Lemuel Racacho - Concepedia

Author

Lemuel Racacho

University of Ottawa ORCID

Also Known As

L. Racacho, Lemuel J. Racacho, Lemuel Racacho, Liu, Hongbin, Racacho, Lemuel J., Racacho, Lemuel Jean

Publications

912

Citations

H-Index

Concepts

All Affiliations

University of Ottawa Ottawa Hospital Children's Hospital of Eastern Ontario Health Sciences Centre Toronto Western Hospital

About

Lemuel Racacho is an author at University of Ottawa specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	468
2	Natural Sciences	2	2	188
3	Public Health	2	2	56
4	Biochemistry	1	1	177
5	Biology	1	1	42

Lemuel Racacho

Publications

895

Citations

H-Index

Page 1

	Year	Citations
Functional alteration of PARL contributes to mitochondrial dysregulation in Parkinson's disease Guang Shi, Jeffrey R. Lee, David A. Grimes, Human Molecular Genetics Functional AlterationMitophagyMitochondrial DysfunctionMolecular BiologyCell Death	2011	177
A novel locus for inherited myoclonus-dystonia on 18p11 David A. Grimes, Fabin Han, Anthony E. Lang, Neurology	2002	116
Translated mutation in the Nurr1 gene as a cause for Parkinson's disease David A. Grimes, Fabin Han, Michel Panisset, Movement Disorders	2006	112
Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog Ashley M Byrnes, Lemuel Racacho, Allison Grimsey, European Journal of Human Genetics Central RegionGeneticsEvolutionary BiologyIndian HedgehogMolecular Genetics	2009	67
A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolved M. Elizabeth McCready, Elizabeth Sweeney, Allan Fryer, Human Genetics Type A1Novel MutationGenetic DisorderGeneticsMolecular Biology	2002	49
Voluntary Running Triggers VGF-Mediated Oligodendrogenesis to Prolong the Lifespan of Snf2h-Null Ataxic Mice Matías Alvarez-Saavedra, Yves De Repentigny, Doo Yang, Cell Reports	2016	47
Refinement of the DYT15 locus in myoclonus dystonia Fabin Han, Lemuel Racacho, Anthony E. Lang, Movement Disorders GeneticsPathologyDisease Gene IdentificationGenomicsDistal Region	2007	42
Mutations in the <b>ε-</b> sarcoglycan gene found to be uncommon in seven myoclonus–dystonia families Fabin Han, Anthony E. Lang, Lemuel Racacho, Neurology Rare DiseasesMendelian DisorderGenetic DisorderTypical MdsGenetics	2003	42
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease Allison A. Dilliott, Sali M.K. Farhan, Mahdi Ghani, Journal of Visualized Experiments GeneticsGenetic EpidemiologyPathologyBioinformatics PipelineDisease Gene Identification	2018	41
The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration Sali M.K. Farhan, Allison A. Dilliott, Mahdi Ghani, npj Genomic Medicine	2016	38

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