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

Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases

全球多族裔全基因组分析鉴定出与甲状腺癌和良性甲状腺疾病相关的基因和生物学通路

White, Samantha L; Brasher, Maizy S; Pattee, Jack; Zhou, Wei; Chapman, Sinéad; Jee, Yon Ho; Bell, Caitlin C; Jamil, Taylor L; Barrio, Martin; Arehart, Christopher H; Evans, Luke M; Hirbo, Jibril; Cox, Nancy J; Straub, Peter; Namba, Shinichi; Bertucci-Richter, Emily; Guare, Lindsay; Edris, Ahmed; Morris, Sam; Mulford, Ashley J; Zhang, Haoyu; Fennessy, Brian; Tobin, Martin D; Chen, Jing; Williams, Alexander T; John, Catherine; van Heel, David A; Mathur, Rohini; Finer, Sarah; Moksnes, Marta R; Brumpton, Ben M; Åsvold, Bjørn Olav; Peculis, Raitis; Rovite, Vita; Konrade, Ilze; Wang, Ying; Crooks, Kristy; Chavan, Sameer; Fisher, Matthew J; Rafaels, Nicholas; Lin, Meng; Shortt, Jonathan A; Sanders, Alan R; Whiteman, David C; MacGregor, Stuart; Medland, Sarah E; Thorsteinsdóttir, Unnur; Stefánsson, Kári; Karaderi, Tugce; Egan, Kathleen M; Bocklage, Therese; McCrary, Hilary C; Riedlinger, Gregory; Salhia, Bodour; Shriver, Craig; Phan, Minh D; Farlow, Janice L; Edge, Stephen; Kaur, Varinder; Churchman, Michelle L; Rounbehler, Robert J; Brock, Pamela L; Ringel, Matthew D; Pividori, Milton; Schweppe, Rebecca; Raeburn, Christopher D; Walters, Robin G; Chen, Zhengming; Li, Liming; Matsuda, Koichi; Okada, Yukinori; Zöllner, Sebastian; Verma, Anurag; Preuss, Michael H; Kenny, Eimear; Hendricks, Audrey E; Fishbein, Lauren; Kraft, Peter; Daly, Mark J; Neale, Benjamin M; Martin, Alicia R; Cole, Joanne B; Haugen, Bryan R; Gignoux, Christopher R; Pozdeyev, Nikita

Mediation of Polygenic Asthma Risk Through Gene Expression

基因表达介导多基因哮喘风险

Natarajan, Rakesh; Szczesny, Brooke; Kanchan, Kanika; Esquinca, Erika; Boorgula, Meher Preethi; Chavan, Sameer; Campbell, Monica; Lorizio, Wendy; Doumatey, Ayo P; Cruz, Alvaro A; Watson, Harold; Naureckas, Edward T; Giles, B Louise; Arinola, Ganiyu; Sogaolu, Olumide; Falade, Adegoke G; Hansel, Nadia N; Olopade, Christopher O; Rotimi, Charles N; Landis, R Clive; Figueiredo, Camila A; Kenny, Eimear E; Ruczinski, Ingo; Liu, Andrew H; Ober, Carole; Taub, Margaret A; Johnson, Randi K; Barnes, Kathleen C; Wojcik, Genevieve L; Mathias, Rasika A

Novel insights into Alzheimer's disease through the study of individuals with Down syndrome

通过对唐氏综合征患者的研究,我们对阿尔茨海默病有了新的认识。

Head, Elizabeth; Cohen, Ann; Fortea, Juan; McGlinchey, Eimear

Factors impacting survival in individuals with Down syndrome-associated Alzheimer's disease

影响唐氏综合征相关阿尔茨海默病患者生存的因素

Benejam, Bessy; McCarron, Mary; Carmona-Iragui, María; Dunne, Pamela; Maure-Blesa, Lucia; Altuna, Miren; Arranz, Javier; Barroeta, Isabel; Bejanin, Alexandre; Soriano, Laura Del Hoyo; Fernández, Susana; Giménez, Sandra; Lleó, Alberto; Lynch, Louise; McCallion, Philip; Mulryan, Niamh; Pertierra, Lucia; Rebillat, Anne-Sophie; Rodríguez-Baz, Íñigo; Hernández, Aida Sanjuan; Vaqué-Alcázar, Lídia; Videla, Laura; Wormald, Andrew; Fortea, Juan; McGlinchey, Eimear

Return of genome-informed risk-assessment results for common conditions to 23,840 adults and children: An eMERGE network study

