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

Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

作者更正:对纤维肌性发育不良的基因研究发现了风险位点以及与常见心血管疾病的共同遗传特征

Georges, Adrien; Yang, Min-Lee; Berrandou, Takiy-Eddine; Bakker, Mark K; Dikilitas, Ozan; Kiando, Soto Romuald; Ma, Lijiang; Satterfield, Benjamin A; Sengupta, Sebanti; Yu, Mengyao; Deleuze, Jean-François; Dupré, Delia; Hunker, Kristina L; Kyryachenko, Sergiy; Liu, Lu; Sayoud-Sadeg, Ines; Amar, Laurence; Brummett, Chad M; Coleman, Dawn M; d'Escamard, Valentina; de Leeuw, Peter; Fendrikova-Mahlay, Natalia; Kadian-Dodov, Daniella; Li, Jun Z; Lorthioir, Aurélien; Pappaccogli, Marco; Prejbisz, Aleksander; Smigielski, Witold; Stanley, James C; Zawistowski, Matthew; Zhou, Xiang; Zöllner, Sebastian; Amouyel, Philippe; De Buyzere, Marc L; Debette, Stéphanie; Dobrowolski, Piotr; Drygas, Wojciech; Gornik, Heather L; Olin, Jeffrey W; Piwonski, Jerzy; Rietzschel, Ernst R; Ruigrok, Ynte M; Vikkula, Miikka; Warchol Celinska, Ewa; Januszewicz, Andrzej; Kullo, Iftikhar J; Azizi, Michel; Jeunemaitre, Xavier; Persu, Alexandre; Kovacic, Jason C; Ganesh, Santhi K; Bouatia-Naji, Nabila

Burden of Rare Genetic Variants in Spontaneous Coronary Artery Dissection With High-risk Features

罕见基因变异在具有高危特征的自发性冠状动脉夹层中的负担

Wang, Yu; Starovoytov, Andrew; Murad, Andrea M; Hunker, Kristina L; Brunham, Liam R; Li, Jun Z; Saw, Jacqueline; Ganesh, Santhi K

Molecular genetic evaluation of pediatric renovascular hypertension due to renal artery stenosis and abdominal aortic coarctation in neurofibromatosis type 1

神经纤维瘤病1型合并肾动脉狭窄和腹主动脉缩窄引起的儿童肾血管性高血压的分子遗传学评估

Coleman, Dawn M; Wang, Yu; Yang, Min-Lee; Hunker, Kristina L; Birt, Isabelle; Bergin, Ingrid L; Li, Jun Z; Stanley, James C; Ganesh, Santhi K

Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

1q21.2染色体及其他基因位点影响自发性冠状动脉夹层和心肌梗死的风险

Saw, Jacqueline; Yang, Min-Lee; Trinder, Mark; Tcheandjieu, Catherine; Xu, Chang; Starovoytov, Andrew; Birt, Isabelle; Mathis, Michael R; Hunker, Kristina L; Schmidt, Ellen M; Jackson, Linda; Fendrikova-Mahlay, Natalia; Zawistowski, Matthew; Brummett, Chad M; Zoellner, Sebastian; Katz, Alexander; Coleman, Dawn M; Swan, Kirby; O'Donnell, Christopher J; Zhou, Xiang; Li, Jun Z; Gornik, Heather L; Assimes, Themistocles L; Stanley, James C; Brunham, Liam R; Ganesh, Santhi K

A Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia

一种新型复发性COL5A1基因变异与一种伴有动脉夹层和纤维肌性发育不良的发育不良相关动脉疾病有关

Richer, Julie; Hill, Hannah L; Wang, Yu; Yang, Min-Lee; Hunker, Kristina L; Lane, Jamie; Blackburn, Susan; Coleman, Dawn M; Eliason, Jonathan; Sillon, Guillaume; D'Agostino, Maria-Daniela; Jetty, Prasad; Mongeon, François-Pierre; Laberge, Anne-Marie; Ryan, Stephen E; Fendrikova-Mahlay, Natalia; Coutinho, Thais; Mathis, Michael R; Zawistowski, Matthew; Hazen, Stanley L; Katz, Alexander E; Gornik, Heather L; Brummett, Chad M; Abecasis, Goncalo; Bergin, Ingrid L; Stanley, James C; Li, Jun Z; Ganesh, Santhi K

Grxcr2 is required for stereocilia morphogenesis in the cochlea.

Grxcr2 是耳蜗立体纤毛形态发生所必需的

Avenarius Matthew R, Jung Jae-Yun, Askew Charles, Jones Sherri M, Hunker Kristina L, Azaiez Hela, Rehman Atteeq U, Schraders Margit, Najmabadi Hossein, Kremer Hannie, Smith Richard J H, Géléoc Gwenaëlle S G, Dolan David F, Raphael Yehoash, Kohrman David C

Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse

Grxcr1基因突变是旋转小鼠内耳功能障碍的根本原因。

Odeh, Hana; Hunker, Kristina L; Belyantseva, Inna A; Azaiez, Hela; Avenarius, Matthew R; Zheng, Lili; Peters, Linda M; Gagnon, Leona H; Hagiwara, Nobuko; Skynner, Michael J; Brilliant, Murray H; Allen, Nicholas D; Riazuddin, Saima; Johnson, Kenneth R; Raphael, Yehoash; Najmabadi, Hossein; Friedman, Thomas B; Bartles, James R; Smith, Richard J H; Kohrman, David C

The transmembrane inner ear (tmie) gene contributes to vestibular and lateral line development and function in the zebrafish (Danio rerio)

跨膜内耳(tmie)基因对斑马鱼(Danio rerio)的前庭和侧线发育和功能有贡献。

Shen, Yu-Chi; Jeyabalan, Anandhi K; Wu, Karen L; Hunker, Kristina L; Kohrman, David C; Thompson, Deborah L; Liu, Dong; Barald, Kate F