Danielle K. Bourque

692 total citations
14 papers, 440 citations indexed

About

Danielle K. Bourque is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Danielle K. Bourque has authored 14 papers receiving a total of 440 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Clinical Biochemistry. Recurrent topics in Danielle K. Bourque's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (3 papers) and Epigenetics and DNA Methylation (3 papers). Danielle K. Bourque is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (3 papers) and Epigenetics and DNA Methylation (3 papers). Danielle K. Bourque collaborates with scholars based in Canada and United States. Danielle K. Bourque's co-authors include Luana Avila, Maria S. Peñaherrera, Peter von Dadelszen, Wendy P. Robinson, Arianne Albert, Sean M. Hemmingsen, Julie van Schalkwyk, Deborah Money, Matthew G. Links and Lohn Zoe and has published in prestigious journals such as Microbiome, Human Mutation and Placenta.

In The Last Decade

Danielle K. Bourque

13 papers receiving 433 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Danielle K. Bourque Canada 9 238 149 123 99 96 14 440
Maarten van Haaften Netherlands 10 82 0.3× 77 0.5× 102 0.8× 61 0.6× 109 1.1× 22 423
Isoken Olomu United States 9 123 0.5× 82 0.6× 40 0.3× 20 0.2× 52 0.5× 16 335
C.R. Juneau United States 13 87 0.4× 312 2.1× 116 0.9× 66 0.7× 48 0.5× 46 801
Joong Shik Lee South Korea 10 115 0.5× 23 0.2× 48 0.4× 109 1.1× 22 0.2× 17 362
Simone Palini Italy 14 272 1.1× 353 2.4× 37 0.3× 105 1.1× 29 0.3× 29 899
Jenny L. Sones United States 17 134 0.6× 297 2.0× 48 0.4× 28 0.3× 44 0.5× 57 745
Sören von Otte Germany 12 111 0.5× 71 0.5× 33 0.3× 25 0.3× 42 0.4× 30 451
Negar Tabatabaei Canada 9 77 0.3× 35 0.2× 108 0.9× 9 0.1× 111 1.2× 15 310
R Ingram Canada 9 156 0.7× 99 0.7× 17 0.1× 83 0.8× 55 0.6× 24 566
Silvia De Stefani Italy 12 93 0.4× 105 0.7× 36 0.3× 41 0.4× 25 0.3× 16 453

Countries citing papers authored by Danielle K. Bourque

Since Specialization
Citations

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

Fields of papers citing papers by Danielle K. Bourque

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Danielle K. Bourque. 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 Danielle K. Bourque. The network helps show where Danielle K. Bourque may publish in the future.

Co-authorship network of co-authors of Danielle K. Bourque

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

All Works

14 of 14 papers shown
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Vincent, Krista M. & Danielle K. Bourque. (2023). A novel splice site CUL3 variant in a patient with neurodevelopmental delay. Brain and Development. 45(4). 244–249. 1 indexed citations
4.
Bourque, Danielle K., Dawn Cordeiro, Graeme Nimmo, Jeff Kobayashi, & Saadet Mercimek‐Andrews. (2021). Phenotypic and Genotypic Spectrum of Glucose Transporter-1 Deficiency Syndrome. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 48(6). 1–5. 8 indexed citations
5.
Bourque, Danielle K., Lynn Meng, Shelley Dougan, et al.. (2021). Gastroschisis in Ontario, Canada: 2012–2018. Birth Defects Research. 113(14). 1044–1051. 11 indexed citations
6.
Bourque, Danielle K., Stacy Hewson, Julian Raiman, et al.. (2020). Outcomes of patients with cobalamin C deficiency: A single center experience. JIMD Reports. 57(1). 102–114. 9 indexed citations
7.
Aref‐Eshghi, Erfan, Danielle K. Bourque, Jennifer Kerkhof, et al.. (2019). Genome‐wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome. Human Mutation. 40(10). 1684–1689. 19 indexed citations
8.
Bourque, Danielle K., M. Cloutier, Kristin D. Kernohan, et al.. (2019). Neu–Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis. American Journal of Medical Genetics Part A. 179(5). 813–816. 12 indexed citations
9.
Bourque, Danielle K., et al.. (2019). Alveolar capillary dysplasia with misalignment of the pulmonary veins and hypoplastic left heart sequence caused by an in frame deletion within FOXF1. American Journal of Medical Genetics Part A. 179(7). 1325–1329. 7 indexed citations
10.
Bourque, Danielle K., David A. Dyment, Ian MacLusky, Kristin D. Kernohan, & Hugh J. McMillan. (2018). Periodic breathing in patients with NALCN mutations. Journal of Human Genetics. 63(10). 1093–1096. 10 indexed citations
11.
Bourque, Danielle K., Taila Hartley, Sarah M. Nikkel, et al.. (2017). A de novo mutation in RPL10 causes a rare X-linked ribosomopathy characterized by syndromic intellectual disability and epilepsy: A new case and review of the literature. European Journal of Medical Genetics. 61(2). 89–93. 14 indexed citations
12.
Chaban, Bonnie, Matthew G. Links, Teenus Paramel Jayaprakash, et al.. (2014). Characterization of the vaginal microbiota of healthy Canadian women through the menstrual cycle. Microbiome. 2(1). 23–23. 187 indexed citations
13.
Bourque, Danielle K., Luana Avila, Maria S. Peñaherrera, Peter von Dadelszen, & Wendy P. Robinson. (2010). Decreased Placental Methylation at the H19/IGF2 Imprinting Control Region is Associated with Normotensive Intrauterine Growth Restriction but not Preeclampsia. Placenta. 31(3). 197–202. 130 indexed citations
14.
Bourque, Danielle K., et al.. (2010). The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders. Clinical Genetics. 79(2). 169–175. 30 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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