Lynette Lau

2.9k total citations
16 papers, 401 citations indexed

About

Lynette Lau is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Lynette Lau has authored 16 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Lynette Lau's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Genetic factors in colorectal cancer (3 papers). Lynette Lau is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Genetic factors in colorectal cancer (3 papers). Lynette Lau collaborates with scholars based in Canada, United States and United Kingdom. Lynette Lau's co-authors include Axel Schumacher, Violeta Popendikytė, James M. Flanagan, Carl Virtanen, Artūras Petronis, Christian R. Marshall, Sun-Chong Wang, Masood Zangeneh, Stephen W. Scherer and Alice A. Kuo and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PEDIATRICS.

In The Last Decade

Lynette Lau

14 papers receiving 397 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lynette Lau Canada	8	197	189	78	70	45	16	401
Jean‐Pierre Frijns Belgium	17	300 1.5×	328 1.7×	114 1.5×	138 2.0×	47 1.0×	23	670
Patricia Robbins‐Furman United States	10	214 1.1×	424 2.2×	71 0.9×	153 2.2×	45 1.0×	17	604
Loretta Thomaidis Greece	14	128 0.6×	205 1.1×	84 1.1×	105 1.5×	15 0.3×	40	452
Amy Turriff United States	14	454 2.3×	178 0.9×	26 0.3×	45 0.6×	15 0.3×	31	668
Christalena Sofocleous Greece	14	218 1.1×	261 1.4×	67 0.9×	81 1.2×	11 0.2×	45	459
Ali Al‐Odaib Saudi Arabia	15	240 1.2×	171 0.9×	28 0.4×	153 2.2×	11 0.2×	34	574
Wilmar Saldarriaga Colombia	11	182 0.9×	343 1.8×	180 2.3×	106 1.5×	21 0.5×	99	586
Tanya N. Eble United States	13	214 1.1×	250 1.3×	54 0.7×	132 1.9×	12 0.3×	24	473
Ellen Taub Israel	8	207 1.1×	263 1.4×	121 1.6×	88 1.3×	13 0.3×	12	446
Laura Conway United States	13	161 0.8×	178 0.9×	33 0.4×	64 0.9×	12 0.3×	25	388

Countries citing papers authored by Lynette Lau

Since Specialization

Citations

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

Fields of papers citing papers by Lynette Lau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lynette Lau

This figure shows the co-authorship network connecting the top 25 collaborators of Lynette Lau. A scholar is included among the top collaborators of Lynette Lau 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 Lynette Lau. Lynette Lau 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

Ungar, Wendy J., Christian R. Marshall, Robin Z. Hayeems, et al.. (2025). A microcosting and cost consequence analysis from a randomized controlled trial comparing genome sequencing with exome sequencing for genetic diagnosis. Genetics in Medicine. 28(2). 101561–101561. 1 indexed citations

Hayeems, Robin Z., Wendy J. Ungar, Christian R. Marshall, et al.. (2025). Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trial. Genetics in Medicine. 28(1). 101605–101605.

Lau, Lynette, Bhooma Thiruvahindrapuram, Wilson W. L. Sung, et al.. (2024). P740: DMD or not DMD? Clinical genome sequencing in the interpretation of complex copy number gains. SHILAP Revista de lepidopterología. 2. 101644–101644. 1 indexed citations

Sjaarda, Calvin, Lynette Lau, Jared T. Simpson, et al.. (2023). Prevalence of Low-Frequency, Antiviral Resistance Variants in SARS-CoV-2 Isolates in Ontario, Canada, 2020-2023. JAMA Network Open. 6(7). e2324963–e2324963. 5 indexed citations

Campigotto, Aaron, Julia Orkin, Lynette Lau, et al.. (2023). Utility of SARS-CoV-2 Genomic Sequencing for Understanding Transmission and School Outbreaks. The Pediatric Infectious Disease Journal. 42(4). 324–331. 3 indexed citations

Couse, Madeline, Jingjing Cao, Lynette Lau, et al.. (2022). Genome-Wide Sequencing Identified Rare Genetic Variants for Childhood-Onset Monogenic Lupus. The Journal of Rheumatology. 50(5). 671–675. 13 indexed citations

Hayeems, Robin Z., Christian R. Marshall, Anna Szuto, et al.. (2022). Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario. CMAJ Open. 10(2). E460–E465. 9 indexed citations

Kuo, Alice A., Tara Crapnell, Lynette Lau, Kristy A. Anderson, & Paul Shattuck. (2018). Stakeholder Perspectives on Research and Practice in Autism and Transition. PEDIATRICS. 141(Supplement_4). S293–S299. 25 indexed citations

Kuo, Alice A., Kristy A. Anderson, Tara Crapnell, Lynette Lau, & Paul Shattuck. (2018). Introduction to Transitions in the Life Course of Autism and Other Developmental Disabilities. PEDIATRICS. 141(Supplement_4). S267–S271. 10 indexed citations

10.

Marshall, Christian R., Stephen W. Scherer, Maimoona A. Zariwala, et al.. (2015). Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia. G3 Genes Genomes Genetics. 5(8). 1775–1781. 50 indexed citations

11.

Basran, Raveen, Christian R. Marshall, Adam Shlien, et al.. (2015). MG-129 Our experience ofin silicogene panel testing for clinically heterogeneous disorders using exome sequencing. Journal of Medical Genetics. 52(Suppl 2). A11.1–A11. 1 indexed citations

12.

Marshall, Christian R., Sandra A. Farrell, Tara Paton, et al.. (2015). Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome. BMC Genomics. 16(S1). S12–S12. 19 indexed citations

13.

Connor, Ashton A., Thomas A. Whelan, Melyssa Aronson, et al.. (2014). Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing. Familial Cancer. 14(1). 69–75. 1 indexed citations

14.

Uddin, Mohammed, Kristiina Tammimies, Giovanna Pellecchia, et al.. (2014). Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder. Nature Genetics. 46(7). 742–747. 98 indexed citations

15.

Buske, Orion J., Misko Dzamba, Justin Foong, et al.. (2011). Variant detection and the Autism sequencing project. BMC Bioinformatics. 12(S11). 3 indexed citations

16.

Flanagan, James M., Violeta Popendikytė, Axel Schumacher, et al.. (2006). Intra- and Interindividual Epigenetic Variation in Human Germ Cells. The American Journal of Human Genetics. 79(1). 67–84. 162 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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