Myeloid pre-leukemia and leukemia of Down syndrome by Cruz Hernandez, D, Vyas, P

Oncogenic drivers and development by Cruz Hernandez, D, Vyas, P

GATA1 and cooperating mutations in myeloid leukaemia of Down syndrome by Garnett, C, Cruz Hernandez, D, Vyas, P

Heterologous vaccination interventions to reduce pandemic morbidity and mortality: modeling the US winter 2020 COVID-19 wave by Hupert, N, Marín-Hernández, D, Gao, B, Águas, R, Nixon, DF

Sensitive, rapid diagnostic test for transient abnormal myelopoiesis and myeloid leukemia of Down syndrome by Cruz Hernandez, D, Metzner, M, de Groot, AP, Usukhbayar, B, Elliott, N, Roberts, I, Vyas, P

Single-cell assessment of transcriptome alterations induced by Scriptaid in early differentiated human haematopoietic progenitors during ex vivo expansion by Hua, P, Kronsteiner, B, Van Der Gard, M, Ashley, N, Hernandez, D, Tarunina, M, Hook, L, Choo, Y, Roberts, I, Mead, A, Watt, S

A novel high throughput screening platform reveals an optimised cytokine formulation for human hematopoietic progenitor cell expansion. by Tarunina, M, Hernandez, D, Kronsteiner-Dobramysl, B, Pratt, P, Watson, T, Hua, P, Gullo, F, Van der Garde, M, Zhang, Y, Hook, L, Choo, Y, Watt, S

A Mendelian randomisation study provides initial evidence that sex hormone binding globulin (SHBG) levels alter type 2 diabetes risk by Perry, J, Melzer, D, Maggio, M, Hernandez, D, Singleton, A, Ferrucci, L, Palmer, C, Bennett, A, Ruokonen, A, Panicker, V, Jarvelin, M, Hattersley, A, Mccarthy, M, Frayling, T

A candidate gene for autoimmune myasthenia gravis. by Landouré, G, Knight, M, Stanescu, H, Taye, A, Shi, Y, Diallo, O, Johnson, J, Hernandez, D, Traynor, B, Biesecker, L, Elkahloun, A, Rinaldi, C, Vincent, A, Willcox, N, Kleta, R, Fischbeck, K, Burnett, BG

Oncogenic Gata1 causes stage-specific megakaryocyte differentiation delay by Juban, G, Nathalie Sakakini, Chagraoui, H, Cruz Hernandez, D, Cheng, Q, Soady, K, Stoilova, B, Garnett, C, Waithe, D, Otto, G, Doondeea, J, Usukhbayar, B, Karkoulia, E, Alexiou, M, Strouboulis, J, Morrissey, E, Roberts, I, Porcher, C, Vyas, P

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. by Chiò, A, Schymick, J, Restagno, G, Scholz, S, Lombardo, F, Lai, S, Mora, G, Fung, H, Britton, A, Arepalli, S, Gibbs, JR, Nalls, M, Berger, S, Kwee, L, Oddone, E, Ding, J, Crews, C, Rafferty, I, Washecka, N, Hernandez, D, Ferrucci, L, Bandinelli, S, Guralnik, J, Macciardi, F, Torri, F

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes. by Wood, A, Tuke, M, Nalls, M, Hernandez, D, Gibbs, JR, Lin, H, Xu, C, Li, Q, Shen, J, Jun, G, Almeida, M, Tanaka, T, Perry, JR, Gaulton, K, Rivas, M, Pearson, R, Curran, J, Johnson, M, Göring, H, Duggirala, R, Blangero, J, Mccarthy, M, Bandinelli, S, Murray, A, Weedon, M

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study by Majounie, E, Renton, A, Mok, K, Dopper, E, Waite, A, Rollinson, S, Chiò, A, Restagno, G, Nicolaou, N, Simon-Sanchez, J, van Swieten, J, Abramzon, Y, Johnson, J, Sendtner, M, Pamphlett, R, Orrell, R, Mead, S, Sidle, K, Houlden, H, Rohrer, J, Morrison, K, Pall, H, Talbot, K, Ansorge, O, Hernandez, D

