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Connection

Dan Liviu Nicolae to Humans

This is a "connection" page, showing publications Dan Liviu Nicolae has written about Humans.
Connection Strength

0.598
  1. Association Tests for Rare Variants. Annu Rev Genomics Hum Genet. 2016 08 31; 17:117-30.
    View in: PubMed
    Score: 0.018
  2. PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population. PLoS Comput Biol. 2015 Mar; 11(3):e1004139.
    View in: PubMed
    Score: 0.016
  3. An exponential combination procedure for set-based association tests in sequencing studies. Am J Hum Genet. 2012 Dec 07; 91(6):977-86.
    View in: PubMed
    Score: 0.014
  4. Replication analysis for severe diabetic retinopathy. Invest Ophthalmol Vis Sci. 2012 Apr 30; 53(4):2377-81.
    View in: PubMed
    Score: 0.013
  5. Accurate imputation of rare and common variants in a founder population from a small number of sequenced individuals. Genet Epidemiol. 2012 May; 36(4):312-9.
    View in: PubMed
    Score: 0.013
  6. Genome-wide meta-analysis for severe diabetic retinopathy. Hum Mol Genet. 2011 Jun 15; 20(12):2472-81.
    View in: PubMed
    Score: 0.012
  7. An evolutionary framework for association testing in resequencing studies. PLoS Genet. 2010 Nov 11; 6(11):e1001202.
    View in: PubMed
    Score: 0.012
  8. You've gotta be lucky: Coverage and the elusive gene-gene interaction. Ann Hum Genet. 2011 Jan; 75(1):105-11.
    View in: PubMed
    Score: 0.012
  9. Gene, region and pathway level analyses in whole-genome studies. Genet Epidemiol. 2010 Apr; 34(3):222-231.
    View in: PubMed
    Score: 0.012
  10. Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS. PLoS Genet. 2010 Apr 01; 6(4):e1000888.
    View in: PubMed
    Score: 0.012
  11. Restricted parameter space models for testing gene-gene interaction. Genet Epidemiol. 2009 Jul; 33(5):386-93.
    View in: PubMed
    Score: 0.011
  12. (Too) great expectations: the challenges in replicating asthma disease genes. Am J Respir Crit Care Med. 2009 Jun 15; 179(12):1078-9.
    View in: PubMed
    Score: 0.011
  13. Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q. J Lipid Res. 2009 May; 50(5):798-806.
    View in: PubMed
    Score: 0.011
  14. Testing untyped alleles (TUNA)-applications to genome-wide association studies. Genet Epidemiol. 2006 Dec; 30(8):718-27.
    View in: PubMed
    Score: 0.009
  15. Quantifying the amount of missing information in genetic association studies. Genet Epidemiol. 2006 Dec; 30(8):703-17.
    View in: PubMed
    Score: 0.009
  16. Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set. PLoS Genet. 2006 May; 2(5):e67.
    View in: PubMed
    Score: 0.009
  17. Phenotype-stratified genetic linkage study demonstrates that IBD2 is an extensive ulcerative colitis locus. Am J Gastroenterol. 2006 Mar; 101(3):572-80.
    View in: PubMed
    Score: 0.009
  18. Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21. Am J Hum Genet. 2005 Feb; 76(2):349-57.
    View in: PubMed
    Score: 0.008
  19. Measuring the relative information in allele-sharing linkage studies. Biometrics. 2004 Jun; 60(2):368-75.
    View in: PubMed
    Score: 0.008
  20. Epigenetic responses to rhinovirus exposure in airway epithelial cells are correlated with key transcriptional pathways in chronic rhinosinusitis. Allergy. 2023 10; 78(10):2698-2711.
    View in: PubMed
    Score: 0.007
  21. Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings. PLoS Genet. 2023 01; 19(1):e1010594.
    View in: PubMed
    Score: 0.007
  22. Fine-mapping studies distinguish genetic risks for childhood- and adult-onset asthma in the HLA region. Genome Med. 2022 05 24; 14(1):55.
