Luis Escobar
Publications by Year
Research Areas
Supramolecular Chemistry and Complexes, Crystallization and Solubility Studies, X-ray Diffraction in Crystallography, Genomic variations and chromosomal abnormalities, Molecular Sensors and Ion Detection
Most-Cited Works
- → A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay(2010)671 cited
- → Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants(2012)626 cited
- → Molecular Recognition in Water Using Macrocyclic Synthetic Receptors(2021)327 cited
- → Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication(2008)305 cited
- → Reanalysis of Clinical Exome Sequencing Data(2019)291 cited
- → High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation(2015)189 cited
- → A prebiotically plausible scenario of an RNA–peptide world(2022)161 cited
- → Investigation ofNRXN1deletions: Clinical and molecular characterization(2013)111 cited
- → Urorectal Septum Malformation Sequence(1987)109 cited
- → Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy(2019)98 cited