N Laflamme

743 total citations
16 papers, 608 citations indexed

About

N Laflamme is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Biological Psychiatry. According to data from OpenAlex, N Laflamme has authored 16 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 3 papers in Biological Psychiatry. Recurrent topics in N Laflamme's work include Sexual Differentiation and Disorders (5 papers), Hormonal and reproductive studies (4 papers) and Hormonal Regulation and Hypertension (4 papers). N Laflamme is often cited by papers focused on Sexual Differentiation and Disorders (5 papers), Hormonal and reproductive studies (4 papers) and Hormonal Regulation and Hypertension (4 papers). N Laflamme collaborates with scholars based in Canada, France and United States. N Laflamme's co-authors include Serge Rivest, Rossella E. Nappi, Jacques Simard, Éric Rhéaume, Fernand Labrie, German Torres, Judith M. Horowitz, François Rousseau, Rocío Sánchez and Denis Richard and has published in prestigious journals such as Journal of Neuroscience, The Journal of Clinical Endocrinology & Metabolism and Neuroscience.

In The Last Decade

N Laflamme

15 papers receiving 590 citations

Peers

Countries citing papers authored by N Laflamme

Since Specialization

Citations

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

Fields of papers citing papers by N Laflamme

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N Laflamme

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	X‐Linked Bilateral Polymicrogyria With Epilepsy and Intellectual Disability Associated With a Novel KIF4A Variant 2024 ·American Journal of Medical Genetics Part A ·N Laflamme, (unknown), (unknown), Dènahin Hinnoutondji Toffa, Laurent Létourneau‐Guillon, Annie Laplante, Patrick Cossette, Éric Samarut, Martine Tétreault, Dang Khoa Nguyen	1
2	Statin withdrawal and health-related quality of life in a primary cardiovascular prevention cohort 2023 ·Quality of Life Research ·(unknown), Pascale Mauriège, Jérôme Frenette, N Laflamme, (unknown), (unknown), Jean Bergeron, Denis R. Joanisse	2
3	Cochlear implantation in patients with chronic otitis media and radical mastoidectomy: A single-stage procedure. 2014 ·PubMed ·Mathieu Piché, (unknown), Daniel J Philippon, N Laflamme, Richard Bussières	0
4	Assessment of the prevalence of the 985A>G MCAD mutation in the French‐Canadian population using allele‐specific PCR 2007 ·Clinical Genetics ·Sylvie Giroux, (unknown), (unknown), Yves Labelle, N Laflamme, Yves Giguère, François Rousseau	13
5	Hereditary hemochromatosis screening: effect of mutation penetrance and prevalence on cost‐effectiveness of testing algorithms 2006 ·Clinical Genetics ·(unknown), Daniel Reinharz, N Laflamme, P C Adams, François Rousseau	28
6	Leisure Physical Activity is Associated with Quantitative Ultrasound Measurements Independently of Bone Mineral Density in Postmenopausal Women 2003 ·Calcified Tissue International ·(unknown), Yves Giguère, Denis Prud’homme, Lucile Turcot-Lemay, Martine Dumont, Geneviève Leduc, Sylvie Côté, N Laflamme, François Rousseau, Sylvie Dodin	37
7	Comparative immunogenicity under field conditions of two recombinant hepatitis B vaccines in 8–10-year-old children 2000 ·Vaccine ·Bernard Duval, Nicole Boulianne, Gaston De Serres, N Laflamme, Philippe De Wals, Raymond Massé, (unknown), Gilles Delage, Laurence Desjardins	23
8	Involvement of serotonergic pathways in mediating the neuronal activity and genetic transcription of neuroendocrine corticotropin-releasing factor in the brain of systemically endotoxin-challenged rats 1999 ·Neuroscience ·N Laflamme, (unknown), Denis Richard, Serge Rivest	35
9	Fluoxetine induces the transcription of genes encoding c-fos, corticotropin-releasing factor and its type 1 receptor in rat brain 1998 ·Neuroscience ·German Torres, Judith M. Horowitz, N Laflamme, Serge Rivest	57
10	Job strain and ambulatory blood pressure among female white-collar workers 1998 ·Scandinavian Journal of Work Environment & Health ·N Laflamme, Chantal Brisson, Jocelyne Moisan, Alain Milot, Benoı̂t Mâsse, M Vézina	49
11	Mutation R96W in cytochrome P450c17 gene causes combined 17 alpha-hydroxylase/17-20-lyase deficiency in two French Canadian patients. 1996 ·The Journal of Clinical Endocrinology & Metabolism ·N Laflamme, J LEBLANC, Jacques Mailloux, Nacia Faure, Fernand Labrie, Jacques Simard	38
12	Immune challenge and immobilization stress induce transcription of the gene encoding the CRF receptor in selective nuclei of the rat hypothalamus 1995 ·Journal of Neuroscience ·Serge Rivest, N Laflamme, Rossella E. Nappi	177
13	Nonsalt-losing male pseudohermaphroditism due to the novel homozygous N100S mutation in the type II 3 beta-hydroxysteroid dehydrogenase gene. 1995 ·The Journal of Clinical Endocrinology & Metabolism ·Farida Mébarki, Rocío Sánchez, Éric Rhéaume, N Laflamme, Jacques Simard, Maguelone G. Forest, (unknown), Muriel D. David, Fernand Labrie, Yves Morel	24
14	Detection and functional characterization of the novel missense mutation Y254D in type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) gene of a female patient with nonsalt-losing 3 beta HSD deficiency. 1994 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Éric Rhéaume, N Laflamme, Robert L. Rosenfield, Fernand Labrie, Jacques Simard	42
15	Molecular basis of congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency. 1993 ·Molecular Endocrinology ·Jacques Simard, Éric Rhéaume, Rocío Sánchez, N Laflamme, Yvan de Launoit, Van Luu‐The, Arnoud P. van Seters, Richard D. Gordon, Markus Bettendorf, U. Heinrich	78
16	MOLECULAR BASIS OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 3β-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY 1993 ·Pediatric Research ·Jacques Simard, Yves Morel, Éric Rhéaume, Rocío Sánchez, Farida Mébarki, N Laflamme, Maria I. New, Fernand Labrie	4

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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