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

Comparative Study Showed Significant Gene Expression Differences in Newborn Infants After Vaginal and Caesarean Deliveries

对比研究显示,阴道分娩和剖腹产后新生儿的基因表达存在显著差异

Carpén, Noora; Helve, Otto; Ericsson, Sabina; Kervinen, Ilona; Stewart-Linnonmaa, Maija; Heinonen, Santtu; Andersson, Sture; Helle, Emmi

The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans.

ERBB2 c.1795C>T,p.Arg599Cys 变异与人类左心室流出道梗阻缺陷有关

Ampuja Minna, Ericsson Sabina, Paatero Ilkka, Chowdhury Iftekhar, Villman Jenna, Broberg Martin, Ramste Amanda, Balboa Diego, Ojala Tiina, Chong Jessica X, Bamshad Michael J, Priest James R, Varjosalo Markku, Kivelä Riikka, Helle Emmi

Association of maternal asthma with congenital heart defects in offspring

母亲哮喘与后代先天性心脏缺陷的关联

Kemppainen, Mari; Kirjavainen, Turkka; Helle, Emmi; Gissler, Mika

Cardiac MRI in patients with Fontan circulation: assessing risk factors for adverse outcomes

Fontan循环患者的心脏磁共振成像:评估不良预后的风险因素

Ericsson, Sabina; Paakkanen, Riitta; Taipale, Marko; Helle, Emmi; Peltonen, Juha; Kormi, Alma; Vepsäläinen, Teemu; Mattila, Ilkka; Pätilä, Tommi; Martelius, Laura; Ojala, Tiina

Maternal Diabetes and Overweight and Congenital Heart Defects in Offspring

母亲患有糖尿病和超重与后代先天性心脏缺陷有关

Turunen, Riitta; Pulakka, Anna; Metsälä, Johanna; Vahlberg, Tero; Ojala, Tiina; Gissler, Mika; Kajantie, Eero; Helle, Emmi

Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects

全基因组关联研究揭示了室间隔缺损和左侧先天性心脏缺陷的新风险位点

Broberg, Martin; Ampuja, Minna; Jones, Samuel; Ojala, Tiina; Rahkonen, Otto; Kivelä, Riikka; Priest, James; Palotie, Aarno; Ollila, Hanna M; Helle, Emmi

Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population

与4p16风险位点相关的自闭症谱系障碍表型以及芬兰人群中自闭症谱系障碍患者的新型全基因组关联研究

Muroke, Valtteri; Jalanko, Mikko; Ruotsalainen, Sanni; Perola, Markus; Helle, Emmi; Sinisalo, Juha

Cardiac MRI and Clinical Outcomes in TMEM43 Arrhythmogenic Cardiomyopathy

TMEM43致心律失常性心肌病的心脏磁共振成像和临床结局

Matos, João; Helle, Emmi; Care, Melanie; Moayedi, Yasbanoo; Gollob, Michael H; Thavendiranathan, Paaladinesh; Spears, Danna; Hanneman, Kate

Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome

CAPN2基因的罕见变异会增加孤立性左心发育不良综合征的风险。

Blue, Elizabeth E; White, Janson J; Dush, Michael K; Gordon, William W; Wyatt, Brent H; White, Peter; Marvin, Colby T; Helle, Emmi; Ojala, Tiina; Priest, James R; Jenkins, Mary M; Almli, Lynn M; Reefhuis, Jennita; Pangilinan, Faith; Brody, Lawrence C; McBride, Kim L; Garg, Vidu; Shaw, Gary M; Romitti, Paul A; Nembhard, Wendy N; Browne, Marilyn L; Werler, Martha M; Kay, Denise M; Mital, Seema; Chong, Jessica X; Nascone-Yoder, Nanette M; Bamshad, Michael J

Risk factors for mortality in patients with hypoplastic left heart syndrome after the Norwood procedure

诺伍德手术后左心发育不良综合征患者的死亡风险因素

Selenius, Sabina; Ilvesvuo, Johanna; Ruotsalainen, Hanna; Mattila, Ilkka; Pätilä, Tommi; Helle, Emmi; Ojala, Tiina