日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A Novel Heterozygous ARL3 Variant in Non-Syndromic Retinitis Pigmentosa: Clinical and Functional Characterization

非综合征型视网膜色素变性中一种新的杂合ARL3变异:临床和功能特征

Stellacci, Emilia; Ziccardi, Lucia; Bruselles, Alessandro; Dell'Aquila, Carmen; Mignini, Luca; Niceta, Marcello; Chiriatti, Luigi; Carvetta, Mattia; Zara, Erika; Leone, Alessandro; Cecchetti, Serena; Coppola, Simona; Parisi, Vincenzo; Tartaglia, Marco; Cordeddu, Viviana

Variable Ophthalmologic Phenotypes Associated with Biallelic Loss-of-Function Variants in POMGNT1

POMGNT1基因双等位基因功能缺失变异与多种眼科表型相关

Ziccardi, Lucia; Barbano, Lucilla; D'Andrea, Mattia; Bruselles, Alessandro; Dell'Aquila, Carmen; Niceta, Marcello; Mancini, Cecilia; Leone, Alessandro; Carvetta, Mattia; Albanese, Maria; Stellacci, Emilia; Tartaglia, Marco; Cordeddu, Viviana

Bridging the educational gaps of health professionals in oncogenomics: results from a pilot e-learning course

弥合卫生专业人员在肿瘤基因组学方面的教育差距:一项试点在线学习课程的结果

Stellacci, Emilia; Martinelli, Simone; Carbone, Pietro; Demuru, Elena; Genuardi, Maurizio; Ghiorzo, Paola; Novelli, Giuseppe; Di Pucchio, Alessandra; Regini, Federica Maria; Guerrera, Debora; Vittozzi, Andrea; Barbina, Donatella; Venanzi, Serenella; van den Bulcke, Marc; Boccia, Stefania; Mazzaccara, Alfonso; De Nicolo, Arcangela; De Angelis, Roberta

Immunological and hematological findings as major features in a patient with a new germline pathogenic CBL variant.

免疫学和血液学发现是具有新的生殖系致病性 CBL 变异的患者的主要特征

Stellacci Emilia, Carter Jennefer N, Pannone Luca, Stevenson David, Moslehi Dorsa, Venanzi Serenella, Bernstein Jonathan A, Tartaglia Marco, Martinelli Simone

Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary Cilium

双等位基因失活的TUB变异体导致视网膜纤毛病,损害初级纤毛的生物发生和结构。

Ziccardi, Lucia; Niceta, Marcello; Stellacci, Emilia; Ciolfi, Andrea; Tatti, Massimo; Bruselles, Alessandro; Mancini, Cecilia; Barbano, Lucilla; Cecchetti, Serena; Costanzo, Eliana; Cappa, Marco; Parravano, Mariacristina; Varano, Monica; Tartaglia, Marco; Cordeddu, Viviana

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

SPEN单倍体不足会导致一种神经发育障碍,该障碍与近端1p36缺失综合征重叠,并在女性中伴有X染色体表观遗传特征。

Radio, Francesca Clementina; Pang, Kaifang; 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; Dentici, Maria Lisa; McWalter, Kirsty; Desai, Megha; Monaghan, Kristin G; Telegrafi, Aida; Philippe, Christophe; Vitobello, Antonio; Au, Margaret; Grand, Katheryn; Sanchez-Lara, Pedro A; 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; Cross, Laura; Zhou, Dihong; Hartley, Taila; Sawyer, Sarah L; Monteiro, Fabíola Paoli; Secches, Tania Vertemati; Kok, Fernando; Schultz-Rogers, Laura E; Macke, Erica L; Morava, Eva; Klee, Eric W; Kemppainen, Jennifer; Iascone, Maria; Selicorni, Angelo; Tenconi, Romano; Amor, David J; Pais, Lynn; Gallacher, Lyndon; Turnpenny, Peter D; Stals, Karen; Ellard, Sian; Cabet, Sara; Lesca, Gaetan; Pascal, Joset; Steindl, Katharina; Ravid, Sarit; Weiss, Karin; Castle, Alison M R; 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; Kingston, Helen M; 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; Hagelstrom, R Tanner; Zanus, Caterina; 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 Jr; Faivre, Laurence; Banka, Siddharth; Wang, Tianyun; Eichler, Evan E; Priolo, Manuela; Dallapiccola, Bruno; Vissers, Lisenka E L M; Sadikovic, Bekim; Scott, Daryl A; Holder, Jimmy Lloyd Jr; Tartaglia, Marco

Mutations in PAX2 associate with adult-onset FSGS

PAX2基因突变与成人发病的局灶节段性肾小球硬化症相关。

Barua, Moumita; Stellacci, Emilia; Stella, Lorenzo; Weins, Astrid; Genovese, Giulio; Muto, Valentina; Caputo, Viviana; Toka, Hakan R; Charoonratana, Victoria T; Tartaglia, Marco; Pollak, Martin R

Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis

RRAS基因的激活突变是RAS病谱系中某种表型的基础,并促进白血病的发生。

Flex, Elisabetta; Jaiswal, Mamta; Pantaleoni, Francesca; Martinelli, Simone; Strullu, Marion; Fansa, Eyad K; Caye, Aurélie; De Luca, Alessandro; Lepri, Francesca; Dvorsky, Radovan; Pannone, Luca; Paolacci, Stefano; Zhang, Si-Cai; Fodale, Valentina; Bocchinfuso, Gianfranco; Rossi, Cesare; Burkitt-Wright, Emma M M; Farrotti, Andrea; Stellacci, Emilia; Cecchetti, Serena; Ferese, Rosangela; Bottero, Lisabianca; Castro, Silvana; Fenneteau, Odile; Brethon, Benoît; Sanchez, Massimo; Roberts, Amy E; Yntema, Helger G; Van Der Burgt, Ineke; Cianci, Paola; Bondeson, Marie-Louise; Cristina Digilio, Maria; Zampino, Giuseppe; Kerr, Bronwyn; Aoki, Yoko; Loh, Mignon L; Palleschi, Antonio; Di Schiavi, Elia; Carè, Alessandra; Selicorni, Angelo; Dallapiccola, Bruno; Cirstea, Ion C; Stella, Lorenzo; Zenker, Martin; Gelb, Bruce D; Cavé, Hélène; Ahmadian, Mohammad R; Tartaglia, Marco

Interaction between the glucocorticoid and erythropoietin receptors in human erythroid cells

人类红细胞中糖皮质激素受体与促红细胞生成素受体的相互作用

Stellacci, Emilia; Di Noia, Antonella; Di Baldassarre, Angela; Migliaccio, Giovanni; Battistini, Angela; Migliaccio, Anna Rita

Interferon regulatory factor-2 drives megakaryocytic differentiation.

干扰素调节因子-2驱动巨核细胞分化

Stellacci Emilia, Testa Ugo, Petrucci Eleonora, Benedetti Eleonora, Orsatti Roberto, Feccia Tiziana, Stafsnes Marit, Coccia Eliana M, Marziali Giovanna, Battistini Angela