| Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease R Soemedi, IJ Wilson, J Bentham, R Darlay, A Töpf, D Zelenika, ... The American Journal of Human Genetics 91 (3), 489-501, 2012 | 335 | 2012 |
| The complexity of the translation ability of circRNAs JT Granados-Riveron, G Aquino-Jarquin Biochimica et Biophysica Acta (BBA)-Gene Regulatory Mechanisms 1859 (10 …, 2016 | 203 | 2016 |
| Rare variants in NR2F2 cause congenital heart defects in humans S Al Turki, AK Manickaraj, CL Mercer, SS Gerety, MP Hitz, S Lindsay, ... The American Journal of Human Genetics 94 (4), 574-585, 2014 | 181 | 2014 |
| Alpha-cardiac actin mutations produce atrial septal defects H Matsson, J Eason, CS Bookwalter, J Klar, P Gustavsson, J Sunnegårdh, ... Human molecular genetics 17 (2), 256-265, 2008 | 179 | 2008 |
| α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects JT Granados-Riveron, TK Ghosh, M Pope, F Bu'Lock, C Thornborough, ... Human molecular genetics 19 (20), 4007-4016, 2010 | 169 | 2010 |
| Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 HJ Cordell, J Bentham, A Topf, D Zelenika, S Heath, C Mamasoula, ... Nature genetics 45 (7), 822-824, 2013 | 158 | 2013 |
| Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls R Soemedi, A Topf, IJ Wilson, R Darlay, T Rahman, E Glen, D Hall, ... Human molecular genetics 21 (7), 1513-1520, 2012 | 132 | 2012 |
| Combined mutation screening of NKX2‐5, GATA4, and TBX5 in congenital heart disease: Multiple heterozygosity and novel mutations JT Granados‐Riveron, M Pope, FA Bu'Lock, C Thornborough, J Eason, ... Congenital heart disease 7 (2), 151-159, 2012 | 103 | 2012 |
| Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot HJ Cordell, A Töpf, C Mamasoula, AV Postma, J Bentham, D Zelenika, ... Human molecular genetics 22 (7), 1473-1481, 2013 | 98 | 2013 |
| The impact of mechanical forces in heart morphogenesis JT Granados-Riveron, JD Brook Circulation: Cardiovascular Genetics 5 (1), 132-142, 2012 | 96 | 2012 |
| High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic … A Ketley, CZ Chen, X Li, S Arya, TE Robinson, J Granados-Riveron, ... Human molecular genetics 23 (6), 1551-1562, 2014 | 77 | 2014 |
| CRISPR–Cas13 precision transcriptome engineering in cancer JT Granados-Riveron, G Aquino-Jarquin Cancer research 78 (15), 4107-4113, 2018 | 76 | 2018 |
| Engineering of the current nucleoside-modified mRNA-LNP vaccines against SARS-CoV-2 JT Granados-Riveron, G Aquino-Jarquin Biomedicine & Pharmacotherapy 142, 111953, 2021 | 75 | 2021 |
| Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects J England, J Granados-Riveron, L Polo-Parada, D Kuriakose, C Moore, ... Journal of molecular and cellular cardiology 106, 1-13, 2017 | 47 | 2017 |
| Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13 125 controls C Mamasoula, RR Prentice, T Pierscionek, F Pangilinan, JL Mills, ... Circulation: Cardiovascular Genetics 6 (4), 347-353, 2013 | 45 | 2013 |
| A Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot JA Goodship, D Hall, A Topf, C Mamasoula, H Griffin, TJ Rahman, E Glen, ... Circulation: Cardiovascular Genetics 5 (3), 287-292, 2012 | 43 | 2012 |
| CRISPR/Cas13-based approaches for ultrasensitive and specific detection of microRNAs JT Granados-Riveron, G Aquino-Jarquin Cells 10 (7), 1655, 2021 | 40 | 2021 |
| MiR-138 indirectly regulates the MDR1 promoter by NF-κB/p65 silencing JL Requenez-Contreras, ES López-Castillejos, R Hernández-Flores, ... Biochemical and biophysical research communications 484 (3), 648-655, 2017 | 26 | 2017 |
| Does the linear Sry transcript function as a ceRNA for miR-138? The sense of antisense JT Granados-Riveron, G Aquino-Jarquin F1000Research 3, 2014 | 25 | 2014 |
| Genetic Variation in VEGF Does Not Contribute Significantly to the Risk of Congenital Cardiovascular Malformation HR Griffin, DH Hall, A Topf, J Eden, AG Stuart, J Parsons, I Peart, ... PLoS One 4 (3), e4978, 2009 | 24 | 2009 |
