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Incidence of second cancers after radiotherapy and systemic chemotherapy in heritable retinoblastoma survivors: A report from the German reference center

Pediatric blood & cancer, 2017-01, Vol.64 (1), p.71-80

2017

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Black carbon concentrations and sources in the marine boundary layer of the tropical Atlantic Ocean using four methodologies

Atmospheric chemistry and physics, 2014-07, Vol.14 (14), p.7431-7443

2014

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Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

Nature genetics, 2011-01, Vol.43 (1), p.20-22

2011

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Levels of PAHs in the Waters, Sediments, and Shrimps of Estero de Urias, an Estuary in Mexico, and Their Toxicological Effects

TheScientificWorld, 2012-01, Vol.2012 (2012), p.1-9

2012

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Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly

American journal of human genetics, 2012-02, Vol.90 (2), p.369-377

2012

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Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study

British journal of cancer, 2012-03, Vol.106 (6), p.1171-1176

2012

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Acrofacial dysostosis, Cincinnati type: a mandibulofacial dysostosis syndrome with limb anomalies caused by POLR1A dysfunction

American journal of human genetics, 2015-05, Vol.96 (5), p.765-774

2015

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Importance of Black Carbon to Sorption of Native PAHs, PCBs, and PCDDs in Boston and New York Harbor Sediments

Environmental science & technology, 2005-01, Vol.39 (1), p.141-148

2005

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Bioremediation of Parboiled Rice Effluent Supplemented with Biodiesel-Derived Glycerol Using Pichia pastoris X-33

TheScientificWorld, 2012-01, Vol.2012 (2012), p.1-5

2012

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Early detection of metastatic uveal melanoma by the analysis of tumor‐specific mutations in cell‐free plasma DNA

Cancer medicine (Malden, MA), 2021-09, Vol.10 (17), p.5974-5982

2021

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X-linked hypophosphatemic rickets and nephrocalcinosis: clinical characteristics of a single-center pediatric cohort in North America before and after burosumab

Frontiers in pediatrics, 2024-08, Vol.12, p.1430921

2024

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Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome

American journal of human genetics, 2014-12, Vol.95 (6), p.698-707

2014

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Retinoblastoma: Revisiting the model prototype of inherited cancer

American journal of medical genetics. Part C, Seminars in medical genetics, 2004-08, Vol.129C (1), p.23-28

2004

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Pediatric second primary malignancies after retinoblastoma treatment

Pediatric blood & cancer, 2015-10, Vol.62 (10), p.1799-1804

2015

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BAP1 germline mutation in two first grade family members with uveal melanoma

British journal of ophthalmology, 2014-02, Vol.98 (2), p.224-227

2014

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A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma

Communications biology, 2024-07, Vol.7 (1), p.919-16, Article 919

2024

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Author Correction: A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma

Communications biology, 2024-09, Vol.7 (1), p.1119-1, Article 1119

2024

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RB1 gene mutations in retinoblastoma

Human mutation, 1999-10, Vol.14 (4), p.283-288

Lohmann, Dietmar R.

1999

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Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

Nature genetics, 2013-08, Vol.45 (8), p.933-936

2013

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EFS shows biallelic methylation in uveal melanoma with poor prognosis as well as tissue-specific methylation

BMC cancer, 2011-08, Vol.11 (1), p.380-380, Article 380

2011

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Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization

Genes chromosomes & cancer, 2005-07, Vol.43 (3), p.294-301

2005

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Psychosocial impact of prognostic genetic testing in uveal melanoma patients: a controlled prospective clinical observational study

BMC Psychology, 2020-01, Vol.8 (1), p.8-8, Article 8

2020

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The impact of RB1 genotype on incidence of second tumours in heritable retinoblastoma

European journal of cancer (1990), 2020-07, Vol.133, p.47-55

2020

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Release of Cell-Free Tumor DNA in the Plasma of Uveal Melanoma Patients Under Radiotherapy

Investigative ophthalmology & visual science, 2023-10, Vol.64 (13), p.35-35

2023

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Comparing the Prognostic Value of BAP1 Mutation Pattern, Chromosome 3 Status, and BAP1 Immunohistochemistry in Uveal Melanoma

The American journal of surgical pathology, 2016-06, Vol.40 (6), p.796-805

2016

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Incidence of second cancers after radiotherapy and systemic chemotherapy in heritable retinoblastoma survivors: A report from the German reference center

Black carbon concentrations and sources in the marine boundary layer of the tropical Atlantic Ocean using four methodologies

Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

Levels of PAHs in the Waters, Sediments, and Shrimps of Estero de Urias, an Estuary in Mexico, and Their Toxicological Effects

Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly

Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study

Acrofacial dysostosis, Cincinnati type: a mandibulofacial dysostosis syndrome with limb anomalies caused by POLR1A dysfunction

Importance of Black Carbon to Sorption of Native PAHs, PCBs, and PCDDs in Boston and New York Harbor Sediments

Bioremediation of Parboiled Rice Effluent Supplemented with Biodiesel-Derived Glycerol Using Pichia pastoris X-33

Early detection of metastatic uveal melanoma by the analysis of tumor‐specific mutations in cell‐free plasma DNA

X-linked hypophosphatemic rickets and nephrocalcinosis: clinical characteristics of a single-center pediatric cohort in North America before and after burosumab

Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome

Retinoblastoma: Revisiting the model prototype of inherited cancer

Pediatric second primary malignancies after retinoblastoma treatment

BAP1 germline mutation in two first grade family members with uveal melanoma

A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma

Author Correction: A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma

RB1 gene mutations in retinoblastoma

Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

EFS shows biallelic methylation in uveal melanoma with poor prognosis as well as tissue-specific methylation

Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization

Psychosocial impact of prognostic genetic testing in uveal melanoma patients: a controlled prospective clinical observational study

The impact of RB1 genotype on incidence of second tumours in heritable retinoblastoma

Release of Cell-Free Tumor DNA in the Plasma of Uveal Melanoma Patients Under Radiotherapy

Comparing the Prognostic Value of BAP1 Mutation Pattern, Chromosome 3 Status, and BAP1 Immunohistochemistry in Uveal Melanoma

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