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

Evaluation of Long-Read Genome Sequencing for Genomic Profiling of Myeloid Cancers

长读长基因组测序在髓系肿瘤基因组分析中的应用评价

Abel, Haley J; Mahgoub, Mohamed; Davarapalli, Nidhi; Kodgule, Rohan; Miller, Christopher A; Fulton, Robert S; Fronick, Catrina; Markovic, Christopher; Heath, Sharon; Payton, Jacqueline E; Jacoby, Meagan A; Link, Daniel C; Walter, Matthew J; Duncavage, Eric J; Ley, Timothy J; Spencer, David H

Intermediately Methylated Regions in Normal Cells Are Epimutation Hotspots in Cancer

正常细胞中甲基化程度中等的区域是癌症中的表观突变热点。

Mahgoub, Mohamed; Abel, Haley; Davarapalli, Nidhi; Struthers, Heidi; Kotnik, Emilee; Johnson, Brittany; Markovic, Christopher; Fronick, Catrina; Fulton, Robert; Meers, Michael P; Spencer, David H

Persistent Molecular Disease in Adult Patients With AML Evaluated With Whole-Exome and Targeted Error-Corrected DNA Sequencing

利用全外显子组测序和靶向纠错DNA测序评估成人急性髓系白血病患者的持续性分子疾病

Slade, Michael J; Ghasemi, Reza; O'Laughlin, Michelle; Burton, Tasha; Fulton, Robert S; Abel, Haley J; Duncavage, Eric J; Ley, Timothy J; Jacoby, Meagan A; Spencer, David H

Ultra-Deep Sequencing Reveals the Mutational Landscape of Classical Hodgkin Lymphoma.

超深度测序揭示经典霍奇金淋巴瘤的突变图谱

Gomez Felicia, Fisk Bryan, McMichael Joshua F, Mosior Matthew, Foltz Jennifer A, Skidmore Zachary L, Duncavage Eric J, Miller Christopher A, Abel Haley, Li Yi-Shan, Russler-Germain David A, Krysiak Kilannin, Watkins Marcus P, Ramirez Cody A, Schmidt Alina, Martins Rodrigues Fernanda, Trani Lee, Khanna Ajay, Wagner Julia A, Fulton Robert S, Fronick Catrina C, O'Laughlin Michelle D, Schappe Timothy, Cashen Amanda F, Mehta-Shah Neha, Kahl Brad S, Walker Jason, Bartlett Nancy L, Griffith Malachi, Fehniger Todd A, Griffith Obi L

Genomic landscape of TP53 -mutated myeloid malignancies

TP53突变髓系恶性肿瘤的基因组图谱

Abel, Haley J; Oetjen, Karolyn A; Miller, Christopher A; Ramakrishnan, Sai M; Day, Ryan B; Helton, Nichole M; Fronick, Catrina C; Fulton, Robert S; Heath, Sharon E; Tarnawsky, Stefan P; Srivatsan, Sridhar Nonavinkere; Duncavage, Eric J; Schroeder, Molly C; Payton, Jacqueline E; Spencer, David H; Walter, Matthew J; Westervelt, Peter; DiPersio, John F; Ley, Timothy J; Link, Daniel C

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

芬兰男性代谢物的全基因组关联研究发现了与疾病相关的基因位点

Yin, Xianyong; Chan, Lap Sum; Bose, Debraj; Jackson, Anne U; VandeHaar, Peter; Locke, Adam E; Fuchsberger, Christian; Stringham, Heather M; Welch, Ryan; Yu, Ketian; Fernandes Silva, Lilian; Service, Susan K; Zhang, Daiwei; Hector, Emily C; Young, Erica; Ganel, Liron; Das, Indraniel; Abel, Haley; Erdos, Michael R; Bonnycastle, Lori L; Kuusisto, Johanna; Stitziel, Nathan O; Hall, Ira M; Wagner, Gregory R; Kang, Jian; Morrison, Jean; Burant, Charles F; Collins, Francis S; Ripatti, Samuli; Palotie, Aarno; Freimer, Nelson B; Mohlke, Karen L; Scott, Laura J; Wen, Xiaoquan; Fauman, Eric B; Laakso, Markku; Boehnke, Michael

Association of structural variation with cardiometabolic traits in Finns

芬兰人结构变异与心血管代谢特征的关联

Chen, Lei; Abel, Haley J; Das, Indraniel; Larson, David E; Ganel, Liron; Kanchi, Krishna L; Regier, Allison A; Young, Erica P; Kang, Chul Joo; Scott, Alexandra J; Chiang, Colby; Wang, Xinxin; Lu, Shuangjia; Christ, Ryan; Service, Susan K; Chiang, Charleston W K; Havulinna, Aki S; Kuusisto, Johanna; Boehnke, Michael; Laakso, Markku; Palotie, Aarno; Ripatti, Samuli; Freimer, Nelson B; Locke, Adam E; Stitziel, Nathan O; Hall, Ira M

Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences

通过DNA测序测量的人类血液中线粒体基因组拷贝数与代谢特征密切相关,这种关联是通过细胞类型组成差异实现的。

Ganel, Liron; Chen, Lei; Christ, Ryan; Vangipurapu, Jagadish; Young, Erica; Das, Indraniel; Kanchi, Krishna; Larson, David; Regier, Allison; Abel, Haley; Kang, Chul Joo; Scott, Alexandra; Havulinna, Aki; Chiang, Charleston W K; Service, Susan; Freimer, Nelson; Palotie, Aarno; Ripatti, Samuli; Kuusisto, Johanna; Boehnke, Michael; Laakso, Markku; Locke, Adam; Stitziel, Nathan O; Hall, Ira M

Mapping and characterization of structural variation in 17,795 human genomes

对17795个人类基因组的结构变异进行定位和表征

Abel, Haley J; Larson, David E; Regier, Allison A; Chiang, Colby; Das, Indraniel; Kanchi, Krishna L; Layer, Ryan M; Neale, Benjamin M; Salerno, William J; Reeves, Catherine; Buyske, Steven; Matise, Tara C; Muzny, Donna M; Zody, Michael C; Lander, Eric S; Dutcher, Susan K; Stitziel, Nathan O; Hall, Ira M

Exome sequencing of Finnish isolates enhances rare-variant association power

对芬兰分离株进行外显子组测序可增强罕见变异关联分析能力。

Locke, Adam E; Steinberg, Karyn Meltz; Chiang, Charleston W K; Service, Susan K; Havulinna, Aki S; Stell, Laurel; Pirinen, Matti; Abel, Haley J; Chiang, Colby C; Fulton, Robert S; Jackson, Anne U; Kang, Chul Joo; Kanchi, Krishna L; Koboldt, Daniel C; Larson, David E; Nelson, Joanne; Nicholas, Thomas J; Pietilä, Arto; Ramensky, Vasily; Ray, Debashree; Scott, Laura J; Stringham, Heather M; Vangipurapu, Jagadish; Welch, Ryan; Yajnik, Pranav; Yin, Xianyong; Eriksson, Johan G; Ala-Korpela, Mika; Järvelin, Marjo-Riitta; Männikkö, Minna; Laivuori, Hannele; Dutcher, Susan K; Stitziel, Nathan O; Wilson, Richard K; Hall, Ira M; Sabatti, Chiara; Palotie, Aarno; Salomaa, Veikko; Laakso, Markku; Ripatti, Samuli; Boehnke, Michael; Freimer, Nelson B