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

Geriatric Syndromes and Mortality Among Hospitalized Older Adults

老年综合征与住院老年患者的死亡率

Avelino-Silva, Thiago J; Roma, Maria Fernanda B; Dutra, Adriana F; Malheiro, Alexandra; Speranza, Ana Cristina C; Casale, Arlety M C; Lopes, Beatriz N A; Almada-Filho, Clineu M; de Sousa, Danilsa V; Marques da Silva, Eduardo; Sepulveda, Fabiola; Garcez, Flavia Barreto; Constantino, Gabriel T; Keller, Gabriela S; Braga, Ianna L S; Gordilho Souza, Jonas; Teixeira, Juliana J M; Rodrigues da Silva Martins, Karoline; Moraes Dias, Laiane; Araujo, Lara M Q; Macedo, Luana A C; de Andrade, Lucas G; Prado, Lucas K P; Venegas-Sanabria, Luis Carlos; Freitas, Marco P D; Saraiva, Marcos D C; Bicalho, Maria Aparecida C; Arbex, Maria Carolyna F B; Pires, Maria E; Guedes, Maria M V; Borges, Marina M G; Gorzoni, Milton L; Bezerra, Mirella R; Garção, Natalia I B; Palmeira, Natascha G F; Lima, Nereida K C; Moreira-Filho, Oberdã G; Villas Boas, Paulo José F; de Almeida, Perola Q; Dip, Renata M; Bandeira de Mello, Renato G; Aruachan, Samir A; Karnakis, Theodora; Pintarelli, Vitor L; Amorim, Welma W C C; Dieguez Ferreira, Yngrid; Covinsky, Kenneth E; Ferriolli, Eduardo; Lee, Sei J; Smith, Alexander K; Suemoto, Claudia K; Aliberti, Marlon J R

Genetic disparities in sleep traits and human capital development: A 25-year study in Finnish population-based cohorts

睡眠特征和人力资本发展中的遗传差异:一项基于芬兰人群队列的25年研究

Hazak, Aaro; Kantojärvi, Katri; Sulkava, Sonja; Kukk, Merike; Jääskeläinen, Tuija; Salomaa, Veikko; Koskinen, Seppo; Perola, Markus; Paunio, Tiina

Real-world comparative effectiveness of SARS-CoV-2 primary vaccination campaigns against SARS-CoV-2 infections: a federated observational study emulating a target trial in three nations

SARS-CoV-2 初次疫苗接种活动预防 SARS-CoV-2 感染的真实世界比较效果:一项在三个国家开展的模拟目标试验的联合观察性研究

Meurisse, Marjan; Estupiñán-Romero, Francisco; Perola, Markus; Paajanen, Teemu; González-Galindo, Javier; Van Goethem, Nina; Bernal-Delgado, Enrique

Polygenic Risks for Mood Disorders and Economic Well-being: Study of Finnish Cohorts

情绪障碍和经济福祉的多基因风险:芬兰队列研究

Hazak, Aaro; Liuhanen, Johanna; Kantojärvi, Katri; Kukk, Merike; Sulkava, Sonja; Jääskeläinen, Tuija; Salomaa, Veikko; Koskinen, Seppo; Perola, Markus; Paunio, Tiina

Risk Haplotype of BTNL2 Predisposes Male Patients to NSTEMI: A Genetic and Functional Study

BTNL2风险单倍型使男性患者易患非ST段抬高型心肌梗死:一项遗传和功能研究

Lokki, A Inkeri; Sinisalo, Juha; Aierken, Kitty; Kalaoja, Marita; Lääperi, Mitja; Koski, Jessica; Salomaa, Veikko; Perola, Markus; Kettunen, Johannes; Varjosalo, Markku; Jarva, Hanna; Pussinen, Pirkko; Klein, Sarah; Öörni, Katariina; Mäyränpää, Mikko; Mack, Steven; Lokki, Marja-Liisa

