Serge B. Melançon

3.6k total citations
48 papers, 1.8k citations indexed

About

Serge B. Melançon is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Serge B. Melançon has authored 48 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 9 papers in Clinical Biochemistry. Recurrent topics in Serge B. Melançon's work include Genetic Neurodegenerative Diseases (10 papers), Metabolism and Genetic Disorders (9 papers) and Mitochondrial Function and Pathology (8 papers). Serge B. Melançon is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Metabolism and Genetic Disorders (9 papers) and Mitochondrial Function and Pathology (8 papers). Serge B. Melançon collaborates with scholars based in Canada, United States and France. Serge B. Melançon's co-authors include Andréa Richter, Louis Dallaire, Kenneth Morgan, C Largillière, Jean‐Pierre Bouchard, Thomas J. Hudson, Jean Mathieu, Michel Potier, Jocelyne Mercier and Bing Ge and has published in prestigious journals such as Science, New England Journal of Medicine and Nature Genetics.

In The Last Decade

Serge B. Melançon

47 papers receiving 1.7k citations

Peers

Countries citing papers authored by Serge B. Melançon

Since Specialization

Citations

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

Fields of papers citing papers by Serge B. Melançon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Serge B. Melançon. 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 Serge B. Melançon. The network helps show where Serge B. Melançon may publish in the future.

Co-authorship network of co-authors of Serge B. Melançon

This figure shows the co-authorship network connecting the top 25 collaborators of Serge B. Melançon. A scholar is included among the top collaborators of Serge B. Melançon 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 Serge B. Melançon. Serge B. Melançon 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

