Klaudia Walter

Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 48 publications

An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.

An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2026

The genetic basis of the immune response to SARS-CoV-2 infection and vaccination in the Italian municipality of Vo'.

The genetic basis of the immune response to SARS-CoV-2 infection and vaccination in the Italian municipality of Vo'.

Journal: Frontiers in immunology

Published: October 03, 2025

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Journal: Nature genetics

Published: June 08, 2025

Integrating natural and engineered genetic variations to decode regulatory influence on blood traits.

Integrating natural and engineered genetic variations to decode regulatory influence on blood traits.

Journal: Cell reports

Published: March 21, 2025

Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity.

Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity.

Journal: American journal of human genetics

Published: April 03, 2024

Misexpression of inactive genes in whole blood is associated with nearby rare structural variants.

Misexpression of inactive genes in whole blood is associated with nearby rare structural variants.

Journal: American journal of human genetics

Published: January 12, 2024

Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations.

Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations.

Journal: Nature genetics

Published: July 24, 2023

Inherited polygenic effects on common hematological traits influence clonal selection on JAK2V617F and the development of myeloproliferative neoplasms.

Inherited polygenic effects on common hematological traits influence clonal selection on JAK2V617F and the development of myeloproliferative neoplasms.

Journal: Nature genetics

Published: December 22, 2022

GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphology.

GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphology.

Journal: Human molecular genetics

Published: May 19, 2022

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

Journal: PLoS genetics

Published: April 06, 2022

Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.

Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.

Journal: American journal of human genetics

Published: August 19, 2021

A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.

A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.

Journal: Nature communications

Published: July 19, 2021

Showing 1-12 of 48

Last Updated: 09/26/2026