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Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|April 1, 2021
SEOM clinical guideline for management of adult medulloblastoma (2020)R Luque, M Benavides, S Del Barco, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 8, 2026
Diagnostic Yield of Exome Reanalysis Over Time: Contribution of Reevaluation Type, Timing, and Patient PhenotypeYi-Lee Ting, Trevor J Williams, Hillery Metz, et al.American Journal of Medical Genetics. Part A|October 7, 2011
A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrumDaniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Analysis of genotype-phenotype correlations in human holoprosencephalyBenjamin D Solomon, Sandra Mercier, Jorge I Vélez, et al.Human Vaccines & Immunotherapeutics|April 7, 2025
Drug survival of omalizumab in atopic asthma: Impact of clinical and genetic variablesSusana Rojo-Tolosa, Alberto Caballero-Vázquez, Laura E Pineda-Lancheros, et al.Nature|February 13, 2015
The formation of a quadruple star system with wide separationJaime E Pineda, Stella S R Offner, Richard J Parker, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|May 25, 2011
De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate geneBenjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, et al.Journal of Immunology (Baltimore, Md. : 1950)|November 11, 2025
STAT3 mediates an inflammation-induced microbial defense response and regulates pathogen control and clearance by macrophagesBhakti Patel, Xiaofeng Zheng, Laura M Kahn, et al.American Journal of Medical Genetics. Part A|October 31, 2009
Compound heterozygosity for mutations in PAX6 in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmiaBenjamin D Solomon, Daniel E Pineda-Alvarez, Joan Z Balog, et al.Molecular Syndromology|May 9, 2013
Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL AssociationB D Solomon, D E Pineda-Alvarez, D W Hadley, et al.Pageof 16