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

The intersection of disorders of sex development and cardiovascular diseases

性发育障碍与心血管疾病的交叉领域

Hashmi, Satwat; Aherrahrou, Rédouane

A prevalent disease-associated SNP in the human ID3 gene regulates E-protein activity and cellular proliferation.

人类 ID3 基因中常见的与疾病相关的 SNP 调节 E 蛋白活性和细胞增殖。

Henderson Christopher A, Ransegnola Brett P, Garmey James, Khan Ali, Aherrahrou Rédouane, Purdy Michael, Wu Shijie, Zhou Andrea, Kirby Jennifer L, Lipinski Michael J, Gordon Vicki, Yeager Mark, Civelek Mete, McNamara Coleen A

Artificial intelligence for comprehensive DNA methylation analysis: overview, challenges, and future directions

人工智能在DNA甲基化综合分析中的应用:概述、挑战与未来方向

Aghziel, Aymane; Mahraz, Mohamed Adnane; Tairi, Hamid; Aherrahrou, Noura

Artery segmentation and atherosclerotic plaque quantification using AI for murine whole slide images stained with oil red O

利用人工智能对油红O染色的鼠类全切片图像进行动脉分割和动脉粥样硬化斑块定量分析

Engster, Johann Christopher; Reinberger, Tobias; Blum, Nele; Stagge, Pascal; Buzug, Thorsten M; Aherrahrou, Zouhair; Stille, Maik

Genome-wide association study of borderline personality disorder identifies 11 loci and highlights shared risk with mental and somatic disorders

全基因组关联研究发现边缘型人格障碍存在11个致病基因位点,并强调了其与精神和躯体疾病的共同风险。

Streit, Fabian; Awasthi, Swapnil; Hall, Alisha Sm; Braun, Alice; Niarchou, Maria; Marouli, Eirini; Babajide, Oladapo; Frank, Josef; Zillich, Lea; Callies, Carolin M; Avetyan, Diana; Zillich, Eric; Naamanka, Joonas; Gonzalez, Jean; Harder, Arvid; Lu, Yi; Aherrahrou, Zouhair; Ahmad, Zain-Ul-Abideen; Ask, Helga; Batzler, Anthony; Benros, Michael E; Brand-de Wilde, Odette M; Brunak, Søren; Bruun, Mie T; Christoffersen, Lea An; Colodro-Conde, Lucía; Coombes, Brandon J; Corfield, Elizabeth C; Dahmen, Norbert; Didriksen, Maria; Dinh, Khoa M; Djurovic, Srdjan; Dowsett, Joseph; Drange, Ole Kristian; Dukal, Helene; Edelmann, Susanne; Erikstrup, Christian; Espinola, Mariana K; Fassbinder, Eva; Faucon, Annika; de Sá, Diana S Ferreira; Foo, Jerome C; Gilles, Maria; Gutiérrez-Zotes, Alfonso; Hansen, Thomas F; Haraldsson, Magnus; Harper, R Patrick; Havdahl, Alexandra; Heilbronner, Urs; Herms, Stefan; Hjalgrim, Henrik; Hübel, Christopher; Jacob, Gitta A; Aagaard, Bitten; Jorgensen, Anders; Jungkunz, Martin; Kleindienst, Nikolaus; Knoblich, Nora; Koglin, Stefanie; Kraft, Julia; Krebs, Kristi; Lee, Christopher W; Lin, Yuhao; Lis, Stefanie; Lisoway, Amanda; Malogiannis, Ioannis A; Martinsen, Amy; Maslahati, Tolou; Merz, Katharina; Meyer-Lindenberg, Andreas; Mikkelsen, Susan; Mikkelsen, Christina; Mobascher, Arian; Muntané, Gerard; Oddsson, Asmundur; Ostrowski, Sisse R; Palviainen, Teemu; Pedersen, Ole Bv; Pedersen, Geir; Quinn, Liam; Reinhard, Matthias A; Ruths, Florian A; Schott, Björn H; Schredl, Michael; Schwarz, Emanuel; Schwarze, Cornelia E; Schwinn, Michael; Send, Tabea; Sigurdsson, Engilbert; Simon-Keller, Katja; Skuladottir, Astros T; Soler, Joaquim; Sonley, Anne; Sørensen, Erik; Stefansson, Hreinn; Straub, Peter; Suvisaari, Jaana; Tesli, Martin; Træholt, Jacob; Ullum, Henrik; Völker, Maja P; Walters, G Bragi; Wang, Rujia; Witt, Christian C; Zarbock, Gerhard; Zill, Peter; Zwart, John-Anker; Andreassen, Ole A; Arntz, Arnoud; Biernacka, Joanna M; Bohus, Martin; Breen, Gerome; Chapman, Alexander L; Cichon, Sven; Davis, Lea K; Deuschle, Michael; Euler, Sebastian; Herpertz, Sabine C; Hummelen, Benjamin; Jobst, Andrea; Kaprio, Jaakko; Kennedy, James L; Lehto, Kelli; Lieb, Klaus; Martorell, Lourdes; McMain, Shelley; Musil, Richard; Nieratschker, Vanessa; Nöthen, Markus M; Padberg, Frank; Palotie, Aarno; Pascual, Juan C; Perroud, Nader; Ramos-Quiroga, Josep A; Reichborn-Kjennerud, Ted; Ribases, Marta; Roepke, Stefan; Rujescu, Dan; Sanchez-Roige, Sandra; Schilling, Claudia; Schmahl, Christian; Stefansson, Kari; Thorgeirsson, Thorgeir E; Turecki, Gustavo; Vilella, Elisabet; Werge, Thomas; Winsvold, Bendik S; Wrege, Johannes; Rietschel, Marcella; Ripke, Stephan; Witt, Stephanie H

