M. Corpas

发表

Phenotype-loci associations in networks of patients with rare disorders: application to assist in the diagnosis of novel clinical cases

J. A. Ranea, P. Lapunzina, E. Rojano, 2018, European Journal of Human Genetics.

Systematic identification of phenotypically enriched loci using a patient network of genomic disorders

Manuel Corpas, Armando Reyes-Palomares, Miguel Ángel Medina, 2016, BMC Genomics.

APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Manuel Corpas, Laura Lyman Rodriguez, Jason Bobe, 2018, Human Genomics.

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.

Manuel Corpas, Yves Moreau, Steven Van Vooren, 2009, American journal of human genetics.

DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders.

Manuel Corpas, Matthew E Hurles, Caroline F Wright, 2012, Human molecular genetics.

Interpretation of Genomic Copy Number Variants Using DECIPHER

Manuel Corpas, Stephen Clayton, Eugene Bragin, 2012, Current protocols in human genetics.

PGP-UK: a research and citizen science hybrid project in support of personalized medicine

G. Bignell, S. Beck, J. A. Guerra-Assunção, 2018, bioRxiv.

Genome sequencing of the staple food crop white Guinea yam enables the development of a molecular marker for sex determination

W. Haerty, H. Matsumura, R. Terauchi, 2017, BMC Biology.

Transferability of genetic risk scores in African populations

Opeyemi S. Soremekun, A. Motala, F. Pirie, 2022, Nature Medicine.

Overt aggression and psicosocial adjustment in adolescence

M. Corpas, Belén Martínez Ferrer, David Moreno Ruiz, 2010 .