Research Topics
Genomes and Genes | Terri BeatySummaryAffiliation: Johns Hopkins Bloomberg School of Public Health Country: USA Publications
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Publications
A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11qRasika A Mathias
Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Balitmore, USA
BMC Genet 7:38. 2006..While efficient in screening a region of dense genotyping, this approach does create some problems: high numbers of tests, assimilating thousands of results, and questions about setting priorities on regions with association signals...
Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populationsT H Beaty
Johns Hopkins University, Baltimore, MD, USA
Hum Genet 120:501-18. 2006....- Invited commentary: two studies of genetic control of birth weight where large data sets were availableT H Beaty
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA
Am J Epidemiol 165:753-5. 2007..Both of these studies confirm that birth weight is not simply due to the direct effects of the baby's genes but is a complex phenotype reflecting the effects of maternal genes and environments... - Testing candidate genes for non-syndromic oral clefts using a case-parent trio designTerri H Beaty
Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, 615 N Wolfe Street, Baltimore, MD 21205, USA
Genet Epidemiol 22:1-11. 2002..03). Using a conditional logistic model to test for gene-gene interaction showed no evidence of interaction between TGFbeta3 and MSX1, with both seeming to contribute independently to risk of isolated, non-syndromic oral clefts... 
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4Terri H Beaty
Johns Hopkins University, School of Public Health, Baltimore, Maryland, USA
Nat Genet 42:525-9. 2010..Expression studies support a role for MAFB in palatal development...- Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palateTerri H Beaty
School of Public Health, Johns Hopkins University, 615 N Wolfe St, Baltimore, Maryland, USA
Genet Epidemiol 35:469-78. 2011..8. These results emphasize the need to consider G × E interaction when searching for genes influencing risk to complex and heterogeneous disorders, such as nonsyndromic CP... - Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populationsJi Wan Park
Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205, USA, and Department of Medical Research and Craniofacial Center, Chang Gung Memorial Hospital, Taoyuan, Taiwan
Genet Med 9:219-27. 2007..This study aimed to confirm the contribution of IRF6 to cleft lip with or without palate risk in additional Asian populations... - Differential parental transmission of markers in RUNX2 among cleft case-parent trios from four populationsJae Woong Sull
Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, 615 North Wolfe Street, Baltimore, MD 21205, USA
Genet Epidemiol 32:505-12. 2008..Thus, RUNX2 appears to influence risk of CL/P through a parent-of-origin effect with excess maternal transmission... - Excess maternal transmission of markers in TCOF1 among cleft palate case-parent trios from three populationsJae Woong Sull
Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA
Am J Med Genet A 146:2327-31. 2008..136), analysis of haplotypes of rs2255796 and rs15251 suggested excess maternal transmission. Therefore, these data suggest TCOF1 may influence risk of cleft palate through a parent-of-origin effect... - Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populationsRoxann G Ingersoll
Johns Hopkins Bloomberg School of Public Health, Department of Epidemiology, Baltimore, MD 21287, USA
Eur J Hum Genet 18:726-32. 2010..These two genes plus EVC2 also yielded suggestive evidence for linkage and disequilibrium among cleft palate trios. This analysis suggests that several genes, not just MSX1, in this region may influence risk of oral clefts... - Oral clefts, maternal smoking, and TGFA: a meta-analysis of gene-environment interactionJoanna S Zeiger
Johns Hopkins Bloomberg School of Hygiene and Public Health, Baltimore, Maryland, USA
Cleft Palate Craniofac J 42:58-63. 2005.... - Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2Joanna S Zeiger
Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA
