Literature DB >> 34983941

The simplest explanation does not have to be preferred: co-occurrence of pathogenic variants in cancer-predisposing genes.

Sergi Castellví-Bel1.   

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Year:  2022        PMID： 34983941      PMCID： PMC8904836          DOI： 10.1038/s41431-021-01031-4

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN： 1018-4813            Impact factor:   4.246


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  5 in total

Review 1.  Sequencing technologies - the next generation.

Authors:  Michael L Metzker
Journal:  Nat Rev Genet       Date:  2009-12-08       Impact factor: 53.242

2.  Digenic inheritance and Mendelian disease.

Authors:  James R Lupski
Journal:  Nat Genet       Date:  2012-12       Impact factor: 38.330

Review 3.  Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and Review.

Authors:  James Whitworth; Anne-Bine Skytte; Lone Sunde; Derek H Lim; Mark J Arends; Lisa Happerfield; Ian M Frayling; Rick van Minkelen; Emma R Woodward; Marc D Tischkowitz; Eamonn R Maher
Journal:  JAMA Oncol       Date:  2016-03       Impact factor: 31.777

4.  The repertoire of mutational signatures in human cancer.

Authors:  Ludmil B Alexandrov; Jaegil Kim; Gad Getz; Steven G Rozen; Michael R Stratton; Nicholas J Haradhvala; Mi Ni Huang; Alvin Wei Tian Ng; Yang Wu; Arnoud Boot; Kyle R Covington; Dmitry A Gordenin; Erik N Bergstrom; S M Ashiqul Islam; Nuria Lopez-Bigas; Leszek J Klimczak; John R McPherson; Sandro Morganella; Radhakrishnan Sabarinathan; David A Wheeler; Ville Mustonen
Journal:  Nature       Date:  2020-02-05       Impact factor: 49.962

Review 5.  Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update.

Authors:  Anthony McGuigan; James Whitworth; Avgi Andreou; Timothy Hearn; Marc Tischkowitz; Eamonn R Maher
Journal:  Eur J Hum Genet       Date:  2022-01-04       Impact factor: 4.246
  5 in total

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