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Acquired and hereditary prosopagnosia in history, fiction literature, biographies, and live celebrities of the present
Kennerknecht, Ingo
2022
An intronic COL1A1 Sp1-Polymorphism but not Vitamin D Receptor Gene Polymorphisms Relates to the Phenotypic Expression of Osteogenesis imperfecta
Trummer, Tatjana ; Kennerknecht, Ingo
2022
Extreme founder effect associated with oculocutaneous albinism type 1 (OCA1) on the island of Nias/Indonesia
How clinical genetics may help population genetics
Kennerknecht, Ingo ; Zühlke, Christine ; Hämmerle, Johannes M.
2021
Hereditary prosopagnosia in self reports
Kennerknecht, Ingo ; Trostmann, Ulrike
2022
Klinik des 5p-minus Syndroms (syn. Cri-du-Chat Syndrom)
Daten einer Fragebogenerhebung (2010 – 2019)
Kennerknecht, Ingo ; Kröll-Schulte, Agnes ; Schulte, Hans Reiner
2021
Prevalence of hereditary prosopagnosia – a worldwide survey
Kennerknecht, Ingo ; Edwards, Steve D. ; Van Belle, Goedele ; Wang-Elze, Zhi ; Wang, Hui ; Hämmerle, Johannes M. ; Aras, Beyhan Durak ; Thomas, Claudia ; Thomas, Christian ; Thomas, Christian Alexander ; Thomas, C.
2021
Prosopagnosie (syn. Gesichtsblindheit) – Berichte von Betroffenen
Kennerknecht, Ingo
2022

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