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

Understanding the Borderline Brain: A Review of Neurobiological Findings in Borderline Personality Disorder (BPD)

了解边缘型人格障碍患者的大脑:边缘型人格障碍(BPD)神经生物学研究综述

Giannoulis, Eleni; Nousis, Christos; Sula, Ioanna-Jonida; Georgitsi, Maria-Evangelia; Malogiannis, Ioannis

Psychometric Properties of the Greek Version of the BPDSI-IV: Insights into Borderline Personality Disorder Severity

希腊语版BPDSI-IV的心理测量学特性:对边缘型人格障碍严重程度的深入了解

Malogiannis, Ioannis; Soultani, Irini; Zikou, Ifigeneia; Georgitsi, Maria-Evangelia; Dimitriou, Ioanna; Triantafyllou, Alexandra; Tsionis, Antonis; Giannoulis, Eleni

Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

全基因组关联研究揭示吉尔·德·拉·图雷特综合征的新基因位点

Tsetsos, Fotis; Topaloudi, Apostolia; Jain, Pritesh; Yang, Zhiyu; Yu, Dongmei; Kolovos, Petros; Tumer, Zeynep; Rizzo, Renata; Hartmann, Andreas; Depienne, Christel; Worbe, Yulia; Müller-Vahl, Kirsten R; Cath, Danielle C; Boomsma, Dorret I; Wolanczyk, Tomasz; Zekanowski, Cezary; Barta, Csaba; Nemoda, Zsofia; Tarnok, Zsanett; Padmanabhuni, Shanmukha S; Buxbaum, Joseph D; Grice, Dorothy; Glennon, Jeffrey; Stefansson, Hreinn; Hengerer, Bastian; Yannaki, Evangelia; Stamatoyannopoulos, John A; Benaroya-Milshtein, Noa; Cardona, Francesco; Hedderly, Tammy; Heyman, Isobel; Huyser, Chaim; Mir, Pablo; Morer, Astrid; Mueller, Norbert; Munchau, Alexander; Plessen, Kerstin J; Porcelli, Cesare; Roessner, Veit; Walitza, Susanne; Schrag, Anette; Martino, Davide; Tischfield, Jay A; Heiman, Gary A; Willsey, A Jeremy; Dietrich, Andrea; Davis, Lea K; Crowley, James J; Mathews, Carol A; Scharf, Jeremiah M; Georgitsi, Marianthi; Hoekstra, Pieter J; Paschou, Peristera

Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

基于多基因风险评分的全表型关联研究发现了图雷特综合征的新关联。

Jain, Pritesh; Miller-Fleming, Tyne; Topaloudi, Apostolia; Yu, Dongmei; Drineas, Petros; Georgitsi, Marianthi; Yang, Zhiyu; Rizzo, Renata; Müller-Vahl, Kirsten R; Tumer, Zeynep; Mol Debes, Nanette; Hartmann, Andreas; Depienne, Christel; Worbe, Yulia; Mir, Pablo; Cath, Danielle C; Boomsma, Dorret I; Roessner, Veit; Wolanczyk, Tomasz; Janik, Piotr; Szejko, Natalia; Zekanowski, Cezary; Barta, Csaba; Nemoda, Zsofia; Tarnok, Zsanett; Buxbaum, Joseph D; Grice, Dorothy; Glennon, Jeffrey; Stefansson, Hreinn; Hengerer, Bastian; Benaroya-Milshtein, Noa; Cardona, Francesco; Hedderly, Tammy; Heyman, Isobel; Huyser, Chaim; Morer, Astrid; Mueller, Norbert; Munchau, Alexander; Plessen, Kerstin J; Porcelli, Cesare; Walitza, Susanne; Schrag, Anette; Martino, Davide; Dietrich, Andrea; Mathews, Carol A; Scharf, Jeremiah M; Hoekstra, Pieter J; Davis, Lea K; Paschou, Peristera

