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Franziska Schnabel
Franziska Schnabel
Institute of Human Genetics Leipzig
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Zitiert von
Zitiert von
Jahr
The influence of olfactory loss on dietary behaviors
K Aschenbrenner, C Hummel, K Teszmer, F Krone, T Ishimaru, HS Seo, ...
The Laryngoscope 118 (1), 135-144, 2008
2792008
A study about the frequency of taste disorders
A Welge-Lüssen, P Dörig, M Wolfensberger, F Krone, T Hummel
Journal of neurology 258, 386-392, 2011
1532011
Novel humanized and highly efficient bispecific antibodies mediate killing of prostate stem cell antigen-expressing tumor cells by CD8+ and CD4+ T cells
A Feldmann, C Arndt, K Töpfer, S Stamova, F Krone, M Cartellieri, ...
The Journal of Immunology 189 (6), 3249-3259, 2012
1162012
Comparison between odor thresholds for phenyl ethyl alcohol and butanol
I Croy, K Lange, F Krone, S Negoias, HS Seo, T Hummel
Chemical senses 34 (6), 523-527, 2009
1022009
Impact of chemotherapy for childhood leukemia on brain morphology and function
M Genschaft, T Huebner, F Plessow, VN Ikonomidou, N Abolmaali, ...
PloS one 8 (11), e78599, 2013
892013
Androstadienone odor thresholds in adolescents
T Hummel, F Krone, JN Lundström, O Bartsch
Hormones and behavior 47 (3), 306-310, 2005
742005
Patient adjustment to reduced olfactory function
I Croy, BN Landis, T Meusel, HS Seo, F Krone, T Hummel
Archives of Otolaryngology–Head & Neck Surgery 137 (4), 377-382, 2011
462011
Premature aging disorders: A clinical and genetic compendium
F Schnabel, U Kornak, B Wollnik
Clinical Genetics 99 (1), 3-28, 2021
342021
Olfactory processing: Detection of rapid changes
I Croy, F Krone, S Walker, T Hummel
Chemical Senses 40 (5), 351-355, 2015
272015
Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22
F Schnabel, M Smogavec, R Funke, S Pauli, P Burfeind, I Bartels
Molecular Cytogenetics 11, 1-5, 2018
122018
GestaltMatcher Database-a FAIR database for medical imaging data of rare disorders
H Lesmann, GJ Lyon, P Caro, IM Abdelrazek, S Moosa, JT Pantel, ...
MedRxiv, 2023
92023
Beurteilung der chemosensorischen Funktion mit validierten Riech-und Schmecktests
Ö Göktas, S Fräßdorf, U Walliczek-Dworschak, P Han, T Hummel
Laryngo-Rhino-Otologie 97 (05), 344-356, 2018
92018
Topographical differences in the sensitivity of the human nasal mucosa to olfactory and trigeminal stimuli
T Ishimaru, J Reden, F Krone, M Scheibe
Neuroscience letters 493 (3), 136-139, 2011
62011
Aplasia cutis congenita in a CDC42related developmental phenotype
F Schnabel, SB Kamphausen, R Funke, S Kaulfuß, B Wollnik, M Zenker
American Journal of Medical Genetics Part A 185 (3), 850-855, 2021
42021
Intrinsic chemosensory signal recorded from the human nasal mucosa in patients with smell loss
T Ishimaru, F Krone, M Scheibe, V Gudziol, S Negoias, T Hummel
European Archives of Oto-Rhino-Laryngology 270, 1335-1338, 2013
42013
Optical recordings from the human nasal mucosa in response to olfactory stimulation
T Ishimaru, J Reden, F Krone, M Scheibe
Neuroscience letters 423 (3), 231-235, 2007
42007
Der Geruchssinn
F Krone, V Gudziol, T Hummel
Ernährung & Medizin 26 (03), 120-123, 2011
12011
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features
X Pan, AM Tao, S Lu, M Ma, SB Hannan, R Slaugh, SD Williams, ...
The American Journal of Human Genetics 111 (4), 742-760, 2024
2024
GestaltMatcher Database-A global reference for the facial phenotypic variability of rare human diseases.
H Lesmann, A Hustinx, S Moosa, E Marchi, P Caro, IM Abdelrazek, ...
Medrxiv: the Preprint Server for Health Sciences, 2023.06. 06.23290887-2023 …, 2024
2024
Bi-allelic loss-of-function variants of FILIP1 encoding a filamin A binding protein cause autosomal recessive arthrogryposis multiplex congenita with microcephaly
F Schnabel, E Schuler, A Al-Maawali, A Chaurasia, S Syrbe, A Al-Kindi, ...
European Journal of Human Genetics 32, 520-520, 2024
2024
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