PubRank

Terri H Beaty

Author PubWeight™ 170.52‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genetic epidemiology of COPD (COPDGene) study design. COPD 2010 7.67
2 Sensitive detection of chromosomal segments of distinct ancestry in admixed populations. PLoS Genet 2009 6.36
3 Pulmonary arterial enlargement and acute exacerbations of COPD. N Engl J Med 2012 5.54
4 Cleft lip and palate: understanding genetic and environmental influences. Nat Rev Genet 2011 5.41
5 The PhenX Toolkit: get the most from your measures. Am J Epidemiol 2011 4.19
6 Variants of DENND1B associated with asthma in children. N Engl J Med 2009 4.18
7 GOLD 2011 disease severity classification in COPDGene: a prospective cohort study. Lancet Respir Med 2012 3.98
8 Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet 2012 3.68
9 Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nat Genet 2011 3.68
10 The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genet Epidemiol 2010 3.48
11 Variants in FAM13A are associated with chronic obstructive pulmonary disease. Nat Genet 2010 3.44
12 Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. Am J Hum Genet 2004 2.65
13 A genome-wide association study on African-ancestry populations for asthma. J Allergy Clin Immunol 2009 2.53
14 Filaggrin mutations that confer risk of atopic dermatitis confer greater risk for eczema herpeticum. J Allergy Clin Immunol 2009 2.20
15 The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. Dev Biol 2011 2.16
16 Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet 2012 2.15
17 A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. Hum Mol Genet 2011 1.98
18 Novel polymorphisms in the myosin light chain kinase gene confer risk for acute lung injury. Am J Respir Cell Mol Biol 2006 1.88
19 Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. Am J Respir Crit Care Med 2014 1.80
20 Tight junction defects in patients with atopic dermatitis. J Allergy Clin Immunol 2010 1.77
21 Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations. Genet Med 2007 1.75
22 Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2012 1.72
23 Adiponectin concentrations: a genome-wide association study. Am J Hum Genet 2010 1.70
24 Innate and acquired resistance to amebiasis in bangladeshi children. J Infect Dis 2002 1.68
25 Recombination rates in admixed individuals identified by ancestry-based inference. Nat Genet 2011 1.64
26 Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns. Am J Respir Crit Care Med 2014 1.57
27 Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. Am J Respir Crit Care Med 2012 1.49
28 Defining complex contributions of NOD2/CARD15 gene mutations, age at onset, and tobacco use on Crohn's disease phenotypes. Inflamm Bowel Dis 2003 1.42
29 Genetic variants in thymic stromal lymphopoietin are associated with atopic dermatitis and eczema herpeticum. J Allergy Clin Immunol 2010 1.38
30 IL6 -174 G/C promoter polymorphism influences susceptibility to mucosal but not localized cutaneous leishmaniasis in Brazil. J Infect Dis 2006 1.38
31 Evidence for a major gene influencing risk of pancreatic cancer. Genet Epidemiol 2002 1.36
32 A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q. BMC Genet 2006 1.33
33 A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity. J Allergy Clin Immunol 2006 1.32
34 Influence of human leukocyte antigen class II alleles on susceptibility to Entamoeba histolytica infection in Bangladeshi children. J Infect Dis 2004 1.31
35 Evaluation of the CD14/-260 polymorphism and house dust endotoxin exposure in the Barbados Asthma Genetics Study. J Allergy Clin Immunol 2005 1.31
36 Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure. J Allergy Clin Immunol 2003 1.27
37 Oral clefts, maternal smoking, and TGFA: a meta-analysis of gene-environment interaction. Cleft Palate Craniofac J 2005 1.25
38 Guidelines for the design and analysis of studies on nonsyndromic cleft lip and cleft palate in humans: summary report from a Workshop of the International Consortium for Oral Clefts Genetics. Cleft Palate Craniofac J 2002 1.23
39 Associations between total serum IgE levels and the 6 potentially functional variants within the genes IL4, IL13, and IL4RA in German children: the German Multicenter Atopy Study. J Allergy Clin Immunol 2003 1.20
40 Genetic variants of the T-cell immunoglobulin mucin 1 but not the T-cell immunoglobulin mucin 3 gene are associated with asthma in an African American population. J Allergy Clin Immunol 2005 1.20
41 Genome-wide association study of smoking behaviours in patients with COPD. Thorax 2011 1.18
42 Rapid testing of SNPs and gene-environment interactions in case-parent trio data based on exact analytic parameter estimation. Biometrics 2011 1.18
43 The association of genome-wide significant spirometric loci with chronic obstructive pulmonary disease susceptibility. Am J Respir Cell Mol Biol 2011 1.17
44 Comparing whole-genome amplification methods and sources of biological samples for single-nucleotide polymorphism genotyping. Clin Chem 2005 1.17
45 Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22. Birth Defects Res A Clin Mol Teratol 2012 1.16
