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

Risk of pre-eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case-control study

具有常见疾病母体遗传倾向的患者发生先兆子痫的风险:一项病例对照研究

Gray, K J; Kovacheva, V P; Mirzakhani, H; Bjonnes, A C; Almoguera, B; Wilson, M L; Ingles, S A; Lockwood, C J; Hakonarson, H; McElrath, T F; Murray, J C; Norwitz, E R; Karumanchi, S A; Bateman, B T; Keating, B J; Saxena, R

Chronotype Genetic Variant in PER2 is Associated with Intrinsic Circadian Period in Humans

PER2基因的昼夜节律类型遗传变异与人类的内在昼夜节律周期相关

Chang, Anne-Marie; Duffy, Jeanne F; Buxton, Orfeu M; Lane, Jacqueline M; Aeschbach, Daniel; Anderson, Clare; Bjonnes, Andrew C; Cain, Sean W; Cohen, Daniel A; Frayling, Timothy M; Gooley, Joshua J; Jones, Samuel E; Klerman, Elizabeth B; Lockley, Steven W; Munch, Mirjam; Rajaratnam, Shantha M W; Rueger, Melanie; Rutter, Martin K; Santhi, Nayantara; Scheuermaier, Karine; Van Reen, Eliza; Weedon, Michael N; Czeisler, Charles A; Scheer, Frank A J L; Saxena, Richa

Gene-Centric Analysis of Preeclampsia Identifies Maternal Association at PLEKHG1

以基因为中心的子痫前期分析发现PLEKHG1基因与母体相关

Gray, Kathryn J; Kovacheva, Vesela P; Mirzakhani, Hooman; Bjonnes, Andrew C; Almoguera, Berta; DeWan, Andrew T; Triche, Elizabeth W; Saftlas, Audrey F; Hoh, Josephine; Bodian, Dale L; Klein, Elisabeth; Huddleston, Kathi C; Ingles, Sue Ann; Lockwood, Charles J; Hakonarson, Hakon; McElrath, Thomas F; Murray, Jeffrey C; Wilson, Melissa L; Norwitz, Errol R; Karumanchi, S Ananth; Bateman, Brian T; Keating, Brendan J; Saxena, Richa

Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men

多民族荟萃分析发现 RAI1 可能是男性阻塞性睡眠呼吸暂停相关的数量性状基因座

Chen, Han; Cade, Brian E; Gleason, Kevin J; Bjonnes, Andrew C; Stilp, Adrienne M; Sofer, Tamar; Conomos, Matthew P; Ancoli-Israel, Sonia; Arens, Raanan; Azarbarzin, Ali; Bell, Graeme I; Below, Jennifer E; Chun, Sung; Evans, Daniel S; Ewert, Ralf; Frazier-Wood, Alexis C; Gharib, Sina A; Haba-Rubio, José; Hagen, Erika W; Heinzer, Raphael; Hillman, David R; Johnson, W Craig; Kutalik, Zoltan; Lane, Jacqueline M; Larkin, Emma K; Lee, Seung Ku; Liang, Jingjing; Loredo, Jose S; Mukherjee, Sutapa; Palmer, Lyle J; Papanicolaou, George J; Penzel, Thomas; Peppard, Paul E; Post, Wendy S; Ramos, Alberto R; Rice, Ken; Rotter, Jerome I; Sands, Scott A; Shah, Neomi A; Shin, Chol; Stone, Katie L; Stubbe, Beate; Sul, Jae Hoon; Tafti, Mehdi; Taylor, Kent D; Teumer, Alexander; Thornton, Timothy A; Tranah, Gregory J; Wang, Chaolong; Wang, Heming; Warby, Simon C; Wellman, D Andrew; Zee, Phyllis C; Hanis, Craig L; Laurie, Cathy C; Gottlieb, Daniel J; Patel, Sanjay R; Zhu, Xiaofeng; Sunyaev, Shamil R; Saxena, Richa; Lin, Xihong; Redline, Susan

Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations

跨种族评估确定了与25-羟基维生素D浓度相关的低频基因位点

Hong, Jaeyoung; Hatchell, Kathryn E; Bradfield, Jonathan P; Bjonnes, Andrew; Chesi, Alessandra; Lai, Chao-Qiang; Langefeld, Carl D; Lu, Lingyi; Lu, Yingchang; Lutsey, Pamela L; Musani, Solomon K; Nalls, Mike A; Robinson-Cohen, Cassianne; Roizen, Jeffery D; Saxena, Richa; Tucker, Katherine L; Ziegler, Julie T; Arking, Dan E; Bis, Joshua C; Boerwinkle, Eric; Bottinger, Erwin P; Bowden, Donald W; Gilsanz, Vicente; Houston, Denise K; Kalkwarf, Heidi J; Kelly, Andrea; Lappe, Joan M; Liu, Yongmei; Michos, Erin D; Oberfield, Sharon E; Palmer, Nicholette D; Rotter, Jerome I; Sapkota, Bishwa; Shepherd, John A; Wilson, James G; Basu, Saonli; de Boer, Ian H; Divers, Jasmin; Freedman, Barry I; Grant, Struan F A; Hakanarson, Hakon; Harris, Tamara B; Kestenbaum, Bryan R; Kritchevsky, Stephen B; Loos, Ruth J F; Norris, Jill M; Norwood, Arnita F; Ordovas, Jose M; Pankow, James S; Psaty, Bruce M; Sanghera, Dharambir K; Wagenknecht, Lynne E; Zemel, Babette S; Meigs, James; Dupuis, Josée; Florez, Jose C; Wang, Thomas; Liu, Ching-Ti; Engelman, Corinne D; Billings, Liana K

