Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset by Agnoletto, Chiara, Corrà, Fabio, Minotti, Linda, Baldassari, Federica, Crudele, Francesca, Cook, William Joseph James, Di Leva, Gianpiero, d'Adamo, Adamo Pio, Gasparini, Paolo, Volinia, Stefano

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TBL1Y: a new gene involved in syndromic hearing loss by Di Stazio, Mariateresa, Collesi, Chiara, Vozzi, Diego, Liu, Wei, Myers, Mike, Morgan, Anna, D Adamo, Pio Adamo, Girotto, Giorgia, Rubinato, Elisa, Giacca, Mauro, Gasparini, Paolo

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Notch Signaling Regulation in Autoinflammatory Diseases by Gratton, Rossella, Tricarico, Paola Maura, d'Adamo, Adamo Pio, Bianco, Anna Monica, Moura, Ronald, Agrelli, Almerinda, Brandão, Lucas, Zupin, Luisa, Crovella, Sergio

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Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique by Di Stazio, Mariateresa, Foschi, Nicola, Athanasakis, Emmanouil, Gasparini, Paolo, d'Adamo, Adamo Pio

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GNE-related thrombocytopenia: evidence for a mutational hotspot in the ADP/substrate domain of the GNE bifunctional enzyme by Bottega, Roberta, Marzollo, Antonio, Marinoni, Maddalena, Athanasakis, Emmanouil, Persico, Ilaria, Bianco, Anna Monica, Faleschini, Michela, Valencic, Erica, Simoncini, Daniela, Rossini, Linda, Corsolini, Fabio, La Bianca, Martina, Robustelli, Giuseppe, Gabelli, Maria, Agosti, Massimo, Biffi, Alessandra, Grotto, Paolo, Bozzi, Valeria, Noris, Patrizia, Burlina, Alberto B, D'Adamo, Adamo Pio, Tommasini, Alberto, Faletra, Flavio, Pastore, Annalisa, Savoia, Anna

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Genetic bases of C7 deficiency: systematic review and report of a novel deletion determining functional hemizygosity by Balduit, Andrea, Bianco, Anna Monica, Mangogna, Alessandro, Zicari, Anna Maria, Leonardi, Lucia, Cinicola, Bianca Laura, Capponi, Martina, Tommasini, Alberto, Agostinis, Chiara, d'Adamo, Adamo Pio, Bulla, Roberta

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Unraveling the Epigenetic Tapestry: Decoding the Impact of Epigenetic Modifications in Hidradenitis Suppurativa Pathogenesis by Nardacchione, Elena Maria, Tricarico, Paola Maura, Moura, Ronald, d'Adamo, Adamo Pio, Thasneem, Ayshath, Suleman, Muhammad, Marzano, Angelo Valerio, Crovella, Sergio, Moltrasio, Chiara

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A rare loss-of-function genetic mutation suggest a role of dermcidin deficiency in hidradenitis suppurativa pathogenesis by Tricarico, Paola Maura, Gratton, Rossella, Dos Santos-Silva, Carlos André, de Moura, Ronald Rodrigues, Ura, Blendi, Sommella, Eduardo, Campiglia, Pietro, Del Vecchio, Cecilia, Moltrasio, Chiara, Berti, Irene, D'Adamo, Adamo Pio, Elsherbini, Ahmed M A, Staudenmaier, Lena, Chersi, Karin, Boniotto, Michele, Krismer, Bernhard, Schittek, Birgit, Crovella, Sergio

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Plant Antimicrobial Peptides as Potential Tool for Topic Treatment of Hidradenitis Suppurativa by Dos Santos-Silva, Carlos André, Tricarico, Paola Maura, Vilela, Lívia Maria Batista, Roldan-Filho, Ricardo Salas, Amador, Vinícius Costa, d'Adamo, Adamo Pio, Rêgo, Mireli de Santana, Benko-Iseppon, Ana Maria, Crovella, Sergio

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Could the MED13 mutations manifest as a Kabuki‐like syndrome? by De Nardi, Laura, Faletra, Flavio, D'Adamo, Adamo Pio, Bianco, Anna Monica Rosaria, Athanasakis, Emmanouil, Bruno, Irene, Barbi, Egidio

