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

A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF

一项多中心研究揭示了OTOF基因中一种新的致病性剪接位点创始变异。

Brownstein, Zippora; Kamal, Lara; Mishan-Montefiori, Shir; Hoffman, Yael; Fine, Dina; Hirsch, Yoel; Weiden, Tzvi; Birnbaum, Rivka; Mor-Shaked, Hagar; Davidov, Bella; Yaron, Yuval; Avraham, Karen B

Why coaching matters: exploring the interplay of teacher self-regulation and well-being with a longitudinal multigroup model

为什么辅导至关重要:运用纵向多组模型探索教师自我调节与幸福感之间的相互作用

Bührer, Zippora; Wolfgramm, Christine; Berweger, Simone; Keck Frei, Andrea; Bieri Buschor, Christine

Synthetic biodegradable microporous hydrogels for in vitro 3D culture of functional human bone cell networks

合成可生物降解微孔水凝胶用于体外三维培养功能性人体骨细胞网络

Doris Zauchner, Monica Zippora Müller, Marion Horrer, Leana Bissig, Feihu Zhao, Philipp Fisch, Sung Sik Lee, Marcy Zenobi-Wong, Ralph Müller, Xiao-Hua Qin

Heat Stress Tolerance: A Prerequisite for the Selection of Drought- and Low Phosphorus-Tolerant Common Beans for Equatorial Tropical Regions Such as Ghana

耐热性:为加纳等赤道热带地区选择耐旱、耐低磷的普通豆类品种的先决条件

Appiah-Kubi, David; Asibuo, James Yaw; Butare, Louis; Yeboah, Stephen; Appiah-Kubi, Zippora; Kena, Alexander Wireko; Tuffour, Henry Oppong; Akromah, Richard

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

常染色体显性非综合征性听力损失定位于 DFNA33 (13q34),并与磷脂翻转酶基因 ATP11A 中的剪接和移码变异共分离

Justin A Pater, Cindy Penney, Darren D O'Rielly, Anne Griffin, Lara Kamal, Zippora Brownstein, Barbara Vona, Chana Vinkler, Mordechai Shohat, Ortal Barel, Curtis R French, Sushma Singh, Salem Werdyani, Taylor Burt, Nelly Abdelfatah, Jim Houston, Lance P Doucette, Jessica Squires, Fabian Glaser, Nico

COVID-19 in Patients with Inflammatory Bowel Disease: The Israeli Experience

新冠肺炎在炎症性肠病患者中的应用:以色列的经验

Lichtenstein, Lev; Koslowsky, Benjamin; Ben Ya'acov, Ami; Avni-Biron, Irit; Ovadia, Baruch; Ben-Bassat, Ofer; Naftali, Timna; Kopylov, Uri; Haberman, Yael; Eran, Hagar Banai; Eliakim, Rami; Lahat-Zok, Adi; Hirsch, Ayal; Zittan, Eran; Maharshak, Nitsan; Waterman, Matti; Israeli, Eran; Goren, Idan; Ollech, Jacob E; Yanai, Henit; Ungar, Bella; Avidan, Benjamin; Ben Hur, Dana; Melamud, Bernardo; Segol, Ori; Shalem, Zippora; Dotan, Iris; Odes, Selwyn H; Ben-Horin, Shomron; Snir, Yf'at; Milgrom, Yael; Broide, Efrat; Goldin, Eran; Delgado, Shmuel; Ron, Yulia; Cohen, Nathaniel Aviv; Maoz, Eran; Zborovsky, Maya; Odeh, Safwat; Abu Freha, Naim; Shachar, Eyal; Chowers, Yehuda; Engel, Tal; Reiss-Mintz, Hila; Segal, Arie; Zinger, Adar; Bar-Gil Shitrit, Ariella

Molecular Features of SLC26A4 Common Variant p.L117F

SLC26A4 常见变异 p.L117F 的分子特征

Arnoldas Matulevičius, Emanuele Bernardinelli, Zippora Brownstein, Sebastian Roesch, Karen B Avraham, Silvia Dossena

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

MYO15A基因的一个同义变异在德系犹太人群体中富集,由于异常剪接导致常染色体隐性遗传性听力损失。

Hirsch, Yoel; Tangshewinsirikul, Chayada; Booth, Kevin T; Azaiez, Hela; Yefet, Devorah; Quint, Adina; Weiden, Tzvi; Brownstein, Zippora; Macarov, Michal; Davidov, Bella; Pappas, John; Rabin, Rachel; Kenna, Margaret A; Oza, Andrea M; Lafferty, Katherine; Amr, Sami S; Rehm, Heidi L; Kolbe, Diana L; Frees, Kathy; Nishimura, Carla; Luo, Minjie; Farra, Chantal; Morton, Cynthia C; Scher, Sholem Y; Ekstein, Josef; Avraham, Karen B; Smith, Richard J H; Shen, Jun

Stress in teachers of children with neuro-developmental disorders: Effect of blended rational emotive behavioral therapy

神经发育障碍儿童教师的压力:混合式理性情绪行为疗法的效果

Obiweluozo, Patience E; Dike, Ibiwari C; Ogba, Francisca N; Elom, Chinyere O; Orabueze, Florence O; Okoye-Ugwu, Stella; Ani, Casmir Kc; Onu, Augustine O; Ukaogo, Victor; Obayi, Loveline N; Abonyi, Sunday E; Onu, Janefrancis; Omenma, Zippora O; Okoro, Ifeanyichukwu D; Eze, Angela; Igu, Ntasiobi Cn; Onuigbo, Liziana N; Umeano, Elsie C; Onyishi, Charity N

Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder

NOG 相关指关节综合征谱系障碍的遗传异质性和核心临床特征

Ryan J Carlson, Alicia Quesnel, Dawson Wells, Zippora Brownstein, Dror Gilony, Suleyman Gulsuner, Kathleen A Leppig, Karen B Avraham, Mary-Claire King, Tom Walsh, Jay Rubinstein