Khan S N相关文献与解析，生知库 | 链接生命科学的每一步

Multi-objective optimization of laser machining parameters for carbon-glass reinforced hybrid composites: Integrating gray relational analysis, regression, and ANN

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

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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Prevalence and antibiotic susceptibility pattern of uropathogens in outpatients at a tertiary care hospital

一家三级医院门诊患者泌尿道病原体的流行情况及抗生素敏感性模式

期刊:New Microbes and New Infections

影响因子:5.4

doi:10.1016/j.nmni.2020.100716

Muhammad, A; Khan, S N; Ali, N; Rehman, M U; Ali, I

微生物学

发表日期：2020

文献求助收藏

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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exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels

exomeSuite：用于快速识别潜在致病性SNV/indel的全外显子组序列变异过滤工具

期刊:Genomics

影响因子:3

doi:10.1016/j.ygeno.2014.02.006

Maranhao, B; Biswas, P; Duncan, J L; Branham, K E; Silva, G A; Naeem, M A; Khan, S N; Riazuddin, S; Hejtmancik, J F; Heckenlively, J R; Riazuddin, S A; Lee, P L; Ayyagari, R

发表日期：2014

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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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Multi-objective optimization of laser machining parameters for carbon-glass reinforced hybrid composites: Integrating gray relational analysis, regression, and ANN

碳-玻璃增强混合复合材料激光加工参数的多目标优化：灰色关联分析、回归分析和人工神经网络的融合

Antibiotic resistance in patients with urinary tract infections in Pakistan

巴基斯坦尿路感染患者的抗生素耐药性

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

Prevalence and antibiotic susceptibility pattern of uropathogens in outpatients at a tertiary care hospital

一家三级医院门诊患者泌尿道病原体的流行情况及抗生素敏感性模式

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

exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels

exomeSuite：用于快速识别潜在致病性SNV/indel的全外显子组序列变异过滤工具

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