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

Understanding how gene-disease relationships can impact clinical utility: adaptations and challenges in hereditary cancer testing

了解基因-疾病关系如何影响临床应用:遗传性癌症检测的适应与挑战

Herrera-Mullar, Jennifer; Horton, Carolyn; Weaver, Amybeth; Towne, Meghan; Huang, Jennifer M; VanNoy, Grace E; Harrison, Steven M; Wayburn, Bess

The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the clinical validity of 111 gene-disease relationships

ClinGen综合征疾病基因注释专家组:评估111个基因-疾病关系的临床有效性

Broeren, Eleanor C; Gitau, Vanessa N; Byrne, Alicia B; Ajuyah, Pamela; Balzotti, Marie B; Berg, Jonathan S; Bluske, Krista; Bowen, B Monica; Brown, Matthew P; Buchanan, Amanda; Burns, Brendan T; Burns, Nicole J; Chandrasekhar, Anjana; Chawla, Aditi; Chong, Jessica X; Chopra, Maya; Clause, Amanda R; DiStefano, Marina T; DiTroia, Stephanie; Elnagheeb, Marwa A; Girod, Amanda N; Goel, Himanshu; Golden-Grant, Katie L; Ha, Thuong; Hamosh, Ada; Huang, Jennifer M; Hughes, Madeline Y; Jamuar, Saumya S; Kam, Sylvia; Kesari, Akanchha; Koh, Ai Ling; Lassiter, Rhonda N T; Leigh, Sarah E; Lemire, Gabrielle; Lim, Jiin Ying; Malhotra, Alka; McCurry, Hannah R; Milewski, Becky; Moosa, Shahida; Murray, Stephen A; Owens, Emma H; Palmer, Elizabeth E; Palus, Brooke C; Patel, Mayher J; Rajkumar, Revathi; Ratliff, Julie C; Raymond, F Lucy; Della Ripa Rodrigues Assis, Bruno; Sajan, Samin A; Schlachetzki, Zinayida; Schmidt, Sarah A; Stark, Zornitza; Strom, Samuel P; Taylor, Julie P; Thaxton, Courtney; Thrush, Devon L; Toro, Sabrina; Tshering, Kezang C; Vasilevsky, Nicole A; Wayburn, Bess; Webb, Ryan F; O'Donnell-Luria, Anne; Coffey, Alison J

CTCF blocks antisense transcription initiation at divergent promoters

CTCF 阻断不同启动子处的反义转录起始

Jing Luan #, Marit W Vermunt #, Camille M Syrett, Allison Coté, Jacob M Tome, Haoyue Zhang, Anran Huang, Jennifer M Luppino, Cheryl A Keller, Belinda M Giardine, Shiping Zhang, Margaret C Dunagin, Zhe Zhang, Eric F Joyce, John T Lis, Arjun Raj, Ross C Hardison, Gerd A Blobel

Diagnostic testing laboratories are valuable partners for disease gene discovery: 5-year experience with GeneMatcher

诊断检测实验室是疾病基因发现的重要合作伙伴:GeneMatcher 五年经验

Towne, Meghan C; Rossi, Mari; Wayburn, Bess; Huang, Jennifer M; Radtke, Kelly; Alcaraz, Wendy; Farwell Hagman, Kelly D; Shinde, Deepali N

Melanocytic Nevi and the Genetic and Epigenetic Control of Oncogene-Induced Senescence

黑素细胞痣与癌基因诱导衰老的遗传和表观遗传控制

Huang, Jennifer M; Chikeka, Ijeuru; Hornyak, Thomas J

Polycomb group proteins--epigenetic repressors with emerging roles in melanocytes and melanoma

多梳蛋白——表观遗传抑制因子,在黑素细胞和黑色素瘤中发挥着新兴作用

Huang, Jennifer M; Hornyak, Thomas J

Imprinting control region (ICR) of the Peg3 domain

Peg3结构域的印记控制区(ICR)

Kim, Joomyeong; Ekram, Muhammad B; Kim, Hana; Faisal, Mohammad; Frey, Wesley D; Huang, Jennifer M; Tran, KimNgoc; Kim, Michelle M; Yu, Sungryul

Identification of an antisense transcript to ZIM2 in the primate lineage

在灵长类谱系中鉴定出ZIM2的反义转录本

Huang, Jennifer M; Yu, Sungryul; Kim, Joomyeong

DNA methylation analysis of the mammalian PEG3 imprinted domain.

哺乳动物PEG3印迹域的DNA甲基化分析

Huang Jennifer M, Kim Joomyeong