Nancy Laurin

1.9k total citations
26 papers, 1.2k citations indexed

About

Nancy Laurin is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Nancy Laurin has authored 26 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 8 papers in Psychiatry and Mental health. Recurrent topics in Nancy Laurin's work include Attention Deficit Hyperactivity Disorder (8 papers), Molecular Biology Techniques and Applications (7 papers) and Forensic and Genetic Research (6 papers). Nancy Laurin is often cited by papers focused on Attention Deficit Hyperactivity Disorder (8 papers), Molecular Biology Techniques and Applications (7 papers) and Forensic and Genetic Research (6 papers). Nancy Laurin collaborates with scholars based in Canada, South Korea and France. Nancy Laurin's co-authors include Jacques P. Brown, Jean Morissette, Vincent Raymond, Grant A. Mitchell, Shu Pei Wang, Chantal J. Frégeau, Michael A. Rudnicki, Marie‐France Robert, Luc L. Oligny and Jean Himms‐Hagen and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Lipid Research and Journal of Bone and Mineral Research.

In The Last Decade

Nancy Laurin

26 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nancy Laurin Canada 16 464 449 215 171 162 26 1.2k
G. T. Hradek United States 11 364 0.8× 241 0.5× 82 0.4× 41 0.2× 28 0.2× 14 936
Josée Prud’homme Canada 13 490 1.1× 129 0.3× 85 0.4× 9 0.1× 149 0.9× 14 1.1k
Anthony J. Griswold United States 18 651 1.4× 119 0.3× 118 0.5× 13 0.1× 82 0.5× 75 1.4k
Fanglin Guan China 23 544 1.2× 102 0.2× 105 0.5× 8 0.0× 165 1.0× 47 1.2k
Berkley R. Powell United States 22 1.0k 2.3× 43 0.1× 149 0.7× 89 0.5× 83 0.5× 32 1.7k
Maddalena Ruggieri Italy 21 501 1.1× 132 0.3× 104 0.5× 13 0.1× 132 0.8× 55 1.4k
Jon Neumann United States 16 1.7k 3.7× 95 0.2× 136 0.6× 28 0.2× 53 0.3× 21 2.2k
Miao-Hsueh Chen United States 20 1.3k 2.9× 181 0.4× 203 0.9× 23 0.1× 62 0.4× 25 1.9k
Andrea Vettori Italy 20 597 1.3× 67 0.1× 123 0.6× 20 0.1× 20 0.1× 43 1.5k
Pascale Vertongen Belgium 21 678 1.5× 295 0.7× 84 0.4× 14 0.1× 24 0.1× 35 1.2k

Countries citing papers authored by Nancy Laurin

Since Specialization
Citations

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

Fields of papers citing papers by Nancy Laurin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy Laurin

