FORABOSCO, PAOLA
FORABOSCO, PAOLA
Istituto di Ricerca Genetica e Biomedica - IRGB
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset
2024 Forabosco, P.; Pala, M.; Crobu, F.; Diana, M. A.; Marongiu, M.; Cusano, R.; Angius, A.; Steri, M.; Orru, V.; Schlessinger, D.; Fiorillo, E.; Devoto, M.; Cucca, F.
A Sardinian founder mutation in glycoprotein Ib platelet subunit beta(GP1BB) that impacts thrombocytopenia
2020 Busonero, Fabio; Steri, Maristella; Orru, Valeria; Sole, Gabriella; Olla, Stefania; Marongiu, Michele; Maschio, Andrea; Sidore, Carlo; Lai, Sandra; Mulas, Antonella; Zoledziewska, Magdalena; Floris, Matteo; Pala, Mauro; Forabosco, Paola; Asunis, Isadora; Pitzalis, Maristella; Deidda, Francesca; Masala, Marco; Caria, Cristian Antonio; Barella, Susanna; Abecasis, Goncalo R.; Schlessinger, David; Sanna, Serena; Fiorillo, Edoardo; Cucca, Francesco
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders
2020 Mencacci N.E.; Reynolds R.; Ruiz S.G.; Vandrovcova J.; Forabosco P.; SanchezFerrer A.; Volpato V.; Weale M.E.; Bhatia K.P.; Webber C.; Hardy J.; Botia J.A.; Ryten M.; Botia J.A.; D'Sa K.; Forabosco P.; Guelfi S.; Hardy J.; Vandrovcova J.; Mackenzie C.A.; Ramasamy A.; Ryten M.; Smith C.; Trabzuni D.; Weale M.E.; Noyce A.J.; Kaiyrzhanov R.; Middlehurst B.; Kia D.A.; Tan M.; Houlden H.; Morris H.R.; PlunFavreau H.; Holmans P.; Hardy J.; Trabzuni D.; Bras J.; Quinn J.; Mok K.Y.; Kinghorn K.J.; Billingsley K.; Wood N.W.; Lewis P.; Guerreiro R.; Lovering R.; R'Bibo L.; Manzoni C.; Rizig M.; Ryten M.; Guelfi S.; EscottPrice V.; Chelban V.; Foltynie T.; Williams N.; Shashakin C.; Zharkinbekova N.; Zholdybayeva E.; Aitkulova A.; Harvey K.; Brice A.; Danjou F.; Lesage S.; Corvol J.C.; Martinez M.; Giri A.; Schulte C.; Brockmann K.; SimonSanchez J.; Heutink P.; Rizzu P.; Sharma M.; Gasser T.; Nicolas A.; Cookson M.R.; BandresCiga S.; Blauwendraat C.; Craig D.W.; Faghri F.; Raphael Gibbs J.; Hernandez D.G.; van KeurenJensen K.; Shulman J.M.; Leonard H.L.; Nalls M.A.; Robak L.; Lubbe S.; Finkbeiner S.; Mencacci N.E.; Lungu C.; Singleton A.B.; Scholz S.W.; Reed X.; van KeurenJensen K.; GanOr Z.; Rouleau G.A.; van Hilten J.J.; Marinus J.; AdarmesGomez A.D.; Aguilar M.; Alvarez I.; Alvarez V.; Barrero F.J.; Yarza J.A.B.; BernalBernal I.; Blazquez M.; BonillaToribio M.; Botia J.A.; Boungiorno M.T.; BuizaRueda D.; Camara A.; Carcel M.; Carrillo F.; CarrionClaro M.; Cerdan D.; Clarimon J.; Compta Y.; DiezFairen M.; DolsIcardo O.; Duarte J.; Duran R.; EscamillaSevilla F.; Ezquerra M.; Fernandez M.; FernandezSantiago R.; Garcia C.; GarciaRuiz P.; GomezGarre P.; Heredia M.J.G.; GonzalezAramburu I.; Pagola A.G.; Hoenicka J.; Infante J.; Jesus S.; JimenezEscrig A.; Kulisevsky J.; LabradorEspinosa M.A.; LopezSendon J.L.; de Munain Arregui A.L.; Macias D.; Marin J.; Marti M.J.; MartinezCastrillo J.C.; MendezDelBarrio C.; Gonzalez M.M.; Minguez A.; Mir P.; Rezola E.M.; Munoz E.; Pagonabarraga J.; Pastor P.; Errazquin F.P.; PerinanTocino T.; RuizMartinez J.; Ruz C.; Rodriguez A.S.; Sierra M.; SuarezSanmartin E.; Tabernero C.; Tartari J.P.; TejeraParrado C.; Tolosa E.; Valldeoriola F.; VargasGonzalez L.; Vela L.; Vives F.; Zimprich A.; Pihlstrom L.; Taba P.; Koks S.