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes

全基因组关联研究荟萃分析为心力衰竭及其亚型的病因学提供了新的见解

Henry, Albert; Mo, Xiaodong; Finan, Chris; Chaffin, Mark D; Speed, Doug; Issa, Hanane; Denaxas, Spiros; Ware, James S; Zheng, Sean L; Malarstig, Anders; Gratton, Jasmine; Bond, Isabelle; Roselli, Carolina; Miller, David; Chopade, Sandesh; Schmidt, A Floriaan; Abner, Erik; Adams, Lance; Andersson, Charlotte; Aragam, Krishna G; Ärnlöv, Johan; Asselin, Geraldine; Raja, Anna Axelsson; Backman, Joshua D; Bartz, Traci M; Biddinger, Kiran J; Biggs, Mary L; Bloom, Heather L; Boersma, Eric; Brandimarto, Jeffrey; Brown, Michael R; Brunak, Søren; Bruun, Mie Topholm; Buckbinder, Leonard; Bundgaard, Henning; Carey, David J; Chasman, Daniel I; Chen, Xing; Cook, James P; Czuba, Tomasz; de Denus, Simon; Dehghan, Abbas; Delgado, Graciela E; Doney, Alexander S; Dörr, Marcus; Dowsett, Joseph; Dudley, Samuel C; Engström, Gunnar; Erikstrup, Christian; Esko, Tõnu; Farber-Eger, Eric H; Felix, Stephan B; Finer, Sarah; Ford, Ian; Ghanbari, Mohsen; Ghasemi, Sahar; Ghouse, Jonas; Giedraitis, Vilmantas; Giulianini, Franco; Gottdiener, John S; Gross, Stefan; Guðbjartsson, Daníel F; Gui, Hongsheng; Gutmann, Rebecca; Hägg, Sara; Haggerty, Christopher M; Hedman, Åsa K; Helgadottir, Anna; Hemingway, Harry; Hillege, Hans; Hyde, Craig L; Aagaard Jensen, Bitten; Jukema, J Wouter; Kardys, Isabella; Karra, Ravi; Kavousi, Maryam; Kizer, Jorge R; Kleber, Marcus E; Køber, Lars; Koekemoer, Andrea; Kuchenbaecker, Karoline; Lai, Yi-Pin; Lanfear, David; Langenberg, Claudia; Lin, Honghuang; Lind, Lars; Lindgren, Cecilia M; Liu, Peter P; London, Barry; Lowery, Brandon D; Luan, Jian'an; Lubitz, Steven A; Magnusson, Patrik; Margulies, Kenneth B; Marston, Nicholas A; Martin, Hilary; März, Winfried; Melander, Olle; Mordi, Ify R; Morley, Michael P; Morris, Andrew P; Morrison, Alanna C; Morton, Lori; Nagle, Michael W; Nelson, Christopher P; Niessner, Alexander; Niiranen, Teemu; Noordam, Raymond; Nowak, Christoph; O'Donoghue, Michelle L; Ostrowski, Sisse Rye; Owens, Anjali T; Palmer, Colin N A; Paré, Guillaume; Pedersen, Ole Birger; Perola, Markus; Pigeyre, Marie; Psaty, Bruce M; Rice, Kenneth M; Ridker, Paul M; Romaine, Simon P R; Rotter, Jerome I; Ruff, Christian T; Sabatine, Marc S; Sallah, Neneh; Salomaa, Veikko; Sattar, Naveed; Shalaby, Alaa A; Shekhar, Akshay; Smelser, Diane T; Smith, Nicholas L; Sørensen, Erik; Srinivasan, Sundararajan; Stefansson, Kari; Sveinbjörnsson, Garðar; Svensson, Per; Tammesoo, Mari-Liis; Tardif, Jean-Claude; Teder-Laving, Maris; Teumer, Alexander; Thorgeirsson, Guðmundur; Thorsteinsdottir, Unnur; Torp-Pedersen, Christian; Tragante, Vinicius; Trompet, Stella; Uitterlinden, Andre G; Ullum, Henrik; van der Harst, Pim; van Heel, David; van Setten, Jessica; van Vugt, Marion; Veluchamy, Abirami; Verschuuren, Monique; Verweij, Niek; Vissing, Christoffer Rasmus; Völker, Uwe; Voors, Adriaan A; Wallentin, Lars; Wang, Yunzhang; Weeke, Peter E; Wiggins, Kerri L; Williams, L Keoki; Yang, Yifan; Yu, Bing; Zannad, Faiez; Zheng, Chaoqun; Asselbergs, Folkert W; Cappola, Thomas P; Dubé, Marie-Pierre; Dunn, Michael E; Lang, Chim C; Samani, Nilesh J; Shah, Svati; Vasan, Ramachandran S; Smith, J Gustav; Holm, Hilma; Shah, Sonia; Ellinor, Patrick T; Hingorani, Aroon D; Wells, Quinn; Lumbers, R Thomas

