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

Postmortem analyses of myocardial microRNA expression in sepsis

脓毒症患者心肌microRNA表达的尸检分析

Lehto, Pasi; Skarp, Sini; Saukko, Taru; Säkkinen, Hanna; Syrjälä, Hannu; Kerkelä, Risto; Saarimäki, Samu; Bläuer, Sonja; Porvari, Katja; Pakanen, Lasse; Karhu, Jaana; Ala-Kokko, Tero

Novel Genetic Variants Associated with Primary Myocardial Fibrosis in Sudden Cardiac Death Victims

与猝死患者原发性心肌纤维化相关的新型基因变异

Skarp, Sini; Doedens, Anne; Holmström, Lauri; Izzi, Valerio; Saarimäki, Samu; Sliz, Eeva; Kettunen, Johannes; Pakanen, Lasse; Kerkelä, Risto; Pylkäs, Katri; Huikuri, Heikki V; Myerburg, Robert J; Junttila, Juhani

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

子宫内膜异位症的遗传基础及其与其他疼痛和炎症性疾病的合并症

Rahmioglu, Nilufer; Mortlock, Sally; Ghiasi, Marzieh; Møller, Peter L; Stefansdottir, Lilja; Galarneau, Geneviève; Turman, Constance; Danning, Rebecca; Law, Matthew H; Sapkota, Yadav; Christofidou, Paraskevi; Skarp, Sini; Giri, Ayush; Banasik, Karina; Krassowski, Michal; Lepamets, Maarja; Marciniak, Błażej; Nõukas, Margit; Perro, Danielle; Sliz, Eeva; Sobalska-Kwapis, Marta; Thorleifsson, Gudmar; Topbas-Selcuki, Nura F; Vitonis, Allison; Westergaard, David; Arnadottir, Ragnheidur; Burgdorf, Kristoffer S; Campbell, Archie; Cheuk, Cecilia S K; Clementi, Caterina; Cook, James; De Vivo, Immaculata; DiVasta, Amy; Dorien, O; Donoghue, Jacqueline F; Edwards, Todd; Fontanillas, Pierre; Fung, Jenny N; Geirsson, Reynir T; Girling, Jane E; Harkki, Paivi; Harris, Holly R; Healey, Martin; Heikinheimo, Oskari; Holdsworth-Carson, Sarah; Hostettler, Isabel C; Houlden, Henry; Houshdaran, Sahar; Irwin, Juan C; Jarvelin, Marjo-Riitta; Kamatani, Yoichiro; Kennedy, Stephen H; Kepka, Ewa; Kettunen, Johannes; Kubo, Michiaki; Kulig, Bartosz; Kurra, Venla; Laivuori, Hannele; Laufer, Marc R; Lindgren, Cecilia M; MacGregor, Stuart; Mangino, Massimo; Martin, Nicholas G; Matalliotaki, Charoula; Matalliotakis, Michail; Murray, Alison D; Ndungu, Anne; Nezhat, Camran; Olsen, Catherine M; Opoku-Anane, Jessica; Padmanabhan, Sandosh; Paranjpe, Manish; Peters, Maire; Polak, Grzegorz; Porteous, David J; Rabban, Joseph; Rexrode, Kathyrn M; Romanowicz, Hanna; Saare, Merli; Saavalainen, Liisu; Schork, Andrew J; Sen, Sushmita; Shafrir, Amy L; Siewierska-Górska, Anna; Słomka, Marcin; Smith, Blair H; Smolarz, Beata; Szaflik, Tomasz; Szyłło, Krzysztof; Takahashi, Atsushi; Terry, Kathryn L; Tomassetti, Carla; Treloar, Susan A; Vanhie, Arne; Vincent, Katy; Vo, Kim C; Werring, David J; Zeggini, Eleftheria; Zervou, Maria I; Adachi, Sosuke; Buring, Julie E; Ridker, Paul M; D'Hooghe, Thomas; Goulielmos, George N; Hapangama, Dharani K; Hayward, Caroline; Horne, Andrew W; Low, Siew-Kee; Martikainen, Hannu; Chasman, Daniel I; Rogers, Peter A W; Saunders, Philippa T; Sirota, Marina; Spector, Tim; Strapagiel, Dominik; Tung, Joyce Y; Whiteman, David C; Giudice, Linda C; Velez-Edwards, Digna R; Uimari, Outi; Kraft, Peter; Salumets, Andres; Nyholt, Dale R; Mägi, Reedik; Stefansson, Kari; Becker, Christian M; Yurttas-Beim, Piraye; Steinthorsdottir, Valgerdur; Nyegaard, Mette; Missmer, Stacey A; Montgomery, Grant W; Morris, Andrew P; Zondervan, Krina T