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
2020 Guelfi, S; D'Sa, K; Botia, Ja; Vandrovcova, J; Reynolds, Rh; Zhang, D; Trabzuni, D; Colladotorres, L; Thomason, A; Quijada Leyton, P; Gagliano Taliun, Sa; Nalls, Ma; Noyce, Aj; Nicolas, A; Cookson, Mr; Bandresciga, S; Gibbs, Jr; Hernandez, Dg; Singleton, Ab; Reed, X; Leonard, H; Blauwendraat, C; Faghri, F; Bras, J; Guerreiro, R; Tucci, A; Kia, Da; Houlden, H; Plunfavreau, H; Mok, Ky; Wood, Nw; Lovering, R; R'Bibo, L; Rizig, M; Chelban, V; Tan, M; Morris, Hr; Middlehurst, B; Quinn, J; Billingsley, K; Holmans, P; Kinghorn, Kj; Lewis, P; Escottprice, V; Williams, N; Foltynie, T; Brice, A; Danjou, F; Lesage, S; Corvol, Jc; Martinez, M; Giri, A; Schulte, C; Brockmann, K; Simonsanchez, J; Heutink, P; Gasser, T; Rizzu, P; Sharma, M; Shulman, Jm; Robak, L; Lubbe, S; Mencacci, Ne; Finkbeiner, S; Lungu, C; Scholz, Sw; Ganor, Z; Rouleau, Ga; Krohan, L; van Hilten, Jj; Marinus, J; Adarmesgomez, Ad; Bernalbernal, I; Bonillatoribio, M; Buizarueda, D; Carrillo, F; Carrionclaro, M; Mir, P; Gomezgarre, P; Jesus, S; Labradorespinosa, Ma; Macias, D; Vargasgonzalez, L; Mendezdelbarrio, C; Perinantocino, T; Tejeraparrado, C; Diezfairen, M; Aguilar, M; Alvarez, I; Boungiorno, Mt; Carcel, M; Pastor, P; Tartari, Jp; Alvarez, V; Gonzalez, Mm; Blazquez, M; Garcia, C; Suarezsanmartin, E; Barrero, Fj; Rezola, Em; Yarza, Jab; Pagola, Ag; Arregui, Alm; Ruizmartinez, J; Cerdan, D; Duarte, J; Clarimon, J; Dolsicardo, O; Infante, J; Marin, J; Kulisevsky, J; Pagonabarraga, J; Gonzalezaramburu, I; Rodriguez, As; Sierra, M; Duran, R; Ruz, C; Vives, F; Escamillasevilla, F; Minguez, A; Camara, A; Compta, Y; Ezquerra, M; Marti, Mj; Fernandez, M; Munoz, E; Fernandezsantiago, R; Tolosa, E; Valldeoriola, F; Garciaruiz, P; Heredia, Mjg; Errazquin, Fp; Hoenicka, J; Jimenezescrig, A; Martinezcastrillo, Jc; Lopezsendon, Jl; Torres, Im; Tabernero, C; Vela, L; Zimprich, A; Pihlstrom, L; Koks, S; Taba, P; Majamaa, K; Siitonen, A; Okubadejo, Nu; Ojo, Oo; Forabosco, P; Walker, R; Small, Ks; Smith, C; Ramasamy, A; Hardy, J; Weale, Me; Ryten, M
Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity
2018 Ip, Hf; Jansen, R; Abdellaoui, A; Bartels, M; Ryten, M; Hardy, J; Weale, Me; Ramasamy, A; Forabosco, P; Matarin, M; Vandrovcova, J; Botia, Ja; D'Sa, K; Guelfi, S; Smith, C; Walker, R; Reynolds, Rh; Zhang, D; Trabzuni, D; Boomsma, Di; Nivard, Mg
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks
2017 Botia, Ja; Vandrovcova, J; Forabosco, P; Guelfi, S; D'Sa, K; Hardy, J; Lewis, Cm; Ryten, M; Weale, Me; Ramasamy, A; Trabzuni, D; Smith, C; Walker, R
Frontotemporal dementia: Insights into the biological underpinnings of disease through gene co-expression network analysis
2016 Ferrari, R; Forabosco, P; Vandrovcova, J; Botia, Ja; Guelfi, S; Warren, Jd; Momeni, P; Weale, Me; Ryten, M; Hardy, J
Gene co-expression networks shed light into diseases of brain iron accumulation
2016 Bettencourt, C; Forabosco, P; Wiethoff, S; Heidari, M; Johnstone, Dm; Botia, Ja; Collingwood, Jf; Hardy, J; Milward, Ea; Ryten, M; Houlden, H; for the UK Brain Expression Consortium, Ukbec
A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia
2015 Mencacci N.E.; RubioAgusti I.; Zdebik A.; Asmus F.; Ludtmann M.H.R.; Ryten M.; Plagnol V.; Hauser A.K.; BandresCiga S.; Bettencourt C.; Forabosco P.; Hughes D.; Soutar M.M.P.; Peall K.; Morris H.R.; Trabzuni D.; Tekman M.; Stanescu H.C.; Kleta R.; Carecchio M.; Zorzi G.; Nardocci N.; Garavaglia B.; Lohmann E.; Weissbach A.; Klein C.; Hardy J.; Pittman A.M.; Foltynie T.; Abramov A.Y.; Gasser T.; Bhatia K.P.; Wood N.W.