Eur J Hum Genet 11:835-9. 2003..022 and 0.006, respectively). A subset of these 26 families provided additional evidence for a susceptibility gene for CL/P on 2q, suggesting that further studies of genes in this region are warranted... - Influence of human leukocyte antigen class II alleles on susceptibility to Entamoeba histolytica infection in Bangladeshi childrenPriya Duggal
Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland, USA
J Infect Dis 189:520-6. 2004..This association may explain why amebiasis does not occur in some children who are exposed to the parasite and implicates HLA class II-restricted immune responses in protection against E. histolytica infection... - Multipoint linkage disequilibrium mapping for complex diseasesKung Yee Liang
Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205, USA
Genet Epidemiol 25:285-92. 2003..Furthermore, such discrepancy in preferential transmission was most evident among probands with early onset age (6 years old or younger)... - Evidence of gene-environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palateTao Wu
Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA
Hum Genet 128:401-10. 2010..These results suggest IRF6 gene may influence risk of CL/P through interaction with multivitamin supplementation and ETS in the Chinese population... - Family-based analysis of MSX1 haplotypes for association with oral cleftsM Daniele Fallin
Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland 21205, USA
Genet Epidemiol 25:168-75. 2003..This study encourages further focus on the MSX1 gene region to ultimately determine specific variants predisposing to oral clefts... - 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 StudyXin Liu
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
J Allergy Clin Immunol 112:382-8. 2003.... - Polymorphisms in the novel gene acyloxyacyl hydroxylase (AOAH) are associated with asthma and associated phenotypesKathleen C Barnes
Division of Allergy and Clinical Immunology, Department of Medicine, The Johns Hopkins University, 5501 Hopkins Bayview Circle, Baltimore, MD 21224, USA
J Allergy Clin Immunol 118:70-7. 2006.... - Familial aggregation of bothersome benign prostatic hyperplasia symptomsJay D Pearson
Department of Epidemiology, Merck Research Laboratories, Merck and Co, Inc, West Point, Pennsylvania 19486-0004, USA
Urology 61:781-5. 2003..Thus, linkage studies are more likely to be successful if they focus on stricter definitions of hereditary BPH (eg, early onset, large volume, strong family history) rather than symptomatic or clinical BPH... - Genetic and environmental risk factors for sagittal craniosynostosisJoanna S Zeiger
Johns Hopkins Bloomberg School of Hygiene and Public Health, Johns Hopkins School of Medicine, Baltimore, MD, USA
J Craniofac Surg 13:602-6. 2002..Parental education and alcohol consumption were associated with sagittal craniosynostosis in this study... - Gene encoding Duffy antigen/receptor for chemokines is associated with asthma and IgE in three populationsCandelaria Vergara
Department of Medicine, Division of Allergy and Clinical Immunology, Johns Hopkins University, Baltimore, Maryland 21224, USA
Am J Respir Crit Care Med 178:1017-22. 2008..This variant provides an evolutionary advantage in malaria-endemic regions, because Duffy antigen/receptor for chemokines-negative erythrocytes are more resistant to infection by P. vivax... - Polymorphisms in Toll-like receptor genes influence antibody responses to cytomegalovirus glycoprotein B vaccineRavit Arav-Boger
Department of Pediatrics, Division of Infectious Diseases, Johns Hopkins Hospital, Baltimore, Maryland 21287 4933, USA
BMC Res Notes 5:140. 2012..A clinical trial of CMV glycoprotein B (gB) vaccine in young women showed promising efficacy. Improved understanding of the basis for prevention of CMV infection is essential for developing improved vaccines... - Unified sampling approach for multipoint linkage disequilibrium mapping of qualitative and quantitative traitsFang-Chi Hsu
Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA
Genet Epidemiol 22:298-312. 2002..84, 43.02) through the 20-cM region framed by markers D12S1052 and D12S1064 on chromosome 12. The test statistic shows strong evidence of linkage and LD (chi-square statistic = 18.39 with 2 df, P-value = 0.0001)... 