Genetic Variants Associated With Sudden Cardiac Death in Victims With Single Vessel Coronary Artery Disease and Left Ventricular Hypertrophy With or Without Fibrosis

与单支冠状动脉疾病和左心室肥厚(伴或不伴纤维化)患者猝死相关的基因变异

Vähätalo, Juha H; Holmström, Lauri T A; Pylkäs, Katri; Skarp, Sini; Porvari, Katja; Pakanen, Lasse; Kaikkonen, Kari S; Perkiömäki, Juha S; Kerkelä, Risto; Huikuri, Heikki V; Myerburg, Robert J; Junttila, M Juhani

Exome Sequencing Reveals a Phenotype Modifying Variant in ZNF528 in Primary Osteoporosis With a COL1A2 Deletion

外显子组测序揭示了原发性骨质疏松症伴COL1A2缺失患者中ZNF528的表型修饰变异

Skarp, Sini; Xia, Ji-Han; Zhang, Qin; Löija, Marika; Costantini, Alice; Ruddock, Lloyd W; Mäkitie, Outi; Wei, Gong-Hong; Männikkö, Minna

A single genetic locus associated with pediatric fractures: A genome-wide association study on 3,230 patients

与儿童骨折相关的单个基因位点:一项针对 3230 名患者的全基因组关联研究

Parviainen, Roope; Skarp, Sini; Korhonen, Linda; Serlo, Willy; Männikkö, Minna; Sinikumpu, Juha-Jaakko

NRF1 and NRF2 mRNA and Protein Expression Decrease Early during Melanoma Carcinogenesis: An Insight into Survival and MicroRNAs.

NRF1 和 NRF2 mRNA 和蛋白质表达在黑色素瘤发生早期下降:对生存和微RNA的见解

Hämäläinen Mari, Teppo Hanna-Riikka, Skarp Sini, Haapasaari Kirsi-Maria, Porvari Katja, Vuopala Katri, Kietzmann Thomas, Karihtala Peeter

Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility

早期骨骼脆性症中基于芯片的比较基因组杂交的罕见拷贝数变异

Costantini, Alice; Skarp, Sini; Kämpe, Anders; Mäkitie, Riikka E; Pettersson, Maria; Männikkö, Minna; Jiao, Hong; Taylan, Fulya; Lindstrand, Anna; Mäkitie, Outi

Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis

芬兰家族的全外显子组测序发现了骨关节炎的新候选基因

Skarp, Sini; Kämäräinen, Olli-Pekka; Wei, Gong-Hong; Jakkula, Eveliina; Kiviranta, Ilkka; Kröger, Heikki; Auvinen, Juha; Lehenkari, Petri; Ala-Kokko, Leena; Männikkö, Minna

TUFT1, a novel candidate gene for metatarsophalangeal osteoarthritis, plays a role in chondrogenesis on a calcium-related pathway

TUFT1是跖趾关节骨关节炎的一个新候选基因,它在钙相关通路中参与软骨形成。

Sliz, Eeva; Taipale, Mari; Welling, Maiju; Skarp, Sini; Alaraudanjoki, Viivi; Ignatius, Jaakko; Ruddock, Lloyd; Nissi, Ritva; Männikkö, Minna