Louisa Goumidi

2.0k total citations
47 papers, 1.0k citations indexed

About

Louisa Goumidi is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Physiology. According to data from OpenAlex, Louisa Goumidi has authored 47 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Endocrinology, Diabetes and Metabolism, 13 papers in Genetics and 11 papers in Physiology. Recurrent topics in Louisa Goumidi's work include Genetic Associations and Epidemiology (9 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (8 papers) and Alzheimer's disease research and treatments (6 papers). Louisa Goumidi is often cited by papers focused on Genetic Associations and Epidemiology (9 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (8 papers) and Alzheimer's disease research and treatments (6 papers). Louisa Goumidi collaborates with scholars based in France, Algeria and United States. Louisa Goumidi's co-authors include Philippe Amouyel, Helen M. Roche, Catherine M. Phillips, Denis Lairon, Sandrine Bertrais, Richard Planells, Aline Meirhaeghe, Ross McManus, Serge Herçberg and Martyn R. Field and has published in prestigious journals such as American Journal of Clinical Nutrition, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

Louisa Goumidi

46 papers receiving 1.0k citations

Peers

Louisa Goumidi

PHYSI

GENET

EDM

EPIDE

Ana Alonso Spain

María Luisa Mansego Spain

Takaya Nakane Japan

Paúl Cordero United Kingdom

Tarunveer S. Ahluwalia Denmark

Michael T. Pedrini Austria

Jina Hong United States

Fiona McMurray United Kingdom

Masayo Yamada Japan

Jan B. van Klinken Netherlands

Ana Alonso Spain

Louisa Goumidi

227 ×0.6

PHYSI

310 ×0.9

301 ×1.2

GENET

347 ×1.6

EDM

151 ×1.1

EPIDE

Citations per year, relative to Louisa Goumidi Louisa Goumidi (= 1×) peers Ana Alonso

Countries citing papers authored by Louisa Goumidi

Since Specialization

Citations

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

Fields of papers citing papers by Louisa Goumidi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louisa Goumidi

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

Goumidi, Louisa, Astrid van Hylckama Vlieg, Maria Bruzelius, et al.. (2023). Association of ABO blood groups with venous thrombosis recurrence in middle-aged patients: insights from a weighted Cox analysis dedicated to ambispective design. BMC Medical Research Methodology. 23(1). 99–99. 2 indexed citations

Thibord, Florian, Noémie Saut, Louisa Goumidi, et al.. (2019). A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process. Journal of Thrombosis and Haemostasis. 17(11). 1808–1814. 4 indexed citations

Suchon, Pierre, Françis Couturaud, David M. Smadja, et al.. (2019). Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation. Scientific Reports. 9(1). 3750–3750. 4 indexed citations

Pigeyre, Marie, J. Rousseaux, Julie Dumont, et al.. (2016). How obesity relates to socio-economic status: identification of eating behavior mediators. International Journal of Obesity. 40(11). 1794–1801. 48 indexed citations

Houti, Leïla, et al.. (2016). Prevalence of Metabolic Syndrome and its Related Risk Factors in the City of Oran, Algeria: the ISOR Study. Ethnicity & Disease. 26(1). 99–99. 22 indexed citations

Médiène-Benchekor, Sounnia, Xavier Hermant, Nadhira Saïdi‐Mehtar, et al.. (2015). Associations of common SNPs in the SORT1, GCKR, LPL, APOA1, CETP, LDLR, APOE genes with lipid trait levels in an Algerian population sample.. PubMed. 8(6). 7358–63. 11 indexed citations

Médiène-Benchekor, Sounnia, Xavier Hermant, Benjamin Grenier‐Boley, et al.. (2015). Examination of the brain natriuretic peptide rs198389 single-nucleotide polymorphism on type 2 diabetes mellitus and related phenotypes in an Algerian population. Gene. 567(2). 159–163. 6 indexed citations

Médiène-Benchekor, Sounnia, Xavier Hermant, Nadhira Saïdi‐Mehtar, et al.. (2014). The TCF7L2rs7903146 polymorphism, dietary intakes and type 2 diabetes risk in an Algerian population. BMC Genetics. 15(1). 134–134. 30 indexed citations

Goumidi, Louisa, Dominique Cottel, Jean Dallongeville, Philippe Amouyel, & Aline Meirhaeghe. (2014). Effects of established BMI-associated loci on obesity-related traits in a French representative population sample. BMC Genetics. 15(1). 62–62. 19 indexed citations

10.

Goumidi, Louisa, Julie Dumont, D. Cottel, et al.. (2012). Impact of REV-ERB alpha gene polymorphisms on obesity phenotypes in adult and adolescent samples. International Journal of Obesity. 37(5). 666–672. 40 indexed citations

11.

Goumidi, Louisa, Karine Gauthier, Vanessa Legry, et al.. (2011). Association Between a Thyroid Hormone Receptor-α Gene Polymorphism and Blood Pressure but Not With Coronary Heart Disease Risk. American Journal of Hypertension. 24(9). 1027–1034. 8 indexed citations

12.

Phillips, Catherine M., Louisa Goumidi, Sandrine Bertrais, et al.. (2011). Dietary saturated fat, gender and genetic variation at the TCF7L2 locus predict the development of metabolic syndrome. The Journal of Nutritional Biochemistry. 23(3). 239–244. 51 indexed citations

13.

Phillips, Catherine M., Louisa Goumidi, Sandrine Bertrais, et al.. (2010). Gene-nutrient interactions with dietary fat modulate the association between genetic variation of the ACSL1 gene and metabolic syndrome. Journal of Lipid Research. 51(7). 1793–1800. 50 indexed citations

14.

Phillips, Catherine M., Louisa Goumidi, Sandrine Bertrais, et al.. (2010). ACC2 gene polymorphisms, metabolic syndrome, and gene-nutrient interactions with dietary fat. Journal of Lipid Research. 51(12). 3500–3507. 29 indexed citations

15.

Goumidi, Louisa, Frédéric Flamant, Corinne Lendon, et al.. (2009). Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease. Neurobiology of Aging. 32(4). 624–630. 14 indexed citations

16.

Phillips, Catherine M., Louisa Goumidi, Sandrine Bertrais, et al.. (2009). Dietary Saturated Fat Modulates the Association between STAT3 Polymorphisms and Abdominal Obesity in Adults ,. Journal of Nutrition. 139(11). 2011–2017. 38 indexed citations

17.

Legry, Vanessa, Louisa Goumidi, Marlène Huyvaert, et al.. (2009). Association between angiopoietin-like 6 (ANGPTL6) gene polymorphisms and metabolic syndrome-related phenotypes in the French MONICA Study. Diabetes & Metabolism. 35(4). 287–292. 12 indexed citations

18.

Chartier‐Harlin, Marie‐Christine, Louisa Goumidi, & Jean‐Charles Lambert. (2004). Complexité génétique de la maladie d’Alzheimer. Revue Neurologique. 160(2). 251–255. 2 indexed citations

19.

Goumidi, Louisa, Jean‐Charles Lambert, D. Cottel, Philippe Amouyel, & Marie‐Christine Chartier‐Harlin. (2002). No association of the HLA-A2 allele with Alzheimer's disease. Neuroscience Letters. 335(2). 75–78. 18 indexed citations

20.

Lambert, Jean‐Charles, Louisa Goumidi, Fabienne Wavrant‐De Vrièze, et al.. (2000). The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease. Human Molecular Genetics. 9(15). 2275–2280. 62 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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