Esins J, Schultz J, Stemper C, Kennerknecht I, Bülthoff I (2016) Face perception and test reliabilities in congenital prosopagnosia in seven tests. i-Perception January-February 2016: 1-37. DOI: 10.1177/2041669515625797
Esins J, Schultz J, Stemper C, Kennerknecht I, Wallraven C, Bülthoff I (2015) Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same mechanisms? Front Hum Neurosci 9: 27 May 2015 http://dx.doi.org/10.3389/fnhum.2015.00294
A Corrigendum on Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms? Esins, J., Schultz, J., Wallraven, C., and Bülthoff, I. (2014). Front. Hum. Neurosci. 8:759. doi: 10.3389/fnhum.2014.00759
Johnen A, Schmukle SC, Hüttenbrink J, Kischka C, Kennerknecht I, Dobel C (2014) A family at risk: Congenital prosopagnosia, poor face recognition and visuoperceptual deficits within one family. Neuropsychologica 58: 52-63
Esins J, Schultz J, Bülthoff I, Kennerknecht I (2013) Galactose uncovers face recognition and mental images in congenital prosopagnosia: The first case report. Nutritional Neuroscience
Kennerknecht I, Kischka C, Stemper C, Elze T, Stollhoff R (2011) Heritability in face recognition. In Tudor Barbu (ed.)
Face Analysis, Modeling and Recognition Systems, ISBN 978-953-307-738-3, InTech - Open Access Publisher, Rijeka, Croatia, p163-188 Download
Stollhoff R, Elze T, Kennerknecht I, Jost J (2011) A computational model of dysfunctional facial encoding in congenital prosopagnosia. Neural Networks 24: 652-664
Dinkelacker V, Grüter M, Klaver P, Grüter T, Specht K, Weis S, Kennerknecht I, Elger CE, Fernández G. (2011) Congenital prosopagnosia: Multistage anatomical and functional deficits in face processing circuitry . J Neurol 258: 770-782
Stollhoff R, Jost J, Elze T, Kennerknecht I (2011) Deficits in long-term recognition memory reveal dissociated subtypes in congenital prosopagnosia. PLoS ONE 6(1): e15702. doi:10.1371/journal.pone.0015702
Stollhoff R, Jost J, Elze T, Kennerknecht I (2010) The early time course of compensatory face processing in congenital prosopagnosia. PLoS ONE 5(7):e11482
Kennerknecht I, Ho T, Wong VCN (2008) Prevalence of hereditary prosopagnosia in a Hong Kong Chinese population. Am J Med Genet 146A:2860-2862
Kennerknecht, Pluempe N, Welling B (2008) Congenital prosopagnosia - a common hereditary cognitive dysfunction
in humans. Frontiers in Bioscience 13:3150-3158 Grüter M, Grüter T, Bell V, Halligan P W, Horst J, Sperling K,
Laskowski W, Ellis H D, Kennerknecht I (2007) Hereditary prosopagnosia: First case series.
Cortex 43:734-749 Kennerknecht I, Grueter T, Welling B, Wentzek S, Horst J, Edwards S, Grueter M (2006) First report on the prevalence
of non-syndromic hereditary prosopagnosia
(HPA). Am J Med Genet Part A 140A:1617-1622
Schwarzer G, Huber S, Grüter M, Grüter T, Groß C, Hipfel M, Kennerknecht I (2006) Gaze behavior in
hereditary prosopagnosia. Psychol Res 71(5):583-590, DOI 10.1007/s00426-006-0068-0 Kennerknecht I, Grüter T, Welling B, Horst J, Grüter M (
2005) Very high prevalence of hereditary prosopagnosia - a first report. Medgen 17:54
Kennerknecht I, Grüter M, Grüter T, Thakur J, Horst J, Raman R
(2004) First report on congenital prosopagnosia outside the caucasian population.
Eur J Hum Genet 12 (Suppl. 1):102 Kennerknecht I, Grüter M, Grüter T, Otte S, Neumann T, Meyer B,
Sperling K, Nürnberg P, Laskowski W (2002) First report on the genetics of prosopagnosia.
Eur J Hum Genet 10 (Suppl. 1):249 Kennerknecht I, Grüter M, Meyer B, Grüter T, Sperling K,
Laskowski W, Nürnberg P (2002) Congenital prosopagnosia - indicative of simple
autosomal dominant inheritance. Medgen 14:308
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Working group at the Institute of Human Genetics
Cooperations
Germany
Prof. Dr. Peter Nürnberg, Dr. Birgit Budde, Cologne Center for Genomics (CCG), Universität zu
Köln, Zülpicher Strasse 47, 50674 Köln
Prof. Dr. Jürgen Jost, Phone +49 (0)341 / 9959552, jjost@mis.mpg.de
Rainer Stollhoff, Phone +49 (0)341 / 9959549, rainer.stollhoff@mis.mpg.de
Tobias Elze, Phone +49 (0)341 / 9959575, tobias-elze@tobias-elze.de
Max Planck Institute for Mathematics in the Sciences, Inselstr. 22, 04103 Leipzig
Dr. med. Vera Dinkelacker, Prof. Dr. med. Elger, Medizinische Einrichtungen der Universität Bonn,
Klinik für Epileptologie, Sigmund-Freud-Str. 25, 53105 Bonn, Direktor; Projektleiterin, Tel: 0228 287 9345,
vera.dinkelacker@ukb.uni-bonn.de
Belgium
Goedele Van Belle, Prof. Dr. Karl Verfaillie, Laboratory of Experimental Psychology,
University of Leuven, Tiensestraat 102, B-3000 Leuven, Phone +32 (0)16 / 326039
Great Britain
Prof. HD Ellis, Prof. Peter Halligan, Dr. Vaughan Bell, Institute of
Psychology, Cardiff University, Cardiff CF10 3AT
Turkey
Osmangazi Üniversitesi Eskisehir
Yrd.Doç.Dr. Beyhan Durak, Tip Fakültesi, Tibbi Genetik BD, TR-26480 Eskisehir und
Dr. med. Neumann, Institute for Human Genetics-University of Muenster
Banaras Hindu University (BHU), Varanasi
Prof. Dr. Rajiva Raman, Banaras Hindu University, Department of Zoology, Varanasi - 221005
Indonesia
Nias Heritage Foundation (Yayasan Pusaka Nias, YPN)
Pastor Johannes M. Hämmerle, Biara Laverna, Kotak Pos 1, Gunungsitoli 22815
and
The Nias Government through Nias Health Office
Dr. Ama Idaman Zega,, Pemerintah Kabupaten Nias, Dinas Kesehatan, Jl. Kartini I
No. 7 Gunungsitoli 22815, Sumatra Utara, Indonesia
China
Prof. Dr. Jia Liu, State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, PR China
Hui Wang, Social Science Department, Chang Chun Taxation College, Jilin, PR China
Prof. Dr. Virginia Wong and Terri Ho, The University of Hong Kong, Queen Mary Hospital, Division of Neurodevelopmental Paediatrics, Department of
Paediatrics & Adolescent Medicine, Faculty of Medicine
Peru
Sara Narro Vigil, Leticia Aliaga Camacho , Instituto National de Cultura
and
P. Alois Eichenlaub, Jr. La Mar 450; Cajamarca, Peru
Zululand, South Africa
Professor Dr. Steve D. Edwards and Dr. Bui Mbele, Zululand
University, Department of Psychology