46 Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations. Eur J Hum Genet 2009 1.14
47 Sequence variants of the gene encoding chemoattractant receptor expressed on Th2 cells (CRTH2) are associated with asthma and differentially influence mRNA stability. Hum Mol Genet 2004 1.11
48 Genetics of sputum gene expression in chronic obstructive pulmonary disease. PLoS One 2011 1.11
49 A genome-wide scan for loci predisposing to non-syndromic cleft lip with or without cleft palate in two large Syrian families. Am J Med Genet A 2003 1.10
50 Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2. Eur J Hum Genet 2003 1.10
51 Genetic predisposition to self-curing infection with the protozoan Leishmania chagasi: a genomewide scan. J Infect Dis 2007 1.09
52 Resequencing candidate genes implicates rare variants in asthma susceptibility. Am J Hum Genet 2012 1.08
53 Clinical and molecular characterization of the bladder exstrophy-epispadias complex: analysis of 232 families. BJU Int 2004 1.08
54 Epidemiology, genetics, and subtyping of preserved ratio impaired spirometry (PRISm) in COPDGene. Respir Res 2014 1.06
55 Polymorphisms in the myosin light chain kinase gene that confer risk of severe sepsis are associated with a lower risk of asthma. J Allergy Clin Immunol 2007 1.05
56 Gene encoding Duffy antigen/receptor for chemokines is associated with asthma and IgE in three populations. Am J Respir Crit Care Med 2008 1.04
57 Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms. Hum Genet 2009 1.01
58 Evidence of gene-environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate. Hum Genet 2010 1.01
59 Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populations. Genet Epidemiol 2008 1.01
60 Genetic and environmental risk factors for sagittal craniosynostosis. J Craniofac Surg 2002 1.01
61 Is there a relationship between risk factors for oral clefts? Teratology 2002 0.99
62 Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans. Genet Epidemiol 2012 0.98
63 Family-based analysis of MSX1 haplotypes for association with oral clefts. Genet Epidemiol 2003 0.98
64 African ancestry is a risk factor for asthma and high total IgE levels in African admixed populations. Genet Epidemiol 2013 0.97
65 The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate. Cleft Palate Craniofac J 2011 0.96
66 Genetic admixture in Brazilians exposed to infection with Leishmania chagasi. Ann Hum Genet 2009 0.96
67 Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P). Am J Med Genet A 2013 0.95
68 Polymorphisms in the novel gene acyloxyacyl hydroxylase (AOAH) are associated with asthma and associated phenotypes. J Allergy Clin Immunol 2006 0.94
69 Major gene evidence after MTHFR-segregation analysis of serum homocysteine in families of patients undergoing coronary arteriography. Hum Genet 2002 0.93
70 African and non-African admixture components in African Americans and an African Caribbean population. Genet Epidemiol 2010 0.93
71 Associations between specific serum IgE response and 6 variants within the genes IL4, IL13, and IL4RA in German children: the German Multicenter Atopy Study. J Allergy Clin Immunol 2004 0.93
72 Dissecting direct and indirect genetic effects on chronic obstructive pulmonary disease (COPD) susceptibility. Hum Genet 2013 0.92
73 Aquaporin 5 polymorphisms and rate of lung function decline in chronic obstructive pulmonary disease. PLoS One 2010 0.92
74 A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma. Hum Genet 2003 0.91
75 Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. Am J Med Genet A 2012 0.90
76 Genetic variants in the mannose receptor gene (MRC1) are associated with asthma in two independent populations. Immunogenetics 2009 0.90
77 Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations. Eur J Hum Genet 2010 0.89
78 Gene expression analysis uncovers novel hedgehog interacting protein (HHIP) effects in human bronchial epithelial cells. Genomics 2013 0.89
79 Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD. Hum Genet 2012 0.88
80 A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk. BMC Genet 2014 0.88
81 Incorporating genotype uncertainties into the genotypic TDT for main effects and gene-environment interactions. Genet Epidemiol 2012 0.88
82 Incorporation of covariates into multipoint linkage disequilibrium mapping in case-control studies. Genet Epidemiol 2008 0.88
83 The effect of RANTES chemokine genetic variants on early HIV-1 plasma RNA among African American injection drug users. J Acquir Immune Defic Syndr 2005 0.88
84 Inheritance of total serum IgE in the isolated Tangier Island population from Virginia: complexities associated with genealogical depth of pedigrees in segregation analyses. Hum Hered 2005 0.87
85 Segregation analysis of 389 Icelandic pedigrees with Breast and prostate cancer. Genet Epidemiol 2002 0.87
86 Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genet Epidemiol 2013 0.87
87 High heritability but uncertain mode of inheritance for total serum IgE level and Schistosoma mansoni infection intensity in a schistosomiasis-endemic Brazilian population. J Infect Dis 2008 0.87
