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

Low-cost generation of clinical-grade, layperson-friendly pharmacogenetic passports using oligonucleotide arrays

利用寡核苷酸芯片低成本生成临床级、非专业人士也能理解的药物遗传学护照

Lanting, Pauline; Warmerdam, Robert; Slager, Jelle; Brugge, Harm; Ochi, Taichi; Benjamins, Marloes; Lopera-Maya, Esteban; Jankipersadsing, Soesma; Gelderloos-Arends, Jody; Teuben, Daphne; Hendriksen, Dennis; Charbon, Bart; Johansson, Lennart; Munnink, Thijs Oude; de Boer-Veger, Nienke; Wilffert, Bob; Swertz, Morris; Touw, Daan; Deelen, Patrick; Knoers, Nine; Dekens, Jackie; Franke, Lude

Host genetic regulation of human gut microbial structural variation

宿主遗传调控人类肠道微生物结构变异

Daria V Zhernakova #, Daoming Wang #, Lei Liu #, Sergio Andreu-Sánchez, Yue Zhang, Angel J Ruiz-Moreno, Haoran Peng, Niels Plomp, Ángela Del Castillo-Izquierdo, Ranko Gacesa, Esteban A Lopera-Maya, Godfrey S Temba, Vesla I Kullaya, Sander S van Leeuwen; Lifelines Cohort Study; Ramnik J Xavier, Quiri

Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation

新的祖先特异性原发性开角型青光眼基因位点及其与血管机制和细胞增殖的共同生物学特征

Lo Faro, Valeria; Bhattacharya, Arjun; Zhou, Wei; Zhou, Dan; Wang, Ying; Läll, Kristi; Kanai, Masahiro; Lopera-Maya, Esteban; Straub, Peter; Pawar, Priyanka; Tao, Ran; Zhong, Xue; Namba, Shinichi; Sanna, Serena; Nolte, Ilja M; Okada, Yukinori; Ingold, Nathan; MacGregor, Stuart; Snieder, Harold; Surakka, Ida; Shortt, Jonathan; Gignoux, Chris; Rafaels, Nicholas; Crooks, Kristy; Verma, Anurag; Verma, Shefali S; Guare, Lindsay; Rader, Daniel J; Willer, Cristen; Martin, Alicia R; Brantley, Milam A Jr; Gamazon, Eric R; Jansonius, Nomdo M; Joos, Karen; Cox, Nancy J; Hirbo, Jibril

Genome-wide Studies Reveal Genetic Risk Factors for Hepatic Fat Content

全基因组研究揭示肝脏脂肪含量的遗传风险因素

Li, Yanni; van den Berg, Eline H; Kurilshikov, Alexander; Zhernakova, Dasha V; Gacesa, Ranko; Hu, Shixian; Lopera-Maya, Esteban A; Zhernakova, Alexandra; de Meijer, Vincent E; Sanna, Serena; Dullaart, Robin P F; Blokzijl, Hans; Festen, Eleonora A M; Fu, Jingyuan; Weersma, Rinse K

Rome III Criteria Capture Higher Irritable Bowel Syndrome SNP-Heritability and Highlight a Novel Genetic Link With Cardiovascular Traits

罗马III标准能够捕捉到更高的肠易激综合征SNP遗传力,并揭示其与心血管性状的新型遗传联系

Camargo Tavares, Leticia; Lopera-Maya, Esteban Alexander; Bonfiglio, Ferdinando; Zheng, Tenghao; Sinha, Trishla; Zanchetta Marques, Francine; Zhernakova, Alexandra; Sanna, Serena; D'Amato, Mauro

