Ingo Kennerknecht

Ingo Kennerknecht

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Ingo Kennerknecht

Ingo Kennerknecht

Publications by authors named "Ingo Kennerknecht"

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Neoplasia in Cri du Chat Syndrome from Italian and German Databases.

Case Rep Genet 2017 24;2017:5181624. Epub 2017 Apr 24.

Dipartimento di Medicina Molecolare, Università di Pavia and IRCCS S. Matteo, Pavia, Italy.

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http://dx.doi.org/10.1155/2017/5181624DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420919PMC
April 2017

Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven Tests.

Iperception 2016 Jan-Feb;7(1):2041669515625797. Epub 2016 Jan 20.

Department of Human Perception, Cognition and Action, Max Planck Institute for Biological Cybernetics, Tübingen, Germany.

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http://dx.doi.org/10.1177/2041669515625797DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4954744PMC
August 2016

Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms?

Front Hum Neurosci 2015 27;9:294. Epub 2015 May 27.

Department of Human Perception, Cognition and Action, Max Planck Institute for Biological Cybernetics Tübingen, Germany ; Department of Brain and Cognitive Engineering, Korea University Seoul, South Korea.

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http://dx.doi.org/10.3389/fnhum.2015.00294DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444816PMC
June 2015

A family at risk: congenital prosopagnosia, poor face recognition and visuoperceptual deficits within one family.

Neuropsychologia 2014 May 3;58:52-63. Epub 2014 Apr 3.

Institute for Biomagnetism and Biosignalanalysis, Westfälische Wilhelms-Universität Münster, Münster, Germany.

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http://dx.doi.org/10.1016/j.neuropsychologia.2014.03.013DOI Listing
May 2014

Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII and variants - update 2012.

Eur J Hum Genet 2013 Jan 15;21(1). Epub 2012 Aug 15.

Molecular Genetics, Center for Human Genetics and Laboratory Medicine Dr. Klein & Dr. Rost, Martinsried, Germany.

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http://dx.doi.org/10.1038/ejhg.2012.162DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533317PMC
January 2013

A computational model of dysfunctional facial encoding in congenital prosopagnosia.

Neural Netw 2011 Aug 11;24(6):652-64. Epub 2011 Mar 11.

Max Planck Institute for Mathematics in the Sciences, Leipzig, Germany.

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http://dx.doi.org/10.1016/j.neunet.2011.03.006DOI Listing
August 2011

Unexpected island effects at an extreme: reduced Y chromosome and mitochondrial DNA diversity in Nias.

Mol Biol Evol 2011 Apr 8;28(4):1349-61. Epub 2010 Nov 8.

Department of Forensic Molecular Biology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1093/molbev/msq300DOI Listing
April 2011

Sorting chromosomes as a software-based exercise.

Med Educ 2010 Nov;44(11):1127

Department of ITZ Forschung und Lehre, University of Münster, Germany.

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http://dx.doi.org/10.1111/j.1365-2923.2010.03845.xDOI Listing
November 2010

Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII.

Eur J Hum Genet 2010 Sep 10;18(9). Epub 2010 Feb 10.

Center for Human Genetics and Laboratory Medicine, Martinsried, Germany.

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http://dx.doi.org/10.1038/ejhg.2009.227DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987428PMC
September 2010

The early time course of compensatory face processing in congenital prosopagnosia.

PLoS One 2010 Jul 21;5(7):e11482. Epub 2010 Jul 21.

Max Planck Institute for Mathematics in the Sciences, Leipzig, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0011482PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908115PMC
July 2010

Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese population.

Am J Med Genet A 2008 Nov;146A(22):2863-70

Institute of Human Genetics, Westfälische Wilhelms-Universität, Münster, Germany.

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http://dx.doi.org/10.1002/ajmg.a.32552DOI Listing
November 2008

Congenital prosopagnosia--a common hereditary cognitive dysfunction in humans.

Front Biosci 2008 Jan 1;13:3150-8. Epub 2008 Jan 1.

Institut fuer Humangenetik, Westfaelische Wilhelms Universitaet, Muenster, Germany.

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http://dx.doi.org/10.2741/2916DOI Listing
January 2008

Gaze behaviour in hereditary prosopagnosia.

Psychol Res 2007 Sep 10;71(5):583-90. Epub 2006 Jun 10.

University of Giessen, Otto-Behaghel-Strasse 10F, 35394 Giessen, Germany.

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http://dx.doi.org/10.1007/s00426-006-0068-0DOI Listing
September 2007

Hereditary prosopagnosia: the first case series.

Cortex 2007 Aug;43(6):734-49

Institute of Human Genetics, Westfälische Wilhelms-University, Münster, Germany.

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http://dx.doi.org/10.1016/s0010-9452(08)70502-1DOI Listing
August 2007

Hereditary prosopagnosia (HPA): the first report outside the Caucasian population.

J Hum Genet 2007 22;52(3):230-6. Epub 2006 Dec 22.

Institut für Humangenetik, Westfälische Wilhelms Universität, Münster, Germany.

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http://dx.doi.org/10.1007/s10038-006-0101-6DOI Listing
April 2007

A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy.

Mol Vis 2006 Dec 2;12:1473-6. Epub 2006 Dec 2.

Institute of Medical Biochemistry, Zentrum für Molekularbiologie der Entzündung (ZMBE), Münster, Germany.

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December 2006

First report of prevalence of non-syndromic hereditary prosopagnosia (HPA).

Am J Med Genet A 2006 Aug;140(15):1617-22

Institute of Human Genetics, Westfälische Wilhelms-Universität, Münster, Germany.

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http://dx.doi.org/10.1002/ajmg.a.31343DOI Listing
August 2006

Multicolor karyotyping in acute myeloid leukemia.

Leuk Lymphoma 2003 Nov;44(11):1843-53

Institut für Humangenetik, Universitätsklinikum Münster, Vesaliusweg 12-14, 48129 Münster, Germany.

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http://dx.doi.org/10.1080/10428190310001603605DOI Listing
November 2003

Novel der(1)t(1;19) in two patients with myeloid neoplasias.

Cancer Genet Cytogenet 2002 Feb;133(1):61-5

Institut für Humangenetik, Westfälische Wilhelms-Universität, Vesaliusweg 12-14, Münster, Germany.

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http://dx.doi.org/10.1016/s0165-4608(01)00505-2DOI Listing
February 2002