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

Genetic analyses across cardiovascular traits: leveraging genetic correlations to empower locus discovery and prediction in common cardiovascular diseases

心血管性状的遗传分析:利用遗传相关性增强常见心血管疾病的基因位点发现和预测

Jordà, Paloma; Lai, Yiwei; Jeuken, Amélie; Lemieux Perreault, Louis-Philippe; Goulet, Elisabeth; Lahrouchi, Najim; Nozza, Anna; Tanck, Michael W; Guerra, Peter; Cadrin-Tourigny, Julia; de Denus, Simon; Bezzina, Connie R; Lettre, Guillaume; Busseuil, David; Dubé, Marie-Pierre; Tardif, Jean-Claude; Tadros, Rafik

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

POPDC2基因的双等位基因变异会导致一种常染色体隐性遗传综合征,其特征为心脏传导缺陷和肥厚型心肌病。

Nicastro, Michele; Vermeer, Alexa M C; Postema, Pieter G; Tadros, Rafik; Bowling, Forrest Z; Aegisdottir, Hildur M; Tragante, Vinicius; Mach, Lukas; Postma, Alex V; Lodder, Elisabeth M; van Duijvenboden, Karel; Zwart, Rob; Beekman, Leander; Wu, Lingshuang; Jurgens, Sean J; van der Zwaag, Paul A; Alders, Mariëlle; Allouba, Mona; Aguib, Yasmine; Santome, J Luis; de Una, David; Monserrat, Lorenzo; Miranda, Antonio M A; Kanemaru, Kazumasa; Cranley, James; van Zeggeren, Ingeborg E; Aronica, Eleonora M A; Ripolone, Michela; Zanotti, Simona; Sveinbjornsson, Gardar; Ivarsdottir, Erna V; Hólm, Hilma; Guðbjartsson, Daníel F; Skúladóttir, Ástrós Th; Stefánsson, Kári; Nadauld, Lincoln; Knowlton, Kirk U; Ostrowski, Sisse Rye; Sørensen, Erik; Vesterager Pedersen, Ole Birger; Ghouse, Jonas; Rand, Søren A; Bundgaard, Henning; Ullum, Henrik; Erikstrup, Christian; Aagaard, Bitten; Bruun, Mie Topholm; Christiansen, Mette; Jensen, Henrik K; Carere, Deanna Alexis; Cummings, Christopher T; Fishler, Kristen; Tørring, Pernille Mathiesen; Brusgaard, Klaus; Juul, Trine Maxel; Saaby, Lotte; Winkel, Bo Gregers; Mogensen, Jens; Fortunato, Francesco; Comi, Giacomo Pietro; Ronchi, Dario; van Tintelen, J Peter; Noseda, Michela; Airola, Michael V; Christiaans, Imke; Wilde, Arthur A M; Wilders, Ronald; Clur, Sally-Ann; Verkerk, Arie O; Bezzina, Connie R; Lahrouchi, Najim

Linguistic disparities in cross-language automatic speech recognition transfer from Arabic to Tashlhiyt

