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Connection

Carole Ober to Male

This is a "connection" page, showing publications Carole Ober has written about Male.
Connection Strength

1.074
  1. Genetic contributions to epigenetic-defined endotypes of allergic phenotypes in children. Am J Hum Genet. 2025 Jul 03; 112(7):1610-1624.
    View in: PubMed
    Score: 0.046
  2. Screening asthmatics for atopic status using the ALergy EXplorer (ALEX2) macroarray. J Asthma. 2024 Sep; 61(9):1050-1057.
    View in: PubMed
    Score: 0.042
  3. 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: 0.032
  4. 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: 0.029
  5. Global DNA methylation changes spanning puberty are near predicted estrogen-responsive genes and enriched for genes involved in endocrine and immune processes. Clin Epigenetics. 2018; 10:62.
    View in: PubMed
    Score: 0.028
  6. 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: 0.027
  7. Host genetic variation in mucosal immunity pathways influences the upper airway microbiome. Microbiome. 2017 02 01; 5(1):16.
    View in: PubMed
    Score: 0.026
  8. 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: 0.025
  9. 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: 0.024
  10. Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma. Nat Commun. 2015 Jan 16; 6:5965.
    View in: PubMed
    Score: 0.022
  11. 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: 0.020
  12. 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: 0.020
  13. Maternal microchimerism protects against the development of asthma. J Allergy Clin Immunol. 2013 Jul; 132(1):39-44.
    View in: PubMed
    Score: 0.019
  14. Rising prevalence of asthma is sex-specific in a US farming population. J Allergy Clin Immunol. 2011 Oct; 128(4):774-9.
    View in: PubMed
    Score: 0.018
  15. IFNG genotype and sex interact to influence the risk of childhood asthma. J Allergy Clin Immunol. 2011 Sep; 128(3):524-31.
    View in: PubMed
    Score: 0.017
  16. A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites. Eur J Hum Genet. 2011 Oct; 19(10):1045-51.
    View in: PubMed
    Score: 0.017
  17. Shades of gray: a comparison of linkage disequilibrium between Hutterites and Europeans. Genet Epidemiol. 2010 Feb; 34(2):133-9.
    View in: PubMed
    Score: 0.016
  18. 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: 0.016
  19. Sex-specific genetic architecture of human disease. Nat Rev Genet. 2008 Dec; 9(12):911-22.
    View in: PubMed
    Score: 0.015
  20. A genomewide screen for chronic rhinosinusitis genes identifies a locus on chromosome 7q. Laryngoscope. 2008 Nov; 118(11):2067-72.
    View in: PubMed
    Score: 0.014
  21. 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: 0.014
  22. A genome-wide screen for hyposmia susceptibility Loci. Chem Senses. 2008 Apr; 33(4):319-29.
    View in: PubMed
    Score: 0.014
  23. CFTR mutations and reproductive outcomes in a population isolate. Hum Genet. 2008 Jan; 122(6):583-8.
    View in: PubMed
    Score: 0.013
  24. 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: 0.013
  25. Correlation of intergenerational family sizes suggests a genetic component of reproductive fitness. Am J Hum Genet. 2007 Jul; 81(1):165-9.
    View in: PubMed
    Score: 0.013
  26. Sex-specific genetic architecture of asthma-associated quantitative trait loci in a founder population. Curr Allergy Asthma Rep. 2006 May; 6(3):241-6.
    View in: PubMed
    Score: 0.012
  27. Rethinking genetic models of asthma: the role of environmental modifiers. Curr Opin Immunol. 2005 Dec; 17(6):670-8.
    View in: PubMed
    Score: 0.012
  28. Prediction and characterization of genetically regulated expression of asthma tissues from African-ancestry populations. J Allergy Clin Immunol. 2026 Jan; 157(1):253-261.
