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Whole-genome sequencing of patients with rare diseases in a national health system.

E. Turro, W. Astle, K. Megy, S. Gräf, D. Greene, O. Shamardina, H. Allen, A. Sanchis-Juan, M. Frontini, C. Thys, J. Stephens, R. Mapeta, O. Burren, K. Downes, M. Haimel, S. Tuna, S. Deevi, T. Aitman, D. Bennett, P. Calleja, K. Carss, M. Caulfield, P. Chinnery, P. Dixon, D. Gale, R. James, A. Koziell, M. Laffan, A. Levine, E. Maher, H. Markus, J. Morales, N. Morrell, A. Mumford, E. Ormondroyd, S. Rankin, A. Rendon, S. Richardson, I. Roberts, N. Roy, M. Saleem, K. Smith, H. Stark, R. Tan, A. Themistocleous, A. Thrasher, H. Watkins, A. Webster, M. Wilkins, C. Williamson, J. Whitworth, S. Humphray, D. Bentley, S. Abbs, L. Abulhoul, J. Adlard, M. Ahmed, H. Alachkar, D. Allsup, J. Almeida-King, P. Ancliff, R. Antrobus, R. Armstrong, G. Arno, S. Ashford, A. Attwood, P. Aurora, C. Babbs, C. Bacchelli, T. Bakchoul, S. Banka, T. Bariana, J. Barwell, J. Batista, H. Baxendale, P. Beales, A. Bierzynska, T. Biss, M. Bitner-Glindzicz, G. Black, M. Bleda, I. Blesneac, D. Bockenhauer, H. Bogaard, C. Bourne, S. Boyce, J. Bradley, E. Bragin, G. Breen, P. Brennan, C. Brewer, M. Brown, A. Browning, M. Browning, R. Buchan, M. Buckland, T. Bueser, C. Diz, J. Burn, S. Burns, N. Burrows, C. Campbell, G. Carr-White, R. Casey, J. Chambers, J. Chambers, M. Chan, C. Cheah, F. Cheng, M. Chitre, M. Christian, C. Church, J. Clayton-Smith, M. Cleary, N. Brod, G. Coghlan, E. Colby, T. Cole, J. Collins, P. Collins, C. Colombo, C. Compton, R. Condliffe, S. Cook, H. Cook, N. Cooper, P. Corris, A. Furnell, F. Cunningham, N. Curry, A. Cutler, M. Daniels, M. Dattani, L. Daugherty, J. Davis, A. Soyza, T. Dent, C. Deshpande, E. Dewhurst, S. Douzgou, A. Drazyk, E. Drewe, D. Duarte, T. Dutt, J. Edgar, K. Edwards, W. Egner, M. Ekani, P. Elliott, W. Erber, M. Erwood, M. Estiu, D. Evans, G. Evans, T. Everington, M. Eyries, H. Fassihi, R. Favier, J. Findhammer, D. Fletcher, F. Flinter, R. Floto, T. Fowler, J. Fox, A. Frary, C. French, K. Freson, H. Gall, V. Ganesan, M. Gattens, C. Geoghegan, T. Gerighty, A. Gharavi, S. Ghio, H. Ghofrani, J. Gibbs, K. Gibson, K. Gilmour, B. Girerd, N. Gleadall, S. Goddard, D. Goldstein, K. Gomez, P. Gordins, D. Gosal, J. Graham, L. Grassi, L. Greenhalgh, A. Greinacher, P. Gresele, P. Griffiths, S. Grigoriadou, R. Grocock, D. Grozeva, M. Gurnell, S. Hackett, C. Hadinnapola, W. Hague, R. Hague, M. Hall, H. Hanson, E. Haque, K. Harkness, A. Harper, C. Harris, D. Hart, A. Hassan, G. Hayman, A. Henderson, A. Herwadkar, J. Hoffman, S. Holden, R. Horvath, H. Houlden, A. Houweling, L. Howard, F. Hu, G. Hudson, J. Hughes, A. Huissoon, M. Humbert, S. Hunter, M. Hurles, M. Irving, L. Izatt, S. Johnson, S. Jolles, J. Jolley, D. Josifova, N. Jurkute, T. Karten, J. Karten, M. Kasanicki, H. Kazkaz, R. Kazmi, P. Kelleher, A. Kelly, W. Kelsall, C. Kempster, D. Kiely, N. Kingston, R. Klima, N. Koelling, M. Kostadima, G. Kovacs, R. Kreuzhuber, T. Kuijpers, A. Kumar, D. Kumararatne, M. Kurian, F. Lalloo, M. Lambert, A. Lawrie, D. Layton, N. Lench, C. Lentaigne, T. Lester, R. Linger, H. Longhurst, L. Lorenzo, E. Louka, P. Lyons, R. Machado, R. Ross, B. Madan, J. Maimaris, S. Malka, S. Mangles, K. Marchbank, S. Marks, H. Marschall, A. Marshall, J. Martin, M. Mathias, E. Matthews, H. Maxwell, P. McAlinden, M. McCarthy, H. McKinney, A. McMahon, S. Meacham, A. Mead, I. Castello, S. Mehta, M. Michaelides, C. Millar, S. Mohammed, S. Moledina, D. Montani, A. Moore, M. Mozere, K. Muir, A. Nemeth, W. Newman, M. Newnham, S. Noorani, P. Nurden, J. O'Sullivan, S. Obaji, C. Odhams, S. Okoli, A. Olschewski, H. Olschewski, K. Ong, S. Oram, W. Ouwehand, C. Palles, S. Papadia, S. Park, D. Parry, S. Patel, J. Paterson, A. Peacock, S. Pearce, J. Peden, K. Peerlinck, C. Penkett, J. Pepke-Zaba, R. Petersen, C. Pilkington, K. Poole, R. Prathalingam, B. Psaila, A. Pyle, R. Quinton, S. Rahman, A. Rao, F. Raymond, P. Rayner-Matthews, C. Rees, T. Renton, C. Rhodes, A. Rice, A. Richter, L. Robert, A. Rogers, S. Rose, R. Ross-Russell, C. Roughley, D. Ruddy, O. Sadeghi-Alavijeh, N. Samani, C. Samarghitean, R. Sargur, R. Sarkany, S. Satchell, S. Savic, J. Sayer, G. Sayer, L. Scelsi, A. Schaefer, S. Schulman, R. Scott, M. Scully, C. Searle, W. Seeger, A. Sen, W. Sewell, D. Seyres, N. Shah, S. Shapiro, A. Shaw, P. Short, K. Sibson, L. Side, I. Simeoni, M. Simpson, M. Sims, S. Sivapalaratnam, D. Smedley, K. Smith, K. Snape, N. Soranzo, F. Soubrier, L. Southgate, O. Spasic-Boskovic, S. Staines, E. Staples, C. Steward, K. Stirrups, A. Stuckey, J. Suntharalingam, E. Swietlik, P. Syrris, R. Tait, K. Talks, K. Tate, J. Taylor, J. Taylor, J. Thaventhiran, E. Thomas, D. Thomas, M. Thomas, P. Thomas, K. Thomson, G. Threadgold, T. Tilly, M. Tischkowitz, C. Titterton, J. Todd, C. Toh, B. Tolhuis, I. Tomlinson, M. Toshner, M. Traylor, C. Treacy, P. Treadaway, R. Trembath, W. Turek, P. Twiss, T. Vale, C. Geet, N. van Zuydam, M. Vandekuilen, A. Vandersteen, M. Vazquez-Lopez, J. von Ziegenweidt, A. Vonk-Noordegraaf, A. Wagner, Q. Waisfisz, S. Walker, N. Walker, K. Walter, J. Ware, C. Watt, L. Wedderburn, W. Wei, S. Welch, J. Wessels, S. Westbury, J. Westwood, J. Wharton, D. Whitehorn, A. Wilkie, B. Wilson, E. Wong, N. Wood, Y. Wood, C. Woods, E. Woodward, S. Wort, A. Worth, M. Wright, K. Yates, P. Yong, T. Young, P. Yu, P. Yu-Wai-Man, and E. Zlamalova. Nat., 583 (7814): 96-102 (2020)

