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

Confirmation of COL4A6 variants in X-linked nonsyndromic hearing loss and its clinical implications

证实 X 连锁非综合征性听力损失中存在 COL4A6 变异及其临床意义

O'Brien, Alexander; Aw, Wen Yih; Tee, Hui Yi; Naegeli, Kaleb M; Bademci, Guney; Tekin, Mustafa; Arnos, Kathleen; Pandya, Arti

Parallel Generalized Suffix Tree Construction for Genomic Data

基因组数据的并行广义后缀树构建

Pandya, Arti; O'Brien, Alexander; Kovasala, Michael; Bademci, Guney; Tekin, Mustafa; Arnos, Kathleen S; Aziz, Md Momin Al; Thulasiraman, Parimala; Mohammed, Noman

Corrigendum: Loss of LDAH associated with prostate cancer and hearing loss

更正:前列腺癌和听力丧失与LDAH丢失有关

Currall, Benjamin B; Chen, Ming; Sallari, Richard C; Cotter, Maura; Wong, Kristen E; Robertson, Nahid G; Penney, Kathryn L; Lunardi, Andrea; Reschke, Markus; Hickox, Ann E; Yin, Yanbo; Wong, Garrett T; Fung, Jacqueline; Brown, Kerry K; Williamson, Robin E; Sinnott-Armstrong, Nicholas A; Kammin, Tammy; Ivanov, Andrew; Zepeda-Mendoza, Cinthya J; Shen, Jun; Quade, Bradley J; Signoretti, Sabina; Arnos, Kathleen S; Banks, Alexander S; Patsopoulos, Nikolaos; Liberman, M Charles; Kellis, Manolis; Pandolfi, Pier Paolo; Morton, Cynthia C

A scoping review of interventions to address intimate partner violence in sub-Saharan African healthcare

对撒哈拉以南非洲医疗保健领域应对亲密伴侣暴力的干预措施进行范围界定综述

Young, Cynthia R; Arnos, Diane M; Matthews, Lynn T

Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

与非综合征性听力损失和前庭导水管扩大相关的低功能性SLC26A4变异体:基因型-表型相关性还是偶然的多态性?

Choi, Byung Yoon; Stewart, Andrew K; Madeo, Anne C; Pryor, Shannon P; Lenhard, Suzanne; Kittles, Rick; Eisenman, David; Kim, H Jeffrey; Niparko, John; Thomsen, James; Arnos, Kathleen S; Nance, Walter E; King, Kelly A; Zalewski, Christopher K; Brewer, Carmen C; Shawker, Thomas; Reynolds, James C; Butman, John A; Karniski, Lawrence P; Alper, Seth L; Griffith, Andrew J

A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart

对相隔一个多世纪收集的两组美国耳聋家系进行遗传流行病学比较分析

Arnos, Kathleen S; Welch, Katherine O; Tekin, Mustafa; Norris, Virginia W; Blanton, Susan H; Pandya, Arti; Nance, Walter E

Ethical and social implications of genetic testing for communication disorders

基因检测在沟通障碍方面的伦理和社会影响

Arnos, Kathleen S

SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities

SLC26A4/PDS基因型-表型相关性在伴有前庭导水管扩大(EVA)的听力损失中的作用:证据表明Pendred综合征和非综合征型EVA是不同的临床和遗传实体。

Pryor, S P; Madeo, A C; Reynolds, J C; Sarlis, N J; Arnos, K S; Nance, W E; Yang, Y; Zalewski, C K; Brewer, C C; Butman, J A; Griffith, A J

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

人类对氨基糖苷类抗生素过敏的分子基础

Hutchin, T; Haworth, I; Higashi, K; Fischel-Ghodsian, N; Stoneking, M; Saha, N; Arnos, C; Cortopassi, G