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

Adult genomic medicine: lessons from a multisite study of 2700 patients

成人基因组医学:一项纳入2700名患者的多中心研究的经验教训

Bakur, Khadijah; Hamid, Halima; Alhaddad, Bader; Alfadhel, Majid; Alhashem, Amal; Eyaid, Wafaa; Alanzi, Talal; Al Mutairi, Fuad; Alswaid, Abdulrahman; Ababneh, Farouq; Al Ghamdi, Malak; Mohamed, Sarar; Alaskar, Ahmed; Alqahtani, Farjah; Alzaidan, Hamad; Al-Owain, Mohammed; Faqeih, Eissa A; Mushiba, Aziza M; Alanazi, Rola; Almoallem, Basamat; Alsaleh, Norah Saleh; Al Tala, Saeed; Alshammari, Muneera; Turkistani, Alyazeed; Gosadi, Ghadah; Hakami, Fahad; Alobaid, Fahad; Al Rukban, Hadeel; Alfaidi, Ahmed; Ba-Abbad, Rola; Almuqbil, Mohammed A; Al-Boukai, Ahmad; Alamri, Abdulrahman Saad; Alshehri, Ali; Sulaiman, Raashda A; Almontasheri, Ali; Danish, Enam; AlSagheir, Afaf; Aljeaid, Deema; Al-Awam, Bashayer S; Shawli, Aiman; Al-Otaibi, Maha; Majdali, Wed Sameer; Azher, Zohor Asaad; Almannai, Mohammed; Baalawi, Wail; AlAbdi, Lama; Benoukraf, Touati; Alkuraya, Fowzan S

Clinical Practice, Challenges, and the Future of Ophthalmic Genetics in Saudi Arabia

沙特阿拉伯眼科遗传学的临床实践、挑战和未来

AlMoallem, Basamat; Alsuwailem, Ghadah; Alqahtani, Nadeef; Alshammari, Layan; Alkhodier, Abeer

Imaging hot photocarrier transfer across a semiconductor heterojunction with ultrafast electron microscopy

利用超快电子显微镜对半导体异质结中的热光载流子转移进行成像

Shaheen, Basamat S; Huynh, Kenny; Quan, Yujie; Choudhry, Usama; Gnabasik, Ryan; Xiang, Zeyu; Goorsky, Mark; Liao, Bolin

In Vitro: The Extraordinary Enhancement in Rutin Accumulation and Antioxidant Activity in Philodendron "Imperial Red" Plantlets Using Ti-Mo-Ni-O Nanotubes as a Novel Elicitor

体外实验:以Ti-Mo-Ni-O纳米管为新型诱导剂,显著提高“帝王红”蔓绿绒幼苗中芦丁的积累和抗氧化活性。

Ebrahim, Hanan S; Deyab, Nourhan M; Shaheen, Basamat S; Gabr, Ahmed M M; Allam, Nageh K

Mapping the pathways of photo-induced ion migration in organic-inorganic hybrid halide perovskites

绘制有机-无机杂化卤化物钙钛矿中光诱导离子迁移的路径

Taeyong Kim, Soyeon Park, Vasudevan Iyer, Basamat Shaheen, Usama Choudhry, Qi Jiang, Gage Eichman, Ryan Gnabasik, Kyle Kelley, Benjamin Lawrie, Kai Zhu, Bolin Liao

Unique phenotypic-genotypic correlation in Saudi patients with ALMS1 mutations

沙特阿拉伯ALMS1突变患者独特的表型-基因型相关性

Almoallem, Basamat M

Unique Roberts syndrome with bilateral congenital glaucoma: A case report

伴有双侧先天性青光眼的独特罗伯茨综合征:病例报告

Almulhim, Amar; Almoallem, Basamat; Alsirrhy, Ehab; Osman, Essam A

Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement

RIMS2功能丧失会导致一种伴有神经发育和胰腺受累的综合征性先天性锥杆突触疾病

Mechaussier, Sabrina; Almoallem, Basamat; Zeitz, Christina; Van Schil, Kristof; Jeddawi, Laila; Van Dorpe, Jo; Rey, Alfredo Dueñas; Condroyer, Christel; Pelle, Olivier; Polak, Michel; Boddaert, Nathalie; Bahi-Buisson, Nadia; Cavallin, Mara; Bacquet, Jean-Louis; Mouallem-Bézière, Alexandra; Zambrowski, Olivia; Sahel, José Alain; Audo, Isabelle; Kaplan, Josseline; Rozet, Jean-Michel; De Baere, Elfride; Perrault, Isabelle

Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement

RIMS2 功能丧失导致综合征性先天性锥杆突触疾病,伴有神经发育和胰腺受累

Sabrina Mechaussier, Basamat Almoallem, Christina Zeitz, Kristof Van Schil, Laila Jeddawi, Jo Van Dorpe, Alfredo Dueñas Rey, Christel Condroyer, Olivier Pelle, Michel Polak, Nathalie Boddaert, Nadia Bahi-Buisson, Mara Cavallin, Jean-Louis Bacquet, Alexandra Mouallem-Bézière, Olivia Zambrowski, José

The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56.

大多数常染色体隐性小眼球症和后部小眼球症可归因于 MFRP 和 PRSS56 的双等位基因序列和结构变异

Almoallem Basamat, Arno Gavin, De Zaeytijd Julie, Verdin Hannah, Balikova Irina, Casteels Ingele, de Ravel Thomy, Hull Sarah, Suzani Martina, Destrée Anne, Peng Michelle, Williams Denise, Ainsworth John R, Webster Andrew R, Leroy Bart P, Moore Anthony T, De Baere Elfride