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D. Lohmann · SciRah

Researcher profile · Semantic Scholar

D. Lohmann

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D. Lohmann — researcher profile on SciRah

h-index: 44
Works: 136
Citations: 11K

Most-cited papers

DNA methylation-based classification of central nervous system tumours
D. Capper, David T. W. Jones, M. Sill, V. Hovestadt +139 more
2018Nature2,577 citations Open access
Semantic Scholar
The landscape of genomic alterations across childhood cancers
S. Gröbner, Barbara C. Worst, J. Weischenfeldt, I. Buchhalter +80 more
2018Nature1,388 citations Open access
Semantic Scholar
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
Marcel Martin, L. Masshöfer, P. Temming, S. Rahmann +8 more
2013Nature Genetics498 citations Open access
Semantic Scholar
Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studies.
D. Rushlow, Berber M. Mol, Jennifer Y. Kennett, Stephanie Yee +21 more
2013The Lancet Oncology360 citations Open access
Semantic Scholar
Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome
J. Dauwerse, Jill Dixon, S. Seland, C. Ruivenkamp +16 more
2011Nature Genetics347 citations
Semantic Scholar
Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
T. Ripperger, S. Bielack, A. Borkhardt, I. Brecht +72 more
2017American Journal of Medical Genetics. Part A247 citations Open access
Semantic Scholar
Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly.
Matthew A. Lines, Li-Jia Huang, J. Schwartzentruber, Stuart Douglas +23 more
2012American Journal of Human Genetics212 citations Open access
Semantic Scholar
Conservative management of retinoblastoma: Challenging orthodoxy without compromising the state of metastatic grace. "Alive, with good vision and no comorbidity".
F. Munier, M. Beck-Popovic, G. Chantada, D. Cobrinik +14 more
2019Progress in retinal and eye research196 citations Open access
Semantic Scholar
Retinoblastoma: Revisiting the model prototype of inherited cancer
D. Lohmann, B. Gallie
2004American Journal of Medical Genetics. Part C, Seminars in Medical Genetics187 citations
Semantic Scholar
Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation
Özge Altug Teber, G. Gillessen-kaesbach, S. Fischer, S. Bohringer +21 more
2004European Journal of Human Genetics179 citations
Semantic Scholar
A novel real-time PCR assay for quantitative analysis of methylated alleles (QAMA): analysis of the retinoblastoma locus.
M. Zeschnigk, S. Bohringer, E. Price, Z. Onadim +2 more
2004Nucleic Acids Research143 citations Open access
Semantic Scholar
The Human Retinoblastoma Gene Is Imprinted
Deniz Kanber, Tea Berulava, O. Ammerpohl, D. Mitter +5 more
2009PLoS Genetics132 citations Open access
Semantic Scholar
Gains and overexpression identify DEK and E2F3 as targets of chromosome 6p gains in retinoblastoma
C. Grasemann, Sandrine Gratias, H. Stephan, A. Schüler +7 more
2005Oncogene129 citations
Semantic Scholar
Detection of chromosomal imbalances in retinoblastoma by matrix‐based comparative genomic hybridization
Boris Zielinski, Sandrine Gratias, G. Toedt, F. Mendrzyk +4 more
2005Genes, Chromosomes and Cancer128 citations
Semantic Scholar
Incidence of second cancers after radiotherapy and systemic chemotherapy in heritable retinoblastoma survivors: A report from the German reference center
P. Temming, Marina Arendt, A. Viehmann, L. Eisele +10 more
2017Pediatric Blood & Cancer104 citations
Semantic Scholar
Comparing the Prognostic Value of BAP1 Mutation Pattern, Chromosome 3 Status, and BAP1 Immunohistochemistry in Uveal Melanoma
J. V. van de Nes, J. Nelles, S. Kreis, C. Metz +3 more
2016American Journal of Surgical Pathology102 citations
Semantic Scholar
Genotype–phenotype correlations in patients with retinoblastoma and interstitial 13q deletions