    View in: PubMed
    Score: 0.007
  23. MERLIN...and the geneticist's stone? Nat Genet. 2002 Jan; 30(1):3-4.
    View in: PubMed
    Score: 0.007
  24. Multi-omics colocalization with genome-wide association studies reveals a context-specific genetic mechanism at a childhood onset asthma risk locus. Genome Med. 2021 10 10; 13(1):157.
    View in: PubMed
    Score: 0.006
  25. Chromosome 17q12-21 Variants Are Associated with Multiple Wheezing Phenotypes in Childhood. Am J Respir Crit Care Med. 2021 04 01; 203(7):864-870.
    View in: PubMed
    Score: 0.006
  26. Altered transcriptional and chromatin responses to rhinovirus in bronchial epithelial cells from adults with asthma. Commun Biol. 2020 11 13; 3(1):678.
    View in: PubMed
    Score: 0.006
  27. On a randomization procedure. Am J Hum Genet. 2000 Nov; 67(5):1352-6.
    View in: PubMed
    Score: 0.006
  28. Epigenetic landscape links upper airway microbiota in infancy with allergic rhinitis at 6 years of age. J Allergy Clin Immunol. 2020 12; 146(6):1358-1366.
    View in: PubMed
    Score: 0.006
  29. Expression quantitative trait locus fine mapping of the 17q12-21 asthma locus in African American children: a genetic association and gene expression study. Lancet Respir Med. 2020 05; 8(5):482-492.
    View in: PubMed
    Score: 0.006
  30. Association of HLA-DRB1*09:01 with tIgE levels among African-ancestry individuals with asthma. J Allergy Clin Immunol. 2020 07; 146(1):147-155.
    View in: PubMed
    Score: 0.006
  31. Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. Lancet Respir Med. 2019 06; 7(6):509-522.
    View in: PubMed
    Score: 0.005
  32. Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. Nat Commun. 2019 02 20; 10(1):880.
    View in: PubMed
    Score: 0.005
  33. Integrating predicted transcriptome from multiple tissues improves association detection. PLoS Genet. 2019 01; 15(1):e1007889.
    View in: PubMed
    Score: 0.005
  34. Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree. Commun Biol. 2019; 2:28.
    View in: PubMed
    Score: 0.005
  35. Assembly of a pan-genome from deep sequencing of 910 humans of African descent. Nat Genet. 2019 01; 51(1):30-35.
    View in: PubMed
    Score: 0.005
  36. Gene Coexpression Networks in Whole Blood Implicate Multiple Interrelated Molecular Pathways in Obesity in People with Asthma. Obesity (Silver Spring). 2018 12; 26(12):1938-1948.
    View in: PubMed
    Score: 0.005
  37. Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions. PLoS One. 2018; 13(9):e0203906.
    View in: PubMed
    Score: 0.005
  38. An admixture mapping meta-analysis implicates genetic variation at 18q21 with asthma susceptibility in Latinos. J Allergy Clin Immunol. 2019 03; 143(3):957-969.
    View in: PubMed
    Score: 0.005
  39. Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat Genet. 2018 08; 50(8):1072-1080.
    View in: PubMed
    Score: 0.005
  40. Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. Nat Genet. 2018 07; 50(7):956-967.
    View in: PubMed
    Score: 0.005
  41. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Nat Commun. 2018 05 08; 9(1):1825.
    View in: PubMed
    Score: 0.005
  42. Role of local CpG DNA methylation in mediating the 17q21 asthma susceptibility gasdermin B (GSDMB)/ORMDL sphingolipid biosynthesis regulator 3 (ORMDL3) expression quantitative trait locus. J Allergy Clin Immunol. 2018 06; 141(6):2282-2286.e6.
    View in: PubMed
    Score: 0.005
  43. A decade of research on the 17q12-21 asthma locus: Piecing together the puzzle. J Allergy Clin Immunol. 2018 09; 142(3):749-764.e3.
    View in: PubMed
    Score: 0.005
  44. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proc Natl Acad Sci U S A. 2018 01 09; 115(2):379-384.
    View in: PubMed
    Score: 0.005
  45. Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nat Genet. 2018 01; 50(1):42-53.
    View in: PubMed
    Score: 0.005
  46. Rare non-coding variants are associated with plasma lipid traits in a founder population. Sci Rep. 2017 11 27; 7(1):16415.
