Sylvie Langlois

5.6k total citations
107 papers, 2.8k citations indexed

About

Sylvie Langlois is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Sylvie Langlois has authored 107 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Genetics, 57 papers in Pediatrics, Perinatology and Child Health and 40 papers in Molecular Biology. Recurrent topics in Sylvie Langlois's work include Prenatal Screening and Diagnostics (53 papers), Genomic variations and chromosomal abnormalities (28 papers) and Genetic Syndromes and Imprinting (23 papers). Sylvie Langlois is often cited by papers focused on Prenatal Screening and Diagnostics (53 papers), Genomic variations and chromosomal abnormalities (28 papers) and Genetic Syndromes and Imprinting (23 papers). Sylvie Langlois collaborates with scholars based in Canada, United States and United Kingdom. Sylvie Langlois's co-authors include Wendy P. Robinson, Dagmar K. Kalousek, Deborah E. McFadden, Irene Barrett, Michael R. Hayden, Irene Yam, P. N. Howard‐Peebles, R. Douglas Wilson, L.E. Bernard and John J.P. Kastelein and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Blood.

In The Last Decade

Sylvie Langlois

100 papers receiving 2.7k citations

Peers

Countries citing papers authored by Sylvie Langlois

Since Specialization

Citations

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

Fields of papers citing papers by Sylvie Langlois

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvie Langlois

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Pathways underlying selective neuronal vulnerability in Alzheimer's disease: Contrasting the vulnerable locus coeruleus to the resilient substantia nigra 2025 ·Alzheimer s & Dementia ·Alexander J. Ehrenberg, Cathrine Petersen, Felipe Luiz Pereira, Song Hua Li, Jessica L. Buxton, Sylvie Langlois, Marena Trinidad, (unknown), Renata Elaine Paraízo Leite, Roberta Diehl Rodriguez, Vítor Ribeiro Paes, Carlos Augusto Pasqualucci, William W. Seeley, Salvatore Spina, Cláudia Kimie Suemoto, Sally Temple, Daniela Kaufer, Lea T. Grinberg	2
2	Characterisation of FLT3 alterations in childhood acute lymphoblastic leukaemia 2023 ·British Journal of Cancer ·Ángela Gutiérrez-Camino, Chantal Richer, Manon Ouimet, (unknown), Sylvie Langlois, (unknown), Maxime Caron, Patrick Beaulieu, Pascal St-Onge, Alain R. Bataille, Daniel Sinnett	5
3	Comprehensive Genomic Analysis of Cemento-Ossifying Fibroma 2023 ·Modern Pathology ·Ricardo Santiago Gomez, (unknown), (unknown), Thaís dos Santos Fontes Pereira, (unknown), Tenzin Gayden, Damien Faury, Emily M. Nakada, Sylvie Langlois, Daniel Sinnett, Wagner Henriques Castro, Marina Gonçalves Diniz, Nada Jabado, Carolina Cavaliéri Gomes	3
4	Out‐of‐pocket and private pay in clinical genetic testing: A scoping review 2021 ·Clinical Genetics ·Peter J. Grant, Sylvie Langlois, Larry D. Lynd, (unknown), Jehannine Austin, Alison M. Elliott	28
5	Effect of preexamination conditions in a centralized-testing model of non-invasive prenatal screening 2021 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·(unknown), Sylvie Giroux, (unknown), (unknown), Jeremy Parker, (unknown), Loubna Jouan, Sylvie Langlois, Guy A. Rouleau, François Rousseau, Aly Karsan	0
6	A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8 2019 ·Journal of Human Genetics ·Heba Yasin, William T. Gibson, Sylvie Langlois, Robert Stowe, Erica S. Tsang, (unknown), (unknown), (unknown), Christine Tyson, Chi Kin Wong, Marco A. Marra, Jan M. Friedman, Farah Zahir	25