D. Mitter, R. Ullmann, A. Muradyan, L. Klein-Hitpass +4 more
2011European Journal of Human Genetics89 citations Open access
Semantic Scholar
Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study
S. Thomas, C. Pütter, S. Weber, N. Bornfeld +2 more
2012British Journal of Cancer86 citations Open access
Semantic Scholar
Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression
P. Albrecht, Birgit Ansperger-Rescher, A. Schüler, M. Zeschnigk +2 more
2005Human Mutation81 citations
Semantic Scholar
Acrofacial Dysostosis, Cincinnati Type, a Mandibulofacial Dysostosis Syndrome with Limb Anomalies, Is Caused by POLR1A Dysfunction.
K. Weaver, Kristin E. Noack Watt, R. Hufnagel, Joaquin Navajas Acedo +11 more
2015American Journal of Human Genetics78 citations Open access
Semantic Scholar
Patterns of missplicing caused by RB1 gene mutations in patients with retinoblastoma and association with phenotypic expression
Katherine Zhang, I. Nowak, D. Rushlow, B. Gallie +1 more
2008Human Mutation73 citations Open access
Semantic Scholar
Molecular subgrouping of primary pineal parenchymal tumors reveals distinct subtypes correlated with clinical parameters and genetic alterations
E. Pfaff, C. Aichmüller, M. Sill, D. Stichel +25 more
2019Acta Neuropathologica71 citations Open access
Semantic Scholar
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome
E. Schaefer, C. Collet, D. Geneviève, M. Vincent +9 more
2014Genetics in Medicine68 citations Open access
Semantic Scholar
Loss of heterozygosity of 1p in uveal melanomas with monosomy 3
Thomas Häusler, A. Stang, G. Anastassiou, K. Jöckel +4 more
2005International Journal of Cancer68 citations Open access
Semantic Scholar
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome.
D. Wieczorek, W. Newman, T. Wieland, Tea Berulava +38 more
2014American Journal of Human Genetics67 citations Open access
Semantic Scholar
Ultradeep sequencing detects GNAQ and GNA11 mutations in cell-free DNA from plasma of patients with uveal melanoma
C. Metz, M. Scheulen, N. Bornfeld, D. Lohmann +1 more
2013Cancer Medicine56 citations Open access
Semantic Scholar
A variant allele of Growth Factor Independence 1 (GFI1) is associated with acute myeloid leukemia.
C. Khandanpour, C. Thiede, P. Valk, E. Sharif-Askari +21 more
2007Blood51 citations Open access
Semantic Scholar
Genomic gains on chromosome 1q in retinoblastoma: Consequences on gene expression and association with clinical manifestation
Sandrine Gratias, A. Schüler, L. Hitpass, H. Stephan +4 more
2005International Journal of Cancer51 citations Open access
Semantic Scholar
How Eye-Preserving Therapy Affects Long-Term Overall Survival in Heritable Retinoblastoma Survivors.
P. Temming, Marina Arendt, A. Viehmann, L. Eisele +10 more
2016Journal of Clinical Oncology47 citations
Semantic Scholar
Age at diagnosis of isolated unilateral retinoblastoma does not distinguish patients with and without a constitutional RB1 gene mutation but is influenced by a parent-of-origin effect.
A. Schüler, S. Weber, M. Neuhäuser, C. Jurklies +6 more
2005European Journal of Cancer42 citations
Semantic Scholar
Imprinting of RB1 (the new kid on the block).
K. Buiting, Deniz Kanber, B. Horsthemke, D. Lohmann
2010Briefings in Functional Genomics37 citations Open access
Semantic Scholar
Pediatric second primary malignancies after retinoblastoma treatment
P. Temming, A. Viehmann, Marina Arendt, L. Eisele +5 more
2015Pediatric Blood & Cancer34 citations Open access
Semantic Scholar
EFS shows biallelic methylation in uveal melanoma with poor prognosis as well as tissue-specific methylation
Lisa C. Neumann, A. Weinhäusel, Stefani N Thomas, B. Horsthemke +2 more
2011BMC Cancer34 citations Open access
Semantic Scholar
