(Q28943387)

14 March 2017

title

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot (English)

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genome-wide association study

14 March 2017

main subject

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32

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Klaartje van Engelen

19

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Anita Rauch

34

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Diana Zelenika

6

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Chrysovalanto Mamasoula

3

Chrysovalanto Mamasoula

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16

Darroch Hall

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28

David Winlaw

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Shoumo Bhattacharya

27

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Alex V Postma

Alex V. Postma

4

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Marc Gewillig

Marc Gewillig

30

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Mark Lathrop

35

G. Mark Lathrop

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25

A. Graham Stuart

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36

Bernard D. Keavney

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37

Judith A. Goodship

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1

Heather J. Cordell

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Javier T Granados-Riveron

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10

Javier Granados Riveron

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5

Jamie Bentham

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9

Catherine Cosgrove

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Jeroen Breckpot

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Kerry Setchfield

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Chris Thornborough

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Rachel Soemedi

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Thahira J. Rahman

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8

Gillian Blue

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2

Ana Töpf

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7

Simon Heath

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Aelko H. Zwinderman

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Seema Mital

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Antoon F. M. Moorman

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Barbara J. M. Mulder

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Rebecca Darlay

11

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Ian J. Wilson

13

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Kristin L. Ayers

14

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J. David Brook

20

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Frances A. Bu'Lock

22

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John O'Sullivan

24

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Jonathan Parsons

26

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publication date

1 April 2013

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14 March 2017

published in

Human Molecular Genetics

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14 March 2017

volume

22

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issue

7

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14 March 2017

page(s)

1473–1481

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describes a project that uses

14 March 2017

genome-wide association study

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based on heuristic

inferred from title

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Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways

3 June 2018

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A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.

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3 June 2018

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3 June 2018

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3 June 2018

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22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia.

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21 January 2018

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inferred from PubMed ID database lookup

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based on heuristic

Identifiers

1 reference

14 March 2017

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