Filaggrin mutations that confer risk of atopic dermatitis confer greater risk for eczema herpeticumPei Song Gao
Johns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA
J Allergy Clin Immunol 124:507-13, 513.e1-7. 2009..Associations have not been reported in African ancestry populations. Atopic dermatitis eczema herpeticum (ADEH) is a rare but serious complication of AD resulting from disseminated cutaneous herpes simplex virus infections...- A genome-wide association study on African-ancestry populations for asthmaRasika A Mathias
Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA
J Allergy Clin Immunol 125:336-346.e4. 2010..Of the limited genetic studies performed on populations of African descent, notable differences in susceptibility allele frequencies have been observed... - Evidence for asthma susceptibility genes on chromosome 11 in an African-American populationShau Ku Huang
Johns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, 5501 Hopkins Bayview Circle, MD 21224 6801, Baltimore, USA
Hum Genet 113:71-5. 2003..8 cM with a confidence interval spanning the linkage peak. Evidence from both linkage and association analyses suggest that this region of chromosome 11 contains one or more susceptibility genes for asthma in these AA families... - Family-based linkage disequilibrium tests using general pedigreesYin Yao Shugart
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
Methods Mol Biol 376:141-9. 2007..However, when the pedigree structure is more complicated, or when the number of informative families is limited, the pseudo-marker approach is anticipated to outperform FBAT... - Comparing whole-genome amplification methods and sources of biological samples for single-nucleotide polymorphism genotypingJi Wan Park
Department of Epidemiology, Bloomberg School of Public Health, McKusick-Nathans Institute of Genetic Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA
Clin Chem 51:1520-3. 2005 - Evaluation of the CD14/-260 polymorphism and house dust endotoxin exposure in the Barbados Asthma Genetics StudyApril Zambelli-Weiner
Division of Allergy and Clinical Immunology, Department of Medicine, Johns Hopkins School of Medicine, 5501 Hopkins Bayview Circle, Baltimore, MD 21224, USA
J Allergy Clin Immunol 115:1203-9. 2005..Both a functional promoter polymorphism in the gene encoding CD14 (C-260T) and exposure to endotoxin are believed to play key roles in modulating the immune response and expression of atopic disease... - 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 populationPei Song Gao
Johns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA
J Allergy Clin Immunol 115:982-8. 2005..The T-cell immunoglobulin mucin ( TIM ) proteins and their genetic variants have been suggested to play a role in regulating allergic diseases... - 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 populationPeter B Chi
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
Genet Epidemiol 30:609-19. 2006..We also found a high degree of consistency between TagSNP and Tagger. Using this set of 713 SNPs on chromosome 12q, our study provides insight towards analytic strategies for future studies of complex traits... - Evidence for a major gene influencing risk of pancreatic cancerAlison P Klein
Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA
Genet Epidemiol 23:133-49. 2002..This hospital-based segregation analysis of pancreatic cancer found evidence supporting the role of a rare major gene influencing risk of pancreatic cancer... - Polymorphisms in the myosin light chain kinase gene that confer risk of severe sepsis are associated with a lower risk of asthmaLi Gao
Division of Allergy and Clinical Immunology, Department of Medicine, Johns Hopkins University, Baltimore, MD 21224, USA
J Allergy Clin Immunol 119:1111-8. 2007..Myosin light chain kinase (MYLK) is a multifunctional protein involved in regulation of airway hyperreactivity and other activities relevant to asthma... - High heritability but uncertain mode of inheritance for total serum IgE level and Schistosoma mansoni infection intensity in a schistosomiasis-endemic Brazilian populationAudrey V Grant
Department of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA
J Infect Dis 198:1227-36. 2008.... - Parent-of-origin effect in the segregation analysis of bipolar affective disorder familiesTsuo Hung Lan
Department of Epidemiology, School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA
Psychiatr Genet 17:93-101. 2007..The purpose of this study is to test for heterogeneity in bipolar families based on the differential parental transmission of disease... - Sensitive detection of chromosomal segments of distinct ancestry in admixed populationsAlkes L Price
Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA
PLoS Genet 5:e1000519. 2009.... - Associations between specific serum IgE response and 6 variants within the genes IL4, IL13, and IL4RA in German children: the German Multicenter Atopy StudyXin Liu
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
J Allergy Clin Immunol 113:489-95. 2004..SNPs were commonly considered individually, and therefore the true effect could be masked by other genes or environmental factors... - Segregation analysis of 389 Icelandic pedigrees with Breast and prostate cancerAgnes B Baffoe-Bonnie
