Gillian M. Belbin

6.4k total citations
24 papers, 442 citations indexed

About

Gillian M. Belbin is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Gillian M. Belbin has authored 24 papers receiving a total of 442 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 3 papers in Epidemiology. Recurrent topics in Gillian M. Belbin's work include Genetic Associations and Epidemiology (9 papers), Forensic and Genetic Research (4 papers) and Genomics and Rare Diseases (3 papers). Gillian M. Belbin is often cited by papers focused on Genetic Associations and Epidemiology (9 papers), Forensic and Genetic Research (4 papers) and Genomics and Rare Diseases (3 papers). Gillian M. Belbin collaborates with scholars based in United States, Japan and France. Gillian M. Belbin's co-authors include Eimear E. Kenny, Christopher R. Gignoux, Noura S. Abul‐Husn, Ruth J. F. Loos, Arden Moscati, Judy H. Cho, Emily R. Soper, Sinéad Cullina, Girish N. Nadkarni and Sabrina A. Suckiel and has published in prestigious journals such as Nature Medicine, Nature Communications and American Journal of Clinical Nutrition.

In The Last Decade

Gillian M. Belbin

23 papers receiving 437 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gillian M. Belbin United States 13 188 142 71 56 49 24 442
Sverrir Thorvaldsson Iceland 6 105 0.6× 117 0.8× 69 1.0× 71 1.3× 52 1.1× 8 511
Sevgi Baǧışlar Türkiye 8 123 0.7× 147 1.0× 45 0.6× 46 0.8× 44 0.9× 8 388
Hye‐Rim Song South Korea 14 36 0.2× 154 1.1× 34 0.5× 108 1.9× 68 1.4× 31 418
Charlotte Gerd Hannibal Denmark 18 72 0.4× 106 0.7× 92 1.3× 73 1.3× 70 1.4× 34 842
Inuk Zandvakili United States 11 173 0.9× 238 1.7× 153 2.2× 75 1.3× 131 2.7× 21 636
Olga L. van der Hel Netherlands 9 67 0.4× 291 2.0× 139 2.0× 33 0.6× 94 1.9× 11 580
Caitlyn Vlasschaert Canada 13 57 0.3× 232 1.6× 30 0.4× 27 0.5× 92 1.9× 46 699
Seon-Hee Yim South Korea 9 51 0.3× 74 0.5× 65 0.9× 26 0.5× 49 1.0× 11 306
Alison Taylor United Kingdom 13 69 0.4× 124 0.9× 28 0.4× 101 1.8× 113 2.3× 15 577
Yoshimasa Asada Japan 15 105 0.6× 250 1.8× 29 0.4× 23 0.4× 26 0.5× 89 911

Countries citing papers authored by Gillian M. Belbin

Since Specialization
Citations

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

Fields of papers citing papers by Gillian M. Belbin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gillian M. Belbin. 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 Gillian M. Belbin. The network helps show where Gillian M. Belbin may publish in the future.

Co-authorship network of co-authors of Gillian M. Belbin

This figure shows the co-authorship network connecting the top 25 collaborators of Gillian M. Belbin. A scholar is included among the top collaborators of Gillian M. Belbin 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 Gillian M. Belbin. Gillian M. Belbin 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.
Mefford, Joel, Ella Petter, Alec Chiu, et al.. (2023). Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region. Nature Medicine. 29(7). 1845–1856. 2 indexed citations
3.
Moscati, Arden, Annika Faucon, Sara Larsson Lönn, et al.. (2023). Life is pain: Fibromyalgia as a nexus of multiple liability distributions. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 192(7-8). 171–182. 1 indexed citations
4.
Cullina, Sinéad, Genevieve L. Wojcik, Derek Klarin, et al.. (2023). Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35. Frontiers in Genetics. 14. 1181167–1181167. 2 indexed citations
5.
Gopalan, Shyamalika, Richard E. W. Berl, Justin W. Myrick, et al.. (2022). Hunter-gatherer genomes reveal diverse demographic trajectories during the rise of farming in Eastern Africa. Current Biology. 32(8). 1852–1860.e5. 14 indexed citations
6.
Belbin, Gillian M., et al.. (2021). Rapid detection of identity-by-descent tracts for mega-scale datasets. Nature Communications. 12(1). 3546–3546. 21 indexed citations
7.
Belbin, Gillian M., Stephanie Rutledge, Tetyana Dodatko, et al.. (2021). Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto Ricans. The American Journal of Human Genetics. 108(11). 2099–2111. 4 indexed citations
8.
Belbin, Gillian M., et al.. (2021). Current Developments in Detection of Identity-by-Descent Methods and Applications. Frontiers in Genetics. 12. 722602–722602. 17 indexed citations
9.
Soper, Emily R., Sinéad Cullina, Gillian M. Belbin, et al.. (2021). CDH1 pathogenic variants and cancer risk in an unselected patient population. Familial Cancer. 21(2). 235–239. 6 indexed citations
10.
Abul‐Husn, Noura S., Emily R. Soper, Jessica Rodriguez, et al.. (2021). Implementing genomic screening in diverse populations. Genome Medicine. 13(1). 17–17. 39 indexed citations
11.
Ang, Celina, Sabrina A. Suckiel, Emily R. Soper, et al.. (2020). Lynch Syndrome–Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank. JCO Precision Oncology. 4(4). 1429–1444. 13 indexed citations
12.
Valencia, Ignacio, Joseph J. Melvin, Agustín Legido, et al.. (2020). Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements. Journal of Child Neurology. 36(2). 93–98. 2 indexed citations
13.
Wenric, Stéphane, Janina M. Jeff, Thomas T. Joseph, et al.. (2020). Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry. The Pharmacogenomics Journal. 21(2). 174–189. 1 indexed citations
14.
Walker, Ryan W., Gillian M. Belbin, Elena P. Sorokin, et al.. (2020). A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobank. Journal of Hepatology. 72(6). 1070–1081. 43 indexed citations
15.
Abul‐Husn, Noura S., Emily R. Soper, Jacqueline A. Odgis, et al.. (2019). Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank. Genome Medicine. 12(1). 2–2. 70 indexed citations
16.
Xu, Ke, Roman Kosoy, Khader Shameer, et al.. (2019). Genome-wide analysis indicates association between heterozygote advantage and healthy aging in humans. BMC Genetics. 20(1). 52–52. 10 indexed citations
17.
Vishnu, Abhishek, Gillian M. Belbin, Genevieve L. Wojcik, et al.. (2019). The role of country of birth, and genetic and self-identified ancestry, in obesity susceptibility among African and Hispanic Americans. American Journal of Clinical Nutrition. 110(1). 16–23. 7 indexed citations
18.
Belbin, Gillian M., María A. Nieves-Colón, Eimear E. Kenny, Andrés Moreno‐Estrada, & Christopher R. Gignoux. (2018). Genetic diversity in populations across Latin America: implications for population and medical genetic studies. Current Opinion in Genetics & Development. 53. 98–104. 28 indexed citations
19.
Serasinghe, Madhavika N., James J. Asciolla, Simona Podgrabinska, et al.. (2014). Anti-apoptotic BCL-2 proteins govern cellular outcome following B-RAFV600E inhibition and can be targeted to reduce resistance. Oncogene. 34(7). 857–867. 47 indexed citations
20.
Asciolla, James J., Esther López-Rivera, Konstantinos V. Floros, et al.. (2012). Sensitization to the mitochondrial pathway of apoptosis augments melanoma tumor cell responses to conventional chemotherapeutic regimens. Cell Death and Disease. 3(11). e420–e420. 24 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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