(Q99243096)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

title

Cytogenetically visible inversions are formed by multiple molecular mechanisms (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

Amy M Breman

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

Christopher M Grochowski

object named as

Christopher M Grochowski

1 reference

12 September 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

Sau Wai Cheung

object named as

Sau Wai Cheung

1 reference

12 September 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

Josephine Wincent

object named as

Josephine Wincent

1 reference

12 September 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

author name string

Ana Cristina Victorino Krepischi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

Carla Rosenberg

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

Jesper Ottosson

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

Lovisa Lovmar

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

Jelena Gacic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

Elisabeth Syk Lundberg

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

Daniel Nilsson

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

publication date

9 September 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

12 September 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32906200%20AND%20SRC:MED&resulttype=core&format=json

CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

12 September 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

MECP2 duplications in six patients with complex sex chromosome rearrangements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Evidence for disease penetrance relating to CNV size: Pelizaeus-Merzbacher disease and manifesting carriers with a familial 11 Mb duplication at Xq22

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Mechanisms underlying structural variant formation in genomic disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Replicative mechanisms for CNV formation are error prone

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Absence of heterozygosity due to template switching during replicative rearrangements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Multi-platform discovery of haplotype-resolved structural variation in human genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

A structural variation reference for medical and population genetics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Recurrent DNA inversion rearrangements in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Chromosomal translocations in human cells are generated by canonical nonhomologous end-joining.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among northern Europeans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

A microhomology-mediated break-induced replication model for the origin of human copy number variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Pericentric inversions. Problems and significance for clinical genetics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

BLAT—The BLAST-Like Alignment Tool

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Mapping and sequencing of structural variation from eight human genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Tabix: fast retrieval of sequence features from generic TAB-delimited files

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

The Sequence Alignment/Map format and SAMtools

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

The Ensembl Variant Effect Predictor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridization

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Human inversions and their functional consequences

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Integrative genomics viewer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Segregation analysis of balanced pericentric inversions in pedigree data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

An integrated map of structural variation in 2,504 human genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Familial pericentric inversion of chromosome 12.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Human Structural Variation: Mechanisms of Chromosome Rearrangements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

ggplot2: Elegant Graphics for Data Analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

Comparative Genomic Analyses of the Human NPHP1 Locus Reveal Complex Genomic Architecture and Its Regional Evolution in Primates.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021

The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.24106

7 January 2021