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

Decentralizing dementia research to the US-Mexico border: the Rio Grande Valley AD-RCMAR as a model for translational equity

将痴呆症研究分散到美墨边境:以格兰德河谷 AD-RCMAR 为例,实现转化公平。

Maestre, Gladys E; Blangero, John; Manusov, Eron G; de Erausquin, Gabriel A; Fernández, Francisco; Mejía-Arango, Silvia; Diego, Vincent; López-Alvarenga, Juan Carlos; Alaniz, Claudia; García, Neyra; Pirela, Rosa V; Tsin, Andrew; Mahaney, Michael C

The RNA-binding protein HuR modulates the expression of the disease-linked CCL2 rs1024611G-rs13900T haplotype

RNA结合蛋白HuR调节与疾病相关的CCL2 rs1024611G-rs13900T单倍型的表达

Akhtar, Feroz; Ruiz, Joselin Hernandez; Liu, Ya-Guang; Resendez, Roy G; Feliers, Denis; Morales, Liza D; Diaz-Badillo, Alvaro; Lehman, Donna M; Arya, Rector; Alvarenga, Juan Carlos Lopez; Blangero, John; Duggirala, Ravindranath; Mummidi, Srinivas

Genetic Variants and Molecular Components Associated with Metabolic Dysfunctional-Associated Steatotic Liver Disease and Depression: Shared Association of ADAMTS7 and THRAP3

与代谢功能障碍相关性脂肪肝和抑郁症相关的遗传变异和分子成分:ADAMTS7 和 THRAP3 的共同关联

Manusov, Eron G; Diego, Vincent P; Almeida, Marcio; Galan, Jacob A; Herklotz, Kathryn; Abrego Iii, Edwardo 2nd; Sultana, Habiba; Pena Marquez, Luis; Arriaga, Marco A; Leandro, Marcelo; Peralta, Juan; C Leandro, Ana; Howard, Tom E; Curran, Joanne E; Laston, Sandra; Blangero, John; Williams-Blangero, Sarah

Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits

针对西班牙裔/拉丁裔人群的大规模多组学分析,鉴定出与心血管代谢特征相关的基因

Petty, Lauren E; Chen, Hung-Hsin; Frankel, Elizabeth G; Zhu, Wanying; Downie, Carolina G; Graff, Mariaelisa; Lin, Phillip; Sharma, Priya; Zhang, Xinruo; Scartozzi, Alyssa C; Roshani, Rashedeh; Landman, Joshua M; Boehnke, Michael; Bowden, Donald W; Chambers, John C; Mahajan, Anubha; McCarthy, Mark I; Ng, Maggie C Y; Sim, Xueling; Spracklen, Cassandra N; Zhang, Weihua; Preuss, Michael; Bottinger, Erwin P; Nadkarni, Girish N; Loos, Ruth J F; Chen, Yii-Der Ida; Tan, Jingyi; Ipp, Eli; Genter, Pauline; Emery, Leslie S; Louie, Tin; Sofer, Tamar; Stilp, Adrienne M; Taylor, Kent D; Xiang, Anny H; Buchanan, Thomas A; Roll, Kathryn; Gao, Chuan; Palmer, Nicholette D; Norris, Jill M; Wagenknecht, Lynne E; Nousome, Darryl; Varma, Rohit; McKean-Cowdin, Roberta; Guo, Xiuqing; Hai, Yang; Hsueh, Willa; Sandow, Kevin; Parra, Esteban J; Cruz, Miguel; Valladares-Salgado, Adan; Wacher-Rodarte, Niels; Rotter, Jerome I; Goodarzi, Mark O; Rich, Stephen S; Bertoni, Alain; Raffel, Leslie J; Nadler, Jerry L; Kandeel, Fouad R; Duggirala, Ravindranath; Blangero, John; Lehman, Donna M; DeFronzo, Ralph A; Thameem, Farook; Wang, Yujie; Gahagan, Sheila; Blanco, Estela; Burrows, Raquel; Huerta-Chagoya, Alicia; Florez, Jose C; Tusie-Luna, Teresa; González-Villalpando, Clicerio; Orozco, Lorena; Haiman, Christopher A; Hanis, Craig L; Rohde, Rebecca; Whitsel, Eric A; Reiner, Alexander P; Kooperberg, Charles; Li, Yun; Duan, Qing; Lee, Miryoung; Correa-Burrows, Paulina; Fried, Susan K; North, Kari E; McCormick, Joseph B; Fisher-Hoch, Susan P; Gamazon, Eric R; Morris, Andrew P; Mercader, Josep M; Highland, Heather M; Below, Jennifer E

