Amanda Clause - Publications

Affiliations: 
MEEI 
Area:
plasticity, auditory system, development

11/26 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 Lee J, Clause A, Kandler K. Structural and functional development of inhibitory connections from the medial nucleus of the trapezoid body to the superior paraolivary nucleus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 37734946 DOI: 10.1523/JNEUROSCI.0920-23.2023  0.661
2017 Clause A, Lauer AM, Kandler K. Mice Lacking the Alpha9 Subunit of the Nicotinic Acetylcholine Receptor Exhibit Deficits in Frequency Difference Limens and Sound Localization. Frontiers in Cellular Neuroscience. 11: 167. PMID 28663725 DOI: 10.3389/fncel.2017.00167  0.675
2017 Guo W, Clause AR, Barth-Maron A, Polley DB. A Corticothalamic Circuit for Dynamic Switching between Feature Detection and Discrimination. Neuron. PMID 28625486 DOI: 10.1016/J.Neuron.2017.05.019  0.618
2015 Hackett TA, Guo Y, Clause A, Hackett NJ, Garbett K, Zhang P, Polley DB, Mirnics K. Transcriptional maturation of the mouse auditory forebrain. Bmc Genomics. 16: 606. PMID 26271746 DOI: 10.1186/S12864-015-1709-8  0.643
2015 Hackett TA, Clause AR, Takahata T, Hackett NJ, Polley DB. Differential maturation of vesicular glutamate and GABA transporter expression in the mouse auditory forebrain during the first weeks of hearing. Brain Structure & Function. PMID 26159773 DOI: 10.1007/S00429-015-1062-3  0.629
2015 Hackett TA, Guo Y, Clause A, Hackett NJ, Garbett K, Zhang P, Polley DB, Mirnics K. Transcriptional maturation of the mouse auditory forebrain Bmc Genomics. 16. DOI: 10.1186/s12864-015-1709-8  0.65
2014 Clause A, Kim G, Sonntag M, Weisz CJ, Vetter DE, Rűbsamen R, Kandler K. The precise temporal pattern of prehearing spontaneous activity is necessary for tonotopic map refinement. Neuron. 82: 822-35. PMID 24853941 DOI: 10.1016/J.Neuron.2014.04.001  0.527
2014 Clause A, Sturm J, Altieri SC, Maricich SM, Kandler K. Development of Mammalian Primary Sound Localization Circuits Development of Auditory and Vestibular Systems: Fourth Edition. 249-285. DOI: 10.1016/B978-0-12-408088-1.00009-9  0.568
2011 Clause A, Nguyen T, Kandler K. An acoustic startle-based method of assessing frequency discrimination in mice. Journal of Neuroscience Methods. 200: 63-7. PMID 21672556 DOI: 10.1016/j.jneumeth.2011.05.027  0.642
2009 Kandler K, Clause A, Noh J. Tonotopic reorganization of developing auditory brainstem circuits. Nature Neuroscience. 12: 711-7. PMID 19471270 DOI: 10.1038/nn.2332  0.675
2008 Seal RP, Akil O, Yi E, Weber CM, Grant L, Yoo J, Clause A, Kandler K, Noebels JL, Glowatzki E, Lustig LR, Edwards RH. Sensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3. Neuron. 57: 263-75. PMID 18215623 DOI: 10.1016/J.Neuron.2007.11.032  0.591
Low-probability matches (unlikely to be authored by this person)
2006 Clause AR, Capaldi EA. Caudal autotomy and regeneration in lizards. Journal of Experimental Zoology. Part a, Comparative Experimental Biology. 305: 965-73. PMID 17068798 DOI: 10.1002/jez.a.346  0.121
2021 Schmidt L, Wain KE, Hajek C, Estrada-Veras JI, Guillen Sacoto MJ, Wentzensen IM, Malhotra A, Clause A, Perry D, Moreno-De-Luca A, Bell M. Expanding the Phenotype of -Related Tubulinopathy: Three Cases of a Novel, Heterozygous Pathogenic Variant p.Gly98Arg. Molecular Syndromology. 12: 33-40. PMID 33776625 DOI: 10.1159/000512160  0.11
2014 Pierson TW, Stratmann T, White EC, Clause AG, Carter C, Herr MW, Jenkins AJ, Vogel H, Knoerr M, Folt B. New county records of amphibians and reptiles resulting from a bioblitz competition in North-Central Georgia, USA Herpetological Review. 45: 296-297.  0.089
