BARLASSINA, MARIA CRISTINA
BARLASSINA, MARIA CRISTINA
Dipartimento di Scienze della Salute
A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility
2022 M. Sorosina, N. Barizzone, F. Clarelli, S. Anand, S. Lupoli, E. Salvi, E. Mangano, R. Bordoni, T. Roostaei, E. Mascia, M. Zuccalà, D. Vecchio, P. Cavalla, S. Santoro, L. Ferrè, A. Zollo, C. Barlassina, D. Cusi, V. Martinelli, G. Comi, M. Leone, M. Filippi, N.A. Patsopoulos, P.L. De Jager, G. De Bellis, F. Esposito, S. D'Alfonso, F. Martinelli Boneschi
Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation
2020 L. Calzari, M. Barcella, V. Alari, D. Braga, R. Munoz-Viana, C. Barlassina, P. Finelli, C. Gervasini, A. Barco, S. Russo, L. Larizza
Immune signature drives leukemia escape and relapse after hematopoietic cell transplantation
2019 C. Toffalori, L. Zito, V. Gambacorta, M. Riba, G. Oliveira, G. Bucci, M. Barcella, O. Spinelli, R. Greco, L. Crucitti, N. Cieri, M. Noviello, F. Manfredi, E. Montaldo, R. Ostuni, M.M. Naldini, B. Gentner, M. Waterhouse, R. Zeiser, J. Finke, M. Hanoun, D.W. Beelen, I. Gojo, L. Luznik, M. Onozawa, T. Teshima, R. Devillier, D. Blaise, C.J.M. Halkes, M. Griffioen, M.G. Carrabba, M. Bernardi, J. Peccatori, C. Barlassina, E. Stupka, D. Lazarevic, G. Tonon, A. Rambaldi, D. Cittaro, C. Bonini, K. Fleischhauer, F. Ciceri, L. Vago
GDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML
2018 A. Rainero, F. Angaroni, A. Conti, C. Pirrone, G. Micheloni, L. Tararà, G. Millefanti, E. Maserati, R. Valli, O. Spinelli, K. Buklijas, A. Michelato, R. Casalone, C. Barlassina, M. Barcella, S. Sirchia, E. Piscitelli, M. Caccia, G. Porta
Self-renewal and phenotypic conversion are the main physiological responses of macrophages to the endogenous estrogen surge
2017 G. Pepe, D. Braga, T.A. Renzi, A. Villa, C. Bolego, F. D'Avila, C. Barlassina, A. Maggi, M. Locati, E. Vegeto
PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population
2017 W. Yang, T. Petit, N. Cauwenberghs, Z. Zhang, C. Sheng, L. Thijs, E. Salvi, B. Izzi, C. Vandenbriele, F. Wei, Y. Gu, L. Jacobs, L. Citterio, S. Delli Carpini, C. Barlassina, D. Cusi, M.F. Hoylaerts, P. Verhamme, T. Kuznetsova, J.A. Staessen
Next-generation sequencing of a family with a high penetrance of monoclonal gammopathies for the identification of candidate risk alleles
2017 N. Bolli, M. Barcella, E. Salvi, F. D'Avila, A. Vendramin, C. De Philippis, N.C. Munshi, H. Avet Loiseau, P.J. Campbell, A. Mussetti, C. Carniti, F. Maura, C. Barlassina, P. Corradini, V. Montefusco
Preliminary profiling of blood transcriptome in a rat model of hemorrhagic shock
2017 D. Braga, M. Barcella, F. D'Avila, S. Lupoli, F. Tagliaferri, M.H. Santamaria, F.A. Delano, G. Baselli, G.W. Schmid Schoenbein, E.B. Kistler, F. Aletti, C. Barlassina
