Carolina Haefliger

BioPharmaceuticals R&D
Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 16 publications

Pharmacogenomic study of the effects of saxagliptin on glucose control and hypoglycemic events.

Pharmacogenomic study of the effects of saxagliptin on glucose control and hypoglycemic events.

Journal: BMC medical genomics

Published: December 24, 2025

Body Mass Index, Clinical Outcomes, and Mortality in Heart Failure: A Mendelian Randomization Study.

Body Mass Index, Clinical Outcomes, and Mortality in Heart Failure: A Mendelian Randomization Study.

Journal: Journal of the American College of Cardiology

Published: November 24, 2025

Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Journal: medRxiv : the preprint server for health sciences

Published: May 20, 2024

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Journal: Nature communications

Published: May 10, 2024

Selecting the right therapeutic target for kidney disease.

Selecting the right therapeutic target for kidney disease.

Journal: Frontiers in pharmacology

Published: June 16, 2022

Rare and Common Variants in KIF15 Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis.

Rare and Common Variants in KIF15 Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis.

Journal: American journal of respiratory and critical care medicine

Published: April 13, 2022

Metabolic dysfunction-related liver disease as a risk factor for cancer.

Metabolic dysfunction-related liver disease as a risk factor for cancer.

Journal: BMJ open gastroenterology

Published: October 25, 2021

Pharmacogenomic study of heart failure and candesartan response from the CHARM programme.

Pharmacogenomic study of heart failure and candesartan response from the CHARM programme.

Journal: ESC heart failure

Published: September 23, 2021

Assessing the Role of Rare Genetic Variation in Patients With Heart Failure.

Assessing the Role of Rare Genetic Variation in Patients With Heart Failure.

Journal: JAMA cardiology

Published: December 16, 2020

Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank.

Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank.

Journal: Nature genetics

Published: November 06, 2020

Rare variant contribution to human disease in 281,104 UK Biobank exomes.

Rare variant contribution to human disease in 281,104 UK Biobank exomes.

Journal: Nature

Published: November 03, 2020

Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing.

Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing.

Journal: Circulation. Genomic and precision medicine

Published: October 30, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026