ZFIN Person: Fish, Richard

ZFIN ID: ZDB-PERS-120302-3

Fish, Richard

Email:	Richard.Fish@unige.ch
URL:
Affiliation:	Zebrafish Core Facility, Faculty of Medicine, University of Geneva and also: Neerman-Arbez Lab
Address:	University Medical Centre 1, rue Michel Servet Geneva 1211 Switzerland
Country:	Switzerland
Phone:
Fax:
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Li, L., Krasnykov, K., Homolka, D., Gos, P., Mendel, M., Fish, R.J., Pandey, R.R., Pillai, R.S. (2022) The XRN1-regulated RNA helicase activity of YTHDC2 ensures mouse fertility independently of m⁶A recognition. Molecular Cell. 82(9):1678-1690.e12

Fish, R.J., Freire, C., Di Sanza, C., Neerman-Arbez, M. (2021) Venous Thrombosis and Thrombocyte Activity in Zebrafish Models of Quantitative and Qualitative Fibrinogen Disorders. International Journal of Molecular Sciences. 22(2):

Vilar, R., Lukowski, S.W., Garieri, M., Di Sanza, C., Neerman-Arbez, M., Fish, R.J. (2020) Chemical Modulators of Fibrinogen Production and Their Impact on Venous Thrombosis. Thrombosis and haemostasis. 121(4):433-448

Freire, C., Fish, R.J., Vilar, R., Di Sanza, C., Grzegorski, S.J., Richter, C.E., Shavit, J.A., Neerman-Arbez, M. (2020) A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasis. Blood advances. 4:5480-5491

Brillatz, T.E.O., Kubo, M., Takahashi, S., Jozukuri, N., Takechi, K., Queiroz, E.F., Marcourt, L., Allard, P.M., Fish, R., Harada, K., Ishizawa, K., Crawford, A.D., Fukuyama, Y., Wolfender, J.L. (2020) Metabolite profiling of Javanese ginger Zingiber purpureum and identification of antiseizure metabolites via a low-cost open-source zebrafish bioassay-guided isolation. Journal of Agricultural and Food Chemistry. 68(30):7904-7915

Zapilko, V., Fish, R.J., Garcia, A., Reny, J.L., Dunoyer-Geindre, S., Lecompte, T., Neerman-Arbez, M., Fontana, P. (2020) MicroRNA-126 is a regulator of platelet-supported thrombin generation. Platelets. 31(6):746-755

Gueneau, L., Fish, R.J., Shamseldin, H.E., Voisin, N., Tran Mau-Them, F., Preiksaitiene, E., Monroe, G.R., Lai, A., Putoux, A., Allias, F., Ambusaidi, Q., Ambrozaityte, L., Cimbalistienė, L., Delafontaine, J., Guex, N., Hashem, M., Kurdi, W., Jamuar, S.S., Ying, L.J., Bonnard, C., Pippucci, T., Pradervand, S., Roechert, B., van Hasselt, P.M., Wiederkehr, M., Wright, C.F., DDD Study, Xenarios, I., van Haaften, G., Shaw-Smith, C., Schindewolf, E.M., Neerman-Arbez, M., Sanlaville, D., Lesca, G., Guibaud, L., Reversade, B., Chelly, J., Kučinskas, V., Alkuraya, F.S., Reymond, A. (2017) KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis. American journal of human genetics. 102(1):116-132

Moysés-Oliveira, M., Giannuzzi, G., Fish, R.J., Rosenfeld, J.A., Petit, F., de Fatima Soares, M., Kulikowski, L.D., Battista, A.D., Zamariolli, M., Xia, F., Liehr, T., Kosyakova, N., Carvalheira, G., Parker, M., Seaby, E.G., Ennis, S., Gilbert, R.D., Hagelstrom, R.T., Cremona, M.L., Li, W.L., Malhotra, A., Chandrasekhar, A., Perry, D.L., Taft, R.J., McCarrier, J., Basel, D.G., Andrieux, J., Stumpp, T., Antunes, F., Pereira, G.J., Neerman-Arbez, M., Meloni, V.A., Drummond-Borg, M., Melaragno, M.I., Reymond, A. (2017) Inactivation of AMMECR1 is associated with growth, bone and heart alterations. Human Mutation. 39(2):281-291

Meta, E., Imhof, B.A., Ropraz, P., Fish, R.J., Brullo, C., Bruno, O., Sidibé, A. (2017) The pyrazolyl-urea GeGe3 inhibits tumor angiogenesis and reveals dystrophia myotonica protein kinase (DMPK)1 as a novel angiogenesis target. Oncotarget. 8:108195-108212

Lodder, E.M., De Nittis, P., Koopman, C.D., Wiszniewski, W., Moura de Souza, C.F., Lahrouchi, N., Guex, N., Napolioni, V., Tessadori, F., Beekman, L., Nannenberg, E.A., Boualla, L., Blom, N.A., de Graaff, W., Kamermans, M., Cocciadiferro, D., Malerba, N., Mandriani, B., Akdemir, Z.H., Fish, R.J., Eldomery, M.K., Ratbi, I., Wilde, A.A., de Boer, T., Simonds, W.F., Neerman-Arbez, M., Sutton, V.R., Kok, F., Lupski, J.R., Reymond, A., Bezzina, C.R., Bakkers, J., Merla, G. (2016) GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability. American journal of human genetics. 99(3):704-10

Fish, R.J., Di Sanza, C., Neerman-Arbez, M. (2014) Targeted mutation of zebrafish fga models human congenital afibrinogenemia. Blood. 123:2278-81

Bontems, F., Fish, R.J., Borlat, I., Lembo, F., Chocu, S., Chalmel, F., Borg, J.P., Pineau, C., Neerman-Arbez, M., Bairoch, A., and Lane, L. (2014) C2orf62 and TTC17 Are Involved in Actin Organization and Ciliogenesis in Zebrafish and Human. PLoS One. 9(1):e86476

Vorjohann, S., Pitetti, J.L., Nef, S., Gonelle-Gispert, C., Buhler, L., Fish, R.J., and Neerman-Arbez, M. (2013) DNA Methylation Profiling of the Fibrinogen Gene Landscape in Human Cells and during Mouse and Zebrafish Development. PLoS One. 8(8):e73089

Fish, R.J., and Neerman-Arbez, M. (2012) A novel regulatory element between the human FGA and FGG genes. Thrombosis and haemostasis. 108(3):427-434

Fish, R.J., Vorjohann, S., Béna, F., Fort, A., and Neerman-Arbez, M. (2012) Developmental expression and organisation of fibrinogen genes in the zebrafish. Thrombosis and haemostasis. 107(1):158-66

NON-ZEBRAFISH PUBLICATIONS