BetterScholar BetterScholar
11
Role
Title
Level Year L/R
🐜 Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study
20 auth. P. Talmud, Sonia H. Shah, R. Whittall, M. Futema, Philip N. Howard, J. Cooper, S. Harrison, Kawah Li, F. Drenos, F. Karpe, ... H. Neil, O. Descamps, C. Langenberg, N. Lench, M. Kivimäki, J. Whittaker, J. Whittaker, A. Hingorani, M. Kumari, S. Humphries
9 2013
9
🐜
🐜 Whole-genome sequencing of patients with rare diseases in a national health system
452 auth. E. Turro, W. Astle, K. Megy, S. Gräf, D. Greene, O. Shamardina, H. L. Allen, Alba Sanchis-Juan, M. Frontini, C. Thys, J. Stephens, R. Mapeta, O. Burren, K. Downes, M. Haimel, ... Salih Tuna, Sri V. V. Deevi, T. Aitman, David L. 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, Joannella Morales, N. Morrell, A. Mumford, E. Ormondroyd, Stuart Rankin, A. Rendon, S. Richardson, I. Roberts, N. Roy, M. Saleem, Kenneth G. C. Smith, H. Stark, R. Tan, Andreas C Themistocleous, A. Thrasher, H. Watkins, A. Webster, M. Wilkins, C. Williamson, J. Whitworth, S. Humphray, D. Bentley, S. Abbs, L. Abulhoul, J. Adlard, Munaza Ahmed, H. Alachkar, D. Allsup, J. Almeida-King, P. Ancliff, R. Antrobus, R. Armstrong, G. Arno, Sofie Ashford, A. Attwood, P. Aurora, C. Babbs, C. Bacchelli, T. Bakchoul, S. Banka, T. Bariana, J. Barwell, Joana Batista, H. Baxendale, P. Beales, A. Bierzynska, T. Biss, M. Bitner-Glindzicz, G. Black, M. Bleda, Iulia Blesneac, D. Bockenhauer, H. Bogaard, Christian J. Bourne, S. Boyce, J. Bradley, E. Bragin, G. Breen, P. Brennan, C. Brewer, Matthew Brown, A. Browning, M. Browning, R. Buchan, M. Buckland, T. Bueser, Carmen Bugarin Diz, J. Burn, S. Burns, N. Burrows, Carolyn Campbell, G. Carr-White, R. Casey, Jenny Chambers, John Chambers, M. Chan, Calvin Cheah, F. Cheng, M. Chitre, M. Christian, C. Church, J. Clayton-Smith, M. Cleary, Naomi Clements Brod, G. Coghlan, Elizabeth Colby, T. Cole, J. Collins, P. Collins, Camilla Colombo, C. Compton, R. Condliffe, S. Cook, H. Cook, Nichola H Cooper, P. Corris, A. Furnell, Fiona Cunningham, N. Curry, A. Cutler, M. Daniels, M. Dattani, L. Daugherty, John Davis, A. De Soyza, Timothy Dent, C. Deshpande, Eleanor F. Dewhurst, S. Douzgou, A. Drazyk, E. Drewe, Daniel Duarte, T. Dutt, J. Edgar, Karen E. Edwards, W. Egner, Melanie N. Ekani, P. Elliott, W. Erber, M. Erwood, M. Estiú, D. G. Evans, G. Evans, T. Everington, M. Eyries, H. Fassihi, R. Favier, J. Findhammer, Debra Fletcher, F. Flinter, R. Floto, T. Fowler, James C. Fox, Amy J. Frary, Courtney E. French, K. Freson, H. Gall, V. Ganesan, M. Gattens, C. Geoghegan, Terence S. A. Gerighty, A. Gharavi, S. Ghio, H. Ghofrani, J. Gibbs, Kate Gibson, K. Gilmour, B. Girerd, Nicholas S. Gleadall, S. Goddard, D. Goldstein, K. Gomez, Pavels 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, Eshika Haque, K. Harkness, A. Harper, Claire L. Harris, D. Hart, Ahamad Hassan, G. Hayman, A. Henderson, A. Herwadkar, Jonathan Hoffman, S. Holden, R. Horvath, H. Houlden, A. Houweling, L. Howard, Fengyuan Hu, G. Hudson, J. Hughes, A. Huissoon, M. Humbert, Sarah Hunter, Matthew Hurles, M. Irving, L. Izatt, Sally A. Johnson, S. Jolles, J. Jolley, D. Josifova, Neringa Jurkute, Tim Karten, J. Karten, Mary