DNA hydroxymethylation controls cardiomyocyte gene expression in development and hypertrophy von Greco, Carolina M., Kunderfranco, Paolo, Rubino, Marcello, Larcher, Veronica, Carullo, Pierluigi, Anselmo, Achille, Kurz, Kerstin, Carell, Thomas, Angius, Andrea, Latronico, Michael V. G., Papait, Roberto, Condorelli, Gianluigi

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Genetic Variants Regulating Immune Cell Levels in Health and Disease von Orrù, Valeria, Steri, Maristella, Sole, Gabriella, Sidore, Carlo, Virdis, Francesca, Dei, Mariano, Lai, Sandra, Zoledziewska, Magdalena, Busonero, Fabio, Mulas, Antonella, Floris, Matteo, Mentzen, Wieslawa I., Urru, Silvana A.M., Olla, Stefania, Marongiu, Michele, Piras, Maria G., Lobina, Monia, Maschio, Andrea, Pitzalis, Maristella, Urru, Maria F., Marcelli, Marco, Cusano, Roberto, Deidda, Francesca, Serra, Valentina, Oppo, Manuela, Pilu, Rosella, Reinier, Frederic, Berutti, Riccardo, Pireddu, Luca, Zara, Ilenia, Porcu, Eleonora, Kwong, Alan, Brennan, Christine, Tarrier, Brendan, Lyons, Robert, Kang, Hyun M., Uzzau, Sergio, Atzeni, Rossano, Valentini, Maria, Firinu, Davide, Leoni, Lidia, Rotta, Gianluca, Naitza, Silvia, Angius, Andrea, Congia, Mauro, Whalen, Michael B., Jones, Chris M., Schlessinger, David, Abecasis, Gonçalo R., Fiorillo, Edoardo, Sanna, Serena, Cucca, Francesco

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Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools von Ding, Jun, Sidore, Carlo, Butler, Thomas J, Wing, Mary Kate, Qian, Yong, Meirelles, Osorio, Busonero, Fabio, Tsoi, Lam C, Maschio, Andrea, Angius, Andrea, Kang, Hyun Min, Nagaraja, Ramaiah, Cucca, Francesco, Abecasis, Gonçalo R, Schlessinger, David

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Loss of Mismatched HLA in Leukemia after Stem-Cell Transplantation von Vago, Luca, Perna, Serena Kimi, Zanussi, Monica, Mazzi, Benedetta, Barlassina, Cristina, Stanghellini, Maria Teresa Lupo, Perrelli, Nicola Flavio, Cosentino, Cristian, Torri, Federica, Angius, Andrea, Forno, Barbara, Casucci, Monica, Bernardi, Massimo, Peccatori, Jacopo, Corti, Consuelo, Bondanza, Attilio, Ferrari, Maurizio, Rossini, Silvano, Roncarolo, Maria Grazia, Bordignon, Claudio, Bonini, Chiara, Ciceri, Fabio, Fleischhauer, Katharina

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Biomarker dynamics affecting neoadjuvant therapy response and outcome of HER2-positive breast cancer subtype von Orrù, Sandra, Pascariello, Emanuele, Pes, Barbara, Rallo, Vincenzo, Barbara, Raffaele, Muntoni, Marta, Notari, Francesca, Fancello, Gianfranco, Mocci, Cristina, Muroni, Maria Rosaria, Cossu-Rocca, Paolo, Angius, Andrea, De Miglio, Maria Rosaria

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The Changing Landscape of Naive T Cell Receptor Repertoire With Human Aging von Egorov, Evgeny S, Kasatskaya, Sofya A, Zubov, Vasiliy N, Izraelson, Mark, Nakonechnaya, Tatiana O, Staroverov, Dmitriy B, Angius, Andrea, Cucca, Francesco, Mamedov, Ilgar Z, Rosati, Elisa, Franke, Andre, Shugay, Mikhail, Pogorelyy, Mikhail V, Chudakov, Dmitriy M, Britanova, Olga V

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Assessing the Predictive Power of the Hemoglobin/Red Cell Distribution Width Ratio in Cancer: A Systematic Review and Future Directions von Coradduzza, Donatella, Medici, Serenella, Chessa, Carla, Zinellu, Angelo, Madonia, Massimo, Angius, Andrea, Carru, Ciriaco, De Miglio, Maria Rosaria

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A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy von Pippucci, Tommaso, Parmeggiani, Antonia, Palombo, Flavia, Maresca, Alessandra, Angius, Andrea, Crisponi, Laura, Cucca, Francesco, Liguori, Rocco, Valentino, Maria Lucia, Seri, Marco, Carelli, Valerio

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Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset von Forabosco, Paola, Pala, Mauro, Crobu, Francesca, Diana, Maria Antonietta, Marongiu, Mara, Cusano, Roberto, Angius, Andrea, Steri, Maristella, Orrù, Valeria, Schlessinger, David, Fiorillo, Edoardo, Devoto, Marcella, Cucca, Francesco

