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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
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
err2026-05-05
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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
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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
err2025-12-01
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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
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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。
err2025-11-25
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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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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
err2025-05-21
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errOAAI
errKanwal, Ambreen; Zulfiqar, Rimsha; Cheema, Husnain Arshad; Jabbar, Nauman; Iftikhar, Amina; Butt, Amina Iftikhar; Sheikh, Sohail A.; Pardo, Jose V.; Naz, Sadaf
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Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss
err2024-09-13
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errOAAI
errKhan, Hina; Muzaffar, Fariha; Salman, Midhat; Bashir, Rasheeda; Seo, Go Hun; Naz, Sadaf
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In vivo evaluation of efficacy and safety of Coagulansin-A in treating arthritis
err2024-08-01
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PREAI
errNaz, Sadaf; Mazhar, Muhammad Usama; Faiz, Sidra; Malik, Maria Nawaz; Khan, Jehan Zeb; Ul Haq, Ihsan; Zhu, Lin; Tipu, Muhammad Khalid
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Identification and analyses of exonic and copy number variants in spastic paraplegia
err2024-06-21
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errOAAI
errShafique, Anum; Nadeem, Ayesha; Aslam, Faiza; Manzoor, Humera; Noman, Muhammad; Wohler, Elizabeth; Witmer, P. Dane; Sobreira, Nara; Naz, Sadaf
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PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss
err2024-03-09
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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
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Raveling out the effect of Pr3+ ions substitution on different properties of nano-sized hexagonal ferrites
err2023-11-01
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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
err2023-02-17
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PREAI
errManzoor, Humera; Zahid, Hafsa; Emerling, Christopher A.; Kumar, Kishore R.; Hussain, Hafiz Muhammad Jafar; Seo, Go Hun; Wajid, Muhammad; Naz, Sadaf
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Preliminary studies on apparent mendelian psychotic disorders in consanguineous families
err2022-11-16
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errKanwal, Ambreen; Sheikh, Sohail A.; Iftikhar, Amina; Naz, Sadaf; Pardo, Jose, V
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MRM2 variants in families with complex dystonic syndromes: evidence for phenotypic heterogeneity
err2022-08-24
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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
err2022-06-24
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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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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
err2021-08-02
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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.
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