从阿拉伯语到塔什利特语的跨语言自动语音识别迁移中的语言差异

Zellou, Georgia; Lahrouchi, Mohamed

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

常见基因变异会增加大动脉转位的风险

Škorić-Milosavljević, Doris; Tadros, Rafik; Bosada, Fernanda M; Tessadori, Federico; van Weerd, Jan Hendrik; Woudstra, Odilia I; Tjong, Fleur V Y; Lahrouchi, Najim; Bajolle, Fanny; Cordell, Heather J; Agopian, A J; Blue, Gillian M; Barge-Schaapveld, Daniela Q C M; Gewillig, Marc; Preuss, Christoph; Lodder, Elisabeth M; Barnett, Phil; Ilgun, Aho; Beekman, Leander; van Duijvenboden, Karel; Bokenkamp, Regina; Müller-Nurasyid, Martina; Vliegen, Hubert W; Konings, Thelma C; van Melle, Joost P; van Dijk, Arie P J; van Kimmenade, Roland R J; Roos-Hesselink, Jolien W; Sieswerda, Gertjan T; Meijboom, Folkert; Abdul-Khaliq, Hashim; Berger, Felix; Dittrich, Sven; Hitz, Marc-Phillip; Moosmann, Julia; Riede, Frank-Thomas; Schubert, Stephan; Galan, Pilar; Lathrop, Mark; Munter, Hans M; Al-Chalabi, Ammar; Shaw, Christopher E; Shaw, Pamela J; Morrison, Karen E; Veldink, Jan H; van den Berg, Leonard H; Evans, Sylvia; Nobrega, Marcelo A; Aneas, Ivy; Radivojkov-Blagojević, Milena; Meitinger, Thomas; Oechslin, Erwin; Mondal, Tapas; Bergin, Lynn; Smythe, John F; Altamirano-Diaz, Luis; Lougheed, Jane; Bouma, Berto J; Chaix, Marie-A; Kline, Jennie; Bassett, Anne S; Andelfinger, Gregor; van der Palen, Roel L F; Bouvagnet, Patrice; Clur, Sally-Ann B; Breckpot, Jeroen; Kerstjens-Frederikse, Wilhelmina S; Winlaw, David S; Bauer, Ulrike M M; Mital, Seema; Goldmuntz, Elizabeth; Keavney, Bernard; Bonnet, Damien; Mulder, Barbara J; Tanck, Michael W T; Bakkers, Jeroen; Christoffels, Vincent M; Boogerd, Cornelis J; Postma, Alex V; Bezzina, Connie R

