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

Assessing genetic counseling efficiency with natural language processing

利用自然语言处理评估遗传咨询效率

Nguyen, Michelle H; Applegate, Carolyn D; Murray, Brittney; Zirikly, Ayah; Tichnell, Crystal; Gordon, Catherine; Yanek, Lisa R; James, Cynthia A; Taylor, Casey Overby

Improved Cardiometabolic Health with Uterine-Preserving Fibroid Treatment Compared to Hysterectomy

与子宫切除术相比,保留子宫的子宫肌瘤治疗可改善心血管代谢健康

Michel, Rachel; Kirschen, Gregory W; Stukel, Caitlin S; Olson, Sydney L; Yanek, Lisa; Cameron, Katie; Bennett, Wendy L; Borahay, Mostafa A

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

Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants

通过常见和罕见的结构变异揭示冠状动脉疾病的遗传图谱

Iyer, Kruthika R; Clarke, Shoa L; Guarischi-Sousa, Rodrigo; Gjoni, Ketrin; Heath, Adam S; Young, Erica P; Stitziel, Nathan O; Laurie, Cecelia; Broome, Jai G; Khan, Alyna T; Lewis, Joshua P; Xu, Huichun; Montasser, May E; Ashley, Kellan E; Hasbani, Natalie R; Boerwinkle, Eric; Morrison, Alanna C; Chami, Nathalie; Do, Ron; Rocheleau, Ghislain; Lloyd-Jones, Donald M; Lemaitre, Rozenn N; Bis, Joshua C; Floyd, James S; Kinney, Gregory L; Bowden, Donald W; Palmer, Nicholette D; Benjamin, Emelia J; Nayor, Matthew; Yanek, Lisa R; Kral, Brian G; Becker, Lewis C; Kardia, Sharon L R; Smith, Jennifer A; Bielak, Lawrence F; Norwood, Arnita F; Min, Yuan-I; Carson, April P; Post, Wendy S; Rich, Stephen S; Herrington, David; Guo, Xiuqing; Taylor, Kent D; Manson, JoAnn E; Franceschini, Nora; Pollard, Katherine S; Mitchell, Braxton D; Loos, Ruth J F; Fornage, Myriam; Hou, Lifang; Psaty, Bruce M; Young, Kendra A; Regan, Elizabeth A; Freedman, Barry I; Vasan, Ramachandran S; Levy, Daniel; Mathias, Rasika A; Peyser, Patricia A; Raffield, Laura M; Kooperberg, Charles; Reiner, Alex P; Rotter, Jerome I; Jun, Goo; de Vries, Paul S; Assimes, Themistocles L

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

Genome-wide association study provides novel insight into the genetic architecture of severe obesity

全基因组关联研究为重度肥胖的遗传结构提供了新的见解。

Krishnan, Mohanraj; Anwar, Mohammad Yaser; Justice, Anne E; Chittoor, Geetha; Chen, Hung-Hsin; Roshani, Rashedeh; Scartozzi, Alyssa; Dickerson, Rachel R; Smit, Roelof A J; Preuss, Michael H; Chami, Nathalie; Hadad, Benjamin S; Parra, Esteban J; Cruz, Miguel; Hui, Qin; Wilson, Peter W F; Sun, Yan V; Zhang, Xiaoyu; Linchangco, Gregorio V; Kardia, Sharon L R; Faul, Jessica D; Weir, David R; Bielak, Lawrence F; Highland, Heather M; Young, Kristin L; Qi, Baiyu; Wang, Yujie; Fornage, Myriam; Haiman, Christopher; Cheng, Iona; Peters, Ulrike; Kooperberg, Charles; Buyske, Steven; McCormick, Joseph B; Fisher-Hoch, Susan P; Lona-Durazo, Frida; Peralta, Jesus; Gomez-Zamudio, Jamie; Rich, Stephen S; Ferrier, Kendra R; Lange, Ethan M; Gignoux, Christopher R; Kenny, Eimear E; Wojcik, Genevieve L; Cho, Kelly; Gaziano, Michael J; Djousse, Luc; Liu, Shuwei; Vaidya, Dhananjay; de Mutsert, Renée; Josyula, Navya S; Bauer, Christopher R; Zhao, Wei; Walker, Ryan W; Smith, Jennifer A; Lange, Leslie A; Meyer, Mariah C; Liu, Ching-Ti; Yanek, Lisa R; Lee, Miryoung; Raffield, Laura M; Loos, Ruth J F; Gordon-Larsen, Penny; Below, Jennifer E; North, Kari E; Graff, Mariaelisa

ESPGHAN 57th Annual Meeting Abstracts

ESPGHAN 第 57 届年会摘要

Jiang, Min-Zhi; Gaynor, Sheila M; Li, Xihao; Van Buren, Eric; Stilp, Adrienne; Buth, Erin; Wang, Fei Fei; Manansala, Regina; Gogarten, Stephanie M; Li, Zilin; Polfus, Linda M; Salimi, Shabnam; Bis, Joshua C; Pankratz, Nathan; Yanek, Lisa R; Durda, Peter; Tracy, Russell P; Rich, Stephen S; Rotter, Jerome I; Mitchell, Braxton D; Lewis, Joshua P; Psaty, Bruce M; Pratte, Katherine A; Silverman, Edwin K; Kaplan, Robert C; Avery, Christy; North, Kari E; Mathias, Rasika A; Faraday, Nauder; Lin, Honghuang; Wang, Biqi; Carson, April P; Norwood, Arnita F; Gibbs, Richard A; Kooperberg, Charles; Lundin, Jessica; Peters, Ulrike; Dupuis, Josée; Hou, Lifang; Fornage, Myriam; Benjamin, Emelia J; Reiner, Alexander P; Bowler, Russell P; Lin, Xihong; Auer, Paul L; Raffield, Laura M

Insulin-like growth factor (IGF) and Insulin-like growth factor binding proteins (IGFBP) as predictors of type 2 diabetes risk in obese adults

胰岛素样生长因子 (IGF) 和胰岛素样生长因子结合蛋白 (IGFBP) 作为肥胖成人 2 型糖尿病风险的预测因子

Maurya, Priyanshi; Yang, Jun; Barnes, Allan; Yanek, Lisa R; Becker, Lewis C; Everett, Allen D; Vaidya, Dhananjay

Threshold Effects, Cognitive Decline, and Longitudinal Changes in White Matter Hyperintensity Volume

阈值效应、认知衰退和白质高信号体积的纵向变化

Sasannia, Sarvin; Matsyuk, Mykola; Wang, Shimeng; Zhang, Jinwei; Walker, Keenan A; Shin, Hyeong-Geol; Leigh, Richard; Prince, Jerry L; Becker, Lewis C; Yanek, Lisa R; Armstrong, Nicola J; van Zijl, Peter; Vaidya, Dhananjay; Knutsson, Linda; Nyquist, Paul A