Raquel Rabionet Janssen
Jefe de Grupo
Research group
Raquel Rabionet graduated in Biology in 1996 from the University of Barcelona and obtained her degree in Biology from the University of Barcelona in 2002.
Between 2002 and 2005, she undertook a postdoctoral stay at Duke University in Durham, NC, where she studied the genetic bases of autism. From 2005 to 2017 she worked at the Center for Genomic Regulation in Barcelona, investigating the genetic bases of intellectual disability or the recovery of stroke, among other complex phenotypes.
Since 2015 she has been an Associate Professor at the University of Barcelona.
In 2017, she joined the research group as a researcher of the PERIS program.
She is currently leading the research line on the genetic bases of stroke recovery, where she studies whether low frequency genetic variants can modulate the inflammatory and neurogenesis response, affecting the functional state after stroke, The aim is to understand better these processes and to apply them to the development of therapies.
Professional network profiles
Last Publications
- Strom NI, Gerring ZF, Galimberti M, Yu D, Halvorsen MW, Abdellaoui A, Rodriguez-Fontenla C, Sealock JM, Bigdeli T, Coleman JR, Mahjani B, Thorp JG, Bey K, Burton CL, Luykx JJ, Zai G, Alemany S, Andre C, Askland KD, Bäckman J, Banaj N, Barlassina C, Nissen JB, Bienvenu OJ, Black D, Bloch MH, Børte S, Rosa Bosch Munsó, Breen M, Brennan BP, Brentani H, Buxbaum JD, Bybjerg-Grauholm J, Byrne EM, Cabana-Domínguez J, Camarena B, Camarena A, Cappi C, Carracedo A, Miguel Casas Brugué, Cavallini MC, Ciullo V, Cook EH, Crosby J, Cullen BA, De Schipper EJ, Delorme R, Djurovic S, Elias JA, Estivill X, Falkenstein MJ, Fundin BT, Garner L, Gironda C, Goes FS, Grados MA, Grove J, Guo W, Haavik J, Hagen K, Harrington K, Havdahl A, Höffler KD, Hounie AG, Hucks D, Hultman C, Janecka M, Jenike E, Karlsson EK, Kelley K, Klawohn J, Krasnow JE, Krebs K, Lange C, Lanzagorta N, Levey D, Lindblad-Toh K, Macciardi F, Maher B, Mathes B, McArthur E, McGregor N, McLaughlin NC, Meier S, Miguel EC, Mulhern M, Nestadt PS, Nurmi EL, O'Connell KS, Osiecki L, Ousdal OT, Palviainen T, Pedersen NL, Piras F, Piras F, Potluri S, Rabionet-Janssen R, Ramirez A, Rauch S, Reichenberg A, Riddle MA, Ripke S, Rosário MC, Sampaio AS, Schiele MA, Skogholt AH, Sloofman LG, Smit J, Artigas MS, Thomas LF, Tifft E, Vallada H, van Kirk N, Veenstra-VanderWeele J, Vulink NN, Walker CP, Wang Y, Wendland JR, Winsvold BS, Yao Y, Zhou H, Agrawal A, Alonso P, Berberich G, Bucholz KK, Bulik CM, Cath D, Denys D, Eapen V, Edenberg H, Falkai P, Fernandez TV, Fyer AJ, Gaziano JM, Geller DA, Grabe HJ, Greenberg BD, Hanna GL, Hickie IB, Hougaard DM, Kathmann N, Kennedy J, Lai D, Landén M, Hellard SL, Leboyer M, Lochner C, McCracken JT, Medland SE, Mortensen PB, Neale BM, Nicolini H, Nordentoft M, Pato M, Pato C, Pauls DL, Piacentini J, Pittenger C, Posthuma D, Ramos-Quiroga JA, Rasmussen SA, Richter MA, Rosenberg DR, Ruhrmann S, Samuels JF, Sandin S, Sandor P, Spalletta G, Stein DJ, Stewart SE, Storch EA, Stranger BE, Turiel M, Werge T, Andreassen OA, Børglum AD, Walitza S, Hveem K, Hansen BK, Rück C, Martin NG, Milani L, Mors O, Reichborn-Kjennerud T, Ribasés M, Kvale G, Mataix-Cols D, Domschke K, Grünblatt E, Wagner M, Zwart JA, Breen G, Nestadt G, Kaprio J, Arnold PD, Grice DE, Knowles JA, Ask H, Verweij KJ, Davis LK, Smit DJ, Crowley JJ, Scharf JM, Stein MB, Gelernter J, Mathews CA, Derks EM and Mattheisen M Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. NATURE GENETICS . 57(6): 1389-1401.
- Urreizti R, Vissicchio J, Idries M, Cozar M, Rabionet-Janssen R, Donald T, Bhoj EJ, Nomakuchi TT, Shipley SC, Timms AE, Mirzaa GM, Serrano M and Sobering AK Two New Cases Expand the Phenotypic Spectrum of TUBG1 Missense Variants AMERICAN JOURNAL OF MEDICAL GENETICS PART A . : .
- Patiño-Salazar JD, Ovejero D, Gabernet M, Martinez-Gil N, Alcaide E, Mellibovsky L, Nogués X, Grinberg-Vaisman DR, Balcells S, Rabionet-Janssen R and Garcia-Giralt N Identifying rare variants in genes related to bone phenotypes in a cohort of postmenopausal women OSTEOPOROSIS INTERNATIONAL . 36(4): 637-644.
Projects
- Project name:
- GENIUS: GENetic Influences on functional oUtcome after Stroke
- Leader
- Raquel Rabionet Janssen
- Funding entities:
- Fundació La Marató de TV3
- Code
- Reg. 70/307 Proj. 201726
- Starting - finishing date:
- 2018 - 2021
- Project name:
- Incorporació de R. Rabionet al projecte d'anàlisi d'exomes en síndrome d'Opitz i Fractura atípica. Beneficiari: Raquel Rabionet
- Leader
- Daniel Raúl Grinberg Vaisman
- Funding entities:
- Generalitat de Catalunya
- Code
- SLT002/16/00310
- Starting - finishing date:
- 2017 - 2019
News
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New advances in Schaaf-Yang syndrome research
A team led by researchers from the Institut de Recerca Sant Joan de Déu · IBUB discover that mutations in the MAGEL2 gene generate non-functional truncated proteins that tend to accumulate in the cell nucleus.