Elisa Docampo

Avenue De L'Hôpital 1
Liege, WAL 4000, Belgium

Last Updated: 09/26/2026

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Found 20 publications

Shprintzen - Goldberg syndrome without intellectual disability: A clinical report and review of literature.

Shprintzen - Goldberg syndrome without intellectual disability: A clinical report and review of literature.

Journal: European journal of medical genetics

Published: September 10, 2024

Interest in the use of polygenic risk scores in breast cancer screening and preventive medicine

Interest in the use of polygenic risk scores in breast cancer screening and preventive medicine

Journal: Revue medicale de Liege

Published: June 13, 2024

Hypophosphatasia Presenting as a Chronic Diffuse Pain Syndrome with Extra-Articular Calcifications.

Hypophosphatasia Presenting as a Chronic Diffuse Pain Syndrome with Extra-Articular Calcifications.

Journal: Journal of clinical medicine

Published: February 14, 2024

The Ehlers Danlos syndrome : a rare disease although commonly suspected

The Ehlers Danlos syndrome : a rare disease although commonly suspected

Journal: Revue medicale de Liege

Published: November 13, 2023

Heredity and cancer

Heredity and cancer

Journal: Revue medicale de Liege

Published: June 03, 2021

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.

Journal: Addiction biology

Published: August 21, 2019

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

Journal: Nature genetics

Published: June 09, 2018

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes.

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes.

Journal: Nature communications

Published: September 01, 2017

Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications.

Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications.

Journal: Annals of the rheumatic diseases

Published: August 05, 2016

Analysis of shared heritability in common disorders of the brain.

Analysis of shared heritability in common disorders of the brain.

Journal: Science (New York, N.Y.)

Published: April 15, 2016

Genome-Wide Association Study of Acute Renal Graft Rejection.

Genome-Wide Association Study of Acute Renal Graft Rejection.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Published: February 18, 2016

HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis.

HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: November 25, 2015

Showing 1-12 of 20

Last Updated: 09/26/2026