| Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands SC Jin, J Homsy, S Zaidi, Q Lu, S Morton, SR DePalma, X Zeng, H Qi, ... Nature genetics 49 (11), 1593-1601, 2017 | 721 | 2017 |
| Mutations disrupting neuritogenesis genes confer risk for cerebral palsy SC Jin, SA Lewis, S Bakhtiari, X Zeng, MC Sierant, S Shetty, SM Nordlie, ... Nature genetics 52 (10), 1046-1056, 2020 | 125 | 2020 |
| Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus SC Jin, W Dong, AJ Kundishora, S Panchagnula, A Moreno-De-Luca, ... Nature medicine 26 (11), 1754-1765, 2020 | 102 | 2020 |
| Somatic PIK3CA Mutations in Sporadic Cerebral Cavernous Malformations M Peyre, D Miyagishima, F Bielle, F Chapon, M Sierant, Q Venot, ... New England Journal of Medicine 385 (11), 996-1004, 2021 | 66 | 2021 |
| Developmental transcriptome analysis of human erythropoiesis L Shi, YH Lin, MC Sierant, F Zhu, S Cui, Y Guan, MA Sartor, O Tanabe, ... Human molecular genetics 23 (17), 4528-4542, 2014 | 59 | 2014 |
| Exome sequencing implicates impaired GABA signaling and neuronal ion transport in trigeminal neuralgia W Dong, SC Jin, A Allocco, X Zeng, AH Sheth, S Panchagnula, ... IScience 23 (10), 2020 | 26 | 2020 |
| Compound loss of function of nuclear receptors Tr2 and Tr4 leads to induction of murine embryonic β-type globin genes S Cui, O Tanabe, M Sierant, L Shi, A Campbell, KC Lim, JD Engel Blood, The Journal of the American Society of Hematology 125 (9), 1477-1487, 2015 | 24 | 2015 |
| Single-cell sequencing in cancer: recent applications to immunogenomics and multi-omics tools MC Sierant, J Choi Genomics & informatics 16 (4), 2018 | 15 | 2018 |
| Biased, non-equivalent gene-proximal and-distal binding motifs of orphan nuclear receptor TR4 in primary human erythroid cells L Shi, MC Sierant, K Gurdziel, F Zhu, S Cui, KE Kolodziej, J Strouboulis, ... PLoS Genetics 10 (5), e1004339, 2014 | 8 | 2014 |
| Genomic Analysis of 11,555 Probands Provides a Framework for Congenital Heart Disease Genetics M Sierant | | 2021 |
