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

Modeling evapotranspiration in diverse climatic zones of Pakistan using Surface Energy Balance Algorithm for Land (SEBAL) through geospatial technologies

利用地理空间技术,采用陆地表面能量平衡算法(SEBAL)对巴基斯坦不同气候带的蒸散量进行建模

Islam, Aneeza; Ali, Syeda Maria; Alamery, Eman Rafi; Faqeih, Khadeijah Yahya; Aldhobaihy, Maha Abdullah; Somayah Moshrif Alamri; Ali, Iftikhar

A novel homozygous CA5A gene deletion in carbonic anhydrase VA deficiency presenting as developmental delay without metabolic crisis

一种新型的碳酸酐酶VA缺乏症纯合CA5A基因缺失,表现为发育迟缓,但无代谢危机。

Bin Hadyan, Maryam F; Saleh, Mohammed A; Aldalaqan, Saad; Mushiba, Aziza M; Alasmari, Ali M; Faqeih, Eissa A; Peer-Zada, Abdul A

Saul Wilson Syndrome: A Case Report With New Features in Saudi Arabia

索尔·威尔逊综合征:沙特阿拉伯一例具有新特征的病例报告

Bin Owaimer, Saad A; Abusrair, Fatimah H; Mutlaq, May R; Faqeih, Eissa A; Abu-Safieh, Leen

Recessive PPTC7 deficiency triggers excessive mitophagy to cause a severe inborn error of metabolism with hypomyelinating leukodystrophy.

隐性 PPTC7 缺陷会引发过度线粒体自噬,从而导致严重的先天性代谢缺陷,并伴有髓鞘形成不足的脑白质营养不良。

Kozul Keri-Lyn, AlAsmari Ali, Alharby Essa, Zakzouk Reem, Yan Youmian, Mushiba Aziza, Alhamad Anwar, Harrelson Emily, Ayach Maya, Cho Kevin, Zahid Heba, Vitorino Francisca De Luna, Searfoss Richard, Liu Xingyu, Saleh Mohammed A, Latif Muhammad, Wei Lianjie, Aldawood Ali, Alsuhaibani Laila, Bafail Mohammed Abdulhafith, Menezes Thiago, Samman Manar, Pletcher Hannah, Sandokji Ibrahim, Borhan Walaa, Lochetto Tessa, Alamri Abrar, Mudayfin Wedad, Syed Mazin, Shriver Leah, Garcia Benjamin, Faqeih Eissa, Patti Gary, Niemi Natalie, Almontashiri Naif

Inherited deficiency of DIAPH1 identifies a DNA double strand break repair pathway regulated by γ-actin.

DIAPH1 的遗传性缺陷揭示了由 α-肌动蛋白调控的 DNA 双链断裂修复途径

Woodward Beth L, Lahiri Sudipta, Chauhan Anoop S, Garcia Marcos Rios, Goodley Lucy E, Clarke Thomas L, Pal Mohinder, Agathanggelou Angelo, Jhujh Satpal S, Ganesh Anil N, Hollins Fay M, Deforie Valentina Galassi, Maroofian Reza, Efthymiou Stephanie, Meinhardt Andrea, Mathew Christopher G, Simpson Michael A, Mefford Heather C, Faqeih Eissa A, Rosenzweig Sergio D, Volpi Stefano, Di Matteo Gigliola, Cancrini Caterina, Scardamaglia Annarita, Shackley Fiona, Davies E Graham, Ibrahim Shahnaz, Arkwright Peter D, Zaki Maha S, Stankovic Tatjana, Taylor A Malcolm R, Mazur Antonina J, Di Donato Nataliya, Houlden Henry, Rothenberg Eli, Stewart Grant S

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

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature

FBXO22 缺陷是一种多效性综合征,表现为生长受限和多系统异常,并伴有独特的表观遗传特征。

Ramakrishna, Navin B; Mohamad Sahari, Umar Bin; Johmura, Yoshikazu; Ali, Nur Ain; Alghamdi, Malak; Bauer, Peter; Khan, Suliman; Ordoñez, Natalia; Ferreira, Mariana; Pinto Basto, Jorge; Alkuraya, Fowzan S; Faqeih, Eissa Ali; Mori, Mari; Almontashiri, Naif A M; Al Shamsi, Aisha; ElGhazali, Gehad; Abu Subieh, Hala; Al Ojaimi, Mode; El-Hattab, Ayman W; Said Al-Kindi, Said Ahmed; Alhashmi, Nadia; Alhabshan, Fahad; Al Saman, Abdulaziz; Tfayli, Hala; Arabi, Mariam; Khalifeh, Simone; Taylor, Alan; Alfadhel, Majid; Jain, Ruchi; Sinha, Shruti; Shenbagam, Shruti; Ramachandran, Revathy; Altunoğlu, Umut; Jacob, Anju; Thalange, Nandu; El Bejjani, Mireille; Perrin, Arnaud; Shin, Jay W; Al-Maawali, Almundher; Al-Shidhani, Azza; Al-Futaisi, Amna; Rabea, Fatma; Chekroun, Ikram; Almarri, Mohamed A; Ohta, Tomohiko; Nakanishi, Makoto; Alsheikh-Ali, Alawi; Ali, Fahad R; Bertoli-Avella, Aida M; Reversade, Bruno; Abou Tayoun, Ahmad

Deep learning framework for mapping nitrate pollution in coastal aquifers under land use pressure

利用深度学习框架绘制土地利用压力下沿海含水层硝酸盐污染图

Chahid, Morad; El-Messari, Jamal Eddine Stitou; Hilal, Ismail; Abdi, Nouhayla; Ali, Tarig; Chakrabortty, Rabin; Faqeih, Khadeijah Yahya; Alamri, Somayah Moshrif; Alamery, Eman Rafi; Tariq, Aqil; Aqnouy, Mourad

Integrating RUSLE, AHP, GIS, and cloud-based geospatial analysis for soil erosion assessment under mediterranean conditions

整合RUSLE、AHP、GIS和基于云的地理空间分析方法,用于地中海地区土壤侵蚀评估

Fadl, Mohamed E; Zekari, Mohammedi; Labad, Rima; Faqeih, Khadeijah Yahya; Abou El-Fadl, Doaa M; Zahra, Wessam R; Mansour, Mohsen M A; Rebouh, Nazih Y; Kucher, Dmitry E; Poddubsky, Anton; Elnagar, Ahmed S; Ali, Elsherbiny A

AHP multi criteria analysis for landslide susceptibility mapping in the Tellian Atlas chain

利用层次分析法(AHP)对泰利安山脉滑坡易发性进行制图

Zighmi, Karim; Zahri, Farid; Faqeih, Khadeijah; Al Amri, Afaf; Riheb, Hadji; Alamri, Somayah Moshrif; Alamery, Eman