Luis H. Ospina - Concepedia

Author

Luis H. Ospina

Centre Hospitalier Universitaire Sainte-Justine ORCID

Also Known As

Adolfo Guemes, L H Ospina, L. Ospina, L.H. Ospina, Luis Fernando Ospina, Luis H Ospina, Luis H. Ospina, Luis Humberto Ospina, Luis Ospina, Luis Ospina-Forero

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Centre Hospitalier Universitaire Sainte-Justine Université de Montréal McGill University BC Children's Hospital University of Manchester

About

Luis H. Ospina is an author at Centre Hospitalier Universitaire Sainte-Justine specializing in medicine, ophthalmology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	3	3	420
2	Business	2	2	90
3	Education	1	1	15
4	Language Studies	1	1	13
5	Management	1	1	28

Luis H. Ospina

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Avoiding False Positive Conclusions in Molecular Simulation: The Importance of Replicas Bernhard Knapp, Luis H. Ospina, Charlotte M. Deane Journal of Chemical Theory and Computation EngineeringMolecular BiologyComputational ChemistryBiological ComputingMolecular Dynamics	2018	330
Neurodevelopmental Outcomes Following Bevacizumab Injections for Retinopathy of Prematurity Julie Morin, Thuy Mai Luu, Rosanne Superstein, PEDIATRICS	2016	285
CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms Léna Damaj, Alexis Lupien‐Meilleur, Anne Lortie, European Journal of Human Genetics Neurodevelopmental DisordersEpileptic EncephalopathyCorticobasal DegenerationNeurological DisorderSyndromic Autism	2015	206
Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population Myriam Srour, Jeremy Schwartzentruber, Fadi F. Hamdan, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsFrench Canadian PopulationGenetic Epidemiology	2012	136
Mutations in <i>TMEM231</i> cause Joubert syndrome in French Canadians Myriam Srour, Fadi F. Hamdan, Jeremy Schwartzentruber, Journal of Medical Genetics	2012	74
Joubert Syndrome in French Canadians and Identification of Mutations in CEP104 Myriam Srour, Fadi F. Hamdan, Dianalee McKnight, The American Journal of Human Genetics Mendelian DisorderJoubert SyndromeFrench CanadiansGeneticsGenetic Disorder	2015	70
Treatment of Periocular Infantile Hemangiomas with Propranolol: Case Series of 18 Children Rola Al Dhaybi, Rosanne Superstein, Ariane Milet, Ophthalmology Periocular Infantile HemangiomasPediatricsVascular MalformationCase SeriesSurgery	2011	64
Estimating networks of sustainable development goals Luis H. Ospina, Gonzalo Castañeda, Omar Guerrero Information & Management EngineeringDevelopment EconomicsSustainable DevelopmentAgricultural EconomicsSustainability Indicator	2020	62
Clinical Presentation and Outcome of Patients With Optic Pathway Glioma Viviane Robert‐Boire, Lorena Rosca, Yvan Samson, Pediatric Neurology Neuro-oncologyOptic Pathway GliomaOcular DiseaseOphthalmologyNeurology	2017	59
Visual acuity of children treated with chemotherapy for optic pathway gliomas Evan Kalin-Hajdu, Jean‐Claude Décarie, Monia Marzouki, Pediatric Blood & Cancer	2013	49

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