Characterising the functional role of GATA1short isoform in normal and malignant haematopoiesis por Cruz Hernandez, D

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

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

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

Heterologous vaccination interventions to reduce pandemic morbidity and mortality: modeling the US winter 2020 COVID-19 wave por 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 por 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 por 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. por 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 por 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. por 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 por 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. por 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. por 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 por 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. por 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. por 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 por 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 por 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 por 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). por 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