    View in: PubMed
    Score: 0.012
  29. Genetic characterization of preschool wheeze phenotypes. J Allergy Clin Immunol. 2025 Dec; 156(6):1537-1546.
    View in: PubMed
    Score: 0.012
  30. Genetic risk for adult obstructive lung function and its early life associations. J Allergy Clin Immunol. 2025 Oct; 156(4):937-947.
    View in: PubMed
    Score: 0.012
  31. Association of 17q12-q21 Asthma Risk Locus with Clinical Severity of Infant Respiratory Syncytial Virus Infection. Biomolecules. 2025 Jul 22; 15(8).
    View in: PubMed
    Score: 0.012
  32. Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample. Hum Genet. 2005 Jun; 117(1):81-7.
    View in: PubMed
    Score: 0.011
  33. Newborn blood DNA methylation and childhood asthma: findings from the ECHO program. Int J Epidemiol. 2025 Apr 12; 54(3).
    View in: PubMed
    Score: 0.011
  34. EndoPRS: Incorporating endophenotype information to improve polygenic risk scores for clinical endpoints-A study in asthma. Am J Hum Genet. 2025 May 01; 112(5):1199-1214.
    View in: PubMed
    Score: 0.011
  35. Early-life wheeze trajectories are associated with distinct asthma transcriptomes later in life. J Allergy Clin Immunol. 2025 Sep; 156(3):640-650.
    View in: PubMed
    Score: 0.011
  36. Human body scents: conscious perceptions and biological effects. Chem Senses. 2005 Jan; 30 Suppl 1:i135-7.
    View in: PubMed
    Score: 0.011
  37. 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: 0.011
  38. Sex-specific genetic architecture of whole blood serotonin levels. Am J Hum Genet. 2005 Jan; 76(1):33-41.
    View in: PubMed
    Score: 0.011
  39. Are common disease susceptibility alleles the same in outbred and founder populations? Eur J Hum Genet. 2004 Jul; 12(7):584-90.
    View in: PubMed
    Score: 0.011
  40. Multi-omics in nasal epithelium reveals three axes of dysregulation for asthma risk in the African Diaspora populations. Nat Commun. 2024 May 28; 15(1):4546.
    View in: PubMed
    Score: 0.011
  41. Does HLA-dependent chimerism underlie the pathogenesis of juvenile dermatomyositis? J Immunol. 2004 Apr 15; 172(8):5041-6.
    View in: PubMed
    Score: 0.011
  42. Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy. J Allergy Clin Immunol. 2004 Mar; 113(3):511-8.
    View in: PubMed
    Score: 0.010
  43. Paternally inherited HLA alleles are associated with women's choice of male odor. Nat Genet. 2002 Feb; 30(2):175-9.
    View in: PubMed
    Score: 0.009
  44. HLA-G genotypes and pregnancy outcome in couples with unexplained recurrent miscarriage. Mol Hum Reprod. 2001 Dec; 7(12):1167-72.
    View in: PubMed
    Score: 0.009
  45. Asthma-associated genetic variants induce IL33 differential expression through an enhancer-blocking regulatory region. Nat Commun. 2021 10 21; 12(1):6115.
    View in: PubMed
    Score: 0.009
  46. 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: 0.009
  47. The genetic dissection of complex traits in a founder population. Am J Hum Genet. 2001 Nov; 69(5):1068-79.
    View in: PubMed
    Score: 0.009
  48. Multiethnic genome-wide and HLA association study of total serum IgE level. J Allergy Clin Immunol. 2021 12; 148(6):1589-1595.
    View in: PubMed
    Score: 0.009
  49. Extensive pleiotropism and allelic heterogeneity mediate metabolic effects of IRX3 and IRX5. Science. 2021 06 04; 372(6546):1085-1091.
    View in: PubMed
    Score: 0.009
  50. Enhanced Neutralizing Antibody Responses to Rhinovirus C and Age-Dependent Patterns of Infection. Am J Respir Crit Care Med. 2021 04 01; 203(7):822-830.
