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Items where Author is "Peyvandi, F"

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Article

Donadon, Irving, McVey, John, Garagiola, Isabella, Branchini, Alessio, Mortarino, Mimosa, Peyvandi, Flora, Bernardi, Francesco and Pinotti, Mirko (2017) Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis/activity Haematologica.

Hampshire, DJ, Cairo, A, Dolan, G, Giansily-Blaizot, M, Gomez, K, Goodeve, AC, Kemball-Cook, G, Ludlam, CA, Mcvey, JH, Oldenburg, J, Perkins, SJ, Peyvandi, F and Rallapalli, PM (2015) Eahad-DB: a combined coagulation factor variant databases resource for the clinical and scientificcommunities JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 13. p. 997.

Hampshire, DJ, Gomez, K, Goodeve, AC, Kemball-Cook, G, Ludlam, CA, McVey, JH, Oldenburg, J, Perkins, SJ, Peyvandi, F and Rallapalli, PM (2014) The EAHAD coagulation factor variant databases JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 12. pp. 105-106.

Butterworth, AS, Saleheen, D, Thompson, SG, Danesh, J, Braund, PS, Hardwick, RJ, Barnes, TA, Codd, V, Goodall, AH, Musameh, MD, Nelson, CP, Tomaszewski, M, van der Harst, P, Samani, NJ, Farrall, M, Peden, JF, Goel, A, Ongen, H, Watkins, H, Frossard, P, Rasheed, A, Zaidi, M, Soranzo, N, Hunt, SE, Potter, S, Rice, C, Deloukas, P, Ouwehand, WH, Chambers, JC, Zhang, W, Sivapalaratnam, S, Basart, H, Kastelein, JJP, Trip, MD, Kleber, ME, Keating, B, Qasim, A, Rader, DJ, Reilly, MP, Klopp, N, Baumert, J, Peters, A, Erdmann, J, Diemert, P, Willenborg, C, Schunkert, H, Assimes, TL, Ball, SG, Balmforth, AJ, Bezzina, CR, de Jong, JS, Wilde, AAM, Boerwinkle, E, Boehm, BO, Brocheton, J, Cambien, F, Bugert, P, Klüterr, H, Clarke, R, Collins, R, Couper, D, Adrienne Cupples, L, O'Donnell, CJ, Ejebe, K, Kathiresan, S, Elbers, CC, van der Schouw, YT, de Bakker, PIW, Elliott, P, Fornage, M, Franzosi, M-G, Garner, S, Koch, K, Stephens, J, Hengstenberg, C, Stark, K, Klungel, OH, Peters, BJM, König, IR, Ziegler, A, Kooner, AS, Scott, J, Sehmi, JS, Kooner, JS, Laaksonen, R, Lathrop, M, Li, M, Qu, L, Liu, K, McPherson, R, Musani, S, Papanicolaou, G, Psaty, BM, Seedorf, U, Sotoodehnia, N, van der Schoot, CE, Thorsteinsdottir, U, Vasan, RS, Winkelmann, BR, Koenig, W, März, W, Hamsten, A, Hall, AS, Thompson, JR, Barnes, T, Rafelt, S, Bruinsma, N, Dekker, LR, Henriques, JP, Koch, KT, de Winter, RJ, Alings, M, Allaart, CF, Gorgels, AP, Verheugt, FW, Mueller, M, Meisinger, C, DerOhannessian, S, Mehta, NN, Ferguson, J, Hakonarson, H, Matthai, W, Wilensky, R, Hopewell, JC, Parish, S, Linksted, P, Notman, J, Gonzalez, H, Young, A, Ostley, T, Munday, A, Goodwin, N, Verdon, V, Shah, S, Cobb, L, Edwards, C, Mathews, C, Gunter, R, Benham, J, Davies, C, Cobb, M, Crowther, J, Richards, A, Silver, M, Tochlin, S, Mozley, S, Clark, S, Radley, M, Kourellias, K, Olsson, P, Barlera, S, Tognoni, G, Rust, S, Assmann, G, Heath, S, Zelenika, D, Gut, I, Green, F, Peden, J, Aly, A, Anner, K, Björklund, K, Blomgren, G, Cederschiöld, B, Danell-Toverud, K, Eriksson, P, Grundstedt, U, Heinonen, M, Hellénius, M-L, van't