Exome sequencing identifies variants in two genes encoding the lim-proteins n-rap and fhl1 in a bag3 myofibrillar myopathy
2016 F. De Santis, M. Meregalli, F. D’Avila, S. Luppoli, M. Barcella, A. Orro, C. Sitzia, A. Farini, P. D’Ursi, S. Erratico, L. Milanesi, D. Braga, D. Cusi, C. Barlassina, Y. Torrente
ShockOmics : multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock
2016 F. Aletti, C. Conti, M. Ferrario, V. Ribas, B. Bollen Pinto, A. Herpain, E. Post, E. Romay Medina, C. Barlassina, E. de Oliveira, R. Pastorelli, G. Tedeschi, G. Ristagno, F.S. Taccone, G.W. Schmid Schönbein, R. Ferrer, D. De Backer, K. Bendjelid, G. Baselli
Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy
2016 F. D’Avila, M. Meregalli, S. Lupoli, M. Barcella, A. Orro, F. DE SANTIS, C. Sitzia, A. Farini, P. D’Ursi, S. Erratico, R. Cristofani, L. Milanesi, D. Braga, D. Cusi, A. Poletti, C. Barlassina, Y. Torrente
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
2016 J.S. Ried, J. Jeff M, A.Y. Chu, J.L. Bragg Gresham, J. van Dongen, J.E. Huffman, T.S. Ahluwalia, G. Cadby, N. Eklund, J. Eriksson, T. Esko, M.F. Feitosa, A. Goel, M. Gorski, C. Hayward, N.L. Heard Costa, A.U. Jackson, E. Jokinen, S. Kanoni, K. Kristiansson, Z. Kutalik, J. Lahti, J. Luan, R. Mägi, A. Mahajan, M. Mangino, C. Medina Gomez, K.L. Monda, I.M. Nolte, L. Pérusse, I. Prokopenko, L. Qi, L.M. Rose, E. Salvi, M.T. Smith, H. Snieder, A. Stančáková, Y. Ju Sung, I. Tachmazidou, A. Teumer, G. Thorleifsson, P. van der Harst, R.W. Walker, S.R. Wang, S.H. Wild, S.M. Willems, A. Wong, W. Zhang, E. Albrecht, A. Couto Alves, S.J.L. Bakker, C. Barlassina, T.M. Bartz, J. Beilby, C. Bellis, R.N. Bergman, S. Bergmann, J. Blangero, M. Blüher, E. Boerwinkle, L.L. Bonnycastle, S.R. Bornstein, M. Bruinenberg, H. Campbell, Y.I. Chen, C.W.K. Chiang, P.S. Chines, F.S. Collins, F. Cucca, L.A. Cupples, F. D'Avila, E.J.C. de Geus, G. Dedoussis, M. Dimitriou, A. Döring, J.G. Eriksson, A. Farmaki, M. Farrall, T. Ferreira, K. Fischer, N.G. Forouhi, N. Friedrich, A.P. Gjesing, N. Glorioso, M. Graff, H. Grallert, N. Grarup, J. Gräßler, J. Grewal, A. Hamsten, M.N. Harder, C.A. Hartman, M. Hassinen, N. Hastie, A.T. Hattersley, A.S. Havulinna, M. Heliövaara, H. Hillege, A. Hofman, O. Holmen, G. Homuth, J. Hottenga, J. Hui, L.L. Husemoen, P.G. Hysi, A. Isaacs, T. Ittermann, S. Jalilzadeh, A.L. James, T. Jørgensen, P. Jousilahti, A. Jula, J. Marie Justesen, A.E. Justice, M. Kähönen, M. Karaleftheri, K. Tee Khaw, S.M. Keinanen