Search filters

List of works by Michael Stratton

A 45-year follow-up of kindred 107 and the search for BRCA2

scientific article published on 01 January 1995

A case of cerebellar medulloblastoma with a single chromosome abnormality.

scientific article published in May 1991

A census of amplified and overexpressed human cancer genes

scientific article

A census of human cancer genes

scientific article

A common coding variant in CASP8 is associated with breast cancer risk

article

A comprehensive catalogue of somatic mutations from a human cancer genome

scientific article

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

scientific article

A gene for lymphedema-distichiasis maps to 16q24.3.

scientific article

A genome wide linkage search for breast cancer susceptibility genes

scientific article published on July 2006

A genome-wide association study of testicular germ cell tumor

scientific article

A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome

scientific article (publication date: October 1992)

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

scientific article

A missense mutation in the BRCA2 gene in three siblings with ovarian cancer

scientific article

A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers

scientific article published on December 2006

A mutational signature in gastric cancer suggests therapeutic strategies

scientific article published on 29 October 2015

A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A.

scientific article

A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencing

scientific article

A physical analysis of the Y chromosome shows no additional deletions, other than Gr/Gr, associated with testicular germ cell tumour

scientific article published on 9 January 2007

A polymorphic stop codon in BRCA2

scientific article published on 01 November 1996

A proteomic chronology of gene expression through the cell cycle in human myeloid leukemia cells

scientific article (publication date: 2014)

A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer

scientific article published on 22 May 2005

A small-cell lung cancer genome with complex signatures of tobacco exposure

scientific article

A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers

scientific article published on 23 January 2017

A survey of RNA editing in human brain

scientific article

A survey of homozygous deletions in human cancer genomes

scientific article

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

scientific article

A whole-genome sequence and transcriptome perspective on HER2-positive breast cancers

scientific article published on 13 July 2016

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

scientific article

Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22

article

Absence of linkage to the ataxia telangiectasia locus in familial breast cancer

scientific article published in August 1993

Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers ⬇️

scientific article published on January 1, 1997

Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells

scientific article published on 3 January 2018

Allelotype of uterine leiomyomas

scientific article published on 01 October 1999

Analysis of the DND1 gene in men with sporadic and familial testicular germ cell tumors

scientific article

Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

scientific article

Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

scientific article

Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer

scientific article

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

scientific article

Atypical ductal hyperplasia of the breast: clonal proliferation with loss of heterozygosity on chromosomes 16q and 17p.

scientific article published on July 1995

Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences

scientific article published on 01 February 2019

Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors

scientific article published in Nature Communications

Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors

scholarly article published in Nature Communications

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

scientific article published on 7 May 2007

BHPR research: qualitative * 1. Complex reasoning determines patients' perception of outcome following foot surgery in rheumatoid arhtritis

scientific article published on 3 April 2012

BLUEPRINT to decode the epigenetic signature written in blood.

scientific article

BRAF gene is somatically mutated but does not make a major contribution to malignant melanoma susceptibility: the Italian Melanoma Intergroup Study

scientific article

BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers

article published in 2000

BRCA2 mutations in primary breast and ovarian cancers

scientific article

Bayesian refinement of association signals for 14 loci in 3 common diseases

scientific article published on 28 October 2012

Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour

scientific article published in February 2005

C. elegans whole-genome sequencing reveals mutational signatures related to carcinogens and DNA repair deficiency

scientific article

CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes

scientific article

COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer

scientific article

COSMIC 2005

scientific article

COSMIC: exploring the world's knowledge of somatic mutations in human cancer

scientific article (publication date: 2015)

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

scientific article

COSMIC: the catalogue of somatic mutations in cancer.

scientific article published on 19 September 2011

Cancer Risks in Two Large Breast Cancer Families Linked to BRCA2 on Chromosome 13q12‐13 ⬇️

scientific article published on July 1, 1997

Cancer and genomics

scientific article

Cancer: understanding the target

scientific article published in July 2004

Case of interstitial 12q deletion in association with Wilms tumor

Case of interstitial 12q deletion in association with Wilms tumor

Characterization of the human cell line TE671.

scientific article published on May 1989

Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis

Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancers

scientific article published on 21 May 2007

Clinical and biological implications of driver mutations in myelodysplastic syndromes

scientific article published on 12 September 2013

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

scientific article

Clock-like mutational processes in human somatic cells

scientific article published on 9 November 2015

Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene

scientific article

Combinations of PARP Inhibitors with Temozolomide Drive PARP1 Trapping and Apoptosis in Ewing's Sarcoma

scientific article

Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

scientific article

Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population

scientific article published on 01 February 1997

Complex landscapes of somatic rearrangement in human breast cancer genomes

scientific article

Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1

scientific article (publication date: November 1998)

Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findings

article

Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene

scientific article

Corrigendum: A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers

scientific article published in October 2017

Corrigendum: Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

scientific article published in Nature

Corrigendum: Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells

scientific article published on May 2016

DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome

scientific article

DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis

scientific article

Data mining using the Catalogue of Somatic Mutations in Cancer BioMart

scientific article

Deciphering signatures of mutational processes operative in human cancer

scientific article

Decoding the fine-scale structure of a breast cancer genome and transcriptome

scientific article

Detection of allelic imbalance indicates that a proportion of mammary hyperplasia of usual type are clonal, neoplastic proliferations.

scientific article

Detection of point mutations in N-ras and K-ras genes of human embryonal rhabdomyosarcomas using oligonucleotide probes and the polymerase chain reaction.

scientific article published in November 1989

Detection of transforming genes by transfection of DNA from primary soft-tissue tumours

scientific article published on September 1991

Dinucleotide repeat polymorphism at the SIS locus

scientific article published on October 1990

Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer

scientific article published on 03 August 2016

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

scientific article

Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone

scientific article

Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridization

scientific article published on September 2005

Does a genotoxic carcinogen contribute to human breast cancer? The value of mutational spectra in unravelling the aetiology of cancer.

scientific article

Embryonal precursors of Wilms tumor

scientific article published on 01 December 2019

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families

scientific article

Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk

scholarly article published in Nature Genetics

Erratum: Corrigendum: Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

scholarly article by Colin S Cooper et al published June 2015 in Nature Genetics

Erratum: Corrigendum: Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone

scholarly article published in Nature Genetics

Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

scholarly article published in Nature Genetics

Erratum: Corrigendum: Signatures of mutational processes in human cancer

scientific article published in Nature

Erratum: Identification of the breast cancer susceptibility gene BRCA2

scientific article published in Nature

Estimation of rearrangement phylogeny for cancer genomes

scientific article

Estrogen Receptor Status Could Modulate the Genomic Pattern in Familial and Sporadic Breast Cancer

Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium

scientific article

Evaluation ofRAD50 in familial breast cancer predisposition

Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21

scientific article (publication date: August 1996)

Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2

scientific article published on July 2000

Exclusion of biglycan mutations in a cohort of patients with neuromuscular disorders

scientific article

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

scientific article

Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets

scientific article

Exploring the Genomes of Cancer Cells: Progress and Promise ⬇️

scientific article published on March 25, 2011

Extensive heterogeneity in somatic mutation and selection in the human bladder

scientific article published on 01 October 2020

Familial cancer syndromes

scientific article published in The Lancet

Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism

scientific article published in November 2000

Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene

scientific article

Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q.

scientific article

Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer

scientific article

Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one family

scientific article published in April 1999

Feedback circuit among INK4 tumor suppressors constrains human glioblastoma development

scientific article

Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability

scientific article

Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes

scientific article

Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma

scientific article published on 16 June 2013

Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells

scientific article published on 11 May 2015

GLO1-A novel amplified gene in human cancer

scientific article

Gene-gene interactions in breast cancer susceptibility

scientific article

Genetic alterations in 'normal' luminal and myoepithelial cells of the breast

scientific article published on 01 December 1999

Genetic heterogeneity and localization of a familial breast-ovarian cancer gene on chromosome 17q12-q21

scientific article

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

scientific article (publication date: March 1998)

Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer

scientific article published in February 2012

Genome sequencing of normal cells reveals developmental lineages and mutational processes

scientific article published on 29 June 2014

Genome-wide association study identifies five new breast cancer susceptibility loci

scientific article

Genome-wide association study identifies novel breast cancer susceptibility loci

scientific article published on 28 June 2007

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

scientific article

Genome-wide linkage screen for testicular germ cell tumour susceptibility loci

scientific article published on 11 January 2006

Genome-wide mutational signatures of aristolochic acid and its application as a screening tool

scientific article

Genome-wide screening for complete genetic loss in prostate cancer by comparative hybridization onto cDNA microarrays

scientific article published on February 2003

Genomic Evolution of Breast Cancer Metastasis and Relapse

scientific article published on August 2017

Genomic architecture characterizes tumor progression paths and fate in breast cancer patients

scientific article published on June 2010

Genomics and the continuum of cancer care

scientific article published on January 2011

Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells

scientific article

Germline mutations in BRCA1 and BRCA2 in breast-ovarian families from a breast cancer risk evaluation clinic

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

article

HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease

scientific article published on October 2002

HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures

scientific article published on 13 March 2017

Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

scientific article

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study

scientific article published in February 1996

Hereditary predisposition to breast cancer

scientific article published on February 1996

Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients ⬇️

scientific article published on October 1, 1998

High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison

scientific article

High-resolution analysis of DNA copy number using oligonucleotide microarrays

scientific article published on February 2004

High-throughput epitope discovery reveals frequent recognition of neo-antigens by CD4+ T cells in human melanoma

scientific article published on 22 December 2014

Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome

scientific article

Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation

scientific article

Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation.