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank
2015 Wain L.V.; Shrine N.; Miller S.; Jackson V.E.; Ntalla I.; Artigas M.S.; Billington C.K.; Kheirallah A.K.; Allen R.; Cook J.P.; Probert K.; Obeidat M.; Bosse Y.; Hao K.; Postma D.S.; Pare P.D.; Ramasamy A.; Magi R.; Mihailov E.; Reinmaa E.; Melen E.; O'Connell J.; Frangou E.; Delaneau O.; Freeman C.; Petkova D.; McCarthy M.; Sayers I.; Deloukas P.; Hubbard R.; Pavord I.; Hansell A.L.; Thomson N.C.; Zeggini E.; Morris A.P.; Marchini J.; Strachan D.P.; Tobin M.D.; Hall I.P.; Farrall M.; Barroso I.; Anderson C.A.; Botia J.; Vandrocova J.; Guelfi S.; D'Sa K.; Ryten M.; Trabzuni D.; Matarin M.; Hardy J.A.; Weale M.E.; Varghese V.; Forabosco P.; Farmer A.; McGuffin P.; Zgaga L.; Wilson J.F.; Wild S.H.; Campbell H.; Rudan I.; Smith C.; Walker R.; Liu J.Z.; Tozzi F.; Muglia P.; Waterworth D.M.; Pillai S.G.; Yuan X.; Mooser V.; Middleton L.; Kooner J.; Chambers J.C.; Berrettini W.; Knouff C.W.; Waeber G.; Vollenweider P.; Preisig M.; Wareham N.J.; Zhao J.H.; Loos R.J.F.; Khaw K.T.; Grundy S.; Barter P.; Mahley R.; Kesaniemi A.; McPherson R.; Vincent J.B.; Strauss J.; Kennedy J.L.; Day R.; Matthews K.; Bakke P.; Gulsvik A.; Lucae S.; Ising M.; Brueckl T.; Horstmann S.; Wichmann H.E; Rawal R.; Wichmann H.E.; Lamina C.; Dahmen N.; Polasek O.; Kolcic I.; Huffman J.; Campbell S.; Vitart V.; Hayward C.; Wright A.F.; Burnett M.S.; Devaney J.M.; Pichard A.D.; Kent K.M.; Satler L.; Lindsay J.M.; Waksman R.; Epstein S.; Reilly M.P.; Li M.; Qu L.; Wilensky R.; Matthai W.; Hakonarson H.H.; Rader D.J.; Ellinghaus D.; Lieb W.; Franke A.; Uda M.; Busonero F.; Terracciano A.; Schlessinger D.; Xiao X.; Scheet P.; St Clair D.; Rujescu D.; Abecasis G.R.; Grabe H.J.; Teumer A.; Volzke H.; Petersmann A.; John U.; Wright B.J.; Thompson J.R.; Balmforth A.J.; Hall A.S.; Samani N.J.; Ahmad T.; Mathew C.G.; Parkes M.; Satsangi J.; Caulfield M.; Munroe P.B.; Dominiczak A.; Worthington J.; Thomson W.; Eyre S.; Barton A.; Francks C.
Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis
2014 Ramasamy A.; Trabzuni D.; Forabosco P.; Smith C.; Walker R.; Dillman A.; Sveinbjornsdottir S.; Hardy J.; Weale M.E.; Ryten M.
Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia
2014 Bettencourt, Conceicao; Ryten, Mina; Forabosco, Paola; Schorge, Stephanie; Hersheson, Joshua; Hardy, John; Houlden, Henry
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease
2014 Cruchaga, Carlos; Karch Celeste, M; Jin Sheng, Chih; Benitez Bruno, A; Cai, Yefei; Guerreiro, Rita; Harari, Oscar; Norton, Joanne; Budde, John; Bertelsen, Sarah; Jeng Amanda, T; Cooper, Breanna; Skorupa, Tara; Carrell, David; Levitch, Denise; Hsu, Simon; Choi, Jiyoon; Ryten, Mina; Sassi, Celeste; Bras, Jose; Gibbs, J Raphael; Hernandez Dena, G; Lupton Michelle, K; Powell, John; Forabosco, Paola; Ridge Perry, G; Corcoran Christopher, D; Tschanz Joann, T; Norton Maria, C; Munger Ronald, G; Schmutz, Cameron; Leary, Maegan; Demirci, F Yesim; Bamne Mikhil, N; Wang, Xingbin; Lopez Oscar, L; Ganguli, Mary; Medway, Christopher; Turton, James; Lord, Jenny; Braae, Anne; Barber, Imelda; Brown, Kristelle; Pastor, Pau; Lorenzobetancor, Oswaldo; Brkanac, Zoran; Scott, Erick; Topol, Eric; Morgan, Kevin; Rogaeva, Ekaterina; Singleton Andrew, B; Hardy, John; Kamboh, M Ilyas; St GeorgeHyslop, Peter; Cairns, Nigel; Morris John, C; Kauwe John, S K; Goate Alison, M
Insights into TREM2 biology by network analysis of human brain gene expression data
2013 Forabosco, Paola; Ramasamy, Adaikalavan; Trabzuni, Daniah; Walker, Robert; Smith, Colin; Bras, Jose; Levine Adam, P; Hardy, John; Pocock Jennifer, M; Guerreiro, Rita; Weale Michael, E; Ryten, Mina
Predicting the Risk of Rheumatoid Arthritis and Its Age of Onset through Modelling Genetic Risk Variants with Smoking
2013 Scott Ian, C; Seegobin Seth, D; Steer, Sophia; Tan, Rachael; Forabosco, Paola; Hinks, Anne; Eyre, Stephen; Morgan Ann, W; Wilson Anthony, G; Hocking Lynne, J; Wordsworth, Paul; Barton, Anne; Worthington, Jane; Cope Andrew, P; Lewis Cathryn, M
Prediction model for rheumatoid arthritis: modelling 46 genetic risk variants with smoking
2013 Scott, Ian C.; Steer, Sophia; Tan, Rachael; Forabosco, Paola; Morgan, Ann W.; Hinks, Anne; Thomson, Wendy; Barton, Anne; Worthington, Jane; Cope, Andrew P.; Lewis, Cathryn M.
Association of the IL-10 Gene Family Locus on Chromosome 1 with Juvenile Idiopathic Arthritis (JIA)
2012 Ebun Omoyinmi; Paola Forabosco;Raja Hamaoui; Annette Bryant; Anne Hinks; Simona Ursu; Childhood Arthritis Prospective Study CAPS; BSPAR study group;Childhood Arthritis Response to Medication Study CHARMS; Lucy R. Wedderburn; Wendy Thomson; Cathryn M. Lewis;Patricia Woo
Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis.
2011 Tore S; Casula S; Casu G; Concas MP; Pistidda P; Persico I; Sassu A; Maestrale GB; Mele C; Caruso MR; Bonerba B; Usai P; Deiana I; Thornton T; Pirastu M; Forabosco P
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy
2010 Bouzigon, E; Forabosco, P; Koppelman, Gh; Cookson, Wo; Dizier, Mh; Duffy, Dl; Evans, Dm; Ferreira, Ma; Kere, J; Laitinen, T; Malerba, G; Meyers, Da; Moffatt, M; Martin, Ng; Ng, My; Pignatti, Pf; Wjst, M; Kauffmann, F; Demenais, F; Lewis, Cm
Meta-analysis of 32 genome-wide linkage studies of schizophreniaGenome-wide linkage studies of SCZ
