Andrea Guerin

1.2k total citations
30 papers, 336 citations indexed

About

Andrea Guerin is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Andrea Guerin has authored 30 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 12 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Andrea Guerin's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (2 papers). Andrea Guerin is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (3 papers) and BRCA gene mutations in cancer (2 papers). Andrea Guerin collaborates with scholars based in Canada, United States and France. Andrea Guerin's co-authors include Rosane Nisenbaum, Joel G. Ray, Grace Yoon, Elizabeth Donner, Annette Feigenbaum, David Chitayat, Dimitri J. Stavropoulos, Saadet Mercimek‐Mahmutoglu, Cristina Go and Yaser Diab and has published in prestigious journals such as Gastroenterology, Brain and Diabetes Care.

In The Last Decade

Andrea Guerin

24 papers receiving 324 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrea Guerin Canada 8 103 99 94 69 57 30 336
Ewa Emich‐Widera Poland 12 39 0.4× 96 1.0× 27 0.3× 66 1.0× 27 0.5× 55 353
Anna Klukovits Hungary 11 32 0.3× 104 1.1× 24 0.3× 28 0.4× 38 0.7× 18 341
Austin Larson United States 11 80 0.8× 179 1.8× 12 0.1× 35 0.5× 28 0.5× 36 329
Tiina Kahre Estonia 13 133 1.3× 146 1.5× 17 0.2× 75 1.1× 28 0.5× 30 328
Yen‐Yin Chou Taiwan 8 72 0.7× 175 1.8× 14 0.1× 29 0.4× 20 0.4× 39 308
H. G. Dörr Germany 10 112 1.1× 100 1.0× 8 0.1× 89 1.3× 52 0.9× 19 302
In Goo Lee South Korea 12 126 1.2× 107 1.1× 8 0.1× 151 2.2× 17 0.3× 31 411
Ahmad Ebrahimi Iran 9 81 0.8× 149 1.5× 17 0.2× 25 0.4× 33 0.6× 46 367
Sukanta Jash United States 13 17 0.2× 163 1.6× 70 0.7× 34 0.5× 25 0.4× 24 367
O. Vérier‐Mine France 8 80 0.8× 77 0.8× 200 2.1× 69 1.0× 121 2.1× 18 396

Countries citing papers authored by Andrea Guerin

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Guerin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Guerin

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Guerin. A scholar is included among the top collaborators of Andrea Guerin 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 Andrea Guerin. Andrea Guerin 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.
2.
Brown, Pierre Antoine, George S. Charames, Mathieu Lemaire, et al.. (2025). Framework for standardized genetic testing recommendations for chronic kidney disease in Ontario. Genetics in Medicine Open. 3. 103442–103442.
3.
Misceo, Doriana, Lisa Lirussi, Petter Strømme, et al.. (2023). A homozygous POLR1A variant causes leukodystrophy and affects protein homeostasis. Brain. 146(8). 3513–3527. 3 indexed citations
4.
Faghfoury, Hanna & Andrea Guerin. (2023). Ensuring timely genetic diagnosis in adults. Canadian Medical Association Journal. 195(11). E413–E414. 6 indexed citations
5.
Lapointe, Julie, et al.. (2022). Scope of coverage of medical genetics and genomics in pre‐clerkship programs of Canadian faculties of medicine: A curriculum analysis. American Journal of Medical Genetics Part A. 191(1). 13–21. 2 indexed citations
6.
Dobson, Stephanie M., Courtney Kiss, Daniel Borschneck, et al.. (2022). Novel FGF9 variant contributes to multiple synostoses syndrome 3. American Journal of Medical Genetics Part A. 188(7). 2162–2167. 4 indexed citations
7.
Guerin, Andrea, et al.. (2022). Prenatal phenotype analysis and mutation identification of a fetus with meckel gruber syndrome. Frontiers in Genetics. 13. 982127–982127. 1 indexed citations
8.
Dentici, Maria Lisa, Viola Alesi, Mathieu Quinodoz, et al.. (2021). Biallelic variants in ZNF526 cause a severe neurodevelopmental disorder with microcephaly, bilateral cataract, epilepsy and simplified gyration. Journal of Medical Genetics. 59(3). 262–269. 4 indexed citations
9.
Siddiqui, Iram, Andrea Guerin, Neal Sondheimer, et al.. (2020). Liver transplantation for Gaucher disease presenting as neonatal cholestasis: Case report and literature review. Pediatric Transplantation. 24(4). e13718–e13718. 3 indexed citations
10.
Guerin, Andrea, et al.. (2020). Polycystic Ovary Syndrome and Incidental Diagnosis of Mosaic Turner Syndrome. Journal of Obstetrics and Gynaecology Canada. 43(6). 756–759.
11.
Sjaarda, Calvin, et al.. (2020). De novo duplication on Chromosome 19 observed in nuclear family displaying neurodevelopmental disorders. Molecular Case Studies. 6(3). a004721–a004721.
12.
13.
14.
Sjaarda, Calvin, Amy J. M. McNaughton, S. Paige Taylor, et al.. (2019). Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism. Journal of Human Genetics. 65(3). 287–296. 7 indexed citations
15.
Guerin, Andrea, et al.. (2014). Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld‐anomaly in a child with PTPN11 mutation. American Journal of Medical Genetics Part A. 167(2). 403–406. 5 indexed citations
16.
Siriwardena, Komudi, Almundher Al‐Maawali, Andrea Guerin, Susan Blasér, & David Chitayat. (2013). XY sex reversal, pontocerebellar hypoplasia and intellectual disability: Confirmation of a new syndrome. American Journal of Medical Genetics Part A. 161(7). 1714–1717. 7 indexed citations
17.
Guerin, Andrea, Dimitri J. Stavropoulos, Yaser Diab, et al.. (2012). Interstitial deletion of 11q‐implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndrome. American Journal of Medical Genetics Part A. 158A(10). 2551–2556. 43 indexed citations
18.
Guerin, Andrea, Annette Feigenbaum, Elizabeth Donner, & Grace Yoon. (2008). Stepwise Developmental Regression Associated With Novel CACNA1A Mutation. Pediatric Neurology. 39(5). 363–364. 33 indexed citations
19.
Guerin, Andrea, Rosane Nisenbaum, & Joel G. Ray. (2007). Use of Maternal GHb Concentration to Estimate the Risk of Congenital Anomalies in the Offspring of Women with Prepregnancy Diabetes. Diabetes Care. 30(7). 1920–1925. 119 indexed citations
20.
Paulmyer‐Lacroix, Odile, et al.. (1998). [Intrauterine insemination with the husband's sperm: conclusions of five years experience].. PubMed. 26(4). 300–6. 9 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Ewa Emich‐Widera Breakdown of academic impact, for papers by Anna Klukovits Breakdown of academic impact, for papers by Austin Larson Breakdown of academic impact, for papers by Tiina Kahre Breakdown of academic impact, for papers by Yen‐Yin Chou Breakdown of academic impact, for papers by H. G. Dörr Breakdown of academic impact, for papers by In Goo Lee Breakdown of academic impact, for papers by Ahmad Ebrahimi Breakdown of academic impact, for papers by Sukanta Jash Breakdown of academic impact, for papers by O. Vérier‐Mine
Rankless by CCL
2026