Jessica Gardner, Ph.D - Related publications

Affiliations: 
Pharmacology & Experimental Neuroscience University of Nebraska Medical Center, Omaha, NE, United States 
Area:
neuroinflammation, astrocytes, glia
Website:
http://www.unmc.edu/research_editorial.htm
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
50 most relevant papers in past 60 days:
Year Citation  Score
2021 Habibi I, Falfoul Y, Tran HV, El Matri K, Chebil A, El Matri L, Schorderet DF. Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies. Frontiers in Cell and Developmental Biology. 9: 625560. PMID 33634125 DOI: 10.3389/fcell.2021.625560   
2021 Guo LJ, Jiang XH, He WF, Yu P, Wan R, Kong QL, Liu C, Yu JH, You ZG, Chen Q, Zhu B, Wu YQ, Xu JS, Hong K. [Prevalence of CYP2C19 gene mutations in patients with coronary heart disease and its biological activation effect in clopidogrel antiplatelet response]. Zhonghua Xin Xue Guan Bing Za Zhi. 49: 43-48. PMID 33429485 DOI: 10.3760/cma.j.cn112148-20200424-00345   
2021 Souza LS, Calyjur P, Ribeiro AF, Gurgel-Giannetti J, Pavanello RCM, Zatz M, Vainzof M. Association of Three Different Mutations in the CLCN1 Gene Modulating the Phenotype in a Consanguineous Family with Myotonia Congenita. Journal of Molecular Neuroscience : Mn. PMID 33464536 DOI: 10.1007/s12031-020-01785-4   
2021 Stutterd CA, Brock S, Stouffs K, Fanjul-Fernandez M, Lockhart PJ, McGillivray G, Mandelstam S, Pope K, Delatycki MB, Jansen A, Leventer RJ. Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing. Brain Communications. 3: fcaa221. PMID 33604570 DOI: 10.1093/braincomms/fcaa221   
2021 Zeitz C, Nassisi M, Laurent-Coriat C, Andrieu C, Boyard F, Condroyer C, Démontant V, Antonio A, Lancelot ME, Frederiksen H, Kloeckener-Gruissem B, El-Shamieh S, Zanlonghi X, Meunier I, Roux AF, et al. CHM mutation spectrum and disease: an update at the time of human therapeutic trials. Human Mutation. PMID 33538369 DOI: 10.1002/humu.24174   
2021 Sen S, Kannan SK, Shanmugam U, Rajan R, Babu N, Vanniarajan A. Variable phenotypes of gyrate atrophy in siblings with a nonsense mutation in gene. Ophthalmic Genetics. 1-4. PMID 33463379 DOI: 10.1080/13816810.2020.1870149   
2021 Malekzadeh H, Shakiba M, Yasaei M. A Novel Mutation in PEX11β Gene. Iranian Journal of Child Neurology. 15: 93-100. PMID 33558817 DOI: 10.22037/ijcn.v15i1.26129   
2021 Ma J, Ming C, Lin K, Zhao LP, Bi XY, Li G, Zhang TS, Ruan B. [Analysis of genetic characteristics in two Chinese children of type Ⅱ Waardenburg syndrome]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery. 56: 47-54. PMID 33472302 DOI: 10.3760/cma.j.cn115330-20200121-00041   
2021 Sharifi Z, Taheri M, Fallah MS, Abiri M, Golnabi F, Bagherian H, Zeinali R, Farahzadi H, Alborji M, Tehrani PG, Amini M, Asnavandi S, Hashemi M, Forouzesh F, Zeinali S. Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran. Journal of Molecular Neuroscience : Mn. PMID 33481221 DOI: 10.1007/s12031-020-01789-0   
2021 Pagnamenta AT, Kaiyrzhanov R, Zou Y, Da'as SI, Maroofian R, Donkervoort S, Dominik N, Lauffer M, Ferla MP, Orioli A, Giess A, Tucci A, Beetz C, Sedghi M, Ansari B, ... , et al. An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy. Brain : a Journal of Neurology. PMID 33559681 DOI: 10.1093/brain/awaa420   