    View in: PubMed
    Score: 0.009
  51. 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: 0.009
  52. Sex-specific differences in peripheral blood leukocyte transcriptional response to LPS are enriched for HLA region and X chromosome genes. Sci Rep. 2021 01 13; 11(1):1107.
    View in: PubMed
    Score: 0.008
  53. Unconjugated bilirubin is associated with protection from early-life wheeze and childhood asthma. J Allergy Clin Immunol. 2021 07; 148(1):128-138.
    View in: PubMed
    Score: 0.008
  54. FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses. Nat Commun. 2020 12 16; 11(1):6398.
    View in: PubMed
    Score: 0.008
  55. Transcriptome and regulatory maps of decidua-derived stromal cells inform gene discovery in preterm birth. Sci Adv. 2020 12; 6(49).
    View in: PubMed
    Score: 0.008
  56. A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. Am J Hum Genet. 2000 Nov; 67(5):1154-62.
    View in: PubMed
    Score: 0.008
  57. A comparison of humans and baboons suggests germline mutation rates do not track cell divisions. PLoS Biol. 2020 08; 18(8):e3000838.
    View in: PubMed
    Score: 0.008
  58. Cytokine-induced molecular responses in airway smooth muscle cells inform genome-wide association studies of asthma. Genome Med. 2020 07 20; 12(1):64.
    View in: PubMed
    Score: 0.008
  59. 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: 0.008
  60. Estimation of variance components of quantitative traits in inbred populations. Am J Hum Genet. 2000 Feb; 66(2):629-50.
    View in: PubMed
    Score: 0.008
  61. 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: 0.008
  62. T-cell phenotypes are associated with serum IgE levels in Amish and Hutterite children. J Allergy Clin Immunol. 2019 11; 144(5):1391-1401.e10.
    View in: PubMed
    Score: 0.008
  63. Mononuclear-cell immunisation in prevention of recurrent miscarriages: a randomised trial. Lancet. 1999 Jul 31; 354(9176):365-9.
    View in: PubMed
    Score: 0.008
  64. Associations between fungal and bacterial microbiota of airways and asthma endotypes. J Allergy Clin Immunol. 2019 11; 144(5):1214-1227.e7.
    View in: PubMed
    Score: 0.008
  65. 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: 0.007
  66. Inbreeding effects on fertility in humans: evidence for reproductive compensation. Am J Hum Genet. 1999 Jan; 64(1):225-31.
    View in: PubMed
    Score: 0.007
  67. Effect of inbreeding avoidance on Hardy-Weinberg expectations: examples of neutral and selected loci. Genet Epidemiol. 1999; 17(3):165-73.
    View in: PubMed
    Score: 0.007
  68. Transmission disequilibrium of maternally-inherited CTLA-4 microsatellite alleles in idiopathic recurrent miscarriage. J Reprod Immunol. 1998 Nov; 40(2):147-57.
    View in: PubMed
    Score: 0.007
  69. HLA-G1 protein expression is not essential for fetal survival. Placenta. 1998 Mar-Apr; 19(2-3):127-32.
    View in: PubMed
    Score: 0.007
  70. HLA and mate choice in humans. Am J Hum Genet. 1997 Sep; 61(3):497-504.
    View in: PubMed
    Score: 0.007
  71. Innate Immunity and Asthma Risk in Amish and Hutterite Farm Children. N Engl J Med. 2016 Aug 04; 375(5):411-421.
    View in: PubMed
    Score: 0.006
  72. Genome-Wide Association Studies of the Human Gut Microbiota. PLoS One. 2015; 10(11):e0140301.
    View in: PubMed
    Score: 0.006
  73. HLA-DQA1 and HLA-DQB1 haplotypes in aborted fetuses and couples with recurrent spontaneous abortion. J Reprod Immunol. 1995 Jul; 29(2):95-104.
