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

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

欧洲和中亚女性的高血压遗传倾向与先兆子痫有关。

Steinthorsdottir, Valgerdur; McGinnis, Ralph; Williams, Nicholas O; Stefansdottir, Lilja; Thorleifsson, Gudmar; Shooter, Scott; Fadista, João; Sigurdsson, Jon K; Auro, Kirsi M; Berezina, Galina; Borges, Maria-Carolina; Bumpstead, Suzannah; Bybjerg-Grauholm, Jonas; Colgiu, Irina; Dolby, Vivien A; Dudbridge, Frank; Engel, Stephanie M; Franklin, Christopher S; Frigge, Michael L; Frisbaek, Yr; Geirsson, Reynir T; Geller, Frank; Gretarsdottir, Solveig; Gudbjartsson, Daniel F; Harmon, Quaker; Hougaard, David Michael; Hegay, Tatyana; Helgadottir, Anna; Hjartardottir, Sigrun; Jääskeläinen, Tiina; Johannsdottir, Hrefna; Jonsdottir, Ingileif; Juliusdottir, Thorhildur; Kalsheker, Noor; Kasimov, Abdumadjit; Kemp, John P; Kivinen, Katja; Klungsøyr, Kari; Lee, Wai K; Melbye, Mads; Miedzybrodska, Zosia; Moffett, Ashley; Najmutdinova, Dilbar; Nishanova, Firuza; Olafsdottir, Thorunn; Perola, Markus; Pipkin, Fiona Broughton; Poston, Lucilla; Prescott, Gordon; Saevarsdottir, Saedis; Salimbayeva, Damilya; Scaife, Paula Juliet; Skotte, Line; Staines-Urias, Eleonora; Stefansson, Olafur A; Sørensen, Karina Meden; Thomsen, Liv Cecilie Vestrheim; Tragante, Vinicius; Trogstad, Lill; Simpson, Nigel A B; Aripova, Tamara; Casas, Juan P; Dominiczak, Anna F; Walker, James J; Thorsteinsdottir, Unnur; Iversen, Ann-Charlotte; Feenstra, Bjarke; Lawlor, Deborah A; Boyd, Heather Allison; Magnus, Per; Laivuori, Hannele; Zakhidova, Nodira; Svyatova, Gulnara; Stefansson, Kari; Morgan, Linda

Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12

对罕见编码变异进行全外显子组分析,发现 MOCS3、IFIT3 和 SERPINA12 基因与 COPD 和气流受限存在新的关联

Jackson, Victoria E; Ntalla, Ioanna; Sayers, Ian; Morris, Richard; Whincup, Peter; Casas, Juan-Pablo; Amuzu, Antoinette; Choi, Minkyoung; Dale, Caroline; Kumari, Meena; Engmann, Jorgen; Kalsheker, Noor; Chappell, Sally; Guetta-Baranes, Tamar; McKeever, Tricia M; Palmer, Colin N A; Tavendale, Roger; Holloway, John W; Sayer, Avan A; Dennison, Elaine M; Cooper, Cyrus; Bafadhel, Mona; Barker, Bethan; Brightling, Chris; Bolton, Charlotte E; John, Michelle E; Parker, Stuart G; Moffat, Miriam F; Wardlaw, Andrew J; Connolly, Martin J; Porteous, David J; Smith, Blair H; Padmanabhan, Sandosh; Hocking, Lynne; Stirrups, Kathleen E; Deloukas, Panos; Strachan, David P; Hall, Ian P; Tobin, Martin D; Wain, Louise V

Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS)

影响人类衰老的遗传变异:晚发性阿尔茨海默病(LOAD)全基因组关联研究(GWAS)

Shi, Hui; Belbin, Olivia; Medway, Christopher; Brown, Kristelle; Kalsheker, Noor; Carrasquillo, Minerva; Proitsi, Petroula; Powell, John; Lovestone, Simon; Goate, Alison; Younkin, Steven; Passmore, Peter; Morgan, Kevin

A multi-center study of ACE and the risk of late-onset Alzheimer's disease

一项关于童年期不良经历与晚发性阿尔茨海默病风险的多中心研究

Belbin, Olivia; Brown, Kristelle; Shi, Hui; Medway, Christopher; Abraham, Richard; Passmore, Peter; Mann, David; Smith, A David; Holmes, Clive; McGuinness, Bernadette; Craig, David; Warden, Donald; Heun, Reinhard; Kölsch, Heike; Love, Seth; Kalsheker, Noor; Williams, Julie; Owen, Michael J; Carrasquillo, Minerva; Younkin, Steven; Morgan, Kevin; Kehoe, Patrick G