A. Kasanicki, H. Kazkaz, R. Kazmi, P. Kelleher, A. Kelly, W. Kelsall, Carly Kempster, D. Kiely, N. Kingston, R. Klima, Nils Koelling, Myrto A. Kostadima, G. Kovacs, Roman Kreuzhuber, T. Kuijpers, Ajith Kumar, D. Kumararatne, M. Kurian, F. Lalloo, Michele P. Lambert, A. Lawrie, D. M. Layton, N. Lench, C. Lentaigne, T. Lester, R. Linger, H. Longhurst, Lorena E. Lorenzo, E. Louka, P. Lyons, R. Machado, R. M. MacKenzie Ross, B. Madan, Jesmeen Maimaris, S. Malka, S. Mangles, K. Marchbank, S. Marks, H. Marschall, Andrew Marshall, Jennifer M. Martin, M. Mathias, E. Matthews, H. Maxwell, P. Mcalinden, Mark I. McCarthy, H. McKinney, A. McMahon, Stuart Meacham, A. Mead, Ignacio Castelló, S. Mehta, M. Michaelides, C. Millar, S. Mohammed, S. Moledina, D. Montani, A. Moore, M. Mozere, K. Muir, A. Nemeth, W. G. 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, Soo-Mi Park, D. Parry, Smita Y. Patel, J. Paterson, A. Peacock, S. H. Pearce, J. Peden, K. Peerlinck, C. Penkett, J. Pepke-Zaba, Romina Petersen, C. Pilkington, Ken Poole, Radhika Prathalingam, B. Psaila, A. Pyle, R. Quinton, S. Rahman, A. Rao, F. Raymond, Paula Rayner-Matthews, Christine Rees, T. Renton, Christopher J. Rhodes, Andrew S C Rice, A. Richter, L. Robert, Anthony Rogers, S. Rose, R. Ross-Russell, Catherine 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, Sol Schulman, R. Scott, M. Scully, C. Searle, W. Seeger, Arjune Sen, W. Sewell, Denis Seyres, N. Shah, S. Shapiro, A. Shaw, Patrick J. Short, Keith R Sibson, L. Side, Ilenia Simeoni, Michael Simpson, M. C. Sims, S. Sivapalaratnam, D. Smedley, Katherine R. Smith, K. Snape, N. Soranzo, F. Soubrier, L. Southgate, O. Spasic-Boskovic, Simon Staines, E. Staples, C. Steward, K. Stirrups, A. Stuckey, J. Suntharalingam, E. Swietlik, P. Syrris, R. Tait, K. Talks, Katie Tate, John M. Taylor, Jenny C. Taylor, James E. D. Thaventhiran, E. Thomas, D. Thomas, Moira J. Thomas, Patrick Thomas, K. Thomson, Glen Threadgold, T. Tilly, M. Tischkowitz, Catherine Titterton, J. Todd, C. Toh, B. Tolhuis, I. Tomlinson, M. Toshner, M. Traylor, C. Treacy, Paul Treadaway, R. Trembath, Wojciech Turek, E. Turro, Philip Twiss, Tom A Vale, C. Geet, N. Zuydam, Maarten Vandekuilen, A. Vandersteen, Marta Vazquez-Lopez, J. von Ziegenweidt, A. Vonk Noordegraaf, Annette Wagner, Q. Waisfisz, S. Walker, Neil E. Walker, Klaudia Walter, J. Ware, C. Watt, L. Wedderburn, Wei Wei, S. Welch, Julie Wessels, S. Westbury, J. Westwood, J. Wharton, Deborah Whitehorn, A. Wilkie, Brian T. Wilson, E. Wong, N. Wood, Y. Wood, C. Woods, E. Woodward, S. Wort, A. Worth, Michael Wright, Katherine Yates, P. Yong, Tim Young, Ping Yu, P. Yu-Wai-Man, Eliska Zlamalova, F. Raymond, W. Ouwehand
8 2020
8
🐜
🐜 Positional cloning of a novel gene influencing asthma from Chromosome 2q14
30 auth. Maxine Allen, A. Heinzmann, E. Noguchi, G. Abecasis, J. Broxholme, C. Ponting, Sumit Bhattacharyya, J. Tinsley, Youming Zhang, R. Holt, E. Jones, N. Lench, A. Carey, Helene Jones, N. Dickens, ... Claire Dimon, R. Nicholls, C. Baker, Luzheng Xue, Elizabeth R. Townsend, M. Kabesch, S. Weiland, D. Carr, E. von Mutius, I. Adcock, P. Barnes, G. Lathrop, M. Edwards, M. Moffatt, W. Cookson
8 2003
8
🐜
🐜 Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF(-kappa)B transcription factors.
