Prioritizing the detection of rare pathogenic variants in population screening

Paul Lacaze; Ranjit Manchanda; Robert C. Green

doi:10.1038/s41576-022-00571-9

Prioritizing the detection of rare pathogenic variants in population screening

Paul Lacaze, Ranjit Manchanda, Robert C. Green

Research output: Contribution to journal › Comment / Debate › Other › peer-review

Original language	English
Pages (from-to)	205-206
Number of pages	2
Journal	Nature Reviews Genetics
Volume	24
Issue number	4
DOIs	https://doi.org/10.1038/s41576-022-00571-9
Publication status	Published - Apr 2023

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title = "Prioritizing the detection of rare pathogenic variants in population screening",

author = "Paul Lacaze and Ranjit Manchanda and Green, {Robert C.}",

note = "Funding Information: The authors thank J. Tiller for her input into this article. P.L. is supported by a National Heart Foundation Future Leader Fellowship (102604) and grants from the Australian Government Department of Health, Medical Research Future Fund, Genomics Health Futures Mission (APP2009024) and National Institutes of Health (1127060). R.M. is funded by the Yorkshire Cancer Research and Eve Appeal into Population testing and has been supported by an NHS Innovation Accelerator (NIA) Fellowship for population testing. R.C.G. is funded by NIH grants: TR003201, HG008685, HL143295, OD026553 and by the Franca Sozzani Fund for Preventive Genomics. ",

year = "2023",

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doi = "10.1038/s41576-022-00571-9",

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T1 - Prioritizing the detection of rare pathogenic variants in population screening

AU - Lacaze, Paul

AU - Manchanda, Ranjit

AU - Green, Robert C.

N1 - Funding Information: The authors thank J. Tiller for her input into this article. P.L. is supported by a National Heart Foundation Future Leader Fellowship (102604) and grants from the Australian Government Department of Health, Medical Research Future Fund, Genomics Health Futures Mission (APP2009024) and National Institutes of Health (1127060). R.M. is funded by the Yorkshire Cancer Research and Eve Appeal into Population testing and has been supported by an NHS Innovation Accelerator (NIA) Fellowship for population testing. R.C.G. is funded by NIH grants: TR003201, HG008685, HL143295, OD026553 and by the Franca Sozzani Fund for Preventive Genomics.

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DO - 10.1038/s41576-022-00571-9

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VL - 24

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EP - 206

JO - Nature Reviews Genetics

JF - Nature Reviews Genetics

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ER -

Prioritizing the detection of rare pathogenic variants in population screening

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