2009 Ng MY; Levinson DF; Faraone SV; Suarez BK; DeLisi LE; Arinami T; Riley B; Paunio T; Pulver AE; Irmansyah; Holmans PA; Escamilla M; Wildenauer DB; Williams NM; Laurent C; Mowry BJ; Brzustowicz LM; Maziade M; Sklar P; Garver DL; Abecasis GR; Lerer B; Fallin MD; Gurling HM; Gejman PV; Lindholm E; Moises HW; Byerley W; Wijsman EM; Forabosco P; Tsuang MT; Hwu HG; Okazaki Y; Kendler KS; Wormley B; Fanous A; Walsh D; O'Neill FA; Peltonen L; Nestadt G; Lasseter VK; Liang KY; Papadimitriou GM; Dikeos DG; Schwab SG; Owen MJ; O'Donovan MC; Norton N; Hare E; Raventos H; Nicolini H; Albus M; Maier W; Nimgaonkar VL; Terenius L; Mallet J; Jay M; Godard S; Nertney D; Alexander M; Crowe RR; Silverman JM; Bassett AS; Roy MA; Mérette C; Pato CN; Pato MT; Roos JL; Kohn Y; AmannZalcenstein D; Kalsi G; McQuillin A; Curtis D; Brynjolfson J; Sigmundsson T; Petursson H; Sanders AR; Duan J; Jazin E; MylesWorsley M; Karayiorgou M; Lewis CM
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset | 1-gen-2024 | Forabosco, P.; Pala, M.; Crobu, F.; Diana, M. A.; Marongiu, M.; Cusano, R.; Angius, A.; Steri, M.; Orru, V.; Schlessinger, D.; Fiorillo, E.; Devoto, M.; Cucca, F. | |
| A Sardinian founder mutation in glycoprotein Ib platelet subunit beta(GP1BB) that impacts thrombocytopenia | 1-gen-2020 | Busonero, Fabio; Steri, Maristella; Orru, Valeria; Sole, Gabriella; Olla, Stefania; Marongiu, Michele; Maschio, Andrea; Sidore, Carlo; Lai, Sandra; Mulas, Antonella; Zoledziewska, Magdalena; Floris, Matteo; Pala, Mauro; Forabosco, Paola; Asunis, Isadora; Pitzalis, Maristella; Deidda, Francesca; Masala, Marco; Caria, Cristian Antonio; Barella, Susanna; Abecasis, Goncalo R.; Schlessinger, David; Sanna, Serena; Fiorillo, Edoardo; Cucca, Francesco | |
| Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders | 1-gen-2020 | Mencacci N.E.; Reynolds R.; Ruiz S.G.; Vandrovcova J.; Forabosco P.; SanchezFerrer A.; Volpato V.; Weale M.E.; Bhatia K.P.; Webber C.; Hardy J.; Botia J.A.; Ryten M.; Botia J.A.; D'Sa K.; Forabosco P.; Guelfi S.; Hardy J.; Vandrovcova J.; Mackenzie C.A.; Ramasamy A.; Ryten M.; Smith C.; Trabzuni D.; Weale M.E.; Noyce A.J.; Kaiyrzhanov R.; Middlehurst B.; Kia D.A.; Tan M.; Houlden H.; Morris H.R.; PlunFavreau H.; Holmans P.; Hardy J.; Trabzuni D.; Bras J.; Quinn J.; Mok K.Y.; Kinghorn K.J.; Billingsley K.; Wood N.W.; Lewis P.; Guerreiro R.; Lovering R.; R'Bibo L.; Manzoni C.; Rizig M.; Ryten M.; Guelfi S.; EscottPrice V.; Chelban V.; Foltynie T.; Williams N.; Shashakin C.; Zharkinbekova N.; Zholdybayeva E.; Aitkulova A.; Harvey K.; Brice A.; Danjou F.; Lesage S.; Corvol J.C.; Martinez M.; Giri A.; Schulte C.; Brockmann K.; SimonSanchez J.; Heutink P.; Rizzu P.; Sharma M.; Gasser T.; Nicolas A.; Cookson M.R.; BandresCiga S.; Blauwendraat C.; Craig D.W.; Faghri F.; Raphael Gibbs J.; Hernandez D.G.; van KeurenJensen K.; Shulman J.M.; Leonard H.L.; Nalls M.A.; Robak L.; Lubbe S.; Finkbeiner S.; Mencacci N.E.; Lungu C.; Singleton A.B.; Scholz S.W.; Reed X.; van KeurenJensen K.; GanOr Z.; Rouleau G.A.; van Hilten J.J.; Marinus J.; AdarmesGomez A.D.; Aguilar M.; Alvarez I.; Alvarez V.; Barrero F.J.; Yarza J.A.B.; BernalBernal I.; Blazquez M.; BonillaToribio M.; Botia J.A.; Boungiorno M.T.; BuizaRueda D.; Camara A.; Carcel M.; Carrillo F.; CarrionClaro M.; Cerdan D.; Clarimon J.; Compta Y.; DiezFairen M.; DolsIcardo O.; Duarte J.; Duran R.; EscamillaSevilla F.; Ezquerra M.; Fernandez M.; FernandezSantiago R.; Garcia C.; GarciaRuiz P.; GomezGarre P.; Heredia M.J.G.; GonzalezAramburu I.; Pagola A.G.; Hoenicka J.; Infante J.; Jesus S.; JimenezEscrig A.; Kulisevsky J.; LabradorEspinosa M.A.; LopezSendon J.L.; de Munain Arregui A.L.; Macias D.; Marin J.; Marti M.J.; MartinezCastrillo J.C.; MendezDelBarrio C.; Gonzalez M.M.; Minguez A.; Mir P.; Rezola E.M.; Munoz E.; Pagonabarraga J.; Pastor P.; Errazquin F.P.; PerinanTocino T.; RuizMartinez J.; Ruz C.; Rodriguez A.S.; Sierra M.; SuarezSanmartin E.; Tabernero C.; Tartari J.P.; TejeraParrado C.; Tolosa E.; Valldeoriola F.; VargasGonzalez L.; Vela L.; Vives F.; Zimprich A.; Pihlstrom L.; Taba P.; Koks S. | |
| Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information | 1-gen-2020 | Guelfi, S; D'Sa, K; Botia, Ja; Vandrovcova, J; Reynolds, Rh; Zhang, D; Trabzuni, D; Colladotorres, L; Thomason, A; Quijada Leyton, P; Gagliano Taliun, Sa; Nalls, Ma; Noyce, Aj; Nicolas, A; Cookson, Mr; Bandresciga, S; Gibbs, Jr; Hernandez, Dg; Singleton, Ab; Reed, X; Leonard, H; Blauwendraat, C; Faghri, F; Bras, J; Guerreiro, R; Tucci, A; Kia, Da; Houlden, H; Plunfavreau, H; Mok, Ky; Wood, Nw; Lovering, R; R'Bibo, L; Rizig, M; Chelban, V; Tan, M; Morris, Hr; Middlehurst, B; Quinn, J; Billingsley, K; Holmans, P; Kinghorn, Kj; Lewis, P; Escottprice, V; Williams, N; Foltynie, T; Brice, A; Danjou, F; Lesage, S; Corvol, Jc; Martinez, M; Giri, A; Schulte, C; Brockmann, K; Simonsanchez, J; Heutink, P; Gasser, T; Rizzu, P; Sharma, M; Shulman, Jm; Robak, L; Lubbe, S; Mencacci, Ne; Finkbeiner, S; Lungu, C; Scholz, Sw; Ganor, Z; Rouleau, Ga; Krohan, L; van Hilten, Jj; Marinus, J; Adarmesgomez, Ad; Bernalbernal, I; Bonillatoribio, M; Buizarueda, D; Carrillo, F; Carrionclaro, M; Mir, P; Gomezgarre, P; Jesus, S; Labradorespinosa, Ma; Macias, D; Vargasgonzalez, L; Mendezdelbarrio, C; Perinantocino, T; Tejeraparrado, C; Diezfairen, M; Aguilar, M; Alvarez, I; Boungiorno, Mt; Carcel, M; Pastor, P; Tartari, Jp; Alvarez, V; Gonzalez, Mm; Blazquez, M; Garcia, C; Suarezsanmartin, E; Barrero, Fj; Rezola, Em; Yarza, Jab; Pagola, Ag; Arregui, Alm; Ruizmartinez, J; Cerdan, D; Duarte, J; Clarimon, J; Dolsicardo, O; Infante, J; Marin, J; Kulisevsky, J; Pagonabarraga, J; Gonzalezaramburu, I; Rodriguez, As; Sierra, M; Duran, R; Ruz, C; Vives, F; Escamillasevilla, F; Minguez, A; Camara, A; Compta, Y; Ezquerra, M; Marti, Mj; Fernandez, M; Munoz, E; Fernandezsantiago, R; Tolosa, E; Valldeoriola, F; Garciaruiz, P; Heredia, Mjg; Errazquin, Fp; Hoenicka, J; Jimenezescrig, A; Martinezcastrillo, Jc; Lopezsendon, Jl; Torres, Im; Tabernero, C; Vela, L; Zimprich, A; Pihlstrom, L; Koks, S; Taba, P; Majamaa, K; Siitonen, A; Okubadejo, Nu; Ojo, Oo; Forabosco, P; Walker, R; Small, Ks; Smith, C; Ramasamy, A; Hardy, J; Weale, Me; Ryten, M | |
| Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity | 1-gen-2018 | Ip, Hf; Jansen, R; Abdellaoui, A; Bartels, M; Ryten, M; Hardy, J; Weale, Me; Ramasamy, A; Forabosco, P; Matarin, M; Vandrovcova, J; Botia, Ja; D'Sa, K; Guelfi, S; Smith, C; Walker, R; Reynolds, Rh; Zhang, D; Trabzuni, D; Boomsma, Di; Nivard, Mg | |
| An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks | 1-gen-2017 | Botia, Ja; Vandrovcova, J; Forabosco, P; Guelfi, S; D'Sa, K; Hardy, J; Lewis, Cm; Ryten, M; Weale, Me; Ramasamy, A; Trabzuni, D; Smith, C; Walker, R | |
| Frontotemporal dementia: Insights into the biological underpinnings of disease through gene co-expression network analysis | 1-gen-2016 | Ferrari, R; Forabosco, P; Vandrovcova, J; Botia, Ja; Guelfi, S; Warren, Jd; Momeni, P; Weale, Me; Ryten, M; Hardy, J | |
| Gene co-expression networks shed light into diseases of brain iron accumulation | 1-gen-2016 | Bettencourt, C; Forabosco, P; Wiethoff, S; Heidari, M; Johnstone, Dm; Botia, Ja; Collingwood, Jf; Hardy, J; Milward, Ea; Ryten, M; Houlden, H; for the UK Brain Expression Consortium, Ukbec | |
