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

The early injected genomic region determines sensitivity to Type I restriction-modification defence against Autographiviridae phages

早期注入的基因组区域决定了对I型限制修饰防御机制对抗自噬噬菌体的敏感性。

Martinez-Cazorla, Andrea; Martinez-Jimenez, Christian; Elio-Lucas, Patricia; Fineran, Peter C; Jackson, Simon; Sanchez-Amat, Antonio

In silico, in vitro, and in vivo characterization of thiamin-binding proteins from plant seeds.

对植物种子中硫胺素结合蛋白进行计算机模拟、体外和体内表征

Faustino Maria, Strobbe Simon, Sanchez-Muñoz Raul, Cao Da, Mishra Ratnesh C, Lourenço Tiago, Oliveira M Margarida, Van Der Straeten Dominique

A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes

用于分析额颞叶痴呆症基因亚型的多组学数据集

Kevin Menden, Margherita Francescatto, Tenzin Nyima, Cornelis Blauwendraat, Ashutosh Dhingra, Melissa Castillo-Lizardo, Noémia Fernandes, Lalit Kaurani, Deborah Kronenberg-Versteeg, Burcu Atasu, Eldem Sadikoglou, Barbara Borroni, Salvador Rodriguez-Nieto, Javier Simon-Sanchez, Andre Fischer, David W

Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation

Shariant平台:促进澳大利亚临床基因检测实验室间的证据共享,以支持变异解读。

Tudini, Emma; Andrews, James; Lawrence, David M; King-Smith, Sarah L; Baker, Naomi; Baxter, Leanne; Beilby, John; Bennetts, Bruce; Beshay, Victoria; Black, Michael; Boughtwood, Tiffany F; Brion, Kristian; Cheong, Pak Leng; Christie, Michael; Christodoulou, John; Chong, Belinda; Cox, Kathy; Davis, Mark R; Dejong, Lucas; Dinger, Marcel E; Doig, Kenneth D; Douglas, Evelyn; Dubowsky, Andrew; Ellul, Melissa; Fellowes, Andrew; Fisk, Katrina; Fortuno, Cristina; Friend, Kathryn; Gallagher, Renee L; Gao, Song; Hackett, Emma; Hadler, Johanna; Hipwell, Michael; Ho, Gladys; Hollway, Georgina; Hooper, Amanda J; Kassahn, Karin S; Krishnaraj, Rahul; Lau, Chiyan; Le, Huong; San Leong, Huei; Lundie, Ben; Lunke, Sebastian; Marty, Anthony; McPhillips, Mary; Nguyen, Lan T; Nones, Katia; Palmer, Kristen; Pearson, John V; Quinn, Michael C J; Rawlings, Lesley H; Sadedin, Simon; Sanchez, Louisa; Schreiber, Andreas W; Sigalas, Emanouil; Simsek, Aygul; Soubrier, Julien; Stark, Zornitza; Thompson, Bryony A; U, James; Vakulin, Cassandra G; Wells, Amanda V; Wise, Cheryl A; Woods, Rick; Ziolkowski, Andrew; Brion, Marie-Jo; Scott, Hamish S; Thorne, Natalie P; Spurdle, Amanda B

Cross-sectional study of antimicrobial use and treatment decision for preweaning Canadian dairy calves

加拿大断奶前奶牛犊抗菌药物使用及治疗决策的横断面研究

Uyama, Tamaki; Kelton, David F; Morrison, Emma I; de Jong, Ellen; McCubbin, Kayley D; Barkema, Herman W; Dufour, Simon; Sanchez, Javier; Heider, Luke C; LeBlanc, Stephen J; Winder, Charlotte B; McClure, J T; Renaud, David L

Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia

TSPOAP1 中的双等位基因变异(编码活性区蛋白 RIMBP1)可导致常染色体隐性肌张力障碍

Niccolò E Mencacci, Marisa M Brockmann, Jinye Dai, Sander Pajusalu, Burcu Atasu, Joaquin Campos, Gabriela Pino, Paulina Gonzalez-Latapi, Christopher Patzke, Michael Schwake, Arianna Tucci, Alan Pittman, Javier Simon-Sanchez, Gemma L Carvill, Bettina Balint, Sarah Wiethoff, Thomas T Warner, Apostolos

