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Sadaf Naz

university of the punjab

26H指数
145论文数
3.3K被引数
收录论文 46
发表时间
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Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from Pakistan遗传学研究确定了巴基斯坦近亲结婚家庭中隐性遗传中度至重度听力损失的已知和新型变异体
errScientific Reports
IF3.9
err2026-05-05
err0
errOAAI
errMemoona Ramzan; Hafiza Idrees; Hina Khan; Rabia Faridi; Zunaira Munir; Fariha Muzaffar; Kanwal Shabbir; Ayesha Imtiaz; Muhammad Noman; Alina Ahmed; Rasheeda Bashir; Niaz Muhammad Khan; Azra Maqsood; Ghulam Mujtaba; Midhat Salman; Ihtisham Bukhari; Hafiz Muhammad Waqas Munir; Huma Tariq; Muhammad Waqas; Muhammad N. Iqbal; Elizabeth Wohler; P. Dane Witmer; Nara Sobreira; Robert J. Morell; Go Hun Seo; Sayaka Inagaki; Thomas B. Friedman; Sadaf Naz
err分享
err收藏
Assessment of Coagulansin-A’s therapeutic potential and safety in an ovalbumin (OVA) induced airway inflammation model评估凝血素-A在卵清蛋白（OVA）诱导的气道炎症模型中的治疗潜力和安全性
errInflammopharmacology
IF5.3
err2026-04-17
err0
PREAI
errSadaf Naz; Muhammad Usama Mazhar; Aimen Wajid; Rimsha Noor; Lin Zhu; Muhammad Khalid Tipu
err分享
err收藏
Exploration of structural, magnetic, electrical polarization, optical and microwave absorption properties of rGO/hexaferrites composites研究rGO/六方铁氧体复合材料的结构、磁学、电学极化、光学和微波吸收性能
errPOLYHEDRON
IF2.6
err2025-12-01
err0
PREAI
errAli, Mehboob; Sharif, Saba; Sadiq, Farhan; Aslam, Humaira; Altaf, Zainab; Naz, Sadaf; Sadiq, Imran; Alghamdi, Eman. A.; Raheel, Muhammad; Shahbaz, Muhammad; Riaz, Saira; Naseem, Shahzad
err分享
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A truncated CDC14A retains catalytic structure and phosphatase activity preserving male fertility but causes nonsyndromic deafness截断的CDC14A保留了催化结构和磷酸酶活性，保留了男性生育能力，但导致了非综合征性耳聋。
errJournal of Biological Chemistry
IF3.9
err2025-11-25
err0
errOAAI
errKanwal Shabbir; Gina Jackisch; Inna A. Belyantseva; Muhammad Imran; Sadaf Naz; Céleste Sele; Victoriia Murina; Wolfgang Knecht; Thomas B. Friedman; Derek T. Logan; Ayesha Imtiaz
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Insights on inflammatory pathways and their cross-talk: a comprehensive review on asthma炎症通路及其相互作用的研究进展：哮喘的全面综述
errMolecular Biology Reports
IF2.8
err2025-11-01
err0
PREAI
errSadaf Naz; Aimen Wajid; Marya Nawaz Malik; Muhammad Khalid Tipu
err分享
err收藏
Synergistic effects of selected ethnomedicinal plants with Metronidazole against resistant H. Pylori, and their urease inhibition mechanism所选用民族药物植物与甲硝唑协同对抗耐药性幽门螺杆菌的效果及其脲酶抑制机制
errSouth African Journal of Botany
IF2.7
err2025-10-14
err0
PREAI
errSania Atta; Marya Nawaz Malik; Muhammad Tahir Aqeel; Iffat Naz; Nadeem Irshad; Sadaf Naz; Nadeem ul Hassan Khan; Faisal Rasheed; Humaira Fatima
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err收藏
Synthesis and Characterization of V2O5/rGO Hybrid Nanowire Composites as Electrode Materials for Energy Storage ApplicationsV2O5/rGO杂化纳米线复合材料的合成与表征及其在储能应用中的电极材料研究
errJournal of Inorganic and Organometallic Polymers and Materials
IF4.9
err2025-08-28
err0
PREAI
errN. A. Niaz; Sadaf Naz; Abdul Shakoor Khan; Fayyaz Hussain; Mudasra Kanwal; Aqsa Arooj; Sarfraz Ahmad; Demet Ozer; Munazza Tariq; Ammar Mohamed Tighezza
err分享
err收藏
Rare Homozygous Variants in INSR and NFXL1 Are Associated with Severe Treatment-Resistant PsychosisINSR和NFXL1基因中的罕见纯合子变异与严重难治性精神病相关联
errINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
IF4.9
err2025-05-21
err0
errOAAI
errKanwal, Ambreen; Zulfiqar, Rimsha; Cheema, Husnain Arshad; Jabbar, Nauman; Iftikhar, Amina; Butt, Amina Iftikhar; Sheikh, Sohail A.; Pardo, Jose V.; Naz, Sadaf
err分享
err收藏
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss
errSCIENTIFIC REPORTS
IF3.9
err2024-09-13
err0
errOAAI
errKhan, Hina; Muzaffar, Fariha; Salman, Midhat; Bashir, Rasheeda; Seo, Go Hun; Naz, Sadaf
err分享
err收藏
In vivo evaluation of efficacy and safety of Coagulansin-A in treating arthritis
errTOXICOLOGY AND APPLIED PHARMACOLOGY
IF3.4
err2024-08-01
err0
PREAI
errNaz, Sadaf; Mazhar, Muhammad Usama; Faiz, Sidra; Malik, Maria Nawaz; Khan, Jehan Zeb; Ul Haq, Ihsan; Zhu, Lin; Tipu, Muhammad Khalid
