PubRank

Daniel F Gudbjartsson

Author PubWeight™ 260.30‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A high-resolution recombination map of the human genome. Nat Genet 2002 28.66
2 A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 2007 18.96
3 A common inversion under selection in Europeans. Nat Genet 2005 13.66
4 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. Nat Genet 2008 12.43
5 Rate of de novo mutations and the importance of father's age to disease risk. Nature 2012 11.92
6 Detection of sharing by descent, long-range phasing and haplotype imputation. Nat Genet 2008 9.69
7 Genetic determinants of hair, eye and skin pigmentation in Europeans. Nat Genet 2007 8.79
8 Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science 2007 7.55
9 Parental origin of sequence variants associated with complex diseases. Nature 2009 7.21
10 Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Nat Genet 2009 6.91
11 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat Genet 2010 6.49
12 Multiple genetic loci for bone mineral density and fractures. N Engl J Med 2008 6.35
13 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. Nat Genet 2009 5.06
14 Fine-scale recombination rate differences between sexes, populations and individuals. Nature 2010 4.74
15 A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction. Nat Genet 2005 4.45
16 BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes. J Clin Oncol 2002 4.38
17 New common variants affecting susceptibility to basal cell carcinoma. Nat Genet 2009 4.15
18 A rare variant in MYH6 is associated with high risk of sick sinus syndrome. Nat Genet 2011 3.94
19 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. Nat Genet 2009 3.46
20 New sequence variants associated with bone mineral density. Nat Genet 2008 3.43
21 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet 2010 3.37
22 Several common variants modulate heart rate, PR interval and QRS duration. Nat Genet 2010 3.34
23 Two newly identified genetic determinants of pigmentation in Europeans. Nat Genet 2008 3.31
24 Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nat Genet 2011 3.18
25 Mutations in BRIP1 confer high risk of ovarian cancer. Nat Genet 2011 3.06
26 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. Science 2008 3.00
27 Allegro version 2. Nat Genet 2005 2.98
28 Genetic correction of PSA values using sequence variants associated with PSA levels. Sci Transl Med 2010 2.83
29 Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family. PLoS Med 2004 2.67
30 Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche. Nat Genet 2009 2.58
31 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. Nat Genet 2010 2.56
32 Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits. Nature 2013 2.55
33 Recombination rate and reproductive success in humans. Nat Genet 2004 2.52
34 Familial risk of lung carcinoma in the Icelandic population. JAMA 2004 2.50
35 Identification of low-frequency variants associated with gout and serum uric acid levels. Nat Genet 2011 2.48
36 A germline variant in the TP53 polyadenylation signal confers cancer susceptibility. Nat Genet 2011 2.43
37 A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer. Nat Genet 2012 2.29
38 Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet 2012 2.12
39 Subclinical intestinal inflammation: an inherited abnormality in Crohn's disease relatives? Gastroenterology 2003 2.03
40 Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proc Natl Acad Sci U S A 2011 2.01
41 Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. Nat Genet 2008 1.84
42 Discovery of common variants associated with low TSH levels and thyroid cancer risk. Nat Genet 2012 1.81
43 A sequence variant on 17q21 is associated with age at onset and severity of asthma. Eur J Hum Genet 2010 1.74
44 Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus. PLoS Genet 2010 1.74
45 Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. Nat Genet 2009 1.73
46 A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting. Am J Hum Genet 2002 1.45
47 European bone mineral density loci are also associated with BMD in East-Asian populations. PLoS One 2010 1.29
48 Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene. PLoS Genet 2010 1.25
49 A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration. Nat Genet 2013 1.23
50 Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. J Am Coll Cardiol 2012 1.14
51 Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies. PLoS One 2010 1.05
52 Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. PLoS Genet 2013 1.04
53 Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. Hum Mol Genet 2011 1.03
54 A common variant at 8q24.21 is associated with renal cell cancer. Nat Commun 2013 0.96
55 Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk. Cancer Res 2011 0.92
56 Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. Hum Mol Genet 2014 0.90
57 "Bias toward the null" means reduced power. Am J Hum Genet 2004 0.79
58 Predicting atrial fibrillation. Lancet 2009 0.79
59 A genetic contribution to inflammatory bowel disease in Iceland: a genealogic approach. Clin Gastroenterol Hepatol 2004 0.77
60 Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat Commun 2015 0.75
61 Evaluating differences in linkage disequilibrium between populations. Ann Hum Genet 2010 0.75