日期 影响因子
日期:
2020 年 — 2026 年
2020
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2026
影响因子:
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An open-source tool for automated human-level circling behavior detection

一款用于自动检测人类水平绕圈行为的开源工具

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-71665-z
Stanley, O R; Swaminathan, A; Wojahn, E; Bao, C; Ahmed, Z M; Cullen, K E
发表日期：2024
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An Open-Source Tool for Automated Human-Level Circling Behavior Detection

一款用于自动检测人类水平绕圈行为的开源工具

期刊:
影响因子:
doi:10.1101/2023.05.30.540066
Stanley, O R; Swaminathan, A; Wojahn, E; Ahmed, Z M; Cullen, K E
Human
发表日期：2023
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Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

更正：对巴基斯坦近亲结婚家庭进行外显子组测序，发现了30个与隐性智力障碍相关的新候选基因

期刊:Molecular Psychiatry
影响因子:10.1
doi:10.1038/s41380-018-0128-z
Riazuddin, S; Hussain, M; Razzaq, A; Iqbal, Z; Shahzad, M; Polla, D L; Song, Y; van Beusekom, E; Khan, A A; Tomas-Roca, L; Rashid, M; Zahoor, M Y; Wissink-Lindhout, W M; Basra, M A R; Ansar, M; Agha, Z; van Heeswijk, K; Rasheed, F; Van de Vorst, M; Veltman, J A; Gilissen, C; Akram, J; Kleefstra, T; Assir, M Z; Grozeva, D; Carss, K; Raymond, F L; O'Connor, T D; Riazuddin, S A; Khan, S N; Ahmed, Z M; de Brouwer, A P M; van Bokhoven, H; Riazuddin, S
发表日期：2020
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Prevention of stone retropulsion during ureteroscopy: Limitations in resources invites revival of old techniques

输尿管镜检查中结石逆行的预防：资源有限促使人们重新采用旧技术

期刊:Arab Journal of Urology
影响因子:1.2
doi:10.1080/2090598X.2020.1805966
Fathelbab, Tarek K; Abdelhamid, Amr M; Anwar, Ahmed Z M; Galal, Ehab M; El-Hawy, Mamdouh M; Abdelgawad, Ahmed H; Tawfiek, Ehab R
发表日期：2020
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Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

对巴基斯坦近亲结婚家庭的外显子组测序发现了30个与隐性智力障碍相关的新候选基因

期刊:Molecular Psychiatry
影响因子:10.1
doi:10.1038/mp.2016.109
Riazuddin, S; Hussain, M; Razzaq, A; Iqbal, Z; Shahzad, M; Polla, D L; Song, Y; van Beusekom, E; Khan, A A; Tomas-Roca, L; Rashid, M; Zahoor, M Y; Wissink-Lindhout, W M; Basra, M A R; Ansar, M; Agha, Z; van Heeswijk, K; Rasheed, F; Van de Vorst, M; Veltman, J A; Gilissen, C; Akram, J; Kleefstra, T; Assir, M Z; Grozeva, D; Carss, K; Raymond, F L; O'Connor, T D; Riazuddin, S A; Khan, S N; Ahmed, Z M; de Brouwer, A P M; van Bokhoven, H; Riazuddin, S
发表日期：2017
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Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.

人类TMHS基因突变会导致隐性遗传的非综合征性听力损失

期刊:Journal of Medical Genetics
影响因子:3.7
doi:10.1136/jmg.2005.039834
Shabbir M I, Ahmed Z M, Khan S Y, Riazuddin Saima, Waryah A M, Khan S N, Camps R D, Ghosh M, Kabra M, Belyantseva I A, Friedman T B, Riazuddin Sheikh
Human
发表日期：2006
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