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Hofrichter, Michaela A. H.
46
results:
Search for persons
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Format
Online (46)
Mediatypes
Articles (Online) (30)
OpenAccess-fulltext (15)
Thesis (Online) (1)
Languages
german (3)
english (43)
Sorted by: Relevance
Sorted by: Year
?
1
Unraveling the genetic complexities of combined retinal dys..:
Bahena, Paulina
;
Daftarian, Narsis
;
Maroofian, Reza
...
Human Genetics. 141 (2021) 3-4 - p. 785-803 , 2021
Link:
https://doi.org/10.1007/..
?
2
Small fish, big prospects: using zebrafish to unravel the m..:
Vona, Barbara
;
Doll, Julia
;
Hofrichter, Michaela A.H.
..
Hearing Research. 397 (2020) - p. 107906 , 2020
Link:
https://doi.org/10.1016/..
?
3
Non-syndromic hearing loss: clinical and diagnostic challen..:
Vona, Barbara
;
Doll, Julia
;
Hofrichter, Michaela A. H.
.
Medizinische Genetik. 32 (2020) 2 - p. 117-129 , 2020
Link:
https://doi.org/10.1515/..
?
4
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Los..:
Doll, Julia
;
Vona, Barbara
;
Schnapp, Linda
...
Genes. 11 (2020) 11 - p. 1329 , 2020
Link:
https://doi.org/10.3390/..
?
5
A novel missense variant in MYO3A is associated with autoso..:
Doll, Julia
;
Hofrichter, Michaela A. H.
;
Bahena, Paulina
...
Molecular Genetics & Genomic Medicine. 8 (2020) 8 - p. , 2020
Link:
https://doi.org/10.1002/..
?
6
Exome-wide copy number variation analysis identifies a COL9..:
Hofrichter, Michaela A.H.
;
Doll, Julia
;
Habibi, Haleh
...
European Journal of Medical Genetics. 62 (2019) 10 - p. 103724 , 2019
Link:
https://doi.org/10.1016/..
?
7
The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundame..:
Hofrichter, Michaela A. H.
;
Mojarad, Majid
;
Doll, Julia
...
BMC Medical Genetics. 19 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
8
Hereditary hearing loss SNP-microarray pilot study:
Vona, Barbara
;
Hofrichter, Michaela A. H.
;
Schröder, Jörg
...
BMC Research Notes. 11 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
9
Confirmation of PDZD7 as a Nonsyndromic Hearing Loss Gene:
Vona, Barbara
;
Lechno, Stanislav
;
Hofrichter, Michaela A. H.
...
Ear & Hearing. 37 (2016) 4 - p. e238-e246 , 2016
Link:
https://doi.org/10.1097/..
?
10
Non-syndromic hearing loss gene identification: A brief his..:
Vona, Barbara
;
Nanda, Indrajit
;
Hofrichter, Michaela A.H.
..
Molecular and Cellular Probes. 29 (2015) 5 - p. 260-270 , 2015
Link:
https://doi.org/10.1016/..
?
11
Targeted next-generation sequencing of deafness genes in he..:
Vona, Barbara
;
Müller, Tobias
;
Nanda, Indrajit
...
Genetics in Medicine. 16 (2014) 12 - p. 945-953 , 2014
Link:
https://doi.org/10.1038/..
?
12
Unraveling the genetic complexities of combined retinal dys..:
Bahena, Paulina
;
Daftarian, Narsis
;
Maroofian, Reza
...
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/26775. , 2022
Link:
https://opus.bibliothek...
?
13
Unraveling the genetic complexities of combined retinal dys..:
Bahena, Paulina
;
Daftarian, Narsis
;
Maroofian, Reza
...
https://repository.publisso.de/resource/frl:6446836. , 2021
Link:
https://repository.publi..
?
14
A novel missense variant in MYO3A is associated with autoso..:
Doll, Julia
;
Hofrichter, Michaela A. H
;
Bahena, Paulina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434730/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
15
Small fish, big prospects: using zebrafish to unravel the m..:
Vona, Barbara
;
Doll, Julia
;
Hofrichter, Michaela A. H
..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415493/. , 2020
Link:
http://www.ncbi.nlm.nih...
1-15
