Nicole Soranzo - Selected Publications#

Chen, L., [67 authors, Soranzo, N.: 63], and Rendon, A. (2014). Transcriptional diversity during lineage commitment of human blood progenitors. Science 345, 1251033.

Huang, J., [17 authors], and Soranzo, N. (2015). Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nat Commun 6, 8111.

UK10K Consortium, [29 authors], and Soranzo, N. (2015). The UK10K project identifies rare variants in health and disease. Nature 526, 82-90.

Chen, L., [80 authors], and Soranzo, N. (2016) Genetic drivers of epigenetic and transcriptional variation in human immune cells. Cell 167;5;1398-1414.e24.

Astle, W.J., [45 authors], and Soranzo, N. (2016) The allelic landscape of human blood cell trait variation and links to common complex disease. Cell 167;5;1415-1429.e19.

Iotchkova, V., Ritchie, G.R.S, Geihs, M., Morganella, S., Min, J.L., Walter, K., Timpson, N.J.; UK10K Consortium, Dunham, I., Birney, E., Soranzo, N. (2019) GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals. Nat Genet. Feb;51(2):343-353.

Vuckovic D., [110 authors] and Soranzo, N. (2020) The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 3;182(5):1214-1231.e11.

Watt S., [25 authors] and Soranzo N. (2021) Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease. Nat Commun. 16;12(1):2298.

Cai N., [26 authors], and Soranzo N. (2021) Mitochondrial DNA variants modulate N-formyl methionine, proteostasis and risk of late-onset human diseases. Nat Med. 27(9):1564-1575.

Kundu K., Tardaguila M., Mann A.L., Watt S., Ponstingl H., Vasquez L., Von Schiller D., Morrell N.W., Stegle O., Pastinen T., Sawcer S.J., Anderson C.A., Walter K., Soranzo N. (2022) Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases. Nat Genet. 54(3):251-262.

H-index: 126,
Citations: 87,584