| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Actionable, pathogenic incidental findings in 1,000 participants' exomes.
|
Am J Hum Genet
|
2013
|
4.06
|
|
2
|
Priorities and standards in pharmacogenetic research.
|
Nat Genet
|
2005
|
2.65
|
|
3
|
Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors.
|
J Genet Couns
|
2002
|
1.51
|
|
4
|
X-linked high myopia associated with cone dysfunction.
|
Arch Ophthalmol
|
2004
|
1.23
|
|
5
|
Small, dense LDL and elevated apolipoprotein B are the common characteristics for the three major lipid phenotypes of familial combined hyperlipidemia.
|
Arterioscler Thromb Vasc Biol
|
2003
|
1.03
|
|
6
|
Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan.
|
Arterioscler Thromb Vasc Biol
|
2004
|
0.96
|
|
7
|
Human genetics. Mapping human history.
|
Science
|
2002
|
0.95
|
|
8
|
Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment.
|
Hum Genet
|
2003
|
0.95
|
|
9
|
Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia.
|
Hum Genet
|
2005
|
0.92
|
|
10
|
Linkage and association of phospholipid transfer protein activity to LASS4.
|
J Lipid Res
|
2011
|
0.91
|
|
11
|
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia.
|
Am J Hum Genet
|
2013
|
0.87
|
|
12
|
Genetic and nongenetic sources of variation in phospholipid transfer protein activity.
|
J Lipid Res
|
2009
|
0.87
|
|
13
|
'Drug reactions, enzymes, and biochemical genetics': 50 years later.
|
Pharmacogenomics
|
2007
|
0.85
|
|
14
|
Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.
|
Hum Genet
|
2010
|
0.84
|
|
15
|
Genome-wide scan for quantitative trait loci influencing LDL size and plasma triglyceride in familial hypertriglyceridemia.
|
J Lipid Res
|
2003
|
0.82
|
|
16
|
Genome-environment interactions and prospective technology assessment: evolution from pharmacogenomics to nutrigenomics and ecogenomics.
|
OMICS
|
2009
|
0.79
|
|
17
|
Response of serum and red blood cell folate concentrations to folic acid supplementation depends on methylenetetrahydrofolate reductase C677T genotype: results from a crossover trial.
|
Mol Nutr Food Res
|
2013
|
0.78
|
|
18
|
Enhancing recruitment of healthy African American volunteers in a city with a small African American community: results from a dietary supplement crossover trial.
|
Ethn Dis
|
2007
|
0.78
|
|
19
|
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria.
|
Proc Natl Acad Sci U S A
|
2011
|
0.77
|
|
20
|
Frequent detection of familial hypercholesterolemia mutations in familial combined hyperlipidemia.
|
J Am Coll Cardiol
|
2008
|
0.76
|
|
21
|
Equal proportion of adult male and female homozygous for the 677C --> T mutation in the methylenetetrahydrofolate reductase polymorphism.
|
Am J Med Genet A
|
2005
|
0.75
|
|
22
|
Giblett ER, Coleman DH, Pirzio-Biroli G, Donohue DM, Motulsky AG, Finch CA. Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia. Blood. 1956;11(4):291-309.
|
Blood
|
2016
|
0.75
|
|
23
|
Letter to the Editor: Reply to Becker and Morgan.
|
J Genet Couns
|
2002
|
0.75
|