Karin Wadt

Karin Wadt

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Karin Wadt

Karin Wadt

Publications by authors named "Karin Wadt"

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35Publications

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Germline variants in oculocutaneous albinism genes and predisposition to familial cutaneous melanoma.

Pigment Cell Melanoma Res 2019 Nov 6;32(6):854-863. Epub 2019 Jul 6.

QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1111/pcmr.12804DOI Listing
November 2019

Global microRNA profiling of metastatic conjunctival melanoma.

Melanoma Res 2019 Oct;29(5):465-473

Department of Pathology, Eye Pathology Section.

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http://dx.doi.org/10.1097/CMR.0000000000000606DOI Listing
October 2019

A new family with a homozygous nonsense variant in further delineated the clinical phenotype of -associated polyposis.

Hum Genome Var 2019 10;6:46. Epub 2019 Oct 10.

Department of Clinical Genetics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

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http://dx.doi.org/10.1038/s41439-019-0077-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804823PMC
October 2019

The genetic evolution of metastatic uveal melanoma.

Nat Genet 2019 Jul 28;51(7):1123-1130. Epub 2019 Jun 28.

Department of Ophthalmology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

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http://www.nature.com/articles/s41588-019-0440-9
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http://dx.doi.org/10.1038/s41588-019-0440-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6632071PMC
July 2019

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.

Genet Med 2019 Jul 24. Epub 2019 Jul 24.

Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.

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http://dx.doi.org/10.1038/s41436-019-0596-9DOI Listing
July 2019

Novel Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome.

Case Rep Genet 2019 28;2019:9650184. Epub 2019 Jul 28.

Department of Clinical Genetics, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

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http://dx.doi.org/10.1155/2019/9650184DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702821PMC
July 2019

Putative new childhood leukemia cancer predisposition syndrome caused by germline bi-allelic missense mutations in DDX41.

Genes Chromosomes Cancer 2018 12 11;57(12):670-674. Epub 2018 Oct 11.

Department of Clinical Genetics, University Hospital Rigshospitalet, Copenhagen, Denmark.

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http://dx.doi.org/10.1002/gcc.22680DOI Listing
December 2018

Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide.

J Natl Cancer Inst 2018 12;110(12):1328-1341

QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

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http://dx.doi.org/10.1093/jnci/djy171DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292796PMC
December 2018

Pediatric cancer families' participation in whole-genome sequencing research in Denmark: Parent perspectives.

Eur J Cancer Care (Engl) 2018 Nov 17;27(6):e12877. Epub 2018 Jul 17.

Department of Anthropology, University of Copenhagen, Copenhagen, Denmark.

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http://dx.doi.org/10.1111/ecc.12877DOI Listing
November 2018

[A family with a congenital DICER1 mutation].

Ugeskr Laeger 2018 Jun;180(25)

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June 2018

Melanoma genetics.

J Med Genet 2016 Jan 3;53(1):1-14. Epub 2015 Sep 3.

QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1136/jmedgenet-2015-103150DOI Listing
January 2016

High accuracy of family history of melanoma in Danish melanoma cases.

Fam Cancer 2015 Dec;14(4):609-13

Department of Clinical Genetics, 4062, University Hospital of Copenhagen, Blegdamsvej 9, 2100, Copenhagen, Denmark.

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http://dx.doi.org/10.1007/s10689-015-9820-1DOI Listing
December 2015

Germline RAD51B truncating mutation in a family with cutaneous melanoma.

Fam Cancer 2015 Jun;14(2):337-40

Department of Clinical Genetics, Rigshospitalet, 4062, Blegdamsvej 9, 2100, Copenhagen, Denmark,

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http://dx.doi.org/10.1007/s10689-015-9781-4DOI Listing
June 2015

Genetics of familial melanoma: 20 years after CDKN2A.

Pigment Cell Melanoma Res 2015 Mar 5;28(2):148-60. Epub 2015 Jan 5.

QIMR Berghofer Medical Research Institute, Brisbane, Qld, Australia; University of Queensland, Brisbane, Qld, Australia.

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http://dx.doi.org/10.1111/pcmr.12333DOI Listing
March 2015

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

J Natl Cancer Inst 2015 Feb 13;107(2). Epub 2014 Dec 13.

Affiliations of authors: QIMR Berghofer Medical Research Institute, Brisbane, Australia (LGA, ALP, MG, PJ, JMP, JS, VB, SW, KDR, MSS, GWM, NGM, NKH); Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK (CDRE, TMK, DJA); Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark (KW, AMG); Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK (MH, HSn, DTB, JANB); Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD (JC, KMB); Departamento de Bioquímica y Biología Molecular, Instituto Universitario de Oncología del Principado de Asturias (IUOPA) Universidad de Oviedo, Oviedo, Spain (VQ, AJR, CLO); Cancer Genomics Research Laboratory, NCI Frederick, SAIC-Frederick Inc., Frederick MD (XZ, KJ); Department of Dermatology, Leiden University Medical Centre, Leiden, the Netherlands (RvD, NAG); Department of Clinical Sciences Lund, Division of Oncology and Pathology, Lund University, Lund, Sweden (HO, CI, ÅB, GJ); Translational Genomics Institute, Phoenix, AZ (JMT); University of Sydney at Westmead Millennium Institute, Westmead, Sydney, NSW, Australia (EAH, HSc, GJM); Melanoma Institute Australia, North Sydney, NSW, Australia (EAH, HSc, GJM).

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http://dx.doi.org/10.1093/jnci/dju408DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334787PMC
February 2015

[CDKN2A-mutation in a family with hereditary malignant melanoma].

Ugeskr Laeger 2014 Sep;176(40)

Klinisk Genetisk Afdeling, Rigshospitalet, Blegdamsvej 9, 2100 København Ø. E-mail:

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September 2014

A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancers.

PLoS One 2013 19;8(8):e72144. Epub 2013 Aug 19.

Oncogenomics Laboratory, Queensland Institute of Medical Research, Brisbane, Queensland, Australia ; University of Queensland, Brisbane, Queensland, Australia.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0072144PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3747051PMC
April 2014

A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma.

Pigment Cell Melanoma Res 2012 Nov 1;25(6):815-8. Epub 2012 Oct 1.

Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.

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http://dx.doi.org/10.1111/pcmr.12006DOI Listing
November 2012

Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma.

Fam Cancer 2012 Sep;11(3):535-7

Department of Clinical Genetics, Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen, Denmark.

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http://dx.doi.org/10.1007/s10689-012-9542-6DOI Listing
September 2012

[A new genetic diagnosis of familiar gastrointestinal stromal tumour].

Ugeskr Laeger 2012 May;174(21):1462-4

Klinisk Genetisk Afdeling, Rigshospitalet, Blegdamsvej 9, 2100 København Ø.

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May 2012

[The genes disposing to malignant melanoma--a systematic review].

Ugeskr Laeger 2012 Feb;174(8):493-7

Klinisk Genetisk Afdeling 4062, Blegdamsvej 9, Rigshospitalet, 2100 København Ø, Denmark.

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February 2012