ZFIN Publication ID	PubMed ID	Authors	Title	Journal	Year	Volume	Pages
ZDB-PUB-051214-11	16327777	Badano, J.L., Leitch, C.C., Ansley, S.J., May-Simera, H., Lawson, S., Lewis, R.A., Beales, P.L., Dietz, H.C., Fisher, S., and Katsanis, N.	Dissection of epistasis in oligogenic Bardet-Biedl syndrome	Nature	2006	439(7074)	326-30
ZDB-PUB-060412-8	16582908	Stoetzel, C., Laurier, V., Davis, E.E., Muller, J., Rix, S., Badano, J.L., Leitch, C.C., Salem, N., Chouery, E., Corbani, S., Jalk, N., Vicaire, S., Sarda, P., Hamel, C., Lacombe, D., Holder, M., Odent, S., Holder, S., Brooks, A.S., Elcioglu, N.H., Da Silva, E., Rossillion, B., Sigaudy, S., de Ravel, T.J., Alan Lewis, R., Leheup, B., Verloes, A., Amati-Bonneau, P., Megarbane, A., Poch, O., Bonneau, D., Beales, P.L., Mandel, J.L., Katsanis, N., and Dollfus, H.	BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus	Nature Genetics	2006	38(5)	521-524
ZDB-PUB-071009-3	17906624	Gerdes, J.M., Liu, Y., Zaghloul, N.A., Leitch, C.C., Lawson, S.S., Kato, M., Beachy, P.A., Beales, P.L., Demartino, G.N., Fisher, S., Badano, J.L., and Katsanis, N.	Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response	Nature Genetics	2007	39(11)	1350-1360
ZDB-PUB-131107-5	21552264	Putoux, A., Thomas, S., Coene, K.L.M., Davis, E.E., Alanay, Y., Ogur, G., Uz, E., Buzas, D., Gomes, C., Patrier, S., Bennett, C.L., Elkhartoufi, N., Saint Frison, M.H., Rigonnot, L., Joye, N., Pruvost, S., Utine, G.E., Boduroglu, K., Nitschke, P., Fertitta, L., Thauvin-Robinet, C., Munnich, A., Cormier-Daire, V., Hennekam, R., Colin, E., Akarsu, N.A., Bole-Feysot, C., Cagnard, N., Schmitt, A., Goudin, N., Lyonnet, S., Encha-Razavi, F., Siffroi, J.P., Winey, M., Katsanis, N., Gonzales, M., Vekemans, M., Beales, P.L., and Attie-Bitach, T.	KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes	Nature Genetics	2011	43	601-606
ZDB-PUB-131205-1	20498079	Zaghloul, N.A., Liu, Y., Gerdes, J.M., Gascue, C., Oh, E.C., Leitch, C.C., Bromberg, Y., Binkley, J., Leibel, R.L., Sidow, A., Badano, J.L., and Katsanis, N.	Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome	Proceedings of the National Academy of Sciences of the United States of America	2010	107(23)	10602-10607
ZDB-PUB-140513-124	24746959	Lindstrand, A., Davis, E.E., Carvalho, C.M., Pehlivan, D., Willer, J.R., Tsai, I.C., Ramanathan, S., Zuppan, C., Sabo, A., Muzny, D., Gibbs, R., Liu, P., Lewis, R.A., Banin, E., Lupski, J.R., Clark, R., Katsanis, N.	Recurrent CNVs and SNVs at the NPHP1 Locus Contribute Pathogenic Alleles to Bardet-Biedl Syndrome	American journal of human genetics	2014	94	745-54
ZDB-PUB-140513-249	24681783	Leitch, C.C., Lodh, S., Prieto-Echagüe, V., Badano, J.L., Zaghloul, N.A.	Basal body proteins regulate Notch signaling via endosomal trafficking	Journal of Cell Science	2014	127(Pt 11)	2407-19
ZDB-PUB-151024-3	26494903	Lodh, S., Hostelley, T.L., Leitch, C.C., O'Hare, E.A., Zaghloul, N.A.	Differential effects on β-cell mass by disruption of Bardet-Biedl Syndrome or Alstrom Syndrome genes	Human molecular genetics	2016	25(1)	57-68
ZDB-PUB-160505-4	27142762	Hostelley, T.L., Lodh, S., Zaghloul, N.A.	Whole organism transcriptome analysis of zebrafish models of Bardet-Biedl Syndrome and Alström Syndrome provides mechanistic insight into shared and divergent phenotypes	BMC Genomics	2016	17	318
ZDB-PUB-190912-3	31506453	Castro-Sánchez, S., Suarez-Bregua, P., Novas, R., Álvarez-Satta, M., Badano, J.L., Rotllant, J., Valverde, D.	Functional analysis of new human Bardet-Biedl syndrome loci specific variants in the zebrafish model	Scientific Reports	2019	9	12936
ZDB-PUB-210616-19	34125181	Hostelley, T.L., Nesmith, J.E., Larkin, E., Jones, A., Boyes, D., Leitch, C.C., Fontaine, M., Zaghloul, N.A.	Exocrine pancreas proteases regulate β-cell proliferation in zebrafish ciliopathy models and in murine systems	Biology Open	2021	10(6)