    View in: PubMed
    Score: 0.005
  47. Host genetic variation in mucosal immunity pathways influences the upper airway microbiome. Microbiome. 2017 02 01; 5(1):16.
    View in: PubMed
    Score: 0.005
  48. Gene Expression Profiling in Blood Provides Reproducible Molecular Insights into Asthma Control. Am J Respir Crit Care Med. 2017 01 15; 195(2):179-188.
    View in: PubMed
    Score: 0.005
  49. DNA methylation in lung cells is associated with asthma endotypes and genetic risk. JCI Insight. 2016 12 08; 1(20):e90151.
    View in: PubMed
    Score: 0.005
  50. Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues. PLoS Genet. 2016 Nov; 12(11):e1006423.
    View in: PubMed
    Score: 0.005
  51. A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome. Nat Commun. 2016 10 11; 7:12522.
    View in: PubMed
    Score: 0.005
  52. Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx. Am J Hum Genet. 2016 Apr 07; 98(4):697-708.
    View in: PubMed
    Score: 0.004
  53. Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic Airways. Am J Respir Crit Care Med. 2016 Feb 15; 193(4):376-85.
    View in: PubMed
    Score: 0.004
  54. Genetic associations with viral respiratory illnesses and asthma control inĀ children. Clin Exp Allergy. 2016 Jan; 46(1):112-24.
    View in: PubMed
    Score: 0.004
  55. A gene-based association method for mapping traits using reference transcriptome data. Nat Genet. 2015 Sep; 47(9):1091-8.
    View in: PubMed
    Score: 0.004
  56. Stress and Bronchodilator Response in Children with Asthma. Am J Respir Crit Care Med. 2015 Jul 01; 192(1):47-56.
    View in: PubMed
    Score: 0.004
  57. Noninvasive analysis of the sputum transcriptome discriminates clinical phenotypes of asthma. Am J Respir Crit Care Med. 2015 May 15; 191(10):1116-25.
    View in: PubMed
    Score: 0.004
  58. Genome-wide association study of recalcitrant atopic dermatitis in Korean children. J Allergy Clin Immunol. 2015 Sep; 136(3):678-684.e4.
    View in: PubMed
    Score: 0.004
  59. Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma. Nat Commun. 2015 Jan 16; 6:5965.
    View in: PubMed
    Score: 0.004
  60. Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos. J Allergy Clin Immunol. 2015 Jun; 135(6):1502-10.
    View in: PubMed
    Score: 0.004
  61. Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis. BMC Med Genomics. 2014 Aug 02; 7:48.
    View in: PubMed
    Score: 0.004
  62. Prenatal tobacco smoke exposure is associated with childhood DNA CpG methylation. PLoS One. 2014; 9(6):e99716.
    View in: PubMed
    Score: 0.004
  63. A genome-wide survey of CD4(+) lymphocyte regulatory genetic variants identifies novel asthma genes. J Allergy Clin Immunol. 2014 Nov; 134(5):1153-62.
    View in: PubMed
    Score: 0.004
  64. Genome-wide interaction studies reveal sex-specific asthma risk alleles. Hum Mol Genet. 2014 Oct 01; 23(19):5251-9.
    View in: PubMed
    Score: 0.004
  65. A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. Cancer Epidemiol Biomarkers Prev. 2014 Apr; 23(4):658-69.
    View in: PubMed
    Score: 0.004
  66. A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk. Cell. 2013 Sep 26; 155(1):70-80.
    View in: PubMed
    Score: 0.004
  67. Ethnicity-specific pharmacogenetics: the case of warfarin in African Americans. Pharmacogenomics J. 2014 Jun; 14(3):223-8.
    View in: PubMed
    Score: 0.004
  68. Genome-wide association study of lung function phenotypes in a founder population. J Allergy Clin Immunol. 2014 Jan; 133(1):248-55.e1-10.
    View in: PubMed
    Score: 0.004
  69. Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. Lancet Respir Med. 2013 Jun; 1(4):309-317.
    View in: PubMed
    Score: 0.004
  70. Genome-wide association study of body mass index in 23 000 individuals with and without asthma. Clin Exp Allergy. 2013 Apr; 43(4):463-74.