Functional Role of Single-Nucleotide Polymorphisms on IFNG and IFNGR1 in Humans with Cardiovascular Disease

单核苷酸多态性对人类心血管疾病中 IFNG 和 IFNGR1 的功能作用

Mehta, Megh; Li, Yang; Parashar, Smriti; Ramirez, Catalina; McKay, Heather; Landay, Alan; Aherrahrou, Redouane; Advani, Aarushi; Patel, Raag; Kaplan, Robert; Lazar, Jason; Anastos, Kathryn; Hanna, David B; Qi, Qibin; Ley, Klaus

Single-Cell Gene-Regulatory Networks of Advanced Symptomatic Atherosclerosis

晚期症状性动脉粥样硬化的单细胞基因调控网络

Mocci, Giuseppe; Sukhavasi, Katyayani; Örd, Tiit; Bankier, Sean; Singha, Prosanta; Arasu, Uma Thanigai; Agbabiaje, Olayinka Oluwasegun; Mäkinen, Petri; Ma, Lijiang; Hodonsky, Chani J; Aherrahrou, Redouane; Muhl, Lars; Liu, Jianping; Gustafsson, Sonja; Byandelger, Byambajav; Wang, Ying; Koplev, Simon; Lendahl, Urban; Owens, Gary K; Leeper, Nicholas J; Pasterkamp, Gerard; Vanlandewijck, Michael; Michoel, Tom; Ruusalepp, Arno; Hao, Ke; Ylä-Herttuala, Seppo; Väli, Marika; Järve, Heli; Mokry, Michal; Civelek, Mete; Miller, Clint J; Kovacic, Jason C; Kaikkonen, Minna U; Betsholtz, Christer; Björkegren, Johan L M

Translatome profiling reveals Itih4 as a novel smooth muscle cell-specific gene in atherosclerosis

翻译组分析揭示 Itih4 是动脉粥样硬化中一种新的平滑肌细胞特异性基因

Aarthi Ravindran, Lari Holappa, Henri Niskanen, Ilya Skovorodkin, Susanna Kaisto, Mustafa Beter, Miika Kiema, Ilakya Selvarajan, Valtteri Nurminen, Einari Aavik, Rédouane Aherrahrou, Sanna Pasonen-Seppänen, Vittorio Fortino, Johanna P Laakkonen, Seppo Ylä-Herttuala, Seppo Vainio, Tiit Örd, Minna U K

Genomic privacy preservation in genome-wide association studies: taxonomy, limitations, challenges, and vision

全基因组关联研究中的基因组隐私保护:分类、局限性、挑战和展望

Aherrahrou, Noura; Tairi, Hamid; Aherrahrou, Zouhair

Secreted Protein Profiling of Human Aortic Smooth Muscle Cells Identifies Vascular Disease Associations.

人主动脉平滑肌细胞分泌蛋白谱分析揭示血管疾病关联

Aherrahrou Rédouane, Baig Ferheen, Theofilatos Konstantinos, Lue Dillon, Beele Alicia, Örd Tiit, Kaikkonen Minna U, Aherrahrou Zouhair, Cheng Qi, Ghosh Saikat Kumar B, Karnewar Santosh, Karnewar Vaishnavi, Finn Aloke V, Owens Gary K, Joner Michael, Mayr Manuel, Civelek Mete