Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations (Q57178727)

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6 April 2020

title

Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations (English)

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6 April 2020

1 reference

3

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6 April 2020

Brenda M Birmann

7

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6 April 2020

author name string

Po-Ru Loh

1

1 reference

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6 April 2020

Giulio Genovese

2

1 reference

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6 April 2020

Hilary K Finucane

4

1 reference

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6 April 2020

Yakir A Reshef

5

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6 April 2020

Pier Francesco Palamara

6

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6 April 2020

Michael E Talkowski

8

1 reference

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6 April 2020

Samuel F Bakhoum

9

1 reference

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6 April 2020

Steven A McCarroll

10

1 reference

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6 April 2020

Alkes L Price

11

1 reference

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6 April 2020

language of work or name

English

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publication date

11 July 2018

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6 April 2020

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6 April 2020

volume

559

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issue

7714

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6 April 2020

page(s)

350-355

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Landscape of X chromosome inactivation across human tissues

6 April 2020

cites work

1 reference

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Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life

2 November 2018

1 reference

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Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular Disease.

2 November 2018

1 reference

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Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly

2 November 2018

1 reference

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Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility

2 November 2018

1 reference

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Mosaicism in health and disease - clones picking up speed

2 November 2018

1 reference

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Reference-based phasing using the Haplotype Reference Consortium panel

2 November 2018

1 reference

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Next-generation genotype imputation service and methods

2 November 2018

1 reference

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Clonal haematopoiesis harbouring AML-associated mutations is ubiquitous in healthy adults

2 November 2018

1 reference

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Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms

2 November 2018

1 reference

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Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

2 November 2018

1 reference

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Fast and accurate long-range phasing in a UK Biobank cohort

2 November 2018

1 reference

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Developing and evaluating polygenic risk prediction models for stratified disease prevention

2 November 2018

1 reference

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The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia

2 November 2018

1 reference

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Mosaic loss of chromosome Y is associated with common variation near TCL1A

2 November 2018

1 reference

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Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia

2 November 2018

1 reference

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Extensive Hidden Genomic Mosaicism Revealed in Normal Tissue

2 November 2018

1 reference

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Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

2 November 2018

1 reference

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Mutations driving CLL and their evolution in progression and relapse

2 November 2018

1 reference

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Tools and best practices for data processing in allelic expression analysis

2 November 2018

1 reference

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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

2 November 2018

1 reference

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Non-coding recurrent mutations in chronic lymphocytic leukaemia

2 November 2018

1 reference

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Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locus

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age

2 November 2018

1 reference

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Characterization of large structural genetic mosaicism in human autosome

2 November 2018

1 reference

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Leukemia-associated somatic mutations drive distinct patterns of age-related clonal hemopoiesis

2 November 2018

1 reference

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Second-generation PLINK: rising to the challenge of larger and richer datasets

2 November 2018

1 reference

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Efficient Bayesian mixed-model analysis increases association power in large cohorts.

2 November 2018

1 reference

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Mutagenesis. Smoking is associated with mosaic loss of chromosome Y.

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence

2 November 2018

1 reference

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2 November 2018

1 reference

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Genetic variation in human DNA replication timing

2 November 2018

1 reference

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2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

Monoclonal B-cell lymphocytosis is characterized by mutations in CLL putative driver genes and clonal heterogeneity many years before disease progression

2 November 2018

1 reference

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The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

2 November 2018

1 reference

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Cumulative haploinsufficiency and triplosensitivity drive aneuploidy patterns and shape the cancer genome

2 November 2018

1 reference

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Transcriptome and genome sequencing uncovers functional variation in humans

2 November 2018

1 reference

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Evolution and impact of subclonal mutations in chronic lymphocytic leukemia

2 November 2018

1 reference

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Haplotype-based profiling of subtle allelic imbalance with SNP arrays

2 November 2018

1 reference

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The life history of 21 breast cancers

2 November 2018

1 reference

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Detectable clonal mosaicism and its relationship to aging and cancer

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

Detectable clonal mosaicism from birth to old age and its relationship to cancer

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

2 November 2018

1 reference

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Estimating missing heritability for disease from genome-wide association studies

2 November 2018

1 reference

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The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors

2 November 2018

1 reference

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Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations in KRT10

2 November 2018

1 reference

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InterLymph hierarchical classification of lymphoid neoplasms for epidemiologic research based on the WHO classification (2008): update and future directions

2 November 2018

1 reference

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R-Gada: a fast and flexible pipeline for copy number analysis in association studies

2 November 2018

1 reference

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Improved IBD detection using incomplete haplotype information

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

The landscape of somatic copy-number alteration across human cancers

2 November 2018

1 reference

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Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

A common JAK2 haplotype confers susceptibility to myeloproliferative neoplasms.

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

B-cell clones as early markers for chronic lymphocytic leukemia

2 November 2018

1 reference

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Whole population, genome-wide mapping of hidden relatedness

2 November 2018

1 reference

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Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

2 November 2018

1 reference

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Monoclonal B-cell lymphocytosis and chronic lymphocytic leukemia

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

2 November 2018

1 reference

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Circular binary segmentation for the analysis of array-based DNA copy number data

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis.

2 November 2018

1 reference

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Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

2 November 2018

1 reference

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Thrombocytopenia in c-mpl-deficient mice

2 November 2018

1 reference

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Heritable fragile sites on human chromosomes. V. A new class of fragile site requiring BrdU for expression

2 November 2018

1 reference

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Dynamic mutations: a new class of mutations causing human disease

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6054542

Mosaic chromosome 20q deletions are more frequent in the aging population

2 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FS41586-018-0321-X

inferred from DOI database lookup

7 January 2021

based on heuristic

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FS41586-018-0321-X

inferred from DOI database lookup

7 January 2021

based on heuristic

Trisomy 15 associated with loss of the Y chromosome in bone marrow: a possible new aging effect

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FS41586-018-0321-X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/S41586-018-0321-X

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29995854%20AND%20SRC:MED&resulttype=core&format=json

journals/nature/LohGHFRPBTBMP18

6 April 2020

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29995854%20AND%20SRC:MED&resulttype=core&format=json

6 April 2020

PubMed publication ID

29995854

1 reference