DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome von 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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OC.16.10: FATTY LIVER IN IBD PATIENTS: FINDINGS FROM AN OBSERVATIONAL RETROSPECTIVE CROSS-SECTIONAL STUDY von Abenavoli Montebianco, L., Spagnuolo, R., Scarlata, G.G.M., Suraci, E., Marasco, R., Imeneo, M.G., Scarpellini, E., Boccuto, L., Luzza, F.

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Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome von Lyons, M J, Graham, J M, Neri, G, Hunter, A G W, Clark, R D, Rogers, R C, Moscarda, M, Boccuto, L, Simensen, R, Dodd, J, Robertson, S, DuPont, B R, Friez, M J, Schwartz, C E, Stevenson, R E

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Individuals with SATB2-associated syndrome with and without autism have a recognizable metabolic profile and distinctive cellular energy metabolism alterations von Zarate, Yuri A., Örsell, Jenny-Li, Bosanko, Katherine, Srikanth, Sujata, Cascio, Lauren, Pauly, Rini, Boccuto, Luigi

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Association between deletion size and important phenotypes expands the genomic region of interest in Phelan–McDermid syndrome (22q13 deletion syndrome) von Sarasua, Sara M, Dwivedi, Alka, Boccuto, Luigi, Rollins, Jonathan D, Chen, Chin-Fu, Rogers, R Curtis, Phelan, Katy, DuPont, Barbara R, Collins, Julianne S

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Correction to “Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic POLR2A variant”

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Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith–Wiedemann syndrome and Wilms' tumour von Cerrato, Flavia, Sparago, Angela, Verde, Gaetano, De Crescenzo, Agostina, Citro, Valentina, Cubellis, Maria Vittoria, Rinaldi, Maria Michela, Boccuto, Luigi, Neri, Giovanni, Magnani, Cinzia, D'Angelo, Paolo, Collini, Paola, Perotti, Daniela, Sebastio, Gianfranco, Maher, Eamonn R., Riccio, Andrea

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Additional file 3 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome von L. C. Schenkel, E. Aref-Eshghi, K. Rooney, J. Kerkhof, M. A. Levy, H. McConkey, R. C. Rogers, K. Phelan, S. M. Sarasua, L. Jain, R. Pauly, L. Boccuto, B. DuPont, G. Cappuccio, N. Brunetti-Pierri, C. E. Schwartz, Sadikovic, B.

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Additional file 4 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome von L. C. Schenkel, E. Aref-Eshghi, K. Rooney, J. Kerkhof, M. A. Levy, H. McConkey, R. C. Rogers, K. Phelan, S. M. Sarasua, L. Jain, R. Pauly, L. Boccuto, B. DuPont, G. Cappuccio, N. Brunetti-Pierri, C. E. Schwartz, Sadikovic, B.

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Additional file 5 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome von L. C. Schenkel, E. Aref-Eshghi, K. Rooney, J. Kerkhof, M. A. Levy, H. McConkey, R. C. Rogers, K. Phelan, S. M. Sarasua, L. Jain, R. Pauly, L. Boccuto, B. DuPont, G. Cappuccio, N. Brunetti-Pierri, C. E. Schwartz, Sadikovic, B.

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Additional file 1 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome von L. C. Schenkel, E. Aref-Eshghi, K. Rooney, J. Kerkhof, M. A. Levy, H. McConkey, R. C. Rogers, K. Phelan, S. M. Sarasua, L. Jain, R. Pauly, L. Boccuto, B. DuPont, G. Cappuccio, N. Brunetti-Pierri, C. E. Schwartz, Sadikovic, B.

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Additional file 6 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome von L. C. Schenkel, E. Aref-Eshghi, K. Rooney, J. Kerkhof, M. A. Levy, H. McConkey, R. C. Rogers, K. Phelan, S. M. Sarasua, L. Jain, R. Pauly, L. Boccuto, B. DuPont, G. Cappuccio, N. Brunetti-Pierri, C. E. Schwartz, Sadikovic, B.

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Additional file 2 of DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome von L. C. Schenkel, E. Aref-Eshghi, K. Rooney, J. Kerkhof, M. A. Levy, H. McConkey, R. C. Rogers, K. Phelan, S. M. Sarasua, L. Jain, R. Pauly, L. Boccuto, B. DuPont, G. Cappuccio, N. Brunetti-Pierri, C. E. Schwartz, Sadikovic, B.

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P-460 SARS-CoV-2 infection of human ovarian cells: an in vitro model for the detection of the virus entry into the host cells von Piomboni, P, Luongo, F.P, Dragoni, F, Gentile, M, Boccuto, A, Boschi, L, Morgante, G, Vicenti, I, Zazzi, M, Luddi, A

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P10-07: Sunscreen accumulation in North Adriatic Sea mussels (Mytilus galloprovincialis) von Rubini, S., Dall'Ara, S., Calfapietra, A., Milandri, S., Baruffaldi, M., Barsi, F., Bernardi, T., Boccuto, F., Munari, M., Fiorentini, L., Tosi, G., Baldini, E., Vertuani, S., Manfredini, S.

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Gene Variant Frequencies of IDO1 , IDO2 , TDO , and KMO in Substance Use Disorder Cohorts von Contella, Lindsey, Farrell, Christopher L, Boccuto, Luigi, Litwin, Alain, Snyder, Marion L

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Clinical and genomic evaluation of 201 patients with Phelan–McDermid syndrome von Sarasua, Sara M., Boccuto, Luigi, Sharp, Julia L., Dwivedi, Alka, Chen, Chin-Fu, Rollins, Jonathan D., Rogers, R. Curtis, Phelan, Katy, DuPont, Barbara R.

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Exploring the Therapeutic Potential for Breast Cancer of Phytochemicals and Secondary Metabolites in Marjoram, Thyme, and Persimmon von Mattingly, Aubrey, Vickery, Zoe, Ivankovic, Diana, Farrell, Christopher L., Hakonarson, Hakon, Nguyen, Katie, Boccuto, Luigi

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Impact of Substance Use Disorder on Tryptophan Metabolism Through the Kynurenine Pathway: A Narrative Review von Contella, Lindsey, Farrell, Christopher L, Boccuto, Luigi, Litwin, Alain H, Snyder, Marion L

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22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan–McDermid syndrome von Sarasua, Sara M., Dwivedi, Alka, Boccuto, Luigi, Chen, Chin-Fu, Sharp, Julia L., Rollins, Jonathan D., Collins, Julianne S., Rogers, R. Curtis, Phelan, Katy, DuPont, Barbara R.

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