, S, MacLean, K, Cardle, L, Fuller, J, Edwards, K. J, Tuvesson, S, Morgante, M, Massari, A, Maestri, E, Marmiroli, N, Sjakste, T, Ganal, M, Powell, W, Waugh, R

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Cross-species amplification of soybean (Glycine max) simple sequence repeats (SSRs) within the genus and other legume genera: implications for the transferability of SSRs in plants von Peakall, R, Gilmore, S, Keys, W, Morgante, M, Rafalski, A

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Alexithymia and personality traits of patients with inflammatory bowel disease von La Barbera, D., Bonanno, B., Rumeo, M. V., Alabastro, V., Frenda, M., Massihnia, E., Morgante, M. C., Sideli, L., Craxì, A., Cappello, M., Tumminello, M., Miccichè, S., Nastri, L.

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