MARONGIU, MARA

MARONGIU, MARA  

Istituto di Ricerca Genetica e Biomedica - IRGB  

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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.
Editorial: Female Infertility: Genetics of Reproductive Ageing, Menopause and Primary Ovarian Insufficiency 1-gen-2022 Marongiu, Mara; Crisponi, Laura; Uda, Manuela; Pelosi, Emanuele
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy 1-gen-2020 Orrù, V; Steri, M; Sidore, C; Marongiu, M; Serra, V; Olla, S; Sole, G; Lai, S; Dei, M; Mulas, A; Virdis, F; Piras, Mg; Lobina, M; Marongiu, M; Pitzalis, M; Deidda, F; Loizedda, A; Onano, S; Zoledziewska, M; Sawcer, S; Devoto, M; Gorospe, M; Abecasis, Gr; Floris, M; Pala, M; Schlessinger, D; Fiorillo, E; Cucca, F
Erratum: Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa (The American Journal of Human Genetics (2016) 99(1) (236-245) (S0002929716301616) (10.1016/j.ajhg.2016.05.026)) 1-gen-2018 Angius, Andrea; Uva, Paolo; Buers, Insa; Oppo, Manuela; Puddu, Alessandro; Onano, Stefano; Persico, Ivana; Loi, Angela; Marcia, Loredana; Höhne, Wolfgang; Cuccuru, Gianmauro; Fotia, Giorgio; Deiana, Manila; Marongiu, Mara; Atalay, Hatice Tuba; Inan, Sibel; El Assy, Osama; Smit, Leo M.E.; Okur, Ilyas; Boduroglu, Koray; Utine, Gülen Eda; Klç, Esra; Zampino, Giuseppe; Crisponi, Giangiorgio; Crisponi, Laura; Rutsch, Frank
Population- and individual-specific regulatory variation in Sardinia. 1-gen-2017 Pala, Mauro; Zappala, Zachary; Marongiu, Mara; Li, Xin; Davis Joe, R; Cusano, Roberto; Crobu, Francesca; Kukurba Kimberly, R; Gloudemans Michael, J; Reinier, Frederic; Berutti, Riccardo; Piras Maria, G; Mulas, Antonella; Zoledziewska, Magdalena; Marongiu, Michele; Sorokin Elena, P; Hess Gaelen, T; Smith Kevin, S; Busonero, Fabio; Maschio, Andrea; Steri, Maristella; Sidore, Carlo; Sanna, Serena; Fiorillo, Edoardo; Bassik Michael, C; Sawcer Stephen, J; Battle, Alexis; Novembre, John; Jones, Chris; Angius, Andrea; Abecasis Goncalo, R; Schlessinger, David; Cucca, Francesco; Montgomery Stephen, B
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa 1-gen-2016 Angius, Andrea; Uva, Paolo; Buers, Insa; Oppo, Manuela; Puddu, Alessandro; Onano, Stefano; Persico, Ivana; Loi, Angela; Marcia, Loredana; Hoehne, Wolfgang; Cuccuru, Gianmauro; Fotia, Giorgio; Deiana, Manila; Marongiu, Mara; Atalay Hatice, Tuba; Inan, Sibel; El Assy, Osama; Smit Leo, M E; Okur, Ilyas; Boduroglu, Koray; Utine Gulen, Eda; Kilic, Esra; Zampino, Giuseppe; Crisponi, Giangiorgio; Crisponi, Laura; Rutsch, Frank
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation 1-gen-2016 Marongiu, Mara; Deiana, Manila; Marcia, Loredana; Sbardellati, Andrea; Asunis, Isadora; Meloni, Alessandra; Angius, Andrea; Cusano, Roberto; Loi, Angela; Crobu, Francesca; Fotia, Giorgio; Cucca, Francesco; Schlessinger, David; Crisponi, Laura
FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice 1-gen-2015 Marongiu, Mara; Marcia, Loredana; Pelosi, Emanuele; Lovicu, Mario; Deiana, Manila; Zhang, Yonqing; Puddu, Alessandro; Loi, Angela; Uda, Manuela; Forabosco, Antonino; Schlessinger, David; Crisponi, Laura
