Suzanne Cheng

4.6k total citations
64 papers, 2.7k citations indexed

About

Suzanne Cheng is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Surgery. According to data from OpenAlex, Suzanne Cheng has authored 64 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 15 papers in Cardiology and Cardiovascular Medicine and 12 papers in Surgery. Recurrent topics in Suzanne Cheng's work include Blood Coagulation and Thrombosis Mechanisms (9 papers), Genetic Associations and Epidemiology (9 papers) and Lipoproteins and Cardiovascular Health (7 papers). Suzanne Cheng is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (9 papers), Genetic Associations and Epidemiology (9 papers) and Lipoproteins and Cardiovascular Health (7 papers). Suzanne Cheng collaborates with scholars based in United States, Switzerland and France. Suzanne Cheng's co-authors include Robert Y.L. Zee, Paul M. Ridker, Michael Grow, William Klitz, Lori Steiner, Sheng-Yung Chang, Patti E. Gravitt, Richard Respess, Klaus Lindpaintner and David M. Iovannisci and has published in prestigious journals such as Nature, Nucleic Acids Research and Circulation.

In The Last Decade

Suzanne Cheng

63 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Suzanne Cheng United States	32	890	527	420	410	395	64	2.7k
Lin Zuo China	19	1.4k 1.6×	398 0.8×	266 0.6×	376 0.9×	434 1.1×	42	3.0k
Chung-Ming Hsieh United States	22	2.2k 2.4×	339 0.6×	464 1.1×	339 0.8×	219 0.6×	29	3.8k
Andrew Shenker United States	36	2.2k 2.5×	1.1k 2.0×	504 1.2×	711 1.7×	699 1.8×	53	5.7k
N. Saha Singapore	25	642 0.7×	376 0.7×	1.1k 2.7×	710 1.7×	938 2.4×	91	3.3k
Karlhans Endlich Germany	35	1.4k 1.6×	428 0.8×	283 0.7×	460 1.1×	286 0.7×	109	3.7k
Arto Orpana Finland	26	2.0k 2.2×	177 0.3×	391 0.9×	316 0.8×	299 0.8×	65	3.6k
Jacob Schneiderman Israel	28	614 0.7×	407 0.8×	672 1.6×	159 0.4×	100 0.3×	100	3.0k
Mukesh K. Jain United States	38	2.2k 2.4×	491 0.9×	589 1.4×	392 1.0×	159 0.4×	68	4.1k
Ethan J. Weiss United States	20	538 0.6×	807 1.5×	355 0.8×	177 0.4×	435 1.1×	39	3.3k
Nicole Endlich Germany	34	1.6k 1.8×	243 0.5×	281 0.7×	465 1.1×	184 0.5×	118	3.5k

Countries citing papers authored by Suzanne Cheng

Since Specialization

Citations

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

Fields of papers citing papers by Suzanne Cheng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suzanne Cheng

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

All Works

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20 of 20 papers shown

Cheng, Suzanne, Gudula Kirtschig, Susan M. Cooper, et al.. (2012). Interventions for erosive lichen planus affecting mucosal sites. Cochrane Database of Systematic Reviews. 2015(12). CD008092–CD008092. 91 indexed citations

Cheng, Suzanne, Walter Koch, & Lin Wu. (2012). Co-development of a companion diagnostic for targeted cancer therapy. New Biotechnology. 29(6). 682–688. 32 indexed citations

Galgani, Andrea, Ana M. Valdes, M Kellis, et al.. (2010). Homozygosity for the Ala allele of the PPARγ2 Pro12Ala polymorphism is associated with reduced risk of coronary artery disease.. SHILAP Revista de lepidopterología. 29(5). 259–64. 12 indexed citations

Brown, Benjamin, Jérémie Nsengimana, Jennifer H. Barrett, et al.. (2010). An evaluation of inflammatory gene polymorphisms in sibships discordant for premature coronary artery disease: the GRACE-IMMUNE study. BMC Medicine. 8(1). 5–5. 19 indexed citations

Green, Deanna, Lori L. Vanscoy, M. Daniele Fallin, et al.. (2010). Use of a modeling framework to evaluate the effect of a modifier gene (MBL2) on variation in cystic fibrosis. European Journal of Human Genetics. 18(6). 680–684. 20 indexed citations

