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Dislocation density assessment via X-ray GaN rocking curve scans

Physica status solidi. C, 2010-07, Vol.7 (7-8), p.1787-1789

2010

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Quaternary nitride heterostructure field effect transistors

Physica status solidi. C, 2010-07, Vol.7 (7-8), p.2001-2003

2010

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Epitaxy and characterisation of AlInGaN heterostructures for HEMT application

Physica status solidi. C, 2009-06, Vol.6 (S2), p.S470-S473

2009

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MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: a pooled analysis from the M-SKIP project

Cancer management and research, 2018-01, Vol.10, p.1143-1154

2018

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Storage protein accumulation in the absence of the vacuolar processing enzyme family of cysteine proteases

The Plant cell, 2004-01, Vol.16 (1), p.270-290

2004

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Registration of Seville st. Augustinegrass1 (Reg. No. 66)

Crop science, 1980-11, Vol.20 (6), p.824-825

1980

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GNAQ and GNA11 mutations and downstream YAP activation in choroidal nevi

British journal of cancer, 2017-09, Vol.117 (6), p.884-887

2017

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Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non‐CDKN2A/CDK4 melanoma families

International journal of cancer, 2019-05, Vol.144 (10), p.2453-2464

2019

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Magnetic Resonance Imaging Surveillance Detects Early-Stage Pancreatic Cancer in Carriers of a p16-Leiden Mutation

Gastroenterology (New York, N.Y. 1943), 2011-03, Vol.140 (3), p.850-856

2011

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Activation of the MAPK pathway is a common event in uveal melanomas although it rarely occurs through mutation of BRAF or RAS

British journal of cancer, 2005-06, Vol.92 (11), p.2032-2038

2005

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Promoter CpG Island Hypermethylation in Dysplastic Nevus and Melanoma: CLDN11 as an Epigenetic Biomarker for Malignancy

Journal of investigative dermatology, 2014-12, Vol.134 (12), p.2957-2966

2014

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Sun exposure and melanoma risk at different latitudes: a pooled analysis of 5700 cases and 7216 controls

International journal of epidemiology, 2009-06, Vol.38 (3), p.814-830

2009

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Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma

JNCI : Journal of the National Cancer Institute, 2015-02, Vol.107 (2), p.1

2015

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CM-Score: a validated scoring system to predict CDKN2A germline mutations in melanoma families from Northern Europe

Journal of medical genetics, 2018-10, Vol.55 (10), p.661

2018

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A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor Types

Science (American Association for the Advancement of Science), 1994-04, Vol.264 (5157), p.436-440

1994

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Loss of Wild-Type CDKN2A Is an Early Event in the Development of Melanoma in FAMMM Syndrome

Journal of investigative dermatology, 2020-11, Vol.140 (11), p.2298-2301.e3

2020

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Melanocortin-1 Receptor Gene Variants Determine the Risk of Nonmelanoma Skin Cancer Independently of Fair Skin and Red Hair

American journal of human genetics, 2001-04, Vol.68 (4), p.884-894

2001

Volltextzugriff (PDF)

MC1R variants in relation to naevi in melanoma cases and controls: a pooled analysis from the M‐SKIP project

Journal of the European Academy of Dermatology and Venereology, 2021-02, Vol.35 (2), p.e135-e138

2021

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Increased Risk of Cancer Other Than Melanoma in CDKN2A Founder Mutation (p16-Leiden)-Positive Melanoma Families

Clinical cancer research, 2008-11, Vol.14 (21), p.7151-7157

2008

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Predictors of Sun Protection Behaviors and Severe Sunburn in an International Online Study

Cancer epidemiology, biomarkers & prevention, 2010-09, Vol.19 (9), p.2199-2210

2010

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Cutaneous melanoma: Medical specialists' opinions on follow-up and sentinel lymph node biopsy

European journal of surgical oncology, 2014-10, Vol.40 (10), p.1276-1283

2014

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Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma

Journal of medical genetics, 2021-11, Vol.58 (11), p.760

2021

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Registration of Seville St. Augustinegrass: (Reg. No. 66) [Stenotaphrum secundatum, cultivars]

Crop science, 1980, Vol.20

1980

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Dislocation density assessment via X-ray GaN rocking curve scans

Quaternary nitride heterostructure field effect transistors

Epitaxy and characterisation of AlInGaN heterostructures for HEMT application

MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: a pooled analysis from the M-SKIP project

Storage protein accumulation in the absence of the vacuolar processing enzyme family of cysteine proteases

Registration of Seville st. Augustinegrass1 (Reg. No. 66)

GNAQ and GNA11 mutations and downstream YAP activation in choroidal nevi

Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non‐CDKN2A/CDK4 melanoma families

POT1 loss-of-function variants predispose to familial melanoma

Magnetic Resonance Imaging Surveillance Detects Early-Stage Pancreatic Cancer in Carriers of a p16-Leiden Mutation

Activation of the MAPK pathway is a common event in uveal melanomas although it rarely occurs through mutation of BRAF or RAS

Promoter CpG Island Hypermethylation in Dysplastic Nevus and Melanoma: CLDN11 as an Epigenetic Biomarker for Malignancy

Sun exposure and melanoma risk at different latitudes: a pooled analysis of 5700 cases and 7216 controls

Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma

CM-Score: a validated scoring system to predict CDKN2A germline mutations in melanoma families from Northern Europe

A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor Types

Loss of Wild-Type CDKN2A Is an Early Event in the Development of Melanoma in FAMMM Syndrome

Melanocortin-1 Receptor Gene Variants Determine the Risk of Nonmelanoma Skin Cancer Independently of Fair Skin and Red Hair

MC1R variants in relation to naevi in melanoma cases and controls: a pooled analysis from the M‐SKIP project

Increased Risk of Cancer Other Than Melanoma in CDKN2A Founder Mutation (p16-Leiden)-Positive Melanoma Families

Predictors of Sun Protection Behaviors and Severe Sunburn in an International Online Study

Cutaneous melanoma: Medical specialists' opinions on follow-up and sentinel lymph node biopsy

Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma

MC1R variants increased the risk of sporadic cutaneous melanoma in darker‐pigmented Caucasians: A pooled‐analysis from the M‐SKIP project

Registration of Seville St. Augustinegrass: (Reg. No. 66) [Stenotaphrum secundatum, cultivars]

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