Liu, Chunyu
Deep sequencing of the mitochondrial genome reveals common heteroplasmic sites in NADH dehydrogenase genes
Human Genetics
2018
29423652
Hu, Yao
A common TCN1 loss of function variant is associated with lower vitamin B12 level in African Americans
Blood
2018
29764838
Mitchell, Braxton
An APOO pseudogene on chromosome 5q regulates LDL-C levels
Circulation
2018
29593015
Silverman, Edwin
Whole Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease
American Journal of Respiratory and Critical Care Medicine
2018
29949718
Natarajan, Pradeep
Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
Nature Communications
2018
30140000
Wheeler, Marsha
Genomic characterization of the RH locus detects common, complex and novel structural variation in two multi-ethnic cohorts
Nature Genetics in Medicine
2018
29955105
Natarajan, Pradeep
Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries
Nature Communications
2018
29973585
Ellinor, Patrick
Association between titin loss-of-function variants and early-onset atrial fibrillation.
JAMA: The Journal of the American Medical Association
2018
30535219
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
Reiner, Alex
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease
PLOS Genetics
2018
29590102