2022 Taylor JP, Malhotra A, Burns NJ, Clause AR, Brown CM, Burns BT, Chandrasekhar A, Schlachetzki Z, Bennett M, Thorpe E, Taft RJ, Perry DL, Coffey AJ. A clinical laboratory's experience using GeneMatcher - building stronger gene-disease relationships. Human Mutation. PMID 35181961 DOI: 10.1002/humu.24356  0.08
2015 Clause AG, Becker RN. Temperature shock as a mechanism for color pattern aberrancy in Snakes Herpetology Notes. 8: 331-334.  0.078
2021 Muirhead KJ, Clause AR, Schlachetzki Z, Dubbs H, Perry DL, Hagelstrom RT, Taft RJ, Vanderver A. Genome sequencing identifies three molecular diagnoses including a mosaic variant in the gene in an individual with Pol III-related leukodystrophy and Feingold syndrome. Cold Spring Harbor Molecular Case Studies. 7. PMID 34737199 DOI: 10.1101/mcs.a006143  0.07
2023 Clause AR, Taylor JP, Rajkumar R, Bluske K, Bennett M, Amendola LM, Bentley DR, Taft RJ, Perry DL, Coffey AJ. Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases. Cell Genomics. 3: 100258. PMID 36819666 DOI: 10.1016/j.xgen.2023.100258  0.068
2014 Clause AL, Coche E, Hantson P, Jacquet LM. Spontaneous pneumomediastinum and epidural pneumatosis after oral ecstasy consumption. Acta Clinica Belgica. 69: 146-8. PMID 24724761 DOI: 10.1179/0001551213Z.00000000019  0.056
2022 Riggs ER, Bingaman TI, Barry CA, Behlmann A, Bluske K, Bostwick B, Bright A, Chen CA, Clause AR, Dharmadhikari AV, Ganapathi M, Gonzaga-Jauregui C, Grant AR, Hughes MY, Kim SR, et al. Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 35616647 DOI: 10.1016/j.gim.2022.05.001  0.051
2000 Poehlau D, Dapprich M, Gerlach W, Thielert L, Welter FL, Albrecht H, Feneberg W, Konig N, Ortmaier A, Pollmann W, Boegner F, Carbon M, Marx P, Nohr R, Hellwig K, ... ... Clause A, et al. Treatment of chronic progressive multiple sclerosis with intravenous immunoglobulins - Interim results on drug safety of an ongoing study Multiple Sclerosis. 6: S21-S23. PMID 11188774  0.039
2023 McCormick EM, Keller K, Taylor JP, Coffey AJ, Shen L, Krotoski D, Harding B, Alves CAPF, Ardissone A, Bai R, de Barcelos IP, Bertini E, Bluske K, Christodoulou J, Clause AR, et al. Expert panel curation of 113 primary mitochondrial disease genes for the Leigh syndrome spectrum. Annals of Neurology. PMID 37255483 DOI: 10.1002/ana.26716  0.034
2014 Clause AL, Vanderheyde K, Pieters T. [Safety of reintroduction of erlotinib at low doses following hand-foot syndrome induced by erlotinib treatment for a Pancoast-Tobias tumour]. Revue Des Maladies Respiratoires. 31: 628-31. PMID 25239586 DOI: 10.1016/j.rmr.2013.11.006  0.029
2022 Mori M, Clause AR, Truxal K, Hagelstrom RT, Manickam K, Kaler SG, Prasad V, Windster J, Alves MM, Di Lorenzo C. Autosomal Recessive ACTG2-Related Visceral Myopathy in Brothers. Jpgn Reports. 3: e258. PMID 37168481 DOI: 10.1097/PG9.0000000000000258  0.023
2010 Verschuren F, Vandenbussche M, Rozencweig S, Stroobant D, Bernard D, Mitri S, Seront B, Nosaradan S, Rougui I, Clause AL, Thys F. Medical trainees participate in the optimization of a recourse in organ and tissue donation following a death that occurred in the emergency service | Les stagiaires en médecine participent à l'optimalisation du recours au don d'organe et de tissus suite à un décès survenu au service des urgences Louvain Medical. 129: 219-223.  0.021
1989 Lahey RT, Clause A, DiMarco P. Chaos and non-linear dynamics of density-wave instabilities in a boiling channel Aiche Symposium Series. 85: 256-261.  0.01
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