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Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations by O'Seaghdha, Conall M, Wu, Hongsheng, Yang, Qiong, Kapur, Karen, Zuber, Annie Mercier, Köttgen, Anna, Stoudmann, Candice, Teumer, Alexander, Kutalik, Zoltán, Mangino, Massimo, Dehghan, Abbas, Eiriksdottir, Gudny, Li, Guo, Tanaka, Toshiko, Lopez, Lorna M, Hayward, Caroline, Lohman, Kurt, Matsuda, Koichi, Padmanabhan, Sandosh, Firsov, Dmitri, Ulivi, Sheila, Brockhaus, A Catharina, Kleber, Marcus E, Mahajan, Anubha, Ernst, Florian D, Gudnason, Vilmundur, Launer, Lenore J, Mace, Aurelien, Boerwinckle, Eric, Arking, Dan E, Tanikawa, Chizu, Brown, Morris J, Gaspoz, Jean-Michel, Theler, Jean-Marc, Siscovick, David S, Psaty, Bruce M, Bergmann, Sven, Vollenweider, Peter, Vitart, Veronique, Wright, Alan F, Zemunik, Tatijana, Boban, Mladen, Kolcic, Ivana, Brown, Edward M, Estrada, Karol, Ding, Jingzhong, Harris, Tamara B, Bandinelli, Stefania, Hernandez, Dena, Singleton, Andrew B, Girotto, Giorgia, Ruggiero, Daniela, d'Adamo, Adamo Pio, Robino, Antonietta, Meitinger, Thomas, Meisinger, Christa, Davies, Gail, Starr, John M, Chambers, John C, Boehm, Bernhard O, Huang, Jie, Murgia, Federico, Campbell, Harry, Morris, Andrew P, Franco, Oscar H, Hofman, Albert, Uitterlinden, Andre G, Rivadeneira, Fernando, Völker, Uwe, Hannemann, Anke, Biffar, Reiner, Hoffmann, Wolfgang, Shin, So-Youn, Lescuyer, Pierre, Henry, Hughes, Munroe, Patricia B, Gasparini, Paolo, Pirastu, Nicola, Ciullo, Marina, Gieger, Christian, März, Winfried, Lind, Lars, Spector, Tim D, Smith, Albert V, Rudan, Igor, Wilson, James F, Polasek, Ozren, Deary, Ian J, Pirastu, Mario, Ferrucci, Luigi, Liu, Yongmei, Kestenbaum, Bryan, Kooner, Jaspal S, Witteman, Jacqueline C M, Nauck, Matthias, Kao, W H Linda, Wallaschofski, Henri, Bonny, Olivier, Fox, Caroline S, Bochud, Murielle

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A loss‐of‐function NCSTN mutation associated with familial Dowling Degos disease and hidradenitis suppurativa by de Oliveira, Ana Sofia Lima Estevao, de Siqueira, Roberta Cardoso, Nait‐Meddour, Cécile, Tricarico, Paola Maura, Moura, Ronald, Agrelli, Almerinda, d'Adamo, Adamo Pio, Jamain, Stéphane, Crovella, Sergio, de Fátima Medeiros Brito, Maria, Boniotto, Michele, Brandão, Lucas André Cavalcanti

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Neuron-Derived Extracellular Vesicles miRNA Profiles Identify Children Who Experience Adverse Events after Ketamine Administration for Procedural Sedation by Lucafò, Marianna, Bidoli, Carlotta, Franzin, Martina, Eitan, Erez, Rau, Sara, Amaddeo, Alessandro, Fachin, Alice, d'Adamo, Adamo Pio, Decorti, Giuliana, Stocco, Gabriele, Barbi, Egidio, Cozzi, Giorgio

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Systematic analysis of factors that improve homologous direct repair by Di Stazio, Mariateresa, Foschi, Nicola, Athanasakis, Emmanouil, Gasparini, Paolo, d'Adamo, Adamo Pio