11 auth. D. V. van Heel, I. Udalova, A. de Silva, D. McGovern, Y. Kinouchi, J. Hull, ... N. Lench, L. Cardon, A. Carey, D. Jewell, D. Kwiatkowski
8 2002
8
🐜
🐜 Low‐Density Lipoprotein Receptor Gene Familial Hypercholesterolemia Variant Database: Update and Pathological Assessment
10 auth. Ebele Usifo, S. Leigh, R. Whittall, N. Lench, Alison Taylor, C. Yeats, ... C. Orengo, Andrew C. R. Martin, J. Celli, S. Humphries
7 2012
7
🐜
🐜 Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities
7 auth. S. Drury, Hywel Williams, N. Trump, Christopher Boustred, N. Lench, R. Scott, ... L. Chitty
7 2015
7
🐜
🐜 Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next-generation sequencing allows for a safer, more accurate, and comprehensive approach
7 auth. L. Chitty, S. Mason, A. Barrett, Fiona McKay, N. Lench, R. Daley, ... L. Jenkins
7 2015
7
🐜
🦁 The clinical implementation of non‐invasive prenatal diagnosis for single‐gene disorders: challenges and progress made
8 auth. N. Lench, A. Barrett, S. Fielding, Fiona McKay, M. Hill, L. Jenkins, ... H. White, L. Chitty
7 2013
7
🦁
🦁 Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
N. Lench, M. Houseman, V. Newton, G. Camp, R. Mueller
7 1998
7
🦁
🐜 CHD2 variants are a risk factor for photosensitivity in epilepsy
47 auth. E. Galizia, Candace T. Myers, C. Leu, C. D. de Kovel, T. Afrikanova, M. L. Cordero-Maldonado, T. Martins, M. Jacmin, S. Drury, V. Krishna Chinthapalli, H. Muhle, Manuela Pendziwiat, T. Sander, Ann-Kathrin Ruppert, R. Møller, ... H. Thiele, R. Krause, J. Schubert, A. Lehesjoki, P. Nürnberg, H. Lerche, A. Palotie, A. Coppola, S. Striano, Luigi del Gaudio, Christopher Boustred, Amy L. Schneider, N. Lench, B. Jocić-Jakubi, A. Covanis, G. Capovilla, P. Veggiotti, M. Piccioli, P. Parisi, L. Cantonetti, L. Sadleir, S. Mullen, S. Berkovic, U. Stephani, I. Helbig, A. Crawford, Camila V. Esguerra, D. Kasteleijn-Nolst Trenité, B. Koeleman, H. Mefford, I. Scheffer, S. Sisodiya
6 2015
6
🐜
🐜 Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations
19 auth. M. Futema, V. Plagnol, Kawah Li, R. Whittall, H. A. W. Neil, M. Seed, S. Bertolini, S. Calandra, Olivier S. Descamps, Colin A Graham, ... Robert A. Hegele, F. Karpe, R. Durst, E. Leitersdorf, N. Lench, Devaki Nair, H. Soran, F M van Bockxmeer, S. Humphries
6 2014
6
🐜