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. 1-gen-2012 Stolk L; Perry JR; Chasman DI; He C; Mangino M; Sulem P; Barbalic M; Broer L; Byrne EM; Ernst F; Esko T; Franceschini N; Gudbjartsson DF; Hottenga JJ; Kraft P; McArdle PF; Porcu E; Shin SY; Smith AV; van Wingerden S; Zhai G; Zhuang WV; Albrecht E; Alizadeh BZ; Aspelund T; Bandinelli S; Lauc LB; Beckmann JS; Boban M; Boerwinkle E; Broekmans FJ; Burri A; Campbell H; Chanock SJ; Chen C; Cornelis MC; Corre T; Coviello AD; d'Adamo P; Davies G; de Faire U; de Geus EJ; Deary IJ; Dedoussis GV; Deloukas P; Ebrahim S; Eiriksdottir G; Emilsson V; Eriksson JG; Fauser BC; Ferreli L; Ferrucci L; Fischer K; Folsom AR; Garcia ME; Gasparini P; Gieger C; Glazer N; Grobbee DE; Hall P; Haller T; Hankinson SE; Hass M; Hayward C; Heath AC; Hofman A; Ingelsson E; Janssens AC; Johnson AD; Karasik D; Kardia SL; Keyzer J; Kiel DP; Kolcic I; Kutalik Z; Lahti J; Lai S; Laisk T; Laven JS; Lawlor DA; Liu J; Lopez LM; Louwers YV; Magnusson PK; Marongiu M; Martin NG; Klaric IM; Masciullo C; McKnight B; Medland SE; Melzer D; Mooser V; Navarro P; Newman AB; Nyholt DR; OnlandMoret NC; Palotie A; Paré G; Parker AN; Pedersen NL; Peeters PH; Pistis G; Plump AS; Polasek O; Pop VJ; Psaty BM; Räikkönen K; Rehnberg E; Rotter JI; Rudan I; Sala C; Salumets A; Scuteri A; Singleton A; Smith JA; Snieder H; Soranzo N; Stacey SN; Starr JM; Stathopoulou MG; Stirrups K; Stolk RP; Styrkarsdottir U; Sun YV; Tenesa A; Thorand B; Toniolo D; Tryggvadottir L; Tsui K; Ulivi S; van Dam RM; van der Schouw YT; van Gils CH; van Nierop P; Vink JM; Visscher PM; Voorhuis M; Waeber G; Wallaschofski H; Wichmann HE; Widen E; Wijnandsvan Gent CJ; Willemsen G; Wilson JF; Wolffenbuttel BH; Wright AF; YergesArmstrong LM; Zemunik T; Zgaga L; Zillikens MC; Zygmunt M; Study TL; Arnold AM; Boomsma DI; Buring JE; Crisponi L; Demerath EW; Gudnason V; Harris TB; Hu FB; Hunter DJ; Launer LJ; Metspalu A; Montgomery GW; Oostra BA; Ridker PM; Sanna S; Schlessinger D; Spector TD; Stefansson K; Streeten EA; Thorsteinsdottir U; Uda M; Uitterlinden AG; van Duijn CM; Völzke H; Murray A; Murabito JM; Visser JA; Lunetta KL.
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders 1-gen-2011 Herholz, Jana; Meloni, Alessandra; Marongiu, Mara; Chiappe, Francesca; Chiappe, Francesca; Deiana, Manila; Herrero Carmen, Roche; Zampino, Giuseppe; Hamamy, Hanan; Zalloum, Yusra; Waaler Per, Erik; Crisponi, Giangiorgio; Crisponi, Laura; Rutsch, Frank
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders. 1-gen-2011 Herholz J; Meloni A; Marongiu M; Chiappe F; Deiana M; Herrero CR; Zampino G; Hamamy H; Zalloum Y; Waaler PE; Crisponi G; Crisponi L; Rutsch F.
SUMOylation of the Forkhead transcription factor FOXL2 promotes its stabilization/activation through transient recruitment to PML bodies. 1-gen-2011 Georges, A; Benayoun, Ba; Marongiu, M; Dipietromaria, A; L'Hôte, D; Todeschini, Al; Auer, J; Crisponi, L; Veitia, Ra
The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity. 1-gen-2010 Mara Marongiu,; Manila Deiana,; Alessandra Meloni,; Loredana Marcia,; Alessandro Puddu,,; Antonio Cao,; David Schlessinger,; Laura Crisponi
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. 1-gen-2010 Cathy E. Elks,; John R.B. Perry,; Patrick Sulem,; Daniel I. Chasman,,; Nora Franceschini,; Chunyan He,,; Kathryn L. Lunetta,,; Jenny A. Visser,; Enda M. Byrne,,; Diana L. Cousminer,; Daniel F. Gudbjartsson,; Tõnu Esko,,,; Bjarke Feenstra,; JoukeJan Hottenga,; Daniel L. Koller,; Zoltán Kutalik,,; Peng Lin,; Massimo Mangino,; Mara Marongiu,; Patrick F. McArdle,; Albert V. Smith,,; Lisette Stolk,,; Sophie W. van Wingerden,; Jing Hua Zhao,; Eva Albrecht,; Tanguy Corre,; Erik Ingelsson,; Caroline Hayward,; Patrik K.E. Magnusson,; Erin N. Smith,; Shelia Ulivi,; Nicole M. Warrington,; Lina Zgaga,; Helen Alavere,; Najaf Amin,; Thor Aspelund,,; Stefania Bandinelli,; Ines Barroso,; Gerald S. Berenson,; Sven Bergmann,,; Hannah Blackburn,; Eric Boerwinkle,; Julie