Zee, Anke H. Maitland‐van der, Bas Peters, Amy I. Lynch, et al.. (2009). The effect of nine common polymorphisms in coagulation factor genes (F2, F5, F7, F12 and F13) on the effectiveness of statins: the GenHAT study. Pharmacogenetics and Genomics. 19(5). 338–344. 14 indexed citations

Conen, David, Suzanne Cheng, Lori Steiner, et al.. (2008). Abstract 3135: Association of 77 Polymorphisms in 52 Candidate Genes with Blood Pressure Progression and Incident Hypertension: The Women's Genome Health Study. Circulation. 118. 1 indexed citations

Martinelli, Nicola, Elisabetta Trabetti, Mirko Pinotti, et al.. (2008). Combined Effect of Hemostatic Gene Polymorphisms and the Risk of Myocardial Infarction in Patients with Advanced Coronary Atherosclerosis. PLoS ONE. 3(2). e1523–e1523. 33 indexed citations

Iovannisci, David M., Edward J. Lammer, Lori Steiner, et al.. (2006). Association Between A Leukotriene C ₄ Synthase Gene Promoter Polymorphism and Coronary Artery Calcium in Young Women. Arteriosclerosis Thrombosis and Vascular Biology. 27(2). 394–399. 36 indexed citations

10.

Carmichael, Suzan L., Gary M. Shaw, David M. Iovannisci, et al.. (2006). Risks of human limb deficiency anomalies associated with 29 SNPs of genes involved in homocysteine metabolism, coagulation, cell–cell interactions, inflammatory response, and blood pressure regulation. American Journal of Medical Genetics Part A. 140A(22). 2433–2440. 14 indexed citations

11.

Berger, Klaus, Florian Stögbauer, Monika Stoll, et al.. (2006). The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case–control studies. Human Genetics. 121(2). 169–178. 65 indexed citations

12.

Cohen, Emily, Angelique C.M. Jansen, S. Matthijs Boekholdt, et al.. (2005). Genetic determinants of plasma HDL-cholesterol levels in familial hypercholesterolemia. European Journal of Human Genetics. 13(10). 1137–1142. 22 indexed citations

13.

Newman, Dina L., Sabine Hoffjan, Catherine Bourgain, et al.. (2004). Are common disease susceptibility alleles the same in outbred and founder populations?. European Journal of Human Genetics. 12(7). 584–590. 21 indexed citations

14.

Gršković, Branka, et al.. (2003). Polymorphisms of PON1 and PON2 genes in patients with coronary artery disease (Zagreb cohort). Clinical Chemistry and Laboratory Medicine (CCLM). 41. 1 indexed citations

15.

Ng, Maggie, Ying Wang, Wing‐Yee So, et al.. (2003). Ethnic differences in the linkage disequilibrium and distribution of single-nucleotide polymorphisms in 35 candidate genes for cardiovascular diseases. Genomics. 83(4). 559–565. 26 indexed citations

16.

Cheng, Suzanne, Michael Grow, Céline Pallaud, et al.. (1999). A Multilocus Genotyping Assay for Candidate Markers of Cardiovascular Disease Risk. Genome Research. 9(10). 936–949. 189 indexed citations

17.

Cheng, Suzanne, Juana Barceló, & Robert G. Korneluk. (1996). Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCR. Human Mutation. 7(4). 304–310. 29 indexed citations

18.

Cheng, Suzanne, Sheng-Yung Chang, Patti E. Gravitt, & Richard Respess. (1994). Long PCR. Nature. 369(6482). 684–685. 158 indexed citations

19.

Cheng, Suzanne, Georges Lutfalla, Gilles Uzé, Ilya Chumakov, & Katheleen Gardiner. (1993). GART, SON, IFNAR, and CRF2-4 genes cluster on human Chromosome 21 and mouse Chromosome 16. Mammalian Genome. 4(6). 338–342. 25 indexed citations

20.

Cheng, Suzanne, Aziz Sancar, & John E. Hearst. (1991). RecA-dependent incision of psoralen-crosslinked DNA by (A)BC excinuclease. Nucleic Acids Research. 19(3). 657–663. 56 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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