The prevalence and phenotypic characteristics of spontaneous premature ovarian failure: a general population registry-based study by Haller-Kikkatalo, K., Uibo, R., Kurg, A., Salumets, A.

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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 by Froguel, P, Beckmann, J. S, Walters, R. G, Jacquemont, S, Valsesia, A, de Smith, A. J, Martinet, D, Andersson, J, Falchi, M, Chen, F, Andrieux, J, Lobbens, S, Delobel, B, Stutzmann, F, El-Sayed Moustafa, J. S, Chèvre, J.-C, Lecoeur, C, Vatin, V, Bouquillon, S, Buxton, J. L, Boute, O, Holder-Espinasse, M, Cuisset, J.-M, Lemaitre, M.-P, Ambresin, A.-E, Brioschi, A, Gaillard, M, Giusti, V, Fellmann, F, Ferrarini, A, Hadjikhani, N, Campion, D, Guilmatre, A, Goldenberg, A, Calmels, N, Mandel, J.-L, Le Caignec, C, David, A, Isidor, B, Cordier, M.-P, Dupuis-Girod, S, Labalme, A, Sanlaville, D, Béri-Dexheimer, M, Jonveaux, P, Leheup, B, Õunap, K, Bochukova, E. G, Henning, E, Keogh, J, Ellis, R. J, MacDermot, K. D, van Haelst, M. M, Vincent-Delorme, C, Plessis, G, Touraine, R, Philippe, A, Malan, V, Mathieu-Dramard, M, Chiesa, J, Blaumeiser, B, Kooy, R. F, Caiazzo, R, Pigeyre, M, Balkau, B, Sladek, R, Bergmann, S, Mooser, V, Waterworth, D, Reymond, A, Vollenweider, P, Waeber, G, Kurg, A, Palta, P, Esko, T, Metspalu, A, Nelis, M, Elliott, P, Hartikainen, A.-L, McCarthy, M. I, Peltonen, L, Carlsson, L, Jacobson, P, Sjöström, L, Huang, N, Hurles, M. E, O'Rahilly, S, Farooqi, I. S, Männik, K, Jarvelin, M.-R, Pattou, F, Meyre, D, Walley, A. J, Coin, L. J. M, Blakemore, A. I. F

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Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases by Tšuiko, O., Nõukas, M., Žilina, O., Hensen, K., Tapanainen, J.S., Mägi, R., Kals, M., Kivistik, P.A., Haller-Kikkatalo, K., Salumets, A., Kurg, A.

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Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families by Žilina, O., Reimand, T., Zjablovskaja, P., Männik, K., Männamaa, M., Traat, A., Puusepp-Benazzouz, H., Kurg, A., Õunap, K.

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A novel de novo 1.8 Mb microdeletion of 17q21.33 associated with intellectual disability and dysmorphic features by Preiksaitiene, E, Männik, K, Dirse, V, Utkus, A, Ciuladaite, Z, Kasnauskiene, J, Kurg, A, Kučinskas, V

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A 2-week maintenance regimen of intravesical instillation of bacillus Calmette-Guerin is safe, adherent and effective in patients with non-muscle-invasive bladder cancer: a prospec... by Kanagawa Urological Research Group (KURG), Kanagawa Urological Research Group (KURG)

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A speculative outlook on embryonic aneuploidy: Can molecular pathways be involved? by Tšuiko, Olga, Jatsenko, Tatjana, Parameswaran Grace, Lalit Kumar, Kurg, Ants, Vermeesch, Joris Robert, Lanner, Fredrik, Altmäe, Signe, Salumets, Andres

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Sol–gel films for DNA microarray applications by Saal, K., Tätte, T., Tulp, I., Kink, I., Kurg, A., Mäeorg, U., Rinken, A., Lõhmus, A.

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Preparation of smooth siloxane surfaces for AFM visualization of immobilized biomolecules by Tätte, T., Saal, K., Kink, I., Kurg, A., Lõhmus, R., Mäeorg, U., Rahi, M., Rinken, A., Lõhmus, A.

