Elisa Contini

The Frontier Fields lens modelling comparison project

M. Meneghetti, Priyamvada Natarajan, Dan Coe et al. · Monthly Notices of the Royal Astronomical Society · 2017 · 227 citations · Full text

Sequencing of a ‘mouse azoospermia’ gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest

Antoni Riera‐Escamilla, Andrea Enguita-Marruedo, Daniel Moreno‐Mendoza et al. · Human Reproduction · 2019 · 96 citations · Full text

Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center

Francesco Mazzarotto, Francesca Girolami, Beatrice Boschi et al. · Genetics in Medicine · 2018 · 71 citations · Full text

A novel <i><scp>PAX1</scp></i> null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency

Irene Paganini, Roberta Sestini, Gabriele Lorenzo Capone et al. · Clinical Genetics · 2017 · 55 citations

Developmental Anomaly, Otofaciocervical Syndrome, Developmental Biology +15

Semi-analytic model predictions of the galaxy population in protoclusters

Elisa Contini, G. De Lucia, N. A. Hatch et al. · Monthly Notices of the Royal Astronomical Society · 2015 · 37 citations · Full text