scientific article published on 16 August 2012

Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14

scientific article published on 12 May 2013

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

scientific article

Imidazopurinones are markers of physiological genomic damage linked to DNA instability and glyoxalase 1-associated tumour multidrug resistance

scientific article

In vitro differential sensitivity of melanomas to phenothiazines is based on the presence of codon 600 BRAF mutation

scientific article published on 04 June 2008

International network of cancer genome projects

scientific article

JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis

scientific article

Journeys into the genome of cancer cells ⬇️

scientific article published on January 22, 2013

LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition

scientific article published in January 2009

Landscape of somatic mutations in 560 breast cancer whole-genome sequences

scientific article

Lessons learnt from large-scale exon re-sequencing of the X chromosome

scientific article published on April 2009

Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancer.

scientific article published in September 1999

Lobular carcinoma in situ of the breast is not caused by constitutional mutations in the E-cadherin gene

scientific article published on February 2000

Localisation of susceptibility genes for familial testicular germ cell tumour

scientific article published in January 2003

Localisation of the breast-ovarian cancer susceptibility gene (BRCAI) on 17q12–21 to an interval of IcM

article

Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours

scientific article

Loss of heterozygosity in ductal carcinoma in situ of the breast.

scientific article published in February 1995

Loss of heterozygosity in lobular carcinoma in situ of the breast

scientific article

Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13.

scientific article

Loss of the mismatch repair protein MSH6 in human glioblastomas is associated with tumor progression during temozolomide treatment

scientific article

Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer ⬇️

scientific article published on April 1, 1998

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

scientific article (publication date: May 2002)

Lung cancer: intragenic ERBB2 kinase mutations in tumours

scientific article

Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro

scientific article published on 02 December 2021

Massive genomic rearrangement acquired in a single catastrophic event during cancer development

scientific article

Mining cancer genomes in COSMIC.

scientific article published in October 2012

Misidentified cell

scientific article published on January 1989

Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes

scientific article

Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25 ⬇️

scientific article

Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations

scientific article published in August 1998

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.

scientific article

Mutation and association analysis of GEN1 in breast cancer susceptibility

scientific article published on 30 May 2010

Mutation of the p53 gene in human soft tissue sarcomas: association with abnormalities of the RB1 gene

scientific article published in September 1990

Mutational processes molding the genomes of 21 breast cancers

scientific article

Mutational signatures associated with tobacco smoking in human cancer

Mutational signatures of ionizing radiation in second malignancies

scientific article

Mutational signatures: the patterns of somatic mutations hidden in cancer genomes

scientific article

Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor

scientific article

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

scientific article

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

scientific article

Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus

scientific article

Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly

scientific article

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation

scientific article

Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation

scientific article

Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation

scientific article

Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability

scientific article

Mutations in the p53 gene in schistosomal bladder cancer: a study of 92 tumours from Egyptian patients and a comparison between mutational spectra from schistosomal and non-schistosomal urothelial tumours

scientific article published on May 1995

Mutations of the BRAF gene in human cancer

scientific article (publication date: 27 June 2002)

Natural history of Christianson syndrome ⬇️

scientific article published on 01 November 2010

Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

scientific article published on 29 March 2009

Novel candidate cancer genes identified by a large-scale cross-species comparative oncogenomics approach

scientific article

Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation

scientific article

Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer

scientific article

Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus

scientific article published on 01 March 1996

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

scientific article

PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data

scientific article

Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors.

scientific article published on 31 October 2017

Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation

article

Patterns of somatic mutation in human cancer genomes

scientific article (publication date: 8 March 2007)

Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype

scientific article published on July 2005

Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer

scientific article published on 18 April 2012

Processed pseudogenes acquired somatically during cancer development

scientific article published on 09 April 2014

RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia

scientific article

RNA editing of human microRNAs

scientific article published on 4 April 2006

Rapid detection of DNA sequence variants by conformation-sensitive capillary electrophoresis

scientific article published in November 2000

Recurrent KRAS codon 146 mutations in human colorectal cancer

scientific article published on August 2006

Recurrent PTPRB and PLCG1 mutations in angiosarcoma

scientific article

Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma

scientific article

Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes

scientific article

SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome

scientific article published on 13 March 2008

Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families

scientific article published on January 2000

Screening for ESR mutations in breast and ovarian cancer patients

scientific article published on 01 January 1997

Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults

scientific article

Short inverted repeats contribute to localized mutability in human somatic cells

scientific article published on 22 August 2017

Signatures of mutation and selection in the cancer genome

scientific article

Signatures of mutational processes in human cancer

scientific article (publication date: 22 August 2013)