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele

通过对体重指数进行全基因组测序分析,发现了一种新的非洲血统特异性风险等位基因。

Zhang, Xinruo; Brody, Jennifer A; Graff, Mariaelisa; Highland, Heather M; Chami, Nathalie; Xu, Hanfei; Wang, Zhe; Ferrier, Kendra R; Chittoor, Geetha; Josyula, Navya Shilpa; Meyer, Mariah; Gupta, Shreyash; Li, Xihao; Li, Zilin; Allison, Matthew A; Becker, Diane M; Bielak, Lawrence F; Bis, Joshua C; Boorgula, Meher Preethi; Bowden, Donald W; Broome, Jai G; Buth, Erin J; Carlson, Christopher S; Chang, Kyong-Mi; Chavan, Sameer; Chiu, Yen-Feng; Chuang, Lee-Ming; Conomos, Matthew P; DeMeo, Dawn L; Du, Mengmeng; Duggirala, Ravindranath; Eng, Celeste; Fohner, Alison E; Freedman, Barry I; Garrett, Melanie E; Guo, Xiuqing; Haiman, Chris; Heavner, Benjamin D; Hidalgo, Bertha; Hixson, James E; Ho, Yuk-Lam; Hobbs, Brian D; Hu, Donglei; Hui, Qin; Hwu, Chii-Min; Jackson, Rebecca D; Jain, Deepti; Kalyani, Rita R; Kardia, Sharon L R; Kelly, Tanika N; Lange, Ethan M; LeNoir, Michael; Li, Changwei; Le Marchand, Loic; McDonald, Merry-Lynn N; McHugh, Caitlin P; Morrison, Alanna C; Naseri, Take; O'Connell, Jeffrey; O'Donnell, Christopher J; Palmer, Nicholette D; Pankow, James S; Perry, James A; Peters, Ulrike; Preuss, Michael H; Rao, D C; Regan, Elizabeth A; Reupena, Sefuiva M; Roden, Dan M; Rodriguez-Santana, Jose; Sitlani, Colleen M; Smith, Jennifer A; Tiwari, Hemant K; Vasan, Ramachandran S; Wang, Zeyuan; Weeks, Daniel E; Wessel, Jennifer; Wiggins, Kerri L; Wilkens, Lynne R; Wilson, Peter W F; Yanek, Lisa R; Yoneda, Zachary T; Zhao, Wei; Zöllner, Sebastian; Arnett, Donna K; Ashley-Koch, Allison E; Barnes, Kathleen C; Blangero, John; Boerwinkle, Eric; Burchard, Esteban G; Carson, April P; Chasman, Daniel I; Ida Chen, Yii-Der; Curran, Joanne E; Fornage, Myriam; Gordeuk, Victor R; He, Jiang; Heckbert, Susan R; Hou, Lifang; Irvin, Marguerite R; Kooperberg, Charles; Minster, Ryan L; Mitchell, Braxton D; Nouraie, Mehdi; Psaty, Bruce M; Raffield, Laura M; Reiner, Alexander P; Rich, Stephen S; Rotter, Jerome I; Benjamin Shoemaker, M; Smith, Nicholas L; Taylor, Kent D; Telen, Marilyn J; Weiss, Scott T; Zhang, Yingze; Heard-Costa, Nancy; Sun, Yan V; Lin, Xihong; Cupples, L Adrienne; Lange, Leslie A; Liu, Ching-Ti; Loos, Ruth J F; North, Kari E; Justice, Anne E

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

罕见的有害CCR2变异与较低的终生心血管风险相关。

Georgakis, Marios K; Malik, Rainer; Bounkari, Omar El; Hasbani, Natalie R; Li, Jiang; Huffman, Jennifer E; Shakt, Gabrielle; Tack, Reinier W P; Kimball, Tamara N; Asare, Yaw; Morrison, Alanna C; Tsao, Noah L; Judy, Renae; Mitchell, Braxton D; Xu, Huichun; Montasser, May E; Do, Ron; Kenny, Eimear E; Loos, Ruth J F; Terry, James G; Carr, John Jeffrey; Bis, Joshua C; Psaty, Bruce M; Longstreth, W T; Young, Kendra A; Lutz, Sharon M; Cho, Michael H; Broome, Jai; Khan, Alyna T; Wang, Fei Fei; Heard-Costa, Nancy; Seshadri, Sudha; Vasan, Ramachandran S; Palmer, Nicholette D; Freedman, Barry I; Bowden, Donald W; Yanek, Lisa R; Kral, Brian G; Becker, Lewis C; Peyser, Patricia A; Bielak, Lawrence F; Ammous, Farah; Carson, April P; Hall, Michael E; Raffield, Laura M; Rich, Stephen S; Post, Wendy S; Tracy, Russel P; Taylor, Kent D; Guo, Xiuqing; Mahaney, Michael C; Curran, Joanne E; Blangero, John; Clarke, Shoa L; Haessler, Jeffrey W; Hu, Yao; Assimes, Themistocles L; Kooperberg, Charles; Bernhagen, Jürgen; Anderson, Christopher D; Damrauer, Scott M; Zand, Ramin; Rotter, Jerome I; de Vries, Paul S; Dichgans, Martin

