Ingo Kennerknecht

Summary

Country: Germany

Publications

  1. ncbi request reprint First report of prevalence of non-syndromic hereditary prosopagnosia (HPA)
    Ingo Kennerknecht
    Institute of Human Genetics, Westfalische Wilhelms Universitat, Munster, Germany
    Am J Med Genet A 140:1617-22. 2006
  2. ncbi request reprint Hereditary prosopagnosia: the first case series
    Martina Grueter
    Institute of Human Genetics, Westfalische Wilhelms University, Munster, Germany
    Cortex 43:734-49. 2007
  3. ncbi request reprint Hereditary prosopagnosia (HPA): the first report outside the Caucasian population
    Ingo Kennerknecht
    Institut fur Humangenetik, Westfalische Wilhelms Universitat, Munster, Germany
    J Hum Genet 52:230-6. 2007
  4. ncbi request reprint Congenital prosopagnosia--a common hereditary cognitive dysfunction in humans
    Ingo Kennerknecht
    Institut fuer Humangenetik, Westfaelische Wilhelms Universitaet, Muenster, Germany
    Front Biosci 13:3150-8. 2008
  5. doi request reprint Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese population
    Ingo Kennerknecht
    Institute of Human Genetics, Westfalische Wilhelms Universitat, Munster, Germany
    Am J Med Genet A 146:2863-70. 2008
  6. ncbi request reprint Novel der(1)t(1;19) in two patients with myeloid neoplasias
    Joelle Tchinda
    Institut fur Humangenetik, Westfalische Wilhelms Universitat, Vesaliusweg 12 14, Munster, Germany
    Cancer Genet Cytogenet 133:61-5. 2002
  7. ncbi request reprint A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy
    Arseni Markoff
    Institute of Medical Biochemistry, Zentrum für Molekularbiologie der Entzündung ZMBE, Munster, Germany
    Mol Vis 12:1473-6. 2006
  8. ncbi request reprint Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies
    Daniela Ehling
    Praenadia GmbH, Muenster, Germany
    Am J Med Genet A 131:265-72. 2004
  9. ncbi request reprint Multicolor karyotyping in acute myeloid leukemia
    Joelle Tchinda
    Institut fur Humangenetik, Universitatsklinikum Munster, Vesaliusweg 12 14, 48129 Munster, Germany
    Leuk Lymphoma 44:1843-53. 2003
  10. ncbi request reprint Gaze behaviour in hereditary prosopagnosia
    Gudrun Schwarzer
    University of Giessen, Otto Behaghel Strasse 10F, 35394 Giessen, Germany
    Psychol Res 71:583-90. 2007

Collaborators

Detail Information

Publications11

  1. ncbi request reprint First report of prevalence of non-syndromic hereditary prosopagnosia (HPA)
    Ingo Kennerknecht
    Institute of Human Genetics, Westfalische Wilhelms Universitat, Munster, Germany
    Am J Med Genet A 140:1617-22. 2006
    ..The segregation pattern of this hereditary prosopagnosia (HPA) is fully compatible with autosomal dominant inheritance...
  2. ncbi request reprint Hereditary prosopagnosia: the first case series
    Martina Grueter
    Institute of Human Genetics, Westfalische Wilhelms University, Munster, Germany
    Cortex 43:734-49. 2007
    ..The results provide compelling evidence for significant genetic contribution to face recognition skills and contribute to the promise offered by the emerging field of cognitive neurogenetics...
  3. ncbi request reprint Hereditary prosopagnosia (HPA): the first report outside the Caucasian population
    Ingo Kennerknecht
    Institut fur Humangenetik, Westfalische Wilhelms Universitat, Munster, Germany
    J Hum Genet 52:230-6. 2007
    ..Several other members of her large family reported the same impairment of face recognition. The segregation pattern of PA in this family is also compatible with autosomal-dominant inheritance...
  4. ncbi request reprint Congenital prosopagnosia--a common hereditary cognitive dysfunction in humans
    Ingo Kennerknecht
    Institut fuer Humangenetik, Westfaelische Wilhelms Universitaet, Muenster, Germany
    Front Biosci 13:3150-8. 2008
    ..Still fitting the concept of autosomal dominant inheritance, we have evidence for a slightly reduced penetrance (4 normal transmitters from distinct families) and one or two de novo mutations...
  5. doi request reprint Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese population
    Ingo Kennerknecht
    Institute of Human Genetics, Westfalische Wilhelms Universitat, Munster, Germany
    Am J Med Genet A 146:2863-70. 2008
    ..Each had other first-degree relatives with the same visual cognitive dysfunction. Thus, as in the Caucasians, regular autosomal dominant inheritance might best explain the segregation pattern...
  6. ncbi request reprint Novel der(1)t(1;19) in two patients with myeloid neoplasias
    Joelle Tchinda
    Institut fur Humangenetik, Westfalische Wilhelms Universitat, Vesaliusweg 12 14, Munster, Germany
    Cancer Genet Cytogenet 133:61-5. 2002
    ..Translocation (1;19)(p13;p13.1) may play a role in the leukemogenesis of myeloid diseases...
  7. ncbi request reprint A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy
    Arseni Markoff
    Institute of Medical Biochemistry, Zentrum für Molekularbiologie der Entzündung ZMBE, Munster, Germany
    Mol Vis 12:1473-6. 2006
    ..To identify the molecular defect causing gelatinous drop-like corneal dystrophy in a Turkish family and assign affected and carriership status...
  8. ncbi request reprint Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies
    Daniela Ehling
    Praenadia GmbH, Muenster, Germany
    Am J Med Genet A 131:265-72. 2004
    ..9 Mb of 21q, may result in mild phenotypes comprising facial anomalies, thin marfanoid build, and mild MR, with or without signs of holoprosencephaly...
  9. ncbi request reprint Multicolor karyotyping in acute myeloid leukemia
    Joelle Tchinda
    Institut fur Humangenetik, Universitatsklinikum Munster, Vesaliusweg 12 14, 48129 Munster, Germany
    Leuk Lymphoma 44:1843-53. 2003
    ..Since, more than 600 cases of AML and MDS have been analyzed. Herein, we attempt to summarize the data published and discuss what has been achieved towards realization of these goals...
  10. ncbi request reprint Gaze behaviour in hereditary prosopagnosia
    Gudrun Schwarzer
    University of Giessen, Otto Behaghel Strasse 10F, 35394 Giessen, Germany
    Psychol Res 71:583-90. 2007
    ..They had a more dispersed gaze and also fixated external facial features. Thus, the face recognition impairment of the hereditary prosopagnosics is reflected in their gaze behaviour...
  11. ncbi request reprint Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene?
    Barbara Fritz
    Institut für Klinische Genetik der Philipps Universität Marburg, Germany
    Eur J Hum Genet 13:34-40. 2005
    ..A positional effect caused by the balanced (X;21) translocation may be responsible for functional nullisomy of ZIC3 and thus explain the situs and cardiac abnormalities in the fetus...