Toni I. Pollin

18.5k total citations · 3 hit papers
129 papers, 6.7k citations indexed

About

Toni I. Pollin is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Toni I. Pollin has authored 129 papers receiving a total of 6.7k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Genetics, 40 papers in Molecular Biology and 39 papers in Surgery. Recurrent topics in Toni I. Pollin's work include Pancreatic function and diabetes (29 papers), Genetic Associations and Epidemiology (23 papers) and Diabetes and associated disorders (13 papers). Toni I. Pollin is often cited by papers focused on Pancreatic function and diabetes (29 papers), Genetic Associations and Epidemiology (23 papers) and Diabetes and associated disorders (13 papers). Toni I. Pollin collaborates with scholars based in United States, Sweden and Canada. Toni I. Pollin's co-authors include Alan R. Shuldiner, Braxton D. Mitchell, Jeffrey R. O’Connell, William C. Knowler, Coleen Damcott, José C. Florez, Kathleen A. Jablonski, John C. McLenithan, David Altshuler and Sandra Ott and has published in prestigious journals such as Science, New England Journal of Medicine and Journal of Clinical Investigation.

In The Last Decade

Toni I. Pollin

123 papers receiving 6.5k citations

Hit Papers

3 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

TCF7L2 Polymorphisms and Progression to Diabetes in the Diabetes Prevention Program

2006 627 citations José C. Florez, Kathleen A. Jablonski et al. profile →
Omentin Plasma Levels and Gene Expression Are Decreased in Obesity

2007 617 citations Alan R. Shuldiner, Toni I. Pollin et al. profile →
A Null Mutation in Human APOC3 Confers a Favorable Plasma Lipid Profile and Apparent Cardioprotection

2008 517 citations Toni I. Pollin, Coleen Damcott et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Toni I. Pollin United States	39	2.2k	2.0k	1.6k	1.6k	1.4k	129	6.7k
Mark Walker United Kingdom	50	2.4k 1.1×	3.0k 1.5×	1.9k 1.2×	2.2k 1.4×	1.0k 0.7×	169	7.5k
Guillaume Paré Canada	53	2.7k 1.2×	2.8k 1.4×	2.1k 1.3×	1.5k 0.9×	1.3k 0.9×	268	10.6k
J. Brent Richards Canada	44	3.3k 1.5×	2.6k 1.3×	852 0.5×	913 0.6×	1.2k 0.9×	156	9.7k
Marie‐Claude Vohl Canada	50	2.3k 1.0×	3.8k 1.9×	1.8k 1.1×	1.8k 1.1×	1.6k 1.2×	327	10.2k
Pierre Bougnères France	44	2.4k 1.1×	2.3k 1.2×	1.5k 0.9×	2.3k 1.4×	862 0.6×	153	7.7k
Ηλίας Ζιντζαράς Greece	48	1.3k 0.6×	1.5k 0.8×	1.3k 0.8×	598 0.4×	985 0.7×	213	8.3k
Kari E. North United States	45	1.6k 0.7×	1.6k 0.8×	522 0.3×	1.1k 0.7×	1.1k 0.8×	298	6.7k
Pierre Gourdy France	45	1.9k 0.8×	1.9k 1.0×	986 0.6×	1.9k 1.2×	1.2k 0.9×	190	8.1k
Ron Do United States	27	3.8k 1.7×	2.5k 1.2×	932 0.6×	576 0.4×	1.1k 0.8×	90	8.1k
Jaroslav A. Hubáček Czechia	35	848 0.4×	1.3k 0.7×	1.6k 1.0×	1.2k 0.7×	862 0.6×	294	5.3k

Countries citing papers authored by Toni I. Pollin

Since Specialization

Citations

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

Fields of papers citing papers by Toni I. Pollin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Toni I. Pollin. 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 Toni I. Pollin. The network helps show where Toni I. Pollin may publish in the future.

Co-authorship network of co-authors of Toni I. Pollin

This figure shows the co-authorship network connecting the top 25 collaborators of Toni I. Pollin. A scholar is included among the top collaborators of Toni I. Pollin 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 Toni I. Pollin. Toni I. Pollin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Mercader, Josep M., Amy K. Mottl, Rachelle Gandica, et al.. (2024). Genetic architecture and biology of youth-onset type 2 diabetes. UNC Libraries.