    View in: PubMed
    Score: 0.006
  74. Host genetic variation influences gene expression response to rhinovirus infection. PLoS Genet. 2015 Apr; 11(4):e1005111.
    View in: PubMed
    Score: 0.006
  75. Association of common filaggrin null mutations with atopy but not chronic rhinosinusitis. Ann Allergy Asthma Immunol. 2015 May; 114(5):420-421.
    View in: PubMed
    Score: 0.006
  76. 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: 0.006
  77. Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma. PLoS One. 2014; 9(8):e104396.
    View in: PubMed
    Score: 0.005
  78. Genome-wide interaction studies reveal sex-specific asthma risk alleles. Hum Mol Genet. 2014 Oct 01; 23(19):5251-9.
    View in: PubMed
    Score: 0.005
  79. Seasonal variation in human gut microbiome composition. PLoS One. 2014; 9(3):e90731.
    View in: PubMed
    Score: 0.005
  80. MHC class II compatibility in aborted fetuses and term infants of couples with recurrent spontaneous abortion. J Reprod Immunol. 1993 Dec; 25(3):195-207.
    View in: PubMed
    Score: 0.005
  81. 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: 0.005
  82. Genome-wide association study identifies candidate genes for male fertility traits in humans. Am J Hum Genet. 2012 Jun 08; 90(6):950-61.
    View in: PubMed
    Score: 0.005
  83. Evaluating the evidence for transmission distortion in human pedigrees. Genetics. 2012 May; 191(1):215-32.
    View in: PubMed
    Score: 0.005
  84. 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: 0.004
  85. The CFTR Met 470 allele is associated with lower birth rates in fertile men from a population isolate. PLoS Genet. 2010 Jun 03; 6(6):e1000974.
    View in: PubMed
    Score: 0.004
  86. Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes. Eur J Hum Genet. 2010 Apr; 18(4):463-70.
    View in: PubMed
    Score: 0.004
  87. Colloquium papers: Heritability of reproductive fitness traits in a human population. Proc Natl Acad Sci U S A. 2010 Jan 26; 107 Suppl 1:1772-8.
    View in: PubMed
    Score: 0.004
  88. Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13. Am J Med Genet A. 2008 Jun 01; 146A(11):1414-22.
    View in: PubMed
    Score: 0.004
  89. High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans. Science. 2008 Mar 07; 319(5868):1395-8.
    View in: PubMed
    Score: 0.003
  90. Heritability estimation of sex-specific effects on human quantitative traits. Genet Epidemiol. 2007 May; 31(4):338-47.
    View in: PubMed
    Score: 0.003
  91. ITGB3 shows genetic and expression interaction with SLC6A4. Hum Genet. 2006 Aug; 120(1):93-100.
    View in: PubMed
    Score: 0.003
  92. Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility. Eur J Hum Genet. 2006 Aug; 14(8):923-31.
    View in: PubMed
    Score: 0.003
  93. Adverse effects of human leukocyte antigen-DR sharing on fertility: a cohort study in a human isolate. Fertil Steril. 1985 Aug; 44(2):227-32.
    View in: PubMed
    Score: 0.003
  94. Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin. Eur J Hum Genet. 2004 Nov; 12(11):949-54.
    View in: PubMed
    Score: 0.003
  95. Evidence for extensive transmission distortion in the human genome. Am J Hum Genet. 2004 Jan; 74(1):62-72.
    View in: PubMed
    Score: 0.003
  96. Shared HLA antigens and reproductive performance among Hutterites. Am J Hum Genet. 1983 Sep; 35(5):994-1004.
    View in: PubMed
    Score: 0.003
  97. Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the Hutterites. Am J Hum Genet. 2002 Apr; 70(4):920-34.
    View in: PubMed
    Score: 0.002
  98. Genetic analysis of HLA in the U.S. Schmiedenleut Hutterites. Am J Hum Genet. 1989 Aug; 45(2):261-9.
    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.