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy Laurin. A scholar is included among the top collaborators of Nancy Laurin 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 Nancy Laurin. Nancy Laurin 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.
Frégeau, Chantal J. & Nancy Laurin. (2023). Processing biological samples from simulated radiological terrorist events using Rapid DNA instruments. Forensic Science International. 354. 111887–111887. 1 indexed citations
2.
Laurin, Nancy, et al.. (2023). Comparative analysis of two Rapid DNA technologies for the processing of blood and saliva-based samples. Forensic Science International Genetics. 67. 102928–102928. 7 indexed citations
3.
Laurin, Nancy, et al.. (2015). New incompatibilities uncovered using the Promega DNA IQ™ chemistry. Forensic Science International. 257. 134–141. 19 indexed citations
4.
Laurin, Nancy & Chantal J. Frégeau. (2015). An Accelerated Analytical Process for the Development of STR Profiles for Casework Samples. Journal of Forensic Sciences. 60(4). 983–989. 2 indexed citations
5.
Frégeau, Chantal J. & Nancy Laurin. (2014). The Qiagen Investigator® Quantiplex HYres as an alternative kit for DNA quantification. Forensic Science International Genetics. 16. 148–162. 14 indexed citations
6.
Laurin, Nancy & Emmanuel Milot. (2013). Population genetic data of the AmpFℓSTR® Identifiler® Plus and PowerPlex® 16 HS STR loci in four Canadian populations. International Journal of Legal Medicine. 128(2). 277–278. 2 indexed citations
7.
Laurin, Nancy & Chantal J. Frégeau. (2011). Optimization and validation of a fast amplification protocol for AmpFlSTR® Profiler Plus® for rapid forensic human identification. Forensic Science International Genetics. 6(1). 47–57. 22 indexed citations
8.
Bonnelye, Edith, Nancy Laurin, Pierre Jurdic, David A. Hart, & Jane E. Aubin. (2008). Estrogen receptor-related receptor-  (ERR- ) is dysregulated in inflammatory arthritis. Lara D. Veeken. 47(12). 1785–1791. 20 indexed citations
9.
Laurin, Nancy, Karen Wigg, Yu Feng, Paul Sandor, & Cathy L. Barr. (2008). Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(1). 95–103. 15 indexed citations
10.
Laurin, Nancy, Abel Ickowicz, Molly Malone, et al.. (2007). Association study for genes at chromosome 5p13‐q11 in attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(5). 600–605. 11 indexed citations
11.
Laurin, Nancy, Abel Ickowicz, Molly Malone, et al.. (2007). No evidence for genetic association between DARPP‐32 (PP1R1B) polymorphisms and attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(3). 339–342. 2 indexed citations
12.
Luca, Pietro De, Nancy Laurin, Virginia L. Misener, et al.. (2007). Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems. Molecular Psychiatry. 12(8). 776–785. 27 indexed citations
13.
Laurin, Nancy, Jennifer Crosbie, Abel Ickowicz, et al.. (2007). Association study of the nicotinic acetylcholine receptor α4 subunit gene, CHRNA4, in attention‐deficit hyperactivity disorder. Genes Brain & Behavior. 7(1). 53–60. 25 indexed citations
14.
Laurin, Nancy, Abel Ickowicz, Molly Malone, et al.. (2006). Investigation of the G protein subunit Gαolf gene (GNAL) in attention deficit/hyperactivity disorder. Journal of Psychiatric Research. 42(2). 117–124. 20 indexed citations
15.
Laurin, Nancy, Virginia L. Misener, Jennifer Crosbie, et al.. (2005). Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder. Molecular Psychiatry. 10(12). 1117–1125. 34 indexed citations
16.
Laurin, Nancy, Jacques P. Brown, Jean Morissette, & Vincent Raymond. (2002). Recurrent Mutation of the Gene Encoding sequestosome 1 (SQSTM1/p62) in Paget Disease of Bone. The American Journal of Human Genetics. 70(6). 1582–1588. 425 indexed citations
17.
Laurin, Nancy, Jacques P. Brown, Arnaud Lemainque, et al.. (2001). Paget Disease of Bone: Mapping of Two Loci at 5q35-qter and 5q31. The American Journal of Human Genetics. 69(3). 528–543. 106 indexed citations
18.
Wang, Shu Pei, Nancy Laurin, Jean Himms‐Hagen, et al.. (2001). The Adipose Tissue Phenotype of Hormone‐Sensitive Lipase Deficiency in Mice. Obesity Research. 9(2). 119–128. 185 indexed citations
19.
Laurin, Nancy, Shu Pei Wang, & Grant A. Mitchell. (2000). The hormone-sensitive lipase gene is transcribed from at least five alternative first exons in mouse adipose tissue. Mammalian Genome. 11(11). 972–978. 25 indexed citations
20.
Mitchell, Grant A., L.I. Ashmarina, M.F. Robert, et al.. (1998). Inborn errors of ketogenesis. Biochemical Society Transactions. 26(2). 136–140. 7 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by G. T. Hradek Breakdown of academic impact, for papers by Josée Prud’homme Breakdown of academic impact, for papers by Anthony J. Griswold Breakdown of academic impact, for papers by Fanglin Guan Breakdown of academic impact, for papers by Berkley R. Powell Breakdown of academic impact, for papers by Maddalena Ruggieri Breakdown of academic impact, for papers by Jon Neumann Breakdown of academic impact, for papers by Miao-Hsueh Chen Breakdown of academic impact, for papers by Andrea Vettori Breakdown of academic impact, for papers by Pascale Vertongen
Rankless by CCL
2026