Astrid Golla

Summary

Affiliation: University of Bonn
Country: Germany

Publications

  1. ncbi Quantitative trait linkage analysis of longitudinal change in body weight
    Astrid Golla
    Institut fur Medizinische Biometrie, Informatik und Epidemiologie, Sigmund Freud Strasse 25, 53105 Bonn, Universitat Bonn, Bonn, Germany
    BMC Genet 4:S7. 2003
  2. ncbi Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22
    Astrid Golla
    Abteilung Medizinische Genetik der Kinderklinik und Kinderpoliklinik im Dr von Haunerschen Kinderspital, Universitat Munchen, Munchen, Germany
    Eur J Hum Genet 10:217-21. 2002
  3. ncbi Genetic analysis of phenotypes derived from longitudinal data: Presentation Group 1 of Genetic Analysis Workshop 13
    Konstantin Strauch
    Institute for Medical Biometry, Informatics, and Epidemiology, University of Bonn, Bonn, Germany
    Genet Epidemiol 25:S5-17. 2003
  4. ncbi Family-based association studies of alpha-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder
    Rami Abou Jamra
    Institute of Human Genetics, University of Bonn, Wilhelmstrasse 31, 53111 Bonn, Germany
    Am J Med Genet B Neuropsychiatr Genet 126:79-81. 2004
  5. ncbi Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26
    Axel M Hillmer
    Department of Genomics, Life and Brain Center, University of Bonn, D 53127 Bonn, Germany
    Am J Hum Genet 82:737-43. 2008
  6. ncbi MRX42: two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation
    Astrid Golla
    Department of Medical Genetics, University of Munich, Munich, Germany
    Am J Med Genet 107:18-25. 2002
  7. ncbi Heritability of carotid artery atherosclerotic lesions: an ultrasound study in 154 families
    Susanna Moskau
    Department of Neurology, University Hospital Bonn, Sigmund-Freud-Str. 25, D-53105 Bonn, Germany
    Stroke 36:5-8. 2005

Collaborators

Detail Information

Publications7

  1. ncbi Quantitative trait linkage analysis of longitudinal change in body weight
    Astrid Golla
    Institut fur Medizinische Biometrie, Informatik und Epidemiologie, Sigmund Freud Strasse 25, 53105 Bonn, Universitat Bonn, Bonn, Germany
    BMC Genet 4:S7. 2003
    ..We conclude that the chromosome 8 region may harbor a gene acting on long-term body weight regulation, thereby contributing to the development of the metabolic syndrome...
  2. ncbi Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22
    Astrid Golla
    Abteilung Medizinische Genetik der Kinderklinik und Kinderpoliklinik im Dr von Haunerschen Kinderspital, Universitat Munchen, Munchen, Germany
    Eur J Hum Genet 10:217-21. 2002
    ..Mutation screening in RANK and the genes PIGN and KIAA1468 led to detection of two variants (one in RANK and one in PIGN), which are in linkage disequilibrium with the rare D18S60 allele, but not independently associated with CRMO...
  3. ncbi Genetic analysis of phenotypes derived from longitudinal data: Presentation Group 1 of Genetic Analysis Workshop 13
    Konstantin Strauch
    Institute for Medical Biometry, Informatics, and Epidemiology, University of Bonn, Bonn, Germany
    Genet Epidemiol 25:S5-17. 2003
    ..Haseman-Elston regression methods, applied to the same phenotype, had low power, but the above-mentioned chromosome 5 locus was not included in this analysis...
  4. ncbi Family-based association studies of alpha-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder
    Rami Abou Jamra
    Institute of Human Genetics, University of Bonn, Wilhelmstrasse 31, 53111 Bonn, Germany
    Am J Med Genet B Neuropsychiatr Genet 126:79-81. 2004
    ..Using the Transmission Disequilibrium Test (TDT), no significant differences in transmissions were observed for any of the three ADRA genes...
  5. ncbi Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26
    Axel M Hillmer
    Department of Genomics, Life and Brain Center, University of Bonn, D 53127 Bonn, Germany
    Am J Hum Genet 82:737-43. 2008
    ..97 (empirical p value = 0.00055). This is the first step toward the identification of new susceptibility genes in AGA, a process which will provide important insights into the molecular and cellular basis of scalp hair loss...
  6. ncbi MRX42: two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation
    Astrid Golla
    Department of Medical Genetics, University of Munich, Munich, Germany
    Am J Med Genet 107:18-25. 2002
    ..Carrier risk estimation using pedigree and haplotype data for five females at risk is presented, and the difficulties of prenatal diagnosis given linkage to two different regions is discussed...
  7. ncbi Heritability of carotid artery atherosclerotic lesions: an ultrasound study in 154 families
    Susanna Moskau
    Department of Neurology, University Hospital Bonn, Sigmund-Freud-Str. 25, D-53105 Bonn, Germany
    Stroke 36:5-8. 2005
    ..This makes IMT a promising candidate for use as an intermediate phenotype in genetic studies aiming to identify novel genes for atherosclerosis...