Isabella Borg

557 total citations
20 papers, 315 citations indexed

About

Isabella Borg is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Isabella Borg has authored 20 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Surgery. Recurrent topics in Isabella Borg's work include Hidradenitis Suppurativa and Treatments (6 papers), Colorectal and Anal Carcinomas (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Isabella Borg is often cited by papers focused on Hidradenitis Suppurativa and Treatments (6 papers), Colorectal and Anal Carcinomas (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Isabella Borg collaborates with scholars based in Malta, United Kingdom and Germany. Isabella Borg's co-authors include Nikolai Paul Pace, Dillon Mintoff, Joy Delhanty, M Baraitser, Sally Ann Lynch, Corinna Menzel, Kristine Freude, Hans‐Hilger Ropers, Niels Tommerup and M.A. Ferguson‐Smith and has published in prestigious journals such as International Journal of Molecular Sciences, International Journal of Environmental Research and Public Health and Journal of Medical Genetics.

In The Last Decade

Isabella Borg

20 papers receiving 310 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabella Borg Malta 10 133 102 71 60 40 20 315
Louisa S. Tang United States 10 65 0.5× 184 1.8× 61 0.9× 60 1.0× 73 1.8× 12 454
Andrew Wang United States 6 93 0.7× 146 1.4× 22 0.3× 17 0.3× 29 0.7× 10 328
Yukiko Kuroda Japan 11 178 1.3× 127 1.2× 10 0.1× 27 0.5× 12 0.3× 40 271
Florencia Giliberto Argentina 11 68 0.5× 312 3.1× 46 0.6× 29 0.5× 14 0.3× 28 409
M. G. Daker United Kingdom 13 333 2.5× 225 2.2× 9 0.1× 41 0.7× 13 0.3× 28 538
Nathalie Marle France 11 237 1.8× 170 1.7× 10 0.1× 29 0.5× 8 0.2× 23 373
Kyoko Hirano Japan 8 22 0.2× 82 0.8× 17 0.2× 23 0.4× 35 0.9× 27 244
Jessica Smith United States 9 16 0.1× 139 1.4× 11 0.2× 23 0.4× 39 1.0× 17 267
Helle Lybæk Norway 10 162 1.2× 114 1.1× 5 0.1× 19 0.3× 11 0.3× 15 282
Avinash M. Veerappa India 10 112 0.8× 148 1.5× 3 0.0× 28 0.5× 43 1.1× 27 280

Countries citing papers authored by Isabella Borg

Since Specialization
Citations

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

Fields of papers citing papers by Isabella Borg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabella Borg

This figure shows the co-authorship network connecting the top 25 collaborators of Isabella Borg. A scholar is included among the top collaborators of Isabella Borg 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 Isabella Borg. Isabella Borg 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.
Mintoff, Dillon, Nikolai Paul Pace, & Isabella Borg. (2023). NCSTN In-Frame Deletion in Maltese Patients With Hidradenitis Suppurativa. JAMA Dermatology. 159(9). 939–939. 12 indexed citations
2.
Mintoff, Dillon, Nikolai Paul Pace, & Isabella Borg. (2022). Management of patients with hidradenitis suppurativa having underlying genetic variation: a systematic review and a call for precision medicine. Clinical and Experimental Dermatology. 48(2). 67–72. 3 indexed citations
3.
Mintoff, Dillon, Isabella Borg, & Nikolai Paul Pace. (2022). Serum Immunoglobulin G Is a Marker of Hidradenitis Suppurativa Disease Severity. International Journal of Molecular Sciences. 23(22). 13800–13800. 8 indexed citations
4.
Mintoff, Dillon, Nikolai Paul Pace, & Isabella Borg. (2022). Interpreting the spectrum of gamma-secretase complex missense variation in the context of hidradenitis suppurativa—An in-silico study. Frontiers in Genetics. 13. 9 indexed citations
5.
Pace, Nikolai Paul, Dillon Mintoff, & Isabella Borg. (2022). The Genomic Architecture of Hidradenitis Suppurativa—A Systematic Review. Frontiers in Genetics. 13. 861241–861241. 44 indexed citations
6.
Formosa, Melissa M., et al.. (2021). Hypermobile Ehlers–Danlos syndrome: A review and a critical appraisal of published genetic research to date. Clinical Genetics. 101(1). 20–31. 10 indexed citations
7.
Mintoff, Dillon, et al.. (2021). A novel SPINK5 donor splice site variant in a child with Netherton syndrome. Molecular Genetics & Genomic Medicine. 9(3). e1611–e1611. 2 indexed citations
8.
Mintoff, Dillon, Isabella Borg, & Nikolai Paul Pace. (2021). The Clinical Relevance of the Microbiome in Hidradenitis Suppurativa: A Systematic Review. Vaccines. 9(10). 1076–1076. 21 indexed citations
9.
Gallagher, Louise, Severin Rakić, Paula Jorge, et al.. (2020). Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4–BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature. International Journal of Environmental Research and Public Health. 17(24). 9253–9253. 4 indexed citations
10.
Pace, Nikolai Paul, et al.. (2020). A respiratory/Hirschsprung phenotype in a three‐generation family associated with a novel pathogenic PHOX2B splice donor mutation. Molecular Genetics & Genomic Medicine. 8(12). e1528–e1528. 3 indexed citations
11.
Mintoff, Dillon, et al.. (2020). A novel c.916C>A EDA gene pathogenic variant in a boy with X‐linked hypohidrotic ectodermal dysplasia. Clinical and Experimental Dermatology. 46(3). 618–620. 1 indexed citations
12.
Pace, Nikolai Paul, et al.. (2019). Two novel GJA1 variants in oculodentodigital dysplasia. Molecular Genetics & Genomic Medicine. 7(9). e882–e882. 6 indexed citations
13.
Sodi, Andrea, Daniela Bacherini, Lucia Finocchio, et al.. (2019). Quantitative Analysis of Conjunctival and Retinal Vessels in Fabry Disease. Journal of Ophthalmology. 2019. 1–6. 10 indexed citations
14.
Mucciolo, Dario Pasquale, Andrea Sodi, Ilaria Passerini, et al.. (2018). Fundus phenotype in retinitis pigmentosa associated with EYS mutations. Ophthalmic Genetics. 39(5). 589–602. 8 indexed citations
15.
16.
Lynch, Sally Ann & Isabella Borg. (2015). Wide disparity of clinical genetics services and EU rare disease research funding across Europe. Journal of Community Genetics. 7(2). 119–126. 19 indexed citations
17.
Borg, Isabella, Kristine Freude, Kirsten Hoffmann, et al.. (2005). Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome. European Journal of Human Genetics. 13(8). 921–927. 67 indexed citations
18.
Borg, Isabella, et al.. (2002). A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation. Journal of Medical Genetics. 39(6). 391–399. 39 indexed citations
19.
Borg, Isabella, Mario Valentino, Ana C. Fiorini, & Alex E. Felice. (1997). HB Setif [α94(GI)ASPàTYR] in Malta. Hemoglobin. 21(1). 91–96. 5 indexed citations
20.
Borg, Isabella, Joy Delhanty, & M Baraitser. (1995). Detection of hemizygosity at the elastin locus by FISH analysis as a diagnostic test in both classical and atypical cases of Williams syndrome.. Journal of Medical Genetics. 32(9). 692–696. 33 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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