Soranzo, Nicole

Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases

Cai, N., Gomez-Duran, A., Yonova-Doing, E., Kundu, K., Burgess, A. I., Golder, Z. J., Calabrese, C., Bonder, M. J., Camacho, M., Lawson, R. A., et al. (2021) · Nature Medicine

Mitochondrial Function and PathologyGenetic Associations and Epidemiology

Cited by 73

Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease

Watt, S., Vasquez, L., Walter, K., Mann, A. L., Kundu, K., Chen, L., Sims, Y., Ecker, S., Burden, F., Farrow, S., et al. (2021) · Nature Communications

Genomics and Chromatin DynamicsGenetic Associations and Epidemiology

Cited by 63

Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits

Boraska, V., Davis, O. S. P., Cherkas, L. F., Helder, S. G., Harris, J., Krug, I., Pei‐Chi Liao, T., Treasure, J., Ntalla, I., Karhunen, L., et al. (2012) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Eating Disorders and BehaviorsGenetic Associations and Epidemiology

Cited by 61

Personalized and graph genomes reveal missing signal in epigenomic data

Groza, C., Kwan, T., Soranzo, N., Pastinen, T., & Bourque, G. (2020) · Genome Biology

Genomics and Phylogenetic StudiesGenomics and Chromatin Dynamics

Cited by 57

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

Polfus, L. M., Khajuria, R. K., Schick, U. M., Pankratz, N., Pazoki, R., Brody, J. A., Chen, M.-H., Auer, P. L., Floyd, J. S., Huang, J., et al. (2016) · The American Journal of Human Genetics

Platelet Disorders and TreatmentsGenetic Associations and Epidemiology

Cited by 54