Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.

Wainschtein P, Jain D, Zheng Z, TOPMed Anthropometry Working Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Cupples LA, Shadyab AH, McKnight B, Shoemaker BM, Mitchell BD, Psaty BM, Kooperberg C, Liu CT, Albert CM, Roden D, Chasman DI, Darbar D, Lloyd-Jones DM, Arnett DK, Regan EA, Boerwinkle E, Rotter JI, O'Connell JR, Yanek LR, de Andrade M, Allison MA, McDonald MN, Chung MK, Fornage M, Chami N, Smith NL, Ellinor PT, Vasan RS, Mathias RA, Loos RJF, Rich SS, Lubitz SA, Heckbert SR, Redline S, Guo X, Chen Y-I, Laurie CA, Hernandez RD, McGarvey ST, Goddard ME, Laurie CC, North KE, Lange LA, Weir BS, Yengo L, Yang J, Visscher PM

Open source

DOI
10.1038/s41588-021-00997-7
Published
2022 Mar
Container
Nature genetics
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1038/s41588-021-00997-7,
  title = {Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.},
  author = {Wainschtein P and Jain D and Zheng Z and TOPMed Anthropometry Working Group and NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium and Cupples LA and Shadyab AH and McKnight B and Shoemaker BM and Mitchell BD and Psaty BM and Kooperberg C and Liu CT and Albert CM and Roden D and Chasman DI and Darbar D and Lloyd-Jones DM and Arnett DK and Regan EA and Boerwinkle E and Rotter JI and O'Connell JR and Yanek LR and de Andrade M and Allison MA and McDonald MN and Chung MK and Fornage M and Chami N and Smith NL and Ellinor PT and Vasan RS and Mathias RA and Loos RJF and Rich SS and Lubitz SA and Heckbert SR and Redline S and Guo X and Chen Y-I and Laurie CA and Hernandez RD and McGarvey ST and Goddard ME and Laurie CC and North KE and Lange LA and Weir BS and Yengo L and Yang J and Visscher PM},
  year = {2022},
  journal = {Nature genetics},
  doi = {10.1038/s41588-021-00997-7},
  url = {https://doi.org/10.1038/s41588-021-00997-7}
}

RIS

TY  - JOUR
TI  - Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.
AU  - Wainschtein P
AU  - Jain D
AU  - Zheng Z
AU  - TOPMed Anthropometry Working Group
AU  - NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
AU  - Cupples LA
AU  - Shadyab AH
AU  - McKnight B
AU  - Shoemaker BM
AU  - Mitchell BD
AU  - Psaty BM
AU  - Kooperberg C
AU  - Liu CT
AU  - Albert CM
AU  - Roden D
AU  - Chasman DI
AU  - Darbar D
AU  - Lloyd-Jones DM
AU  - Arnett DK
AU  - Regan EA
AU  - Boerwinkle E
AU  - Rotter JI
AU  - O'Connell JR
AU  - Yanek LR
AU  - de Andrade M
AU  - Allison MA
AU  - McDonald MN
AU  - Chung MK
AU  - Fornage M
AU  - Chami N
AU  - Smith NL
AU  - Ellinor PT
AU  - Vasan RS
AU  - Mathias RA
AU  - Loos RJF
AU  - Rich SS
AU  - Lubitz SA
AU  - Heckbert SR
AU  - Redline S
AU  - Guo X
AU  - Chen Y-I
AU  - Laurie CA
AU  - Hernandez RD
AU  - McGarvey ST
AU  - Goddard ME
AU  - Laurie CC
AU  - North KE
AU  - Lange LA
AU  - Weir BS
AU  - Yengo L
AU  - Yang J
AU  - Visscher PM
PY  - 2022
JO  - Nature genetics
DO  - 10.1038/s41588-021-00997-7
UR  - https://doi.org/10.1038/s41588-021-00997-7
ER  -

APA

P, W., D, J., Z, Z., Group, T. A. W., Consortium, N. T. F. P. M. (., LA, C., AH, S., B, M., BM, S., BD, M., BM, P., C, K., CT, L., CM, A., D, R., DI, C., D, D., DM, L., DK, A., EA, R., E, B., JI, R., JR, O., LR, Y., M, D. A., MA, A., MN, M., MK, C., M, F., N, C., NL, S., PT, E., RS, V., RA, M., RJF, L., SS, R., SA, L., SR, H., S, R., X, G., Y-I, C., CA, L., RD, H., ST, M., ME, G., CC, L., KE, N., LA, L., BS, W., L, Y., J, Y., & PM, V. (2022). Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.. Nature genetics. https://doi.org/10.1038/s41588-021-00997-7

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