In-feed supplementation of clinoptilolite favourably modulates intestinal and systemic immunity and some production parameters in weaned pigs by Valpotic, H., Terzic, S., Vince, S., Samardzija, M., Turk, R., Lackovic, G., Habrun, B., Djuricic, D., Sadikovic, M., Valpotic, I.

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Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer by Sadikovic, B, Al-Romaih, K, Squire, J A, Zielenska, M

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Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes by Aref-Eshghi, Erfan, Rodenhiser, David I., Schenkel, Laila C., Lin, Hanxin, Skinner, Cindy, Ainsworth, Peter, Paré, Guillaume, Hood, Rebecca L., Bulman, Dennis E., Kernohan, Kristin D., Boycott, Kym M., Campeau, Philippe M., Schwartz, Charles, Sadikovic, Bekim

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Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1 by Martin-Herranz, Daniel E, Aref-Eshghi, Erfan, Bonder, Marc Jan, Stubbs, Thomas M, Choufani, Sanaa, Weksberg, Rosanna, Stegle, Oliver, Sadikovic, Bekim, Reik, Wolf, Thornton, Janet M

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A genome-wide DNA methylation signature for SETD1B-related syndrome by Krzyzewska, I M, Maas, S M, Henneman, P, Lip, K V D, Venema, A, Baranano, K, Chassevent, A, Aref-Eshghi, E, van Essen, A J, Fukuda, T, Ikeda, H, Jacquemont, M, Kim, H-G, Labalme, A, Lewis, S M E, Lesca, G, Madrigal, I, Mahida, S, Matsumoto, N, Rabionet, R, Rajcan-Separovic, E, Qiao, Y, Sadikovic, B, Saitsu, H, Sweetser, D A, Alders, M, Mannens, M M A M

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Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseases by van Karnebeek, Clara D M, O'Donnell-Luria, Anne, Baynam, Gareth, Baudot, Anaïs, Groza, Tudor, Jans, Judith J M, Lassmann, Timo, Letinturier, Mary Catherine V, Montgomery, Stephen B, Robinson, Peter N, Sansen, Stefaan, Mehrian-Shai, Ruty, Steward, Charles, Kosaki, Kenjiro, Durao, Patricia, Sadikovic, Bekim

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Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome by Kumps, Candy, D'haenens, Erika, Kerkhof, Jennifer, McConkey, Haley, Alders, Marielle, Sadikovic, Bekim, Vanakker, Olivier M

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Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature by van der Laan, Liselot, Rooney, Kathleen, Haghshenas, Sadegheh, Silva, Ananília, McConkey, Haley, Relator, Raissa, Levy, Michael A., Valenzuela, Irene, Trujillano, Laura, Lasa-Aranzasti, Amaia, Campos, Berta, Castells, Neus, Verberne, Eline A., Maas, Saskia, Alders, Mariëlle, Mannens, Marcel M. A. M., van Haelst, Mieke M., Sadikovic, Bekim, Henneman, Peter

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Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome by Connaughton, Dervla M., Bhai, Pratibha, Isenring, Paul, Mahdi, Mohammed, Sadikovic, Bekim, Schenkel, Laila C.

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Incidental findings from cancer next generation sequencing panels by Maani, Nika, Panabaker, Karen, McCuaig, Jeanna M., Buckley, Kathleen, Semotiuk, Kara, Farncombe, Kirsten M., Ainsworth, Peter, Panchal, Seema, Sadikovic, Bekim, Armel, Susan Randall, Lin, Hanxin, Kim, Raymond H.

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Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature by Hoogenboom, Amarens, Falix, Farah A, van der Laan, Liselot, Kerkhof, Jennifer, Alders, Mariëlle, Sadikovic, Bekim, van Haelst, Mieke M

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DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome by Schenkel, L C, Aref-Eshghi, E, Rooney, K, Kerkhof, J, Levy, M A, McConkey, H, Rogers, R C, Phelan, K, Sarasua, S M, Jain, L, Pauly, R, Boccuto, L, DuPont, B, Cappuccio, G, Brunetti-Pierri, N, Schwartz, C E, Sadikovic, B

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Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy by Kernohan, Kristin D, Cigana Schenkel, Laila, Huang, Lijia, Smith, Amanda, Pare, Guillaume, Ainsworth, Peter, Boycott, Kym M, Warman-Chardon, Jodi, Sadikovic, Bekim

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Myelodysplastic Neoplasms (MDS) with Ring Sideroblasts or SF3B1 Mutations: The Improved Clinical Utility of World Health Organization and International Consensus Classification 202... by Mortuza, Shamim, Chin-Yee, Benjamin, James, Tyler E, Chin-Yee, Ian H, Hedley, Benjamin D, Ho, Jenny M, Saini, Lalit, Lazo-Langner, Alejandro, Schenkel, Laila, Bhai, Pratibha, Sadikovic, Bekim, Keow, Jonathan, Sangle, Nikhil, Hsia, Cyrus C

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The defining DNA methylation signature of Floating-Harbor Syndrome by Hood, Rebecca L., Schenkel, Laila C., Nikkel, Sarah M., Ainsworth, Peter J., Pare, Guillaume, Boycott, Kym M., Bulman, Dennis E., Sadikovic, Bekim

