Lab
Erica Davis Lab
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Statement of Research Interest
Lab Members
- Dharmadhikari, A.V., Abad, M.A., Khan, S., Maroofian, R., Sands, T.T., Ullah, F., Samejima, I., Shen, Y., Wear, M.A., Moore, K.E., Kondakova, E., Mitina, N., Schaub, T., Lee, G.K., Umandap, C.H., Berger, S.M., Iglesias, A.D., Popp, B., Abou Jamra, R., Gabriel, H., Rentas, S., Rippert, A.L., Gray, C., Izumi, K., Conlin, L.K., Koboldt, D.C., Mosher, T.M., Hickey, S.E., Albert, D.V.F., Norwood, H., Lewanda, A.F., Dai, H., Liu, P., Mitani, T., Marafi, D., Eker, H.K., Pehlivan, D., Posey, J.E., Lippa, N.C., Vena, N., Heinzen, E.L., Goldstein, D.B., Mignot, C., de Sainte Agathe, J.M., Al-Sannaa, N.A., Zamani, M., Sadeghian, S., Azizimalamiri, R., Seifia, T., Zaki, M.S., Abdel-Salam, G.M.H., Abdel-Hamid, M.S., Alabdi, L., Alkuraya, F.S., Dawoud, H., Lofty, A., Bauer, P., Zifarelli, G., Afzal, E., Zafar, F., Efthymiou, S., Gossett, D., Towne, M.C., Yeneabat, R., Perez-Duenas, B., Cazurro-Gutierrez, A., Verdura, E., Cantarin-Extremera, V., Marques, A.D.V., Helwak, A., Tollervey, D., Wontakal, S.N., Aggarwal, V.S., Rosenfeld, J.A., Tarabykin, V., Ohta, S., Lupski, J.R., Houlden, H., Earnshaw, W.C., Davis, E.E., Jeyaprakash, A.A., Liao, J. (2025) RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS. Nature communications. 16:17031703
- Fellmann, F., Saunders, C., O'Donohue, M.F., Reid, D.W., McFadden, K.A., Montel-Lehry, N., Yu, C., Fang, M., Zhang, J., Royer-Bertrand, B., Farinelli, P., Karboul, N., Willer, J.R., Fievet, L., Bhuiyan, Z.A., Kleinhenz, A.L., Jadeau, J., Fulbright, J., Rivolta, C., Renella, R., Katsanis, N., Beckmann, J.S., Nicchitta, C.V., Da Costa, L., Davis, E.E., Gleizes, P.E. (2024) An atypical form of 60S ribosomal subunit in Diamond-Blackfan anemia linked to RPL17 variants. JCI insight. 9(17):
- Levic, D.S., Niedzwiecki, D., Kandakatla, A., Karlovich, N.S., Juneja, A., Park, J., Stolarchuk, C., Adams, S., Willer, J.R., Schaner, M.R., Lian, G., Beasley, C., Marjoram, L., Flynn, A.D., Valentine, J.F., Onken, J.E., Sheikh, S.Z., Davis, E.E., Evason, K.J., Garman, K.S., Bagnat, M. (2024) TNF Promoter Hypomethylation Is Associated With Mucosal Inflammation in IBD and Anti-TNF Response. Gastro hep advances. 3:888898888-898
- Yang, S., Zhang, L., Khan, K., Travers, J., Huang, R., Jovanovic, V.M., Veeramachaneni, R., Sakamuru, S., Tristan, C.A., Davis, E.E., Klumpp-Thomas, C., Witt, K.L., Simeonov, A., Shaw, N.D., Xia, M. (2024) Identification of Environmental Compounds That May Trigger Early Female Puberty by Activating Human GnRHR and KISS1R. Endocrinology. 165(10):
- Scala, M., Khan, K., Beneteau, C., Fox, R.G., von Hardenberg, S., Khan, A., Joubert, M., Fievet, L., Musquer, M., Le Vaillant, C., Holsclaw, J.K., Lim, D., Berking, A.C., Accogli, A., Giacomini, T., Nobili, L., Striano, P., Zara, F., Torella, A., Nigro, V., Cogné, B., Salick, M.R., Kaykas, A., Eggan, K., Capra, V., Bézieau, S., Davis, E.E., Wells, M.F. (2023) Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities. Genetics in medicine : official journal of the American College of Medical Genetics. 26(4):101057
- Lippincott, M.F., Xu, W., Smith, A.A., Miao, X., Lafont, A., Shennib, O., Farley, G.J., Sabbagh, R., Delaney, A., Stamou, M., Plummer, L., Salnikov, K., Georgopoulos, N.A., Mericq, V., Quinton, R., Mau-Them, F.T., Nambot, S., Hamad, A., Brittain, H., Tooze, R.S., Calpena, E., Wilkie, A.O.M., Willems, M., Crowley, W.F., Balasubramanian, R., Lamarche-Vane, N., Davis, E.E., Seminara, S.B. (2022) The p190 RhoGAPs, ARHGAP35, and ARHGAP5 are implicated in GnRH neuronal development: Evidence from patients with idiopathic hypogonadotropic hypogonadism, zebrafish, and in vitro GAP activity assay. Genetics in medicine : official journal of the American College of Medical Genetics. 24(12):2501-2515
- Chen, C., Gu, Y., Philippe, J., Zhang, P., Bachman, H., Zhang, J., Mai, J., Rufo, J., Rawls, J.F., Davis, E.E., Katsanis, N., Huang, T.J. (2021) Acoustofluidic rotational tweezing enables high-speed contactless morphological phenotyping of zebrafish larvae. Nature communications. 12:1118
- Ullah, F., Rauf, W., Khan, K., Khan, S., Bell, K.M., de Oliveira, V.C., Tariq, M., Bakhshalizadeh, S., Touraine, P., Katsanis, N., Sinclair, A., He, S., Tucker, E.J., Baig, S.M., Davis, E.E. (2021) A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss. Human genetics. 140(12):1733-1751
- Cogné, B., Latypova, X., Senaratne, L.D.S., Martin, L., Koboldt, D.C., Kellaris, G., Fievet, L., Le Meur, G., Caldari, D., Debray, D., Nizon, M., Frengen, E., Bowne, S.J., 99 Lives Consortium, Cadena, E.L., Daiger, S.P., Bujakowska, K.M., Pierce, E.A., Gorin, M., Katsanis, N., Bézieau, S., Petersen-Jones, S.M., Occelli, L.M., Lyons, L.A., Legeai-Mallet, L., Sullivan, L.S., Davis, E.E., Isidor, B. (2020) Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy. American journal of human genetics. 106(6):893-904
- Davis, E.E., Balasubramanian, R., Kupchinsky, Z.A., Keefe, D.L., Plummer, L., Khan, K., Meczekalski, B., Heath, K.E., Lopez-Gonzalez, V., Ballesta-Martinez, M.J., Margabanthu, G., Price, S., Greening, J., Brauner, R., Valenzuela, I., Cusco, I., Fernandez-Alvarez, P., Wierman, M.E., Li, T., Lage, K., Barroso, P.S., Chan, Y.M., Crowley, W.F., Katsanis, N. (2020) TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci. Human molecular genetics. 29(14):2435-2450
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