2021 Layalle S, They L, Ourghani S, Raoul C, Soustelle L. Amyotrophic Lateral Sclerosis Genes in . International Journal of Molecular Sciences. 22. PMID 33477509 DOI: 10.3390/ijms22020904   
2021 Wang SJ, Xiong WY, Ma YY, Peng X, Yang F, Chen ZQ, Yu FH, Cheng J, Yuan HJ, Kang HY, Lu Y. [Mutation analysis and prenatal diagnosis of MYO7A gene in a case of Usher syndrome type 1]. Zhonghua Yi Xue Za Zhi. 101: 122-126. PMID 33455127 DOI: 10.3760/cma.j.cn112137-20201010-02801   
2021 Borg R, Farrugia Wismayer M, Bonavia K, Farrugia Wismayer A, Vella M, van Vugt JJFA, Kenna BJ, Kenna KP, Vassallo N, Veldink JH, Cauchi RJ. Genetic analysis of ALS cases in the isolated island population of Malta. European Journal of Human Genetics : Ejhg. PMID 33414559 DOI: 10.1038/s41431-020-00767-9   
2021 Greenberg MJ, Tardiff JC. Complexity in genetic cardiomyopathies and new approaches for mechanism-based precision medicine. The Journal of General Physiology. 153. PMID 33512404 DOI: 10.1085/jgp.202012662   
2021 Lizarraga SB, Ma L, Maguire AM, van Dyck LI, Wu Q, Ouyang Q, Kavanaugh BC, Nagda D, Livi LL, Pescosolido MF, Schmidt M, Alabi S, Cowen MH, Brito-Vargas P, Hoffman-Kim D, et al. Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13. PMID 33568516 DOI: 10.1126/scitranslmed.aaw0682   
2021 Hegde S, Hegde R, Kulkarni SS, Das KK, Gai PB, Bulgouda R. Molecular alteration in the Gap Junction Beta 2 () gene associated with non-syndromic sensorineural hearing impairment. Intractable & Rare Diseases Research. 10: 31-36. PMID 33614373 DOI: 10.5582/irdr.2020.03157   
2021 Chang YH, Yu CH, Jou ST, Lin CY, Lin KH, Lu MY, Wu KH, Chang HH, Lin DT, Lin SW, Chen HY, Yang YL. Targeted sequencing to identify genetic alterations and prognostic markers in pediatric T-cell acute lymphoblastic leukemia. Scientific Reports. 11: 769. PMID 33436855 DOI: 10.1038/s41598-020-80613-6   
2021 Micaglio E, Monasky MM, Bernardini A, Mecarocci V, Borrelli V, Ciconte G, Locati ET, Piccoli M, Ghiroldi A, Anastasia L, Pappone C. Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel Frameshift Mutation. International Journal of Molecular Sciences. 22. PMID 33445410 DOI: 10.3390/ijms22020670   
2021 Tong TM, Dao TTH, Doan LP, Nguyen DT, Nguyen QT, Do TT, Truong KD, Phan MD, Nguyen HN, Tran TC, Giang H. Genetic analysis of vietnamese patients with early-onset alzheimer's disease. The International Journal of Neuroscience. 1-10. PMID 33397166 DOI: 10.1080/00207454.2020.1870974   
2021 Tong Y, Zhang Y, Luo J, Hong Z, Chen X, Bi Q. Identification of Novel Mutations in the and Genes of Chinese Patients with Hereditary Multiple Osteochondromas. Genetic Testing and Molecular Biomarkers. 25: 145-151. PMID 33596140 DOI: 10.1089/gtmb.2020.0098   
2021 Yan L, Shen R, Cao Z, Han C, Zhang Y, Liu Y, Yang X, Xie M, Li H. A Novel Missense Variant in the Gene Causes a Rare Neurodevelopmental Disorder with Increased Phenotype. Biomed Research International. 2021: 6661860. PMID 33628804 DOI: 10.1155/2021/6661860   
2021 Chen J, Zheng H, Wang Z, Wang J, He F, Zhang C, Xiong F. A female carrier of a novel DMD mutation with slightly skewed X-chromosome inactivation shows a suspected case of Becker muscular dystrophy in a Chinese family. Molecular Genetics and Genomics : Mgg. PMID 33566169 DOI: 10.1007/s00438-020-01757-8   
