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

Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis.

GWAS、QTL 和角质形成细胞功能检测的整合揭示了特应性皮炎的分子机制

Oliva Meritxell, Sarkar Mrinal K, March Michael E, Saeidian Amir Hossein, Mentch Frank D, Hsieh Chen-Lin, Tang Fanying, Uppala Ranjitha, Patrick Matthew T, Li Qinmengge, Bogle Rachael, Kahlenberg J Michelle, Watson Deborah, Glessner Joseph T, Youssefian Leila, Vahidnezhad Hassan, Tsoi Lam C, Hakonarson Hakon, Gudjonsson Johann E, Smith Kathleen M, Riley-Gillis Bridget

Copy Number Variant Architecture of Child Psychopathology and Cognitive Development in the ABCD Study

ABCD研究中儿童精神病理学和认知发展的拷贝数变异结构

Sha, Zhiqiang; Sun, Kevin Y; Jung, Benjamin; Barzilay, Ran; Moore, Tyler M; Almasy, Laura; Forsyth, Jennifer K; Prem, Smrithi; Gandal, Michael J; Seidlitz, Jakob; Glessner, Joseph T; Alexander-Bloch, Aaron F

Natural killer cell subpopulations in the peripheral blood of single ventricle/hypoplastic left heart syndrome patients via single-cell RNA sequencing

通过单细胞RNA测序分析单心室/左心发育不全综合征患者外周血中自然杀伤细胞亚群

Qu, Hui-Qi; Goel, Kushagra; Ostberg, Kayleigh; Slater, Diana J; Wang, Fengxiang; Snyder, James; Hou, Cuiping; Eister, Garnet; Connolly, John J; March, Michael; Glessner, Joseph T; Kao, Charlly; Hakonarson, Hakon

Single-Cell RNA Sequencing of Peripheral Blood Mononuclear Cells in Patients With Single Ventricle/Hypoplastic Left Heart Syndrome

单心室/左心发育不全综合征患者外周血单核细胞的单细胞RNA测序

Qu, Hui-Qi; Ostberg, Kayleigh; Slater, Diana J; Wang, Fengxiang; Snyder, James; Hou, Cuiping; Connolly, John J; March, Michael; Glessner, Joseph T; Kao, Charlly; Hakonarson, Hakon

Data-informed insights into sex differences in peripheral blood mononuclear cells from single-cell transcriptomics

基于单细胞转录组学的外周血单核细胞性别差异数据洞察

Qu, Hui-Qi; Glessner, Joseph T; Kao, Charlly; Hakonarson, Hakon

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

针对美国不同人群,筛选、优化和验证十种慢性病多基因风险评分,以用于临床应用

Lennon, Niall J; Kottyan, Leah C; Kachulis, Christopher; Abul-Husn, Noura S; Arias, Josh; Belbin, Gillian; Below, Jennifer E; Berndt, Sonja I; Chung, Wendy K; Cimino, James J; Clayton, Ellen Wright; Connolly, John J; Crosslin, David R; Dikilitas, Ozan; Velez Edwards, Digna R; Feng, QiPing; Fisher, Marissa; Freimuth, Robert R; Ge, Tian; Glessner, Joseph T; Gordon, Adam S; Patterson, Candace; Hakonarson, Hakon; Harden, Maegan; Harr, Margaret; Hirschhorn, Joel N; Hoggart, Clive; Hsu, Li; Irvin, Marguerite R; Jarvik, Gail P; Karlson, Elizabeth W; Khan, Atlas; Khera, Amit; Kiryluk, Krzysztof; Kullo, Iftikhar; Larkin, Katie; Limdi, Nita; Linder, Jodell E; Loos, Ruth J F; Luo, Yuan; Malolepsza, Edyta; Manolio, Teri A; Martin, Lisa J; McCarthy, Li; McNally, Elizabeth M; Meigs, James B; Mersha, Tesfaye B; Mosley, Jonathan D; Musick, Anjene; Namjou, Bahram; Pai, Nihal; Pesce, Lorenzo L; Peters, Ulrike; Peterson, Josh F; Prows, Cynthia A; Puckelwartz, Megan J; Rehm, Heidi L; Roden, Dan M; Rosenthal, Elisabeth A; Rowley, Robb; Sawicki, Konrad Teodor; Schaid, Daniel J; Smit, Roelof A J; Smith, Johanna L; Smoller, Jordan W; Thomas, Minta; Tiwari, Hemant; Toledo, Diana M; Vaitinadin, Nataraja Sarma; Veenstra, David; Walunas, Theresa L; Wang, Zhe; Wei, Wei-Qi; Weng, Chunhua; Wiesner, Georgia L; Yin, Xianyong; Kenny, Eimear E