A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner

基因组和外显子组混合测序方法能够以无偏倚、高质量且经济高效的方式捕获遗传变异。

Boltz, Toni A; Chu, Benjamin B; Liao, Calwing; Sealock, Julia M; Ye, Robert; Majara, Lerato; Fu, Jack M; Service, Susan; Zhan, Lingyu; Medland, Sarah E; Chapman, Sinéad B; Rubinacci, Simone; DeFelice, Matthew; Grimsby, Jonna L; Abebe, Tamrat; Alemayehu, Melkam; Ashaba, Fred K; Atkinson, Elizabeth G; Bigdeli, Tim; Bradway, Amanda B; Brand, Harrison; Chibnik, Lori B; Fekadu, Abebaw; Gatzen, Michael; Gelaye, Bizu; Gichuru, Stella; Gildea, Marissa L; Hill, Toni C; Huang, Hailiang; Hubbard, Kalyn M; Injera, Wilfred E; James, Roxanne; Joloba, Moses; Kachulis, Christopher; Kalmbach, Phillip R; Kamulegeya, Rogers; Kigen, Gabriel; Kim, Soyeon; Koen, Nastassja; Kwobah, Edith K; Kyebuzibwa, Joseph; Lee, Seungmo; Lennon, Niall J; Lind, Penelope A; Lopera-Maya, Esteban A; Makale, Johnstone; Mangul, Serghei; McMahon, Justin; Mowlem, Pierre; Musinguzi, Henry; Mwema, Rehema M; Nakasujja, Noeline; Newman, Carter P; Nkambule, Lethukuthula L; O'Neil, Conor R; Olivares, Ana Maria; Olsen, Catherine M; Ongeri, Linnet; Parsa, Sophie J; Pretorius, Adele; Ramesar, Raj; Reagan, Faye L; Sabatti, Chiara; Schneider, Jacquelyn A; Shiferaw, Welelta; Stevenson, Anne; Stricker, Erik; Stroud, Rocky E 2nd; Tang, Jessie; Whiteman, David; Yohannes, Mary T; Yu, Mingrui; Yuan, Kai; Akena, Dickens; Atwoli, Lukoye; Kariuki, Symon M; Koenen, Karestan C; Newton, Charles R J C; Stein, Dan J; Teferra, Solomon; Zingela, Zukiswa; Pato, Carlos N; Pato, Michele T; Lopez-Jaramillo, Carlos; Freimer, Nelson; Ophoff, Roel A; Olde Loohuis, Loes M; Talkowski, Michael E; Neale, Benjamin M; Howrigan, Daniel P; Martin, Alicia R

Phenotypic and Genetic Factors Associated with Absence of Cardiomyopathy Symptoms in PLN:c.40_42delAGA Carriers

PLN:c.40_42delAGA 携带者无心肌病症状的表型和遗传因素

Lopera-Maya, Esteban A; Li, Shuang; de Brouwer, Remco; Nolte, Ilja M; van Breen, Justin; Jongbloed, Jan D H; Swertz, Morris A; Snieder, Harold; Franke, Lude; Wijmenga, Cisca; de Boer, Rudolf A; Deelen, Patrick; van der Zwaag, Paul A; Sanna, Serena

