Borck, G., Rehman, A.U., Lee, K., Pogoda, H.M., Kakar, N., von Ameln, S., Grillet, N., Hildebrand, M.S., Ahmed, Z.M., Nürnberg, G., Ansar, M., Basit, S., Javed, Q., Morell, R.J., Nasreen, N., Shearer, A.E., Ahmad, A., Kahrizi, K., Shaikh, R.S., Ali, R.A., Khan, S.N., Goebel, I., Meyer, N.C., Kimberling, W.J., Webster, J.A., Stephan, D.A., Schiller, M.R., Bahlo, M., Najmabadi, H., Gillespie, P.G., Nürnberg, P., Wollnik, B., Riazuddin, S., Smith, R.J., Ahmad, W., Müller, U., Hammerschmidt, M., Friedman, T.B., Riazuddin, S., Leal, S.M., Ahmad, J., and Kubisch, C. (2011) Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42. American journal of human genetics. 88(2):127-137

Gasanov, E.V., Jędrychowska, J., Kuźnicki, J., Korzh, V. (2021) Evolutionary context can clarify gene names: Teleosts as a case study. BioEssays : news and reviews in molecular, cellular and developmental biology. 43(6):e2000258

Strausberg,R.L., Feingold,E.A., Grouse,L.H., Derge,J.G., Klausner,R.D., Collins,F.S., Wagner,L., Shenmen,C.M., Schuler,G.D., Altschul,S.F., Zeeberg,B., Buetow,K.H., Schaefer,C.F., Bhat,N.K., Hopkins,R.F., Jordan,H., Moore,T., Max,S.I., Wang,J., Hsieh,F., Diatchenko,L., Marusina,K., Farmer,A.A., Rubin,G.M., Hong,L., Stapleton,M., Soares,M.B., Bonaldo,M.F., Casavant,T.L., Scheetz,T.E., Brownstein,M.J., Usdin,T.B., Toshiyuki,S., Carninci,P., Prange,C., Raha,S.S., Loquellano,N.A., Peters,G.J., Abramson,R.D., Mullahy,S.J., Bosak,S.A., McEwan,P.J., McKernan,K.J., Malek,J.A., Gunaratne,P.H., Richards,S., Worley,K.C., Hale,S., Garcia,A.M., Gay,L.J., Hulyk,S.W., Villalon,D.K., Muzny,D.M., Sodergren,E.J., Lu,X., Gibbs,R.A., Fahey,J., Helton,E., Ketteman,M., Madan,A., Rodrigues,S., Sanchez,A., Whiting,M., Madan,A., Young,A.C., Shevchenko,Y., Bouffard,G.G., Blakesley,R.W., Touchman,J.W., Green,E.D., Dickson,M.C., Rodriguez,A.C., Grimwood,J., Schmutz,J., Myers,R.M., Butterfield,Y.S., Krzywinski,M.I., Skalska,U., Smailus,D.E., Schnerch,A., Schein,J.E., Jones,S.J., and Marra,M.A. (2002) Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proceedings of the National Academy of Sciences of the United States of America. 99(26):16899-903

Gasanov, E.V., Jędrychowska, J., Kuźnicki, J., Korzh, V. (2021) Evolutionary context can clarify gene names: Teleosts as a case study. BioEssays : news and reviews in molecular, cellular and developmental biology. 43(6):e2000258

Varshney, G.K., Pei, W., LaFave, M.C., Idol, J., Xu, L., Gallardo, V., Carrington, B., Bishop, K., Jones, M., Li, M., Harper, U., Huang, S.C., Prakash, A., Chen, W., Sood, R., Ledin, J., Burgess, S.M. (2015) High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9. Genome research. 25(7):1030-42

Borck, G., Rehman, A.U., Lee, K., Pogoda, H.M., Kakar, N., von Ameln, S., Grillet, N., Hildebrand, M.S., Ahmed, Z.M., Nürnberg, G., Ansar, M., Basit, S., Javed, Q., Morell, R.J., Nasreen, N., Shearer, A.E., Ahmad, A., Kahrizi, K., Shaikh, R.S., Ali, R.A., Khan, S.N., Goebel, I., Meyer, N.C., Kimberling, W.J., Webster, J.A., Stephan, D.A., Schiller, M.R., Bahlo, M., Najmabadi, H., Gillespie, P.G., Nürnberg, P., Wollnik, B., Riazuddin, S., Smith, R.J., Ahmad, W., Müller, U., Hammerschmidt, M., Friedman, T.B., Riazuddin, S., Leal, S.M., Ahmad, J., and Kubisch, C. (2011) Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42. American journal of human genetics. 88(2):127-137