Ryan E. Lamont

2.4k total citations
35 papers, 850 citations indexed

About

Ryan E. Lamont is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Ryan E. Lamont has authored 35 papers receiving a total of 850 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Clinical Biochemistry. Recurrent topics in Ryan E. Lamont's work include Genomics and Rare Diseases (8 papers), Metabolism and Genetic Disorders (6 papers) and RNA modifications and cancer (6 papers). Ryan E. Lamont is often cited by papers focused on Genomics and Rare Diseases (8 papers), Metabolism and Genetic Disorders (6 papers) and RNA modifications and cancer (6 papers). Ryan E. Lamont collaborates with scholars based in Canada, United States and Germany. Ryan E. Lamont's co-authors include Sarah J. Childs, Jillian S. Parboosingh, A. Micheil Innes, François P. Bernier, Teresa Zelinski, Marion E. Reid, Christopher Smith, Lennart Lögdberg, Klaus Wrogemann and Cheryl R. Greenberg and has published in prestigious journals such as The American Journal of Human Genetics, Developmental Biology and Human Mutation.

In The Last Decade

Ryan E. Lamont

33 papers receiving 836 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ryan E. Lamont Canada 16 611 165 148 133 78 35 850
Shamir Zenvirt Israel 16 618 1.0× 367 2.2× 173 1.2× 205 1.5× 109 1.4× 22 1.2k
Haike Reznik‐Wolf Israel 15 554 0.9× 171 1.0× 118 0.8× 95 0.7× 52 0.7× 39 888
Jean‐Pierre Desvignes France 17 603 1.0× 324 2.0× 96 0.6× 99 0.7× 56 0.7× 31 1.0k
Ortal Barel Israel 15 450 0.7× 247 1.5× 58 0.4× 78 0.6× 48 0.6× 63 868
Steffen Uebe Germany 22 819 1.3× 507 3.1× 134 0.9× 80 0.6× 55 0.7× 58 1.3k
Emma L. Baple United Kingdom 18 547 0.9× 373 2.3× 137 0.9× 64 0.5× 128 1.6× 59 902
Mei-Yao Lin United States 12 695 1.1× 68 0.4× 147 1.0× 219 1.6× 103 1.3× 14 1.2k
Jinmin Miao United States 13 578 0.9× 408 2.5× 90 0.6× 136 1.0× 27 0.3× 22 1.1k
Wojciech Wiszniewski United States 18 509 0.8× 320 1.9× 144 1.0× 343 2.6× 47 0.6× 42 1.1k
Louise Ocaka United Kingdom 19 729 1.2× 420 2.5× 107 0.7× 41 0.3× 36 0.5× 30 1.2k

Countries citing papers authored by Ryan E. Lamont

Since Specialization
Citations

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

Fields of papers citing papers by Ryan E. Lamont

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryan E. Lamont. 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 Ryan E. Lamont. The network helps show where Ryan E. Lamont may publish in the future.

