J N Painter

Summary

Affiliation: University of Helsinki
Country: Finland

Publications

  1. ncbi request reprint Complex social organization reflects genetic structure and relatedness in the cooperatively breeding bell miner, Manorina melanophrys
    J N Painter
    Department of Genetics and Evolution, La Trobe University, Bundoora, Victoria 3083 Australia
    Mol Ecol 9:1339-47. 2000
  2. ncbi request reprint A known polymorphism in the bile salt export pump gene is not a risk allele for intrahepatic cholestasis of pregnancy
    J N Painter
    The Folkhälsan Institute of Genetics and Dept of Medical Genetics, Biomedicum Helsinki, Haartmaninkatu 8, P O Box 63, University of Helsinki, Finland
    Scand J Gastroenterol 39:694-5. 2004
  3. ncbi request reprint Sequence variation in the ATP8B1 gene and intrahepatic cholestasis of pregnancy
    Jodie N Painter
    Folkhalsan Institute of Genetics, Biomedicum Helsinki, University of Helsinki, Helsinki, Finland
    Eur J Hum Genet 13:435-9. 2005
  4. pmc A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax
    Jodie N Painter
    Folkhalsan Institute of Genetics, University of Helsinki, Helsinki, Finland
    Am J Hum Genet 76:522-7. 2005
  5. doi request reprint Sex chromosome characteristics and recurrent miscarriage
    Milja Kaare
    Folkhalsan Institute of Genetics, University of Helsinki, Helsinki, Finland
    Fertil Steril 90:2328-33. 2008
  6. ncbi request reprint Variations of the Amnionless gene in recurrent spontaneous abortions
    Milja Kaare
    Folkhalsan Institute of Genetics, University of Helsinki, Finland
    Mol Hum Reprod 12:25-9. 2006
  7. ncbi request reprint Ural owl sex allocation and parental investment under poor food conditions
    Jon E Brommer
    Department of Ecology and Systematics, Bird Ecology Unit, University of Helsinki, Viikinkaari 1, P O Box 65, 00014 Helsinki, Finland
    Oecologia 137:140-7. 2003
  8. ncbi request reprint Study of p53 gene mutations and placental expression in recurrent miscarriage cases
    Milja Kaare
    Folkhalsan Institute of Genetics, University of Helsinki, PO Box 63, 00014 Helsinki, Finland
    Reprod Biomed Online 18:430-5. 2009
  9. ncbi request reprint Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome
    Anne M Wikström
    Hospital for Children and Adolescents, Helsinki University Central Hospital, University of Helsinki, Helsinki, Finland
    Clin Endocrinol (Oxf) 65:92-7. 2006
  10. pmc The search for genes contributing to endometriosis risk
    Grant W Montgomery
    Genetic and Molecular Epidemiology Laboratories, Queensland Institute of Medical Research, Royal Brisbane Hospital, 300 Herston Road, Brisbane, QLD 4029, Australia
    Hum Reprod Update 14:447-57. 2008

Detail Information

Publications10

  1. ncbi request reprint Complex social organization reflects genetic structure and relatedness in the cooperatively breeding bell miner, Manorina melanophrys
    J N Painter
    Department of Genetics and Evolution, La Trobe University, Bundoora, Victoria 3083 Australia
    Mol Ecol 9:1339-47. 2000
    ..Similarly, the contingent of individuals attending a nest were generally close relatives of the young they were aiding, supporting models invoking kin selection as the selective agency mediating helping...
  2. ncbi request reprint A known polymorphism in the bile salt export pump gene is not a risk allele for intrahepatic cholestasis of pregnancy
    J N Painter
    The Folkhälsan Institute of Genetics and Dept of Medical Genetics, Biomedicum Helsinki, Haartmaninkatu 8, P O Box 63, University of Helsinki, Finland
    Scand J Gastroenterol 39:694-5. 2004
  3. ncbi request reprint Sequence variation in the ATP8B1 gene and intrahepatic cholestasis of pregnancy
    Jodie N Painter
    Folkhalsan Institute of Genetics, Biomedicum Helsinki, University of Helsinki, Helsinki, Finland
    Eur J Hum Genet 13:435-9. 2005
    ..In conclusion, although the exon 2 and 7 changes may have functioned as risk alleles, ATP8B1 is probably not a major gene contributing to the occurrence of ICP...
  4. pmc A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax
    Jodie N Painter
    Folkhalsan Institute of Genetics, University of Helsinki, Helsinki, Finland
    Am J Hum Genet 76:522-7. 2005
    ..Additionally, given the strong association of PSP and BHD, the connection between these conditions needs to be investigated further, particularly in patients with familial PSP, who may be at a greater risk of developing renal cancer...
  5. doi request reprint Sex chromosome characteristics and recurrent miscarriage
    Milja Kaare
    Folkhalsan Institute of Genetics, University of Helsinki, Helsinki, Finland
    Fertil Steril 90:2328-33. 2008
    ..To investigate whether skewed X chromosome inactivation (XCI) and Y chromosome microdeletions are associated with recurrent miscarrige (RM)...
  6. ncbi request reprint Variations of the Amnionless gene in recurrent spontaneous abortions
    Milja Kaare
    Folkhalsan Institute of Genetics, University of Helsinki, Finland
    Mol Hum Reprod 12:25-9. 2006
    ..In addition, birthplaces of the patients' ancestors revealed some clustering, suggesting that some patients may carry a founder mutation in another gene which may contribute to RSA...
  7. ncbi request reprint Ural owl sex allocation and parental investment under poor food conditions
    Jon E Brommer
    Department of Ecology and Systematics, Bird Ecology Unit, University of Helsinki, Viikinkaari 1, P O Box 65, 00014 Helsinki, Finland
    Oecologia 137:140-7. 2003
    ..We discuss, in relation to published studies, the possibility of a sex-allocation scenario where, under poor food conditions, a daughter's long-term fitness is reduced more than a son's...
  8. ncbi request reprint Study of p53 gene mutations and placental expression in recurrent miscarriage cases
    Milja Kaare
    Folkhalsan Institute of Genetics, University of Helsinki, PO Box 63, 00014 Helsinki, Finland
    Reprod Biomed Online 18:430-5. 2009
    ..Further studies are, however, necessary to define whether the intronic polymorphism has functional consequences. The immunohistochemical staining of placental tissues revealed no abnormal p53 expression patterns in the samples studied...
  9. ncbi request reprint Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome
    Anne M Wikström
    Hospital for Children and Adolescents, Helsinki University Central Hospital, University of Helsinki, Helsinki, Finland
    Clin Endocrinol (Oxf) 65:92-7. 2006
    ..Previous studies have suggested that genetic features of the X chromosome may contribute to the wide phenotypic variation in KS...
  10. pmc The search for genes contributing to endometriosis risk
    Grant W Montgomery
    Genetic and Molecular Epidemiology Laboratories, Queensland Institute of Medical Research, Royal Brisbane Hospital, 300 Herston Road, Brisbane, QLD 4029, Australia
    Hum Reprod Update 14:447-57. 2008
    ..Genetic variation contributes to the risk of developing endometriosis. This review summarizes gene mapping studies in endometriosis and the prospects of finding gene pathways contributing to disease using the latest genome-wide strategies...