88 Fast detection of de novo copy number variants from SNP arrays for case-parent trios. BMC Bioinformatics 2012 0.86
89 BMP4 was associated with NSCL/P in an Asian population. PLoS One 2012 0.86
90 Homocysteine levels--before and after methionine loading--in 51 Dutch families. Eur J Hum Genet 2005 0.86
91 Excess maternal transmission of markers in TCOF1 among cleft palate case-parent trios from three populations. Am J Med Genet A 2008 0.85
92 Candidate pathway based analysis for cleft lip with or without cleft palate. Stat Appl Genet Mol Biol 2012 0.85
93 Family history of diabetes and risk of atherosclerotic cardiovascular disease in Korean men and women. Atherosclerosis 2007 0.85
94 Functional polymorphisms in IL13 are protective against high Schistosoma mansoni infection intensity in a Brazilian population. PLoS One 2012 0.84
95 MSX1 polymorphism associated with risk of oral cleft in Korea: evidence from case-parent trio and case-control studies. Yonsei Med J 2007 0.84
96 Comparison of SNP tagging methods using empirical data: association study of 713 SNPs on chromosome 12q14.3-12q24.21 for asthma and total serum IgE in an African Caribbean population. Genet Epidemiol 2006 0.84
97 Genetic variants in interferon regulatory factor 2 (IRF2) are associated with atopic dermatitis and eczema herpeticum. J Invest Dermatol 2011 0.84
98 Familial aggregation of bothersome benign prostatic hyperplasia symptoms. Urology 2003 0.83
99 Evidence for asthma susceptibility genes on chromosome 11 in an African-American population. Hum Genet 2003 0.82
100 Admixture mapping identifies a quantitative trait locus associated with FEV1/FVC in the COPDGene Study. Genet Epidemiol 2014 0.82
101 Differential parental transmission of markers in BCL3 among Korean cleft case-parent trios. J Prev Med Public Health 2009 0.81
102 Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis. BMC Med Genomics 2014 0.81
103 X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts. Eur J Oral Sci 2013 0.81
104 Segregation analysis of 231 Ashkenazi Jewish families for evidence of additional breast cancer susceptibility genes. Cancer Epidemiol Biomarkers Prev 2003 0.81
105 Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods. Hum Genet 2003 0.81
106 Multipoint linkage disequilibrium mapping approach: incorporating evidence of linkage and linkage disequilibrium from unlinked region. Genet Epidemiol 2003 0.80
107 Phenotypic discordance in a family with monozygotic twins and nonsyndromic cleft lip and palate: follow-up. Am J Med Genet 2002 0.80
108 Both rare and common variants in PCSK9 influence plasma low-density lipoprotein cholesterol level in American Indians. J Clin Endocrinol Metab 2014 0.79
109 Model comparison and the likelihood ratio test in segregation analysis. Genet Epidemiol 2003 0.78
110 Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studies. Biom J 2014 0.78
111 Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate. Birth Defects Res A Clin Mol Teratol 2012 0.78
112 Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease. Am J Respir Cell Mol Biol 2014 0.78
113 Beyond GWAS in COPD: probing the landscape between gene-set associations, genome-wide associations and protein-protein interaction networks. Hum Hered 2014 0.77
114 Nitric oxide synthase polymorphisms, gene expression and lung function in chronic obstructive pulmonary disease. BMC Pulm Med 2013 0.77
115 A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts. Birth Defects Res A Clin Mol Teratol 2015 0.76
116 Correlates of sensitization to Blomia tropicalis and Dermatophagoides pteronyssinus in asthma in Barbados. Int Arch Allergy Immunol 2003 0.76
117 ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population. Chin Med J (Engl) 2012 0.76
118 Parent-of-origin effect in the segregation analysis of bipolar affective disorder families. Psychiatr Genet 2007 0.76
119 Spouse controls in family case-control studies: a methodological consideration. Fam Cancer 2003 0.76
120 Detecting disease variants in case-parent trio studies using the bioconductor software package trio. Genet Epidemiol 2014 0.75
121 Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations. Eur J Hum Genet 2013 0.75
122 Correction: Susceptibility to chronic mucus hypersecretion, a genome wide association study. PLoS One 2015 0.75
123 Detecting familial aggregation. Methods Mol Biol 2012 0.75
124 Multipoint linkage disequilibrium mapping for complex diseases. Genet Epidemiol 2003 0.75
125 Genetic Epidemiology and Public Health: The Evolution From Theory to Technology. Am J Epidemiol 2016 0.75
126 Transmission/disequilibrium tests of androgen receptor and glutathione S-transferase pi variants in prostate cancer families. Int J Cancer 2002 0.75
127 Multipoint linkage detection in the presence of heterogeneity. Biostatistics 2002 0.75
128 Unified sampling approach for multipoint linkage disequilibrium mapping of qualitative and quantitative traits. Genet Epidemiol 2002 0.75
129 Theory and methodology for utilizing genes as biomarkers to determine potential biological mixtures. Ann Epidemiol 2005 0.75