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

Sex-specific cardiometabolic multimorbidity, metabolic syndrome and left ventricular function in heart failure with preserved ejection fraction in the UK Biobank

英国生物银行中射血分数保留型心力衰竭患者的性别特异性心血管代谢多重疾病、代谢综合征和左心室功能

Bertrand, Ambre; Zhou, Xin; Lewis, Andrew; Monfeuga, Thomas; Gupta, Ramneek; Grau, Vicente; Rodriguez, Blanca

Data-driven identification of predictive risk biomarkers for subgroups of osteoarthritis using interpretable machine learning

利用可解释的机器学习方法,基于数据识别骨关节炎亚组的预测风险生物标志物

Nielsen, Rikke Linnemann; Monfeuga, Thomas; Kitchen, Robert R; Egerod, Line; Leal, Luis G; Schreyer, August Thomas Hjortshøj; Gade, Frederik Steensgaard; Sun, Carol; Helenius, Marianne; Simonsen, Lotte; Willert, Marianne; Tahrani, Abd A; McVey, Zahra; Gupta, Ramneek

Evaluation of long acting GLP1R/GCGR agonist in a DIO and biopsy-confirmed mouse model of NASH suggest a beneficial role of GLP-1/glucagon agonism in NASH patients

在DIO和经活检证实的NASH小鼠模型中对长效GLP1R/GCGR激动剂的评估表明,GLP-1/胰高血糖素激动剂在NASH患者中具有有益作用。

Thomas Monfeuga ,Jenny Norlin ,Anne Bugge ,Elisabeth D Gaalsgaard ,Cesar A Prada-Medina ,Markus Latta ,Sanne S Veidal ,Pia S Petersen ,Michael Feigh ,Dorte Holst

MLX plays a key role in lipid and glucose metabolism in humans: Evidence from in vitro and in vivo studies

MLX在人体脂质和葡萄糖代谢中发挥关键作用:来自体外和体内研究的证据

Shilpa R Nagarajan ,Eilidh J Livingstone ,Thomas Monfeuga ,Lara C Lewis ,Shahul Hameed Liyakath Ali ,Anandhakumar Chandran ,David J Dearlove ,Matt J Neville ,Lingyan Chen ,Cyrielle Maroteau ,Maxwell A Ruby ,Leanne Hodson

Central androgen action reverses hypothalamic astrogliosis and atherogenic risk factors induced by orchiectomy and high-fat diet feeding in male mice

中枢雄激素作用可逆转雄性小鼠睾丸切除术和高脂饮食喂养引起的下丘脑星形胶质增生和动脉粥样硬化危险因素

Mauricio D Dorfman, Thomas Monfeuga, Susan J Melhorn, Jenny E Kanter, Jeremy M Frey, Rachael D Fasnacht, Anandhakumar Chandran, Emaad Lala, Inmaculada Velasco, Katya B Rubinow, Thomas H Meek, Ellen A Schur, Karin E Bornfeldt, Joshua P Thaler

Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets

通过对代谢功能障碍相关脂肪肝疾病的基因组和蛋白质组进行分析,可以识别潜在的治疗靶点。

Liu, Jun; Hu, Sile; Chen, Lingyan; Daly, Charlotte; Prada Medina, Cesar Augusto; Richardson, Tom G; Traylor, Matthew; Dempster, Niall J; Mbasu, Richard; Monfeuga, Thomas; Vujkovic, Marijana; Tsao, Philip S; Lynch, Julie A; Voight, Benjamin F; Chang, Kyong-Mi; Million, V A; Cobbold, Jeremy F; Tomlinson, Jeremy W; van Duijn, Cornelia M; Howson, Joanna M M

NMDA Receptor Antagonists Increase the Release of GLP-1 From Gut Endocrine Cells

NMDA 受体拮抗剂增加肠内分泌细胞释放 GLP-1

Malgorzata Cyranka, Thomas Monfeuga, Natascia Vedovato, Chelsea M Larabee, Anandhakumar Chandran, Enrique M Toledo, Heidi de Wet

