Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.

Audain E, Wilsdon A, Breckpot J, Izarzugaza JMG, Fitzgerald TW, Kahlert AK, Sifrim A, Wünnemann F, Perez-Riverol Y, Abdul-Khaliq H, Bak M, Bassett AS, Benson DW, Berger F, Daehnert I, Devriendt K, Dittrich S, Daubeney PE, Garg V, Hackmann K, Hoff K, Hofmann P, Dombrowsky G, Pickardt T, Bauer U, Keavney BD, Klaassen S, Kramer HH, Marshall CR, Milewicz DM, Lemaire S, Coselli JS, Mitchell ME, Tomita-Mitchell A, Prakash SK, Stamm K, Stewart AFR, Silversides CK, Siebert R, Stiller B, Rosenfeld JA, Vater I, Postma AV, Caliebe A, Brook JD, Andelfinger G, Hurles ME, Thienpont B, Larsen LA, Hitz MP

Open source

DOI
10.1371/journal.pgen.1009679
Published
2021 Jul
Container
PLoS genetics
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1371/journal.pgen.1009679,
  title = {Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.},
  author = {Audain E and Wilsdon A and Breckpot J and Izarzugaza JMG and Fitzgerald TW and Kahlert AK and Sifrim A and Wünnemann F and Perez-Riverol Y and Abdul-Khaliq H and Bak M and Bassett AS and Benson DW and Berger F and Daehnert I and Devriendt K and Dittrich S and Daubeney PE and Garg V and Hackmann K and Hoff K and Hofmann P and Dombrowsky G and Pickardt T and Bauer U and Keavney BD and Klaassen S and Kramer HH and Marshall CR and Milewicz DM and Lemaire S and Coselli JS and Mitchell ME and Tomita-Mitchell A and Prakash SK and Stamm K and Stewart AFR and Silversides CK and Siebert R and Stiller B and Rosenfeld JA and Vater I and Postma AV and Caliebe A and Brook JD and Andelfinger G and Hurles ME and Thienpont B and Larsen LA and Hitz MP},
  year = {2021},
  journal = {PLoS genetics},
  doi = {10.1371/journal.pgen.1009679},
  url = {https://doi.org/10.1371/journal.pgen.1009679}
}

RIS

TY  - JOUR
TI  - Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
AU  - Audain E
AU  - Wilsdon A
AU  - Breckpot J
AU  - Izarzugaza JMG
AU  - Fitzgerald TW
AU  - Kahlert AK
AU  - Sifrim A
AU  - Wünnemann F
AU  - Perez-Riverol Y
AU  - Abdul-Khaliq H
AU  - Bak M
AU  - Bassett AS
AU  - Benson DW
AU  - Berger F
AU  - Daehnert I
AU  - Devriendt K
AU  - Dittrich S
AU  - Daubeney PE
AU  - Garg V
AU  - Hackmann K
AU  - Hoff K
AU  - Hofmann P
AU  - Dombrowsky G
AU  - Pickardt T
AU  - Bauer U
AU  - Keavney BD
AU  - Klaassen S
AU  - Kramer HH
AU  - Marshall CR
AU  - Milewicz DM
AU  - Lemaire S
AU  - Coselli JS
AU  - Mitchell ME
AU  - Tomita-Mitchell A
AU  - Prakash SK
AU  - Stamm K
AU  - Stewart AFR
AU  - Silversides CK
AU  - Siebert R
AU  - Stiller B
AU  - Rosenfeld JA
AU  - Vater I
AU  - Postma AV
AU  - Caliebe A
AU  - Brook JD
AU  - Andelfinger G
AU  - Hurles ME
AU  - Thienpont B
AU  - Larsen LA
AU  - Hitz MP
PY  - 2021
JO  - PLoS genetics
DO  - 10.1371/journal.pgen.1009679
UR  - https://doi.org/10.1371/journal.pgen.1009679
ER  -

APA

E, A., A, W., J, B., JMG, I., TW, F., AK, K., A, S., F, W., Y, P., H, A., M, B., AS, B., DW, B., F, B., I, D., K, D., S, D., PE, D., V, G., K, H., K, H., P, H., G, D., T, P., U, B., BD, K., S, K., HH, K., CR, M., DM, M., S, L., JS, C., ME, M., A, T., SK, P., K, S., AFR, S., CK, S., R, S., B, S., JA, R., I, V., AV, P., A, C., JD, B., G, A., ME, H., B, T., LA, L., & MP, H. (2021). Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.. PLoS genetics. https://doi.org/10.1371/journal.pgen.1009679

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