Lemuel Racacho

913 total citations
18 papers, 547 citations indexed

About

Lemuel Racacho is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Lemuel Racacho has authored 18 papers receiving a total of 547 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Neurology. Recurrent topics in Lemuel Racacho's work include Glycogen Storage Diseases and Myoclonus (4 papers), Hedgehog Signaling Pathway Studies (4 papers) and Neurological disorders and treatments (4 papers). Lemuel Racacho is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (4 papers), Hedgehog Signaling Pathway Studies (4 papers) and Neurological disorders and treatments (4 papers). Lemuel Racacho collaborates with scholars based in Canada, United States and United Kingdom. Lemuel Racacho's co-authors include Dennis E. Bulman, David A. Grimes, Fabin Han, Anthony E. Lang, Owen A. Ross, Jeffrey R. Lee, G. Angus McQuibban, Guang Shi, Matthew J. Farrer and Fengxia Xiao and has published in prestigious journals such as Neurology, Human Molecular Genetics and Cell Reports.

In The Last Decade

Lemuel Racacho

17 papers receiving 526 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lemuel Racacho Canada 14 262 192 164 116 80 18 547
Anita E. Harding United Kingdom 13 419 1.6× 145 0.8× 297 1.8× 96 0.8× 29 0.4× 15 710
Jenny E.V. Morton United Kingdom 7 360 1.4× 64 0.3× 71 0.4× 211 1.8× 16 0.2× 11 574
Fabin Han China 16 180 0.7× 219 1.1× 171 1.0× 87 0.8× 85 1.1× 29 516
Yoshio Morimatsu Japan 15 391 1.5× 102 0.5× 181 1.1× 140 1.2× 45 0.6× 28 605
Cíntia Barros Santos-Rebouças Brazil 17 378 1.4× 162 0.8× 76 0.5× 311 2.7× 80 1.0× 64 767
Hanna Mierzewska Poland 15 444 1.7× 98 0.5× 105 0.6× 127 1.1× 30 0.4× 57 728
Janel O. Johnson United States 10 153 0.6× 163 0.8× 94 0.6× 58 0.5× 31 0.4× 11 364
Niranjanan Nirmalananthan United Kingdom 11 293 1.1× 177 0.9× 159 1.0× 30 0.3× 28 0.3× 23 537
Fabienne Wavrant De Vrieze United States 5 232 0.9× 181 0.9× 90 0.5× 250 2.2× 10 0.1× 6 543
Jyrki Kaukonen Finland 6 1.1k 4.2× 136 0.7× 234 1.4× 144 1.2× 34 0.4× 7 1.2k

Countries citing papers authored by Lemuel Racacho

Since Specialization
Citations

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

Fields of papers citing papers by Lemuel Racacho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lemuel Racacho

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

All Works

18 of 18 papers shown
1.
Groopman, Emily, Shruthi Mohan, Raquel Fernández, et al.. (2024). Assessment of genes involved in lysosomal diseases using the ClinGen clinical validity framework. Molecular Genetics and Metabolism. 143(3). 108593–108593.
2.
Dickson, Alexa, Marcus J. Miller, Elaine Spector, et al.. (2023). Specifications of the ACMG/AMP guidelines for ACADVL variant interpretation. Molecular Genetics and Metabolism. 140(3). 107668–107668. 1 indexed citations
3.
Farhan, Sali M.K., Allison A. Dilliott, Mahdi Ghani, et al.. (2016). The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration. npj Genomic Medicine. 1(1). 16032–16032. 15 indexed citations
4.
Alvarez-Saavedra, Matías, Yves De Repentigny, Ryan W. O’Meara, et al.. (2016). Voluntary Running Triggers VGF-Mediated Oligodendrogenesis to Prolong the Lifespan of Snf2h-Null Ataxic Mice. Cell Reports. 17(3). 862–875. 39 indexed citations
5.
Han, Fabin, David A. Grimes, Fang Li, et al.. (2015). Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada. International Journal of Neuroscience. 126(5). 415–421. 19 indexed citations
6.
Racacho, Lemuel, H. Robson MacDonald, Helen J. Dranse, et al.. (2015). Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1. European Journal of Human Genetics. 23(12). 1640–1645. 18 indexed citations
7.
Lahiry, Piya, Lemuel Racacho, Jian Wang, et al.. (2013). A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorder. Orphanet Journal of Rare Diseases. 8(1). 5 indexed citations
8.
Shi, Guang, Jeffrey R. Lee, David A. Grimes, et al.. (2011). Functional alteration of PARL contributes to mitochondrial dysregulation in Parkinson's disease. Human Molecular Genetics. 20(10). 1966–1974. 128 indexed citations
9.
Racacho, Lemuel, Sarah M. Nikkel, Fengxia Xiao, et al.. (2010). Mutations in GDF5 presenting as semidominant brachydactyly A1. Human Mutation. 31(10). 1155–1162. 21 indexed citations
10.
Racacho, Lemuel, Louanne Hudgins, Andrea Kwan, et al.. (2009). Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog. European Journal of Human Genetics. 17(9). 1112–1120. 43 indexed citations
11.
Han, Fabin, Lemuel Racacho, Anthony E. Lang, Dennis E. Bulman, & David A. Grimes. (2007). Refinement of the DYT15 locus in myoclonus dystonia. Movement Disorders. 22(6). 888–892. 27 indexed citations
12.
Han, Fabin, Lemuel Racacho, Howard H. Yang, et al.. (2007). Large deletions account for an increasing number of mutations in SGCE. Movement Disorders. 23(3). 456–460. 15 indexed citations
13.
Grimes, David A., Lemuel Racacho, Fabin Han, Michel Panisset, & Dennis E. Bulman. (2007). LRRK2 Screening in a Canadian Parkinson's Disease Cohort. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 34(3). 336–338. 9 indexed citations
14.
Grimes, David A., Fabin Han, Michel Panisset, et al.. (2006). Translated mutation in the Nurr1 gene as a cause for Parkinson's disease. Movement Disorders. 21(7). 906–909. 80 indexed citations
15.
Han, Fabin, Anthony E. Lang, Lemuel Racacho, Dennis E. Bulman, & David A. Grimes. (2003). Mutations in the ε- sarcoglycan gene found to be uncommon in seven myoclonus–dystonia families. Neurology. 61(2). 244–246. 21 indexed citations
16.
McCready, M. Elizabeth, Elizabeth Sweeney, Dian Donnai, et al.. (2002). A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolved. Human Genetics. 111(4-5). 368–375. 29 indexed citations
17.
Grimes, David A., et al.. (2002). A novel locus for inherited myoclonus-dystonia on 18p11. Neurology. 59(8). 1183–1186. 63 indexed citations
18.
Racacho, Lemuel, Richard S. McLachlan, George C. Ebers, John Maher, & Dennis E. Bulman. (2000). Evidence Favoring Genetic Heterogeneity for Febrile Convulsions. Epilepsia. 41(2). 132–139. 14 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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