    View in: PubMed
    Score: 0.004
  71. Rhinovirus wheezing illness and genetic risk of childhood-onset asthma. N Engl J Med. 2013 Apr 11; 368(15):1398-407.
    View in: PubMed
    Score: 0.004
  72. Maternal asthma and microRNA regulation of soluble HLA-G in the airway. J Allergy Clin Immunol. 2013 Jun; 131(6):1496-503.
    View in: PubMed
    Score: 0.004
  73. Marbled inflation from population structure in gene-based association studies with rare variants. Genet Epidemiol. 2013 Apr; 37(3):286-92.
    View in: PubMed
    Score: 0.004
  74. Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene. PLoS One. 2013; 8(2):e56179.
    View in: PubMed
    Score: 0.004
  75. A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations. J Allergy Clin Immunol. 2013 Apr; 131(4):1176-84.
    View in: PubMed
    Score: 0.003
  76. Further replication studies of the EVE Consortium meta-analysis identifies 2 asthma risk loci in European Americans. J Allergy Clin Immunol. 2012 Dec; 130(6):1294-301.
    View in: PubMed
    Score: 0.003
  77. Increased protein-coding mutations in the mitochondrial genome of African American women with preeclampsia. Reprod Sci. 2012 Dec; 19(12):1343-51.
    View in: PubMed
    Score: 0.003
  78. Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases. J Allergy Clin Immunol. 2012 Oct; 130(4):861-8.e7.
    View in: PubMed
    Score: 0.003
  79. Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects. J Allergy Clin Immunol. 2012 Sep; 130(3):622-629.e9.
    View in: PubMed
    Score: 0.003
  80. On sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacy. Am J Hum Genet. 2012 Apr 06; 90(4):591-8.
    View in: PubMed
    Score: 0.003
  81. Resequencing candidate genes implicates rare variants in asthma susceptibility. Am J Hum Genet. 2012 Feb 10; 90(2):273-81.
    View in: PubMed
    Score: 0.003
  82. Finding disease variants in Mendelian disorders by using sequence data: methods and applications. Am J Hum Genet. 2011 Dec 09; 89(6):701-12.
    View in: PubMed
    Score: 0.003
  83. Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nat Genet. 2011 Jul 31; 43(9):887-92.
    View in: PubMed
    Score: 0.003
  84. Recombination rates in admixed individuals identified by ancestry-based inference. Nat Genet. 2011 Jul 20; 43(9):847-53.
    View in: PubMed
    Score: 0.003
  85. Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals. Diabetologia. 2011 Aug; 54(8):2047-55.
    View in: PubMed
    Score: 0.003
  86. A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci. PLoS Genet. 2011 Feb 03; 7(2):e1001292.
    View in: PubMed
    Score: 0.003
  87. The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans. Clin Pharmacol Ther. 2011 Mar; 89(3):408-15.
    View in: PubMed
    Score: 0.003
  88. Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13. Hum Mol Genet. 2011 Apr 01; 20(7):1285-9.
    View in: PubMed
    Score: 0.003
  89. Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping. Am J Hum Genet. 2010 Jul 09; 87(1):123-8.
    View in: PubMed
    Score: 0.003
  90. Shades of gray: a comparison of linkage disequilibrium between Hutterites and Europeans. Genet Epidemiol. 2010 Feb; 34(2):133-9.
    View in: PubMed
    Score: 0.003
  91. Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors. Hum Immunol. 2010 Jan; 71(1):100-3.
    View in: PubMed
    Score: 0.003
  92. Common variants at five new loci associated with early-onset inflammatory bowel disease. Nat Genet. 2009 Dec; 41(12):1335-40.
    View in: PubMed
    Score: 0.003
  93. A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose. Diabetes. 2010 Feb; 59(2):539-49.
    View in: PubMed
    Score: 0.003
  94. Ethnic differences and functional analysis of MET mutations in lung cancer. Clin Cancer Res. 2009 Sep 15; 15(18):5714-23.