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. by Keller, M, Saad, M, Bras, J, Bettella, F, Nicolaou, N, Simón-Sánchez, J, Mittag, F, Büchel, F, Sharma, M, Gibbs, JR, Schulte, C, Moskvina, V, Durr, A, Holmans, P, Kilarski, L, Guerreiro, R, Hernandez, D, Brice, A, Ylikotila, P, Stefánsson, H, Majamaa, K, Morris, H, Williams, N, Gasser, T, Heutink, P

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. by Majounie, E, Renton, A, Mok, K, Dopper, E, Waite, A, Rollinson, S, Chiò, A, Restagno, G, Nicolaou, N, Simon-Sanchez, J, van Swieten, J, Abramzon, Y, Johnson, J, Sendtner, M, Pamphlett, R, Orrell, R, Mead, S, Sidle, K, Houlden, H, Rohrer, J, Morrison, K, Pall, H, Talbot, K, Ansorge, O, Hernandez, D

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies by Nalls, M, Plagnol, V, Hernandez, D, Sharma, M, Sheerin, U, Saad, M, Simon-Sanchez, J, Schulte, C, Lesage, S, Sveinbjornsdottir, S, Arepalli, S, Barker, R, Ben-Shlomo, Y, Berendse, H, Berg, D, Bhatia, K, de Bie, R, Biffi, A, Bloem, B, Bochdanovits, Z, Bonin, M, Bras, J, Brockmann, K, Brooks, J, Burn, D

Mechanisms of progression of myeloid preleukemia to transformed myeloid leukemia in children with Down syndrome by Labuhn, M, Perkins, K, Matzk, S, Varghese, L, Garnett, C, Papaemmanuil, E, Metzner, M, Kennedy, A, Amstislavskiy, V, Risch, T, Bhayadia, R, Samulowski, D, Hernandez, D, Stoilova, B, Iotchkova, V, Oppermann, U, Scheer, C, Yoshida, K, Schwarzer, A, Taub, J, Crispino, J, Weiss, M, Hayashi, A, Taga, T, Ito, E, Ogawa, S, Reinhardt, D, Yaspo, M, Campbell, P, Roberts, I, Constantinescu, S, Vyas, P, Heckl, D, Klusmann, J

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases by Nalls, M, Bras, J, Hernandez, D, Keller, M, Majounie, E, Renton, A, Saad, M, Jansen, I, Guerreiro, R, Lubbe, S, Plagnol, V, Gibbs, J, Schulte, C, Pankratz, N, Sutherland, M, Bertram, L, Lill, C, DeStefano, A, Faroud, T, Eriksson, N, Tung, J, Edsall, C, Nichols, N, Brooks, J, Arepalli, S, Pliner, H, Letson, C, Heutink, P, Martinez, M, Gasser, T, Traynor, B, Wood, N, Hardy, J, Singleton, A

A genome-wide association study identifies protein quantitative trait loci (pQTLs). by Melzer, D, Perry, JR, Hernandez, D, Corsi, A, Stevens, K, Rafferty, I, Lauretani, F, Murray, A, Gibbs, JR, Paolisso, G, Rafiq, S, Simon-Sanchez, J, Lango, H, Scholz, S, Weedon, M, Arepalli, S, Rice, N, Washecka, N, Hurst, A, Britton, A, Henley, W, van de Leemput, J, Li, R, Newman, AB, Tranah, G, Harris, T, Panicker, V, Dayan, C, Bennett, A, McCarthy, M, Ruokonen, A, Jarvelin, MR, Guralnik, J, Bandinelli, S, Frayling, T, Singleton, A, Ferrucci, L

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. by Bras, J, Guerreiro, R, Darwent, L, Parkkinen, L, Ansorge, O, Escott-Price, V, Hernandez, D, Nalls, M, Clark, L, Honig, L, Marder, K, Van Der Flier, WM, Lemstra, A, Scheltens, P, Rogaeva, E, St George-Hyslop, P, Londos, E, Zetterberg, H, Ortega-Cubero, S, Pastor, P, Ferman, T, Graff-Radford, N, Ross, O, Barber, I, Braae, A, Brown, K, Morgan, K, Maetzler, W, Berg, D, Troakes, C, Al-Sarraj, S, Lashley, T, Compta, Y, Revesz, T, Lees, A, Cairns, N, Halliday, G, Mann, D, Pickering-Brown, S, Dickson, D, Singleton, A, Hardy, J