ZMB Member Dietmar Lohmann
ZMB Member
Dietmar Lohmann
Next ZMB-Member
Prof. Dr. Dietmar Lohmann
Institute of Human Genetics
University Hospital Essen
Hufelandstr. 55
45122 Essen
- +49 201 723 4562
- Website
- Selected Publications
- Publication Metrics
-
- ZMB Research Program
Molecular and Chemical Cell Biology
Research Overview
Retinoblastoma
- Determining the genetic architecture underlying predisposition to retinoblastoma
- Identification of risk factors for development of extraocular neoplasms in patients with retinoblastoma
- Analysis of changes of the genetic landscape during retinoblastoma progression
Uveal Melanoma
- Identification of heritable genetic alterations that alter the risk for uveal melanoma
- Development of prognostic and predictive biomarkers
- Determining somatic genetic alterations linked to metastasizing uveal melanoma
Selected Publications
-
Molecular subgrouping of primary pineal parenchymal tumors reveals distinct subtypes correlated with clinical parameters and genetic alterationsIn: Acta Neuropathologica Vol. 139 (2020) Nr. 2, pp. 243 - 257
ISSN: 1432-0533; 0001-6322Online Full Text: dx.doi.org/ -
Ectopic intracranial retinoblastoma in a 3.5-month-old infant without eye involvement and without evidence of heritabilityIn: Pediatric Blood and Cancer Vol. 66 (2019) Nr. 5, pp. e27599
ISSN: 1545-5009; 1545-5017Online Full Text: dx.doi.org/ -
GNAQ Q209R Mutations Are Highly Specific for Circumscribed Choroidal HemangiomaIn: Cancers Vol. 11 (2019) Nr. 7, pp. 1031
ISSN: 2072-6694Online Full Text: dx.doi.org/ Online Full Text (Open Access) -
Retinoblastoma with late metastatic spread : a case reportIn: Pediatric Blood and Cancer Vol. 66 (2019) Nr. 6, pp. e27656
ISSN: 1545-5017; 1545-5009Online Full Text: dx.doi.org/ -
Author Correction : The landscape of genomic alterations across childhood cancersIn: Nature Vol. 559 (2018) Nr. 7714, pp. E10
ISSN: 0028-0836; 1476-4687Online Full Text: dx.doi.org/ -
DNA methylation-based classification of central nervous system tumoursIn: Nature Vol. 555 (2018) Nr. 7697, pp. 469 - 474
ISSN: 0028-0836; 1476-4687Online Full Text: dx.doi.org/ (Open Access) -
The landscape of genomic alterations across childhood cancersIn: Nature Vol. 555 (2018) Nr. 7696, pp. 321 - 327
ISSN: 0028-0836; 1476-4687Online Full Text: dx.doi.org/ (Open Access) -
First Prospective National Registry for Pediatric Eye Cancer in Germany and AustriaIn: Pediatric Blood and Cancer Vol. 64 (2017) Nr. Suppl. 3, pp. S276 - S277
ISSN: 1545-5009; 1545-5017 -
Incidence of second cancers after radiotherapy and systemic chemotherapy in heritable retinoblastoma survivors : a report from the German reference centerIn: Pediatric Blood and Cancer Vol. 64 (2017) Nr. 1, pp. 71 - 80
ISSN: 1545-5009; 1545-5017Online Full Text: dx.doi.org/ -
How Eye-Preserving Therapy Affects Long-Term Overall Survival in Heritable Retinoblastoma SurvivorsIn: Journal of Clinical Oncology Vol. 34 (2016) Nr. 26, pp. 3183 - 3188
ISSN: 0732-183X; 1527-7755Online Full Text: dx.doi.org/ -
Pediatric second primary malignancies after retinoblastoma treatmentIn: Pediatric Blood and Cancer Vol. 62 (2015) Nr. 10, pp. 1799 - 1804
ISSN: 1545-5009; 1545-5017; 0098-1532; 1096-911XOnline Full Text: dx.doi.org/ (Open Access) -
Characterisation of retinoblastomas without RB1 mutations: Genomic, gene expression, and clinical studiesIn: The Lancet Oncology Vol. 14 (2013) Nr. 4, pp. 327 - 334
ISSN: 1470-2045; 1474-5488Online Full Text: dx.doi.org/ -
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3In: Nature Genetics Vol. 45 (2013) Nr. 8, pp. 933 - 936
ISSN: 1061-4036; 1546-1718Online Full Text: dx.doi.org/ -
Sporadic unilateral retinoblastoma or first sign of bilateral disease?In: Pediatric Blood and Cancer Vol. 59 (2012) Nr. 6, pp. 1064 - 1064
ISSN: 1545-5009; 1545-5017 -
Anthropogenic greenhouse gas contribution to flood risk in England and Wales in autumn 2000In: Nature Vol. 470 (2011) Nr. 7334, pp. 382 - 385
ISSN: 0028-0836; 1476-4687Online Full Text: dx.doi.org/ -
Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndromeIn: Nature Genetics Vol. 43 (2011) Nr. 1, pp. 20 - 22
ISSN: 1061-4036; 1546-1718Online Full Text: dx.doi.org/ -
A variant allele of Growth Factor Independence 1 (GFI1) is associated with acute myeloid leukemiaIn: Blood Vol. 115 (2010) Nr. 12, pp. 2462 - 2472
ISSN: 0006-4971; 1528-0020Online Full Text: dx.doi.org/