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

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

非编码RNA基因RNU4-2的双等位基因变异会导致一种隐性遗传的神经发育综合征,并伴有明显的白质改变。

Rius, Rocio; Blakes, Alexander J M; Chen, Yuyang; De Jonghe, Joachim; Lecoquierre, François; Dawes, Ruebena; Cogne, Benjamin; Kim, Hyung Chul; Alvi, Javeria R; Amblard, Florence; Ansari, Morad; Arlt, Annabelle; Austin-Tse, Christina; Baer, Sarah; Balasubramanian, Meena; Balton, Elsa V; Barcia, Giulia; Beleza-Meireles, Ana; Bernstein, Jonathan A; Beygo, Jasmin; Blanc, Pierre; Bramswig, Nuria C; Braun, Frederik; Buchzik, Daniel; Calame, Daniel G; Campbell, Jamie; Coutton, Charles; Cunningham, Chloe A; Dargie, Nitsuh; Depienne, Christel; Dipple, Katrina M; Dieux, Anne; Dixit, Abhijit; Dreyer, Lauren; Du, Haowei; El Chehadeh, Salima; Field, Michael; Ewans, Lisa J; Geiger, Vanessa; Gibbs, Richard A; Glass, Ian; Grunewald, Olivier; Gueguen, Paul; Haack, Tobias B; Hadj Abdallah, Hamza; Harbuz, Radu; Helbig, Ingo; Horvath, Judit; Hustinx, Alexander; Isidor, Bertrand; Jacquemont, Marie-Line; Jamie, Fraser; Jeanne, Médéric; Kessler, Riley; Klinkhammer, Hannah; Korenke, G Christoph; Kotzaeridou, Urania; Krawitz, Peter; Laurie, Steven; Leventer, Richard J; Levy, Rebecca J; Lupski, James R; Marijon, Pierre; McGinnis, Kaitlin E; Mendez, Rodrigo; Messaoud, Olfa; Nava, Caroline; Nizard, Mevyn; O'Donnell-Luria, Anne; O'Leary, Melanie C; Olivieri, Simone; Parida, Amitav; Pehlivan, Davut; Prentice, Anna Jenne; Posey, Jennifer E; Reuter, Chloe M; Satre, Véronique; Schluth-Bolard, Caroline; Smol, Thomas; Sultan, Tipu; Taylor, John; Thauvin-Robinetvin, Christel; Thevenon, Julien; Uebergang, Eloise; Ueberberg, Sandra; Vincent-Delorme, Catherine; Wassmer, Evangeline; Westwood, Emma; Wheeler, Matthew T; Gulec, Elif Yilmaz; Vanderver, Adeline; Vossough, Arastoo; Sanders, Stephan J; Banka, Siddharth; Findlay, Gregory M; MacArthur, Daniel G; Simons, Cas; Whiffin, Nicola

Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene

利用 Eye2Gene 进行多模态成像,实现遗传性视网膜疾病的下一代表型分析

Pontikos, Nikolas; Woof, William A; Lin, Siying; Ghoshal, Biraja; Mendes, Bernardo S; Veturi, Advaith; Nguyen, Quang; Javanmardi, Behnam; Georgiou, Michalis; Hustinx, Alexander; Ibarra-Arellano, Miguel A; Moghul, Ismail; Liu, Yichen; Pfau, Kristina; Pfau, Maximilian; Shah, Mital; Yu, Jing; Al-Khuzaei, Saoud; Wagner, Siegfried K; Daich Varela, Malena; Cabral de Guimarães, Thales Antonio; Sen, Sagnik; Naik, Gunjan; Sumodhee, Dayyanah; Fu, Dun Jack; Kabiri, Nathaniel; Furman, Jennifer; Liefers, Bart; Lee, Aaron Y; De Silva, Samantha R; Marques, Caio; Motta, Fabiana; Fujinami-Yokokawa, Yu; Hardcastle, Alison J; Arno, Gavin; Lorenz, Birgit; Herrmann, Philipp; Fujinami, Kaoru; Sallum, Juliana; Madhusudhan, Savita; Downes, Susan M; Holz, Frank G; Balaskas, Konstantinos; Webster, Andrew R; Mahroo, Omar A; Krawitz, Peter M; Michaelides, Michel

GestaltGAN: synthetic photorealistic portraits of individuals with rare genetic disorders