向 23,840 名成人和儿童反馈常见疾病的基因组信息风险评估结果:一项 eMERGE 网络研究

Lawson, Lucinda P; Prows, Cynthia A; Cortopassi, Josh; Davis, Kyle W; Head, Madilyn; Martin, Lisa J; Perez, Emma F; Sobowale, Agboade; Abul-Husn, Noura S; Bangash, Hana; Bland, Harris T; Bonini, Katherine E; Chisholm, Rex L; Chung, Wendy K; Cimino, James J; Connolly, John J; Crosslin, David R; Freimuth, Robert R; Goff, Blake; Gordon, Adam S; Hakonarson, Hakon; Harr, Margaret H; Henricks, Emma; Hernandez, Valentina; Hoell, Christin; Holm, Ingrid A; Hripcsak, George; Karlson, Elizabeth W; Kenny, Eimear E; Khan, Atlas; Kiryluk, Krzysztof; Kottyan, Leah C; Lennon, Niall J; Limdi, Nita; Linder, Jodell E; Liu, Cong; Manolio, Teri A; Maradik, Mary A; Marathe, Priya N; Maripuri, Devi P; McNally, Elizabeth M; Murphy, Shawn N; Naderian, Mohammadreza; Namjou, Bahram; Odgis, Jacqueline A; Peterson, Josh F; Pineda-Alvarez, Daniel E; Puckelwartz, Megan; Purcell, Jasmine; Rasmussen-Torvik, Laura J; Roden, Dan M; Rosenthal, Elisabeth A; Rowley, Robb; Sabatello, Maya; Scherr, Courtney L; Shaibi, Gabriel Q; Sharp, Richard R; Smoller, Jordan W; Sterling, Rene; Suckiel, Sabrina A; Terek, Shannon; Ting, Yi-Lee; Velez Edwards, Digna R; Walunas, Theresa L; Wei, Wei-Qi; Weng, Chunhua; Wiesner, Georgia L; Xian, Su; Jarvik, Gail P; Kullo, Iftikhar

The Electronic Medical Records and Genomics study: Design and analytic framework for assessing the impact of genome-informed risk assessments

电子病历与基因组学研究:评估基因组信息风险评估影响的设计和分析框架

Limdi, Nita; Beasley, T Mark; Cortopassi, Josh; Davis, Brittney; Bangash, Hana; Chen, Jingheng; Chisholm, Rex L; Chung, Wendy K; Cimino, James J; Connolly, John; Crosslin, David R; Davis, Kyle W; DiVietro, Alanna; Esplin, Edward D; Freimuth, Bob; Gordon, Adam; Hakonarson, Hakon; Hamed, Marwan; He, Megan; Hoell, Christin; Holm, Ingrid; Hripscak, George; Irvin, Margurite R; Jarvik, Gail P; Karavite, Dean; Karlson, Elizabeth W; Kenny, Eimear E; Khan, Atlas; Kiryluk, Krzysztof; Knerr, Sarah; Korf, Bruce; Kottyan, Leah; Kullo, Iftikhar; Larkin, Katie; Lennon, Niall; Linder, Jodell E; Manolio, Teri; Martin, Lisa J; McNally, Elizabeth M; Morse, Jennifer; Murphy, Shawn; Namjou, Bahram; Odgis, Jacqueline A; Orlando, Lori; Pacheco, Jennifer; Peterson, Josh F; Pineda-Alvarez, Daniel E; Prows, Cindy; Puckelwartz, Megan; Purcell, Jasmine; Rasmussen-Torvik, Laura; Rehm, Heidi; Roden, Dan M; Rosenthal, Elisabeth A; Rowley, Robb; Sabatello, Maya; Schaid, Daniel; Sharp, Richard; Smith, Johanna L; Smoller, Jordan W; Soper, Emily R; Sterling, Rene; Suckiel, Sabrina A; Terek, Shannon; Thayer, Jeritt; Ting, Yi-Lee; Tiwari, Hemant; Velez-Edwards, Digna; Wagholikar, Kavishwar B; Walunas, Theresa; Wei, Wei-Qi; Weng, Chunua; Wiesner, Georgia; Abul-Husn, Noura S; Veenstra, David L

A spectral component approach leveraging identity-by-descent graphs to address recent population structure in genomic analysis

利用同源性图的谱成分方法解决基因组分析中近期群体结构问题

Shemirani, Ruhollah; Belbin, Gillian M; Cullina, Sinead; Caggiano, Christa; Gignoux, Christopher R; Zaitlen, Noah; Kenny, Eimear E

Mitochondrial impairment and mTORC1 signalling exhaustion define NK Cell dysfunction progression in melanoma

线粒体功能障碍和 mTORC1 信号通路耗竭是黑色素瘤中 NK 细胞功能障碍进展的特征。

Mylod, Eimear; Behan, Jack; Baier, Dina; Kelleher, Fergal C; Gardiner, Clair M

Signal Transducer and Activator of Transcription (STAT) Proteins Regulate Mucosal-Associated Invariant T (MAIT) Cell Function

信号转导和转录激活因子 (STAT) 蛋白调节黏膜相关不变 T (MAIT) 细胞功能

Cheng, Olivia J; Ryan, Eimear K; Bennett, Michael; Clutter, Christy; Cacioppo, Jackson G; Aubé, Jeffrey; Hogan, Andy E; Leung, Daniel T

A Paediatric Perspective: Opportunities and Challenges in Emergency Department Antimicrobial Stewardship

儿科视角:急诊科抗菌药物管理的机遇与挑战

McCarthy, Karen N; Tedford, Kara; Kitt, Eimear