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

更正:PLCG2 中的非同义突变可降低阿尔茨海默病、路易体痴呆和额颞叶痴呆的风险,并增加长寿的可能性。

van der Lee, Sven J; Conway, Olivia J; Jansen, Iris; Carrasquillo, Minerva M; Kleineidam, Luca; van den Akker, Erik; Hernández, Isabel; van Eijk, Kristel R; Stringa, Najada; Chen, Jason A; Zettergren, Anna; Andlauer, Till F M; Diez-Fairen, Monica; Simon-Sanchez, Javier; Lleó, Alberto; Zetterberg, Henrik; Nygaard, Marianne; Blauwendraat, Cornelis; Savage, Jeanne E; Mengel-From, Jonas; Moreno-Grau, Sonia; Wagner, Michael; Fortea, Juan; Keogh, Michael J; Blennow, Kaj; Skoog, Ingmar; Friese, Manuel A; Pletnikova, Olga; Zulaica, Miren; Lage, Carmen; de Rojas, Itziar; Riedel-Heller, Steffi; Illán-Gala, Ignacio; Wei, Wei; Jeune, Bernard; Orellana, Adelina; Then Bergh, Florian; Wang, Xue; Hulsman, Marc; Beker, Nina; Tesi, Niccolo; Morris, Christopher M; Indakoetxea, Begoña; Collij, Lyduine E; Scherer, Martin; Morenas-Rodríguez, Estrella; Ironside, James W; van Berckel, Bart N M; Alcolea, Daniel; Wiendl, Heinz; Strickland, Samantha L; Pastor, Pau; Rodríguez Rodríguez, Eloy; Boeve, Bradley F; Petersen, Ronald C; Ferman, Tanis J; van Gerpen, Jay A; Reinders, Marcel J T; Uitti, Ryan J; Tárraga, Lluís; Maier, Wolfgang; Dols-Icardo, Oriol; Kawalia, Amit; Dalmasso, Maria Carolina; Boada, Mercè; Zettl, Uwe K; van Schoor, Natasja M; Beekman, Marian; Allen, Mariet; Masliah, Eliezer; de Munain, Adolfo López; Pantelyat, Alexander; Wszolek, Zbigniew K; Ross, Owen A; Dickson, Dennis W; Graff-Radford, Neill R; Knopman, David; Rademakers, Rosa; Lemstra, Afina W; Pijnenburg, Yolande A L; Scheltens, Philip; Gasser, Thomas; Chinnery, Patrick F; Hemmer, Bernhard; Huisman, Martijn A; Troncoso, Juan; Moreno, Fermin; Nohr, Ellen A; Sørensen, Thorkild I A; Heutink, Peter; Sánchez-Juan, Pascual; Posthuma, Danielle; Clarimón, Jordi; Christensen, Kaare; Ertekin-Taner, Nilüfer; Scholz, Sonja W; Ramirez, Alfredo; Ruiz, Agustín; Slagboom, Eline; van der Flier, Wiesje M; Holstege, Henne

Clinical Protocol for a Longitudinal Cohort Study Employing Systems Biology to Identify Markers of Vaccine Immunogenicity in Newborn Infants in The Gambia and Papua New Guinea

一项采用系统生物学方法,在冈比亚和巴布亚新几内亚开展的纵向队列研究的临床方案,旨在识别新生儿疫苗免疫原性的标志物。

Idoko, Olubukola T; Smolen, Kinga K; Wariri, Oghenebrume; Imam, Abdulazeez; Shannon, Casey P; Dibassey, Tida; Diray-Arce, Joann; Darboe, Alansana; Strandmark, Julia; Ben-Othman, Rym; Odumade, Oludare A; McEnaney, Kerry; Amenyogbe, Nelly; Pomat, William S; van Haren, Simon; Sanchez-Schmitz, Guzmán; Brinkman, Ryan R; Steen, Hanno; Hancock, Robert E W; Tebbutt, Scott J; Richmond, Peter C; van den Biggelaar, Anita H J; Kollmann, Tobias R; Levy, Ofer; Ozonoff, Al; Kampmann, Beate