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P–381 Deciphering the genetic cause of recurrent and sporadic pregnancy loss by Essers, R, Acharya, G, Al-Nasiry, S, Brunner, H, Deligiannis, S P, Fonova, E A, Kurg, A, Lebedev, I N, Macville, M V E, Nikitina, T V, Salumets, A, Sazhenova, E A, Stevens, S J C, Tolmacheva, E N, Zaman. Esteki, M

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Creating basis for introducing non‐invasive prenatal testing in the Estonian public health setting by Žilina, Olga, Rekker, Kadri, Kaplinski, Lauris, Sauk, Martin, Paluoja, Priit, Teder, Hindrek, Ustav, Eva‐Liina, Tõnisson, Neeme, Reimand, Tiia, Ridnõi, Konstantin, Palta, Priit, Vermeesch, Joris Robert, Krjutškov, Kaarel, Kurg, Ants, Salumets, Andres

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NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies by Sauk, Martin, Žilina, Olga, Kurg, Ants, Ustav, Eva-Liina, Peters, Maire, Paluoja, Priit, Roost, Anne Mari, Teder, Hindrek, Palta, Priit, Brison, Nathalie, Vermeesch, Joris R., Krjutškov, Kaarel, Salumets, Andres, Kaplinski, Lauris

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Experimental validation of PRD-like homeobox genes expressed in bovine oocytes and early IVF embryos by Yasar, B, Boskovic, N, Jouhilahti, EM, Vill, P, Burglin, T, Katayama, S, Org, T, Kere, J, Kurg, A

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A first-generation linkage disequilibrium map of human chromosome 22 by Cardon, Lon R, Dunham, Ian, Dawson, Elisabeth, Abecasis, Gonçalo R, Bumpstead, Suzannah, Chen, Yuan, Hunt, Sarah, Beare, David M, Pabial, Jagjit, Dibling, Thomas, Tinsley, Emma, Kirby, Susan, Carter, David, Papaspyridonos, Marianna, Livingstone, Simon, Ganske, Rocky, Lõhmussaar, Elin, Zernant, Jana, Tõnisson, Neeme, Remm, Maido, Mägi, Reedik, Puurand, Tarmo, Vilo, Jaak, Kurg, Ants, Rice, Kate, Deloukas, Panos, Mott, Richard, Metspalu, Andres, Bentley, David R

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The nature and prevalence of chromosomal dynamics in early spontaneous pregnancy loss by Essers, R, Lebedev, I, Kurg, A, Fonova, E, Stevens, S, von Rango, U, Deligiannis, SP, Nikitina, T, Sazhenova, E, Tolmacheva, E, Kashevarova, A, Koeck, R, Al-Nasiry, S, Dreesen, JCMF, Paulussen, ADC, Macville, M, Hoischen, A, Acharya, G, Brunner, H, Salumets, A, Esteki, MZ

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Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays by Pastinen, T, Kurg, A, Metspalu, A, Peltonen, L, Syvänen, A C

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Deciphering the genetic cause of recurrent and sporadic pregnancy loss by Essers, R, Acharya, G, Al-Nasiry, S, Brunner, HG, Deligiannis, SP, Fonova, EA, Hoischen, A, Kurg, A, Lebedev, IN, Macville, MVE, Nikitina, TV, Salumets, A, Sazhenova, EA, Stevens, SJC, Tolmacheva, EN, Esteki, MZ

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A hybrid approach to device integration on a genetic analysis platform by Brennan, Des, Jary, Dorothee, Kurg, Ants, Berik, Evgeny, Justice, John, Aherne, Margaret, Macek, Milan, Galvin, Paul

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Evaluating the Arrayed Primer Extension Resequencing Assay of TP53 Tumor Suppressor Gene by Tõnisson, Neeme, Zernant, Jana, Kurg, Ants, Pavel, Hendrik, Slavin, Georg, Roomere, Hanno, Meiel, Aune, Hainaut, Pierre, Metspalu, Andres

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Deciphering the genetic cause of recurrent and sporadic pregnancy loss by Essers, R, Acharya, G, Al-Nasiry, S, Brunner, H, Deligiannis, SP, Fonova, EA, Kurg, A, Lebedev, IN, Macville, MVE, Nikitina, TV, Salumets, A, Sazhenova, EA, Stevens, SJC, Tolmacheva, EN, Esteki, MZ

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