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BAFopathies’ DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin–Siris and Nicolaides–Baraitser syndromes by Aref-Eshghi, Erfan, Bend, Eric G., Hood, Rebecca L., Schenkel, Laila C., Carere, Deanna Alexis, Chakrabarti, Rana, Nagamani, Sandesh C. S., Cheung, Sau Wai, Campeau, Philippe M., Prasad, Chitra, Siu, Victoria Mok, Brady, Lauren, Tarnopolsky, Mark A., Callen, David J., Innes, A. Micheil, White, Susan M., Meschino, Wendy S., Shuen, Andrew Y., Paré, Guillaume, Bulman, Dennis E., Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Hennekam, Raoul C., Boycott, Kym M., Schwartz, Charles E., Sadikovic, Bekim

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SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females by Radio, Francesca Clementina, Ciolfi, Andrea, Levy, Michael A., Hernández-García, Andrés, Pedace, Lucia, Pantaleoni, Francesca, Liu, Zhandong, de Boer, Elke, Jackson, Adam, Bruselles, Alessandro, McConkey, Haley, Stellacci, Emilia, Lo Cicero, Stefania, Motta, Marialetizia, Carrozzo, Rosalba, McWalter, Kirsty, Desai, Megha, Monaghan, Kristin G., Telegrafi, Aida, Philippe, Christophe, Vitobello, Antonio, Au, Margaret, Grand, Katheryn, Baez, Joanne, Lindstrom, Kristin, Kulch, Peggy, Sebastian, Jessica, Madan-Khetarpal, Suneeta, Roadhouse, Chelsea, MacKenzie, Jennifer J., Monteleone, Berrin, Saunders, Carol J., Jean Cuevas, July K., Zhou, Dihong, Sawyer, Sarah L., Monteiro, Fabíola Paoli, Secches, Tania Vertemati, Kok, Fernando, Schultz-Rogers, Laura E., Morava, Eva, Klee, Eric W., Kemppainen, Jennifer, Iascone, Maria, Selicorni, Angelo, Tenconi, Romano, Pais, Lynn, Gallacher, Lyndon, Turnpenny, Peter D., Stals, Karen, Ellard, Sian, Cabet, Sara, Lesca, Gaetan, Pascal, Joset, Steindl, Katharina, Weiss, Karin, Carter, Melissa T., Kalsner, Louisa, de Vries, Bert B.A., van Bon, Bregje W., Wevers, Marijke R., Pfundt, Rolph, Stegmann, Alexander P.A., Kerr, Bronwyn, Chandler, Kate E., Sheehan, Willow, Elias, Abdallah F., Shinde, Deepali N., Towne, Meghan C., Robin, Nathaniel H., Goodloe, Dana, Vanderver, Adeline, Sherbini, Omar, Bluske, Krista, Faletra, Flavio, Musante, Luciana, Kurtz-Nelson, Evangeline C., Earl, Rachel K., Anderlid, Britt-Marie, Morin, Gilles, van Slegtenhorst, Marjon, Diderich, Karin E.M., Brooks, Alice S., Gribnau, Joost, Boers, Ruben G., Finestra, Teresa Robert, Carter, Lauren B., Rauch, Anita, Gasparini, Paolo, Boycott, Kym M., Barakat, Tahsin Stefan, Graham, John M., Faivre, Laurence, Banka, Siddharth, Wang, Tianyun, Eichler, Evan E., Dallapiccola, Bruno, Vissers, Lisenka E.L.M., Sadikovic, Bekim, Holder, Jimmy Lloyd, Tartaglia, Marco

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Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile by Ciolfi, Andrea, Foroutan, Aidin, Capuano, Alessandro, Pedace, Lucia, Travaglini, Lorena, Pizzi, Simone, Andreani, Marco, Miele, Evelina, Invernizzi, Federica, Reale, Chiara, Panteghini, Celeste, Iascone, Maria, Niceta, Marcello, Gavrilova, Ralitza H, Schultz-Rogers, Laura, Agolini, Emanuele, Bedeschi, Maria Francesca, Prontera, Paolo, Garibaldi, Matteo, Galosi, Serena, Leuzzi, Vincenzo, Soliveri, Paola, Olson, Rory J, Zorzi, Giovanna S, Garavaglia, Barbara M, Tartaglia, Marco, Sadikovic, Bekim

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Double heterozygosity for germline mutations in BRCA1 and p53 in a woman with early onset breast cancer by Bell, K., Hodgson, N., Levine, M., Sadikovic, B., Zbuk, K.

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Clinical Features and Long-Term Outcomes of a Pan-Canadian Cohort of Adolescents and Young Adults with Myeloproliferative Neoplasms: A Canadian MPN Group Study by England, James T., Szuber, Natasha, Sirhan, Shireen, Dunne, Tom, Cerquozzi, Sonia, Hill, Madeleine, Villeneuve, Pierre J. A., Ho, Jenny M., Sadikovic, Bekim, Bhai, Pratibha, Krishnan, Nupur, Dowhanik, Sebastian, Hillis, Chris, Capo-Chichi, Jose-Mario, Tsui, Hubert, Cheung, Verna, Gauthier, Karine, Sibai, Hassan, Davidson, Marta B., Bankar, Aniket, Kotchetkov, Rouslan, Gupta, Vikas, Maze, Dawn

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