Kwak, Soo Heon, Shylaja Srinivasan, Ling Chen, et al.. (2024). Genetic architecture and biology of youth-onset type 2 diabetes. Nature Metabolism. 6(2). 226–237. 16 indexed citations

Tosur, Mustafa, Ashok Balasubramanyam, Rochelle N. Naylor, et al.. (2023). Enrollment of underrepresented racial and ethnic groups in the Rare and Atypical Diabetes Network (RADIANT). Journal of Clinical and Translational Science. 7(1). e47–e47. 3 indexed citations

Humphries, Elizabeth, Kwangmi Ahn, Rachel L. Kember, et al.. (2023). Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population. Molecular Psychiatry. 28(12). 5262–5271. 1 indexed citations

Maloney, Kristin A., et al.. (2023). Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors. Journal of Genetic Counseling. 33(3). 493–505. 3 indexed citations

Todd, Jennifer N., Jeffrey W. Kleinberger, Haichen Zhang, et al.. (2021). Monogenic Diabetes in Youth With Presumed Type 2 Diabetes: Results From the Progress in Diabetes Genetics in Youth (ProDiGY) Collaboration. Diabetes Care. 44(10). 2312–2319. 18 indexed citations

Reyes‐Soffer, Gissette, et al.. (2020). Abstract 219: Effects of Homozygosity for the P.e167k Variant in Tm6sf2 on Lipid and Lipoprotein Metabolism in Humans. Arteriosclerosis Thrombosis and Vascular Biology. 1 indexed citations

Guan, Yue, Kristin A. Maloney, & Toni I. Pollin. (2020). Patient perspectives on the diagnostic journey to a monogenic diabetes diagnosis: Barriers and facilitators. Journal of Genetic Counseling. 29(6). 1106–1113. 8 indexed citations

Huang, Xuemei, Honglei Chen, Lan Kong, et al.. (2020). Parkinson’s Disease-Related Motor and Nonmotor Symptoms in the Lancaster Amish. Neuroepidemiology. 54(5). 392–397. 1 indexed citations

10.

Orlando, Lori A., Nina Sperber, Corrine I. Voils, et al.. (2017). Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network’s Common Measures Working Group. Genetics in Medicine. 20(6). 655–663. 49 indexed citations

11.

Wadhawan, Abhishek, Allyson Duffy, Kathleen A. Ryan, et al.. (2017). Positive association between Toxoplasma gondii IgG serointensity and current dysphoria/hopelessness scores in the Old Order Amish: a preliminary study. Pteridines. 28(3-4). 185–194. 8 indexed citations

12.

Billings, Liana K., Kathleen A. Jablonski, Jarred B. McAteer, et al.. (2017). Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention. The Journal of Clinical Endocrinology & Metabolism. 102(8). 2678–2689. 13 indexed citations

13.

Ramos‐Molina, Bruno, et al.. (2017). Functional analysis of PCSK2 coding variants: A founder effect in the Old Order Amish population. Diabetes Research and Clinical Practice. 131. 82–90. 9 indexed citations

14.

Overby, Casey Lynnette, et al.. (2017). Using Workflow Modeling to Identify Areas to Improve Genetic Test Processes in the University of Maryland Translational Pharmacogenomics Project.. PubMed. 2015. 466–74. 5 indexed citations

15.

Beitelshees, Amber L., James J. Cimino, Guilherme Del Fiol, et al.. (2016). User-centered design of multi-gene sequencing panel reports for clinicians. Journal of Biomedical Informatics. 63. 1–10. 15 indexed citations

16.

Kleinberger, Jeffrey W., Kristin A. Maloney, & Toni I. Pollin. (2016). The Genetic Architecture of Diabetes in Pregnancy: Implications for Clinical Practice. American Journal of Perinatology. 33(13). 1319–1326. 16 indexed citations

17.

Reed, Robert M., Patrick F. McArdle, Michael Miller, et al.. (2014). Vitamin and Supplement Use among Old Order Amish: Sex-Specific Prevalence and Associations with Use. Journal of the Academy of Nutrition and Dietetics. 115(3). 397–405.e3. 10 indexed citations

18.

Pollin, Toni I., Coleen Damcott, Haiqing Shen, et al.. (2008). A Null Mutation in Human APOC3 Confers a Favorable Plasma Lipid Profile and Apparent Cardioprotection. Science. 322(5908). 1702–1705. 517 indexed citations breakdown →

19.

Awomoyi, Agnes A., Prasad Rallabhandi, Toni I. Pollin, et al.. (2007). Association of TLR4 Polymorphisms with Symptomatic Respiratory Syncytial Virus Infection in High-Risk Infants and Young Children. The Journal of Immunology. 179(5). 3171–3177. 146 indexed citations

20.

Steinle, Nanette, Wen‐Chi Hsueh, Søren Snitker, et al.. (2002). Eating behavior in the Old Order Amish: heritability analysis and a genome-wide linkage analysis. American Journal of Clinical Nutrition. 75(6). 1098–1106. 93 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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