Genome-wide association study of pulpal and apical diseases

牙髓和根尖疾病的全基因组关联研究

Salminen, Aino; Hyvärinen, Kati; Ritari, Jarmo; Leppilahti, Jussi M; Palotie, Ulla; Vuollo, Ville; Kambur, Oleg; Reis, Kadri; Reigo, Anu; Palta, Priit; Perola, Markus; Sinisalo, Juha; Havulinna, Aki S; Mäntylä, Päivi; Gürsoy, Ulvi Kahraman; Suominen, A Liisa; Rice, David P; Anttonen, Vuokko; Nieminen, Pekka; Pussinen, Pirkko J

Effects of parental autoimmune diseases on type 1 diabetes in offspring can be partially explained by HLA and non-HLA polymorphisms

父母自身免疫性疾病对后代1型糖尿病的影响可部分地用HLA和非HLA多态性来解释。

Wang, Feiyi; Liu, Aoxing; Yang, Zhiyu; Vartiainen, Pekka; Jukarainen, Sakari; Koskela, Satu; Oram, Richard; Allen, Lowri; Ritari, Jarmo; Partanen, Jukka; Perola, Markus; Tuomi, Tiinamaija; Ganna, Andrea

Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study.

芬兰和挪威特发性正常压力脑积水患者中 CWH43 变异体的患病率较低:一项基于队列的观察性研究

Räsänen Joel, Helisalmi Seppo, Heikkinen Sami, Raivo Joose, Korhonen Ville E, Martiskainen Henna, Junkkari Antti, Grenier-Boley Benjamin, Bellenguez Céline, Oinas Minna, Avellan Cecilia, Frantzen Janek, Kotkansalo Anna, Rinne Jaakko, Ronkainen Antti, Kauppinen Mikko, von Und Zu Fraunberg Mikael, Lönnrot Kimmo, Satopää Jarno, Perola Markus, Koivisto Anne M, Julkunen Valtteri, Portaankorva Anne M, Mannermaa Arto, Soininen Hilkka, Jääskeläinen Juha E, Lambert Jean-Charles, Eide Per K, Palotie Aarno, Kurki Mitja I, Hiltunen Mikko, Leinonen Ville, Lipponen Anssi

Value of Pharmacogenetic Testing Assessed with Real-World Drug Utilization and Genotype Data

基于真实世界药物利用和基因型数据评估药物基因组学检测的价值

Litonius, Kaisa; Kulla, Noora; Falkenbach, Petra; Kristiansson, Kati; Tarkiainen, E Katriina; Ukkola-Vuoti, Liisa; Cajanus, Kristiina; Korhonen, Mari; Khan, Sofia; Sistonen, Johanna; Orpana, Arto; Lindstedt, Mats; Nyrönen, Tommi; Perola, Markus; Turpeinen, Miia; Kytö, Ville; Tornio, Aleksi; Niemi, Mikko