|
Hu, Yao |
A common TCN1 loss of function variant is associated with lower vitamin B12 level in African Americans |
Blood |
2018 |
29764838 |
|
|
Sofer, Tamar |
A Fully-Adjusted Two-Stage Procedure for Rank Normalization in Genetic Association Studies |
Genet Epidemiol. |
2019 |
30653739 |
|
|
Mitchell, Braxton |
An APOO pseudogene on chromosome 5q regulates LDL-C levels |
Circulation |
2018 |
29593015 |
|
|
Brody, Jennifer |
Analysis Commons: A Team Approach to Discovery in a Big-Data Environment for Genetic Epidemiology |
Nature Genetics |
2017 |
29074945 |
|
|
Szpiech, Zachary |
Ancestry-dependent Enrichment of Deleterious Homozygotes in Runs of Homozygosity |
AJHG |
2019 |
31543216 |
|
|
Ellinor, Patrick |
Association between titin loss-of-function variants and early-onset atrial fibrillation. |
JAMA |
2018 |
30535219 |
|
|
Reiner, Alex |
Common α-globin and β-globin variants in African Americans and their interaction on red cell and other clinical phenotypes |
PLOS Genetics |
2018 |
29590102 |
|
|
Raffield, Laura |
D-dimer in African Americans: Whole Genome Sequence Analysis and Relationship to CVD Risk in the Jackson Heart Study |
ATVB |
2017 |
28912365 |
|
|
Natarajan, Pradeep |
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries |
Nature Communications |
2018 |
29973585 |
|
|
Natarajan, Pradeep |
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals |
Nature Communications |
2018 |
30140000 |
|
|
Chen, Han |
Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies |
The American Journal of Human Genetics |
2018 |
30639324 |
|
|
Mak, Angel CY |
Identification of CFTR Variants in Hispanic Patients with Cystic Fibrosis from the Dominican Republic and Puerto Rico |
Pediatric Pulmonology |
2019 |
31665830 |
|
|
Sarnowski, Chloé |
Impact of rare and common genetic variants on type 2 diabetes diagnosis by hemoglobin A1c in multi-ancestry populations from the Trans-Omics for Precision Medicine (TOPMed) Program |
American Journal of Human Genetics |
2019 |
31564435 |
|
|
Zhu, Xiaofeng |
Leveraging linkage evidence to identify low frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data |
Human Genetics |
2019 |
30671673 |
|
|
Sarnowski, Chloe |
Whole genome sequence analyses of brain imaging measures in the Framingham Study |
Neurology |
2017 |
29282330 |
|
|
Auer, Paul |
Whole genome sequences association with E-selectin levels reveals Loss-of-function variant in African Americans |
Human Molecular Genetics |
2018 |
30307499 |
|
|
Weiss, Scott |
Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with Airway Hyperresponsive Asthma |
Chest |
2019 |
31557467 |
|
|
Silverman, Edwin |
Whole Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease |
American Journal of Respiratory and Critical Care Medicine |
2018 |
29949718 |
|
|
Oh, Sam |
Whole genome sequencing of pharmacogenetic drug response in racially and ethnically diverse children with asthma |
American Journal of Respiratory and Critical Care Medicine |
2018 |
29509491 |
|