PheWAS and cross-disorder analysis reveal genetic architecture, pleiotropic loci and phenotypic correlations across 11 autoimmune disorders

表型组关联分析(PheWAS)和跨疾病分析揭示了11种自身免疫性疾病的遗传结构、多效性基因位点和表型相关性。

Topaloudi, Apostolia; Jain, Pritesh; Martinez, Melanie B; Bryant, Josephine K; Reynolds, Grace; Zagoriti, Zoi; Lagoumintzis, George; Zamba-Papanicolaou, Eleni; Tzartos, John; Poulas, Konstantinos; Kleopa, Kleopas A; Tzartos, Socrates; Georgitsi, Marianthi; Drineas, Petros; Paschou, Peristera

The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder

特定学习障碍的多基因性质和复杂遗传结构

Georgitsi, Marianthi; Dermitzakis, Iasonas; Soumelidou, Evgenia; Bonti, Eleni

Association of rs11780592 Polymorphism in the Human Soluble Epoxide Hydrolase Gene (EPHX2) with Oxidized LDL and Mortality in Patients with Diabetic Chronic Kidney Disease

人类可溶性环氧化物水解酶基因(EPHX2)rs11780592多态性与糖尿病慢性肾病患者氧化型低密度脂蛋白和死亡率的相关性

Roumeliotis, Stefanos; Roumeliotis, Athanasios; Stamou, Aikaterini; Panagoutsos, Stylianos; Manolopoulos, Vangelis G; Tsetsos, Fotis; Georgitsi, Marianthi; Liakopoulos, Vassilios

Oxidative Stress Genes in Diabetes Mellitus Type 2: Association with Diabetic Kidney Disease

2型糖尿病中的氧化应激基因:与糖尿病肾病的关联

Roumeliotis, Athanasios; Roumeliotis, Stefanos; Tsetsos, Fotis; Georgitsi, Marianthi; Georgianos, Panagiotis I; Stamou, Aikaterini; Vasilakou, Anna; Kotsa, Kalliopi; Tsekmekidou, Xanthippi; Paschou, Peristera; Panagoutsos, Stylianos; Liakopoulos, Vassilios

Genetic variation in CARD8, a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 diabetes mellitus

CARD8基因(编码NLRP3炎症小体相关蛋白)的遗传变异会改变2型糖尿病患者发生糖尿病肾病的遗传风险。

Tsetsos, Fotis; Roumeliotis, Athanasios; Tsekmekidou, Xanthippi; Alexouda, Sophia; Roumeliotis, Stefanos; Theodoridis, Marios; Thodis, Elias; Panagoutsos, Stylianos; Papanas, Nikolaos; Papazoglou, Dimitrios; Kotsa, Kalliopi; Yovos, John G; Maltezos, Efstratios; Passadakis, Ploumis; Paschou, Peristera; Georgitsi, Marianthi

European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents

欧洲儿童抽动症多中心研究(EMTICS):两项队列研究方案,旨在评估儿童和青少年抽动症发作和加重的风险因素

Schrag, Anette; Martino, Davide; Apter, Alan; Ball, Juliane; Bartolini, Erika; Benaroya-Milshtein, Noa; Buttiglione, Maura; Cardona, Francesco; Creti, Roberta; Efstratiou, Androulla; Gariup, Maria; Georgitsi, Marianthi; Hedderly, Tammy; Heyman, Isobel; Margarit, Immaculada; Mir, Pablo; Moll, Natalie; Morer, Astrid; Müller, Norbert; Müller-Vahl, Kirsten; Münchau, Alexander; Orefici, Graziella; Plessen, Kerstin J; Porcelli, Cesare; Paschou, Peristera; Rizzo, Renata; Roessner, Veit; Schwarz, Markus J; Steinberg, Tamar; Tagwerker Gloor, Friederike; Tarnok, Zsanett; Walitza, Susanne; Dietrich, Andrea; Hoekstra, Pieter J