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

Local ancestry modulates gene expression: shifting our understanding of genetic regulation and disease association within and across populations

局部祖先特征调节基因表达:改变我们对群体内部和群体间基因调控和疾病关联的理解

Chen, Hung-Hsin; Cai, Yanwei; Graff, MariaElisa; Zhu, Wanying; Petty, Lauren E; Highland, Heather M; Roshani, Rashedah; Polikowsky, Hannah G; Lorenz, Anna S; Frankel, Elizabeth; Landman, Joshua M; Anwar, Mohammad Y; Franson, Elyn E; Haessler, Jeffrey; Avery, Christy L; Young, Kristin L; Fernandez-Rhodes, Lindsay; Reiner, Alexander P; Peters, Ulrike; Gordon-Larsen, Penny; Gamazon, Eric R; Pereira, Alexandre C; Kooperberg, Charles; Huff, Chad D; Fisher-Hoch, Susan P; McCormick, Joseph B; North, Kari E; Below, Jennifer E

Large-scale genome-wide analyses of stuttering

大规模全基因组口吃分析

Polikowsky, Hannah G; Scartozzi, Alyssa C; Shaw, Douglas M; Pruett, Dillon G; Chen, Hung-Hsin; Petty, Lauren E; Petty, Alexander S; Lowther, Emily J; Cho, Shu-Hsien; Yu, Yao; Mozaffari, Sahar; Avery, Christy L; Harris, Kathleen Mullan; Gordon, Reyna L; Beilby, Janet M; Viljoen, Kathryn Z; Jones, Robin M; Huff, Chad D; Highland, Heather M; Kraft, Shelly Jo; Below, Jennifer E

Genomic Characterization of High-Grade Serous Ovarian Carcinoma Reveals Distinct Somatic Features in Black Individuals

高级别浆液性卵巢癌的基因组特征分析揭示了黑人个体独特的体细胞特征

Lawson-Michod, Katherine A; Marks, Jeffrey R; Collin, Lindsay J; Nix, David A; Davidson, Natalie R; Huff, Chad D; Yu, Yao; Atkinson, Aaron; Johnson, Courtney E; Salas, Lucas A; Peres, Lauren C; Greene, Casey S; Schildkraut, Joellen M; Doherty, Jennifer A

Co-occurrence of congenital anomalies and childhood brain tumors in 22 million live births

2200万活产婴儿中先天性异常与儿童脑肿瘤同时发生

Hoang, Thanh T; Schraw, Jeremy M; Shumate, Charles; Desrosiers, Tania A; Nembhard, Wendy N; Yazdy, Mahsa; Nestoridi, Eirini; Janitz, Amanda E; Kirby, Russell S; Salemi, Jason L; Tanner, Jean Paul; Chambers, Tiffany M; Taylor, Michael D; Huff, Chad D; Plon, Sharon E; Lupo, Philip J; Scheurer, Michael E

COMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstruction

COMPADRE:结合谱系信息的远亲关系估计方法,用于改进谱系重建

Evans, Grahame F; Baker, James T; Petty, Lauren E; Petty, Alexander S; Polikowsky, Hannah G; Bohlender, Ryan J; Chen, Hung-Hsin; Chou, Che-Yu; Viljoen, Kathryn Z; Beilby, Janet M; Kraft, Shelly Jo; Zhu, Wanying; Landman, Joshua M; Morrow, Autumn R; Bian, Dayi; Scartozzi, Alyssa C; Huff, Chad D; Below, Jennifer E

Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer

一项针对398,238名女性的全基因组关联研究揭示了与高级别浆液性卵巢癌相关的七个基因位点

Barnes, Daniel R; Tyrer, Jonathan P; Dennis, Joe; Leslie, Goska; Bolla, Manjeet K; Lush, Michael; Aeilts, Amber M; Aittomäki, Kristiina; Andrieu, Nadine; Andrulis, Irene L; Anton-Culver, Hoda; Arason, Adalgeir; Arun, Banu K; Balmaña, Judith; Bandera, Elisa V; Barkardottir, Rosa B; Berger, Lieke P V; Berrington de Gonzalez, Amy; Berthet, Pascaline; Białkowska, Katarzyna; Bjørge, Line; Blanco, Amie M; Blok, Marinus J; Bobolis, Kristie A; Bogdanova, Natalia V; Brenton, James D; Butz, Henriett; Buys, Saundra S; Caligo, Maria A; Campbell, Ian; Castillo, Carmen; Claes, Kathleen B M; Colonna, Sarah V; Cook, Linda S; Daly, Mary B; Dansonka-Mieszkowska, Agnieszka; de la Hoya, Miguel; deFazio, Anna; DePersia, Allison; Ding, Yuan Chun; Doherty, Jennifer A; Domchek, Susan M; Dörk, Thilo; Einbeigi, Zakaria; Engel, Christoph; Evans, D Gareth; Foretova, Lenka; Fortner, Renée T; Fostira, Florentia; Foti, Maria Cristina; Friedman, Eitan; Frone, Megan N; Ganz, Patricia A; Gentry-Maharaj, Aleksandra; Glendon, Gord; Godwin, Andrew K; González-Neira, Anna; Greene, Mark H; Gronwald, Jacek; Guerrieri-Gonzaga, Aliana; Hamann, Ute; Hansen, Thomas V O; Harris, Holly R; Hauke, Jan; Heitz, Florian; Hogervorst, Frans B L; Hooning, Maartje J; Hopper, John L; Huff, Chad D; Huntsman, David G; Imyanitov, Evgeny N; Izatt, Louise; Jakubowska, Anna; James, Paul A; Janavicius, Ramunas; John, Esther M; Kar, Siddhartha; Karlan, Beth Y; Kennedy, Catherine J; Kiemeney, Lambertus A L M; Konstantopoulou, Irene; Kupryjanczyk, Jolanta; Laitman, Yael; Lavie, Ofer; Lawrenson, Kate; Lester, Jenny; Lesueur, Fabienne; Lopez-Pleguezuelos, Carlos; Mai, Phuong L; Manoukian, Siranoush; May, Taymaa; McNeish, Iain A; Menon, Usha; Milne, Roger L; Modugno, Francesmary; Mongiovi, Jennifer M; Montagna, Marco; Moysich, Kirsten B; Neuhausen, Susan L; Nielsen, Finn C; Noguès, Catherine; Oláh, Edit; Olopade, Olufunmilayo I; Osorio, Ana; Papi, Laura; Pathak, Harsh; Pearce, Celeste L; Pedersen, Inge S; Peixoto, Ana; Pejovic, Tanja; Peng, Pei-Chen; Peshkin, Beth N; Peterlongo, Paolo; Powell, C Bethan; Prokofyeva, Darya; Pujana, Miquel Angel; Radice, Paolo; Rashid, Muhammad U; Rennert, Gad; Richenberg, George; Sandler, Dale P; Sasamoto, Naoko; Setiawan, Veronica W; Sharma, Priyanka; Sieh, Weiva; Singer, Christian F; Snape, Katie; Sokolenko, Anna P; Soucy, Penny; Southey, Melissa C; Stoppa-Lyonnet, Dominique; Sutphen, Rebecca; Sutter, Christian; Tan, Yen Y; Teixeira, Manuel R; Terry, Kathryn L; Thomsen, Liv Cecilie V; Tischkowitz, Marc; Toland, Amanda E; Van Gorp, Toon; Vega, Ana; Velez Edwards, Digna R; Webb, Penelope M; Weitzel, Jeffrey N; Wentzensen, Nicolas; Whittemore, Alice S; Winham, Stacey J; Wu, Anna H; Yadav, Siddhartha; Yu, Yao; Ziogas, Argyrios; Berchuck, Andrew; Couch, Fergus J; Goode, Ellen L; Goodman, Marc T; Monteiro, Alvaro N; Offit, Kenneth; Ramus, Susan J; Risch, Harvey A; Schildkraut, Joellen M; Thomassen, Mads; Simard, Jacques; Easton, Douglas F; Jones, Michelle R; Chenevix-Trench, Georgia; Gayther, Simon A; Antoniou, Antonis C; Pharoah, Paul D P

Structural birth defects and leukemia risk in children with Down syndrome

唐氏综合征患儿的结构性出生缺陷和白血病风险

Hsu, Ching-Ju; Schraw, Jeremy M; Rasmussen, Sonja A; Chambers, Tiffany M; Desrosiers, Tania A; Huff, Chad D; Janitz, Amanda E; Kirby, Russell S; Nestoridi, Eirini; Nembhard, Wendy N; Salemi, Jason L; Shumate, Charles; Tanner, Jean Paul; Yazdy, Mahsa M; Scheurer, Michael E; Rabin, Karen R; Lupo, Philip J

Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopies

对 BRCA1/2 阴性家族中遗传性乳腺癌和卵巢癌进行靶向测序,揭示了复杂的遗传结构和表型模拟。

Plowman, Jocelyn N; Matoy, Evanjalina J; Uppala, Lavanya V; Draves, Samantha B; Watson, Cynthia J; Sefranek, Bridget A; Stacey, Mark L; Anderson, Samuel P; Belshan, Michael A; Blue, Elizabeth E; Huff, Chad D; Fu, Yusi; Stessman, Holly A F

The impact of genetic ancestry on survival outcomes in pediatric rhabdomyosarcoma: A report from the Children's Oncology Group

遗传祖先对儿童横纹肌肉瘤生存结局的影响:来自儿童肿瘤协作组的报告

Onwuka, Ekene A; Magyar, Christina L; Martin-Giacalone, Bailey A; Scheurer, Michael E; Marquez-Do, Deborah A; Zobeck, Mark; Atkinson, Elizabeth G; Rudzinski, Erin R; Arnold, Michael A; Barkauskas, Donald A; Hall, David; Khan, Javed; Shern, Jack F; Scheet, Paul; Crompton, Brian; Linardic, Corinne M; Hawkins, Douglas S; Venkatramani, Rajkumar; Mirabello, Lisa; Huff, Chad D; Richard, Melissa A; Lupo, Philip J

Homologous Recombination Deficiency and Survival in Ovarian High-Grade Serous Carcinoma by Self-Reported Race

根据自我报告的种族,同源重组缺陷与卵巢高级别浆液性癌患者的生存率之间的关系

Lawson-Michod, Katherine A; Johnson, Courtney E; Barnard, Mollie E; Davidson, Natalie R; Collin, Lindsay J; Nix, David A; Huff, Chad D; Berchuck, Andrew; Salas, Lucas A; Greene, Casey S; Marks, Jeffrey R; Peres, Lauren C; Doherty, Jennifer A; Schildkraut, Joellen M