Last Updated: 09/26/2026
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Found 35 publications
The clinical utility of sequencing the entirety of CFTR.
Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Published: December 12, 2023
Genetic modifiers of body mass index in individuals with cystic fibrosis.
Journal: American journal of human genetics
Published: December 12, 2023
Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes.
Journal: Nature communications
Published: October 16, 2023
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients.
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients.
Journal: American journal of respiratory and critical care medicine
Published: March 15, 2023
Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries.
Journal: Nature genetics
Published: February 14, 2023
Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium.
Journal: Genes
Published: November 17, 2022
Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis.
Journal: American journal of human genetics
Published: January 21, 2022
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries.
Journal: Nature genetics
Published: November 24, 2021
Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients.
Journal: HGG advances
Published: October 21, 2021
A Custom Genotyping Array Reveals Population-Level Heterogeneity for the Genetic Risks of Prostate Cancer and Other Cancers in Africa.
Journal: Cancer research
Published: July 15, 2019
Genetic Modifiers of Cystic Fibrosis-Related Diabetes Have Extensive Overlap With Type 2 Diabetes and Related Traits.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 04, 2019
ZCCHC8, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation.
Journal: Genes & development
Published: April 19, 2019
Last Updated: 09/26/2026