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

Allogeneic hematopoietic stem cell transplantation in ERCC6L2 disease

ERCC6L2疾病的异基因造血干细胞移植

Hakkarainen, Marja; Sicre de Fontbrune, Flore; Kaaja, Ilse; Douglas, Suvi; Dalle, Jean-Hugues; Risitano, Antonio Maria; Kulasekararaj, Austin; Alsultan, Abdulrahman; Cutler, Corey; Ho, Vincent T; Hellström-Lindberg, Eva; Mielke, Stephan; Myhre, Anders E; Rihani, Rawad; Shanap, Mayada Abu; Hashem, Hasan; Shimamura, Akiko; Rowe, R Grant; Auer, Franziska; Beier, Fabian; Desnica, Lana; Hough, Rachael; Ali Jafri, Syed Rafat; Ayas, Mouhab; Jardine, Laura; Mellid, Eugenia Fernandez; Corrales, Irene; Richardson, Deborah; Özbek, Namik Yasar; Zaniewska-Tekieli, Anna; Gozdzik, Jolanta; Ryhänen, Samppa; Niinimäki, Riitta; Jahnukainen, Kirsi; Salmenniemi, Urpu; Kilpivaara, Outi; Wartiovaara-Kautto, Ulla

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

通过对超过6500个罕见病家族进行外显子组和基因组测序数据的系统分析,检测出线粒体DNA变异,从而解决了未确诊的病例。

Stenton, Sarah L; Laricchia, Kristen; Lake, Nicole J; Chaluvadi, Sushma; Ganesh, Vijay; DiTroia, Stephanie; Osei-Owusu, Ikeoluwa; Pais, Lynn; O'Heir, Emily; Austin-Tse, Christina; O'Leary, Melanie; Abu Shanap, Mayada; Barrows, Chelsea; Berger, Seth; Bönnemann, Carsten G; Bujakowska, Kinga M; Campagna, Dean R; Compton, Alison G; Donkervoort, Sandra; Fleming, Mark D; Gallacher, Lyndon; Gleeson, Joseph G; Haliloglu, Goknur; Pierce, Eric A; Place, Emily M; Sankaran, Vijay G; Shimamura, Akiko; Stark, Zornitza; Tan, Tiong Yang; Thorburn, David R; White, Susan M; Zaki, Maha S; Vilain, Eric; Lek, Monkol; Rehm, Heidi L; O'Donnell-Luria, Anne

Enhancing Early Detection of Pancreatic Cancer in Genetically Predisposed Individuals: Integrating Advanced Imaging Modalities with Emerging Biomarkers and Liquid Biopsy

提高遗传易感人群胰腺癌的早期检出率:整合先进影像技术、新兴生物标志物和液体活检

Abdel-Razeq, Rashid; Mansour, Asem; Barbar, Maha; Abu Shanap, Mayada; Sharaf, Baha; Tamimi, Faris; Mansour, Razan; Muhanna, Adel; Al-Othman, Yazan; Hammad, Hazem; Shakhatreh, Mohammad; Mahafdah, Suleiman; Bani Hani, Hira; Abdel-Razeq, Hikmat

Exploring the aftermath of hematopoietic cell transplantation: 18-year insights into post-transplant neoplasms

探索造血干细胞移植的后续影响:18 年来对移植后肿瘤的深入研究

Rihani, Rawad; Amer, Shrouq; Halahleh, Khalid; Hashem, Hasan; Abdel Rahman, Zaid; Baqain, Laith; Abu Shanap, Mayada; Sultan, Iyad; Qudeimat, Amr

METB-08. CIRCULAR EXTRACHROMOSOMAL DNA IS ASSOCIATED WITH POOR SURVIVAL IN CHILDHOOD CANCER TYPES

METB-08. 环状染色体外DNA与儿童癌症类型预后不良相关

Carty, Ben L; Dubocanin, Danilo; Murillo-Pineda, Marina; Dumont, Marie; Volpe, Emilia; Mikulski, Pawel; Humes, Julia; Whittingham, Oliver; Fachinetti, Daniele; Giunta, Simona; Altemose, Nicolas; Jansen, Lars E T; Sato, Mariko; Sharma, Prachi; Navalkele, Pournima; Pathare, Jody; Abdullae, Zied; Aldape, Ken; Crawford, John; Amer, Shrouq; Shanap, Mayada Abu; Amayiri, Nisreen; Huang, Tina; Piunti, Andrea; Qi, Jin; Bartom, Elizabeth; Saratsis, Amanda; Sridhar, Sunita; Chapman, Owen; Dutta, Aditi; Wang, Shanqing; Kenkre, Rishaan; Luebeck, Jens; Bafna, Vineet; Mesirov, Jill P; Chavez, Lukas

