Julie Lauzon

2.0k total citations
23 papers, 430 citations indexed

About

Julie Lauzon is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Julie Lauzon has authored 23 papers receiving a total of 430 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Julie Lauzon's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Julie Lauzon is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Julie Lauzon collaborates with scholars based in Canada, United States and United Kingdom. Julie Lauzon's co-authors include A. Micheil Innes, Kenneth Lim, Wendy P. Robinson, Deborah E. McFadden, Bob Argiropoulos, Dimitri J. Stavropoulos, Caroline Mackie Ogilvie, Christian R. Marshall, Yan Li and Kunwei Wu and has published in prestigious journals such as Neuron, SHILAP Revista de lepidopterología and Human Reproduction.

In The Last Decade

Julie Lauzon

22 papers receiving 423 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julie Lauzon Canada 10 228 196 126 55 50 23 430
Sophie Dahoun Switzerland 14 271 1.2× 371 1.9× 98 0.8× 92 1.7× 33 0.7× 26 629
Michela Malacarne Italy 16 416 1.8× 282 1.4× 150 1.2× 21 0.4× 53 1.1× 56 626
Sylvie Jaillard France 16 397 1.7× 435 2.2× 148 1.2× 123 2.2× 48 1.0× 54 802
Yingjun Xie China 13 157 0.7× 279 1.4× 138 1.1× 23 0.4× 63 1.3× 65 543
Courtney Sebold United States 16 437 1.9× 216 1.1× 141 1.1× 21 0.4× 52 1.0× 27 616
Renske Oegema Netherlands 13 217 1.0× 245 1.3× 147 1.2× 34 0.6× 28 0.6× 21 534
LaDonna Immken United States 13 339 1.5× 372 1.9× 112 0.9× 25 0.5× 79 1.6× 21 689
Tiia Reimand Estonia 13 291 1.3× 229 1.2× 97 0.8× 20 0.4× 17 0.3× 41 488
Marie Vincent France 16 168 0.7× 422 2.2× 70 0.6× 15 0.3× 55 1.1× 41 635
Atsushi Ieshima Japan 11 205 0.9× 153 0.8× 66 0.5× 77 1.4× 20 0.4× 29 393

Countries citing papers authored by Julie Lauzon

Since Specialization
Citations

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

Fields of papers citing papers by Julie Lauzon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julie Lauzon

This figure shows the co-authorship network connecting the top 25 collaborators of Julie Lauzon. A scholar is included among the top collaborators of Julie Lauzon 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 Julie Lauzon. Julie Lauzon 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.
2.
Chan, Elaine S., David Somerset, Lawrence de Koning, et al.. (2024). Maternal Cytomegalovirus (CMV) Serology: The Diagnostic Limitations of CMV IgM and IgG Avidity in Detecting Congenital CMV Infection. Pediatric and Developmental Pathology. 27(6). 530–544. 2 indexed citations
3.
4.
Kassam, Aliya, et al.. (2024). Ethical issues in residency education related to the COVID-19 pandemic: a narrative inquiry study. Journal of Medical Ethics. 51(11). 778–786. 1 indexed citations
5.
Jia, Xiangbin, Mariëlle Alders, Arjan Bouman, et al.. (2022). De novo variants in the PABP domain of PABPC1 lead to developmental delay. Genetics in Medicine. 24(8). 1761–1773. 4 indexed citations
6.
Elliott, Mark, et al.. (2021). Mainstreaming Genetic Testing for Adult Patients With Autosomal Dominant Polycystic Kidney Disease. Canadian Journal of Kidney Health and Disease. 8. 1015010201–1015010201. 13 indexed citations
7.
Lazier, Joanna, Taila Hartley, Jo‐Ann Brock, et al.. (2021). Clinical application of fetal genome-wide sequencing during pregnancy: position statement of the Canadian College of Medical Geneticists. Journal of Medical Genetics. 59(10). 931–937. 24 indexed citations
8.
Nguyen, Thien, Kunwei Wu, Yan Li, et al.. (2020). A Cluster of Autism-Associated Variants on X-Linked NLGN4X Functionally Resemble NLGN4Y. Neuron. 106(5). 759–768.e7. 60 indexed citations
9.
Lauzon, Julie, et al.. (2020). Perinatal outcome and prognostic factors of fetal megacystis diagnosed at 11–14 week's gestation. Prenatal Diagnosis. 41(3). 308–315. 3 indexed citations
10.
Lauzon, Julie, Gaëtan F. Tremblay, Gilles Bélanger, et al.. (2019). Alfalfa and Timothy Nutritive Value in Contrasting Agroclimatic Regions. Agronomy Journal. 111(3). 1371–1380. 7 indexed citations
11.
Chan, Elaine S., et al.. (2018). Atypical Prenatal Ultrasound Presentation and Neuropathological Findings in a Neonate With Alpha Thalassemia Major: A Case Report. Pediatric and Developmental Pathology. 22(2). 166–170. 3 indexed citations
12.
Potter, Kathryn J., et al.. (2017). Beta cell function and clinical course in three siblings with thiamine-responsive megaloblastic anemia (TRMA) treated with thiamine supplementation. Journal of Pediatric Endocrinology and Metabolism. 30(2). 241–246. 9 indexed citations
13.
Lazier, Joanna, Deborah Fruitman, Julie Lauzon, et al.. (2016). Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies. Journal of Obstetrics and Gynaecology Canada. 38(7). 619–626. 11 indexed citations
14.
Chénier, Sébastien, Grace Yoon, Bob Argiropoulos, et al.. (2014). CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems. Journal of Neurodevelopmental Disorders. 6(1). 9–9. 63 indexed citations
15.
Merner, Nancy D., et al.. (2012). A Novel Deletion inSMPXCauses a Rare form of X-Linked Progressive Hearing Loss in Two Families Due to a Founder Effect. Human Mutation. 34(1). 66–69. 20 indexed citations
16.
Liu, Jing, François P. Bernier, Julie Lauzon, R. Brian Lowry, & Judy Chernos. (2011). Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case Reports. PubMed. 2011. 1–9. 7 indexed citations
17.
Lin, Angela E., Barbara O’Brien, Laurie Demmer, et al.. (2009). Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia. Prenatal Diagnosis. 29(7). 682–690. 43 indexed citations
18.
Mitha, Alim P., et al.. (2009). Endoscopic third ventriculostomy to treat hydrocephalus associated with macrocephaly-cutis marmorata telangiectatica congenita. Journal of Neurosurgery Pediatrics. 4(4). 397–401. 4 indexed citations
19.
Conway, Robert L., Barry D. Pressman, William B. Dobyns, et al.. (2007). Neuroimaging findings in macrocephaly–capillary malformation: A longitudinal study of 17 patients. American Journal of Medical Genetics Part A. 143A(24). 2981–3008. 78 indexed citations
20.
Robinson, Wendy P., et al.. (2006). Origin and outcome of pregnancies affected by androgenetic/biparental chimerism. Human Reproduction. 22(4). 1114–1122. 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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