Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland. (Q64895719)

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English	Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland.	scientific article

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scholarly article

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Europe PubMed Central

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30 June 2019

http://europepmc.org/abstract/PMC/6333986

Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland. (English)

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Europe PubMed Central

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30 June 2019

http://europepmc.org/abstract/PMC/6333986

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Cezary Cybulski

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Cezary Cybulski

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http://europepmc.org/abstract/PMC/6333986

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Jan Lubiński

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http://europepmc.org/abstract/PMC/6333986

Romuald Maleszka

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Romuald Maleszka

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http://europepmc.org/abstract/PMC/6333986

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Dawid Murawa

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http://europepmc.org/abstract/PMC/6333986

Tadeusz Dębniak

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Tadeusz Dębniak

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Bohdan Górski

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Andrzej Kram

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Tomasz Gromowski

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Tomasz Gromowski

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http://europepmc.org/abstract/PMC/6333986

Aniruddh Kashyap

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Aniruddh Kashyap

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http://europepmc.org/abstract/PMC/6333986

Bartłomiej Masojć

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Bartłomiej Masojć

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http://europepmc.org/abstract/PMC/6333986

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Marcin R Lener

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http://europepmc.org/abstract/PMC/6333986

Helena Rudnicka

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Helena Rudnicka

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Katarzyna Paszkowska-Szczur

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Katarzyna Paszkowska-Szczur

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Jakub Deptuła

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author name string

Rodney J Scott

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Karolina Malińska

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Emilia Rogoża

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publication date

14 May 2018

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Cancer Research and Treatment

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http://europepmc.org/abstract/PMC/6333986

51

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1

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http://europepmc.org/abstract/PMC/6333986

337-344

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30 June 2019

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copyright license

Creative Commons Attribution-NonCommercial 3.0 Unported

14 May 2018

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April 2022 Public Data File from Crossref

copyright status

0 references

Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents

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Improved human disease candidate gene prioritization using mouse phenotype

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Fast and accurate short read alignment with Burrows-Wheeler transform

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https://pubmed.ncbi.nlm.nih.gov/29764119

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The Sequence Alignment/Map format and SAMtools

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Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

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https://pubmed.ncbi.nlm.nih.gov/29764119

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Genome-wide association study identifies novel loci predisposing to cutaneous melanoma

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Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

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Genome-wide association study identifies three new melanoma susceptibility loci

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Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/29764119

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TERT promoter mutations in familial and sporadic melanoma

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A variant in FTO shows association with melanoma risk not due to BMI

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Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012

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

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Accurate de novo and transmitted indel detection in exome-capture data using microassembly

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

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Germline RAD51B truncating mutation in a family with cutaneous melanoma

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Analysis of BAP1 Germline Gene Mutation in Young Uveal Melanoma Patients

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Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/29764119

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inferred from PubMed ID database lookup

POLE mutations in families predisposed to cutaneous melanoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/29764119

12 December 2020

based on heuristic

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Familial Risk and Heritability of Cancer Among Twins in Nordic Countries

1 reference

https://pubmed.ncbi.nlm.nih.gov/29764119

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.4143/CRT.2018.157

1 reference

Europe PubMed Central

PMC publication ID

30 June 2019

http://europepmc.org/abstract/PMC/6333986

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

30 June 2019

http://europepmc.org/abstract/PMC/6333986

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

30 June 2019

http://europepmc.org/abstract/PMC/6333986

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