University of Münster
CRIS@UM
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Prof. Dr. Ingo Kennerknecht

No current affiliations available for this person. The person is no longer active at the university.

Curriculum Vitae (CV)

Research Focus

  • Congenital prosopagnosia, genotype- / phenotypkorrelation
  • Population genetics, peopling and clan dispersal of Nias / Indonesia
  • Cri-du-Chat syndrome

Functions and Memberships

Deutsche Gesellschaft für Humangenetik
Berufsverband Deutscher Humangenetiker
Klinische Genetik in der Pädiatrie
Europäische Gesellschaft für Humangenetik
Gesellschaft für Osteogenesis imperfecta
Förderverein für Menschen mit Cri-du-Chat-Syndrom e.V.

Publications

Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome
Neuhaus C., Eisenberger T., Decker C., Nagl S., Blank C., Pfister M., Kennerknecht I., Müller-Hofstede C., Charbel Issa P., Heller R., Beck B., Rüther K., Mitter D., Rohrschneider K., Steinhauer U., Korbmacher H., Huhle D., Elsayed S., Taha H., Baig S., Stöhr H., Preising M., Markus S., Moeller F., Lorenz B., Nagel-Wolfrum K., Khan A., Bolz H. (2017)
In: ((Bitte Journal prüfen)), 5(5), 531-552. doi:10.1002/mgg3.312
Research article (journal) | Peer reviewed | Published
Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome).
Ruggieri M, Roggini M, Kennerknecht I, Polizzi A, Distefano A, Pavone V (2011)
In: Acta Pædiatrica, 100(1), 121-127. doi:10.1111/j.1651-2227.2010.01970.x
Research article (journal) | Published
Congenital prosopagnosia: multistage anatomical and functional deficits in face processing circuitry.
Dinkelacker V, Grüter M, Klaver P, Grüter T, Specht K, Weis S, Kennerknecht I, Elger CE, Fernandez G (2011)
In: Journal of Neurology, 258(5), 770-782. doi:10.1007/s00415-010-5828-5
Research article (journal) | Published
Unexpected island effects at an extreme: reduced y chromosome and mitochondrial DNA diversity in nias.
van Oven M, Hämmerle JM, van Schoor M, Kushnick G, Pennekamp P, Zega I, Lao O, Brown L, Kennerknecht I, Kayser M (2011)
In: Molecular Biology and Evolution, 28(4), 1349-1361.
Research article (journal) | Published
Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII.
Mayer K, Kennerknecht I, Steinmann B (2010)
In: European Journal of Human Genetics, 18(9). doi:10.1038/ejhg.2009.227
Research article (journal) | Published
Show all publications (13)

Doctorates

Hereditäre Prosopagnosie in Brasilien
Candidate: Kotzyba, Ferdinand Sebastian | Supervisors: Kennerknecht, Ingo
Period of time: until 01/06/2010
Doctoral examination procedure finished at: Doctoral examination procedure at University of Münster