Marie Lambert

1.3k total citations
29 papers, 901 citations indexed

About

Marie Lambert is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Marie Lambert has authored 29 papers receiving a total of 901 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 7 papers in Genetics. Recurrent topics in Marie Lambert's work include Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (5 papers) and Obesity, Physical Activity, Diet (4 papers). Marie Lambert is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (5 papers) and Obesity, Physical Activity, Diet (4 papers). Marie Lambert collaborates with scholars based in Canada, United States and Belgium. Marie Lambert's co-authors include Grant A. Mitchell, François‐Guillaume Debray, Pierre Allard, Brian H. Robinson, James A. Hanley, Barbara K. Goodman, Shlomo Almashanu, Cassandra Obie, David Valle and Robin Casey and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and American Journal of Clinical Nutrition.

In The Last Decade

Marie Lambert

29 papers receiving 866 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marie Lambert Canada 16 413 292 180 127 126 29 901
Iris Scala Italy 16 425 1.0× 139 0.5× 69 0.4× 119 0.9× 177 1.4× 37 862
Peter J. Stahl United States 23 402 1.0× 159 0.5× 286 1.6× 217 1.7× 115 0.9× 60 1.4k
Georgianne L. Arnold United States 20 546 1.3× 616 2.1× 119 0.7× 263 2.1× 181 1.4× 56 1.4k
Chi‐Ren Tsai Taiwan 22 431 1.0× 279 1.0× 54 0.3× 97 0.8× 45 0.4× 54 1.2k
B F Kase Norway 15 378 0.9× 241 0.8× 101 0.6× 40 0.3× 81 0.6× 24 887
Magnhild Rasmussen Norway 18 819 2.0× 179 0.6× 106 0.6× 69 0.5× 38 0.3× 55 1.3k
Andrew A. M. Morris United Kingdom 22 903 2.2× 949 3.3× 103 0.6× 128 1.0× 117 0.9× 45 1.4k
József Kovács Hungary 18 401 1.0× 131 0.4× 46 0.3× 98 0.8× 37 0.3× 46 1.1k
Amy Goldstein United States 15 779 1.9× 532 1.8× 54 0.3× 144 1.1× 59 0.5× 29 1.1k
Anna‐Kaisa Niemi United States 14 501 1.2× 238 0.8× 48 0.3× 321 2.5× 74 0.6× 27 1.1k

Countries citing papers authored by Marie Lambert

Since Specialization
Citations

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

Fields of papers citing papers by Marie Lambert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie Lambert

