De novo mutations in human genetic disease
By J. Veltman, H. Brunner. Nature reviews genetics, 2012
806 citations recorded by the source corpus.
Subfields: Genetics
View Paper: https://www.semanticscholar.org/paper/309e5928360fe9ce56521de3a76d08da6356c503
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Genetics
- Heng Li
- Thorfinn Sand Korneliussen
- Anders Albrechtsen
- Gabor T. Marth
- Erik P. Garrison
- Julian Catchen
- Olivier Delaneau
- Kathryn E. Holt
Citations in the corpus
- Toward better understanding of artifacts in variant calling from high-coverage samples (2014, background): “…(Watson et al., 2013), for the discovery of de novo mutations associated with Mendelian diseases (Bamshad et al., 2011), for the reconstruction of human population history (Li and Durbin, 2011) and for the understanding of mutation processes (Veltman and Brunner, 2012; Campbell and Eichler, 2013).”