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

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity

对 44,028 名具有高纯合性的英国南亚裔人群进行外显子组测序和分析

Kim, Hye In; DeBoever, Christopher; Walter, Klaudia; Kalantzis, Georgios; Li, Chen; Mozaffari, Sahar V; Kundu, Kousik; Jacobs, Benjamin M; Mohammadi-Shemirani, Pedrum; Musolf, Anthony M; Davitte, Jonathan M; Aksit, Melis A; Gafton, Joseph; Catalano, Katrina A; Dawed, Adem Y; Graham, Robert R; Guo, Bin; Gupta, Namrata; Heng, Teng Hiang; Hunt, Karen A; Iyer, Vivek; Langenberg, Claudia; Lassen, Frederik H; MacArthur, Daniel G; Maher, Eamonn R; Maroteau, Cyrielle; Newman, William G; O'Rahilly, Stephen; Palmer, Duncan S; Popov, Iaroslav; Siddiqui, Moneeza K; Simpson, Michael A; Spreckley, Marie; Wright, John; Del Angel, Guillermo; Petrovski, Slavé; Holzinger, Emily R; Maranville, Joseph C; Addis, Laura; Turner, Richard M; Estrada, Karol; Longerich, Simone; Howson, Joanna M M; Jamshidi, Yalda; Fauman, Eric B; Miller, Melissa R; Diogo, Dorothée; Trembath, Richard C; Finer, Sarah; Martin, Hilary C; van Heel, David A

An Advanced 3D Model of Vascularized Epithelial Ovarian Cancer in a Tumor-on-a-Chip System Based on Multi-Cell Culture

基于多细胞培养的肿瘤芯片系统中血管化上皮性卵巢癌的先进3D模型

Flont, Magdalena; Żuchowska, Agnieszka; Tadko, Oliwia; Konopka, Joanna; Musolf, Paulina; Gnyszka, Agnieszka; Baranowska, Patrycja; Jastrzębska, Elżbieta

Next generation sequencing analysis reveals complex genetic architecture of childhood-onset systemic lupus erythematosus

新一代测序分析揭示了儿童期发病系统性红斑狼疮的复杂遗传结构

Lewandowski, Laura; Hiraki, Linda; Scott, Christiaan; Barrera-Vargas, Ana; Romo Tena, Jorge; Gómez-Martín, Diana; Ombrello, Michael J; Aksentijevich, Ivona; Deng, Zuoming; Musolf, Anthony M; Paul, Subrata; Lu, Shajia; Gadina, Massimo; Hupalo, Daniel; Dalgard, Clifton L; Hasni, Sarfaraz; Silverman, Earl D; Kaplan, Mariana J

Quantifying coordinative patterns in steady‐state running: The impact of footwear and foot strike on joint coupling variability

量化稳态跑步中的协调模式:鞋类和足部着地方式对关节耦合变异性的影响

Seiferheld, Bo Eitel; Lindvald, Martin Vorup; Theodorakos, Ilias; Musolf, Brett Michael; Simonsen, Morten Bilde; Andersen, Michael Skipper; Einafshar, Mohammadjavad Matin; Garofolini, Alessandro; Mickle, Karen J; McLaughlin, Patrick; Taylor, Simon

Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428

全基因组测序发现非综合征性矢状缝早闭与BMP2基因间区和非编码RNA基因LINC01428相关

Musolf, Anthony M; Justice, Cristina M; Erdogan-Yildirim, Zeynep; Goovaerts, Seppe; Cuellar, Araceli; Shaffer, John R; Marazita, Mary L; Claes, Peter; Weinberg, Seth M; Li, Jae; Senders, Craig; Zwienenberg, Marike; Simeonov, Emil; Kaneva, Radka; Roscioli, Tony; Di Pietro, Lorena; Barba, Marta; Lattanzi, Wanda; Cunningham, Michael L; Romitti, Paul A; Boyadjiev, Simeon A

Microresonator photonic wire bond integration for Kerr-microcomb generation

用于克尔微梳生成的微谐振器光子线键合集成

Takabayashi, Alain Yuji; Pavlov, Nikolay; Rosborough, Victoria; Hoffman, Galen; Kanger, Lou; Koushyar, Farzad Mokhtari; Huffman, Taran; Nelson, Mike; Turner, Charles; Johansson, Leif; Musolf, Juergen; Garrett, Henry; Liu, Thomas; Morrison, Gordon; Chembo, Yanne; Mattis, Brian; Nguyen, Thien-An; Van Camp, Mackenzie; Turner, Steven Eugene; Karpov, Maxim; Jost, John; Burkley, Zakary

Double-layer optical fiber interferometer with bio-layer-modified reflector for label-free biosensing of inflammatory proteins

带有生物层改性反射器的双层光纤干涉仪用于炎症蛋白的无标记生物传感

Dariusz Burnat #, Monika Janik #, Norbert Kwietniewski, Agnieszka Martychowiec, Paulina Musolf, Krzysztof Bartnik, Marcin Koba, Tomasz P Rygiel, Joanna Niedziółka-Jönsson, Mateusz Śmietana

Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape

联合多祖源和混合全基因组关联研究揭示了人类颅骨形状背后复杂的遗传机制

Goovaerts, Seppe; Hoskens, Hanne; Eller, Ryan J; Herrick, Noah; Musolf, Anthony M; Justice, Cristina M; Yuan, Meng; Naqvi, Sahin; Lee, Myoung Keun; Vandermeulen, Dirk; Szabo-Rogers, Heather L; Romitti, Paul A; Boyadjiev, Simeon A; Marazita, Mary L; Shaffer, John R; Shriver, Mark D; Wysocka, Joanna; Walsh, Susan; Weinberg, Seth M; Claes, Peter

Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

对多民族人群的罕见变异分析发现了与屈光不正相关的新基因。

Musolf, Anthony M; Haarman, Annechien E G; Luben, Robert N; Ong, Jue-Sheng; Patasova, Karina; Trapero, Rolando Hernandez; Marsh, Joseph; Jain, Ishika; Jain, Riya; Wang, Paul Zhiping; Lewis, Deyana D; Tedja, Milly S; Iglesias, Adriana I; Li, Hengtong; Cowan, Cameron S; Biino, Ginevra; Klein, Alison P; Duggal, Priya; Mackey, David A; Hayward, Caroline; Haller, Toomas; Metspalu, Andres; Wedenoja, Juho; Pärssinen, Olavi; Cheng, Ching-Yu; Saw, Seang-Mei; Stambolian, Dwight; Hysi, Pirro G; Khawaja, Anthony P; Vitart, Veronique; Hammond, Christopher J; van Duijn, Cornelia M; Verhoeven, Virginie J M; Klaver, Caroline C W; Bailey-Wilson, Joan E

A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancer

一种罕见的FGF5候选变异体(rs112475347)与非鳞状非小细胞肺癌的易感性相关

Cannon-Albright, Lisa A; Teerlink, Craig C; Stevens, Jeff; Facelli, Julio C; Carr, Shamus R; Allen-Brady, Kristina; Puri, Sonam; Bailey-Wilson, Joan E; Musolf, Anthony M; Akerley, Wallace