Oscar F. Chacón‐Camacho

Author

Universidad Nacional Autónoma de México ORCID

Also Known As

O. F. Chacon-Camacho, O.F. Chacon-Camacho, O.F. Chacón-Camacho, O.F. Chacón‐Camacho, Oscar Chacon-Camacho, Oscar Chacon‐Camacho, Oscar Chacón-Camacho, Oscar F Chacon-Camacho, Oscar F Chacon-camacho, Oscar F Chacon‐Camacho

Publications

814

Citations

H-Index

Concepts

All Affiliations

Universidad Nacional Autónoma de México Institute of Ophthalmology Autonomous University of Tlaxcala Instituto Tecnológico de Oaxaca Instituto Nacional de Neurología y Neurocirugía

About

Oscar F. Chacón‐Camacho is an author at Universidad Nacional Autónoma de México specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	126
2	Molecular Genetics	2	2	58
3	Public Health	1	1	24
4	Epidemiology	1	1	24
5	Molecular Biology	1	1	16

Oscar F. Chacón‐Camacho

Publications

445

Citations

H-Index

Page 1

	Year	Citations
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for <i>IRF6</i> and variants at 8q24 and 10q25 Augusto Rojas-Martı́nez, Heiko Reutter, Oscar F. Chacón‐Camacho, Birth Defects Research Part A Clinical and Molecular Teratology	2010	59
Congenital Hereditary Endothelial Dystrophy Caused by SLC4A11 Mutations Progresses to Harboyan Syndrome Salina Siddiqui, Juan Carlos Zenteno, Aine Rice, Cornea	2013	56
Expansion of the phenotypic spectrum and description of molecular findings in a cohort of patients with oculocutaneous mosaic RASopathies Oscar F. Chacón‐Camacho, Daniel López-Moreno, Martha Alejandra Morales‐Sánchez, Molecular Genetics & Genomic Medicine	2019	56
Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing Juan Carlos Zenteno, Leopoldo A. García‐Montaño, Marisa Cruz‐Aguilar, Molecular Genetics & Genomic Medicine	2019	45
ABCA4 mutational spectrum in Mexican patients with Stargardt disease: Identification of 12 novel mutations and evidence of a founder effect for the common p.A1773V mutation Oscar F. Chacón‐Camacho, Mariella Granillo-Alvarez, Raúl Ayala-Ramírez, Experimental Eye Research Genetic DisorderMedicineGeneticsMexican PatientsGenetic Epidemiology	2013	42
Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing Diana Matías-Pérez, Leopoldo A. García‐Montaño, Marisa Cruz‐Aguilar, Journal of Human Genetics Novel Pathogenic VariantsAllelic VariantMedicineGeneticsPathogenesis	2018	24
Expanding the phenotype of gingival fibromatosis–mental retardation–hypertrichosis (Zimmermann–Laband) syndrome Oscar F. Chacón‐Camacho, Johanna Vázquez, Juan Carlos Zenteno American Journal of Medical Genetics Part A	2011	21
Klippel–Feil syndrome associated with situs inversus: Description of a new case and exclusion of GDF1, GDF3 and GDF6 as causal genes Oscar F. Chacón‐Camacho, Leyla Camarillo-Blancarte, Hugo Peláez‐González, European Journal of Medical Genetics Developmental BiologyCausal GenesGeneticsPathogenesisPathology	2012	19
Exome sequencing identifies RDH12 compound heterozygous mutations in a family with severe retinitis pigmentosa Oscar F. Chacón‐Camacho, Serguei Jitskii, Beatriz Buentello‐Volante, Gene Somatic VariantMendelian DisorderGenetic DisorderMedicineGenetics	2013	16
Nasopalpebral Lipoma‐Coloboma syndrome: Clinical, radiological, and histopathological description of a novel sporadic case Oscar F. Chacón‐Camacho, Monica López‐Martínez, Johanna Vázquez, American Journal of Medical Genetics Part A	2013	14

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