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

全球生物银行荟萃分析计划:助力人类疾病的基因发现

Zhou, Wei; Kanai, Masahiro; Wu, Kuan-Han H; Rasheed, Humaira; Tsuo, Kristin; Hirbo, Jibril B; Wang, Ying; Bhattacharya, Arjun; Zhao, Huiling; Namba, Shinichi; Surakka, Ida; Wolford, Brooke N; Lo Faro, Valeria; Lopera-Maya, Esteban A; Läll, Kristi; Favé, Marie-Julie; Partanen, Juulia J; Chapman, Sinéad B; Karjalainen, Juha; Kurki, Mitja; Maasha, Mutaamba; Brumpton, Ben M; Chavan, Sameer; Chen, Tzu-Ting; Daya, Michelle; Ding, Yi; Feng, Yen-Chen A; Guare, Lindsay A; Gignoux, Christopher R; Graham, Sarah E; Hornsby, Whitney E; Ingold, Nathan; Ismail, Said I; Johnson, Ruth; Laisk, Triin; Lin, Kuang; Lv, Jun; Millwood, Iona Y; Moreno-Grau, Sonia; Nam, Kisung; Palta, Priit; Pandit, Anita; Preuss, Michael H; Saad, Chadi; Setia-Verma, Shefali; Thorsteinsdottir, Unnur; Uzunovic, Jasmina; Verma, Anurag; Zawistowski, Matthew; Zhong, Xue; Afifi, Nahla; Al-Dabhani, Kawthar M; Al Thani, Asma; Bradford, Yuki; Campbell, Archie; Crooks, Kristy; de Bock, Geertruida H; Damrauer, Scott M; Douville, Nicholas J; Finer, Sarah; Fritsche, Lars G; Fthenou, Eleni; Gonzalez-Arroyo, Gilberto; Griffiths, Christopher J; Guo, Yu; Hunt, Karen A; Ioannidis, Alexander; Jansonius, Nomdo M; Konuma, Takahiro; Lee, Ming Ta Michael; Lopez-Pineda, Arturo; Matsuda, Yuta; Marioni, Riccardo E; Moatamed, Babak; Nava-Aguilar, Marco A; Numakura, Kensuke; Patil, Snehal; Rafaels, Nicholas; Richmond, Anne; Rojas-Muñoz, Agustin; Shortt, Jonathan A; Straub, Peter; Tao, Ran; Vanderwerff, Brett; Vernekar, Manvi; Veturi, Yogasudha; Barnes, Kathleen C; Boezen, Marike; Chen, Zhengming; Chen, Chia-Yen; Cho, Judy; Smith, George Davey; Finucane, Hilary K; Franke, Lude; Gamazon, Eric R; Ganna, Andrea; Gaunt, Tom R; Ge, Tian; Huang, Hailiang; Huffman, Jennifer; Katsanis, Nicholas; Koskela, Jukka T; Lajonchere, Clara; Law, Matthew H; Li, Liming; Lindgren, Cecilia M; Loos, Ruth J F; MacGregor, Stuart; Matsuda, Koichi; Olsen, Catherine M; Porteous, David J; Shavit, Jordan A; Snieder, Harold; Takano, Tomohiro; Trembath, Richard C; Vonk, Judith M; Whiteman, David C; Wicks, Stephen J; Wijmenga, Cisca; Wright, John; Zheng, Jie; Zhou, Xiang; Awadalla, Philip; Boehnke, Michael; Bustamante, Carlos D; Cox, Nancy J; Fatumo, Segun; Geschwind, Daniel H; Hayward, Caroline; Hveem, Kristian; Kenny, Eimear E; Lee, Seunggeun; Lin, Yen-Feng; Mbarek, Hamdi; Mägi, Reedik; Martin, Hilary C; Medland, Sarah E; Okada, Yukinori; Palotie, Aarno V; Pasaniuc, Bogdan; Rader, Daniel J; Ritchie, Marylyn D; Sanna, Serena; Smoller, Jordan W; Stefansson, Kari; van Heel, David A; Walters, Robin G; Zöllner, Sebastian; Martin, Alicia R; Willer, Cristen J; Daly, Mark J; Neale, Benjamin M

Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility

利用基于症状的病例预测来识别导致 COVID-19 易感性的宿主遗传因素

van Blokland, Irene V; Lanting, Pauline; Ori, Anil P S; Vonk, Judith M; Warmerdam, Robert C A; Herkert, Johanna C; Boulogne, Floranne; Claringbould, Annique; Lopera-Maya, Esteban A; Bartels, Meike; Hottenga, Jouke-Jan; Ganna, Andrea; Karjalainen, Juha; Hayward, Caroline; Fawns-Ritchie, Chloe; Campbell, Archie; Porteous, David; Cirulli, Elizabeth T; Schiabor Barrett, Kelly M; Riffle, Stephen; Bolze, Alexandre; White, Simon; Tanudjaja, Francisco; Wang, Xueqing; Ramirez, Jimmy M 3rd; Lim, Yan Wei; Lu, James T; Washington, Nicole L; de Geus, Eco J C; Deelen, Patrick; Boezen, H Marike; Franke, Lude H

Lack of Association Between Genetic Variants at ACE2 and TMPRSS2 Genes Involved in SARS-CoV-2 Infection and Human Quantitative Phenotypes

SARS-CoV-2感染相关的ACE2和TMPRSS2基因遗传变异与人类定量表型之间缺乏关联

Lopera Maya, Esteban A; van der Graaf, Adriaan; Lanting, Pauline; van der Geest, Marije; Fu, Jingyuan; Swertz, Morris; Franke, Lude; Wijmenga, Cisca; Deelen, Patrick; Zhernakova, Alexandra; Sanna, Serena