Ingo Kennerknecht

Muenster, NW, Germany

Last Updated: 09/26/2026

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Found 12 publications

Extreme founder effect associated with hyperglycemia and hyperlipidemia on the island of NIAS/Indonesia.

Extreme founder effect associated with hyperglycemia and hyperlipidemia on the island of NIAS/Indonesia.

Journal: Atherosclerosis plus

Published: May 05, 2024

Human genetics of face recognition: discovery of MCTP2 mutations in humans with face blindness (congenital prosopagnosia).

Human genetics of face recognition: discovery of MCTP2 mutations in humans with face blindness (congenital prosopagnosia).

Journal: Genetics

Published: December 24, 2023

Expanding the spectrum of syndromic PPP2R3C-related XY gonadal dysgenesis to XX gonadal dysgenesis.

Expanding the spectrum of syndromic PPP2R3C-related XY gonadal dysgenesis to XX gonadal dysgenesis.

Journal: Clinical genetics

Published: August 23, 2021

Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area.

Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area.

Journal: Frontiers in behavioral neuroscience

Published: July 26, 2021

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

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

Journal: Case reports in genetics

Published: March 02, 2017

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

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

Journal: i-Perception

Published: August 03, 2016

MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta.

MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta.

Journal: Nature communications

Published: December 01, 2015

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

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

Journal: Frontiers in human neuroscience

Published: May 04, 2015

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

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

Journal: Human genetics

Published: January 20, 2015

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

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

Journal: Nutritional neuroscience

Published: October 30, 2013

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

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

Journal: Neuropsychologia

Published: May 25, 2013

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

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

Journal: European journal of human genetics : EJHG

Published: August 16, 2012

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Last Updated: 09/26/2026