Laurence Tiret

30.0k total citations · 5 hit papers
151 papers, 15.5k citations indexed

About

Laurence Tiret is a scholar working on Cardiology and Cardiovascular Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Laurence Tiret has authored 151 papers receiving a total of 15.5k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Cardiology and Cardiovascular Medicine, 39 papers in Genetics and 37 papers in Molecular Biology. Recurrent topics in Laurence Tiret's work include Genetic Associations and Epidemiology (32 papers), Adipokines, Inflammation, and Metabolic Diseases (23 papers) and Atherosclerosis and Cardiovascular Diseases (18 papers). Laurence Tiret is often cited by papers focused on Genetic Associations and Epidemiology (32 papers), Adipokines, Inflammation, and Metabolic Diseases (23 papers) and Atherosclerosis and Cardiovascular Diseases (18 papers). Laurence Tiret collaborates with scholars based in France, Germany and United Kingdom. Laurence Tiret's co-authors include François Cambien, Stefan Blankenberg, Christoph Bickel, Odette Poirier, Florent Soubrier, Hans J. Rupprecht, Dominique Arveiler, Sandrine Barbaux, Viviane Nicaud and Stefan Blankenberg and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

Laurence Tiret

151 papers receiving 15.0k citations

Hit Papers

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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.

Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction

1992 1.6k citations François Cambien, Odette Poirier et al. profile →
Evidence, from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels.

1992 1.0k citations Laurence Tiret, Sophie Visvikis‐Siest et al. profile →
Adhesion molecules and atherosclerosis

2003 869 citations Laurence Tiret et al. Atherosclerosis profile →
Plasma Concentrations and Genetic Variation of Matrix Metalloproteinase 9 and Prognosis of Patients With Cardiovascular Disease

2003 616 citations Stefan Blankenberg, Hans J. Rupprecht et al. Circulation profile →
Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension.

1994 600 citations Alain Bonnardeaux, Laurence Tiret et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laurence Tiret France	65	7.0k	4.2k	3.3k	2.9k	2.2k	151	15.5k
François Cambien France	71	10.0k 1.4×	7.0k 1.7×	3.9k 1.2×	3.2k 1.1×	3.1k 1.4×	229	20.8k
Douglas E. Vaughan United States	70	6.5k 0.9×	2.7k 0.6×	4.0k 1.2×	2.9k 1.0×	828 0.4×	229	17.0k
Agnes B. Fogo United States	86	3.8k 0.5×	3.2k 0.8×	7.1k 2.2×	2.7k 0.9×	1.5k 0.7×	501	23.7k
Merlin C. Thomas Australia	69	3.5k 0.5×	6.1k 1.4×	4.2k 1.3×	2.5k 0.9×	1.3k 0.6×	351	18.8k
Enyu Imai Japan	61	3.6k 0.5×	2.3k 0.5×	4.8k 1.5×	3.0k 1.1×	1.5k 0.7×	324	18.7k
Muredach P. Reilly United States	70	4.2k 0.6×	2.5k 0.6×	4.9k 1.5×	4.0k 1.4×	1.5k 0.7×	302	18.5k
Hirofumi Makino Japan	74	2.9k 0.4×	3.9k 0.9×	7.0k 2.1×	3.3k 1.2×	1.3k 0.6×	672	23.6k
Heribert Schunkert Germany	73	13.2k 1.9×	3.5k 0.8×	3.9k 1.2×	4.2k 1.5×	2.3k 1.0×	602	20.5k
Hermann Haller Germany	80	4.8k 0.7×	3.5k 0.8×	7.0k 2.1×	4.1k 1.4×	744 0.3×	454	23.0k
Danilo Fliser Germany	75	4.3k 0.6×	1.7k 0.4×	4.0k 1.2×	2.7k 1.0×	1.0k 0.5×	301	18.6k

Countries citing papers authored by Laurence Tiret

Since Specialization

Citations

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

Fields of papers citing papers by Laurence Tiret

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurence Tiret

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Tiret. A scholar is included among the top collaborators of Laurence Tiret 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 Laurence Tiret. Laurence Tiret 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

Müller, Christian, Arne Schillert, Caroline Röthemeier, et al.. (2016). Removing Batch Effects from Longitudinal Gene Expression - Quantile Normalization Plus ComBat as Best Approach for Microarray Transcriptome Data. PLoS ONE. 11(6). e0156594–e0156594. 92 indexed citations

Plichart, Matthieu, Jean‐Philippe Empana, Jean‐Charles Lambert, et al.. (2012). Single polymorphism nucleotide rs1333049 on chromosome 9p21 is associated with carotid plaques but not with common carotid intima-media thickness in older adults. A combined analysis of the Three-City and the EVA studies. Atherosclerosis. 222(1). 187–190. 9 indexed citations