A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample

对 SpiroMeta 一般人群样本中潜在的肺功能相关基因进行全面评估

Obeidat, Ma'en; Wain, Louise V; Shrine, Nick; Kalsheker, Noor; Soler Artigas, Maria; Repapi, Emmanouela; Burton, Paul R; Johnson, Toby; Ramasamy, Adaikalavan; Zhao, Jing Hua; Zhai, Guangju; Huffman, Jennifer E; Vitart, Veronique; Albrecht, Eva; Igl, Wilmar; Hartikainen, Anna-Liisa; Pouta, Anneli; Cadby, Gemma; Hui, Jennie; Palmer, Lyle J; Hadley, David; McArdle, Wendy L; Rudnicka, Alicja R; Barroso, Inês; Loos, Ruth J F; Wareham, Nicholas J; Mangino, Massimo; Soranzo, Nicole; Spector, Tim D; Gläser, Sven; Homuth, Georg; Völzke, Henry; Deloukas, Panos; Granell, Raquel; Henderson, John; Grkovic, Ivica; Jankovic, Stipan; Zgaga, Lina; Polašek, Ozren; Rudan, Igor; Wright, Alan F; Campbell, Harry; Wild, Sarah H; Wilson, James F; Heinrich, Joachim; Imboden, Medea; Probst-Hensch, Nicole M; Gyllensten, Ulf; Johansson, Åsa; Zaboli, Ghazal; Mustelin, Linda; Rantanen, Taina; Surakka, Ida; Kaprio, Jaakko; Jarvelin, Marjo-Riitta; Hayward, Caroline; Evans, David M; Koch, Beate; Musk, Arthur William; Elliott, Paul; Strachan, David P; Tobin, Martin D; Sayers, Ian; Hall, Ian P

Opportunities and challenges in the genetics of COPD 2010: an International COPD Genetics Conference report

2010年慢性阻塞性肺疾病遗传学领域的机遇与挑战:国际慢性阻塞性肺疾病遗传学会议报告

Silverman, Edwin K; Vestbo, Jørgen; Agusti, Alvar; Anderson, Wayne; Bakke, Per S; Barnes, Kathleen C; Barr, R Graham; Bleecker, Eugene R; Boezen, H Marike; Burkart, Kristin M; Celli, Bartolome R; Cho, Michael H; Cookson, William O C; Croxton, Thomas; Daley, Denise; DeMeo, Dawn L; Gan, Weiniu; Garcia-Aymerich, Judith; Hall, Ian P; Hansel, Nadia N; Hersh, Craig P; Kalsheker, Noor; Kiley, James P; Kim, Woo Jin; Lambrechts, Diether; Lee, Sang-Do; Litonjua, Augusto A; Lomas, David A; London, Stephanie J; Nishimura, Masaharu; Nørdestgaard, Borge G; O'Donnell, Christopher J; Postma, Dirkje S; Puhan, Milo A; Tesfaigzi, Yohannes; Tobin, Martin D; Vogelmeier, Claus; Wilk, Jemma B; Wouters, Emiel; Young, Robert P; Ziegler-Heitbrock, Loems; MacNee, William; Crapo, James D

The role of IREB2 and transforming growth factor beta-1 genetic variants in COPD: a replication case-control study

IREB2 和转化生长因子β-1基因变异在慢性阻塞性肺疾病中的作用:一项重复病例对照研究

Chappell, Sally L; Daly, Leslie; Lotya, Juzer; Alsaegh, Aiman; Guetta-Baranes, Tamar; Roca, Josep; Rabinovich, Roberto; Morgan, Kevin; Millar, Ann B; Donnelly, Seamas C; Keatings, Vera; MacNee, William; Stolk, Jan; Hiemstra, Pieter S; Miniati, Massimo; Monti, Simonetta; O'Connor, Clare M; Kalsheker, Noor

EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity

EDNRA 变异与平滑肌 mRNA 水平、细胞增殖率和囊性纤维化肺病严重程度相关。

Darrah, Rebecca; McKone, Edward; O'Connor, Clare; Rodgers, Christine; Genatossio, Alan; McNamara, Sharon; Gibson, Ronald; Stuart Elborn, J; Ennis, Madeleine; Gallagher, Charles G; Kalsheker, Noor; Aitken, Moira; Wiese, Dawn; Dunn, John; Smith, Paul; Pace, Rhonda; Londono, Douglas; Goddard, Katrina A B; Knowles, Michael R; Drumm, Mitchell L

Association of MMP-2 polymorphisms with severe and very severe COPD: a case control study of MMPs-1, 9 and 12 in a European population

MMP-2多态性与重度及极重度慢性阻塞性肺疾病的关联:一项针对欧洲人群中MMP-1、9和12的病例对照研究

Haq, Imran; Chappell, Sally; Johnson, Simon R; Lotya, Juzer; Daly, Leslie; Morgan, Kevin; Guetta-Baranes, Tamar; Roca, Josep; Rabinovich, Roberto; Millar, Ann B; Donnelly, Seamas C; Keatings, Vera; MacNee, William; Stolk, Jan; Hiemstra, Pieter S; Miniati, Massimo; Monti, Simonetta; O'Connor, Clare M; Kalsheker, Noor

The SERPINE2 gene and chronic obstructive pulmonary disease

SERPINE2基因与慢性阻塞性肺疾病

Chappell, Sally; Daly, Leslie; Morgan, Kevin; Baranes, Tamar Guetta; Roca, Josep; Rabinovich, Roberto; Millar, Ann; Donnelly, Seamas C; Keatings, Vera; MacNee, William; Stolk, Jan; Hiemstra, Pieter S; Miniati, Massimo; Monti, Simonetta; O'Connor, Clare M; Kalsheker, Noor