Kiukaanniemi, L. Kinnunen, P.B. Knekt, H.A. Koistinen, I. Kolcic, I.K. Kooner, S. Koskinen, P. Kovacs, T. Kyriakou, T. Laitinen, C. Langenberg, A.M. Lewin, P. Lichtner, C.M. Lindgren, J. Lindström, A. Linneberg, R. Lorbeer, M. Lorentzon, R. Luben, V. Lyssenko, S. Männistö, P. Manunta, I.M. Leach, W.L. Mcardle, B. Mcknight, K.L. Mohlke, E. Mihailov, L. Milani, R. Mills, M.E. Montasser, A.P. Morris, G. Müller, A.W. Musk, N. Narisu, K.K. Ong, B.A. Oostra, C. Osmond, A. Palotie, J.S. Pankow, L. Paternoster, B.W. Penninx, I. Pichler, M.G. Pilia, O. Polašek, P.P. Pramstaller, O.T. Raitakari, T. Rankinen, D.C. Rao, N.W. Rayner, R. Ribel Madsen, T.K. Rice, M. Richards, P.M. Ridker, F. Rivadeneira, K.A. Ryan, S. Sanna, M.A. Sarzynski, S. Scholtens, R.A. Scott, S. Sebert, L. Southam, T.H. Sparsø, V. Steinthorsdottir, K. Stirrups, R.P. Stolk, K. Strauch, H.M. Stringham, M.A. Swertz, A.J. Swift, A. Tönjes, E. Tsafantakis, P.J. van der Most, J.V. Van Vliet Ostaptchouk, L. Vandenput, E. Vartiainen, C. Venturini, N. Verweij, J.S. Viikari, V. Vitart, M. Vohl, J.M. Vonk, G. Waeber, E. Widén, G. Willemsen, T. Wilsgaard, T.W. Winkler, A.F. Wright, L.M. Yerges Armstrong, J. Hua Zhao, M. Carola Zillikens, D.I. Boomsma, C. Bouchard, J.C. Chambers, D.I. Chasman, D. Cusi, R.T. Gansevoort, C. Gieger, T. Hansen, A.A. Hicks, F. Hu, K. Hveem, M. Jarvelin, E. Kajantie, J.S. Kooner, D. Kuh, J. Kuusisto, M. Laakso, T.A. Lakka, T. Lehtimäki, A. Metspalu, I. Njølstad, C. Ohlsson, A.J. Oldehinkel, L.J. Palmer, O. Pedersen, M. Perola, A. Peters, B.M. Psaty, H. Puolijoki, R. Rauramaa, I. Rudan, V. Salomaa, P.E.H. Schwarz, A.R. Shudiner, J.H. Smit, T.I.A. Sørensen, T.D. Spector, K. Stefansson, M. Stumvoll, A. Tremblay, J. Tuomilehto, A.G. Uitterlinden, M. Uusitupa, U. Völker, P. Vollenweider, N.J. Wareham, H. Watkins, J.F. Wilson, E. Zeggini, G.R. Abecasis, M. Boehnke, I.B. Borecki, P. Deloukas, C.M. van Duijn, C. Fox, L.C. Groop, I.M. Heid, D.J. Hunter, R.C. Kaplan, M.I. Mccarthy, K.E. North, J.R. O'Connell, D. Schlessinger, U. Thorsteinsdottir, D.P. Strachan, T. Frayling, J.N. Hirschhorn, M. Müller Nurasyid, R.J.F. Loos
Xanthine oxidase gene variants and their association with blood pressure and incident hypertension : A population study
2016 L.E.J.M. Scheepers, F. Wei, K. Stolarz Skrzypek, S. Malyutina, V. Tikhonoff, L. Thijs, E. Salvi, C. Barlassina, J. Filipovský, E. Casiglia, Y. Nikitin, K. Kawecka Jaszcz, P. Manunta, D. Cusi, A. Boonen, J.A. Staessen, I.C.W. Arts
Exome sequencing identifies mutations in two genes encoding the LIM-proteins N-RAP and FHL1 in a BAG3 myofibrillar myopathy
2015 M. Meregalli, F.C. D’Avila, S. Lupoli, M. Barcella, A. Orro, F. De Santis, C. Sitzia, A. Farini, P. D’Ursi, S. Erratico, L. Milanesi, D. Braga, D. Cusi, M.C. Barlassina, Y. Torrente
Inactive matrix gla protein is causally related to adverse health outcomes : a mendelian randomization study in a flemish population
2015 Y. Liu, Y. Gu, L. Thijs, M.H.J. Knapen, E. Salvi, L. Citterio, T. Petit, S. Delli Carpini, Z. Zhang, L. Jacobs, Y. Jin, C. Barlassina, P. Manunta, T. Kuznetsova, P. Verhamme, H.A. Struijker Boudier, D. Cusi, C. Vermeer, J.A. Staessen