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

对心电图QT间期及其组成部分的遗传分析,可以发现其他基因位点和通路。

Young, William J; Lahrouchi, Najim; Isaacs, Aaron; Duong, ThuyVy; Foco, Luisa; Ahmed, Farah; Brody, Jennifer A; Salman, Reem; Noordam, Raymond; Benjamins, Jan-Walter; Haessler, Jeffrey; Lyytikäinen, Leo-Pekka; Repetto, Linda; Concas, Maria Pina; van den Berg, Marten E; Weiss, Stefan; Baldassari, Antoine R; Bartz, Traci M; Cook, James P; Evans, Daniel S; Freudling, Rebecca; Hines, Oliver; Isaksen, Jonas L; Lin, Honghuang; Mei, Hao; Moscati, Arden; Müller-Nurasyid, Martina; Nursyifa, Casia; Qian, Yong; Richmond, Anne; Roselli, Carolina; Ryan, Kathleen A; Tarazona-Santos, Eduardo; Thériault, Sébastien; van Duijvenboden, Stefan; Warren, Helen R; Yao, Jie; Raza, Dania; Aeschbacher, Stefanie; Ahlberg, Gustav; Alonso, Alvaro; Andreasen, Laura; Bis, Joshua C; Boerwinkle, Eric; Campbell, Archie; Catamo, Eulalia; Cocca, Massimiliano; Cutler, Michael J; Darbar, Dawood; De Grandi, Alessandro; De Luca, Antonio; Ding, Jun; Ellervik, Christina; Ellinor, Patrick T; Felix, Stephan B; Froguel, Philippe; Fuchsberger, Christian; Gögele, Martin; Graff, Claus; Graff, Mariaelisa; Guo, Xiuqing; Hansen, Torben; Heckbert, Susan R; Huang, Paul L; Huikuri, Heikki V; Hutri-Kähönen, Nina; Ikram, M Arfan; Jackson, Rebecca D; Junttila, Juhani; Kavousi, Maryam; Kors, Jan A; Leal, Thiago P; Lemaitre, Rozenn N; Lin, Henry J; Lind, Lars; Linneberg, Allan; Liu, Simin; MacFarlane, Peter W; Mangino, Massimo; Meitinger, Thomas; Mezzavilla, Massimo; Mishra, Pashupati P; Mitchell, Rebecca N; Mononen, Nina; Montasser, May E; Morrison, Alanna C; Nauck, Matthias; Nauffal, Victor; Navarro, Pau; Nikus, Kjell; Pare, Guillaume; Patton, Kristen K; Pelliccione, Giulia; Pittman, Alan; Porteous, David J; Pramstaller, Peter P; Preuss, Michael H; Raitakari, Olli T; Reiner, Alexander P; Ribeiro, Antonio Luiz P; Rice, Kenneth M; Risch, Lorenz; Schlessinger, David; Schotten, Ulrich; Schurmann, Claudia; Shen, Xia; Shoemaker, M Benjamin; Sinagra, Gianfranco; Sinner, Moritz F; Soliman, Elsayed Z; Stoll, Monika; Strauch, Konstantin; Tarasov, Kirill; Taylor, Kent D; Tinker, Andrew; Trompet, Stella; Uitterlinden, André; Völker, Uwe; Völzke, Henry; Waldenberger, Melanie; Weng, Lu-Chen; Whitsel, Eric A; Wilson, James G; Avery, Christy L; Conen, David; Correa, Adolfo; Cucca, Francesco; Dörr, Marcus; Gharib, Sina A; Girotto, Giorgia; Grarup, Niels; Hayward, Caroline; Jamshidi, Yalda; Järvelin, Marjo-Riitta; Jukema, J Wouter; Kääb, Stefan; Kähönen, Mika; Kanters, Jørgen K; Kooperberg, Charles; Lehtimäki, Terho; Lima-Costa, Maria Fernanda; Liu, Yongmei; Loos, Ruth J F; Lubitz, Steven A; Mook-Kanamori, Dennis O; Morris, Andrew P; O'Connell, Jeffrey R; Olesen, Morten Salling; Orini, Michele; Padmanabhan, Sandosh; Pattaro, Cristian; Peters, Annette; Psaty, Bruce M; Rotter, Jerome I; Stricker, Bruno; van der Harst, Pim; van Duijn, Cornelia M; Verweij, Niek; Wilson, James F; Arking, Dan E; Ramirez, Julia; Lambiase, Pier D; Sotoodehnia, Nona; Mifsud, Borbala; Newton-Cheh, Christopher; Munroe, Patricia B

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

基于证据的扩张型心肌病基因评估

Jordan, Elizabeth; Peterson, Laiken; Ai, Tomohiko; Asatryan, Babken; Bronicki, Lucas; Brown, Emily; Celeghin, Rudy; Edwards, Matthew; Fan, Judy; Ingles, Jodie; James, Cynthia A; Jarinova, Olga; Johnson, Renee; Judge, Daniel P; Lahrouchi, Najim; Lekanne Deprez, Ronald H; Lumbers, R Thomas; Mazzarotto, Francesco; Medeiros Domingo, Argelia; Miller, Rebecca L; Morales, Ana; Murray, Brittney; Peters, Stacey; Pilichou, Kalliopi; Protonotarios, Alexandros; Semsarian, Christopher; Shah, Palak; Syrris, Petros; Thaxton, Courtney; van Tintelen, J Peter; Walsh, Roddy; Wang, Jessica; Ware, James; Hershberger, Ray E

