Jeremy Cauwels
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View article: Population Genomic Screening and Improved Lipid Management in Patients With Familial Hypercholesterolemia
Population Genomic Screening and Improved Lipid Management in Patients With Familial Hypercholesterolemia Open
BACKGROUND: The Helix Research Network program is a large population genomics initiative that screens an all-comers population of patients for Centers for Disease Control and Prevention Tier 1 genetic conditions, including familial hyperch…
View article: Population genomic screening leads to improved lipid management in patients with familial hypercholesterolemia
Population genomic screening leads to improved lipid management in patients with familial hypercholesterolemia Open
Background The Helix Research Network TM program is a large population genomics initiative that screens an all-comers population of patients for CDC Tier 1 genetic conditions, including familial hypercholesterolemia (FH). We evaluated chan…
View article: P172: A framework to identify individuals at low risk of disease in the population*
P172: A framework to identify individuals at low risk of disease in the population* Open
View article: P580: Comparing automated vs ACMG/AMP-based variant interpretation for the CDC Tier 1 conditions in a clinicogenomic cohort from US-based health systems
P580: Comparing automated vs ACMG/AMP-based variant interpretation for the CDC Tier 1 conditions in a clinicogenomic cohort from US-based health systems Open
View article: O20: Improved clinical management following diagnosis with familial hypercholesterolemia in the Helix Research Network Population Genomics Screening Program
O20: Improved clinical management following diagnosis with familial hypercholesterolemia in the Helix Research Network Population Genomics Screening Program Open
View article: P101: Very low penetrance of loss-of-function variants in PMS2 for all Lynch syndrome relevant cancers in large US biobanks*
P101: Very low penetrance of loss-of-function variants in PMS2 for all Lynch syndrome relevant cancers in large US biobanks* Open
View article: P187: Truncating variants in APOB are not VUS when screening for familial hypercholesterolemia
P187: Truncating variants in APOB are not VUS when screening for familial hypercholesterolemia Open