Microcephaly, microtia, preauricular tags, choanal atresia and developmental delay in three unrelated patients: A mandibulofacial dysostosis distinct from Treacher Collins syndrome
D. Wieczorek, B. Gener, M. González, S. Seland +7 more
2009American Journal of Medical Genetics. Part A34 citations
Semantic Scholar
Allelic loss in a minimal region on chromosome 16q24 is associated with vitreous seeding of retinoblastoma.
Sandrine Gratias, H. Rieder, R. Ullmann, L. Klein-Hitpass +4 more
2007Cancer Research34 citations Open access
Semantic Scholar
GNAQ Q209R Mutations Are Highly Specific for Circumscribed Choroidal Hemangioma
C. L. Le Guin, K. Metz, S. Kreis, N. Bechrakis +3 more
2019Cancers29 citations Open access
Semantic Scholar
Current Concepts for Diagnosis and Treatment of Retinoblastoma in Germany: Aiming for Safe Tumor Control and Vision Preservation
P. Temming, D. Lohmann, N. Bornfeld, W. Sauerwein +2 more
2012Klinische Pädiatrie28 citations
Semantic Scholar
BAP1 germline mutation in two first grade family members with uveal melanoma
D. Maerker, M. Zeschnigk, J. Nelles, D. Lohmann +4 more
2013British Journal of Ophthalmology27 citations Open access
Semantic Scholar
Treacher Collins syndrome: clinical implications for the paediatrician—a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature
J. Schlump, A. Stein, U. Hehr, T. Karen +8 more
2012European Journal of Pediatrics26 citations Open access
Semantic Scholar
Chemoreduction improves eye retention in patients with retinoblastoma: a report from the German Retinoblastoma Reference Centre
A. Künkele, C. Jurklies, R. Wieland, D. Lohmann +3 more
2013British Journal of Ophthalmology25 citations
Semantic Scholar
Establishment and characterization of two uveal melanoma cell lines derived from tumors with loss of one chromosome 3.
G. Nareyeck, M. Zeschnigk, G. Prescher, D. Lohmann +1 more
2006Experimental Eye Research25 citations
Semantic Scholar
Author Correction: The landscape of genomic alterations across childhood cancers
S. Gröbner, Barbara C. Worst, J. Weischenfeldt, I. Buchhalter +80 more
2018Nature24 citations Open access
Semantic Scholar
The Interdisciplinary Diagnosis and Treatment of Intraocular Tumors.
N. Bornfeld, E. Biewald, S. Bauer, P. Temming +2 more
2018Deutsches Ärzteblatt International24 citations Open access
Semantic Scholar
The Origin of the RB1 Imprint
Deniz Kanber, K. Buiting, C. Roos, J. Gromoll +3 more
2013PLoS ONE24 citations Open access
Semantic Scholar
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome
Jasmin Beygo, Karin Buiting, Saskia Seland, H. Lüdecke +5 more
2012Molecular Syndromology24 citations Open access
Semantic Scholar
TFF1 in Aqueous Humor—A Potential New Biomarker for Retinoblastoma
M. Busch, André Haase, Natalia Miroschnikov, Annika Doege +7 more
2022Cancers22 citations Open access
Semantic Scholar
Early detection of metastatic uveal melanoma by the analysis of tumor‐specific mutations in cell‐free plasma DNA
C. L. Le Guin, N. Bornfeld, N. Bechrakis, L. Jabbarli +3 more
2021Cancer Medicine21 citations Open access
Semantic Scholar
Neoadjuvant/adjuvant treatment of high-risk retinoblastoma: a report from the German Retinoblastoma Referral Centre
A. Künkele, J. Wilm, M. Holdt, D. Lohmann +4 more
2015British Journal of Ophthalmology20 citations
Semantic Scholar
Psychosocial impact of prognostic genetic testing in uveal melanoma patients: a controlled prospective clinical observational study
Marietta Lieb, S. Tagay, Anja Breidenstein, Tobias Hepp +6 more
2020BMC Psychology19 citations Open access
Semantic Scholar
Neurotrophin receptor expression in human primary retinoblastomas and retinoblastoma cell lines
H. Stephan, J. Zakrzewski, R. Bölöni, C. Grasemann +2 more
2008Pediatric Blood & Cancer19 citations
Semantic Scholar

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