Schnabel, Renate B., Andreas Schulz, Claudia‐Martina Messow, et al.. (2010). Multiple marker approach to risk stratification in patients with stable coronary artery disease. European Heart Journal. 31(24). 3024–3031. 85 indexed citations

Mazoyer, E., Laurent Ripoll, R Guéguen, et al.. (2009). Prevalence of factor V Leiden and prothrombin G20210A mutation in a large French population selected for nonthrombotic history: geographical and age distribution. Blood Coagulation & Fibrinolysis. 20(7). 503–510. 29 indexed citations

Proust, Carole, Mervi Alanne, Veikko Salomaa, et al.. (2009). Lack of association between polymorphisms of the IL18R1 and IL18RAP genes and cardiovascular risk: the MORGAM Project. BMC Medical Genetics. 10(1). 44–44. 14 indexed citations

Sinning, Jan‐Malte, Christoph Bickel, Claudia‐Martina Messow, et al.. (2006). Impact of C-reactive protein and fibrinogen on cardiovascular prognosis in patients with stable angina pectoris: the AtheroGene study. European Heart Journal. 27(24). 2962–2968. 61 indexed citations

Schnabel, Renate B., Karl J. Lackner, Hans J. Rupprecht, et al.. (2005). Glutathione Peroxidase-1 and Homocysteine for Cardiovascular Risk Prediction. Journal of the American College of Cardiology. 45(10). 1631–1637. 86 indexed citations

Cambien, François & Laurence Tiret. (2005). Atherosclerosis: From Genetic Polymorphisms to System Genetics. Cardiovascular Toxicology. 5(2). 143–152. 12 indexed citations

Batide-Alanore, Agnès La, David‐Alexandre Trégouët, Catherine Sass, et al.. (2003). Family study of the relationship between height and cardiovascular risk factors in the STANISLAS cohort. International Journal of Epidemiology. 32(4). 607–614. 18 indexed citations

10.

Blankenberg, Stefan, Gérald Luc, Pierre Ducimetière, et al.. (2003). Interleukin-18 and the Risk of Coronary Heart Disease in European Men. Circulation. 108(20). 2453–2459. 263 indexed citations

11.

Deakin, Sara, et al.. (2002). Paraoxonase-1 L55M Polymorphism Is Associated with an Abnormal Oral Glucose Tolerance Test and Differentiates High Risk Coronary Disease Families. The Journal of Clinical Endocrinology & Metabolism. 87(3). 1268–1273. 28 indexed citations

12.

Donger, Claire, Viviane Nicaud, Caroline Morrison, et al.. (2001). New polymorphisms in the interleukin‐10 gene – relationships to myocardial infarction. European Journal of Clinical Investigation. 31(1). 9–15. 63 indexed citations

13.

Cambien, François, Odette Poirier, Viviane Nicaud, et al.. (1999). Sequence Diversity in 36 Candidate Genes for Cardiovascular Disorders. The American Journal of Human Genetics. 65(1). 183–191. 124 indexed citations

14.

Brazier, Lionel, Laurence Tiret, Gérald Luc, et al.. (1999). Sequence polymorphisms in the apolipoprotein(a) gene and their association with lipoprotein(a) levels and myocardial infarction. The ECTIM Study. Atherosclerosis. 144(2). 323–333. 46 indexed citations

15.

Kee, Frank, et al.. (1997). Short stature and heart disease: nature or nurture? The EARS Group. International Journal of Epidemiology. 26(4). 748–756. 24 indexed citations

16.

Tiret, Laurence. (1997). The Renin-Angiotensin System Gene Polymorphism and Left Ventricular Hypertrophy. Advances in experimental medicine and biology. 432. 111–115. 5 indexed citations

17.

Tiret, Laurence, Pierre Ducimetière, Alain Bonnardeaux, et al.. (1994). Synergistic effects of angiotensin-converting enzyme and angiotensin-II type 1 receptor gene polymorphisms on risk of myocardial infarction. The Lancet. 344(8927). 910–913. 356 indexed citations

18.

Kee, Frank, Laurence Tiret, Viviane Nicaud, et al.. (1993). Reliability of reported family history of myocardial infarction.. BMJ. 307(6918). 1528–1530. 118 indexed citations

19.

Tiret, Laurence, et al.. (1992). Segregation analysis of height‐adjusted weight with generation‐ and age‐dependent effects: The Nancy family study. Genetic Epidemiology. 9(6). 389–403. 25 indexed citations

20.

Tiret, Laurence, Pierre Ducimetière, Jean-Luc André, et al.. (1991). Family resemblance in body circumferences and their ratios: the Nancy family study. Annals of Human Biology. 18(3). 259–271. 13 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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