A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

PLCG2基因的非同义突变可降低阿尔茨海默病、路易体痴呆和额颞叶痴呆的风险,并增加长寿的可能性。

van der Lee, Sven J; Conway, Olivia J; Jansen, Iris; Carrasquillo, Minerva M; Kleineidam, Luca; van den Akker, Erik; Hernández, Isabel; van Eijk, Kristel R; Stringa, Najada; Chen, Jason A; Zettergren, Anna; Andlauer, Till F M; Diez-Fairen, Monica; Simon-Sanchez, Javier; Lleó, Alberto; Zetterberg, Henrik; Nygaard, Marianne; Blauwendraat, Cornelis; Savage, Jeanne E; Mengel-From, Jonas; Moreno-Grau, Sonia; Wagner, Michael; Fortea, Juan; Keogh, Michael J; Blennow, Kaj; Skoog, Ingmar; Friese, Manuel A; Pletnikova, Olga; Zulaica, Miren; Lage, Carmen; de Rojas, Itziar; Riedel-Heller, Steffi; Illán-Gala, Ignacio; Wei, Wei; Jeune, Bernard; Orellana, Adelina; Then Bergh, Florian; Wang, Xue; Hulsman, Marc; Beker, Nina; Tesi, Niccolo; Morris, Christopher M; Indakoetxea, Begoña; Collij, Lyduine E; Scherer, Martin; Morenas-Rodríguez, Estrella; Ironside, James W; van Berckel, Bart N M; Alcolea, Daniel; Wiendl, Heinz; Strickland, Samantha L; Pastor, Pau; Rodríguez Rodríguez, Eloy; Boeve, Bradley F; Petersen, Ronald C; Ferman, Tanis J; van Gerpen, Jay A; Reinders, Marcel J T; Uitti, Ryan J; Tárraga, Lluís; Maier, Wolfgang; Dols-Icardo, Oriol; Kawalia, Amit; Dalmasso, Maria Carolina; Boada, Mercè; Zettl, Uwe K; van Schoor, Natasja M; Beekman, Marian; Allen, Mariet; Masliah, Eliezer; de Munain, Adolfo López; Pantelyat, Alexander; Wszolek, Zbigniew K; Ross, Owen A; Dickson, Dennis W; Graff-Radford, Neill R; Knopman, David; Rademakers, Rosa; Lemstra, Afina W; Pijnenburg, Yolande A L; Scheltens, Philip; Gasser, Thomas; Chinnery, Patrick F; Hemmer, Bernhard; Huisman, Martijn A; Troncoso, Juan; Moreno, Fermin; Nohr, Ellen A; Sørensen, Thorkild I A; Heutink, Peter; Sánchez-Juan, Pascual; Posthuma, Danielle; Clarimón, Jordi; Christensen, Kaare; Ertekin-Taner, Nilüfer; Scholz, Sonja W; Ramirez, Alfredo; Ruiz, Agustín; Slagboom, Eline; van der Flier, Wiesje M; Holstege, Henne

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

西班牙帕金森病遗传结构:表征人群特异性风险、差异性单倍型结构并提供病因学见解

Bandres-Ciga, Sara; Ahmed, Sarah; Sabir, Marya S; Blauwendraat, Cornelis; Adarmes-Gómez, Astrid D; Bernal-Bernal, Inmaculada; Bonilla-Toribio, Marta; Buiza-Rueda, Dolores; Carrillo, Fátima; Carrión-Claro, Mario; Gómez-Garre, Pilar; Jesús, Silvia; Labrador-Espinosa, Miguel A; Macias, Daniel; Méndez-Del-Barrio, Carlota; Periñán-Tocino, Teresa; Tejera-Parrado, Cristina; Vargas-González, Laura; Diez-Fairen, Monica; Alvarez, Ignacio; Tartari, Juan Pablo; Buongiorno, Mariateresa; Aguilar, Miquel; Gorostidi, Ana; Bergareche, Jesús Alberto; Mondragon, Elisabet; Vinagre-Aragon, Ana; Croitoru, Ioana; Ruiz-Martínez, Javier; Dols-Icardo, Oriol; Kulisevsky, Jaime; Marín-Lahoz, Juan; Pagonabarraga, Javier; Pascual-Sedano, Berta; Ezquerra, Mario; Cámara, Ana; Compta, Yaroslau; Fernández, Manel; Fernández-Santiago, Rubén; Muñoz, Esteban; Tolosa, Eduard; Valldeoriola, Francesc; Gonzalez-Aramburu, Isabel; Sanchez Rodriguez, Antonio; Sierra, María; Menéndez-González, Manuel; Blazquez, Marta; Garcia, Ciara; Suarez-San Martin, Esther; García-Ruiz, Pedro; Martínez-Castrillo, Juan Carlos; Vela-Desojo, Lydia; Ruz, Clara; Barrero, Francisco Javier; Escamilla-Sevilla, Francisco; Mínguez-Castellanos, Adolfo; Cerdan, Debora; Tabernero, Cesar; Gomez Heredia, Maria Jose; Perez Errazquin, Francisco; Romero-Acebal, Manolo; Feliz, Cici; Lopez-Sendon, Jose Luis; Mata, Marina; Martínez Torres, Irene; Kim, Jonggeol Jeffrey; Dalgard, Clifton L; Brooks, Janet; Saez-Atienzar, Sara; Gibbs, J Raphael; Jorda, Rafael; Botia, Juan A; Bonet-Ponce, Luis; Morrison, Karen E; Clarke, Carl; Tan, Manuela; Morris, Huw; Edsall, Connor; Hernandez, Dena; Simon-Sanchez, Javier; Nalls, Mike A; Scholz, Sonja W; Jimenez-Escrig, Adriano; Duarte, Jacinto; Vives, Francisco; Duran, Raquel; Hoenicka, Janet; Alvarez, Victoria; Infante, Jon; Marti, Maria José; Clarimón, Jordi; López de Munain, Adolfo; Pastor, Pau; Mir, Pablo; Singleton, Andrew