KOLF2.1J iPSCs carry CNVs associated with neurodevelopmental disorders

KOLF2.1J iPSCs携带与神经发育障碍相关的拷贝数变异(CNV)。

Gracia-Diaz, Carolina; Perdomo, Jonathan E; Khan, Munir E; Roule, Thomas; Disanza, Brianna L; Cajka, Gregory G; Lei, Sunyimeng; Gagne, Alyssa L; Maguire, Jean Ann; Shalem, Ophir; Bhoj, Elizabeth J; Ahrens-Nicklas, Rebecca C; French, Deborah L; Goldberg, Ethan M; Wang, Kai; Glessner, Joseph T; Akizu, Naiara

Genetic Association of Juvenile Idiopathic Arthritis With Adult Rheumatic Disease

幼年特发性关节炎与成人风湿病的遗传关联

Fan, Jingxian; Hao, Jian; Fu, Yuqiao; Liu, Xiaoyang; Qu, Hui-Qi; Glessner, Joseph T; Ji, Dandan; Liu, Wei; Zheng, Gang; Ding, Zhiyong; Cui, Shuzhong; Xia, Qianghua; Hakonarson, Hakon; Wei, Wei; Li, Jin

Mitochondrial DNA Haplogroup K Is Protective Against Autism Spectrum Disorder Risk in Populations of European Ancestry

线粒体DNA单倍群K对欧洲血统人群的自闭症谱系障碍风险具有保护作用

Chang, Xiao; Qu, Hui-Qi; Liu, Yichuan; Glessner, Joseph T; Hakonarson, Hakon

Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

一项跨祖先全基因组关联研究探讨了青春期身高纵向增长及其与成年期健康结果的共同遗传性

Bradfield, Jonathan P; Kember, Rachel L; Ulrich, Anna; Balkhiyarova, Zhanna; Alyass, Akram; Aris, Izzuddin M; Bell, Joshua A; Broadaway, K Alaine; Chen, Zhanghua; Chai, Jin-Fang; Davies, Neil M; Fernandez-Orth, Dietmar; Bustamante, Mariona; Fore, Ruby; Ganguli, Amitavo; Heiskala, Anni; Hottenga, Jouke-Jan; Íñiguez, Carmen; Kobes, Sayuko; Leinonen, Jaakko; Lowry, Estelle; Lyytikainen, Leo-Pekka; Mahajan, Anubha; Pitkänen, Niina; Schnurr, Theresia M; Have, Christian Theil; Strachan, David P; Thiering, Elisabeth; Vogelezang, Suzanne; Wade, Kaitlin H; Wang, Carol A; Wong, Andrew; Holm, Louise Aas; Chesi, Alessandra; Choong, Catherine; Cruz, Miguel; Elliott, Paul; Franks, Steve; Frithioff-Bøjsøe, Christine; Gauderman, W James; Glessner, Joseph T; Gilsanz, Vicente; Griesman, Kendra; Hanson, Robert L; Kaakinen, Marika; Kalkwarf, Heidi; Kelly, Andrea; Kindler, Joseph; Kähönen, Mika; Lanca, Carla; Lappe, Joan; Lee, Nanette R; McCormack, Shana; Mentch, Frank D; Mitchell, Jonathan A; Mononen, Nina; Niinikoski, Harri; Oken, Emily; Pahkala, Katja; Sim, Xueling; Teo, Yik-Ying; Baier, Leslie J; van Beijsterveldt, Toos; Adair, Linda S; Boomsma, Dorret I; de Geus, Eco; Guxens, Mònica; Eriksson, Johan G; Felix, Janine F; Gilliland, Frank D; Biobank, Penn Medicine; Hansen, Torben; Hardy, Rebecca; Hivert, Marie-France; Holm, Jens-Christian; Jaddoe, Vincent W V; Järvelin, Marjo-Riitta; Lehtimäki, Terho; Mackey, David A; Meyre, David; Mohlke, Karen L; Mykkänen, Juha; Oberfield, Sharon; Pennell, Craig E; Perry, John R B; Raitakari, Olli; Rivadeneira, Fernando; Saw, Seang-Mei; Sebert, Sylvain; Shepherd, John A; Standl, Marie; Sørensen, Thorkild I A; Timpson, Nicholas J; Torrent, Maties; Willemsen, Gonneke; Hypponen, Elina; Power, Chris; McCarthy, Mark I; Freathy, Rachel M; Widén, Elisabeth; Hakonarson, Hakon; Prokopenko, Inga; Voight, Benjamin F; Zemel, Babette S; Grant, Struan F A; Cousminer, Diana L