This figure shows the co-authorship network connecting the top 25 collaborators of Marie Lambert. A scholar is included among the top collaborators of Marie Lambert 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 Marie Lambert. Marie Lambert 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.
Caburet, Sandrine, Elodie Dardillac, Marie Lambert, et al.. (2020). Homozygous hypomorphic BRCA2 variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait. Journal of Medical Genetics. 58(2). 125–134. 24 indexed citations
2.
Charlier, Bernadette & Marie Lambert. (2019). Evaluating the effects of faculty development: theoretical framework and empirical implementation. The International Journal for Academic Development. 25(2). 162–175. 8 indexed citations
3.
Kakinami, Lisa, Lise Gauvin, Louise Séguin, et al.. (2014). Persistent and occasional poverty and children's food consumption: evidence from a longitudinal Québec birth cohort. Journal of Epidemiology & Community Health. 68(10). 987–992. 4 indexed citations
4.
Lundgren, Jennifer D., Kelly C. Allison, Albert J. Stunkard, et al.. (2012). Validity of the night eating questionnaire in children. International Journal of Eating Disorders. 45(7). 861–865. 11 indexed citations
5.
Hulst, Andraea Van, Lise Gauvin, Mark Daniel, et al.. (2012). Associations Between Children’s Diets and Features of Their Residential and School Neighbourhood Food Environments. Canadian Journal of Public Health. 103(S3). S48–S54. 47 indexed citations
6.
Thiel, Christian, Georg F. Hoffmann, Kristen Hanson, et al.. (2011). Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. Human Mutation. 33(3). 485–487. 29 indexed citations
7.
Chaiton, Michael, Jennifer O’Loughlin, Igor Karp, & Marie Lambert. (2010). Depressive Symptoms and C-Reactive Protein Are Not Associated in a Population-Based Sample of Adolescents. International Journal of Behavioral Medicine. 17(3). 216–222. 27 indexed citations
8.
Debray, François‐Guillaume, Aïcha Mérouani, Marie Lambert, et al.. (2008). Acute Tubular Dysfunction With Fanconi Syndrome: A New Manifestation of Mitochondrial Cytopathies. American Journal of Kidney Diseases. 51(4). 691–696. 5 indexed citations
9.
Debray, François‐Guillaume, Marie Lambert, & Grant A. Mitchell. (2008). Disorders of mitochondrial function. Current Opinion in Pediatrics. 20(4). 471–482. 56 indexed citations
10.
Debray, François‐Guillaume, Marie Lambert, Anne Lortie, Michel Vanasse, & Grant A. Mitchell. (2007). Long‐term outcome of Leigh syndrome caused by the NARP‐T8993C mtDNA mutation. American Journal of Medical Genetics Part A. 143A(17). 2046–2051. 38 indexed citations
11.
Debray, François‐Guillaume, Grant A. Mitchell, Pierre Allard, et al.. (2007). Diagnostic Accuracy of Blood Lactate-to-Pyruvate Molar Ratio in the Differential Diagnosis of Congenital Lactic Acidosis. Clinical Chemistry. 53(5). 916–921. 97 indexed citations
12.
Henderson, Mélanie, Émile Lévy, Edgard Delvin, Monique Losekoot, & Marie Lambert. (2006). Prevalence and clinical phenotype of the p.Val226Met glucokinase gene mutation in French Canadians in Quebec, Canada. Molecular Genetics and Metabolism. 90(1). 87–92. 6 indexed citations
13.
Delvin, Edgard, Rima Rozen, Aïcha Mérouani, Jacques Genest, & Marie Lambert. (2000). Influence of methylenetetrahydrofolate reductase genotype, age, vitamin B-12, and folate status on plasma homocysteine in children. American Journal of Clinical Nutrition. 72(6). 1469–1473. 57 indexed citations
14.
Lambert, Marie, Robert Giguère, Christiane Auray‐Blais, et al.. (1999). Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening program. The Journal of Pediatrics. 134(6). 675–680. 51 indexed citations
15.
Obie, Cassandra, Barbara K. Goodman, Chien-an A. Hu, et al.. (1999). Hyperornithinaemia- hyperammonaemia- homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Nature Genetics. 22(2). 151–158. 152 indexed citations
16.
Vohl, Marie‐Claude, Madeleine Roy, Daniel Gaudet, et al.. (1997). Geographic distribution of French‐Canadian low‐density lipoprotein receptor gene mutations in the Province of Quebec. Clinical Genetics. 52(1). 1–6. 35 indexed citations
17.
18.
Matthijs, Gert, Eric Legius, Els Schollen, et al.. (1996). Evidence for Genetic Heterogeneity in the Carbohydrate-Deficient Glycoprotein Syndrome Type I (CDG1). Genomics. 35(3). 597–599. 26 indexed citations
19.
Michaud, Jacques L., D Filiatrault, Louis Dallaire, & Marie Lambert. (1995). New autosomal recessive form of amelia. American Journal of Medical Genetics. 56(2). 164–167. 7 indexed citations
20.
Luks, François I., Dickens St‐Vil, Jean‐Martin Laberge, et al.. (1993). SURGICAL AND METABOLIC ASPECTS OF LIVER TRANSPLANTATION FOR TYROSINEMIA1. Transplantation. 56(6). 1376–1380. 7 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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