Joo Wook Ahn

1.8k total citations
29 papers, 605 citations indexed

About

Joo Wook Ahn is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Joo Wook Ahn has authored 29 papers receiving a total of 605 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 10 papers in Molecular Biology. Recurrent topics in Joo Wook Ahn's work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (10 papers) and Genomics and Rare Diseases (8 papers). Joo Wook Ahn is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (10 papers) and Genomics and Rare Diseases (8 papers). Joo Wook Ahn collaborates with scholars based in United Kingdom, Australia and United States. Joo Wook Ahn's co-authors include Caroline Mackie Ogilvie, Kathy Mann, Frances Flinter, David Collier, M Cafferkey, Kenneth L. Powell, Paul Kellam, Sarah Curran, Dagmar Alber and Celia Donaghue and has published in prestigious journals such as Blood, PLoS ONE and Journal of Virology.

In The Last Decade

Joo Wook Ahn

28 papers receiving 579 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joo Wook Ahn United Kingdom 13 424 232 159 72 57 29 605
Sophia Kitsiou‐Tzeli Greece 16 407 1.0× 422 1.8× 77 0.5× 69 1.0× 28 0.5× 39 656
Isabel Filges Switzerland 18 435 1.0× 338 1.5× 278 1.7× 44 0.6× 28 0.5× 44 773
Margaret Lilley Canada 10 418 1.0× 327 1.4× 110 0.7× 82 1.1× 71 1.2× 20 662
Brian P. Perry United States 12 233 0.5× 137 0.6× 79 0.5× 64 0.9× 44 0.8× 27 509
Céline Dupont France 15 328 0.8× 213 0.9× 123 0.8× 88 1.2× 20 0.4× 38 645
Marsha Speevak Canada 17 420 1.0× 302 1.3× 141 0.9× 96 1.3× 21 0.4× 37 636
Ingrid Simonic United Kingdom 14 331 0.8× 371 1.6× 111 0.7× 47 0.7× 48 0.8× 23 758
María Palomares‐Bralo Spain 13 364 0.9× 339 1.5× 105 0.7× 55 0.8× 68 1.2× 38 540
Dunja Niedrist Switzerland 8 279 0.7× 263 1.1× 119 0.7× 37 0.5× 19 0.3× 11 571
Chansonette Harvard Canada 17 417 1.0× 294 1.3× 185 1.2× 85 1.2× 11 0.2× 19 681

Countries citing papers authored by Joo Wook Ahn

Since Specialization
Citations

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

Fields of papers citing papers by Joo Wook Ahn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joo Wook Ahn. 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 Joo Wook Ahn. The network helps show where Joo Wook Ahn may publish in the future.

Co-authorship network of co-authors of Joo Wook Ahn

This figure shows the co-authorship network connecting the top 25 collaborators of Joo Wook Ahn. A scholar is included among the top collaborators of Joo Wook Ahn 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 Joo Wook Ahn. Joo Wook Ahn 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.
Deans, Zandra C., Joo Wook Ahn, Isabel M. Carreira, et al.. (2022). Recommendations for reporting results of diagnostic genomic testing. European Journal of Human Genetics. 30(9). 1011–1016. 29 indexed citations
2.
Shangaris, Panicos, Alison Ho, Simi George, et al.. (2021). A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report. BMC Medical Genomics. 14(1). 58–58. 1 indexed citations
3.
Sabir, Ataf, et al.. (2021). Automated reanalysis application to assist in detecting novel gene–disease associations after genome sequencing. Genetics in Medicine. 24(4). 811–820. 5 indexed citations
4.
Sabir, Ataf, et al.. (2021). Automated reanalysis, a novel way to diagnose an ultra-rare condition: Fibronectin-1-related spondylometaphyseal dysplasia (SMD-FN1). Clinical Dysmorphology. 30(3). 154–158. 1 indexed citations
5.
Donaghue, Celia, et al.. (2017). Efficient and cost-effective genetic analysis of products of conception and fetal tissues using a QF-PCR/array CGH strategy; five years of data. Molecular Cytogenetics. 10(1). 12–12. 17 indexed citations
6.
Ahn, Joo Wook & Caroline Mackie Ogilvie. (2016). Context and Applications of Targeted Genetic Testing, with Emphasis on Copy Number Variants. Advances in clinical chemistry. 75. 33–51. 1 indexed citations
7.
Liu, Min, Zhenlong Guan, Qin Shen, et al.. (2016). Ulk4 Regulates Neural Stem Cell Pool. Stem Cells. 34(9). 2318–2331. 23 indexed citations
8.
Ahn, Joo Wook, et al.. (2015). Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants. Journal of Visualized Experiments. e51718–e51718. 4 indexed citations
9.
Sagoo, Gurdeep S., Shehla Mohammed, Gail Norbury, et al.. (2015). Cost Effectiveness of Using Array-CGH for Diagnosing Learning Disability. Applied Health Economics and Health Policy. 13(4). 421–432. 12 indexed citations
10.
Ahn, Joo Wook, et al.. (2015). Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants. Journal of Visualized Experiments. 1 indexed citations
11.
Cafferkey, M, Joo Wook Ahn, Frances Flinter, & Caroline Mackie Ogilvie. (2014). Phenotypic features in patients with 15q11.2(BP1‐BP2) deletion: Further delineation of an emerging syndrome. American Journal of Medical Genetics Part A. 164(8). 1916–1922. 53 indexed citations
12.
Chénier, Sébastien, Grace Yoon, Bob Argiropoulos, et al.. (2014). CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems. Journal of Neurodevelopmental Disorders. 6(1). 9–9. 63 indexed citations
13.
Tropeano, Maria, Joo Wook Ahn, Richard Dobson, et al.. (2013). Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders. PLoS ONE. 8(4). e61365–e61365. 102 indexed citations
14.
15.
Curran, Sarah, Joo Wook Ahn, Hannah M. Grayton, David Collier, & Caroline Mackie Ogilvie. (2013). NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders. PubMed. 1(1). 4–4. 28 indexed citations
16.
Ahn, Joo Wook, Abhishek Dixit, Caroline Mackie Ogilvie, et al.. (2013). BBGRE: brain and body genetic resource exchange. Database. 2013. bat067–bat067.
17.
Pichert, Gabriella, et al.. (2011). Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?. Journal of Medical Genetics. 48(8). 535–539. 30 indexed citations
18.
19.
Ahn, Joo Wook, Kathy Mann, Zoe Docherty, & Caroline Mackie Ogilvie. (2008). Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis. Molecular Cytogenetics. 1(1). 2–2. 10 indexed citations
20.

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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