Hooft, F, Husman, K, Lagercrantz, J, Larsson, A, Larsson, M, Mossfeldt, M, Mälarstig, A, Olsson, G, Sabater-Lleal, M, Sennblad, B, Silveira, A, Strawbridge, R, Söderholm, B, Öhrvik, J, Shah Zaman, K, Hayat Mallick, N, Azhar, M, Samad, A, Ishaq, M, Shah, N, Samuel, M, Reilly, M, Holm, H, Preuss, M, Stewart, AFR, Barbalic, M, Gieger, C, Absher, D, Aherrahrou, Z, Allayee, H, Altshuler, D, Anand, S, Andersen, K, Anderson, JL, Ardissino, D, Becker, LC, Becker, DM, Berger, K, Bis, JC, Matthijs Boekholdt, S, Brown, MJ, Susan Burnett, M, Buysschaert, I, Carlquist, JF, Chen, L, Davies, RW, Dedoussis, G, Dehghan, A, Demissie, S, Devaney, J, Do, R, Doering, A, El Mokhtari, NE, Ellis, SG, Elosua, R, Engert, JC, Epstein, S, de Faire, U, Fischer, M, Folsom, AR, Freyer, J, Gigante, B, Girelli, D, Gretarsdottir, S, Gudnason, V, Gulcher, JR, Tennstedt, S, Halperin, E, Hammond, N, Hazen, SL, Hofman, A, Horne, BD, Illig, T, Iribarren, C, Jones, GT, Wouter Jukema, J, Kaiser, MA, Kaplan, LM, Khaw, K-T, Knowles, JW, Kolovou, G, Kong, A, Lambrechts, D, Leander, K, Lieb, W, Lettre, G, Loley, C, Lotery, AJ, Mannucci, PM, Maouche, S, Martinelli, N, McKeown, PP, Meitinger, T, Melander, O, Angelica Merlini, P, Mooser, V, Morgan, T, Mühleisen, TW, Muhlestein, JB, Musunuru, K, Nahrstaedt, J, Nöthen, MM, Olivieri, O, Peyvandi, F, Patel, RS, Patterson, CC, Quyyumi, AA, Rallidis, LS, Roosendaal, FR, Rubin, D, Salomaa, V, Lourdes Sampietro, M, Sandhu, MS, Schadt, E, Schäfer, A, Schillert, A, Schreiber, S, Schrezenmeir, J, Schwartz, SM, Siscovick, DS, Sivananthan, M, Smith, AV, Smith, TB, Snoep, JD, Spertus, JA, Stefansson, K, Stirrups, K, Stoll, M, Wilson Tang, WH, Thorgeirsson, G, Thorleifsson, G, Uitterlinden, AG, van Rij, AM, Voight, BF, Wareham, NJ, Wells, GA, Wichmann, H-E, Witteman, JCM, Wright, BJ, Ye, S, Quertermous, T, Blankenberg, S, Roberts, R, Onland-Moret, NC, van Setten, J, Monique Verschuren, WM, Boer, JMA, Wijmenga, C, Hofker, MH, Maitland-van der Zee, A-H, de Boer, A, Grobbee, DE, Attwood, T, Belz, S, Braund, P, Cooper, J, Crisp-Hihn, A, Foad, N, Gracey, J, Gray, E, Gwilliams, R, Heimerl, S, Jolley, J, Krishnan, U, Lloyd-Jones, H, Lugauer, I, Lundmark, P, Moore, JS, Muir, D, Murray, E, Neudert, J and Niblett, D (2011) Large-scale gene-centric analysis identifies novel variants for coronary artery disease PLoS Genetics, 7 (9).

Neerman-Arbez, M, Johnson, KM, Morris, MA, McVey, JH, Peyvandi, F, Nichols, WC, Ginsburg, D, Rossier, C, Antonarakis, SE and Tuddenham, EGD (1999) Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V factor VIII deficiency BLOOD, 93 (7). pp. 2253-2260.

Conference or Workshop Item

Ludlam, CA, Cairo, A, Dolan, G, Gomez, K, Goodeve, AC, Hampshire, DJ, Kemball-Cook, G, Mcvey, JH, Oldenburg, J, Perkins, SJ, Peyvandi, F and Rallapalli, PM (2015) The European Association for Haemophilia and Allied Disorders Coagulation Factor Variant Databases

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