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Malak El-Quessny - Publications

Affiliations: 
University of California, Berkeley, Berkeley, CA, United States 
Area:
Neural circuit development
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6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Prigge CL, Dembla M, Sharma A, El-Quessny M, Kozlowski C, Paisley CE, Miltner AM, Johnson TM, Della Santina L, Feller MB, Kay JN. Rejection of inappropriate synaptic partners in mouse retina mediated by transcellular FLRT2-UNC5 signaling. Developmental Cell. PMID 37557174 DOI: 10.1016/j.devcel.2023.07.011  0.521
2021 El-Quessny M, Feller MB. Dendrite morphology minimally influences the synaptic distribution of excitation and inhibition in retinal direction selective ganglion cells. Eneuro. PMID 34380656 DOI: 10.1523/ENEURO.0261-21.2021  0.522
2020 El-Quessny M, Maanum K, Feller MB. Visual Experience Influences Dendritic Orientation but Is Not Required for Asymmetric Wiring of the Retinal Direction Selective Circuit. Cell Reports. 31: 107844. PMID 32610144 DOI: 10.1016/j.celrep.2020.107844  0.522
2017 Nakayama T, Wu J, Galvin-Parton P, Weiss J, Andriola MR, Hill RS, Vaughan D, El-Quessny M, Barry BJ, Partlow JN, Barkovich AJ, Ling J, Mochida GH. Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathy. Human Mutation. PMID 28493438 DOI: 10.1002/Humu.23250  0.601
2015 Al-Maawali A, Barry BJ, Rajab A, El-Quessny M, Seman A, Coury SN, Barkovich AJ, Yang E, Walsh CA, Mochida GH, Stoler JM. Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizures. American Journal of Medical Genetics. Part A. PMID 26463574 DOI: 10.1002/Ajmg.A.37422  0.596
2015 Nakayama T, Al-Maawali A, El-Quessny M, Rajab A, Khalil S, Stoler JM, Tan WH, Nasir R, Schmitz-Abe K, Hill RS, Partlow JN, Al-Saffar M, Servattalab S, LaCoursiere CM, Tambunan DE, et al. Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination. American Journal of Human Genetics. 96: 709-19. PMID 25865492 DOI: 10.1016/J.Ajhg.2015.03.003  0.604
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