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

22q11.2缺失存在时,精神分裂症风险的遗传因素

Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S; Heung, Tracy; Holleman, Aaron M; Johnston, H Richard; Monfeuga, Thomas; McDonald-McGinn, Donna M; Gur, Raquel E; Morrow, Bernice E; Swillen, Ann; Vorstman, Jacob A S; Bearden, Carrie E; Chow, Eva W C; van den Bree, Marianne; Emanuel, Beverly S; Vermeesch, Joris R; Warren, Stephen T; Owen, Michael J; Chopra, Pankaj; Cutler, David J; Duncan, Richard; Kotlar, Alex V; Mulle, Jennifer G; Voss, Anna J; Zwick, Michael E; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih-Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold I; Tran, Oanh; Holmans, Peter; Pardinas, Antonio; Walters, James T R; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J; Costain, Gregory A; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A M J; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T Blaine; McGinn, Daniel E; Moss, Edward M; Sharkus, Robert J; Unolt, Marta; Zackai, Elaine H; Calkins, Monica E; Gallagher, Robert S; Gur, Ruben C; Tang, Sunny X; Fritsch, Rosemarie; Ornstein, Claudia; Repetto, Gabriela M; Breetvelt, Elemi; Duijff, Sasja N; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C; Prasad, Sarah E; Daly, Eileen M; Gudbrandsen, Maria; Murphy, Clodagh M; Murphy, Declan G; Buzzanca, Antonio; Fabio, Fabio Di; Digilio, Maria C; Pontillo, Maria; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F; Ousley, Opal Y; Carmel, Miri; Gothelf, Doron; Mekori-Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Weizman, Abraham; Kushan, Leila; Jalbrzikowski, Maria; Armando, Marco; Eliez, Stéphan; Sandini, Corrado; Schneider, Maude; Béna, Frédérique Sloan; Antshel, Kevin M; Fremont, Wanda; Kates, Wendy R; Belzeaux, Raoul; Busa, Tiffany; Philip, Nicole; Campbell, Linda E; McCabe, Kathryn L; Hooper, Stephen R; Schoch, Kelly; Shashi, Vandana; Simon, Tony J; Tassone, Flora; Arango, Celso; Fraguas, David; García-Miñaúr, Sixto; Morey-Canyelles, Jaume; Rosell, Jordi; Suñer, Damià H; Raventos-Simic, Jasna; Epstein, Michael P; Williams, Nigel M; Bassett, Anne S

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

利用常见遗传变异研究22q11.2缺失综合征的表型表达和风险预测

Davies, Robert W; Fiksinski, Ania M; Breetvelt, Elemi J; Williams, Nigel M; Hooper, Stephen R; Monfeuga, Thomas; Bassett, Anne S; Owen, Michael J; Gur, Raquel E; Morrow, Bernice E; McDonald-McGinn, Donna M; Swillen, Ann; Chow, Eva W C; van den Bree, Marianne; Emanuel, Beverly S; Vermeesch, Joris R; van Amelsvoort, Therese; Arango, Celso; Armando, Marco; Campbell, Linda E; Cubells, Joseph F; Eliez, Stephan; Garcia-Minaur, Sixto; Gothelf, Doron; Kates, Wendy R; Murphy, Kieran C; Murphy, Clodagh M; Murphy, Declan G; Philip, Nicole; Repetto, Gabriela M; Shashi, Vandana; Simon, Tony J; Suñer, Damiàn Heine; Vicari, Stefano; Scherer, Stephen W; Bearden, Carrie E; Vorstman, Jacob A S

Functional module detection through integration of single-cell RNA sequencing data with protein-protein interaction networks

通过将单细胞RNA测序数据与蛋白质-蛋白质相互作用网络整合来进行功能模块检测

Klimm, Florian; Toledo, Enrique M; Monfeuga, Thomas; Zhang, Fang; Deane, Charlotte M; Reinert, Gesine