Candidate genes identified by whole-exome sequencing in preeclampsia families : insights into functional annotation and in-silico prediction of deleterious variants

enthalten in: Journal of hypertension | 2020

von Linhares, N. | Conceição, I. | Sandrim, V. | +1

Letter by Linhares et al Regarding Article, "Cardiomyopathy and Preeclampsia : Shared Genetics?"

enthalten in: Circulation | 2019

von Linhares, N. | Conceição, I. | Luizon, M.

"Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis (Linhares et al., 2014)" turns out to be EBV+ leiomyomatosis caused by CARMIL2 mutations

enthalten in: European journal of medical genetics | 2018

von Linhares, N. | Freire, M. | Cardenas, R. | +3