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

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility

大规模测序鉴定出多个与克罗恩病易感性相关的基因和罕见变异

Sazonovs, Aleksejs; Stevens, Christine R; Venkataraman, Guhan R; Yuan, Kai; Avila, Brandon; Abreu, Maria T; Ahmad, Tariq; Allez, Matthieu; Ananthakrishnan, Ashwin N; Atzmon, Gil; Baras, Aris; Barrett, Jeffrey C; Barzilai, Nir; Beaugerie, Laurent; Beecham, Ashley; Bernstein, Charles N; Bitton, Alain; Bokemeyer, Bernd; Chan, Andrew; Chung, Daniel; Cleynen, Isabelle; Cosnes, Jacques; Cutler, David J; Daly, Allan; Damas, Oriana M; Datta, Lisa W; Dawany, Noor; Devoto, Marcella; Dodge, Sheila; Ellinghaus, Eva; Fachal, Laura; Farkkila, Martti; Faubion, William; Ferreira, Manuel; Franchimont, Denis; Gabriel, Stacey B; Ge, Tian; Georges, Michel; Gettler, Kyle; Giri, Mamta; Glaser, Benjamin; Goerg, Siegfried; Goyette, Philippe; Graham, Daniel; Hämäläinen, Eija; Haritunians, Talin; Heap, Graham A; Hiltunen, Mikko; Hoeppner, Marc; Horowitz, Julie E; Irving, Peter; Iyer, Vivek; Jalas, Chaim; Kelsen, Judith; Khalili, Hamed; Kirschner, Barbara S; Kontula, Kimmo; Koskela, Jukka T; Kugathasan, Subra; Kupcinskas, Juozas; Lamb, Christopher A; Laudes, Matthias; Lévesque, Chloé; Levine, Adam P; Lewis, James D; Liefferinckx, Claire; Loescher, Britt-Sabina; Louis, Edouard; Mansfield, John; May, Sandra; McCauley, Jacob L; Mengesha, Emebet; Mni, Myriam; Moayyedi, Paul; Moran, Christopher J; Newberry, Rodney D; O'Charoen, Sirimon; Okou, David T; Oldenburg, Bas; Ostrer, Harry; Palotie, Aarno; Paquette, Jean; Pekow, Joel; Peter, Inga; Pierik, Marieke J; Ponsioen, Cyriel Y; Pontikos, Nikolas; Prescott, Natalie; Pulver, Ann E; Rahmouni, Souad; Rice, Daniel L; Saavalainen, Päivi; Sands, Bruce; Sartor, R Balfour; Schiff, Elena R; Schreiber, Stefan; Schumm, L Philip; Segal, Anthony W; Seksik, Philippe; Shawky, Rasha; Sheikh, Shehzad Z; Silverberg, Mark S; Simmons, Alison; Skeiceviciene, Jurgita; Sokol, Harry; Solomonson, Matthew; Somineni, Hari; Sun, Dylan; Targan, Stephan; Turner, Dan; Uhlig, Holm H; van der Meulen, Andrea E; Vermeire, Séverine; Verstockt, Sare; Voskuil, Michiel D; Winter, Harland S; Young, Justine; Duerr, Richard H; Franke, Andre; Brant, Steven R; Cho, Judy; Weersma, Rinse K; Parkes, Miles; Xavier, Ramnik J; Rivas, Manuel A; Rioux, John D; McGovern, Dermot P B; Huang, Hailiang; Anderson, Carl A; Daly, Mark J

Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study design

高血压的药物表观遗传学:采用双盲交叉研究设计,对四类降压药物的反应进行全基因组甲基化分析

Nuotio, Marja-Liisa; Sánez Tähtisalo, Heini; Lahtinen, Alexandra; Donner, Kati; Fyhrquist, Frej; Perola, Markus; Kontula, Kimmo K; Hiltunen, Timo P

Chromosomal Region 11p14.1 is Associated with Pharmacokinetics and Pharmacodynamics of Bisoprolol

染色体区域 11p14.1 与比索洛尔的药代动力学和药效学相关

Fontana, Vanessa; Turner, Richard Myles; Francis, Ben; Yin, Peng; Pütz, Benno; Hiltunen, Timo P; Ruotsalainen, Sanni; Kontula, Kimmo K; Müller-Myhsok, Bertam; Pirmohamed, Munir

Adverse Cardiovascular Outcomes and Antihypertensive Treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies

不良心血管结局与抗高血压治疗:国际抗高血压药物基因组学研究联盟的全基因组相互作用荟萃分析

McDonough, Caitrin W; Warren, Helen R; Jack, John R; Motsinger-Reif, Alison A; Armstrong, Nicole D; Bis, Joshua C; House, John S; Singh, Sonal; El Rouby, Nihal M; Gong, Yan; Mychaleckyj, Joesyf C; Rotroff, Daniel M; Benavente, Oscar R; Caulfield, Mark J; Doria, Alessandrio; Pepine, Carl J; Psaty, Bruce M; Glorioso, Valeria; Glorioso, Nicola; Hiltunen, Timo P; Kontula, Kimmo K; Arnett, Donna K; Buse, John B; Irvin, Marguerite R; Johnson, Julie A; Munroe, Patricia B; Wagner, Michael J; Cooper-DeHoff, Rhonda M

Human essential hypertension: no significant association of polygenic risk scores with antihypertensive drug responses

人类原发性高血压:多基因风险评分与降压药物反应无显著相关性

Sánez Tähtisalo, Heini; Ruotsalainen, Sanni; Mars, Nina; Porthan, Kimmo; Oikarinen, Lasse; Virolainen, Juha; Fyhrquist, Frej; Ripatti, Samuli; Kontula, Kimmo K; Hiltunen, Timo P

Effect of four classes of antihypertensive drugs on cardiac repolarization heterogeneity: A double-blind rotational study

四类降压药对心脏复极异质性的影响:一项双盲轮换研究

Sánez Tähtisalo, Heini; Hiltunen, Timo P; Kenttä, Tuomas; Junttila, Juhani; Oikarinen, Lasse; Virolainen, Juha; Kontula, Kimmo K; Porthan, Kimmo

Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation.

由兰尼碱受体 2 型 P2328S 突变引起的儿茶酚胺能多形性室性心动过速的谱系和临床过程

Koponen Mikael, Marjamaa Annukka, Tuiskula Annukka M, Viitasalo Matti, Nallinmaa-Luoto Terhi, Leinonen Jaakko T, Widen Elisabeth, Toivonen Lauri, Kontula Kimmo, Swan Heikki

Genome-Wide Meta-Analysis of Blood Pressure Response to β(1)-Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)

β(1)受体阻滞剂血压反应的全基因组荟萃分析:来自ICAPS(国际抗高血压药物基因组学研究联盟)的结果

Singh, Sonal; Warren, Helen R; Hiltunen, Timo P; McDonough, Caitrin W; El Rouby, Nihal; Salvi, Erika; Wang, Zhiying; Garofalidou, Tatiana; Fyhrquist, Frej; Kontula, Kimmo K; Glorioso, Valeria; Zaninello, Roberta; Glorioso, Nicola; Pepine, Carl J; Munroe, Patricia B; Turner, Stephan T; Chapman, Arlene B; Boerwinkle, Eric; Johnson, Julie A; Gong, Yan; Cooper-DeHoff, Rhonda M

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

对阿什肯纳兹犹太人群体中克罗恩病和罕见病的遗传流行病学的深入了解

Rivas, Manuel A; Avila, Brandon E; Koskela, Jukka; Huang, Hailiang; Stevens, Christine; Pirinen, Matti; Haritunians, Talin; Neale, Benjamin M; Kurki, Mitja; Ganna, Andrea; Graham, Daniel; Glaser, Benjamin; Peter, Inga; Atzmon, Gil; Barzilai, Nir; Levine, Adam P; Schiff, Elena; Pontikos, Nikolas; Weisburd, Ben; Lek, Monkol; Karczewski, Konrad J; Bloom, Jonathan; Minikel, Eric V; Petersen, Britt-Sabina; Beaugerie, Laurent; Seksik, Philippe; Cosnes, Jacques; Schreiber, Stefan; Bokemeyer, Bernd; Bethge, Johannes; Heap, Graham; Ahmad, Tariq; Plagnol, Vincent; Segal, Anthony W; Targan, Stephan; Turner, Dan; Saavalainen, Paivi; Farkkila, Martti; Kontula, Kimmo; Palotie, Aarno; Brant, Steven R; Duerr, Richard H; Silverberg, Mark S; Rioux, John D; Weersma, Rinse K; Franke, Andre; Jostins, Luke; Anderson, Carl A; Barrett, Jeffrey C; MacArthur, Daniel G; Jalas, Chaim; Sokol, Harry; Xavier, Ramnik J; Pulver, Ann; Cho, Judy H; McGovern, Dermot P B; Daly, Mark J

Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients

成人长QT综合征1型和2型患者的临床和分子遗传风险决定因素:Koponen等人对成人长QT综合征患者的随访

Koponen, Mikael; Havulinna, Aki S; Marjamaa, Annukka; Tuiskula, Annukka M; Salomaa, Veikko; Laitinen-Forsblom, Päivi J; Piippo, Kirsi; Toivonen, Lauri; Kontula, Kimmo; Viitasalo, Matti; Swan, Heikki