Julie Richer

2.5k total citations
34 papers, 670 citations indexed

About

Julie Richer is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Julie Richer has authored 34 papers receiving a total of 670 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Molecular Biology and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Julie Richer's work include Genomics and Rare Diseases (8 papers), Connective tissue disorders research (6 papers) and Aortic aneurysm repair treatments (4 papers). Julie Richer is often cited by papers focused on Genomics and Rare Diseases (8 papers), Connective tissue disorders research (6 papers) and Aortic aneurysm repair treatments (4 papers). Julie Richer collaborates with scholars based in Canada, United States and Belgium. Julie Richer's co-authors include Nitish Kumar, Kathryn B. Horwitz, Gareth I. Owen, Kimberly K. Leslie, Elizabeth S. Litman, Kym M. Boycott, Tanya N. Nelson, Anne‐Marie Laberge, Christine M. Armour and Michael T. Geraghty and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Julie Richer

33 papers receiving 657 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 Richer Canada 13 399 202 103 89 80 34 670
Jodi D. Hoffman United States 18 365 0.9× 215 1.1× 48 0.5× 119 1.3× 74 0.9× 33 654
Tahsin Yakut Türkiye 15 191 0.5× 315 1.6× 117 1.1× 174 2.0× 72 0.9× 78 762
Carine Courtillot France 13 226 0.6× 206 1.0× 139 1.3× 93 1.0× 30 0.4× 32 774
Shaoke Chen China 17 238 0.6× 326 1.6× 56 0.5× 171 1.9× 49 0.6× 69 778
Martha Salas United States 11 223 0.6× 458 2.3× 112 1.1× 174 2.0× 41 0.5× 18 745
Christine M. Armour Canada 20 435 1.1× 340 1.7× 86 0.8× 358 4.0× 44 0.6× 52 923
Ergül Tunçbılek Türkiye 20 254 0.6× 274 1.4× 82 0.8× 188 2.1× 72 0.9× 55 831
Shimul Chowdhury United States 16 660 1.7× 378 1.9× 60 0.6× 158 1.8× 135 1.7× 32 1.0k
Derek Lim United Kingdom 13 546 1.4× 651 3.2× 63 0.6× 293 3.3× 157 2.0× 24 928
Bo Yu China 14 83 0.2× 303 1.5× 156 1.5× 132 1.5× 45 0.6× 75 695

Countries citing papers authored by Julie Richer

Since Specialization
Citations

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

Fields of papers citing papers by Julie Richer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julie Richer

This figure shows the co-authorship network connecting the top 25 collaborators of Julie Richer. A scholar is included among the top collaborators of Julie Richer 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 Richer. Julie Richer 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.
Richer, Julie, Sharan Goobie, Ingrid M.B.H. van de Laar, et al.. (2025). Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals. Journal of Medical Genetics. 62(3). 199–205.
2.
Miller, Elka, et al.. (2024). Imaging Review of Pediatric Monogenic CNS Vasculopathy with Genetic Correlation. Radiographics. 44(5). e230087–e230087. 1 indexed citations
3.
Goh, Elaine, Lauren Chad, Julie Richer, et al.. (2024). Canadian College of Medical Geneticists: clinical practice advisory document – responsibility to recontact for reinterpretation of clinical genetic testing. Journal of Medical Genetics. 61(12). 1123–1131. 2 indexed citations
4.
5.
Richter, Uwe, Omid Safronov, Lars Paulín, et al.. (2022). Nonstop mRNAs generate a ground state of mitochondrial gene expression noise. Science Advances. 8(46). eabq5234–eabq5234. 10 indexed citations
6.
Richer, Julie, et al.. (2022). NTRK1-related Hereditary Sensory and Autonomic Neuropathy Type 4: The Role of the Histamine Challenge Test. SHILAP Revista de lepidopterología. 9. 2329048X221108826–2329048X221108826. 1 indexed citations
7.
Verstraeten, Aline, Josephina Meester, Peter Ponsaerts, et al.. (2022). Generation and validation of an iPSC line (BBANTWi008-A) from a Loeys-Dietz Syndrome type 3 patient. Stem Cell Research. 64. 102932–102932. 2 indexed citations
8.
Richer, Julie & Anne‐Marie Laberge. (2018). Secondary findings from next-generation sequencing: what does actionable in childhood really mean?. Genetics in Medicine. 21(1). 124–132. 14 indexed citations
9.
McMillan, Hugh J., et al.. (2018). Worster-Drought Syndrome Associated With LINS Mutations. SHILAP Revista de lepidopterología. 5. 2329048X18791083–2329048X18791083. 2 indexed citations
10.
Richer, Julie, et al.. (2018). Valproic acid as a monotherapy in drug-resistant methyl-CpG-binding protein 2 gene (MECP2) duplication-related epilepsy. Epilepsy & Behavior Case Reports. 10. 133–136. 4 indexed citations
11.
Balcı, Tuğçe B., Jorge Dávila, Addo Boafo, et al.. (2017). Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(1). 101–109. 28 indexed citations
12.
Richer, Julie, Hussein Daoud, Pavel Geier, et al.. (2015). Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE. American Journal of Medical Genetics Part A. 167(7). 1654–1658. 12 indexed citations
13.
Richer, Julie & Anne‐Marie Laberge. (2015). Screening Children for Familial Aortopathies: Tread With Caution. Canadian Journal of Cardiology. 32(1). 60–65. 4 indexed citations
14.
Guerin, Andrea, et al.. (2014). Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld‐anomaly in a child with PTPN11 mutation. American Journal of Medical Genetics Part A. 167(2). 403–406. 5 indexed citations
15.
Kleiderman, Erika, Bartha Maria Knoppers, Conrad V. Fernandez, et al.. (2013). Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases. Journal of Medical Ethics. 40(10). 691–696. 65 indexed citations
16.
Richer, Julie, Dianna M. Milewicz, Robert M. Gow, et al.. (2012). R179H mutation in ACTA2 expanding the phenotype to include prune‐belly sequence and skin manifestations. American Journal of Medical Genetics Part A. 158A(3). 664–668. 44 indexed citations
17.
Richer, Julie, et al.. (2012). CCMG statement on gene patents. Clinical Genetics. 82(5). 405–407. 2 indexed citations
18.
Carter, Melissa T., Sarah Dyack, & Julie Richer. (2010). Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1–q26.3. Clinical Dysmorphology. 19(3). 140–145. 12 indexed citations
19.
Richer, Julie & AE Chudley. (2005). The hemoglobinopathies and malaria. Clinical Genetics. 68(4). 332–336. 14 indexed citations
20.
Kumar, Nitish, Julie Richer, Gareth I. Owen, et al.. (1998). Selective down-regulation of progesterone receptor isoform B in poorly differentiated human endometrial cancer cells: implications for unopposed estrogen action.. PubMed. 58(9). 1860–5. 116 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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