Flores, Carlos

Genome-wide association study of susceptibility to idiopathic pulmonary fibrosis

Allen, R. J., Guillen-Guio, B., Oldham, J. M., Ma, S.-F., Dressen, A., Paynton, M. L., Kraven, L. M., Obeidat, M., Li, X., Ng, M., et al. (2020) · American Journal of Respiratory and Critical Care Medicine

Interstitial Lung Diseases and Idiopathic Pulmonary FibrosisGenetic Associations and Epidemiology

Cited by 329

Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study

Allen, R. J., Porte, J., Braybrooke, R., Flores, C., Fingerlin, T. E., Oldham, J. M., Guillen-Guio, B., Ma, S.-F., Okamoto, T., John, A. E., et al. (2017) · The Lancet Respiratory Medicine

Interstitial Lung Diseases and Idiopathic Pulmonary FibrosisGenetic Associations and Epidemiology

Cited by 297

Curated variation benchmarks for challenging medically relevant autosomal genes

Wagner, J., Olson, N. D., Harris, L., McDaniel, J., Cheng, H., Fungtammasan, A., Hwang, Y.-C., Gupta, R., Wenger, A. M., Rowell, W. J., et al. (2022) · Nature Biotechnology

Genomics and Phylogenetic StudiesGenomics and Rare Diseases

Cited by 241

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Pairo-Castineira, E., Rawlik, K., Bretherick, A. D., Qi, T., Wu, Y., Nassiri, I., McConkey, G. A., Zechner, M., Klaric, L., Griffiths, F., et al. (2023) · Nature

Genetic Associations and EpidemiologyCOVID-19 Clinical Research Studies

Cited by 225

PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions

Olson, N. D., Wagner, J., McDaniel, J., Stephens, S. H., Westreich, S. T., Prasanna, A. G., Johanson, E., Boja, E., Maier, E. J., Serang, O., et al. (2022) · Cell Genomics

Genomics and Phylogenetic StudiesGenomics and Rare Diseases

Cited by 202

Gene flow from North Africa contributes to differential human genetic diversity in southern Europe

Botigué, L. R., Henn, B. M., Gravel, S., Maples, B. K., Gignoux, C. R., Corona, E., Atzmon, G., Burns, E., Ostrer, H., Flores, C., et al. (2013) · Proceedings of the National Academy of Sciences

Forensic and Genetic ResearchGenetic diversity and population structure

Cited by 199

Tachykinins and tachykinin receptors in human uterus

Patak, E., Luz Candenas, M., Pennefather, J. N., Ziccone, S., Lilley, A., Martín, J. D., Flores, C., Mantecón, A. G., Story, M. E., & Pinto, F. M. (2003) · British Journal of Pharmacology

Neuropeptides and Animal PhysiologyCardiovascular, Neuropeptides, and Oxidative Stress Research

Cited by 82

Type 2 deiodinase and host responses of sepsis and acute lung injury

Ma, S.-F., Xie, L., Pino-Yanes, M., Sammani, S., Wade, M. S., Letsiou, E., Siegler, J., Wang, T., Infusino, G., Kittles, R. A., et al. (2011) · American Journal of Respiratory Cell and Molecular Biology

Respiratory Support and MechanismsThyroid Disorders and Treatments

Cited by 60

Evaluation of a whole‐exome sequencing pipeline and benchmarking of causal germline variant prioritizers

Tosco‐Herrera, E., Muñoz‐Barrera, A., Jáspez, D., Rubio‐Rodríguez, L. A., Mendoza‐Alvarez, A., Rodriguez‐Perez, H., Jou, J., Iñigo‐Campos, A., Corrales, A., Ciuffreda, L., et al. (2022) · Human Mutation

Genomics and Rare DiseasesGenomics and Phylogenetic Studies

Cited by 20