@article{4bc3eeb6ad224f049f3e39723d3a9ca8,
title = "Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data",
author = "{DDD Study} and Stuart Aitken and Firth, {Helen V.} and Jeremy McRae and Mihail Halachev and Usha Kini and Parker, {Michael J.} and Lees, {Melissa M.} and Katherine Lachlan and Ajoy Sarkar and Shelagh Joss and Miranda Splitt and Shane McKee and N{\'e}meth, {Andrea H.} and Scott, {Richard H.} and Wright, {Caroline F.} and Marsh, {Joseph A.} and Hurles, {Matthew E.} and FitzPatrick, {David R.} and Fitzgerald, {T. W.} and Gerety, {S. S.} and Jones, {W. D.} and {van Kogelenberg}, M. and King, {D. A.} and J. McRae and Morley, {K. I.} and V. Parthiban and S. Al-Turki and K. Ambridge and Barrett, {D. M.} and T. Bayzetinova and S. Clayton and Coomber, {E. L.} and S. Gribble and P. Jones and N. Krishnappa and Mason, {L. E.} and A. Middleton and R. Miller and E. Prigmore and D. Rajan and A. Sifrim and Tivey, {A. R.} and M. Ahmed and N. Akawi and R. Andrews and U. Anjum and H. Archer and R. Armstrong and M. Balasubramanian and R. Banerjee",
note = "Funding Information: The DDD study presents independent research commissioned by the Health Innovation Challenge Fund (grant number HICF-1009-003 ), a parallel funding partnership between Wellcome and the Department of Health , and the Wellcome Sanger Institute (grant number WT098051 ). The views expressed in this publication are those of the author(s) and not necessarily those of Wellcome or the Department of Health. The study has UK Research Ethics Committee approval (10/H0305/83, granted by the Cambridge South REC, and GEN/284/12 granted by the Republic of Ireland REC). The research team acknowledges the support of the National Institute for Health Research, through the Comprehensive Clinical Research Network. This study makes use of DECIPHER, which is funded by the Wellcome . H.V.F. is supported by Wellcome (award 200990/Z/16/Z ) “Designing, developing and delivering integrated foundations for genomic medicine.” The research team acknowledges the support of the National Institute for Health Research, through the Comprehensive Clinical Research Network. Funding for UK10K was provided by Wellcome under award WT091310 . D.R.F. was funded as part of the MRC Human Genetics Unit grant to the University of Edinburgh. M.H. is supported by an IGMM Translational Science Award . J.A.M. is supported by an MRC Career Development Award ( MR/M02122X/1 ) and is a Lister Institute Research Prize Fellow . S.A. is supported by MRC Core funding to the MRC Human Genetics Unit. Funding Information: The DDD study presents independent research commissioned by the Health Innovation Challenge Fund (grant number HICF-1009-003), a parallel funding partnership between Wellcome and the Department of Health, and the Wellcome Sanger Institute (grant number WT098051). The views expressed in this publication are those of the author(s) and not necessarily those of Wellcome or the Department of Health. The study has UK Research Ethics Committee approval (10/H0305/83, granted by the Cambridge South REC, and GEN/284/12 granted by the Republic of Ireland REC). The research team acknowledges the support of the National Institute for Health Research, through the Comprehensive Clinical Research Network. This study makes use of DECIPHER, which is funded by the Wellcome. H.V.F. is supported by Wellcome (award 200990/Z/16/Z) ?Designing, developing and delivering integrated foundations for genomic medicine.? The research team acknowledges the support of the National Institute for Health Research, through the Comprehensive Clinical Research Network. Funding for UK10K was provided by Wellcome under award WT091310. D.R.F. was funded as part of the MRC Human Genetics Unit grant to the University of Edinburgh. M.H. is supported by an IGMM Translational Science Award. J.A.M. is supported by an MRC Career Development Award (MR/M02122X/1) and is a Lister Institute Research Prize Fellow. S.A. is supported by MRC Core funding to the MRC Human Genetics Unit. Publisher Copyright: {\textcopyright} 2019 The Authors",
year = "2019",
month = nov,
day = "7",
doi = "10.1016/j.ajhg.2019.09.015",
language = "English",
volume = "105",
pages = "933--946",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",
number = "5",
}