PubRank

Anders Albrechtsen

Author PubWeight™ 71.95‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genotype and SNP calling from next-generation sequencing data. Nat Rev Genet 2011 8.34
2 Ancient human genome sequence of an extinct Palaeo-Eskimo. Nature 2010 7.51
3 Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants. Nat Genet 2010 5.44
4 Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. Nat Genet 2009 5.43
5 An Aboriginal Australian genome reveals separate human dispersals into Asia. Science 2011 4.84
6 Low physical activity accentuates the effect of the FTO rs9939609 polymorphism on body fat accumulation. Diabetes 2007 4.19
7 Recalibrating Equus evolution using the genome sequence of an early Middle Pleistocene horse. Nature 2013 3.45
8 Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies. Diabetes 2007 3.25
9 Darwinian and demographic forces affecting human protein coding genes. Genome Res 2009 3.01
10 SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing data. PLoS One 2012 2.37
11 Estimation of allele frequency and association mapping using next-generation sequencing data. BMC Bioinformatics 2011 1.93
12 Association testing of novel type 2 diabetes risk alleles in the JAZF1, CDC123/CAMK1D, TSPAN8, THADA, ADAMTS9, and NOTCH2 loci with insulin release, insulin sensitivity, and obesity in a population-based sample of 4,516 glucose-tolerant middle-aged Danes. Diabetes 2008 1.55
13 Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome. PLoS Genet 2011 1.54
14 Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes. Am J Hum Genet 2013 1.43
15 A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics. Genome Res 2011 1.41
16 Quantifying population genetic differentiation from next-generation sequencing data. Genetics 2013 1.41
17 Estimating individual admixture proportions from next generation sequencing data. Genetics 2013 1.32
18 Combined analyses of 20 common obesity susceptibility variants. Diabetes 2010 1.27
19 Estimating inbreeding coefficients from NGS data: Impact on genotype calling and allele frequency estimation. Genome Res 2013 1.12
20 Calculation of Tajima's D and other neutrality test statistics from low depth next-generation sequencing data. BMC Bioinformatics 2013 1.10
21 Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. PLoS Genet 2013 1.04
22 Association testing for next-generation sequencing data using score statistics. Genet Epidemiol 2012 1.00
23 Novel de novo BRCA2 mutation in a patient with a family history of breast cancer. BMC Med Genet 2008 0.99
24 Studies of the common DIO2 Thr92Ala polymorphism and metabolic phenotypes in 7342 Danish white subjects. J Clin Endocrinol Metab 2006 0.98
25 RelateAdmix: a software tool for estimating relatedness between admixed individuals. Bioinformatics 2013 0.97
26 Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families. Breast Cancer Res Treat 2008 0.96
27 A common Greenlandic Inuit BRCA1 RING domain founder mutation. Breast Cancer Res Treat 2008 0.92
28 The -250G>A promoter variant in hepatic lipase associates with elevated fasting serum high-density lipoprotein cholesterol modulated by interaction with physical activity in a study of 16,156 Danish subjects. J Clin Endocrinol Metab 2008 0.91
29 The validation and assessment of machine learning: a game of prediction from high-dimensional data. PLoS One 2009 0.91
30 Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a nucleotide 249T>A/c.130T>A (p.Cys44Ser) mutation in two Greenlandic Inuit families: implications for genetic screening of Greenlandic Inuit families with high risk for breast and/or ovarian cancer. Breast Cancer Res Treat 2010 0.81
31 A novel -192c/g mutation in the proximal P2 promoter of the hepatocyte nuclear factor-4 alpha gene (HNF4A) associates with late-onset diabetes. Diabetes 2006 0.81
32 Genome-Wide Association Study of Genetic Variants in LPS-Stimulated IL-6, IL-8, IL-10, IL-1ra and TNF-α Cytokine Response in a Danish Cohort. PLoS One 2013 0.80
33 Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity. PLoS One 2010 0.77
34 Partial USH2A deletions contribute to Usher syndrome in Denmark. Eur J Hum Genet 2015 0.77