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

Mol2Raman: a graph neural network model for predicting Raman spectra from SMILES representations

Mol2Raman:一种基于SMILES表示预测拉曼光谱的图神经网络模型

Sorrentino, Salvatore; Gussoni, Alessandro; Calcagno, Francesco; Pasotti, Gioele; Avagliano, Davide; Rivalta, Ivan; Garavelli, Marco; Polli, Dario

Diabatization with Electrostatic Embedding for Studying Photophysics in Organic Molecular Crystals

利用静电嵌入进行绝热化以研究有机分子晶体的光物理性质

Ingham, Michael; Aarabi, Mohammad; Giannini, Samuele; Garavelli, Marco; Santoro, Fabrizio; Improta, Roberto; Crespo-Otero, Rachel

Quantum Chemistry-Driven Molecular Inverse Design of Stable Isomers with Data-Free Reinforcement Learning

基于量子化学的稳定异构体分子逆向设计与无数据强化学习

Calcagno, Francesco; Serfilippi, Luca; Franceschelli, Giorgio; Garavelli, Marco; Musolesi, Mirco; Rivalta, Ivan

The LMSz method - an automatable scalable approach to constructing gene-specific growth charts in rare disorders

LMSz 方法——一种用于构建罕见疾病基因特异性生长曲线的自动化、可扩展的方法

Low, Karen J; Foreman, Julia; Hobson, Rachel J; Kwuo, Hannah; Martinez-Cayuelas, Elena; Almoguera, Berta; Marin-Reina, Purin; Caraffi, Stefano G; Garavelli, Livia; Woods, Emily; Balasubramanian, Meena; Bayat, Allan; Ockeloen, Charlotte W; Wright, Caroline M; Firth, Helen V; Cole, Tim J

White-Sutton Syndrome: Insight of an Italian Cohort of 19 Subjects

怀特-萨顿综合征:一项对19名意大利受试者的研究

Facchini, Anna; Concas, Maria Pina; Zampieri, Stefania; Scala, Iris; Graziano, Claudio; Innoceta, Anna Maria; Trivisano, Marina; De Dominicis, Angela; Trimarchi, Gabriele; Garavelli, Livia; Baldassarri, Margherita; De Maggio, Ilaria; Mari, Francesca; Greco, Donatella; Gasparini, Paolo

Transition From Children's to Adults' Healthcare for Youth With (Genetic) Intellectual Disabilities: An ERN-ITHACA Guideline

为患有(遗传性)智力障碍的青少年从儿童医疗保健过渡到成人医疗保健:ERN-ITHACA 指南

Klein Haneveld, Mirthe J; Świeczkowska, Katarzyna; Grybek, Tomasz; Labunets, Kinga; van Amelsvoort, Thérèse A M J; Bedeschi, Maria F; Behan, Claire; Dufke, Andreas; Dupont, Juliette; Gaasterland, Charlotte M W; Garavelli, Livia; Helverschou, Sissel B; McAnallen, Susan; Milska-Musa, Katarzyna A; van Staa, AnneLoes; Streață, Ioana; Stumpel, Connie T R M; Tamburrino, Federica; Vasseghi, Mary; Vyshka, Klea; Wierzba, Jolanta M; van Eeghen, Agnies M

Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases

Telethon 未确诊疾病项目:以结构化方法解决罕见的儿童期发病遗传疾病

Torella, Annalaura; Morleo, Manuela; Spampanato, Carmine; Castello, Raffaele; Zanobio, Mariateresa; Piluso, Giulio; Di Letto, Pasquale; Onore, Maria Elena; Rahman, Sarah Iffat; Musacchia, Francesco; Pinelli, Michele; Vitiello, Giuseppina; De Riso, Giulia; Selicorni, Angelo; Mariani, Milena; Daolio, Cecilia; Capra, Valeria; Scala, Marcello; Nardecchia, Francesca; Galosi, Serena; Mastrangelo, Mario; Manti, Filippo; Milani, Donatella; Romano, Corrado; Greco, Donatella; Ciaccio, Claudia; D'Arrigo, Stefano; De Laurentiis, Arianna; Coppola, Antonietta; Zollino, Marcella; Pasquetti, Domizia; L'Erario, Federica Francesca; Tummolo, Albina; Santoro, Claudia; Garavelli, Livia; Marini, Carla; Bigoni, Stefania; Tirozzi, Alfonsina; Cetrangolo, Viviana; Parenti, Giancarlo; Di Bernardo, Diego; Peron, Angela; Maitz, Silvia; Accogli, Andrea; Cappuccio, Gerarda; Banfi, Sandro; Casari, Giorgio; Ballabio, Andrea; Brunetti-Pierri, Nicola; Nigro, Vincenzo

Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies

ACTB 和 ACTG1 相关非肌肉肌动蛋白病中的分子基因型-表型相关性

Di Donato, Nataliya; Thom, Andrew; Rump, Andreas; Greve, Johannes N; Cadiñanos, Juan; Calabrò, Rocco Salvatore; Cathey, Sara; Chung, Brian; Cope, Heidi; Costales, Maria; Cuvertino, Sara; Dinkel, Philine; Erripi, Kalliopi; Fry, Andrew E; Garavelli, Livia; Hoffjan, Sabine; Janzarik, Wibke G; Kreimer, Insa; Mancini, Grazia; Marin-Reina, Purificacion; Meinhardt, Andrea; Niehaus, Indra; Pilz, Daniela; Ricca, Ivana; Simarro, Fernando Santos; Schrock, Evelin; Marquardt, Anja; Taft, Manuel H; Tezcan, Kamer; Thunström, Sofia; Verhagen, Judith; Verloes, Alain; Wollnik, Bernd; Krawitz, Peter; Hsieh, Tzung-Chien; Seifert, Michael; Heide, Michael; Lawrence, Catherine B; Roberts, Neil A; Manstein, Dietmar J; Woolf, Adrian S; Banka, Siddharth

Photochemical Pathways and Light-Enhanced Radical Scavenging Activity of 1,8-Dihydroxynaphthalene Allomelanin

1,8-二羟基萘异黑素的光化学途径和光增强自由基清除活性

Petropoulos, Vasilis; Mordini, Dario; Montorsi, Francesco; Akturk, Mert; Menichetti, Arianna; Olivati, Andrea; Petrozza, Annamaria; Morandi, Vittorio; Maiuri, Margherita; Gianneschi, Nathan C; Garavelli, Marco; Valgimigli, Luca; Cerullo, Giulio; Montalti, Marco

De novo variants in LRRC8C resulting in constitutive channel activation cause a human multisystem disorder

LRRC8C基因的新生突变导致通道持续激活,从而引发人类多系统疾病。

Mathieu Quinodoz # ,Sonja Rutz # ,Virginie Peter # ,Livia Garavelli # ,A Micheil Innes # ,Elena F Lehmann ,Stephan Kellenberger ,Zhong Peng ,Angelica Barone ,Belinda Campos-Xavier ,Sheila Unger ,Carlo Rivolta ,Raimund Dutzler ,Andrea Superti-Furga