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

Making atomistic materials calculations accessible with the AiiDAlab Quantum ESPRESSO app

借助 AiiDAlab Quantum ESPRESSO 应用程序,原子材料计算变得触手可及。

Wang, Xing; Bainglass, Edan; Bonacci, Miki; Ortega-Guerrero, Andres; Bastonero, Lorenzo; Bercx, Marnik; Bonfà, Pietro; De Renzi, Roberto; Du, Dou; Gillespie, Peter N O; Hernández-Bertrán, Michael A; Hollas, Daniel; Huber, Sebastiaan P; Molinari, Elisa; Onuorah, Ifeanyi J; Paulish, Nataliya; Prezzi, Deborah; Qiao, Junfeng; Reents, Timo; Sewell, Christopher J; Timrov, Iurii; Yakutovich, Aliaksandr V; Yu, Jusong; Marzari, Nicola; Pignedoli, Carlo A; Pizzi, Giovanni

Laterally π-Extended Polyhelicenes

侧向π共轭扩展的聚螺旋烯

Wu, Hao; Qiu, Zijie; Wen, Guanzhao; Hinaut, Antoine; Harano, Koji; Graf, Robert; Prezzi, Deborah; Estaque, Lilian; Tsai, Yu-Liang; Schollmeyer, Dieter; Pieters, Grégory; Molinari, Elisa; Pawlak, Rémy; Meyer, Ernst; Kimoto, Koji; Wang, Hai I; Bonn, Mischa; Müllen, Klaus; Narita, Akimitsu

Urine-derived renal epithelial cells for deep phenotyping and transcriptomic response to therapy in Fabry disease.

尿源性肾上皮细胞用于法布里病的深度表型分析和转录组治疗反应研究

Sudhindar Praveen Dhondurao, Orr Sarah E, Miller-Hodges Eve, Molinari Elisa, Wood Katrina, Srivastava Shalabh, Miles Colin G, Mabillard Holly R, Sentell Zachary T, Trevisan-Herraz Marco, Arcila-Galvis Juliana E, Sayer John A

Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome

CEP164基因的双等位基因变异会导致一种类似运动性纤毛病的综合征。

Devlin, Laura A; Coles, Janice; Jackson, Claire L; Barroso-Gil, Miguel; Green, Ben; Walker, Woolf T; Thomas, N Simon; Thompson, James; Rock, Simon A; Neatu, Ruxandra; Powell, Laura; Molinari, Elisa; Wilson, Ian J; Cordell, Heather J; Olinger, Eric; Miles, Colin G; Sayer, John A; Wheway, Gabrielle; Lucas, Jane S

Gap Opening in Double-Sided Highly Hydrogenated Free-Standing Graphene

双面高氢化自支撑石墨烯中的间隙打开

Betti, Maria Grazia; Placidi, Ernesto; Izzo, Chiara; Blundo, Elena; Polimeni, Antonio; Sbroscia, Marco; Avila, José; Dudin, Pavel; Hu, Kailong; Ito, Yoshikazu; Prezzi, Deborah; Bonacci, Miki; Molinari, Elisa; Mariani, Carlo

Evidence of ideal excitonic insulator in bulk MoS(2) under pressure

压力下块状 MoS₂ 中理想激子绝缘体的证据

Ataei, S Samaneh; Varsano, Daniele; Molinari, Elisa; Rontani, Massimo

A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families

NPHP3基因中一个被弃用的同义变异解释了几个家族的肾痨和先天性肝纤维化。

Olinger, Eric; Alawi, Intisar Al; Al Riyami, Mohammed S; Salmi, Isa Al; Molinari, Elisa; Faqeih, Eissa Ali; Al-Hamed, Mohamed H; Barroso-Gil, Miguel; Powell, Laura; Al-Hussaini, Abdulrahman A; Rahim, Khawla A; Almontashiri, Naif A M; Miles, Colin; Shril, Shirlee; Hildebrandt, Friedhelm; Consortium, Genomics England Research; Wilson, Ian J; Sayer, John A

Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome

小鼠遗传学研究揭示了 Barttin 是 Joubert 综合征的遗传修饰因子。

Ramsbottom, Simon A; Thelwall, Peter E; Wood, Katrina M; Clowry, Gavin J; Devlin, Laura A; Silbermann, Flora; Spiewak, Helena L; Shril, Shirlee; Molinari, Elisa; Hildebrandt, Friedhelm; Gunay-Aygun, Meral; Saunier, Sophie; Cordell, Heather J; Sayer, John A; Miles, Colin G

Disease Modeling To Understand the Pathomechanisms of Human Genetic Kidney Disorders

疾病建模在理解人类遗传性肾脏疾病发病机制中的应用

Molinari, Elisa; Sayer, John A

Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman

阿曼常染色体隐性多囊肾病的临床和遗传特征

Al Alawi, Intisar; Molinari, Elisa; Al Salmi, Issa; Al Rahbi, Fatma; Al Mawali, Adhra; Sayer, John A