| A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia | 1-gen-2015 | Mencacci N.E.; RubioAgusti I.; Zdebik A.; Asmus F.; Ludtmann M.H.R.; Ryten M.; Plagnol V.; Hauser A.K.; BandresCiga S.; Bettencourt C.; Forabosco P.; Hughes D.; Soutar M.M.P.; Peall K.; Morris H.R.; Trabzuni D.; Tekman M.; Stanescu H.C.; Kleta R.; Carecchio M.; Zorzi G.; Nardocci N.; Garavaglia B.; Lohmann E.; Weissbach A.; Klein C.; Hardy J.; Pittman A.M.; Foltynie T.; Abramov A.Y.; Gasser T.; Bhatia K.P.; Wood N.W. | |
| Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): A genetic association study in UK Biobank | 1-gen-2015 | Wain L.V.; Shrine N.; Miller S.; Jackson V.E.; Ntalla I.; Artigas M.S.; Billington C.K.; Kheirallah A.K.; Allen R.; Cook J.P.; Probert K.; Obeidat M.; Bosse Y.; Hao K.; Postma D.S.; Pare P.D.; Ramasamy A.; Magi R.; Mihailov E.; Reinmaa E.; Melen E.; O'Connell J.; Frangou E.; Delaneau O.; Freeman C.; Petkova D.; McCarthy M.; Sayers I.; Deloukas P.; Hubbard R.; Pavord I.; Hansell A.L.; Thomson N.C.; Zeggini E.; Morris A.P.; Marchini J.; Strachan D.P.; Tobin M.D.; Hall I.P.; Farrall M.; Barroso I.; Anderson C.A.; Botia J.; Vandrocova J.; Guelfi S.; D'Sa K.; Ryten M.; Trabzuni D.; Matarin M.; Hardy J.A.; Weale M.E.; Varghese V.; Forabosco P.; Farmer A.; McGuffin P.; Zgaga L.; Wilson J.F.; Wild S.H.; Campbell H.; Rudan I.; Smith C.; Walker R.; Liu J.Z.; Tozzi F.; Muglia P.; Waterworth D.M.; Pillai S.G.; Yuan X.; Mooser V.; Middleton L.; Kooner J.; Chambers J.C.; Berrettini W.; Knouff C.W.; Waeber G.; Vollenweider P.; Preisig M.; Wareham N.J.; Zhao J.H.; Loos R.J.F.; Khaw K.T.; Grundy S.; Barter P.; Mahley R.; Kesaniemi A.; McPherson R.; Vincent J.B.; Strauss J.; Kennedy J.L.; Day R.; Matthews K.; Bakke P.; Gulsvik A.; Lucae S.; Ising M.; Brueckl T.; Horstmann S.; Wichmann H.E; Rawal R.; Wichmann H.E.; Lamina C.; Dahmen N.; Polasek O.; Kolcic I.; Huffman J.; Campbell S.; Vitart V.; Hayward C.; Wright A.F.; Burnett M.S.; Devaney J.M.; Pichard A.D.; Kent K.M.; Satler L.; Lindsay J.M.; Waksman R.; Epstein S.; Reilly M.P.; Li M.; Qu L.; Wilensky R.; Matthai W.; Hakonarson H.H.; Rader D.J.; Ellinghaus D.; Lieb W.; Franke A.; Uda M.; Busonero F.; Terracciano A.; Schlessinger D.; Xiao X.; Scheet P.; St Clair D.; Rujescu D.; Abecasis G.R.; Grabe H.J.; Teumer A.; Volzke H.; Petersmann A.; John U.; Wright B.J.; Thompson J.R.; Balmforth A.J.; Hall A.S.; Samani N.J.; Ahmad T.; Mathew C.G.; Parkes M.; Satsangi J.; Caulfield M.; Munroe P.B.; Dominiczak A.; Worthington J.; Thomson W.; Eyre S.; Barton A.; Francks C. | |
| Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis | 1-gen-2014 | Ramasamy A.; Trabzuni D.; Forabosco P.; Smith C.; Walker R.; Dillman A.; Sveinbjornsdottir S.; Hardy J.; Weale M.E.; Ryten M. | |
| Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia | 1-gen-2014 | Bettencourt, Conceicao; Ryten, Mina; Forabosco, Paola; Schorge, Stephanie; Hersheson, Joshua; Hardy, John; Houlden, Henry | |
| Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease | 1-gen-2014 | Cruchaga, Carlos; Karch Celeste, M; Jin Sheng, Chih; Benitez Bruno, A; Cai, Yefei; Guerreiro, Rita; Harari, Oscar; Norton, Joanne; Budde, John; Bertelsen, Sarah; Jeng Amanda, T; Cooper, Breanna; Skorupa, Tara; Carrell, David; Levitch, Denise; Hsu, Simon; Choi, Jiyoon; Ryten, Mina; Sassi, Celeste; Bras, Jose; Gibbs, J Raphael; Hernandez Dena, G; Lupton Michelle, K; Powell, John; Forabosco, Paola; Ridge Perry, G; Corcoran Christopher, D; Tschanz Joann, T; Norton Maria, C; Munger Ronald, G; Schmutz, Cameron; Leary, Maegan; Demirci, F Yesim; Bamne Mikhil, N; Wang, Xingbin; Lopez Oscar, L; Ganguli, Mary; Medway, Christopher; Turton, James; Lord, Jenny; Braae, Anne; Barber, Imelda; Brown, Kristelle; Pastor, Pau; Lorenzobetancor, Oswaldo; Brkanac, Zoran; Scott, Erick; Topol, Eric; Morgan, Kevin; Rogaeva, Ekaterina; Singleton Andrew, B; Hardy, John; Kamboh, M Ilyas; St GeorgeHyslop, Peter; Cairns, Nigel; Morris John, C; Kauwe John, S K; Goate Alison, M | |