E. Buring,,; Fabio Busonero,; Harry Campbell,; Stephen J. Chanock,; Wei Chen,; Marilyn C. Cornelis,; David Couper,; Andrea D. Coviello,; Pio d'Adamo,; Ulf de Faire,; Eco J.C. de Geus,; Panos Deloukas,; Angela Döring,; George Davey Smith,; Douglas F. Easton,; Gudny Eiriksdottir,; Valur Emilsson,; Johan Eriksson,,,,; Luigi Ferrucci,; Aaron R. Folsom,; Tatiana Foroud,; Melissa Garcia,; Paolo Gasparini,; Frank Geller,; Christian Gieger,; The GIANT Consortium,; Vilmundur Gudnason,,; Per Hall,; Susan E. Hankinson,,; Liana Ferreli,; Andrew C. Heath,; Dena G. Hernandez,; Albert Hofman,; Frank B. Hu,,,; Thomas Illig,; MarjoRiitta Järvelin,; Andrew D. Johnson,,; David Karasik,; KayTee Khaw,; Douglas P. Kiel,; Tuomas O. Kilpeläinen,; Ivana Kolcic,; Peter Kraft,,,; Lenore J. Launer,; Joop S.E. Laven,; Shengxu Li,; Jianjun Liu,; Daniel Levy,,,; Nicholas G. Martin,; Wendy L. McArdle,; Mads Melbye,; Vincent Mooser,; Jeffrey C. Murray,; Sarah S. Murray,; Michael A. Nalls,; Pau Navarro,; Mari Nelis,,,; Andrew R. Ness,; Kate Northstone,; Ben A. Oostra,; Munro Peacock,; Lyle J. Palmer,; Aarno Palotie,,,; Guillaume Paré,,,; Alex N. Parker,; Nancy L. Pedersen,; Leena Peltonen,,,,,; Craig E. Pennell,; Paul Pharoah,; Ozren Polasek,,; Andrew S. Plump,; Anneli Pouta,; Eleonora Porcu,; Thorunn Rafnar,, John P. Rice,; Susan M. Ring,; Fernando Rivadeneira,,,; Igor Rudan,,; Cinzia Sala,; Veikko Salomaa,; Serena Sanna,; David Schlessinger,; Nicholas J. Schork,; Angelo Scuteri,,; Ayellet V. Segrè,,; Alan R. Shuldiner,,; Nicole Soranzo,,; Ulla Sovio,; Sathanur R. Srinivasan,; David P. Strachan,; MarLiis Tammesoo,; Emmi Tikkanen,,; Daniela Toniolo,; Kim Tsui,; Laufey Tryggvadottir,; Jonathon Tyrer,; Manuela Uda,; Rob M. van Dam,,; Joyve B.J. van Meurs,; Peter Vollenweider,; Gerard Waeber,; Nicholas J. Wareham,; Dawn M. Waterworth,; Michael N. Weedon,; H. Erich Wichmann,,,; Gonneke Willemsen,; James F. Wilson,; Alan F. Wright,; Lauren Young,; Guangju Zhai,; Wei Vivian Zhuang,; Laura J. Bierut,; Dorret I. Boomsma,; Heather A. Boyd,; Laura Crisponi,; Ellen W. Demerath,; Cornelia M. van Duijn,; Michael J. Econs,,; Tamara B. Harris,; David J. Hunter,,,,; Ruth J.F. Loos,; Andres Metspalu,,,; Grant W. Montgomery,; Paul M. Ridker,,,,; Tim D. Spector,; Elizabeth A. Streeten,; Kari Stefansson,,; Unnur Thorsteinsdottir,,; André G. Uitterlinden,,,; Elisabeth Widen,; Joanne M. Murabito,,; Ken Ong,, ; Anna Murray
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia 1-gen-2009 Sanna, Serena; Busonero, Fabio; Maschio, Andrea; F McArdle, Patrick; Usala, Gianluca; Dei, Mariano; Lai, Sandra; Mulas, Antonella; Piras, MARIA GRAZIA; Perseu, Lucia; Masala, Marco; Marongiu, Mara; Crisponi, Laura; Naitza, Silvia; Galanello, Renzo; R Abecasis, Gonçalo; R Shuldiner, Alan; Schlessinger, David; Cao, Antonio; Uda, Manuela
Withania somnifera prevents morphine withdrawal-induced decrease in spine density in nucleus accumbens shell of rats: A confocal laser scanning microscopy study 1-gen-2009 Kasture, S; Vinci, S; Ibba, F; Puddu, A; Marongiu, M; Murali, B; Pisanu, A; Lecca, D; Zernig, G; Acquas, E
Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1 1-gen-2007 Crisponi, Laura; Crisponi, Giangiorgio; Meloni, Alessandra; Reza Toliat, Mohammad; Nürnberg, Gudrun; Usala, Gianluca; Uda, Manuela; Masala, Marco; Höhne, Wolfgang; Becker, Christian; Marongiu, Mara; Chiappe, Francesca; Kleta, Robert; Rauch, Anita; Wollnik, Bernd; Strasser, Friedrich; Reese, Thomas; Jakobs, Cornelis; Kurlemann, Gerd; Cao, Antonio; Nürnberg, Peter; Rutsch, Frank