Department of Epidemiology, Johns Hopkins School of Hygiene and Public Health, Baltimore, Maryland 21205, USA
Genet Epidemiol 23:349-63. 2002.... - The effect of RANTES chemokine genetic variants on early HIV-1 plasma RNA among African American injection drug usersPriya Duggal
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
J Acquir Immune Defic Syndr 38:584-9. 2005..Because RANTES is a critical chemokine and competitively inhibits HIV-1 by binding to its receptor CCR5, treatment to enhance RANTES expression may assist in delaying the progression of AIDS by decreasing the initial viral load... - Inheritance of total serum IgE in the isolated Tangier Island population from Virginia: complexities associated with genealogical depth of pedigrees in segregation analysesRasika A Mathias
Department of Epidemiology, Bloomberg School of Hygiene and Public Health, Johns Hopkins University, Baltimore, MD 21224, USA
Hum Hered 59:228-38. 2005.... - 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 GeneticsLaura E Mitchell
Center for Clinical Epidemiology and Biostatistics, The University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104 6021, USA
Cleft Palate Craniofac J 39:93-100. 2002..This report presents summary statements of the four subcommittees... - Phenotypic discordance in a family with monozygotic twins and nonsyndromic cleft lip and palate: follow-upDiego F Wyszynski
Am J Med Genet 110:182-3. 2002 - Multipoint linkage disequilibrium mapping approach: incorporating evidence of linkage and linkage disequilibrium from unlinked regionFang-Chi Hsu
Section on Biostatistics, Department of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, North Carolina 21205, USA
Genet Epidemiol 25:1-13. 2003..67 cM, with a 95% confidence interval of (8.75, 14.59), and the test statistic shows significant evidence of linkage and LD (P-value=0.0198) in this region of chromosome 8... - Incorporation of covariates into multipoint linkage disequilibrium mapping in case-control studiesYen Feng Chiu
Division of Biostatistics and Bioinformatics, National Health Research Institutes, Zhunan, Taiwan
Genet Epidemiol 32:143-51. 2008..Simulation studies and these diabetes data both demonstrate how the efficiency of the estimated location of a disease gene can be improved substantially by incorporating information on covariates... - A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of AsthmaMalcolm N Blumenthal
Department of Medicine, University of Minnesota, MMC 434 Mayo, 420 Delaware SE, Minneapolis, MN 55455, USA
Hum Genet 114:157-64. 2004..65), 8p (D8S1113, lod=1.60), 12p (D12S372, lod=1.54) and 14q (D14S749, lod=1.70). These results suggest that several regions may harbor genes contributing to the risk for atopy and these may interact with one another in a complex manner... - Novel polymorphisms in the myosin light chain kinase gene confer risk for acute lung injuryLi Gao
Department of Medicine, University of Chicago Pritzker School of Medicine, 5841 S Maryland Avenue, W604, Chicago, IL 60637, USA
Am J Respir Cell Mol Biol 34:487-95. 2006..These data strongly implicate MYLK genetic variants to confer increased risk of sepsis and sepsis-associated ALI... - A genome-wide scan for loci predisposing to non-syndromic cleft lip with or without cleft palate in two large Syrian familiesDiego F Wyszynski
Genetics Program, Department of Medicine, Boston University School of Medicine, Boston, MA, USA
Am J Med Genet A 123:140-7. 2003..2 (P < or = 0.01) included 3p21.2, 4q32.1, and 7q34. These data indicate the possible presence of several susceptibility loci for CL/P and identify a strong candidate locus for this common birth defect on chromosome 17p13... - Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35Mary L Marazita
Center for Craniofacial and Dental Genetics, Division of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA 15219, USA
Am J Hum Genet 75:161-73. 2004..0004). These are the first genomewide significant linkage results ever reported for CL/P, and they represent an unprecedented demonstration of the power of linkage analysis to detect multiple genes simultaneously for a complex disorder... - MSX1 polymorphism associated with risk of oral cleft in Korea: evidence from case-parent trio and case-control studiesJungyong Park
Department of Epidemiology and Health Promotion, Graduate School of Public Health, Yonsei University, Seoul 120 752, Korea
Yonsei Med J 48:101-8. 2007..26, 95% CI=0.10-0.99). These results are consistent with evidence from other studies in the US and Chile and confirm the importance of the MSX1 genotype in determining the risk of CL/P and CP in Koreans... - Model comparison and the likelihood ratio test in segregation analysisRasika A Mathias
Genet Epidemiol 25:382-3. 2003 - Sequence variants of the gene encoding chemoattractant receptor expressed on Th2 cells (CRTH2) are associated with asthma and differentially influence mRNA stabilityJing Long Huang
The Division of Allergy, Asthma and Rheumatology, Department of Pediatrics, Chang Gung Children s Hospital, Taoyuan, Taiwan