2021 Chen L, Ding L, Chen X, Zhang X. Resistance to thyroid hormone caused by a mutation of the thyroid β receptor gene (Cys446Ser) in a family over three generations. Endokrynologia Polska. PMID 33619717 DOI: 10.5603/EP.a2020.0089   
2021 Castilla-Vallmanya L, Gürsoy S, Giray-Bozkaya Ö, Prat-Planas A, Bullich G, Matalonga L, Centeno-Pla M, Rabionet R, Grinberg D, Balcells S, Urreizti R. and Mutations in a Highly Consanguineous Family. International Journal of Molecular Sciences. 22. PMID 33557041 DOI: 10.3390/ijms22041549   
2021 Liang L, Shuai R, Yu Y, Qiu W, Shen L, Wu S, Wei H, Chen Y, Yang C, Xu P, Chen X, Zou H, Feng J, Niu T, Hu H, et al. A rare mutation c.1663G > A (p.A555T) in the MMUT gene associated with mild clinical and biochemical phenotypes of methylmalonic acidemia in 30 Chinese patients. Orphanet Journal of Rare Diseases. 16: 22. PMID 33413471 DOI: 10.1186/s13023-020-01632-0   
2021 Zou Y, Li J, Hua P, Liang T, Ji X, Zhao P. Spectrum of germline mutations in RB1 in Chinese patients with retinoblastoma: Application of targeted next-generation sequencing. Molecular Vision. 27: 1-16. PMID 33456302   
2021 Klipfel L, Cordonnier M, Thiébault L, Clérin E, Blond F, Millet-Puel G, Mohand-Saïd S, Goureau O, Sahel JA, Nandrot EF, Léveillard T. A Splice Variant in Gene Leads to Lactate Transport Deficit in Human iPS Cell-Derived Retinal Pigment Epithelial Cells. Cells. 10. PMID 33477551 DOI: 10.3390/cells10010179   
2021 Ramadesikan S, Skiba L, Lee J, Madhivanan K, Sarkar D, De La Fuente A, Hanna CB, Terashi G, Hazbun T, Kihara D, Aguilar RC. Genotype & Phenotype in Lowe Syndrome: Specific OCRL1 patient mutations differentially impact cellular phenotypes. Human Molecular Genetics. PMID 33517444 DOI: 10.1093/hmg/ddab025   
2021 Ghosh S, Tourtellotte WG. The Complex Clinical and Genetic Landscape of Hereditary Peripheral Neuropathy. Annual Review of Pathology. 16: 487-509. PMID 33497257 DOI: 10.1146/annurev-pathol-030320-100822   
2021 Lee H, Kim EN, Lee JY, Kim JH, Oh JH, Kim WK, Cho EJ, Lim J, Chun SM, Sung CO. Characterization of early postzygotic somatic mutations through multi-organ analysis. Journal of Human Genetics. PMID 33611337 DOI: 10.1038/s10038-021-00908-y   
2021 Jang W, Kim SK, Nahm CH, Choi JW, Kim JJ, Moon Y. A Novel Mutation in Gene Identified through Targeted Next-Generation Sequencing in a Neonate with Hereditary Spherocytosis. Annals of Clinical and Laboratory Science. 51: 136-139. PMID 33653793   
2021 Dicipulo R, Norton KA, Fairbridge NA, Kibalnyk Y, Fox SC, Hornberger LK, McDermid HE. Cecr2 mutant mice as a model for human cat eye syndrome. Scientific Reports. 11: 3111. PMID 33542446 DOI: 10.1038/s41598-021-82556-y   
2021 Liu C, Tu C, Wang L, Wu H, Houston BJ, Mastrorosa FK, Zhang W, Shen Y, Wang J, Tian S, Meng L, Cong J, Yang S, Jiang Y, Tang S, et al. Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility. American Journal of Human Genetics. PMID 33472045 DOI: 10.1016/j.ajhg.2021.01.002   
2021 Qiao F, Zhang C, Wang Y, Liu G, Shao B, Hu P, Xu Z. Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome. Frontiers in Genetics. 12: 628890. PMID 33633789 DOI: 10.3389/fgene.2021.628890   
2021 Kim YJ, Lee Y, Zhang H, Song JS, Hu JC, Simmer JP, Kim JW. A Novel de Novo sp6 Mutation Causes Severe Hypoplastic Ame-Logenesis Imperfecta. Genes. 12. PMID 33652941 DOI: 10.3390/genes12030346   
2021 Zhan Z, Shu Y, Zhao Y, Peng J, