LOTTA, LUCA ANDREA
LOTTA, LUCA ANDREA
Universita' degli Studi di MILANO
Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581] (Journal of Hepatology (2021) 75(3) (572–581), (S0168827821003342), (10.1016/j.jhep.2021.04.055))
2022 H.J. Cordell, J.J. Fryett, K. Ueno, R. Darlay, Y. Aiba, Y. Hitomi, M. Kawashima, N. Nishida, S.-. Khor, O. Gervais, Y. Kawai, M. Nagasaki, K. Tokunaga, R. Tang, Y. Shi, Z. Li, B.D. Juran, E.J. Atkinson, A. Gerussi, M. Carbone, R. Asselta, A. Cheung, M. de Andrade, A. Baras, J. Horowitz, M.A.R. Ferreira, D. Sun, D.E. Jones, S. Flack, A. Spicer, V.L. Mulcahy, J. Byun, Y. Han, R.N. Sandford, K.N. Lazaridis, C.I. Amos, G.M. Hirschfield, M.F. Seldin, P. Invernizzi, K.A. Siminovitch, X. Ma, M. Nakamura, G.F. Mells, A. Mason, C. Vincent, G. Xie, J. Zhang, A. Affronti, P.L. Almasio, D. Alvaro, P. Andreone, A. Andriulli, F. Azzaroli, P.M. Battezzati, A. Benedetti, M.C. Bragazzi, M. Brunetto, S. Bruno, V. Calvaruso, V. Cardinale, G. Casella, N. Cazzagon, A. Ciaccio, B. Coco, A. Colli, G. Colloredo, M. Colombo, S. Colombo, L. Cristoferi, C. Cursaro, L.S. Croce, A. Crosignani, D. D'Amato, F. Donato, G. Elia, L. Fabris, S. Fagiuoli, C. Ferrari, A. Floreani, A. Galli, E. Giannini, I. Grattagliano, P. Lampertico, A. Lleo, F. Malinverno, C. Mancuso, F. Marra, M. Marzioni, S. Massironi, A. Mattalia, L. Miele, C. Milani, L. Morini, F. Morisco, L. Muratori, P. Muratori, G.A. Niro, S. O'Donnell, A. Picciotto, P. Portincasa, C. Rigamonti, V. Ronca, F. Rosina, G. Spinzi, M. Strazzabosco, M. Tarocchi, C. Tiribelli, P. Toniutto, L. Valenti, M. Vinci, M. Zuin, H. Nakamura, S. Abiru, S. Nagaoka, A. Komori, H. Yatsuhashi, H. Ishibashi, M. Ito, K. Migita, H. Ohira, S. Katsushima, A. Naganuma, K. Sugi, T. Komatsu, T. Mannami, K. Matsushita, K. Yoshizawa, F. Makita, T. Nikami, H. Nishimura, H. Kouno, H. Kouno, H. Ota, T. Komura, Y. Nakamura, M. Shimada, N. Hirashima, T. Komeda, K. Ario, M. Nakamuta, T. Yamashita, K. Furuta, M. Kikuchi, N. Naeshiro, H. Takahashi, Y. Mano, S. Tsunematsu, I. Yabuuchi, Y. Shimada, K. Yamauchi, R. Sugimoto, H. Sakai, E. Mita, M. Koda, S. Tsuruta, H. Kamitsukasa, T. Sato, N. Masaki, T. Kobata, N. Fukushima, Y. Ohara, T. Muro, E. Takesaki, H. Takaki, T. Yamamoto, M. Kato, Y. Nagaoki, S. Hayashi, J. Ishida, Y. Watanabe, M. Kobayashi, M. Koga, T. Saoshiro, M. Yagura, K. Hirata, A. Tanaka, H. Takikawa, M. Zeniya, M. Abe, M. Onji, S. Kaneko, M. Honda, K. Arai, T. Arinaga-Hino, E. Hashimoto, M. Taniai, T. Umemura, S. Joshita, K. Nakao, T. Ichikawa, H. Shibata, S. Yamagiwa, M. Seike, K. Honda, S. Sakisaka, Y. Takeyama, M. Harada, M. Senju, O. Yokosuka, T. Kanda, Y. Ueno, K. Kikuchi, H. Ebinuma, T. Himoto, M. Yasunami, K. Murata, M. Mizokami, K. Kawata, S. Shimoda, Y. Miyake, A. Takaki, K. Yamamoto, K. Hirano, T. Ichida, A. Ido, H. Tsubouchi, K. Chayama, K. Harada, Y. Nakanuma, Y. Maehara, A. Taketomi, K. Shirabe, Y. Soejima, A. Mori, S. Yagi, S. Uemoto, E. H, T. Tanaka, N. Yamashiki, S. Tamura, Y. Sugawara, N. Kokudo, N. Chalasani, V. Luketic, J. Odin, K. Chopra, G. Abecasis, M. Cantor, G. Coppola, A. Economides, L.A. Lotta, J.D. Overton, J.G. Reid, A. Shuldiner, C. Beechert, C. Forsythe, E.D. Fuller, Z. Gu, M. Lattari, A. Lopez, T.D. Schleicher, M.S. Padilla, K. Toledo, L. Widom, S.E. Wolf, M. Pradhan, K. Manoochehri, R.H. Ulloa, X. Bai, S. Balasubramanian, L. Barnard, A. Blumenfeld, G. Eom, L. Habegger, A. Hawes, S. Khalid, E.K. Maxwell, W. Salerno, J.C. Staples, M.B. Jones, L.J. Mitnaul, R. Sturgess, C. Healey, A. Yeoman, A.V.J. Gunasekera, P. Kooner, K. Kapur, V. Sathyanarayana, Y. Kallis, J. Subhani, R. Harvey, R. Mccorry, P. Rooney, D. Ramanaden, R. Evans, T. Mathialahan, J. Gasem, C. Shorrock, M. Bhalme, P. Southern, J.A. Tibble, D.A. Gorard, S. Jones, G. Mells, V. Mulcahy, B. Srivastava, M.R. Foxton, C.E. Collins, D. Elphick, M. Karmo, F. Porras-Perez, M. Mendall, T. Yapp, M. Patel, R. Ede, J. Sayer, J. Jupp, N. Fisher, M.J. Carter, K. Koss, J. Shah, A. Piotrowicz, G. Scott, C. Grimley, I.R. Gooding, S. Williams, J. Tidbury, G. Lim, K. Cheent, S. Levi, D. Mansour, M. Beckley, C. Hollywood, T. Wong, R. Marley, J. Ramage, H.M. Gordon, J. Ridpath, T. Ngatchu, V.P. Bob Grover, R.G. Shidrawi, G. Abouda, L. Corless, M. Narain, I. Rees, A. Brown, S. Taylor-Robinson, J. Wilkins, L. Grellier, P. Banim, D. Das, M.A. Heneghan, H. Curtis, H.C. Matthews, F. Mohammed, M. Aldersley, R. Srirajaskanthan, G. Walker, A. Mcnair, A. Sharif, S. Sen, G. Bird, M.I. Prince, G. Prasad, P. Kitchen, A. Barnardo, C. Oza, N.N. Sivaramakrishnan, P. Gupta, A. Shah, C.D.J. Evans, S. Saha, K. Pollock, P. Bramley, A. Mukhopadhya, S.T. Barclay, N. Mcdonald, A.J. Bathgate, K. Palmer, J.F. Dillon, S.M. Rushbrook, R. Przemioslo, C. Mcdonald, A. Millar, C. Tai, S. Mitchell, J. Metcalf, S. Shaukat, M. Ninkovic, U. Shmueli, A. Davis, A. Naqvi, T.J.W. Lee, S. Ryder, J. Collier, H. Klass, M.E. Cramp, N. Sharer, R. Aspinall, D. Ghosh, A.C. Douds, J. Booth, E. Williams, H. Hussaini, J. Christie, S. Mann, D. Thorburn, A. Marshall, I. Patanwala, A. Ala, J. Maltby, R. Matthew, C. Corbett, S. Vyas, S. Singhal, D. Gleeson, S. Misra, J. Butterworth, K. George, T. Harding, A. Douglass, H. Mitchison, S. Panter, J. Shearman, G. Bray, M. Roberts, G. Butcher, D. Forton, Z. Mahmood, M. Cowan, D. Das, C.L. Ch'Ng, M. Rahman, G.C.A. Whatley, E. Wesley, A. Mandal, S. Jain, S.P. Pereira, M. Wright, P. Trivedi, F.H. Gordon, E. Unitt, A. Palejwala, A. Austin, V. Vemala, A. Grant, A.D. Higham, A. Brind, R. Mathew, M. Cox, S. Ramakrishnan, A. King, S. Whalley, J. Fraser, S.J. Thomson, A. Bell, V.S. Wong, R. Kia, I. Gee, R. Keld, R. Ransford, J. Gotto, C. Millson
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (Nature Genetics, (2020), 52, 12, (1314-1332), 10.1038/s41588-020-00713-x)
2021 P. Surendran, E.V. Feofanova, N. Lahrouchi, I. Ntalla, S. Karthikeyan, J. Cook, L. Chen, B. Mifsud, C. Yao, A.T. Kraja, J.H. Cartwright, J.N. Hellwege, A. Giri, V. Tragante, G. Thorleifsson, D.J. Liu, B.P. Prins, I.D. Stewart, C.P. Cabrera, J.M. Eales, A. Akbarov, P.L. Auer, L.F. Bielak, J.C. Bis, V.S. Braithwaite, J.A. Brody, E.W. Daw, H.R. Warren, F. Drenos, S.F. Nielsen, J.D. Faul, E.B. Fauman, C. Fava, T. Ferreira, C.N. Foley, N. Franceschini, H. Gao, O. Giannakopoulou, F. Giulianini, D.F. Gudbjartsson, X. Guo, S.E. Harris, A.S. Havulinna, A. Helgadottir, J.E. Huffman, S.-. Hwang, S. Kanoni, J. Kontto, M.G. Larson, R. Li-Gao, J. Lindstrom, L.A. Lotta, Y. Lu, J. Luan, A. Mahajan, G. Malerba, N.G.D. Masca, H. Mei, C. Menni, D.O. Mook-Kanamori, D. Mosen-Ansorena, M. Muller-Nurasyid, G. Pare, D.S. Paul, M. Perola, A. Poveda, R. Rauramaa, M. Richard, T.G. Richardson, N. Sepulveda, X. Sim, A.V. Smith, J.A. Smith, J.R. Staley, A. Stanakova, P. Sulem, S. Theriault, U. Thorsteinsdottir, S. Trompet, T.V. Varga, D.R. Velez Edwards, G. Veronesi, S. Weiss, S.M. Willems, J. Yao, R. Young, B. Yu, W. Zhang, J.-. Zhao, W. Zhao, W. Zhao, E. Evangelou, S. Aeschbacher, E. Asllanaj, S. Blankenberg, L.L. Bonnycastle, J. Bork-Jensen, I. Brandslund, P.S. Braund, S. Burgess, K. Cho, C. Christensen, J. Connell, R. Mutsert, A.F. Dominiczak, M. Dorr, G. Eiriksdottir, A.-. Farmaki, J.M. Gaziano, N. Grarup, M.L. Grove, G. Hallmans, T. Hansen, C.T. Have, G. Heiss, M.E. Jorgensen, P. Jousilahti, E. Kajantie, M. Kamat, A.M. Karajamaki, F. Karpe, H.A. Koistinen, C.P. Kovesdy, K. Kuulasmaa, T. Laatikainen, L. Lannfelt, I.-. Lee, W.-. Lee, R.A. de Boer, P. van der Harst, P. van der Meer, N. Verweij, A. Linneberg, L.W. Martin, M. Moitry, G. Nadkarni, M.J. Neville, C.N.A. Palmer, G.J. Papanicolaou, O. Pedersen, J. Peters, N. Poulter, A. Rasheed, K.L. Rasmussen, N.W. Rayner, R. Magi, F. Renstrom, R. Rettig, J. Rossouw, P.J. Schreiner, P.S. Sever, E.L. Sigurdsson, T. Skaaby, Y.V. Sun, J. Sundstrom, G. Thorgeirsson, T. Esko, E. Trabetti, P.S. Tsao, T. Tuomi, S.T. Turner, I. Tzoulaki, I. Vaartjes, A.-. Vergnaud, C.J. Willer, P.W.F. Wilson, D.R. Witte, E. Yonova-Doing, H. Zhang, N. Aliya, P. Almgren, P. Amouyel, F.W. Asselbergs, M.R. Barnes, A.I. Blakemore, M. Boehnke, M.L. Bots, E.P. Bottinger, J.E. Buring, J.C. Chambers, Y.-.I. Chen, R. Chowdhury, D. Conen, A. Correa, G. Davey Smith, R.A. Boer, I.J. Deary, G. Dedoussis, P. Deloukas, E. Di Angelantonio, P. Elliott, A.S. Butterworth, J. Danesh, C. Langenberg, M.I. Mccarthy, P.W. Franks, O. Rolandsson, N.J. Wareham, S.B. Felix, J. Ferrieres, I. Ford, M. Fornage, P.W. Franks, S. Franks, P. Frossard, G. Gambaro, T.R. Gaunt, L. Groop, V. Gudnason, T.B. Harris, C. Hayward, B.J. Hennig, K.