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Julia Vogt · SciRah

Researcher profile · Semantic Scholar

Julia Vogt

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Julia Vogt — researcher profile on SciRah

h-index: 14
Works: 33
Citations: 648

Most-cited papers

Mosaic type‐1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type‐1 (NF1)
L. Messiaen, Julia Vogt, K. Bengesser, Chuanhua Fu +6 more
2011Human Mutation120 citations Open access
Semantic Scholar
panelcn.MOPS: Copy‐number detection in targeted NGS panel data for clinical diagnostics
G. Povysil, A. Tzika, Julia Vogt, Verena Haunschmid +5 more
2017Human Mutation84 citations Open access
Semantic Scholar
SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints
Julia Vogt, K. Bengesser, K. Claes, K. Wimmer +12 more
2014Genome Biology73 citations Open access
Semantic Scholar
Monozygotic twins discordant for neurofibromatosis type 1 due to a postzygotic NF1 gene mutation
Julia Vogt, J. Kohlhase, S. Morlot, L. Kluwe +3 more
2011Human Mutation40 citations Open access
Semantic Scholar
Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type‐2 NF1 deletions
Angelika C. Roehl, Julia Vogt, Tanja Mussotter, Antje N. Zickler +8 more
2010Human Mutation37 citations
Semantic Scholar
Internal tumor burden in neurofibromatosis Type I patients with large NF1 deletions
L. Kluwe, R. Nguyen, Julia Vogt, K. Bengesser +5 more
2012Genes, Chromosomes and Cancer36 citations
Semantic Scholar
Setting the PAS, the role of circadian PAS domain proteins during environmental adaptation in plants
Julia Vogt, Jos H. M. Schippers
2015Frontiers in Plant Science35 citations Open access
Semantic Scholar
Molecular characterization of Richter syndrome identifies de novo diffuse large B-cell lymphomas with poor prognosis
J. Broséus, Sébastien Hergalant, Julia Vogt, E. Tausch +38 more
2023Nature Communications32 citations Open access
Semantic Scholar
Human Serum Induces Streptococcal C5a Peptidase Expression
Ute Gleich-Theurer, Simone Aymanns, G. Haas, S. Mauerer +2 more
2009Infection and Immunity31 citations Open access
Semantic Scholar
Identification of recurrent type‐2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder
Julia Vogt, Tanja Mussotter, K. Bengesser, K. Claes +8 more
2012Human Mutation26 citations
Semantic Scholar
Tissue‐specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/−) stem cells
Angelika C. Roehl, Tanja Mussotter, D. Cooper, L. Kluwe +6 more
2012Human Mutation25 citations Open access
Semantic Scholar
Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletions
H. Kehrer-Sawatzki, Julia Vogt, Tanja Mussotter, L. Kluwe +2 more
2012Neurogenetics22 citations
Semantic Scholar
Analysis of Crossover Breakpoints Yields New Insights into the Nature of the Gene Conversion Events Associated with Large NF1 Deletions Mediated by Nonallelic Homologous Recombination
K. Bengesser, Julia Vogt, Tanja Mussotter, V. Mautner +3 more
2014Human Mutation19 citations Open access
Semantic Scholar
Expression of ELF1, a lymphoid ETS domain‐containing transcription factor, is recurrently lost in classical Hodgkin lymphoma
J. Paczkowska, Natalia Soloch, M. Bodnar, Katarzyna Kiwerska +9 more
2019British Journal of Haematology15 citations
Semantic Scholar
Delineation of the clinical phenotype associated with non-mosaic type-2 NF1 deletions: two case reports
Julia Vogt, R. Nguyen, L. Kluwe, M. Schuhmann +5 more
2011Journal of Medical Case Reports14 citations Open access
Semantic Scholar
Array‐based profiling of the lymphoma cell DNA methylome does not unequivocally distinguish primary lymphomas of the central nervous system from non‐CNS diffuse large B‐cell lymphomas
Julia Vogt, R. Wagener, M. Montesinos-Rongen, O. Ammerpohl +3 more
2018Genes, Chromosomes and Cancer12 citations Open access
Semantic Scholar
The curious case of Merkel cell carcinoma: epigenetic youth and lack of pluripotency
E. Chteinberg, Julia Vogt, J. Kolarova, Felix Bormann +7 more
2020Epigenetics10 citations Open access
Semantic Scholar
PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1
Julia Vogt, A. Wernstedt, T. Ripperger, B. Pabst +3 more
2016European Journal of Human Genetics9 citations Open access
Semantic Scholar
Two molecularly distinct atypical teratoid/rhabdoid tumors (or tumor components) occurring in an infant with rhabdoid tumor predisposition syndrome 1
C. Thomas, F. Knerlich-Lukoschus, H. Reinhard, P. Johann +17 more
2019Acta Neuropathologica8 citations
Semantic Scholar
ARRAY‐BASED DNA METHYLOME ANALYSES OF PRIMARY LYMPHOMAS OF THE CENTRAL NERVOUS SYSTEM
Julia Vogt, R. Wagener, M. Montesinos-Rongen, O. Ammerpohl +3 more
20170 citations Open access
Semantic Scholar
GSM1395204: atypical NF1 deletion patient_1
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395207: atypical NF1 deletion patient_4
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395210: atypical NF1 deletion patient_7
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395205: atypical NF1 deletion patient_2
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395209: atypical NF1 deletion patient_6
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395208: atypical NF1 deletion patient_5
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395214: atypical NF1 deletion patient_11
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395213: atypical NF1 deletion patient_10
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395215: atypical NF1 deletion patient_12
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395206: atypical NF1 deletion patient_3
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395212: atypical NF1 deletion patient_9
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
GSM1395211: atypical NF1 deletion patient_8
Julia Vogt, H. Kehrer-Sawatzki
20140 citations
Semantic Scholar
Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletions
H. Kehrer-Sawatzki, Julia Vogt, Tanja Mussotter, L. Kluwe +2 more
2012Neurogenetics0 citations
Semantic Scholar

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