Genome-wide association study of kidney function decline in individuals of European descent
2015 M. Gorski, A. Tin, M. Garnaas, G.M. Mcmahon, A.Y. Chu, B.O. Tayo, C. Pattaro, A. Teumer, D.I. Chasman, J. Chalmers, P. Hamet, J. Tremblay, M. Woodward, T. Aspelund, G. Eiriksdottir, V. Gudnason, T.B. Harris, L.J. Launer, A.V. Smith, B.D. Mitchell, J.R. O'Connell, A.R. Shuldiner, J. Coresh, M. Li, P. Freudenberger, E. Hofer, H. Schmidt, R. Schmidt, E.G. Holliday, P. Mitchell, J.J. Wang, I.H. de Boer, G. Li, D.S. Siscovick, Z. Kutalik, T. Corre, P. Vollenweider, G. Waeber, J. Gupta, P.A. Kanetsky, S. Hwang, M. Olden, Q. Yang, M. de Andrade, E.J. Atkinson, S.L.R. Kardia, S.T. Turner, J.M. Stafford, J. Ding, Y. Liu, C. Barlassina, D. Cusi, E. Salvi, J.A. Staessen, P.M. Ridker, H. Grallert, C. Meisinger, M. Müller Nurasyid, B.K. Krämer, H. Kramer, S.E. Rosas, I.M. Nolte, B.W. Penninx, H. Snieder, M. Fabiola Del Greco, A. Franke, U. Nöthlings, W. Lieb, S.J.L. Bakker, R.T. Gansevoort, P. van der Harst, A. Dehghan, O.H. Franco, A. Hofman, F. Rivadeneira, S. Sedaghat, A.G. Uitterlinden, S. Coassin, M. Haun, B. Kollerits, F. Kronenberg, B. Paulweber, N. Aumann, K. Endlich, M. Pietzner, U. Völker, R. Rettig, V. Chouraki, C. Helmer, J. Lambert, M. Metzger, B. Stengel, T. Lehtimäki, L. Lyytikäinen, O. Raitakari, A. Johnson, A. Parsa, M. Bochud, I.M. Heid, W. Goessling, A. Köttgen, W.H.L. Kao, C.S. Fox, C.A. Böger
The -665 C>T polymorphism in the eNOS gene predicts cardiovascular mortality and morbidity in white Europeans
2015 L. Olivi, Y.M. Gu, E. Salvi, Y.P. Liu, L. Thijs, D. Velayutham, Y. Jin, L. Jacobs, F. D'Avila, T. Petit, M. Barcella, C. Lanzani, T. Kuznetsova, P. Manunta, C. Barlassina, D. Cusi, J.A. Staessen
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives
2015 M. Chittani, R. Zaninello, C. Lanzani, F. Frau, M.F. Ortu, E. Salvi, G. Fresu, L. Citterio, D. Braga, D.A. Piras, S.D. Carpini, D. Velayutham, M. Simonini, G. Argiolas, S. Pozzoli, C. Troffa, V. Glorioso, K.K. Kontula, T.P. Hiltunen, K.M. Donner, S.T. Turner, E. Boerwinkle, A.B. Chapman, S. Padmanabhan, A.F. Dominiczak, O. Melander, J.A. Johnson, R.M. Cooper Dehoff, Y. Gong, N.V. Rivera, G. Condorelli, B. Trimarco, P. Manunta, D. Cusi, N. Glorioso, C. Barlassina
Pharmacogenomics considerations in the control of hypertension
2015 S. Lupoli, E. Salvi, M. Barcella, C. Barlassina
Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population
2015 W. Yang, T. Petit, L. Thijs, Z. Zhang, L. Jacobs, A. Hara, F. Wei, E. Salvi, L. Citterio, S.D. Carpini, Y. Gu, J. Knez, N. Cauwenberghs, M. Barcella, C. Barlassina, P. Manunta, G. Coppiello, X.L. Aranguren, T. Kuznetsova, D. Cusi, P. Verhamme, A. Luttun, J.A. Staessen