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List of works by Ingo Kennerknecht

A computational model of dysfunctional facial encoding in congenital prosopagnosia

scientific article published on 11 March 2011

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

scientific article published on 3 April 2014

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

scientific article published on 02 December 2006

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

scientific article

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

scientific article published on 10 February 2010

Congenital prosopagnosia--a common hereditary cognitive dysfunction in humans

scientific article published on 01 January 2008

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

scientific article published on 27 May 2015

Deficits in long-term recognition memory reveal dissociated subtypes in congenital prosopagnosia

scientific article

Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven Tests

scientific article published on 20 January 2016

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

scientific article

Galactose uncovers face recognition and mental images in congenital prosopagnosia: the first case report

scientific article

Gaze behaviour in hereditary prosopagnosia

scientific article published on 10 June 2006

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21

scientific article

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

scientific article published on 22 December 2006

Hereditary prosopagnosia: the first case series

scientific article

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies

scientific article published in December 2004

Multicolor karyotyping in acute myeloid leukemia

scientific article published on November 2003

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

scientific article published on 01 February 2002

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

scientific article published on 01 November 2008

Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene?

scientific article published in January 2005

Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3

scientific journal article

Sorting chromosomes as a software-based exercise ⬇️

scientific article published on 01 November 2010

Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)

scientific article published on 01 January 2011

The early time course of compensatory face processing in congenital prosopagnosia

scientific article

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

scientific article

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