Naz Khan

1.3k total citations
21 papers, 241 citations indexed

About

Naz Khan is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Naz Khan has authored 21 papers receiving a total of 241 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Naz Khan's work include Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (4 papers) and Prenatal Screening and Diagnostics (4 papers). Naz Khan is often cited by papers focused on Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (4 papers) and Prenatal Screening and Diagnostics (4 papers). Naz Khan collaborates with scholars based in United Kingdom, Australia and Austria. Naz Khan's co-authors include Nadeem Qureshi, Helen Kingston, Rhona MacLeod, Victoria G. Woof, Louise S. Donnelly, D. Gareth Evans, David French, Fiona Ulph, Julian Barwell and Michael Parker and has published in prestigious journals such as SHILAP Revista de lepidopterología, Heart and BMJ Open.

In The Last Decade

Naz Khan

19 papers receiving 235 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naz Khan United Kingdom 10 94 42 38 30 27 21 241
Susanne Schweitzer Germany 7 67 0.7× 23 0.5× 76 2.0× 16 0.5× 34 1.3× 11 280
S. A. Borinskaya Russia 11 128 1.4× 23 0.5× 93 2.4× 11 0.4× 18 0.7× 40 492
Paul Brennan United Kingdom 10 76 0.8× 46 1.1× 124 3.3× 15 0.5× 14 0.5× 22 331
Brian M. Faux United States 7 41 0.4× 21 0.5× 153 4.0× 26 0.9× 14 0.5× 13 265
Fleur Vansenne Netherlands 9 119 1.3× 11 0.3× 135 3.6× 24 0.8× 93 3.4× 21 340
Yujuan Xiang China 13 38 0.4× 93 2.2× 61 1.6× 8 0.3× 12 0.4× 25 338
Tan T. Nguyen United States 6 116 1.2× 10 0.2× 67 1.8× 17 0.6× 29 1.1× 7 320
Javier Aisenberg United States 11 91 1.0× 42 1.0× 155 4.1× 14 0.5× 67 2.5× 18 400
Art Cohen United States 7 86 0.9× 136 3.2× 52 1.4× 24 0.8× 20 0.7× 11 364
Thaís Della Manna Brazil 13 224 2.4× 20 0.5× 148 3.9× 25 0.8× 48 1.8× 50 507

Countries citing papers authored by Naz Khan

Since Specialization
Citations

This map shows the geographic impact of Naz Khan'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 Naz Khan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Naz Khan more than expected).

Fields of papers citing papers by Naz Khan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Naz Khan. 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 Naz Khan. The network helps show where Naz Khan may publish in the future.

Co-authorship network of co-authors of Naz Khan

This figure shows the co-authorship network connecting the top 25 collaborators of Naz Khan. A scholar is included among the top collaborators of Naz Khan 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 Naz Khan. Naz Khan 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.
Mamun, Abdullah Al, et al.. (2025). AI-Powered Predictive Analytics in Healthcare Business: Enhancing Operational Efficiency and Patient Outcomes. 7(3). 93–114. 1 indexed citations
2.
Mamun, Abdullah Al, et al.. (2025). Optimizing Revenue Cycle Management in Healthcare: AI and IT Solutions for Business Process Automation. 7(3). 141–162. 3 indexed citations
3.
4.
Gasteiger, Norina, et al.. (2023). Digital interventions for genomics and genetics education, empowerment, and service engagement: A systematic review. Journal of Community Genetics. 14(3). 227–240. 3 indexed citations
5.
Woof, Victoria G., David French, Louise S. Donnelly, et al.. (2023). The role of knowledge, primary care and community engagement to improve breast-screening access for Pakistani women in the United Kingdom: A secondary analysis of a qualitative study. Journal of Health Services Research & Policy. 28(3). 149–156. 3 indexed citations
6.
Gasteiger, Norina, et al.. (2022). Patient-facing genetic and genomic mobile apps in the UK: a systematic review of content, functionality, and quality. Journal of Community Genetics. 13(2). 171–182. 12 indexed citations
7.
Paesschen, Wim Van, Ataf Sabir, Francis H. Sansbury, et al.. (2021). ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsy. European Journal of Human Genetics. 29(9). 1377–1383. 6 indexed citations
8.
Woof, Victoria G., David French, Fiona Ulph, et al.. (2020). The introduction of risk stratified screening into the NHS breast screening Programme: views from British-Pakistani women. BMC Cancer. 20(1). 452–452. 22 indexed citations
9.
Beaman, Glenda M., Kate Chandler, James O’Sullivan, et al.. (2020). Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformations. European Journal of Medical Genetics. 63(9). 103974–103974. 2 indexed citations
10.
11.
Woof, Victoria G., Fiona Ulph, David French, et al.. (2019). Engagement barriers and service inequities in the NHS Breast Screening Programme: Views from British-Pakistani women. Journal of Medical Screening. 27(3). 130–137. 21 indexed citations
12.
Barwell, Julian, et al.. (2017). Inclusion of diverse populations in genomic research and health services: Genomix workshop report. Journal of Community Genetics. 8(4). 267–273. 27 indexed citations
13.
Salway, Sarah, Parveen Ali, Elizabeth Such, et al.. (2016). Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England. Journal of Community Genetics. 7(3). 215–228. 10 indexed citations
14.
Khan, Naz, et al.. (2016). Community engagement and education: addressing the needs of South Asian families with genetic disorders. Journal of Community Genetics. 7(4). 317–323. 8 indexed citations
15.
Goede, Christian de, Wyatt W. Yue, Kate Chandler, et al.. (2015). Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disorders. European Journal of Paediatric Neurology. 20(2). 286–295. 21 indexed citations
16.
Banka, Siddharth, Christian de Goede, Wyatt W. Yue, et al.. (2014). Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: A treatable neurological disorder caused by TPK1 mutations. Molecular Genetics and Metabolism. 113(4). 301–306. 43 indexed citations
17.
Caldwell, Jane C., Naz Khan, L Kerzin-Storrar, et al.. (2012). The clinical management of relatives of young sudden unexplained death victims; implantable defibrillators are rarely indicated. Heart. 98(8). 631–636. 22 indexed citations
18.
Raffan, Eleanor, Liam A. Hurst, Saeed Al Turki, et al.. (2011). Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient. SHILAP Revista de lepidopterología. 2. 8–8. 9 indexed citations
19.
Jenkinson, Emma M., Helen Kingston, Jill Urquhart, et al.. (2011). Newly recognized recessive syndrome characterized by dysmorphic features, hypogonadotropic hypogonadism, severe microcephaly, and sensorineural hearing loss maps to 3p21.3. American Journal of Medical Genetics Part A. 155(12). 2910–2915. 1 indexed citations
20.
Khan, Naz, et al.. (2010). Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families. Journal of Community Genetics. 1(2). 73–81. 22 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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