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Connection

Carole Ober to Pedigree

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

2.014
  1. Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree. Commun Biol. 2019; 2:28.
    View in: PubMed
    Score: 0.562
  2. Best linear unbiased allele-frequency estimation in complex pedigrees. Biometrics. 2004 Jun; 60(2):359-67.
    View in: PubMed
    Score: 0.204
  3. 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: 0.137
  4. 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: 0.107
  5. A population-based study of autosomal-recessive disease-causing mutations in a founder population. Am J Hum Genet. 2012 Oct 05; 91(4):608-20.
    View in: PubMed
    Score: 0.090
  6. Evaluating the evidence for transmission distortion in human pedigrees. Genetics. 2012 May; 191(1):215-32.
    View in: PubMed
    Score: 0.087
  7. A genomewide screen for chronic rhinosinusitis genes identifies a locus on chromosome 7q. Laryngoscope. 2008 Nov; 118(11):2067-72.
    View in: PubMed
    Score: 0.069
  8. A genome-wide screen for hyposmia susceptibility Loci. Chem Senses. 2008 Apr; 33(4):319-29.
    View in: PubMed
    Score: 0.066
  9. 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: 0.062
  10. Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy. Respir Res. 2005 Dec 10; 6:145.
    View in: PubMed
    Score: 0.057
  11. 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: 0.054
  12. Sequence variation in the promoter region of the cholinergic receptor muscarinic 3 gene and asthma and atopy. J Allergy Clin Immunol. 2003 Mar; 111(3):527-32.
    View in: PubMed
    Score: 0.047
  13. Major loci influencing serum triglyceride levels on 2q14 and 9p21 localized by homozygosity-by-descent mapping in a large Hutterite pedigree. Hum Mol Genet. 2003 Jan 15; 12(2):137-44.
    View in: PubMed
    Score: 0.046
  14. The genetic dissection of complex traits in a founder population. Am J Hum Genet. 2001 Nov; 69(5):1068-79.
    View in: PubMed
    Score: 0.042
  15. Broad and narrow heritabilities of quantitative traits in a founder population. Am J Hum Genet. 2001 May; 68(5):1302-7.
    View in: PubMed
    Score: 0.041
  16. 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: 0.040
  17. Estimation of variance components of quantitative traits in inbred populations. Am J Hum Genet. 2000 Feb; 66(2):629-50.
    View in: PubMed
    Score: 0.038
  18. HLA-G1 protein expression is not essential for fetal survival. Placenta. 1998 Mar-Apr; 19(2-3):127-32.
    View in: PubMed
    Score: 0.033
  19. Human leukocyte antigen matching and fetal loss: results of a 10 year prospective study. Hum Reprod. 1998 Jan; 13(1):33-8.
    View in: PubMed
    Score: 0.033
  20. An estimate of the average number of recessive lethal mutations carried by humans. Genetics. 2015 Apr; 199(4):1243-54.
    View in: PubMed
    Score: 0.027
  21. Estimating the human mutation rate using autozygosity in a founder population. Nat Genet. 2012 Nov; 44(11):1277-81.
    View in: PubMed
    Score: 0.023
  22. 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: 0.022
  23. 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: 0.022
  24. 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: 0.020
  25. 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: 0.017
  26. 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: 0.016
  27. 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: 0.015
  28. Multilocus linkage disequilibrium mapping by the decay of haplotype sharing with samples of related individuals. Genet Epidemiol. 2005 Sep; 29(2):128-40.
    View in: PubMed
    Score: 0.014
  29. 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: 0.013
  30. 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: 0.011
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.