Co-authorship network of co-authors of Ryan E. Lamont

This figure shows the co-authorship network connecting the top 25 collaborators of Ryan E. Lamont. A scholar is included among the top collaborators of Ryan E. Lamont 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 Ryan E. Lamont. Ryan E. Lamont 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.
Wade, Andrew, Jillian S. Parboosingh, Ping Yee Billie Au, et al.. (2024). Genome sequencing identifies biallelic variants in SCLT1 in a patient with syndromic nephronophthisis: Reflections on the SCLT1‐related ciliopathy spectrum. American Journal of Medical Genetics Part A. 194(11). e63789–e63789.
2.
Fraser, Sherri D., Oana Caluseriu, Claudia Vivori, et al.. (2022). Hnrnpul1 controls transcription, splicing, and modulates skeletal and limb development in vivo. G3 Genes Genomes Genetics. 12(5). 5 indexed citations
3.
Ridsdale, Ross, Lauren MacNeil, Margaret Lilley, et al.. (2021). The Alberta Newborn Screening Approach for Sickle Cell Disease: The Advantages of Molecular Testing. International Journal of Neonatal Screening. 7(4). 78–78. 7 indexed citations
4.
Eaton, Alison, Taila Hartley, Kristin D. Kernohan, et al.. (2020). When to think outside the autozygome: Best practices for exome sequencing in “consanguineous” families. Clinical Genetics. 97(6). 835–843. 9 indexed citations
5.
Zhao, Tian, Rasha Sabouny, Susanne Lingrell, et al.. (2019). PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes. Life Science Alliance. 2(2). e201900353–e201900353. 45 indexed citations
6.
Eaton, Alison, François P. Bernier, Oana Caluseriu, et al.. (2018). Is PNPT1‐related hearing loss ever non‐syndromic? Whole exome sequencing of adult siblings expands the natural history of PNPT1‐related disorders. American Journal of Medical Genetics Part A. 176(11). 2487–2493. 13 indexed citations
7.
Zambonin, Jessica L., David A. Dyment, Ryan E. Lamont, et al.. (2017). A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsy. Neurogenetics. 19(1). 61–65. 11 indexed citations
8.
Lamont, Ryan E., Chandree L. Beaulieu, François P. Bernier, et al.. (2016). A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite population. American Journal of Medical Genetics Part A. 173(3). 596–600. 13 indexed citations
9.
Gordon, Paul M. K., Anzalee Khan, Nicholas Chang, et al.. (2016). An Algorithm Measuring Donor Cell-Free DNA in Plasma of Cellular and Solid Organ Transplant Recipients That Does Not Require Donor or Recipient Genotyping. Frontiers in Cardiovascular Medicine. 3. 33–33. 26 indexed citations
10.
Lamont, Ryan E., et al.. (2016). The LIM-homeodomain transcription factor Islet2a promotes angioblast migration. Developmental Biology. 414(2). 181–192. 14 indexed citations
11.
Smith, Christopher, Jillian S. Parboosingh, Kym M. Boycott, et al.. (2016). Expansion of the GLE1‐associated arthrogryposis multiplex congenita clinical spectrum. Clinical Genetics. 91(3). 426–430. 14 indexed citations
12.
Argiropoulos, Bob, Xing‐Chang Wei, Jillian S. Parboosingh, et al.. (2016). Two De Novo Mutations in an Autistic Child Who Had Previously Undergone Transplantation for Dilated Cardiomyopathy: The Importance of Keeping an Open Mind. Canadian Journal of Cardiology. 33(2). 292.e5–292.e7. 2 indexed citations
13.
Aldinger, Kimberly A., Martine Tétreault, Jennifer C. Dempsey, et al.. (2014). Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy. The American Journal of Human Genetics. 95(2). 227–234. 78 indexed citations
14.
Buchert, Rebecca, Hasan Tawamie, Christopher Smith, et al.. (2014). A Peroxisomal Disorder of Severe Intellectual Disability, Epilepsy, and Cataracts Due to Fatty Acyl-CoA Reductase 1 Deficiency. The American Journal of Human Genetics. 95(5). 602–610. 95 indexed citations
15.
Lamont, Ryan E., et al.. (2010). Hedgehog signaling via angiopoietin1 is required for developmental vascular stability. Mechanisms of Development. 127(3-4). 159–168. 35 indexed citations
16.
Lamont, Ryan E., et al.. (2009). Antagonistic interactions among Plexins regulate the timing of intersegmental vessel formation. Developmental Biology. 331(2). 199–209. 32 indexed citations
17.
Armistead, Joy, Britta Meyer, Brian L. Mark, et al.. (2009). Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome. The American Journal of Human Genetics. 84(6). 728–739. 98 indexed citations
18.
Lamont, Ryan E., et al.. (2007). Expression of multiple class three semaphorins in the retina and along the path of zebrafish retinal axons. Developmental Dynamics. 236(10). 2918–2924. 20 indexed citations
19.
Lögdberg, Lennart, Marion E. Reid, Ryan E. Lamont, & Teresa Zelinski. (2005). Human Blood Group Genes 2004: Chromosomal Locations and Cloning Strategies. Transfusion Medicine Reviews. 19(1). 45–57. 42 indexed citations
20.
Frosk, Patrick, Cheryl R. Greenberg, Ryan E. Lamont, et al.. (2004). The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations. Human Mutation. 25(1). 38–44. 53 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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