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The Journal of Allergy and Clinical Immunology
Volume 122, Issue 4
, Pages
820-827.e9
, October 2008
Differences in allergic sensitization by self-reported race and genetic ancestry
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Individual admixture estimates for the 385 participants who reported being African American (A) and for the 216 participants who reported being white (B). Each patient number (column) comprises an ind
Individual admixture estimates for the 385 participants who reported being African American (A) and for the 216 participants who reported being white (B). Each patient number (column) comprises an individual and their admixture, where gray represents African ancestry and blue represents European ancestry.
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Distribution of study participants within the city limits of Detroit (also includes Hamtramck and Highland Park shown with bolded outlines). Participants who reported being African American are shownDistribution of study participants within the city limits of Detroit (also includes Hamtramck and Highland Park shown with bolded outlines). Participants who reported being African American are shown against the proportion of individuals within each census tract who reported being African American (A), and participants who reported being white are shown against the proportion of individuals within each census tract who reported being white (B). Census tract proportions are taken from year 2000 US Census data.
Supported by grants from the Fund for Henry Ford Hospital, the Sandler Program for Asthma Research, and the National Institute of Allergy and Infectious Diseases (AI61774, AI50681, and AI59415) and the National Heart, Lung, and Blood Institute (HL79055), National Institutes of Health.
Disclosure of potential conflict of interest: E. G. Burchard has received research support from the National Institutes of Health (NIH) and the Flight Attendants Medical Research Institute and has served as a member of the American Thoracic Society (ATS). S. Choudhry has received research support from the ATS and the TRDRP. C. C. Johnson has received research support from the NIH and Henry Ford Hospital. D. R. Ownby has received research support from the National Institute of Allergy and Infections Diseases (NIAID), the American Academy of Pediatrics, and the Merck Childhood Asthma Network. P.-Y. Kwok has received research support from the NIH and has consulted on DNA analysis technology patent litigation. C. L. Joseph has received research support from the NIH. M. D. Shriver has consulting arrangements with DNAPrint Genomics and has received research support from the National Human Genome Research Institute, the NIH, the National Institute of Child Health and Human Development, the March of Dimes, and the National heart, Lung, and Blood Institute (NHLBI). L. K. Williams has received research support from the NIAID, the NIH, the NHLBI, and the Strategic Program for Asthma Research. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(08)01457-7
doi: 10.1016/j.jaci.2008.07.044
© 2008 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
« Previous
Next »
The Journal of Allergy and Clinical Immunology
Volume 122, Issue 4
, Pages
820-827.e9
, October 2008
