The Validity and Reliability of the Dutch Effort-Reward Imbalance Questionnaire von Hanson, Eamonn K. S, Schaufeli, Wilmar, Vrijkotte, Tanja, Plomp, Nico H, Godaert, Guido L. R

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Cortisol secretion throughout the day, perceptions of the work environment, and negative affect von Hanson, E K, Maas, C J, Meijman, T F, Godaert, G L

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THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Overview von Alexander, Stephen PH, Kelly, Eamonn, Marrion, Neil V, Peters, John A, Faccenda, Elena, Harding, Simon D, Pawson, Adam J, Sharman, Joanna L, Buneman, O Peter, Cidlowski, John A, Christopoulos, Arthur, Davenport, Anthony P, Abbracchio, M‐P, Aldrich, R, Attali, B, Bäck, M, Bathgate, R, Bettler, B, Biel, M, Birdsall, NJ, Boison, D, Bräuner‐osborne, H, Bröer, S, Burnstock, G, Calo, G, Catterall, WA, Chan, SL, Chazot, P, Chiang, N, Chung, J‐J, Clapham, DE, Clapp, L, Connor, MA, Davies, P, Dawson, PA, Dent, G, Fong, TM, Fowler, CJ, Frantz, A, Fuller, P, Gershengorn, MA, Goldstein, SAN, Goudet, C, Hammond, JR, Hancox, JC, Hanson, J, Hanukoglu, I, Hollenberg, AN, Holliday, ND, Hoyer, D, Inui, KI, Irving, AJ, Ishii, S, Jacobson, KA, Jensen, R, Jockers, R, Karnik, S, Kellenberger, S, Kennedy, C, Kerr, ID, Kihara, Y, Larhammar, D, Leach, K, Lecca, D, Leprince, J, Macewan, D, Maguire, JJ, Marshall, F, Mazella, J, Mcardle, CA, Mitolo, V, Mizuno, H, Mouillac, B, Panaro, MA, Perez‐reyes, E, Pertwee, RG, Pisegna, JR, Plant, LD, Poyner, DR, Pyne, S, Ramachandran, R, Ren, D, Sanger, G, Sanguinetti, MC, Schulte, G, Schulz, S, Segaloff, DL, Singh, KD, Slesinger, PA, Sobey, CG, Stoddart, LA, Thwaites, D, Toll, L, Trimmer, JS, Vaudry, H, Vilargada, J‐P, Wei, AD, Woodruff, TM, Ye, RD, Zajac, J‐M

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Cytoplasmic synthesis of endogenous Alu complementary DNA via reverse transcription and implications in age-related macular degeneration von Fukuda, Shinichi, Varshney, Akhil, Fowler, Benjamin J., Wang, Shao-bin, Narendran, Siddharth, Ambati, Kameshwari, Yasuma, Tetsuhiro, Magagnoli, Joseph, Leung, Hannah, Hirahara, Shuichiro, Nagasaka, Yosuke, Yasuma, Reo, Apicella, Ivana, Pereira, Felipe, Makin, Ryan D., Magner, Eamonn, Liu, Xinan, Sun, Jian, Wang, Mo, Baker, Kirstie, Marion, Kenneth M., Huang, Xiwen, Baghdasaryan, Elmira, Ambati, Meenakshi, Ambati, Vidya L., Pandey, Akshat, Pandya, Lekha, Cummings, Tammy, Banerjee, Daipayan, Huang, Peirong, Yerramothu, Praveen, Tolstonog, Genrich V., Held, Ulrike, Erwin, Jennifer A., Paquola, Apua C. M., Herdy, Joseph R., Ogura, Yuichiro, Terasaki, Hiroko, Oshika, Tetsuro, Darwish, Shaban, Singh, Ramendra K., Mozaffari, Saghar, Bhattarai, Deepak, Kim, Kyung Bo, Hardin, James W., Bennett, Charles L., Hinton, David R., Hanson, Timothy E., Röver, Christian, Parang, Keykavous, Kerur, Nagaraj, Liu, Jinze, Werner, Brian C., Sutton, S.Scott, Sadda, Srinivas R., Schumann, Gerald G., Gelfand, Bradley D., Gage, Fred H., Ambati, Jayakrishna

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Hereditary Leiomyomatosis and Renal Cell Cancer: Clinical, Molecular, and Screening Features in a Cohort of 185 Affected Individuals von Forde, Claire, Lim, Derek H.K., Alwan, Yousef, Burghel, George, Butland, Laura, Cleaver, Ruth, Dixit, Abhijit, Evans, D. Gareth, Hanson, Helen, Lalloo, Fiona, Oliveira, Pedro, Vialard, Lindsey, Wallis, Yvonne, Maher, Eamonn R., Woodward, Emma R.

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UK recommendations for SDHA germline genetic testing and surveillance in clinical practice von Hanson, Helen, Durkie, Miranda, Lalloo, Fiona, Izatt, Louise, McVeigh, Terri P, Cook, Jackie A, Brewer, Carole, Drummond, James, Butler, Samantha, Cranston, Treena, Casey, Ruth, Tan, Tricia, Morganstein, Daniel, Eccles, Diana M, Tischkowitz, Marc, Turnbull, Clare, Woodward, Emma Roisin, Maher, Eamonn R, UK Cancer Genetics Centres

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Investigation and Management of Apparently Sporadic Central Nervous System Haemangioblastoma for Evidence of Von Hippel–Lindau Disease von Furness, Hugh, Salfity, Louay, Devereux, Johanna, Halliday, Dorothy, Hanson, Helen, Ruddy, Deborah M, UK VHL Study Group, UK VHL Study Group, Shah, Neha, Sultana, George, Woodward, Emma R, Sandford, Richard N, Snape, Katie M, Maher, Eamonn R

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Quantifying evidence toward pathogenicity for rare phenotypes: The case of succinate dehydrogenase genes, SDHB and SDHD von Garrett, Alice, Loveday, Chey, King, Laura, Butler, Samantha, Robinson, Rachel, Horton, Carrie, Yussuf, Amal, Choi, Subin, Torr, Beth, Durkie, Miranda, Burghel, George J, Drummond, James, Berry, Ian, Wallace, Andrew, Callaway, Alison, Eccles, Diana, Tischkowitz, Marc, Tatton-Brown, Katrina, Snape, Katie, McVeigh, Terri, Izatt, Louise, Woodward, Emma R, Burnichon, Nelly, Gimenez-Roqueplo, Anne-Paule, Mazzarotto, Francesco, Whiffin, Nicola, Ware, James, Hanson, Helen, Pesaran, Tina, LaDuca, Holly, Buffet, Alexandre, Maher, Eamonn R, Turnbull, Clare, Cancer Variant Interpretation Group UK (CanVIG-UK)

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