Hum Mol Genet 13:2691-7. 2004..11q is a strong candidate gene for asthma... - Family history of diabetes and risk of atherosclerotic cardiovascular disease in Korean men and womenJi Wan Park
Department of Molecular and Cellular Biology, Sungkyunkwan University School of Medicine, Suwon, Republic of Korea
Atherosclerosis 197:224-31. 2008.... - Transmission/disequilibrium tests of androgen receptor and glutathione S-transferase pi variants in prostate cancer familiesGloria Y F Ho
Department of Epidemiology and Social Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA
Int J Cancer 98:938-42. 2002..Our findings do not support the hypothesis that familial clustering of prostate cancer in high-risk families is attributable to these genetic variants... - IL6 -174 G/C promoter polymorphism influences susceptibility to mucosal but not localized cutaneous leishmaniasis in BrazilLea Castellucci
Servico de Imunologia, Hospital Universitario Professor Edgard Santos, Universidade Federal da Bahia, Salvador, BA, Brazil
J Infect Dis 194:519-27. 2006..Interleukin (IL)-6 down-regulates T helper (Th) cell type 1 differentiation and drives Th2 cell differentiation. The IL6 -174 G/C polymorphism is associated with proinflammatory diseases and IL-6 regulation... - Major gene evidence after MTHFR-segregation analysis of serum homocysteine in families of patients undergoing coronary arteriographySun Ha Jee
Department of Epidemiology and Health Promotion, Graduate School of Health Science and Management, Yonsei University, Seoul 120 752, South Korea
Hum Genet 111:128-35. 2002..The results of this study also indicated that multifactorial inheritance was supported more strongly than Mendelian inheritance alone. Our findings may have implications for attempts to identify new homocysteine susceptible genes... - Is there a relationship between risk factors for oral clefts?Joanna S Zeiger
Teratology 66:205-8. 2002 - Homocysteine levels--before and after methionine loading--in 51 Dutch familiesMartin den Heijer
Department of Endocrinology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
Eur J Hum Genet 13:753-62. 2005..Further studies are needed to identify the genes responsible for the inheritance of postload homocysteine levels... - Evidence for gene-environment interactions in a linkage study of asthma and smoking exposureSusan Colilla
Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA
J Allergy Clin Immunol 111:840-6. 2003..Asthma, a common and chronic disease of the airways, has a multifactorial cause involving both genetic and environmental factors. As a result, mapping genes that influence asthma susceptibility has been challenging... - Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methodsTeri A Manolio
Division of Epidemiology and Clinical Applications, National Heart, Lung, and Blood Institute, 6701 Rockledge Drive, Rm 8160, Bethesda, MD 20892 7934, USA
Hum Genet 113:437-46. 2003..Adjustment for covariates had minimal impact. This suggests that future investigations of genetic determinants of IgE levels should include approaches that allow for potential sex differences in their expression... - Defining complex contributions of NOD2/CARD15 gene mutations, age at onset, and tobacco use on Crohn's disease phenotypesSteven R Brant
The Harvey M and Lyn P Meyerhoff Inflammatory Bowel Disease Center, Dept of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, U S A
Inflamm Bowel Dis 9:281-9. 2003..Multiple factors, particularly IBD family history, tobacco use, age at diagnosis and recently, NOD2 mutant genotypes may influence Crohn's disease (CD) heterogeneity... - Spouse controls in family case-control studies: a methodological considerationBas A J Verhage
Department of Epidemiology and Biostatistics, University Medical Centre Nijmegen, Nijmegen, The Netherlands
Fam Cancer 2:101-8. 2003..Using a simulation study it is illustrated that even strong assortative mating on a factor, which is strongly correlated with a true risk factor under study, will have a negligible effect on the observed extent of familial aggregation... - Segregation analysis of 231 Ashkenazi Jewish families for evidence of additional breast cancer susceptibility genesDavid J Kaufman
Laboratory of Population Genetics, National Cancer Institute, NIH, Bethesda, Maryland 20892, USA
Cancer Epidemiol Biomarkers Prev 12:1045-52. 2003..The study adds support for a major autosomal recessive component to breast cancer susceptibility... - Genetic predisposition to self-curing infection with the protozoan Leishmania chagasi: a genomewide scanSelma M B Jeronimo
Department of Biochemistry, Universidade Federal do Rio Grande do Norte, Natal, Rio de Grande do Norte, Brazil
J Infect Dis 196:1261-9. 2007..chagasi may identify proteins essential for immune protection against this parasitic disease and reveal strategies for immunotherapy or prevention...
Research Grants
- INTERNATIONAL GENETIC EPIDEMIOLOGY OF ORAL CLEFTSTerri Beaty; Fiscal Year: 2009....
- International Consortium to Identify Genes and Interactions Controlling Oral ClefTerri Beaty; Fiscal Year: 2007....
- INTERNATIONAL GENETIC EPIDEMIOLOGY OF ORAL CLEFTSTerri Beaty; Fiscal Year: 2007....
- INTERNATIONAL GENETIC EPIDEMIOLOGY OF ORAL CLEFTSTerri H Beaty; Fiscal Year: 2010....