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Population genomic analysis of ancient and modern genomes yields new insights into the genetic ancestry of the Tyrolean Iceman and the genetic structure of Europe von Sikora, Martin, Carpenter, Meredith L, Moreno-Estrada, Andres, Henn, Brenna M, Underhill, Peter A, Sánchez-Quinto, Federico, Zara, Ilenia, Pitzalis, Maristella, Sidore, Carlo, Busonero, Fabio, Maschio, Andrea, Angius, Andrea, Jones, Chris, Mendoza-Revilla, Javier, Nekhrizov, Georgi, Dimitrova, Diana, Theodossiev, Nikola, Harkins, Timothy T, Keller, Andreas, Maixner, Frank, Zink, Albert, Abecasis, Goncalo, Sanna, Serena, Cucca, Francesco, Bustamante, Carlos D

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Landscape of transcriptome variations uncovering known and novel driver events in colorectal carcinoma von Pira, Giovanna, Uva, Paolo, Scanu, Antonio Mario, Rocca, Paolo Cossu, Murgia, Luciano, Uleri, Elena, Piu, Claudia, Porcu, Alberto, Carru, Ciriaco, Manca, Alessandra, Persico, Ivana, Muroni, Maria Rosaria, Sanges, Francesca, Serra, Caterina, Dolei, Antonia, Angius, Andrea, De Miglio, Maria Rosaria

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A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy von Serra, Rita, Rallo, Vincenzo, Steri, Maristella, Olla, Stefania, Piras, Maria Grazia, Marongiu, Michele, Gorospe, Myriam, Schlessinger, David, Pinna, Antonio, Fiorillo, Edoardo, Cucca, Francesco, Angius, Andrea

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Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges von Wen, Xiaofen, Coradduzza, Donatella, Shen, Jiaxin, Scanu, Antonio Mario, Muroni, Maria Rosaria, Massidda, Matteo, Rallo, Vincenzo, Carru, Ciriaco, Angius, Andrea, De Miglio, Maria Rosaria

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Environmental and genetic contribution to hypertension prevalence: data from an epidemiological survey on Sardinian genetic isolates von Biino, Ginevra, Parati, Gianfranco, Concas, Maria Pina, Adamo, Mauro, Angius, Andrea, Vaccargiu, Simona, Pirastu, Mario

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A Portrait of Intratumoral Genomic and Transcriptomic Heterogeneity at Single-Cell Level in Colorectal Cancer von Angius, Andrea, Scanu, Antonio Mario, Arru, Caterina, Muroni, Maria Rosaria, Carru, Ciriaco, Porcu, Alberto, Cossu-Rocca, Paolo, De Miglio, Maria Rosaria

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A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman von Palombo, Flavia, Al-Wardy, Nadia, Ruscone, Guido Alberto Gnecchi, Oppo, Manuela, Kindi, Mohammed Nasser Al, Angius, Andrea, Al Lamki, Khalsa, Girotto, Giorgia, Giangregorio, Tania, Benelli, Matteo, Magi, Alberto, Seri, Marco, Gasparini, Paolo, Cucca, Francesco, Sazzini, Marco, Al Khabori, Mazin, Pippucci, Tommaso, Romeo, Giovanni

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Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report von Alves, Rita Maria, Uva, Paolo, Veiga, Marielza F, Oppo, Manuela, Zschaber, Fabiana C R, Porcu, Giampiero, Porto, Henrique P, Persico, Ivana, Onano, Stefano, Cuccuru, Gianmauro, Atzeni, Rossano, Vieira, Lauro C N, Pires, Marcos V A, Cucca, Francesco, Toralles, Maria Betânia P, Angius, Andrea, Crisponi, Laura

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Correction: Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools von Ding, Jun, Sidore, Carlo, Butler, Thomas J, Wing, Mary Kate, Qian, Yong, Meirelles, Osorio, Busonero, Fabio, Tsoi, Lam C, Maschio, Andrea, Angius, Andrea, Kang, Hyun Min, Nagaraja, Ramaiah, Cucca, Francesco, Abecasis, Gonçalo R, Schlessinger, David

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High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis von Pistis, Giorgio, Piras, Ignazio, Pirastu, Nicola, Persico, Ivana, Sassu, Alessandro, Picciau, Andrea, Prodi, Dionigio, Fraumene, Cristina, Mocci, Evelina, Manias, Maria Teresa, Atzeni, Rossano, Cosso, Massimiliano, Pirastu, Mario, Angius, Andrea

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A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman von Palombo, Flavia, Al-Wardy, Nadia, Ruscone, Guido Alberto Gnecchi, Oppo, Manuela, Kindi, Mohammed Nasser Al, Angius, Andrea, Al Lamki, Khalsa, Girotto, Giorgia, Giangregorio, Tania, Benelli, Matteo, Magi, Alberto, Seri, Marco, Gasparini, Paolo, Cucca, Francesco, Sazzini, Marco, Al Khabori, Mazin, Pippucci, Tommaso, Romeo, Giovanni

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