    View in: PubMed
    Score: 0.003
  95. Invasive pneumococcal infections: Austrian syndrome. Rom J Intern Med. 2009; 47(1):93-6.
    View in: PubMed
    Score: 0.003
  96. A signature of evolutionary constraint on a subset of ectopically expressed olfactory receptor genes. Mol Biol Evol. 2009 Mar; 26(3):491-4.
    View in: PubMed
    Score: 0.003
  97. Patient self-report of prior laser treatment reliably indicates presence of severe diabetic retinopathy. Am J Ophthalmol. 2009 Mar; 147(3):501-4.
    View in: PubMed
    Score: 0.003
  98. A common cortactin gene variation confers differential susceptibility to severe asthma. Genet Epidemiol. 2008 Dec; 32(8):757-66.
    View in: PubMed
    Score: 0.003
  99. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet. 2008 Aug; 40(8):955-62.
    View in: PubMed
    Score: 0.003
  100. Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function. N Engl J Med. 2008 Apr 17; 358(16):1682-91.
    View in: PubMed
    Score: 0.003
  101. Allele-specific targeting of microRNAs to HLA-G and risk of asthma. Am J Hum Genet. 2007 Oct; 81(4):829-34.
    View in: PubMed
    Score: 0.002
  102. Integrin beta 3 genotype influences asthma and allergy phenotypes in the first 6 years of life. J Allergy Clin Immunol. 2007 Jun; 119(6):1423-9.
    View in: PubMed
    Score: 0.002
  103. Smoking and inflammatory bowel disease: trends in familial and sporadic cohorts. Inflamm Bowel Dis. 2007 May; 13(5):573-9.
    View in: PubMed
    Score: 0.002
  104. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. Nat Genet. 2007 May; 39(5):596-604.
    View in: PubMed
    Score: 0.002
  105. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science. 2006 Dec 01; 314(5804):1461-3.
    View in: PubMed
    Score: 0.002
  106. Dominant-negative TLR5 polymorphism reduces adaptive immune response to flagellin and negatively associates with Crohn's disease. Am J Physiol Gastrointest Liver Physiol. 2006 Jun; 290(6):G1157-63.
    View in: PubMed
    Score: 0.002
  107. Gene-environment interaction effects on the development of immune responses in the 1st year of life. Am J Hum Genet. 2005 Apr; 76(4):696-704.
    View in: PubMed
    Score: 0.002
  108. A genome scan in 260 inflammatory bowel disease-affected relative pairs. Inflamm Bowel Dis. 2004 Sep; 10(5):513-20.
    View in: PubMed
    Score: 0.002
  109. Regulation of IL-8 and IL-1beta expression in Crohn's disease associated NOD2/CARD15 mutations. Hum Mol Genet. 2004 Aug 15; 13(16):1715-25.
    View in: PubMed
    Score: 0.002
  110. Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy. J Allergy Clin Immunol. 2004 Mar; 113(3):511-8.
    View in: PubMed
    Score: 0.002
  111. A genome scan in 260 inflammatory bowel disease-affected relative pairs. Inflamm Bowel Dis. 2004 Jan; 10(1):15-22.
    View in: PubMed
    Score: 0.002
  112. Association studies for asthma and atopic diseases: a comprehensive review of the literature. Respir Res. 2003; 4:14.
    View in: PubMed
    Score: 0.002
  113. Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure. J Allergy Clin Immunol. 2003 Apr; 111(4):840-6.
    View in: PubMed
    Score: 0.002
  114. Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan. Gastroenterology. 2003 Jan; 124(1):140-6.
    View in: PubMed
    Score: 0.002
  115. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature. 2001 May 31; 411(6837):603-6.
    View in: PubMed
    Score: 0.002
  116. Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease. Hum Mol Genet. 2000 May 22; 9(9):1425-32.
    View in: PubMed
    Score: 0.001
  117. Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans. Nat Genet. 1999 Feb; 21(2):213-5.
    View in: PubMed
    Score: 0.001
  118. Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1. Proc Natl Acad Sci U S A. 1998 Jun 23; 95(13):7502-7.
    View in: PubMed
    Score: 0.001
  119. Effect of subcutaneous recombinant human erythropoietin in cancer patients receiving radiotherapy: final report of a randomized, open-labelled, phase II trial. Br J Cancer. 1998 Jun; 77(11):1996-2002.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.