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

共同的遗传通路会增加肥厚型心肌病和扩张型心肌病的风险,但作用方向相反。

Tadros, Rafik; Francis, Catherine; Xu, Xiao; Vermeer, Alexa M C; Harper, Andrew R; Huurman, Roy; Kelu Bisabu, Ken; Walsh, Roddy; Hoorntje, Edgar T; Te Rijdt, Wouter P; Buchan, Rachel J; van Velzen, Hannah G; van Slegtenhorst, Marjon A; Vermeulen, Jentien M; Offerhaus, Joost Allard; Bai, Wenjia; de Marvao, Antonio; Lahrouchi, Najim; Beekman, Leander; Karper, Jacco C; Veldink, Jan H; Kayvanpour, Elham; Pantazis, Antonis; Baksi, A John; Whiffin, Nicola; Mazzarotto, Francesco; Sloane, Geraldine; Suzuki, Hideaki; Schneider-Luftman, Deborah; Elliott, Paul; Richard, Pascale; Ader, Flavie; Villard, Eric; Lichtner, Peter; Meitinger, Thomas; Tanck, Michael W T; van Tintelen, J Peter; Thain, Andrew; McCarty, David; Hegele, Robert A; Roberts, Jason D; Amyot, Julie; Dubé, Marie-Pierre; Cadrin-Tourigny, Julia; Giraldeau, Geneviève; L'Allier, Philippe L; Garceau, Patrick; Tardif, Jean-Claude; Boekholdt, S Matthijs; Lumbers, R Thomas; Asselbergs, Folkert W; Barton, Paul J R; Cook, Stuart A; Prasad, Sanjay K; O'Regan, Declan P; van der Velden, Jolanda; Verweij, Karin J H; Talajic, Mario; Lettre, Guillaume; Pinto, Yigal M; Meder, Benjamin; Charron, Philippe; de Boer, Rudolf A; Christiaans, Imke; Michels, Michelle; Wilde, Arthur A M; Watkins, Hugh; Matthews, Paul M; Ware, James S; Bezzina, Connie R

Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy

PLD1基因的双等位基因功能缺失变异会导致先天性右侧心脏瓣膜缺陷和新生儿心肌病。

Lahrouchi, Najim; Postma, Alex V; Salazar, Christian M; De Laughter, Daniel M; Tjong, Fleur; Piherová, Lenka; Bowling, Forrest Z; Zimmerman, Dominic; Lodder, Elisabeth M; Ta-Shma, Asaf; Perles, Zeev; Beekman, Leander; Ilgun, Aho; Gunst, Quinn; Hababa, Mariam; Škorić-Milosavljević, Doris; Stránecký, Viktor; Tomek, Viktor; de Knijff, Peter; de Leeuw, Rick; Robinson, Jamille Y; Burn, Sabrina C; Mustafa, Hiba; Ambrose, Matthew; Moss, Timothy; Jacober, Jennifer; Niyazov, Dmitriy M; Wolf, Barry; Kim, Katherine H; Cherny, Sara; Rousounides, Andreas; Aristidou-Kallika, Aphrodite; Tanteles, George; Ange-Line, Bruel; Denommé-Pichon, Anne-Sophie; Francannet, Christine; Ortiz, Damara; Haak, Monique C; Ten Harkel, Arend DJ; Manten, Gwendolyn Tr; Dutman, Annemiek C; Bouman, Katelijne; Magliozzi, Monia; Radio, Francesca Clementina; Santen, Gijs We; Herkert, Johanna C; Brown, H Alex; Elpeleg, Orly; van den Hoff, Maurice Jb; Mulder, Barbara; Airola, Michael V; Kmoch, Stanislav; Barnett, Joey V; Clur, Sally-Ann; Frohman, Michael A; Bezzina, Connie R

