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

Effects of TrkB-related induced metaplasticity within the BLA on anxiety, extinction learning, and plasticity in BLA-modulated brain regions

BLA内TrkB相关诱导的元可塑性对焦虑、消退学习以及BLA调控脑区可塑性的影响

Hazra, Joyeeta Dutta; Shrivastava, Kuldeep; Wüstner, Lisa-Sophie; Anunu, Rachel; Chervinsky, Erez; Hazra, Somoday; Beuter, Simone; Kriebel, Martin; Maroun, Mouna; Volkmer, Hansjuergen; Richter-Levin, Gal

Phenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis

对171例综合征型遗传性视网膜疾病患者的表型和基因型特征分析凸显了基因检测在准确临床诊断中的重要性

Kulyamzin, Sofia; Leibu, Rina; Newman, Hadas; Ehrenberg, Miriam; Goldenberg-Cohen, Nitza; Zayit-Soudry, Shiri; Mezer, Eedy; Rotenstreich, Ygal; Deitch, Iris; Panneman, Daan M; Zur, Dinah; Chervinsky, Elena; Shalev, Stavit A; Cremers, Frans P M; Sharon, Dror; Roosing, Susanne; Ben-Yosef, Tamar

National Rapid Genome Sequencing in Neonatal Intensive Care

新生儿重症监护中的国家快速基因组测序

Marom, Daphna; Mory, Adi; Reytan-Miron, Sivan; Amir, Yam; Kurolap, Alina; Cohen, Julia Grinshpun; Morhi, Yocheved; Smolkin, Tatiana; Cohen, Lior; Zangen, Shmuel; Shalata, Adel; Riskin, Arieh; Peleg, Amir; Lavie-Nevo, Karen; Mandel, Dror; Chervinsky, Elana; Fisch, Clari Felszer; Fleisher Sheffer, Vered; Falik-Zaccai, Tzipora C; Rips, Jonathan; Shlomai, Noa Ofek; Friedman, Smadar Eventov; Shporen, Calanit Hershkovich; Ben-Yehoshua, Sagie Josefsberg; Simmonds, Aryeh; Yaacobi, Racheli Goldfarb; Bauer-Rusek, Sofia; Omari, Hussam; Weiss, Karin; Hochwald, Ori; Koifman, Arie; Globus, Omer; Batzir, Nurit Assia; Yaron, Naveh; Segel, Reeval; Morag, Iris; Reish, Orit; Eliyahu, Aviva; Leibovitch, Leah; Schwartz, Marina Eskin; Abramsky, Ramy; Hochberg, Amit; Oron, Anat; Banne, Ehud; Portnov, Igor; Samra, Nadra Nasser; Singer, Amihood; Baris Feldman, Hagit

Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population

教育工具可帮助以色列异质性人群做出知情的基因携带者筛查决策

Gafni-Amsalem, Chen; Aboleil-Zoubi, Olfat; Chervinsky, Elena; Aleme, Ola; Khayat, Morad; Bashir, Husam; Perets, Lilach Peled; Mamluk, Efrat; Hakrosh, Shadia; Kurtzman, Shoshi; Tamir, Liron; Baram-Tsabari, Ayelet; Shalev, Stavit A

Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry

以色列埃塞俄比亚裔犹太人遗传性视网膜疾病的遗传原因

Ben Yosef, Tamar; Banin, Eyal; Chervinsky, Elana; Shalev, Stavit A; Leibu, Rina; Mezer, Eedy; Rotenstreich, Ygal; Goldenberg-Cohen, Nitza; Weiss, Shirel; Khan, Muhammad Imran; Panneman, Daan M; Hitti-Malin, Rebekkah J; Weiner, Chen; Roosing, Susanne; Cremers, Frans P M; Pras, Eran; Zur, Dinah; Newman, Hadas; Deitch, Iris; Sharon, Dror; Ehrenberg, Miriam

Trajectories of Neurologic Recovery 12 Months After Hospitalization for COVID-19: A Prospective Longitudinal Study

新冠肺炎住院治疗12个月后神经功能恢复轨迹:一项前瞻性纵向研究

Frontera, Jennifer A; Yang, Dixon; Medicherla, Chaitanya; Baskharoun, Samuel; Bauman, Kristie; Bell, Lena; Bhagat, Dhristie; Bondi, Steven; Chervinsky, Alexander; Dygert, Levi; Fuchs, Benjamin; Gratch, Daniel; Hasanaj, Lisena; Horng, Jennifer; Huang, Joshua; Jauregui, Ruben; Ji, Yuan; Kahn, D Ethan; Koch, Ethan; Lin, Jessica; Liu, Susan; Olivera, Anlys; Rosenthal, Jonathan; Snyder, Thomas; Stainman, Rebecca; Talmasov, Daniel; Thomas, Betsy; Valdes, Eduard; Zhou, Ting; Zhu, Yingrong; Lewis, Ariane; Lord, Aaron S; Melmed, Kara; Meropol, Sharon B; Thawani, Sujata; Troxel, Andrea B; Yaghi, Shadi; Balcer, Laura J; Wisniewski, Thomas; Galetta, Steven

Homozygote loss-of-function variants in the human COCH gene underlie hearing loss

人类 COCH 基因的纯合功能丧失变异是听力损失的根本原因

Nada Danial-Farran, Elena Chervinsky, Prathamesh T Nadar-Ponniah, Eran Cohen Barak, Shahar Taiber, Morad Khayat, Karen B Avraham, Stavit A Shalev

Keeping the team together: Transformation of an inpatient neurology service at an urban, multi-ethnic, safety net hospital in New York City during COVID-19

维系团队:新冠疫情期间纽约市一家城市多民族公立医院的住院神经科服务的转型

Lord, Aaron S; Lombardi, Nicole; Evans, Katherine; Deveaux, Dewi; Douglas, Elizabeth; Mansfield, Laura; Zakin, Elina; Jakubowska-Sadowska, Katarzyna; Grayson, Kammi; Omari, Mirza; Yaghi, Shadi; Humbert, Kelley; Sanger, Matt; Kim, Sun; Boffa, Michael; Szuchumacher, Mariana; Jongeling, Amy; Vazquez, Blanca; Berberi, Nisida; Kwon, Patrick; Locascio, Gianna; Chervinsky, Alexander; Frontera, Jennifer; Zhou, Ting; Kahn, D Ethan; Abou-Fayssal, Nada

Combined loss of LAP1B and LAP1C results in an early onset multisystemic nuclear envelopathy

LAP1B 和 LAP1C 的共同缺失导致早发性多系统核膜病

Boris Fichtman, Fadia Zagairy, Nitzan Biran, Yiftah Barsheshet, Elena Chervinsky, Ziva Ben Neriah, Avraham Shaag, Michael Assa, Orly Elpeleg, Amnon Harel, Ronen Spiegel

Genetics of hearing loss in the Arab population of Northern Israel

以色列北部阿拉伯人群听力损失的遗传学研究

Danial-Farran, Nada; Brownstein, Zippora; Gulsuner, Suleyman; Tammer, Luna; Khayat, Morad; Aleme, Ola; Chervinsky, Elena; Zoubi, Olfat Aboleile; Walsh, Tom; Ast, Gil; King, Mary-Claire; Avraham, Karen B; Shalev, Stavit A