Single-cell paired-end genome sequencing reveals structural variation per cell cycle

scientific article

Somatic KIT mutations occur predominantly in seminoma germ cell tumors and are not predictive of bilateral disease: report of 220 tumors and review of literature

scientific article published on January 2008

Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts

scientific article

Somatic evolution and global expansion of an ancient transmissible cancer lineage

scientific article

Somatic mutant clones colonize the human esophagus with age

scientific article

Somatic mutations of KIT in familial testicular germ cell tumours

scientific article published on June 2004

Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

scientific article

Somatic mutations of the protein kinase gene family in human lung cancer

scientific article published on September 2005

Somatic mutations reveal asymmetric cellular dynamics in the early human embryo

scientific article

Somatic structural rearrangements in genetically engineered mouse mammary tumors

scientific article

Statistical analysis of pathogenicity of somatic mutations in cancer

scientific article

Structural alterations of the RB1 gene in human soft tissue tumours

scientific article

Structure of the met protein and variation of met protein kinase activity among human tumour cell lines

scientific article published in July 1988

Subclonal diversification of primary breast cancer revealed by multiregion sequencing

scientific article published on 22 June 2015

Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing

scholarly article

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation

scientific article published on 24 January 2008

Systematic identification of genomic markers of drug sensitivity in cancer cells

scientific article (publication date: 28 March 2012)

Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes

scientific article

THE GENETICS OF BREAST CANCER SUSCEPTIBILITY

article

Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes

scientific article

Testicular microlithiasis as a familial risk factor for testicular germ cell tumour

scientific article published on 30 October 2007

The BRC repeats are conserved in mammalian BRCA2 proteins

scientific article

The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website

scientific article

The Catalogue of Somatic Mutations in Cancer (COSMIC)

scientific article

The Human Cell Atlas

scientific article

The Human Cell Atlas

The Human Cell Atlas White Paper ⬇️

journal article from 'arXiv:1810.05192 [q-bio]' published in 2018

The International Testicular Cancer Linkage Consortium: a clinicopathologic descriptive analysis of 461 familial malignant testicular germ cell tumor kindred

scientific article

The Life History of 21 Breast Cancers

The Repertoire of Mutational Signatures in Human Cancer

The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders

scientific article

The Y deletion gr/gr and susceptibility to testicular germ cell tumor

scientific article

The cancer genome

scientific article (publication date: 9 April 2009)

The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromas

scientific article

The driver landscape of sporadic chordoma

scientific article published on 12 October 2017

The emerging landscape of breast cancer susceptibility

The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor gene

article

The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer. The Cancer Research Campaign/British Prostate Group United Kingdom Familial Prostate Cancer Study Collaborators

article

The genetics of familial breast cancer and their practical implications

scientific article published on January 1994

The genome as a record of environmental exposure

scientific article published on 6 October 2015

The genomic landscape of cutaneous SCC reveals drivers and a novel azathioprine associated mutational signature

scientific article published in Nature Communications

The landscape of cancer genes and mutational processes in breast cancer

scientific article (publication date: 16 May 2012)

The life history of 21 breast cancers

scientific article (publication date: 25 May 2012)

The mutational landscape of normal human endometrial epithelium

scientific article published on 22 April 2020

The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

scientific article published on 16 March 2007

The patterns and dynamics of genomic instability in metastatic pancreatic cancer

scientific article (publication date: 28 October 2010)

The topography of mutational processes in breast cancer genomes

scientific article published on 02 May 2016

Timing, rates and spectra of human germline mutation

scientific article published on 14 December 2015

Tissue-specific mutation accumulation in human adult stem cells during life

scientific article published on 3 October 2016

Transmissible [corrected] dog cancer genome reveals the origin and history of an ancient cell lineage

scientific article

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

article

Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skin

scientific article

Universal Patterns Of Selection In Cancer And Somatic Tissues

Universal Patterns of Selection in Cancer and Somatic Tissues

scientific article published on 18 October 2017

Universal Patterns of Selection in Cancer and Somatic Tissues.

scientific article published in June 2018

Use of cancer-specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors

scientific article

Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes ⬇️

scientific article published on February 1, 1998

Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility

scientific article

Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer

scientific article

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene

scientific article published on 01 January 1997

Whole exome sequencing of adenoid cystic carcinoma

scientific article published on 17 June 2013

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

scientific article

Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency

scientific article

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

scientific article (publication date: 5 June 2011)

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

scientific article

Younger age-at-diagnosis for familial malignant testicular germ cell tumor

scientific article

Paulina is supported by:

About Paulina

Help