-. Herzig, E. Ingelsson, J. Tuomilehto, M.-. Jarvelin, J.W. Jukema, S.L.R. Kardia, F. Kee, J.S. Kooner, C. Kooperberg, L.J. Launer, L. Lind, R.J.F. Loos, A.S. Majumder, M. Laakso, M.I. Mccarthy, O. Melander, K.L. Mohlke, A.D. Murray, B.G. Nordestgaard, M. Orho-Melander, C.J. Packard, S. Padmanabhan, W. Palmas, O. Polasek, D.J. Porteous, A.M. Prentice, M.A. Province, C.L. Relton, K. Rice, P.M. Ridker, O. Rolandsson, F.R. Rosendaal, J.I. Rotter, I. Rudan, V. Salomaa, N.J. Samani, N. Sattar, W.H.-. Sheu, B.H. Smith, N. Soranzo, T.D. Spector, J.M. Starr, S. Sebert, K.D. Taylor, T.A. Lakka, N.J. Timpson, M.D. Tobin, B.P. Prins, E. Zeggini, P. van der Harst, P. van der Meer, V.S. Ramachandran, N. Verweij, J. Virtamo, U. Volker, D.R. Weir, E. Zeggini, F.J. Charchar, J.N. Hellwege, A. Giri, D.R.V. Edwards, K. Cho, J.M. Gaziano, C.P. Kovesdy, Y.V. Sun, P.W.F. Wilson, T.L. Edwards, A.M. Hung, C.J. O'Donnell, M. Tomaszewski, A.S. Butterworth, M.J. Caulfield, T.L. Edwards, H. Holm, C.M. Lindgren, C. Liu, A.K. Manning, A.P. Morris, A.C. Morrison, C.J. O'Donnell, B.M. Psaty, D. Saleheen, K. Stefansson, E. Boerwinkle, D.I. Chasman, D. Levy, C. Newton-Cheh, P.B. Munroe, J.M.M. Howson
Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects
2019 M.M. Gorski, A. Lecchi, E.A. Femia, S. La Marca, A. Cairo, E. Pappalardo, L.A. Lotta, A. Artoni, F. Peyvandi
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes
2018 H.G. de Haan, A. van Hylckama Vlieg, L.A. Lotta, M.M. Gorski, P. Bucciarelli, I. Martinelli, T.P. Baglin, F. Payvandi, F.R. Rosendaal, P. Amouyel, M. de Andrade, S. Basu, C. Berr, J.A. Brody, D.I. Chasman, J.-. Dartigues, A.R. Folsom, M. Germain, J. Heit, J. Houwing-Duitermaat, C. Kabrhel, P. Kraft, G. Le Gal, S. Lindström, R. Monajemi, P.-. Morange, B.M. Psaty, P.H. Reitsma, P.M. Ridker, L.M. Rose, N. Saut, E. Slagboom, D. Smadja, N.L. Smith, P. Suchon, W. Tang, K.D. Taylor, D.-. Trégouët, C. Tzourio, M.C.H. de Visser, L.-. Weng, K.L. Wiggins
Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis
2018 M.M. Gorski, H.G. de Haan, I. Mancini, L.A. Lotta, P. Bucciarelli, S.M. Passamonti, A. Cairo, E. Pappalardo, A. van Hylckama Vlieg, I. Martinelli, F.R. Rosendaal, F. Peyvandi
Next-generation sequencing and in vitro expression study of ADAMTS13 single nucleotide variants in deep vein thrombosis
2016 M.T. Pagliari, L.A. Lotta, H.G. De Haan, C. Valsecchi, G. Casoli, S. Pontiggia, I. Martinelli, S.M. Passamonti, F.R. Rosendaal, F. Peyvandi
Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients
2016 M.M. Gorski, K. Blighe, L.A. Lotta, E. Pappalardo, I. Garagiola, I. Mancini, M.E. Mancuso, M.R. Fasulo, E. Santagostino, F. Peyvandi
A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity
2015 R. Rossio, L.A. Lotta, S. Pontiggia, N. Borsa Ghiringhelli, I. Garagiola, G. Ardissino, D. Mikovic, M. Cugno, F. Peyvandi