| Insights into TREM2 biology by network analysis of human brain gene expression data | 1-gen-2013 | Forabosco, Paola; Ramasamy, Adaikalavan; Trabzuni, Daniah; Walker, Robert; Smith, Colin; Bras, Jose; Levine Adam, P; Hardy, John; Pocock Jennifer, M; Guerreiro, Rita; Weale Michael, E; Ryten, Mina | |
| Predicting the Risk of Rheumatoid Arthritis and Its Age of Onset through Modelling Genetic Risk Variants with Smoking | 1-gen-2013 | Scott Ian, C; Seegobin Seth, D; Steer, Sophia; Tan, Rachael; Forabosco, Paola; Hinks, Anne; Eyre, Stephen; Morgan Ann, W; Wilson Anthony, G; Hocking Lynne, J; Wordsworth, Paul; Barton, Anne; Worthington, Jane; Cope Andrew, P; Lewis Cathryn, M | |
| Prediction model for rheumatoid arthritis: modelling 46 genetic risk variants with smoking | 1-gen-2013 | Scott, Ian C.; Steer, Sophia; Tan, Rachael; Forabosco, Paola; Morgan, Ann W.; Hinks, Anne; Thomson, Wendy; Barton, Anne; Worthington, Jane; Cope, Andrew P.; Lewis, Cathryn M. | |
| Association of the IL-10 Gene Family Locus on Chromosome 1 with Juvenile Idiopathic Arthritis (JIA) | 1-gen-2012 | Ebun Omoyinmi; Paola Forabosco;Raja Hamaoui; Annette Bryant; Anne Hinks; Simona Ursu; Childhood Arthritis Prospective Study CAPS; BSPAR study group;Childhood Arthritis Response to Medication Study CHARMS; Lucy R. Wedderburn; Wendy Thomson; Cathryn M. Lewis;Patricia Woo | |
| Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis. | 1-gen-2011 | Tore S; Casula S; Casu G; Concas MP; Pistidda P; Persico I; Sassu A; Maestrale GB; Mele C; Caruso MR; Bonerba B; Usai P; Deiana I; Thornton T; Pirastu M; Forabosco P | |
| Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy | 1-gen-2010 | Bouzigon, E; Forabosco, P; Koppelman, Gh; Cookson, Wo; Dizier, Mh; Duffy, Dl; Evans, Dm; Ferreira, Ma; Kere, J; Laitinen, T; Malerba, G; Meyers, Da; Moffatt, M; Martin, Ng; Ng, My; Pignatti, Pf; Wjst, M; Kauffmann, F; Demenais, F; Lewis, Cm | |
| Meta-analysis of 32 genome-wide linkage studies of schizophreniaGenome-wide linkage studies of SCZ | 1-gen-2009 | Ng MY; Levinson DF; Faraone SV; Suarez BK; DeLisi LE; Arinami T; Riley B; Paunio T; Pulver AE; Irmansyah; Holmans PA; Escamilla M; Wildenauer DB; Williams NM; Laurent C; Mowry BJ; Brzustowicz LM; Maziade M; Sklar P; Garver DL; Abecasis GR; Lerer B; Fallin MD; Gurling HM; Gejman PV; Lindholm E; Moises HW; Byerley W; Wijsman EM; Forabosco P; Tsuang MT; Hwu HG; Okazaki Y; Kendler KS; Wormley B; Fanous A; Walsh D; O'Neill FA; Peltonen L; Nestadt G; Lasseter VK; Liang KY; Papadimitriou GM; Dikeos DG; Schwab SG; Owen MJ; O'Donovan MC; Norton N; Hare E; Raventos H; Nicolini H; Albus M; Maier W; Nimgaonkar VL; Terenius L; Mallet J; Jay M; Godard S; Nertney D; Alexander M; Crowe RR; Silverman JM; Bassett AS; Roy MA; Mérette C; Pato CN; Pato MT; Roos JL; Kohn Y; AmannZalcenstein D; Kalsi G; McQuillin A; Curtis D; Brynjolfson J; Sigmundsson T; Petursson H; Sanders AR; Duan J; Jazin E; MylesWorsley M; Karayiorgou M; Lewis CM |