#	Work	Indexed citations
1	Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene 2013 ·Molecular Genetics and Metabolism ·Sirisak Chanprasert, Jing Wang, (unknown), Gregory M. Enns, Daniel R. Boué, Brenda Wong, Jerry R. Mendell, Deborah Perry, Zarife Sahenk, William J. Craigen, (unknown), Juan M. Pascual, Serge B. Melançon, Victor Wei Zhang, Fernando Scaglia, Lee-Jun Wong	27
2	A de novo 2.1‐Mb deletion of 13q12.11 in a child with developmental delay and minor dysmorphic features 2011 ·American Journal of Medical Genetics Part A ·Vazken M. Der Kaloustian, Laura Russell, Swaroop Aradhya, Gabriele Richard, Bernard Rosenblatt, Serge B. Melançon	6
3	A Novel Syndrome of Mandibular Hypoplasia, Deafness, and Progeroid Features Associated with Lipodystrophy, Undescended Testes, and Male Hypogonadism 2010 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Vinaya Simha, Koumudi Godbole, Paolo Sbraccia, Serge B. Melançon, Chittaranjan S. Yajnik, Giuseppe Novelli, Matthias Kroiß, Abhimanyu Garg	50
4	FOXE3 plays a significant role in autosomal recessive microphthalmia 2010 ·American Journal of Medical Genetics Part A ·Linda M. Reis, Rebecca C. Tyler, Adele Schneider, Tanya Bardakjian, Joan M. Stoler, Serge B. Melançon, Elena V. Semina	44
5	Tremor–ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3–10q23.31 2010 ·Neurogenetics ·Geneviève Bernard, Isabelle Thiffault, Martine Tétreault, (unknown), (unknown), Michel Sylvain, Serge B. Melançon, Rachel Laframboise, Pierre Langevin, Jean‐Pierre Bouchard, Michel Vanasse, Adeline Vanderver, Guillaume Sébire, Bernard Brais	29
6	Heparin cofactor II–thrombin complex: A biomarker of MPS disease 2008 ·Molecular Genetics and Metabolism ·Derrick R. Randall, (unknown), (unknown), Graham Sinclair, (unknown), Anita C. Thomas, Olaf A. Bodamer, (unknown), Paul M. Fernhoff, Robin Casey, (unknown), Grant A. Mitchell, (unknown), Serge B. Melançon, Tony Rupar, L. Clarke	45
7	Compound heterozygous deletions of PMP22 causing severe Charcot‐Marie‐Tooth disease of the Dejerine‐Sottas disease phenotype 2008 ·American Journal of Medical Genetics Part A ·Khalid Al‐Thihli, (unknown), Nancy Carson, Chantal Poulin, Serge B. Melançon, Vazken M. Der Kaloustian	20
8	Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry disease 2007 ·Molecular Genetics and Metabolism ·Christiane Auray‐Blais, Denis Cyr, (unknown), Michael L. West, Josanne Cox‐Brinkman, Daniel G. Bichet, Dominique P. Germain, Rachel Laframboise, Serge B. Melançon, Tracy Stockley, Joe T.R. Clarke, Régen Drouin	85
9	Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11 1999 ·The American Journal of Human Genetics ·Andréa Richter, John D. Rioux, Jean‐Pierre Bouchard, Jocelyne Mercier, Jean Mathieu, Bing Ge, Josée Poirier, (unknown), Gàbor Gyapay, Jean Weissenbach, Thomas J. Hudson, Serge B. Melançon, Kenneth Morgan	61
10	Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay (ARSACS): High-Resolution Physical and Transcript Map of the Candidate Region in Chromosome Region 13q11 1999 ·Genomics ·James C. Engert, Carole Doré, Jocelyne Mercier, Bing Ge, Christine Bétard, John D. Rioux, Carolyn A. Owen, Pierre Bérubé, (unknown), Bruce W. Birren, Serge B. Melançon, Kenneth Morgan, Thomas J. Hudson, Andréa Richter	20
11	GAA Instability in Friedreich's Ataxia Shares a Common, DNA-Directed and Intraallelic Mechanism with Other Trinucleotide Diseases 1998 ·Molecular Cell ·A. Marquis Gacy, Geoffrey M. Goellner, Craig Spiro, Xian Chen, (unknown), E. Morton Bradbury, Roy B. Dyer, (unknown), Janet Yao, Aaron J. Johnson, Andréa Richter, Serge B. Melançon, Cynthia T. McMurray	145
12	Autosomal recessive spastic ataxia of Charlevoix–Saguenay 1998 ·Neuromuscular Disorders ·Jean‐Pierre Bouchard, Andréa Richter, Jean Mathieu, Denis Brunet, Thomas J. Hudson, Kenneth Morgan, Serge B. Melançon	104
13	Friedreich ataxia in Acadian families from eastern Canada: Clinical diversity with conserved haplotypes 1996 ·American Journal of Medical Genetics ·Andréa Richter, Josée Poirier, Jocelyne Mercier, (unknown), Kenneth Morgan, Madeleine Roy, (unknown), Jean‐Pierre Bouchard, Serge B. Melançon	23
14	Chronic Sodium Benzoate Therapy in Children with Inborn Errors of Urea Synthesis: Effect on Carnitine Metabolism and Ammonia Nitrogen Removal 1996 ·Biochemical and Molecular Medicine ·Juan Carlos Feoli‐Fonseca, Marie Lambert, Grant A. Mitchell, Serge B. Melançon, Louis Dallaire, (unknown), Ijaz A. Qureshi	14
15	Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French — Canadian population 1994 ·Human Molecular Genetics ·Louise R. Simard, (unknown), Camille Rochette, Kenneth Morgan, (unknown), (unknown), Serge B. Melançon, Michel Vanasse	24
16	The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French Canada 1992 ·Human Genetics ·Peter Hechtman, Bernard Boulay, Marc De Braekeleer, (unknown), Serge B. Melançon, Jean Larochelle, Claude Prévost, Feige Kaplan	28
17	Neurologic Crises in Hereditary Tyrosinemia 1990 ·New England Journal of Medicine ·Grant A. Mitchell, Jean Larochelle, Marie Lambert, Jean Michaud, A Grenier, Hélène Ogier, Marie Gauthier, Jacques Lacroix, Michel Vanasse, Albert Larbrisseau, Khazal Paradis, Andrée Weber, (unknown), Serge B. Melançon, Louis Dallaire	147
18	Developmental patterns of intestinal disaccharidases in human amniotic fluid 1978 ·American Journal of Obstetrics and Gynecology ·Michel Potier, Serge B. Melançon, Louis Dallaire	30
19	A syndrome of generalized elastic fiber deficiency with leprechaunoid features: a distinct genetic disease with an autosomal recessive mode of inheritance 1976 ·Clinical Genetics ·Louis Dallaire, Marc Cantin, Serge B. Melançon, Gilles Perreault, Michel Potier	12
20	Acetic and benzoic acids in the urine of patients with chronic schizophrenia 1971 ·Clinica Chimica Acta ·Thomas L. Perry, Shirley Hansen, Sheila Diamond, Serge B. Melançon, (unknown)	15

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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