7	Non-invasive prenatal aneuploidy testing: Critical diagnostic performance parameters predict sample z-score values 2018 ·Clinical Biochemistry ·Jonatan Blais, Sylvie Giroux, (unknown), (unknown), Alexandre Dionne‐Laporte, Loubna Jouan, Julie Gauthier, (unknown), Richard A. Moore, Jeremy Parker, (unknown), Yongjun Zhao, Guy A. Rouleau, Aly Karsan, Sylvie Langlois, François Rousseau	7
8	Attitudes toward prenatal screening for chromosomal abnormalities: A focus group study 2018 ·Women and Birth ·Sarah Munro, (unknown), Wei Zhang, (unknown), Logan Trenaman, Sylvie Langlois, Aslam H. Anis	7
9	Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues 2016 ·The Application of Clinical Genetics ·Jean Gekas, Sylvie Langlois, Vardit Ravitsky, François Audibert, David Van Den Berg, Hazar Haidar, François Rousseau	34
10	Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus? 2015 ·Prenatal Diagnosis ·Lyn S. Chitty, Jan M. Friedman, Sylvie Langlois	10
11	Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsia 2014 ·Placenta ·John D. Blair, Sylvie Langlois, Deborah E. McFadden, Wendy P. Robinson	27
12	Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes 2013 ·European Journal of Human Genetics ·Tracy Tucker, Farah Zahir, Malachi Griffith, Allen Delaney, David Chai, Erica S. Tsang, Emmanuelle Lemyre, Sylvia Dobrzeniecka, Marco A. Marra, Patrice Eydoux, Sylvie Langlois, Fadi F. Hamdan, Jacques L. Michaud, Jan M. Friedman	30
13	An evaluation of the decision‐making process regarding amniocentesis following a screen‐positive maternal serum screen result 2009 ·Prenatal Diagnosis ·Christine Kobelka, André Mattman, Sylvie Langlois	22
14	Patterns of variation in DNA segments upstream of transcription start sites 2007 ·Human Mutation ·Damian Labuda, Catherine Labbé, Sylvie Langlois, Jean‐François Lefebvre, Virginie Freytag, Claudia Moreau, (unknown), Patrick Beaulieu, Tomi Pastinen, Thomas J. Hudson, Daniel Sinnett	3
15	Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes 2006 ·Genomics ·Daniel Sinnett, Patrick Beaulieu, Hélène Bélanger, Jean‐François Lefebvre, Sylvie Langlois, (unknown), Simon Drouin, (unknown), Thomas J. Hudson, Damian Labuda	22
16	Submicroscopic deletions and duplications in individuals with intellectual disability detected by array‐CGH 2005 ·American Journal of Medical Genetics Part A ·Christine Tyson, Chansonette Harvard, (unknown), Jan M. Friedman, Sylvie Langlois, M. E. Suzanne Lewis, Margot Van Allen, Martin J. Somerville, Laura Arbour, L. Clarke, (unknown), Siu Li Yong, (unknown), Evica Rajcan‐Separovic	86
17	Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction. 1997 ·PubMed ·Wendy P. Robinson, Irene Barrett, L.E. Bernard, Adèle Telenius, Fosco Bernasconi, R. Douglas Wilson, Robert G. Best, P. N. Howard‐Peebles, Sylvie Langlois, Dagmar K. Kalousek	164
18	CYTOGENETIC AND AGE-DEPENDENT RISK FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY 15 1996 ·Prenatal Diagnosis ·Wendy P. Robinson, Sylvie Langlois, Simone Schuffenhauer, Bernhard Horsthemke, Ron C. Michaelis, Susan L. Christian, David H. Ledbetter, Albert Schinzel	50
19	Trisomy 7 CVS mosaicism: Pregnancy outcome, placental and DNA analysis in 14 cases 1996 ·American Journal of Medical Genetics ·Dagmar K. Kalousek, Sylvie Langlois, Wendy P. Robinson, Adèle Telenius, L.E. Bernard, Irene Barrett, P. N. Howard‐Peebles, R. Douglas Wilson	46
20	New Mechanisms for Genetic Disease and Nontraditional Modes of Inheritance 1995 ·Advances in Pediatrics ·Sylvie Langlois, Elena Lopez‐Rangel, Judith G. Hall	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.

Explore authors with similar magnitude of impact