Mutational analysis of the RB1 gene in patients with unilateral retinoblastoma

单侧视网膜母细胞瘤患者RB1基因突变分析

Yousef, Yacoub A; Mohammad, Mona; Baqain, Laith; Al-Hussaini, Maysa; Shanap, Mayada Abu; Halalsheh, Hadeel; Khzouz, Jakub; Jaradat, Imad; Mehyar, Mustafa; Sultan, Iyad; AlNawaiseh, Ibrahim; Shawagfeh, Munir

NFS-27. SELUMETINIB FOR SYMPTOMATIC, INOPERABLE PLEXIFORM NEUROFIBROMAS IN NEUROFIBROMATOSIS TYPE 1: A SINGLE-INSTITUTION EXPERIENCE

NFS-27. 塞鲁美替尼治疗1型神经纤维瘤病伴症状性、无法手术的丛状神经纤维瘤:单中心经验

Zhu, Baochen; Xiao, Yang; Liao, Ruiheng; Zhao, Hanxing; Xu, Xuewen; Zhang, Yan'ge; Amer, Shrouq; Shanap, Mayada Abu; Amayiri, Nisreen; Parida, Abhijeet; Jiang, Zhifan; Anwar, Syed Muhammad; Stence, Nicholas; Foreman, Nicholas; Packer, Roger J; Fisher, Michael J; Avery, Robert A; Linguraru, Marius George; Vázquez-Gómez, Felisa; Perez-Somarriba, Marta; Castellano, Serafin; Moreno, José Luis; Cartas, Susana; Cantarín, Verónica; Duat, Anna; Borrego, Pedro; Solís, Inés; Valls, Isabel; Hernández, Ángela; Torrelo, Antonio; Esteso, Borja; Tamariz-Martel, Amalia; Egea, Rosa María; Blasco, Luis; Colmenero, Isabel; Arce, Begoña; Rivero, Belén; Madero, Luis; Lassaletta, Álvaro

METB-13. GERMLINE GENETIC TESTING IN CHILDREN WITH CNS TUMORS; FIRST-EVER EXPERIENCE FROM JORDAN

METB-13. 中枢神经系统肿瘤患儿的生殖系基因检测;来自约旦的首例经验

Petroulia, Stavroula; Hockemeyer, Kathryn; Tiwari, Shashank; Berico, Pietro; Shamloo, Sama; Banijamali, Seyedeh Elnaz; Vega-Saenz de Miera, Eleazar; Gong, Yixiao; Thandapani, Palaniraja; Wang, Eric; Schulz, Michael; Tsirigos, Aristotelis; Osman, Iman; Aifantis, Ioannis; Imig, Jochen; Wang, Jianbo; Campbell, Matthew; Shah, Amishi Y; Goswami, Sangeeta; Msaouel, Pavlos; Alhalabi, Omar; Hahn, Andrew; Kovitz, Craig; Bagi, Jana; Araujo, John; Gao, Jianjun; Lin, John; Zurita, Amado; Jonasch, Eric; Corn, Paul; Tannir, Nizar; Amer, Shrouq; Shanap, Mayada Abu; Amayiri, Nisreen

Early post-induction augmented therapy improves outcome in children and adolescents with T-cell acute lymphoblastic leukemia

早期诱导后强化治疗可改善T细胞急性淋巴细胞白血病患儿和青少年的预后

Abu Shanap, Mayada; Al Jabour, Haytham; Rihani, Rawad; Hashem, Hasan; Abu Ghosh, Amal; Tbakhi, Abdelghani; Kamal, Nazmi; Sultan, Iyad; Madanat, Faris

Using ChatGPT to Predict Cancer Predisposition Genes: A Promising Tool for Pediatric Oncologists

利用 ChatGPT 预测癌症易感基因:儿科肿瘤学家的一项有前景的工具

Sultan, Iyad; Al-Abdallat, Haneen; Alnajjar, Zaina; Ismail, Layan; Abukhashabeh, Razan; Bitar, Layla; Abu Shanap, Mayada