FRETS-VWF73 rather than CBA assay reflects ADAMTS13 proteolytic activity in acquired thrombotic thrombocytopenic purpura patients
2014 I. Mancini, C. Valsecchi, L.A. Lotta, L. Deforche, S. Pontiggia, M. Bajetta, R. Palla, K. Vanhoorelbeke, F. Peyvandi
Measurement and prevalence of circulating ADAMTS13-specific immune complexes in autoimmune thrombotic thrombocytopenic purpura
2014 L.A. Lotta, C. Valsecchi, S. Pontiggia, I. Mancini, A. Cannavò, A. Artoni, D. Mikovic, G. Meloni, F. Peyvandi
Association between thrombin generation and bleeding severity in 41 patients with coagulation factor VII deficiency
2013 L.A. Lotta, S.M. Siboni, L. Lemma, M. Clerici, M. Menegatti, F. Peyvandi
Raised haematocrit concentration and the risk of death and vascular complications after major surgery
2013 K.M. Musallam, J.B. Porter, P.M. Sfeir, H.M. Tamim, T. Richards, L.A. Lotta, F. Peyvandi, F.R. Jamali
Treatment of chronic hepatitis C with pegylated interferon-α in a patient with recurrent autoimmune thrombotic thrombocytopenic purpura
2013 L.A. Lotta, E. Degasperi, A. Aghemo, B. Ferrari, F. Peyvandi, M. Colombo
Prevalence of disease and relationships between laboratory phenotype and bleeding severity in platelet primary secretion defects
2013 L.A. Lotta, A. Maino, G. Tuana, R. Rossio, A. Lecchi, A. Artoni, F. Peyvandi
Drop of residual plasmatic activity of ADAMTS13 to undetectable levels during acute disease in a patient with adult-onset congenital thrombotic thrombocytopenic purpura
2013 L.A. Lotta, H.M. Wu, A. Cairo, G. Bentivoglio, F. Peyvandi
Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis
2013 L.A. Lotta, G. Tuana, J. Yu, I. Martinelli, M. Wang, F. Yu, S.M. Passamonti, E. Pappalardo, C. Valsecchi, S.E. Scherer, W. Hale, D.M. Muzny, G. Randi, F.R. Rosendaal, R.A. Gibbs, F. Peyvandi
Association of a single nucleotide polymorphism of the NPR3 gene promoter with early onset ischemic stroke in an Italian cohort
2013 S. Rubattu, B. Giusti, L.A. Lotta, F. Peyvandi, M. Cotugno, R. Stanzione, S. Marchitti, A.M. Palombella, S. Di Castro, M. Rasura, P.M. Mannucci, M. Volpe
Preoperative hematocrit concentration and the risk of stroke in patients undergoing isolated coronary-artery bypass grafting
2013 K.M. Musallam, F.R. Jamali, F.R. Rosendaal, T. Richards, D.R. Spahn, K. Khavandi, I. Barakat, B. Demoss, L.A. Lotta, F. Peyvandi, P.M. Sfeir
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes
2012 L.A. LOTTA, M. WANG, J. YU, I. MARTINELLI, F. YU, S.M. PASSAMONTI, D. CONSONNI, E. PAPPALARDO, M. MENEGATTI, S.E. SCHERER, L.L. LEWIS, H. AKBAR, Y. WU, M.N. BAINBRIDGE, D.M. MUZNY, P.M. MANNUCCI, R.A. GIBBS, F. PEYVANDI
Case report : use of thienopyridines in a patient with acquired idiopathic thrombotic thrombocytopenic purpura
2012 L.A. Lotta, I. Mancini, G. Tuana, K.M. Musallam, F. Peyvandi