GestaltGAN:合成罕见遗传疾病患者的逼真肖像

Kirchhoff, Aron; Hustinx, Alexander; Javanmardi, Behnam; Hsieh, Tzung-Chien; Brand, Fabian; Hellmann, Fabio; Mertes, Silvan; André, Elisabeth; Moosa, Shahida; Schultz, Thomas; Solomon, Benjamin D; Krawitz, Peter

Machine Learning Model Integrating CT Radiomics of the Lung to Predict Checkpoint Inhibitor Pneumonitis in Patients with Advanced Cancer

整合肺部CT放射组学数据的机器学习模型用于预测晚期癌症患者的免疫检查点抑制剂肺炎

Cousin, François; Louis, Thomas; Frères, Pierre; Guiot, Julien; Occhipinti, Mariaelena; Bottari, Fabio; Vos, Wim; Hustinx, Roland

(18)F-FDG PET/CT discriminates whether rheumatoid arthritis patients are in ultrasound remission or not

(18)F-FDG PET/CT 可以区分类风湿性关节炎患者是否处于超声缓解期

Rinkin, Charline; Malaise, Olivier; Lamaye, Claire; Chauveheid, Florane; Gérard, Caroline; Seidel, Laurence; Malaise, Michel; Hustinx, Roland; Ribbens, Clio

Characterization of exclusive rib lesions detected by [ 68 Ga]Ga-PSMA-11 PET/CT

[68Ga]Ga-PSMA-11 PET/CT 检测到的肋骨特异性病变的特征分析

Stoffels, Marine; Cousin, François; Lamande, Maréva; Denis, Chloé; Waltregny, David; Hustinx, Roland; Sautois, Brieuc; Withofs, Nadia

ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations

ZSCAN10 缺陷会导致一种神经发育障碍,其特征是耳面部畸形。

Laugwitz, Lucia; Cheng, Fubo; Collins, Stephan C; Hustinx, Alexander; Navarro, Nicolas; Welsch, Simon; Cox, Helen; Hsieh, Tzung-Chien; Vijayananth, Aswinkumar; Buchert, Rebecca; Bender, Benjamin; Efthymiou, Stephanie; Murphy, David; Zafar, Faisal; Rana, Nuzhat; Grasshoff, Ute; Falb, Ruth J; Grimmel, Mona; Seibt, Annette; Zheng, Wenxu; Ghaedi, Hamid; Thirion, Marie; Couette, Sébastien; Azizimalamiri, Reza; Sadeghian, Saeid; Galehdari, Hamid; Zamani, Mina; Zeighami, Jawaher; Sedaghat, Alireza; Ramshe, Samira Molaei; Zare, Ali; Alipoor, Behnam; Klee, Dirk; Sturm, Marc; Ossowski, Stephan; Houlden, Henry; Riess, Olaf; Wieczorek, Dagmar; Gavin, Ryan; Maroofian, Reza; Krawitz, Peter; Yalcin, Binnaz; Distelmaier, Felix; Haack, Tobias B

Apomorphine for prolonged disorders of consciousness: a multimodal open-label study

阿扑吗啡治疗持续性意识障碍:一项多模式开放标签研究

Sanz, Leandro R D; Lejeune, Nicolas; Szymkowicz, Emilie; Bonin, Estelle A C; Panda, Rajanikant; Sala, Arianna; Thibaut, Aurore; Huerta-Gutierrez, Rodrigo; Dardenne, Nadia; Dikenstein, David; Van Goethem, Sébastien; Ledoux, Didier; Hustinx, Roland; Stender, Johan; Farber, Neal M; Zafonte, Ross D; Schiff, Nicholas D; Laureys, Steven; Gosseries, Olivia

Correction to: CD38 as theranostic target in oncology

更正:CD38 作为肿瘤学诊疗靶点

Bocuzzi, Valentina; Bridoux, Jessica; Pirotte, Michelle; Withofs, Nadia; Hustinx, Roland; D'Huyvetter, Matthias; Caers, Jo; Marcion, Guillaume

CD38 as theranostic target in oncology

CD38 作为肿瘤学诊疗靶点

Bocuzzi, Valentina; Bridoux, Jessica; Pirotte, Michelle; Withofs, Nadia; Hustinx, Roland; D'Huyvetter, Matthias; Caers, Jo; Marcion, Guillaume