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Doll, Julia
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1

Epithelioid and spindle cell rhabdomyosarcoma with EWSR1::T..:

Haug, Lukas ; Doll, Julia ; Appenzeller, Silke...
Pathology - Research and Practice.  249 (2023)  - p. 154779 , 2023
Link: https://doi.org/10.1016/..
 
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2

mRNA Abundance of Neurogenic Factors Correlates with Hearin..:

Engert, Jonas ; Doll, Julia ; Vona, Barbara...
Life.  13 (2023)  9 - p. 1858 , 2023
Link: https://doi.org/10.3390/..
 
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3

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/..
 
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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/..
 
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5

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/..
 
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6

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/..
 
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7

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/..
 
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8

Novel Loss-of-Function Variants in CDC14A are Associated wi..:

Doll, Julia ; Kolb, Susanne ; Schnapp, Linda...
International Journal of Molecular Sciences.  21 (2020)  1 - p. 311 , 2020
Link: https://doi.org/10.3390/..
 
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9

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/..
 
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10

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/..
 
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11

The CAPOS mutation in ATP1A3 alters Na/K-ATPase function an..:

Tranebjærg, Lisbeth ; Strenzke, Nicola ; Lindholm, Sture...
Human Genetics.  137 (2018)  2 - p. 111-127 , 2018
Link: https://doi.org/10.1007/..
 
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12

Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATP..:

Tranebjærg, Lisbeth ; Strenzke, Nicola ; Lindholm, Sture...
Human Genetics.  137 (2018)  3 - p. 279-280 , 2018
Link: https://doi.org/10.1007/..
 
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13

Electrochemical Degradation of Molecularly Imprinted Polyme..:

Nguyen, Minh-Hai ; Onken, Adrian ; Sündermann, Jan...
ACS Omega.  9 (2024)  23 - p. 25223-25238 , 2024
Link: https://doi.org/10.1021/..
 
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14

A JAGN1-associated severe congenital neutropenia zebrafish ..:

Doll, Larissa ; Welte, Karl ; Skokowa, Julia.
Blood Advances.  , 2024
Link: https://doi.org/10.1182/..
 
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15

P750: A ZEBRAFISH MODEL FOR JAGN1-ASSOCIATED SEVERE CONGENI..:

Doll, Larissa ; Aghaallaei, Narges ; Lengerke, Claudia...
HemaSphere.  7 (2023)  S3 - p. e69758f3 , 2023
Link: https://doi.org/10.1097/..
 
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