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David B Adler

David B Dollenmayer

Erna Goldstein

Franz Goldstein

Walter Goldstein

Other publications of authors with the same name

Focused goodness of fit tests for gene set analyses.M. Zhang, S. Gelfman, C. Moreno, J. McCarthy, M. Harms, D. Goldstein, and A. Allen. Briefings Bioinform., (2022)Whole-genome sequencing of patients with rare diseases in a national health system.E. Turro, W. Astle, K. Megy, S. Gräf, D. Greene, O. Shamardina, H. Allen, A. Sanchis-Juan, M. Frontini, C. Thys and 439 other author(s). Nat., 583 (7814): 96-102 (2020)ATAV: a comprehensive platform for population-scale genomic analyses.Z. Ren, G. Povysil, J. Hostyk, H. Cui, N. Bhardwaj, and D. Goldstein. BMC Bioinform., 22 (1): 149 (2021)A non-equilibrium surface reservoir approach for hybrid DSMC/Navier-Stokes particle generation.K. Stephani, D. Goldstein, and P. Varghese. J. Comput. Phys., 232 (1): 468-481 (2013)Maintenance of Polygenic Variation in Spatially Structured Populations: Roles for Local Mating and Genetic RedundancyD. Goldstein, and K. Holsinger. Evolution, 46 (2): 412--429 (1992)Genomics: Lessons in complexity from yeast.D. Goldstein, and M. Noor. Nature, 464 (7291): 985--986 (Apr 15, 2010)meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays.S. Gelfman, Q. Wang, Y. Lu, D. Hall, C. Bostick, R. Dhindsa, M. Halvorsen, K. McSweeney, E. Cotterill, T. Edinburgh and 7 other author(s). PLoS Comput. Biol., (2018)The All of Us Research Program: Data quality, utility, and diversity.A. Ramirez, L. Sulieman, D. Schlueter, A. Halvorson, J. Qian, F. Ratsimbazafy, R. Loperena-Cortes, K. Mayo, M. Basford, N. Deflaux and 38 other author(s). Patterns, 3 (8): 100570 (2022)Evolution.N. Barton, D. Briggs, J. Eisen, D. Goldstein, and N. Patel. Cold Spring Harbor Laboratory Press, (2007)Monte Carlo solution of the Boltzmann equation via a discrete velocity model.A. Morris, P. Varghese, and D. Goldstein. J. Comput. Phys., 230 (4): 1265-1280 (2011)

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Disambiguation of "Goldstein, David B."

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Whole-genome sequencing of patients with rare diseases in a national health system.

Please choose a person to relate this publication to

David B Adler

David B Dollenmayer

Erna Goldstein

Franz Goldstein

Walter Goldstein

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Goldstein, David B."

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Whole-genome sequencing of patients with rare diseases in a national health system.

Please choose a person to relate this publication to

David B Adler

David B Dollenmayer

Erna Goldstein

Franz Goldstein

Walter Goldstein

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
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MSOffice XML

Whole-genome sequencing of patients with rare diseases in a national health system.