Introduction by Valérie Bourdier, Françoise Doro-Mégy

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KONTESTASI IDENTITAS (Studi Analitis Terhadap Gikiri dan Kekristenan di Kao Halmahera Utara) by , Agnes Megy Takaendengan, , Prof. Dr. Irwan Abdullah

Implementation of individualised polygenic risk score analysis: a test case of a family of four by Manuel Corpas, Karyn Megy, Antonio Metastasio, Edmund Lehmann

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PERAN KEJUT LISTRIK DAN TEMPERATUR SEBAGAI ELISITOR DALAM MENINGKATKAN KANDUNGAN SENYAWA BIOAKTIF DAN AKTIVITAS ANTIOKSIDAN PADA KEDELAI (Glycine max) : KAJIAN PUSTAKA by Megy Wida Fitria, Widya Dwi Rukmi Putri, Jaya Mahar Maligan

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Rift Valley fever virus modulates apoptosis and immune response during infection of human astrocytes by Jordan Quellec, Aurélie Pédarrieu, Camille Piro-Mégy, Jonathan Barthelemy, Yannick Simonin, Sara Salinas, Catherine Cêtre-Sossah

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De novo variant in tyrosine kinase SRC causes thrombocytopenia: case report of a second family by Lore De Kock, Chantal Thys, Kate Downes, Daniel Duarte, Karyn Megy, Chris Van Geet, Kathleen Freson

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Molecular Dynamics Studies of Poly(Lactic Acid) Nanoparticles and Their Interactions with Vitamin E and TLR Agonists Pam₁CSK₄ and Pam₃CSK<sub>4</su... by Simon Megy, Stephanie Aguero, David Da Costa, Myriam Lamrayah, Morgane Berthet, Charlotte Primard, Bernard Verrier, Raphael Terreux

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Heteronuclear proton assisted recoupling by Paepe, Gael De, Lewandowski, Jozef R., Loquet, Antoine, Eddy, Matthew Thomas, Megy, Simon, Bockmann, Anja, Griffin, Robert Guy

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Whole-genome sequencing of patients with rare diseases in a national health system by Turro, E, Astle, WJ, Megy, K, Bennett, DL, Ormondroyd, E, Roberts, I, Roy, NBA, Themistocleous, A, Watkins, H

Glucophosphate isomerase deficiency identified by next‐generation sequencing by Vora, S, Proven, M, Hipkiss, R, Ware, P, Howard, K, Dreau, H, Baird, S, Ouwehand, W, Megy, K, Stirrups, K, Lim, D, Norton, A, Kumar, A, Roberts, I, Layton, M, Roy, N

Genome sequence of Aedes aegypti, a major arbovirus vector. by Nene, V, Wortman, JR, Lawson, D, Haas, B, Kodira, C, Tu, Z, Loftus, B, Xi, Z, Megy, K, Grabherr, M, Ren, Q, Zdobnov, E, Lobo, N, Campbell, K, Brown, SE, Bonaldo, M, Zhu, J, Sinkins, S, Hogenkamp, D, Amedeo, P, Arensburger, P, Atkinson, P, Bidwell, S, Biedler, J, Birney, E

Genome sequence of Aedes aegypti, a major arbovirus vector by Nene, V, Wortman, JR, Lawson, D, Haas, B, Kodira, C, Tu, Z, Loftus, B, Xi, Z, Megy, K, Grabherr, M, Ren, Q, Zdobnov, E, Lobo, N, Campbell, K, Brown, SE, Bonaldo, M, Zhu, J, Sinkins, S, Hogenkamp, D, Amedeo, P, Arensburger, P, Atkinson, P, Bidwell, S, Biedler, J, Birney, E

Investigating genotype–phenotype relationship of extreme neuropathic pain disorders in a UK national cohort by Themistocleous, AC, Baskozos, G, Blesneac, I, Comini, M, Megy, K, Chong, S, Deevi, SVV, Ginsberg, L, Gosal, D, Hadden, RDM, Horvath, R, Mahdi-Rogers, M, Manzur, A, Mapeta, R, Marshall, A, Matthews, E, McCarthy, MI, Reilly, MM, Renton, T, Rice, ASC, Vale, TA, van Zuydam, N, Walker, SM, Woods, CG, Bennett, DLH

