Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. (Q36119845)

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19 February 2020

title

Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects (English)

1 reference

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genome-wide association study

19 February 2020

main subject

0 references

author

Adam E Locke

3

1 reference

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19 February 2020

Clifford L. Cua

8

1 reference

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19 February 2020

Eleanor Feingold

13

1 reference

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19 February 2020

15

Michael E Zwick

1 reference

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19 February 2020

11

Cheryl L Maslen

1 reference

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19 February 2020

author name string

Dhanya Ramachandran

1

1 reference

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19 February 2020

Zhen Zeng

2

1 reference

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19 February 2020

Jennifer G Mulle

4

1 reference

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19 February 2020

Lora J H Bean

5

1 reference

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19 February 2020

Tracie C Rosser

6

1 reference

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19 February 2020

Kenneth J Dooley

7

1 reference

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19 February 2020

George T Capone

9

1 reference

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19 February 2020

Roger H Reeves

10

1 reference

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19 February 2020

David J Cutler

12

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19 February 2020

Stephanie L Sherman

14

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19 February 2020

publication date

20 July 2015

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19 February 2020

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19 February 2020

volume

5

1 reference

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19 February 2020

issue

10

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19 February 2020

page(s)

1961-1971

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describes a project that uses

19 February 2020

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease

2 October 2017

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BAALC, the human member of a novel mammalian neuroectoderm gene lineage, is implicated in hematopoiesis and acute leukemia

2 October 2017

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The C-terminal cytoplasmic Lys-thr-X-X-X-Trp motif in frizzled receptors mediates Wnt/beta-catenin signalling

2 October 2017

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2 October 2017

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Congenital heart disease caused by mutations in the transcription factor NKX2-5

2 October 2017

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2 October 2017

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Evidence of congenital heart disease in the offspring of parents with atrioventricular defects

2 October 2017

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Novel and functional DNA sequence variants within the GATA5 gene promoter in ventricular septal defects.

2 October 2017

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Genetic variants at 10p11 confer risk of Tetralogy of Fallot in Chinese of Nanjing

2 July 2018

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2 July 2018

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Population-based treated prevalence of congenital heart disease in a pediatric cohort

23 September 2018

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Gene expression profiling and qRT-PCR expression of RRP1B, PCNT, KIF21A and ADRB2 in leucocytes of Down's syndrome subjects.

23 September 2018

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A novel GATA6 mutation associated with congenital ventricular septal defect.

23 September 2018

1 reference

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The contribution of chromosomal abnormalities to congenital heart defects: a population-based study

23 September 2018

1 reference

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Depletion of Med10 enhances Wnt and suppresses Nodal signaling during zebrafish embryogenesis

23 September 2018

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Longitudinal development of psychopathology in an adult congenital heart disease cohort.

23 September 2018

1 reference

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The Wnt/beta-catenin pathway regulates cardiac valve formation

23 September 2018

1 reference

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Mortality associated with congenital heart defects in the United States: trends and racial disparities, 1979-1997.

23 September 2018

1 reference

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Population-based study of congenital heart defects in Down syndrome.

23 September 2018

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Estimates of the economic costs of birth defects

23 September 2018

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Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project

21 October 2018

1 reference

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Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study

5 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26194203

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Report of the task force on children and youth. American Heart Association

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26194203

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1534/G3.115.019943

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26194203%20AND%20SRC:MED&resulttype=core&format=json

19 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26194203%20AND%20SRC:MED&resulttype=core&format=json

19 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26194203%20AND%20SRC:MED&resulttype=core&format=json