Sadaf Naz

3.3k total citations
94 papers, 1.8k citations indexed

About

Sadaf Naz is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Sadaf Naz has authored 94 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 26 papers in Genetics and 22 papers in Sensory Systems. Recurrent topics in Sadaf Naz's work include Hearing, Cochlea, Tinnitus, Genetics (22 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Vestibular and auditory disorders (10 papers). Sadaf Naz is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (22 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Vestibular and auditory disorders (10 papers). Sadaf Naz collaborates with scholars based in Pakistan, United States and Finland. Sadaf Naz's co-authors include Thomas B. Friedman, Andrew J. Griffith, Inna A. Belyantseva, Zubair M. Ahmed, Edward R. Wilcox, Robert J. Morell, Sheikh Riazuddin, Tenesha N. Smith, Gregory I. Frolenkov and James R. Sellers and has published in prestigious journals such as Cell, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Sadaf Naz

87 papers receiving 1.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sadaf Naz Pakistan 19 957 863 557 205 179 94 1.8k
Donald Coling United States 25 652 0.7× 904 1.0× 300 0.5× 75 0.4× 184 1.0× 45 1.6k
Kimia Kahrizi Iran 30 1.8k 1.9× 826 1.0× 382 0.7× 835 4.1× 252 1.4× 141 3.0k
Kyu-Yup Lee South Korea 21 542 0.6× 734 0.9× 342 0.6× 81 0.4× 64 0.4× 98 1.4k
Chantal M. Longo-Guess United States 18 1.5k 1.5× 530 0.6× 224 0.4× 291 1.4× 323 1.8× 24 2.2k
Theo Peters Netherlands 25 1.4k 1.5× 417 0.5× 204 0.4× 464 2.3× 401 2.2× 74 2.4k
Hans‐Henrik M. Dahl Australia 23 1.2k 1.2× 392 0.5× 95 0.2× 380 1.9× 73 0.4× 51 1.9k
Susan A. Cook United States 19 1.2k 1.2× 339 0.4× 186 0.3× 305 1.5× 210 1.2× 32 1.8k
Gabriela Pavlínková United States 28 1.0k 1.1× 315 0.4× 62 0.1× 184 0.9× 55 0.3× 65 2.1k
Ruth Chia United States 21 793 0.8× 81 0.1× 396 0.7× 152 0.7× 155 0.9× 34 2.0k
Ji Eun Lee South Korea 22 1.2k 1.2× 140 0.2× 111 0.2× 566 2.8× 289 1.6× 51 1.8k

Countries citing papers authored by Sadaf Naz

Since Specialization
Citations

This map shows the geographic impact of Sadaf Naz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sadaf Naz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sadaf Naz more than expected).

Fields of papers citing papers by Sadaf Naz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sadaf Naz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sadaf Naz. The network helps show where Sadaf Naz may publish in the future.

Co-authorship network of co-authors of Sadaf Naz

This figure shows the co-authorship network connecting the top 25 collaborators of Sadaf Naz. A scholar is included among the top collaborators of Sadaf Naz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sadaf Naz. Sadaf Naz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Naz, Sadaf, et al.. (2024). Anti-inflammatory and anti-arthritic potential of Coagulansin-A: in vitro and in vivo studies. Inflammopharmacology. 32(2). 1225–1238. 5 indexed citations
2.
Seo, Go Hun, et al.. (2023). Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathy. BMC Musculoskeletal Disorders. 24(1). 735–735. 1 indexed citations
3.
Naz, Sadaf, Imran Sadiq, Farhan Sadiq, et al.. (2023). Raveling out the effect of Pr3+ ions substitution on different properties of nano-sized hexagonal ferrites. Materials Science and Engineering B. 297. 116717–116717. 10 indexed citations
4.
Sheikh, Sohail A., et al.. (2022). Preliminary studies on apparent mendelian psychotic disorders in consanguineous families. BMC Psychiatry. 22(1). 709–709. 2 indexed citations
5.
Faridi, Rabia, Cristina Fenollar‐Ferrer, Raymond T. O’Keefe, et al.. (2021). New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human Genetics. 141(3-4). 805–819. 28 indexed citations
6.
Reilly, Madeline Louise, Noor Ul Ain, Céline Huber, et al.. (2020). Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia. Journal of Bone and Mineral Research. 37(9). 1642–1652. 7 indexed citations
7.
Zaki, Maha S., Katherine Johnson, Jennifer McEvoy‐Venneri, et al.. (2020). Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability. Journal of Medical Genetics. 58(4). 237–246. 5 indexed citations
8.
Ain, Noor Ul, Mehdi Dianatpour, Ihtisham Bukhari, et al.. (2020). Biallelic TMEM251 variants in patients with severe skeletal dysplasia and extreme short stature. Human Mutation. 42(1). 89–101. 17 indexed citations
9.
Naz, Sadaf & Thomas B. Friedman. (2019). Growth factor and receptor malfunctions associated with human genetic deafness. Clinical Genetics. 97(1). 138–155. 5 indexed citations
11.
Naz, Sadaf, et al.. (2019). Frequency of Hypogonadism in Type 2 Diabetes Mellitus Patients with and without Coronary Artery Disease. Cureus. 11(12). e6500–e6500. 6 indexed citations
12.
Khan, Khurshid, et al.. (2018). FREQUENCY OF PERIPHERAL ARTERIAL DISEASE IN HIGH RISK TYPE 2 DIABETES MELLITUS USING ANKLE-BRACHIAL INDEX AND ITS ASSOCIATION WITH THE RISK FACTORS AMONG PATIENTS PRESENTING IN JINNAH HOSPITAL, LAHORE. SHILAP Revista de lepidopterología. 2 indexed citations
13.
Ain, Noor Ul, et al.. (2018). Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux. European Journal of Medical Genetics. 62(9). 103554–103554. 12 indexed citations
14.
Naz, Sadaf, et al.. (2017). Biogenic Synthesis of Silver Nanoparticles and Valuation of their Antimicrobial Activity against Dengue Larvae. Journal of Plant Pathology & Microbiology. 8(8). 2 indexed citations
16.
Naz, Sadaf, et al.. (2012). Impact of Teacher Turn over on Students Motivation, Psyche and Performance.. International Review of Management and Business Research. 1(1). 26. 2 indexed citations
17.
Naz, Sadaf, Syeda Hafiza Benish Ali, Saima Riazuddin, et al.. (2011). Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families. British Journal of Ophthalmology. 95(7). 1019–1024. 22 indexed citations
18.
Riazuddin, Saima, Shaheen N. Khan, Zubair M. Ahmed, et al.. (2005). Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness. The American Journal of Human Genetics. 78(1). 137–143. 76 indexed citations
19.
Belyantseva, Inna A., Erich T. Boger, Sadaf Naz, et al.. (2005). Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia. Nature Cell Biology. 7(2). 148–156. 281 indexed citations
20.
Riazuddin, Saima, Zubair M. Ahmed, Anil K. Lalwani, et al.. (2000). Dominant modifier DFNM1 suppresses recessive deafness DFNB26. Nature Genetics. 26(4). 431–434. 104 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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