Whole genome sequencing for the investigation of rare anaemias: challenges and real-world outcomes by Brierley, C, Babbs, C, McGowan, S, Downes, D, Sanchis-Juan, A, Aydinok, Y, Thakur, I, Connor, P, Tedgard, U, Bechensteen, A, Harvet, G, De La Fuente, J, Mettananda, S, Hendricks, M, Carey, P, Lausen, B, Ancliff, P, Qureshi, A, Louka, E, Okoli, S, Psaila, B, O'Sullivan, J, Mead, A, Mapeta, R, Megy, K, Ouwehand, W, Turro, E, Roberts, I, Layton, M, Roy, N

Next‐generation sequencing for the diagnosis of MYH9‐RD: Predicting pathogenic variants by Bury, L, Megy, K, Stephens, JC, Grassi, L, Greene, D, Gleadall, N, Althaus, K, Allsup, D, Bariana, TK, Bonduel, M, Butta, NV, Collins, P, Curry, N, Deevi, SVV, Downes, K, Duarte, D, Elliott, K, Falcinelli, E, Furie, B, Keeling, D, Lambert, MP, Linger, R, Mangles, S, Mapeta, R, Millar, CM, Penkett, C, Perry, DJ, Stirrups, KE, Turro, E, Westbury, SK, Wu, J, Nihr BioResource, Gomez, K, Freson, K, Ouwehand, WH, Gresele, P, Simeoni, I

Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease by Carss, K, Arno, G, Erwood, M, Stephens, J, Sanchis-Juan, A, Hull, S, Megy, K, Grozeva, D, Dewhurst, E, Malka, S, Plagnol, V, Penkett, C, Stirrups, K, Rizzo, R, Wright, G, Josifova, D, Bitner-Glindzicz, M, Scott, R, Clement, E, Allen, L, Armstrong, R, Brady, A, Carmichael, J, Chitre, M, Henderson, R, Hurst, J, Maclaren, R, Murphy, E, Paterson, J, Rosser, E, Thompson, D, Wakeling, E, Ouwehand, W, Michaelides, M, Moore, A, Nihr-Bioresource Rare Diseases Consortium, Webster, A, Raymond, F

Whole-genome sequencing of a sporadic primary immunodeficiency cohort by Thaventhiran, JED, Lango Allen, H, Burren, OS, Rae, W, Greene, D, Staples, E, Zhang, Z, Farmery, JHR, Simeoni, I, Rivers, E, Maimaris, J, Penkett, CJ, Stephens, J, Deevi, SVV, Sanchis-Juan, A, Gleadall, NS, Thomas, MJ, Sargur, RB, Gordins, P, Baxendale, HE, Brown, M, Tuijnenburg, P, Worth, A, Hanson, S, Linger, RJ, Buckland, MS, Rayner-Matthews, PJ, Gilmour, KC, Samarghitean, C, Seneviratne, SL, Sansom, DM, Lynch, AG, Megy, K, Ellinghaus, E, Ellinghaus, D, Jorgensen, SF, Karlsen, TH, Stirrups, KE, Cutler, AJ, Kumararatne, DS, Chandra, A, Edgar, JDM, Herwadkar, A, Cooper, N, Grigoriadou, S, Huissoon, AP, Goddard, S, Jolles, S, Schuetz, C, Boschann, F, Roberts, IAG

The allelic landscape of human blood cell trait variation and links to common complex disease by Astle, WJ, Elding, H, Jiang, T, Allen, D, Ruklisa, D, Mann, AL, Mead, D, Bouman, H, Riveros-Mckay, F, Kostadima, MA, Lambourne, JJ, Sivapalaratnam, S, Downes, K, Kundu, K, Bomba, L, Berentsen, K, Bradley, JR, Daugherty, LC, Delaneau, O, Freson, K, Garner, SF, Grassi, L, Guerrero, J, Haimel, M, Janssen-Megens, EM, Kaan, A, Kamat, M, Kim, B, Mandoli, A, Marchini, J, Martens, JH, Meacham, S, Megy, K, O'Connell, J, Petersen, R, Sharifi, N, Sheard, SM, Staley, JR, Tuna, S, van der Ent, M, Walter, K, Wang, SY, Wheeler, E, Wilder, SP, Iotchkova, V, Moore, C, Sambrook, J, Stunnenberg, HG, Di Angelantonio, E, Kaptoge, S, Kuijpers, TW, Carrillo-de-Santa-Pau, E, Juan, D, Rico, D, Valencia, A, Chen, L, Ge, B, Vasquez, L, Kwan, T, Garrido-Martín, D, Watt, S, Yang, Y, Guigo, R, Beck, S, Paul, DS, Pastinen, T, Bujold, D, Bourque, G, Frontini, M, Danesh, J, Roberts, DJ, Ouwehand, WH, Butterworth, AS, Soranzo, N

Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children by French, CE, Delon, I, Dolling, H, Sanchis-Juan, A, Shamardina, O, Mégy, K, Abbs, S, Austin, T, Bowdin, S, Branco, RG, Firth, H, Tuna, S, Aitman, TJ, Ashford, S, Astle, WJ, Bennet, DL, Bleda, M, Carss, KJ, Chinnery, PF, Deevi, SVV, Fletcher, D, Gale, DP, Gräf, SF, Hu, F, James, R, Kasanicki, MA, Kingston, N, Koziell, AB, Allen, HL, Maher, ER, Markus, HS, Meacham, S, Morrell, NW, Penkett, CJ, Roberts, I, Smith, KGC, Stark, H, Stirrups, KE, Turro, E, Watkins, H, Williamson, C, Young, T, Bradley, JR, Ouwehand, WH, Raymond, FL, Agrawal, S, Armstrong, R, Beardsall, K, Belteki, G, Bohatschek, M, Broster, S, Campbell, R, Chaudhary, R, Costa, C, D’Amore, A, Fitzsimmons, A, Hague, J, Harley, J, Hoodbhoy, S, Kayani, R, Kelsall, W, Mehta, SG, O’Donnell, R, O’Hare, S, Ogilvy-Stuart, A, Papakostas, S, Park, SM, Parker, A, Pathan, N, Prapa, M, Sammut, A, Sandford, R, Schon, K, Singh, Y, Spike, K, Tavares, ALT, Wari-Pepple, D, Wong, HS, Woods, CG, Rowitch, DH, Raymond, FL

Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes by Whitworth, J, Smith, PS, Martin, J-E, West, H, Luchetti, A, Rodger, F, Clark, G, Carss, K, Stephens, J, Stirrups, K, Penkett, C, Mapeta, R, Ashford, S, Megy, K, Shakeel, H, Ahmed, M, Adlard, J, Barwell, J, Brewer, C, Casey, RT, Armstrong, R, Cole, T, Evans, DG, Fostira, F, Greenhalgh, L, Hanson, H, Henderson, A, Hoffman, J, Izatt, L, Kumar, A, Kwong, A, Lalloo, F, Ong, KR, Paterson, J, Park, S-M, Chen-Shtoyerman, R, Searle, C, Side, L, Skytte, A-B, Snape, K, Woodward, ER, Tischkowitz, MD, Maher, ER, Aitman, T, Alachkar, H, Ali, S, Allen, L, Allsup, D, Ambegaonkar, G, Anderson, J, Antrobus, R, Armstrong, R, Arno, G, Arumugakani, G, Ashford, S, Astle, W, Attwood, A, Austin, S, Bacchelli, C, Bakchoul, T, Bariana, TK, Baxendale, H, Bennett, D, Bethune, C, Bibi, S, Bitner-Glindzicz, M, Bleda, M, Boggard, H, Bolton-Maggs, P, Booth, C, Bradley, JR, Brady, A, Brown, M, Browning, M, Bryson, C, Burns, S, Calleja, P, Canham, N, Carmichael, J, Carss, K, Caulfield, M, Chalmers, E, Chandra, A, Chinnery, P, Chitre, M, Church, C, Clement, E, Clements-Brod, N, Clowes, V, Coghlan, G, Collins, P, Cookson, V, Cooper, N, Corris, P, Creaser-Myers, A, Dacosta, R, Daugherty, L, Davies, S, Davis, J, De Vries, M, Deegan, P, Deevi, SVV, Deshpande, C, Devlin, L, Dewhurst, E, Dixon, P, Doffinger, R, Dormand, N, Drewe, E, Edgar, D, Egner, W, Erber, WN, Erwood, M, Erwood, M, Everington, T, Favier, R, Firth, H, Fletcher, D, Flinter, F, Frary, A, Freson, K, Furie, B, Furnell, A, Gale, D, Gardham, A, Gattens, M, Ghali, N, Ghataorhe, PK, Ghurye, R, Gibbs, S, Gilmour, K, Gissen, P, Goddard, S, Gomez, K, Gordins, P, Graf, S, Gräf, S, Greene, D, Greenhalgh, A, Greinacher, A, Grigoriadou, S, Grozeva, D, Hackett, S, Hadinnapola, C, Hague, R, Haimel, M, Halmagyi, C, Hammerton, T, Hart, D, Hayman, G, Heemskerk, JWM, Henderson, R, Hensiek, A, Henskens, Y, Herwadkar, A, Holden, S, Holder, M, Holder, S, Hu, F, Veld, A, Huissoon, A, Humbert, M, Hurst, J, James, R, Jolles, S, Josifova, D, Kazmi, R, Keeling, D, Kelleher, P, Kelly, AM, Kennedy, F, Kiely, D, Kingston, N, Koziell, A, Krishnakumar, D, Kuijpers, TW, Kuijpers, T, Kumararatne, D, Kurian, M, Laffan, MA, Lambert, MP, Allen, HL, Lango-Allen, H, Lawrie, A, Lear, S, Lees, M, Lentaigne, C, Liesner, R, Linger, R, Longhurst, H, Lorenzo, L, Louka, E, Machado, R, Ross, RM, Maclaren, R, Maher, E, Maimaris, J, Mangles, S, Manson, A, Mapeta, R, Markus, HS, Martin, J, Masati, L, Mathias, M, Matser, V, Maw, A, McDermott, E, McJannet, C, Meacham, S, Meehan, S, Megy, K, Mehta, S, Michaelides, M, Millar, CM, Moledina, S, Moore, A, Morrell, N, Mumford, A, Murng, S, Murphy, E, Nejentsev, S, Noorani, S, Nurden, P, Oksenhendler, E, Othman, S, Ouwehand, WH, Ouwehand, WH, Papadia, S, Park, S-M, Parker, A, Pasi, J, Patch, C, Paterson, J, Payne, J, Peacock, A, Peerlinck, K, Penkett, CJ, Pepke-Zaba, J, Perry, D, Perry, DJ, Pollock, V, Polwarth, G, Ponsford, M, Qasim, W, Quinti, I, Rankin, S, Rankin, J, Raymond, FL, Rayner-Matthews, P, Rehnstrom, K, Reid, E, Rhodes, CJ, Richards, M, Richardson, S, Richter, A, Roberts, I, Rondina, M, Rosser, E, Roughley, C, Roy, N, Rue-Albrecht, K, Samarghitean, C, Sanchis-Juan, A, Sandford, R, Santra, S, Sargur, R, Savic, S, Schotte, G, Schulman, S, Schulze, H, Scott, R, Scully, M, Seneviratne, S, Sewell, C, Shamardina, O, Shipley, D, Simeoni, I, Sivapalaratnam, S, Smith, KGC, Sohal, A, Southgate, L, Staines, S, Staples, E, Stark, H, Stauss, H, Stein, P, Stephens, J, Stirrups, K, Stock, S, Suntharalingam, J, Talks, K, Tan, Y, Thachil, J, Thaventhiran, J, Thomas, E, Thomas, M, Thompson, D, Thrasher, A, Tischkowitz, M, Titterton, C, Toh, C-H, Toshner, M, Treacy, C, Trembath, R, Tuna, S, Turek, W, Turro, E, Van Geet, C, Veltman, M, Vogt, J, Von Ziegenweldt, J, Noordegraaf, AV, Wakeling, E, Wanjiku, I, Warner, TQ, Wassmer, E, Watkins, H, Watt, C, Webster, N, Welch, S, Westbury, S, Wharton, J, Whitehorn, D, Wilkins, M, Willcocks, L, Williamson, C, Woods, G, Woods, G, Wort, J, Yeatman, N, Yong, P, Young, T, Yu, P