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

通过对联盟疾病队列和人群对照进行定量分析,增强对遗传性心律失常中罕见变异的解读。

Walsh, Roddy; Lahrouchi, Najim; Tadros, Rafik; Kyndt, Florence; Glinge, Charlotte; Postema, Pieter G; Amin, Ahmad S; Nannenberg, Eline A; Ware, James S; Whiffin, Nicola; Mazzarotto, Francesco; Škorić-Milosavljević, Doris; Krijger, Christian; Arbelo, Elena; Babuty, Dominique; Barajas-Martinez, Hector; Beckmann, Britt M; Bézieau, Stéphane; Bos, J Martijn; Breckpot, Jeroen; Campuzano, Oscar; Castelletti, Silvia; Celen, Candan; Clauss, Sebastian; Corveleyn, Anniek; Crotti, Lia; Dagradi, Federica; de Asmundis, Carlo; Denjoy, Isabelle; Dittmann, Sven; Ellinor, Patrick T; Ortuño, Cristina Gil; Giustetto, Carla; Gourraud, Jean-Baptiste; Hazeki, Daisuke; Horie, Minoru; Ishikawa, Taisuke; Itoh, Hideki; Kaneko, Yoshiaki; Kanters, Jørgen K; Kimoto, Hiroki; Kotta, Maria-Christina; Krapels, Ingrid P C; Kurabayashi, Masahiko; Lazarte, Julieta; Leenhardt, Antoine; Loeys, Bart L; Lundin, Catarina; Makiyama, Takeru; Mansourati, Jacques; Martins, Raphaël P; Mazzanti, Andrea; Mörner, Stellan; Napolitano, Carlo; Ohkubo, Kimie; Papadakis, Michael; Rudic, Boris; Molina, Maria Sabater; Sacher, Frédéric; Sahin, Hatice; Sarquella-Brugada, Georgia; Sebastiano, Regina; Sharma, Sanjay; Sheppard, Mary N; Shimamoto, Keiko; Shoemaker, M Benjamin; Stallmeyer, Birgit; Steinfurt, Johannes; Tanaka, Yuji; Tester, David J; Usuda, Keisuke; van der Zwaag, Paul A; Van Dooren, Sonia; Van Laer, Lut; Winbo, Annika; Winkel, Bo G; Yamagata, Kenichiro; Zumhagen, Sven; Volders, Paul G A; Lubitz, Steven A; Antzelevitch, Charles; Platonov, Pyotr G; Odening, Katja E; Roden, Dan M; Roberts, Jason D; Skinner, Jonathan R; Tfelt-Hansen, Jacob; van den Berg, Maarten P; Olesen, Morten S; Lambiase, Pier D; Borggrefe, Martin; Hayashi, Kenshi; Rydberg, Annika; Nakajima, Tadashi; Yoshinaga, Masao; Saenen, Johan B; Kääb, Stefan; Brugada, Pedro; Robyns, Tomas; Giachino, Daniela F; Ackerman, Michael J; Brugada, Ramon; Brugada, Josep; Gimeno, Juan R; Hasdemir, Can; Guicheney, Pascale; Priori, Silvia G; Schulze-Bahr, Eric; Makita, Naomasa; Schwartz, Peter J; Shimizu, Wataru; Aiba, Takeshi; Schott, Jean-Jacques; Redon, Richard; Ohno, Seiko; Probst, Vincent; Behr, Elijah R; Barc, Julien; Bezzina, Connie R

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

编码 VEGF 受体 2 的 KDR 基因的罕见变异与法洛四联症相关。

Škorić-Milosavljević, Doris; Lahrouchi, Najim; Bosada, Fernanda M; Dombrowsky, Gregor; Williams, Simon G; Lesurf, Robert; Tjong, Fleur V Y; Walsh, Roddy; El Bouchikhi, Ihssane; Breckpot, Jeroen; Audain, Enrique; Ilgun, Aho; Beekman, Leander; Ratbi, Ilham; Strong, Alanna; Muenke, Maximilian; Heide, Solveig; Muir, Alison M; Hababa, Mariam; Cross, Laura; Zhou, Dihong; Pastinen, Tomi; Zackai, Elaine; Atmani, Samir; Ouldim, Karim; Adadi, Najlae; Steindl, Katharina; Rauch, Anita; Brook, David; Wilsdon, Anna; Kuipers, Irene; Blom, Nico A; Mulder, Barbara J; Mefford, Heather C; Keren, Boris; Joset, Pascal; Kruszka, Paul; Thiffault, Isabelle; Sheppard, Sarah E; Roberts, Amy; Lodder, Elisabeth M; Keavney, Bernard D; Clur, Sally-Ann B; Mital, Seema; Hitz, Marc-Philip; Christoffels, Vincent M; Postma, Alex V; Bezzina, Connie R