(Q34165506)

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Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

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Europe PubMed Central

PubMed publication ID

31 July 2017

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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deep vein thrombosis

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based on heuristic

inferred from title

object named as

Jin Yu

3

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Serena M. Passamonti

object named as

Serena M Passamonti

6

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object named as

Luca A Lotta

1

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object named as

Ida Martinelli

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object named as

Dario Consonni

7

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object named as

Flora Peyvandi

18

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Pier Mannuccio Mannucci

16

object named as

Pier M Mannucci

1 reference

Europe PubMed Central

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31 July 2017

15

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Donna M Muzny

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Europe PubMed Central

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31 July 2017

Emanuela Pappalardo

8

object named as

Emanuela Pappalardo

1 reference

Europe PubMed Central

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31 July 2017

Richard A Gibbs

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object named as

Richard A Gibbs

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11

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Lora L Lewis

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31 July 2017

author name string

Mark Wang

2

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31 July 2017

Fuli Yu

5

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Europe PubMed Central

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31 July 2017

Marzia Menegatti

9

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Europe PubMed Central

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31 July 2017

Steven E Scherer

10

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Europe PubMed Central

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31 July 2017

Humeira Akbar

12

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Europe PubMed Central

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31 July 2017

Yuanqing Wu

13

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31 July 2017

Matthew N Bainbridge

14

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31 July 2017

publication date

21 February 2012

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31 July 2017

BMC Medical Genomics

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31 July 2017

5

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Europe PubMed Central

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31 July 2017

7

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Europe PubMed Central

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31 July 2017

Phased whole-genome genetic risk in a family quartet using a major allele reference sequence

1 reference

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5 July 2018

Delineating the Hemostaseome as an aid to individualize the analysis of the hereditary basis of thrombotic and bleeding disorders

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5 July 2018

Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis

1 reference

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5 July 2018

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

1 reference

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5 July 2018

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing.

1 reference

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5 July 2018

A map of human genome variation from population-scale sequencing

1 reference

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5 July 2018

A common variant in the Von Willebrand factor gene is associated with multiple functional consequences.

1 reference

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5 July 2018

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

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A method and server for predicting damaging missense mutations

1 reference

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5 July 2018

A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

5 July 2018

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

1 reference

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5 July 2018

Exome sequencing identifies the cause of a mendelian disorder

1 reference

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5 July 2018

Deciphering the molecular basis of venous thromboembolism: where are we and where should we go?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

5 July 2018

BFAST: an alignment tool for large scale genome resequencing

1 reference

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5 July 2018

Targeted capture and massively parallel sequencing of 12 human exomes

1 reference

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5 July 2018

The Sequence Alignment/Map format and SAMtools

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

5 July 2018

Advances in understanding pathogenic mechanisms of thrombophilic disorders

1 reference

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5 July 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

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5 July 2018

The association of alpha-fibrinogen Thr312Ala polymorphism and venous thromboembolism in the LITE study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

5 July 2018

Functional polymorphisms of FGA, encoding alpha fibrinogen, are associated with susceptibility to venous thromboembolism in a Taiwanese population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

5 July 2018

SNPdetector: a software tool for sensitive and accurate SNP detection

1 reference

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5 July 2018

Accounting for human polymorphisms predicted to affect protein function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

5 July 2018

Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

5 July 2018

Validated questionnaire for the identification of previous personal or familial venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

5 July 2018

Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-7

21 January 2018

The Human Gene Mutation Database: 2008 update

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-7

21 January 2018

Functional analysis of the fibrinogen Aalpha Thr312Ala polymorphism: effects on fibrin structure and function.

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-5-7

21 January 2018

Familial risk of venous thromboembolism: a nationwide cohort study

1 reference

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21 January 2018

Major genetic susceptibility for venous thromboembolism in men: a study of Danish twins

1 reference

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28 October 2018

alpha-fibrinogen Thr312Ala polymorphism and venous thromboembolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3305575

28 October 2018

Familial segregation of venous thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/22353194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene variants associated with venous thrombosis: confirmation in the MEGA study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22353194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene variants associated with deep vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22353194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acute pulmonary embolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/22353194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1755-8794-5-7

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Dimensions Publication ID

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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