err分享
err收藏
Identification and analyses of exonic and copy number variants in spastic paraplegia
errSCIENTIFIC REPORTS
IF3.9
err2024-06-21
err0
errOAAI
errShafique, Anum; Nadeem, Ayesha; Aslam, Faiza; Manzoor, Humera; Noman, Muhammad; Wohler, Elizabeth; Witmer, P. Dane; Sobreira, Nara; Naz, Sadaf
err分享
err收藏
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss
errHUMAN GENETICS
IF3.6
err2024-03-09
err2
errOAAI
errRedfield, Shelby E.; De-la-Torre, Pedro; Zamani, Mina; Wang, Hanjun; Khan, Hina; Morris, Tyler; Shariati, Gholamreza; Karimi, Majid; Kenna, Margaret A.; Seo, Go Hun; Xu, Hongen; Lu, Wei; Naz, Sadaf; Galehdari, Hamid; Indzhykulian, Artur A.; Shearer, A. Eliot; Vona, Barbara
err分享
err收藏
Immunostimulant, hepatoprotective, and nephroprotective potential of Bacillus subtilis (NMCC-path-14) in comparison to dexamethasone in alleviating CFA-induced arthritis
errNAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY
IF3.1
err2023-11-06
err1
PREAI
errMazhar, Muhammad Usama; Naz, Sadaf; Zulfiqar, Tayyaba; Khan, Jehan Zeb; Ghazanfar, Shakira; Tipu, Muhammad Khalid
err分享
err收藏
Raveling out the effect of Pr3+ ions substitution on different properties of nano-sized hexagonal ferrites
errMATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS
IF4.6
err2023-11-01
err7
PREAI
errRamzan, Azka; Naz, Sadaf; Zubair, Azqa; Sadiq, Imran; Abbas, Qammar; Sadiq, Farhan; Shahbaz, Muhammad; Saeed, Samreen; Idrees, Mishal; Hussain, Sajjad; Riaz, Saira; Naseem, Shahzad
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A biallelic variant of DCAF13 implicated in a neuromuscular disorder in humans
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2023-02-17
err4
PREAI
errManzoor, Humera; Zahid, Hafsa; Emerling, Christopher A.; Kumar, Kishore R.; Hussain, Hafiz Muhammad Jafar; Seo, Go Hun; Wajid, Muhammad; Naz, Sadaf
err分享
err收藏
Preliminary studies on apparent mendelian psychotic disorders in consanguineous families
errBMC PSYCHIATRY
IF3.6
err2022-11-16
err2
errOAAI
errKanwal, Ambreen; Sheikh, Sohail A.; Iftikhar, Amina; Naz, Sadaf; Pardo, Jose, V
err分享
err收藏
RGS3 and IL1RAPL1 missense variants implicate defective neurotransmission in early-onset inherited schizophrenias
errJOURNAL OF PSYCHIATRY & NEUROSCIENCE
IF3.3
err2022-11-01
err5
errOAAI
errKanwal, Ambreen; Pardo, Jose V.; Naz, Sadaf
err分享
err收藏
MRM2 variants in families with complex dystonic syndromes: evidence for phenotypic heterogeneity
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2022-08-24
err1
PREAI
errShafique, Anum; Arif, Beenish; Chu, Mary Lynn; Moran, Ellen; Hussain, Tooba; Zamora, Francisca Millan; Wohler, Elizabeth; Sobreira, Nara; Klein, Christine; Lohmann, Katja; Naz, Sadaf
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Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia双等位基因KIF24变体负责一系列骨骼疾病，从致死性骨骼纤毛病到严重的肢端细胞发育不良
errJOURNAL OF BONE AND MINERAL RESEARCH
IF5.9
err2022-06-24
err8
errOAAI
errReilly, Madeline Louise; ul Ain, Noor; Muurinen, Mari; Tata, Alice; Huber, Celine; Simon, Marleen; Ishaq, Tayyaba; Shaw, Nick; Rusanen, Salla; Pekkinen, Minna; Hogler, Wolfgang; Knapen, Maarten F. C. M.; van den Born, Myrthe; Saunier, Sophie; Naz, Sadaf; Cormier-Daire, Valerie; Benmerah, Alexandre; Makitie, Outi
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err收藏
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder对Perrault综合征的新见解，这是一种临床和遗传异质性疾病
errHUMAN GENETICS
IF3.6
err2021-08-02
err34
errOAAI
errFaridi, Rabia; Rea, Alessandro; Fenollar-Ferrer, Cristina; O'Keefe, Raymond T.; Gu, Shoujun; Munir, Zunaira; Khan, Asma Ali; Riazuddin, Sheikh; Hoa, Michael; Naz, Sadaf; Newman, William G.; Friedman, Thomas B.
err分享
err收藏

研究方向

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合作学者
合作期刊
S
Stylianos E. Antonarakis
H 指数: 146 · 论文数: 920
H
Henry Houlden
H 指数: 120 · 论文数: 1.5K
R
Richard J. Smith
H 指数: 118 · 论文数: 1.5K
C
Christine Klein
H 指数: 104 · 论文数: 1.2K
V
Valérie Cormier‐Daire
H 指数: 99 · 论文数: 1.1K
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