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

Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

SEM1-DLX5-DLX6 (7q21.3) 基因座中的调控元件参与冠状非综合征性颅缝早闭和骨密度相关性状的遗传控制。

Nicoletti, Paola; Zafer, Samreen; Matok, Lital; Irron, Inbar; Patrick, Meidva; Haklai, Rotem; Evangelista, John Erol; Marino, Giacomo B; Ma'ayan, Avi; Sewda, Anshuman; Holmes, Greg; Britton, Sierra R; Lee, Won Jun; Wu, Meng; Ru, Ying; Arnaud, Eric; Botto, Lorenzo; Brody, Lawrence C; Byren, Jo C; Caggana, Michele; Carmichael, Suzan L; Cilliers, Deirdre; Conway, Kristin; Crawford, Karen; Cuellar, Araceli; Di Rocco, Federico; Engel, Michael; Fearon, Jeffrey; Feldkamp, Marcia L; Finnell, Richard; Fisher, Sarah; Freudlsperger, Christian; Garcia-Fructuoso, Gemma; Hagge, Rhinda; Heuzé, Yann; Harshbarger, Raymond J; Hobbs, Charlotte; Howley, Meredith; Jenkins, Mary M; Johnson, David; Justice, Cristina M; Kane, Alex; Kay, Denise; Gosain, Arun Kumar; Langlois, Peter; Legal-Mallet, Laurence; Lin, Angela E; Mills, James L; Morton, Jenny E V; Noons, Peter; Olshan, Andrew; Persing, John; Phipps, Julie M; Redett, Richard; Reefhuis, Jennita; Rizk, Elias; Samson, Thomas D; Shaw, Gary M; Sicko, Robert; Smith, Nataliya; Staffenberg, David; Stoler, Joan; Sweeney, Elizabeth; Taub, Peter J; Timberlake, Andrew T; Topczewska, Jolanta; Wall, Steven A; Wilson, Alexander F; Wilson, Louise C; Boyadjiev, Simeon A; Wilkie, Andrew O M; Richtsmeier, Joan T; Jabs, Ethylin Wang; Romitti, Paul A; Karasik, David; Birnbaum, Ramon Y; Peter, Inga

Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays

NR2F2基因的杂合罕见变异会导致一种可识别的多发性先天性异常综合征,并伴有发育迟缓。

Ganapathi, Mythily; Matsuoka, Leticia S; March, Michael; Li, Dong; Brokamp, Elly; Benito-Sanz, Sara; White, Susan M; Lachlan, Katherine; Ahimaz, Priyanka; Sewda, Anshuman; Bastarache, Lisa; Thomas-Wilson, Amanda; Stoler, Joan M; Bramswig, Nuria C; Baptista, Julia; Stals, Karen; Demurger, Florence; Cogne, Benjamin; Isidor, Bertrand; Bedeschi, Maria Francesca; Peron, Angela; Amiel, Jeanne; Zackai, Elaine; Schacht, John P; Iglesias, Alejandro D; Morton, Jenny; Schmetz, Ariane; Seidel, Verónica; Lucia, Stephanie; Baskin, Stephanie M; Thiffault, Isabelle; Cogan, Joy D; Gordon, Christopher T; Chung, Wendy K; Bowdin, Sarah; Bhoj, Elizabeth

Correction to: Genetic architecture of cardiometabolic risks in people living with HIV

更正:HIV感染者心血管代谢风险的遗传结构

Cheng, Haoxiang; Sewda, Anshuman; Marquez-Luna, Carla; White, Sierra R; Whitney, Bridget M; Williams-Nguyen, Jessica; Nance, Robin M; Lee, Won Jun; Kitahata, Mari M; Saag, Michael S; Willig, Amanda; Eron, Joseph J; Mathews, W Christopher; Hunt, Peter W; Moore, Richard D; Webel, Allison; Mayer, Kenneth H; Delaney, Joseph A; Crane, Paul K; Crane, Heidi M; Hao, Ke; Peter, Inga

Genetic architecture of cardiometabolic risks in people living with HIV

艾滋病毒感染者心脏代谢风险的遗传结构

Haoxiang Cheng #, Anshuman Sewda #, Carla Marquez-Luna, Sierra R White, Bridget M Whitney, Jessica Williams-Nguyen, Robin M Nance, Won Jun Lee, Mari M Kitahata, Michael S Saag, Amanda Willig, Joseph J Eron, W Christopher Mathews, Peter W Hunt, Richard D Moore, Allison Webel, Kenneth H Mayer, Joseph

Gene-based analyses of the maternal genome implicate maternal effect genes as risk factors for conotruncal heart defects

基于基因的母体基因组分析表明,母体效应基因是圆锥动脉干心脏缺陷的风险因素。

Sewda, Anshuman; Agopian, A J; Goldmuntz, Elizabeth; Hakonarson, Hakon; Morrow, Bernice E; Musfee, Fadi; Taylor, Deanne; Mitchell, Laura E

Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study

HIF1α基因变异与法洛四联症术后患者右心室纤维化负荷相关:一项心血管磁共振研究

Hoang, Thanh T; Manso, Paulo Henrique; Edman, Sharon; Mercer-Rosa, Laura; Mitchell, Laura E; Sewda, Anshuman; Swartz, Michael D; Fogel, Mark A; Agopian, A J; Goldmuntz, Elizabeth

Gene-based genome-wide association studies and meta-analyses of conotruncal heart defects

基于基因的全基因组关联研究和圆锥动脉干心脏缺陷的荟萃分析

Sewda, Anshuman; Agopian, A J; Goldmuntz, Elizabeth; Hakonarson, Hakon; Morrow, Bernice E; Taylor, Deanne; Mitchell, Laura E

A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure

一项针对以色列基布兹的研究揭示了心血管代谢特征的风险因素和微妙的人口结构。

Granot-Hershkovitz, Einat; Karasik, David; Friedlander, Yechiel; Rodriguez-Murillo, Laura; Dorajoo, Rajkumar; Liu, Jianjun; Sewda, Anshuman; Peter, Inga; Carmi, Shai; Hochner, Hagit

Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects

先天性心脏缺陷的全基因组关联研究和荟萃分析

Agopian, A J; Goldmuntz, Elizabeth; Hakonarson, Hakon; Sewda, Anshuman; Taylor, Deanne; Mitchell, Laura E

Cell-surface markers for colon adenoma and adenocarcinoma

结肠腺瘤和腺癌的细胞表面标志物

Kamini Sewda, Domenico Coppola, Steven Enkemann, Binglin Yue, Jongphil Kim, Alexis S Lopez, Jonathan W Wojtkowiak, Valerie E Stark, Brian Morse, David Shibata, Shivakumar Vignesh, David L Morse