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High prevalence of rare FBLIM1 gene variants in an Italian cohort of patients with Chronic Non-bacterial Osteomyelitis (CNO) by d’Adamo, Adamo Pio, Bianco, Anna Monica, Ferrara, Giovanna, La Bianca, Martina, Insalaco, Antonella, Tommasini, Alberto, Pardeo, Manuela, Cattalini, Marco, La Torre, Francesco, Finetti, Martina, Alizzi, Clotilde, Simonini, Gabriele, Messia, Virginia, Pastore, Serena, Cimaz, Rolando, Gattorno, Marco, Taddio, Andrea

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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche by Ferreira, Teresa, He, Chunyan, Esko, Tõnu, Thorleifsson, Gudmar, Albrecht, Eva, Corre, Tanguy, Franceschini, Nora, Ganna, Andrea, Porcu, Eleonora, Stolk, Lisette, Tšernikova, Natalia, Tikkanen, Emmi, Wagner, Erin K, Hottenga, Jouke-Jan, Mangino, Massimo, Pers, Tune H, Atsma, Femke, Beckmann, Matthias W, Benitez, Javier, Blomqvist, Carl, Bojesen, Stig E, Bolla, Manjeet K, Brauch, Hiltrud, Brenner, Hermann, Buring, Julie E, Chanock, Stephen, Chen, Jinhui, Chenevix-Trench, Georgia, Couch, Fergus J, Czene, Kamila, D'adamo, Adamo Pio, Smith, George Davey, De Vivo, Immaculata, Demerath, Ellen W, Dennis, Joe, Dunning, Alison M, Eriksson, Johan G, Ferrucci, Luigi, Flesch-Janys, Dieter, Flyger, Henrik, Garcia, Melissa E, García-Closas, Montserrat, Gudnason, Vilmundur, Guénel, Pascal, Hall, Per, Hamann, Ute, Haring, Robin, Hartman, Catharina A, Heath, Andrew C, Hofman, Albert, Hu, Frank B, Karasik, David, Kosma, Veli-Matti, Kutalik, Zoltan, Lai, Sandra, Lindblom, Annika, Mägi, Reedik, Melbye, Mads, Michailidou, Kyriaki, Nevanlinna, Heli, Neven, Patrick, Nohr, Ellen A, Oostra, Ben A, Palotie, Aarno, Peterlongo, Paolo, Peto, Julian, Postma, Dirkje S, Pylkäs, Katri, Radice, Paolo, Ring, Susan, Rivadeneira, Fernando, Rose, Lynda M, Rudolph, Anja, Sanna, Serena, Southey, Mellissa C, Visser, Jenny A, Waldenberger, Melanie, Wallaschofski, Henri, Wolffenbuttel, Bruce Hr, Wright, Margaret J, Econs, Michael J, Khaw, Kay-Tee, Montgomery, Grant W, Streeten, Elizabeth A, Thorsteinsdottir, Unnur, Bergmann, Sven, Crisponi, Laura, Gasparini, Paolo, Gieger, Christian, Harris, Tamara B, Ingelsson, Erik, Järvelin, Marjo-Riitta, Kraft, Peter, Lawlor, Debbie, Metspalu, Andres, Pennell, Craig E, Zygmunt, Marek, Murray, Anna, Stefansson, Kari, Ong, Ken K

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Whole-Genome Methylation Study of Congenital Lung Malformations in Children by Patrizi, Sara, Pederiva, Federica, d'Adamo, Adamo Pio

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Incidence of Congenital Clubfoot: Preliminary Data from Italian CeDAP Registry by Dibello, Daniela, Torelli, Lucio, Di Carlo, Valentina, d'Adamo, Adamo Pio, Faletra, Flavio, Mangogna, Alessandro, Colin, Giulia

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Genome‐wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HL... by Magri, Chiara, Marchina, Eleonora, Sansone, Emanuele, D'Adamo, Adamo Pio, Cappellani, Stefania, Bonfanti, Carlo, Terlenghi, Luigina, Biasiotto, Giorgio, Zanella, Isabella, Sala, Emma, Caruso, Arnaldo, Lombardo, Massimo, Gasparini, Paolo, De Palma, Giuseppe, Gennarelli, Massimo

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A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss by Faletra, Flavio, Girotto, Giorgia, D'Adamo, Adamo Pio, Vozzi, Diego, Morgan, Anna, Gasparini, Paolo

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