An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery

一项整合临床项目和众包策略,用于基因组测序和孟德尔遗传病基因发现

Haghighi, Alireza; Krier, Joel B; Toth-Petroczy, Agnes; Cassa, Christopher A; Frank, Natasha Y; Carmichael, Nikkola; Fieg, Elizabeth; Bjonnes, Andrew; Mohanty, Anwoy; Briere, Lauren C; Lincoln, Sharyn; Lucia, Stephanie; Gupta, Vandana A; Söylemez, Onuralp; Sutti, Sheila; Kooshesh, Kameron; Qiu, Haiyan; Fay, Christopher J; Perroni, Victoria; Valerius, Jamie; Hanna, Meredith; Frank, Alexander; Ouahed, Jodie; Snapper, Scott B; Pantazi, Angeliki; Chopra, Sameer S; Leshchiner, Ignaty; Stitziel, Nathan O; Feldweg, Anna; Mannstadt, Michael; Loscalzo, Joseph; Sweetser, David A; Liao, Eric; Stoler, Joan M; Nowak, Catherine B; Sanchez-Lara, Pedro A; Klein, Ophir D; Perry, Hazel; Patsopoulos, Nikolaos A; Raychaudhuri, Soumya; Goessling, Wolfram; Green, Robert C; Seidman, Christine E; MacRae, Calum A; Sunyaev, Shamil R; Maas, Richard L; Vuzman, Dana

Genetic predisposition to elevated levels of C-reactive protein is associated with a decreased risk for preeclampsia

遗传因素导致C反应蛋白水平升高与先兆子痫风险降低相关

Spracklen, Cassandra N; Smith, Caitlin J; Saftlas, Audrey F; Triche, Elizabeth W; Bjonnes, Andrew; Keating, Brendan J; Saxena, Richa; Breheny, Patrick J; Dewan, Andrew T; Robinson, Jennifer G; Hoh, Josephine; Ryckman, Kelli K

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans

西班牙裔/拉丁裔美国人阻塞性睡眠呼吸暂停特征的遗传关联

Cade, Brian E; Chen, Han; Stilp, Adrienne M; Gleason, Kevin J; Sofer, Tamar; Ancoli-Israel, Sonia; Arens, Raanan; Bell, Graeme I; Below, Jennifer E; Bjonnes, Andrew C; Chun, Sung; Conomos, Matthew P; Evans, Daniel S; Johnson, W Craig; Frazier-Wood, Alexis C; Lane, Jacqueline M; Larkin, Emma K; Loredo, Jose S; Post, Wendy S; Ramos, Alberto R; Rice, Ken; Rotter, Jerome I; Shah, Neomi A; Stone, Katie L; Taylor, Kent D; Thornton, Timothy A; Tranah, Gregory J; Wang, Chaolong; Zee, Phyllis C; Hanis, Craig L; Sunyaev, Shamil R; Patel, Sanjay R; Laurie, Cathy C; Zhu, Xiaofeng; Saxena, Richa; Lin, Xihong; Redline, Susan

Relationship between polycystic ovary syndrome and ancestry in European Americans

欧洲裔美国人多囊卵巢综合征与血统的关系

Bjonnes, Andrew C; Saxena, Richa; Welt, Corrine K

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis

一项全面的国际荟萃分析显示,冠状动脉疾病与X染色体变异之间无关联

Loley, Christina; Alver, Maris; Assimes, Themistocles L; Bjonnes, Andrew; Goel, Anuj; Gustafsson, Stefan; Hernesniemi, Jussi; Hopewell, Jemma C; Kanoni, Stavroula; Kleber, Marcus E; Lau, King Wai; Lu, Yingchang; Lyytikäinen, Leo-Pekka; Nelson, Christopher P; Nikpay, Majid; Qu, Liming; Salfati, Elias; Scholz, Markus; Tukiainen, Taru; Willenborg, Christina; Won, Hong-Hee; Zeng, Lingyao; Zhang, Weihua; Anand, Sonia S; Beutner, Frank; Bottinger, Erwin P; Clarke, Robert; Dedoussis, George; Do, Ron; Esko, Tõnu; Eskola, Markku; Farrall, Martin; Gauguier, Dominique; Giedraitis, Vilmantas; Granger, Christopher B; Hall, Alistair S; Hamsten, Anders; Hazen, Stanley L; Huang, Jie; Kähönen, Mika; Kyriakou, Theodosios; Laaksonen, Reijo; Lind, Lars; Lindgren, Cecilia; Magnusson, Patrik K E; Marouli, Eirini; Mihailov, Evelin; Morris, Andrew P; Nikus, Kjell; Pedersen, Nancy; Rallidis, Loukianos; Salomaa, Veikko; Shah, Svati H; Stewart, Alexandre F R; Thompson, John R; Zalloua, Pierre A; Chambers, John C; Collins, Rory; Ingelsson, Erik; Iribarren, Carlos; Karhunen, Pekka J; Kooner, Jaspal S; Lehtimäki, Terho; Loos, Ruth J F; März, Winfried; McPherson, Ruth; Metspalu, Andres; Reilly, Muredach P; Ripatti, Samuli; Sanghera, Dharambir K; Thiery, Joachim; Watkins, Hugh; Deloukas, Panos; Kathiresan, Sekar; Samani, Nilesh J; Schunkert, Heribert; Erdmann, Jeanette; König, Inke R