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List of works by Cecelia A Laurie

1-16 of 16 results

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Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis

scientific article published on 22 December 2012
Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

scientific article
Genome-wide association study of colorectal cancer identifies six new susceptibility loci

scientific article published on 07 July 2015
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

scientific article published on 22 March 2016
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

scientific article published on 30 March 2016
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

scientific article
Discovery of common and rare genetic risk variants for colorectal cancer

scientific article published on 03 December 2018
Novel Common Genetic Susceptibility Loci for Colorectal Cancer

scientific article published on 01 February 2019
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

scientific article
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci

scientific article published on 26 October 2015
Inherited causes of clonal haematopoiesis in 97,691 whole genomes

scientific article published on 14 October 2020
Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants

scientific article published on 14 October 2020
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

scientific article
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program

scientific article published in April 2023
Rare variant contribution to the heritability of coronary artery disease

scientific article published on 9 October 2024

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