Time-Resolved Pump-Probe X-Ray Solution Scattering Capabilities at BioCARS 14 ID Beamline, Advanced Photon Source

BioCARS 14 ID 光束线(先进光子源)的时间分辨泵浦探测 X 射线溶液散射能力

Kochunov, Peter; Glahn, David C; Lancaster, Jack; Winkler, Anderson; Karlsgodt, Kathrin; Olvera, Rene L; Curran, Joanna E; Carless, Melanie A; Dyer, Thomas D; Almasy, Laura; Duggirala, Ravi; Fox, Peter T; Blangero, John; Kosheleva, Irina; Henning, Robert; Kim, Insik; Zoellner, Eric; Srajer, Vukica; Ranganathan, Rama

Lifespan reference curves for harmonizing multi-site regional brain white matter metrics from diffusion MRI

用于协调多部位扩散磁共振成像区域脑白质指标的寿命参考曲线

Zhu, Alyssa H; Nir, Talia M; Javid, Shayan; Villalón-Reina, Julio E; Rodrigue, Amanda L; Strike, Lachlan T; de Zubicaray, Greig I; McMahon, Katie L; Wright, Margaret J; Medland, Sarah E; Blangero, John; Glahn, David C; Kochunov, Peter; Williamson, Douglas E; Håberg, Asta K; Thompson, Paul M; Jahanshad, Neda

Association of genetic scores related to insulin resistance with neurological outcomes in ancestrally diverse cohorts from the Trans-Omics for Precision Medicine (TOPMed) program

来自精准医学跨组学(TOPMed)计划的祖源多样性队列中,与胰岛素抵抗相关的遗传评分与神经系统结局的关联

Sarnowski, Chloé; Zhang, Yixin; Ammous, Farah; Shade, Lincoln M P; DiCorpo, Daniel; Jian, Xueqiu; Arnett, Donna K; Austin, Thomas R; Beiser, Alexa; Bis, Joshua C; Blangero, John; Boerwinkle, Eric; Bressler, Jan; Curran, Joanne E; DeCarli, Charles S; Doddapaneni, Harsha; Dupuis, Josée; Fardo, David W; Florez, Jose C; Gabriel, Stacey; Gibbs, Richard A; Glahn, David C; Gupta, Namrata; González, Hector M; González, Kevin A; Hatzikotoulas, Konstantinos; Hayden, Kathleen M; Heckbert, Susan R; Hidalgo, Bertha; Huerta-Chagoya, Alicia; Hughes, Timothy M; Kardia, Sharon L R; Kooperberg, Charles L; Launer, Lenore J; Longstreth, W T Jr; Mandla, Ravi; Mathias, Rasika A; Morris, Andrew P; Mosley, Thomas H; Nasrallah, Ilya M; Nyquist, Paul; Psaty, Bruce M; Qi, Qibin; Raffield, Laura M; Rayner, Nigel W; Reiner, Alexander P; Satizabal, Claudia L; Selvin, Elizabeth; Sevilla-Gonzalez, Magdalena D R; Smith, Albert V; Smith, Jennifer A; Smith, Kirk; Snively, Beverly M; Southam, Lorraine; Sofer, Tamar; Suzuki, Ken; Taylor, Henry J; Udler, Miriam S; Viaud-Martinez, Karine A; Wassertheil-Smoller, Sylvia; Wood, Alexis C; Yanek, Lisa R; Yin, Xianyong; Manning, Alisa K; Rotter, Jerome I; Rich, Stephen S; Meigs, James B; Fornage, Myriam; Seshadri, Sudha; Morrison, Alanna C

Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleeding

对血管性血友病因子抗原水平≤50 IU/dL的基因研究可识别与血管性血友病和出血风险增加相关的变异。

Friedman, Rachel K; Heath, Adam S; Huffman, Jennifer E; Baker, James T; Hasbani, Natalie R; Gagliano Taliun, Sarah A; Chen, Ming-Huei; Howard, Tom E; Lewis, Joshua P; Pankratz, Nathan; Patil, Snehal; Reiner, Alex P; Thibord, Florian; Yanek, Lisa R; Yao, Jie; Chen, Hung-Hsin; Curran, Joanne E; Faraday, Nauder; Guo, Xiuqing; Wheeler, Marsha M; Ryan, Kathleen A; Zhou, Xiang; Cho, Kelly; Almasy, Laura; Auer, Paul L; Becker, Lewis C; Wilson, Peter W F; Boerwinkle, Eric; O'Connell, Jeffrey R; Rich, Stephen S; Samuels, David C; Blangero, John; Fornage, Myriam; Kooperberg, Charles; Mathias, Rasika A; Mitchell, Braxton D; Rotter, Jerome I; Johnson, Andrew D; Smith, Nicholas L; Coban-Akdemir, Zeynep H; Below, Jennifer E; Morrison, Alanna C; Johnsen, Jill M; de Vries, Paul S