ZFIN Lab: Schimmenti Lab

ZFIN ID: ZDB-LAB-130130-1

Schimmenti Lab

PI/Director:	Schimmenti, Lisa A.
Contact Person:	Schimmenti, Lisa A.
Email:	las@umn.edu
URL:	http://www.med.umn.edu/peds/genetics/faculty/schimmentilisa/home.html
Address:	5-214 MCB (Molecular Cellular Biology) 1231B 420 Washington Ave SE Minneapolis, MN 55455
Country:	United States
Phone:	612-624-5613
Fax:	612-626-2993
Line Designation:	mn

GENOMIC FEATURES ORIGINATING FROM THIS LAB

Show all 2 genomic features

STATEMENT OF RESEARCH INTERESTS

LAB MEMBERS

Pretorius, Pamela Post-Doc	Lerach, Stephanie Graduate Student	Agamawi, Yusuf Research Staff
Seubert, Adam Research Staff	Tye, Marc Fish Facility Staff

ZEBRAFISH PUBLICATIONS OF LAB MEMBERS

Riley, K.C., Koleilat, A., Dugdale, J.A., Cooper, S.A., Christensen, T.A., Schimmenti, L.A. (2023) Three-Dimensional Structure of Inner Ear Hair Cell Ribbon Synapses in a Zebrafish Model of Usher Syndrome Type 1B. Zebrafish. 20:475447-54

Koleilat, A., Dugdale, J.A., Christenson, T.A., Bellah, J.L., Lambert, A.M., Masino, M.A., Ekker, S.C., Schimmenti, L.A. (2020) L-type voltage-gated calcium channel agonists mitigate hearing loss and modify ribbon synapse morphology in the zebrafish model of Usher syndrome type 1. Disease models & mechanisms. 13(11):

Muthusamy, K., Hanna, C., Johnson, D.R., Cramer, C.H., Tebben, P.J., Libi, S.E., Poling, G.L., Lanpher, B.C., Morava, E., Schimmenti, L.A. (2020) Growth hormone deficiency in a child with branchio-oto-renal spectrum disorder: Clinical evidence of EYA1 in pituitary development and a recommendation for pituitary function surveillance. American journal of medical genetics. Part A. 185(1):261-266

Brenes-Soto, A., Tye, M., Esmail, M.Y. (2020) The Role of Feed in Aquatic Laboratory Animal Nutrition and the Potential Impact on Animal Models and Study Reproducibility. ILAR journal. 60:197-215

Ichino, N., Serres, M.R., Urban, R.M., Urban, M.D., Treichel, A.J., Schaefbauer, K.J., Greif, L.E., Varshney, G.K., Skuster, K.J., McNulty, M.S., Daby, C.L., Wang, Y., Liao, H.K., El-Rass, S., Ding, Y., Liu, W., Anderson, J.L., Wishman, M.D., Sabharwal, A., Schimmenti, L.A., Sivasubbu, S., Balciunas, D., Hammerschmidt, M., Farber, S.A., Wen, X.Y., Xu, X., McGrail, M., Essner, J.J., Burgess, S.M., Clark, K.J., Ekker, S.C. (2020) Building the vertebrate codex using the gene breaking protein trap library. eLIFE. 9:

Tye, M., Masino, M.A. (2019) Dietary Contaminants and Their Effects on Zebrafish Embryos. Toxics. 7(3):

Riché, R., Liao, M., Pena, I.A., Leung, K.Y., Lepage, N., Greene, N., Sarafoglou, K., Schimmenti, L.A., Drapeau, P., Samarut, É. (2018) Glycine decarboxylase deficiency-induced motor dysfunction in zebrafish is rescued by counterbalancing glycine synaptic level. JCI insight. 3(21):

Tye, M.T., Montgomery, J.E., Hobbs, M.R., Vanpelt, K.T., Masino, M.A. (2018) An Adult Zebrafish Diet Contaminated with Chromium Reduces the Viability of Progeny. Zebrafish. 15(2):179-187

Schimmenti, L.A. (2017) Tank to Bedside: Zebrafish and the Cancer Moonshot. Zebrafish. 14(4):390-392

Schimmenti, L. (2017) Correction to: Zebrafish 2016;13:545-547. Zebrafish. 14:195

Shaw, N.D., Brand, H., Kupchinsky, Z.A., Bengani, H., Plummer, L., Jones, T.I., Erdin, S., Williamson, K.A., Rainger, J., Stortchevoi, A., Samocha, K., Currall, B.B., Dunican, D.S., Collins, R.L., Willer, J.R., Lek, A., Lek, M., Nassan, M., Pereira, S., Kammin, T., Lucente, D., Silva, A., Seabra, C.M., Chiang, C., An, Y., Ansari, M., Rainger, J.K., Joss, S., Smith, J.C., Lippincott, M.F., Singh, S.S., Patel, N., Jing, J.W., Law, J.R., Ferraro, N., Verloes, A., Rauch, A., Steindl, K., Zweier, M., Scheer, I., Sato, D., Okamoto, N., Jacobsen, C., Tryggestad, J., Chernausek, S., Schimmenti, L.A., Brasseur, B., Cesaretti, C., García-Ortiz, J.E., Buitrago, T.P., Silva, O.P., Hoffman, J.D., Mühlbauer, W., Ruprecht, K.W., Loeys, B.L., Shino, M., Kaindl, A.M., Cho, C.H., Morton, C.C., Meehan, R.R., van Heyningen, V., Liao, E.C., Balasubramanian, R., Hall, J.E., Seminara, S.B., Macarthur, D., Moore, S.A., Yoshiura, K.I., Gusella, J.F., Marsh, J.A., Graham, J.M., Lin, A.E., Katsanis, N., Jones, P.L., Crowley, W.F., Davis, E.E., FitzPatrick, D.R., Talkowski, M.E. (2017) SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nature Genetics. 49(2):238-248

Schimmenti, L.A. (2016) Keep Swimming Toward Precision Medicine Discoveries. Zebrafish. 13:545-547

Pei, W., Xu, L., Varshney, G.K., Carrington, B., Bishop, K., Jones, M., Huang, S.C., Idol, J., Pretorius, P.R., Beirl, A., Schimmenti, L.A., Kindt, K.S., Sood, R., Burgess, S.M. (2016) Additive reductions in zebrafish PRPS1 activity result in a spectrum of deficiencies modeling several human PRPS1-associated diseases. Scientific Reports. 6:29946

Schimmenti, L.A. (2016) Zebrafish: A Functional Refuge at the End of an Odyssey. Zebrafish. 13(3):236-8

Tye, M., Rider, D., Duffy, E.A., Seubert, A., Lothert, B., Schimmenti, L.A. (2015) Nonhatching Decapsulated Artemia Cysts As a Replacement to Artemia Nauplii in Juvenile and Adult Zebrafish Culture. Zebrafish. 12(6):457-61

Duffy, E.A., Pretorius, P.R., Lerach, S., Lohr, J.L., Hirsch, B., Souza, C.M., Veillette, A., Schimmenti, L.A. (2015) Mosaic partial deletion of PTPN12 in a child with interrupted aortic arch type A. American journal of medical genetics. Part A. 167(11):2674-83

Pretorius, P.R. (2010) Elucidating a role for BBS3 in syndromic and non-syndromic retinal disease. Ph.D. Thesis. :133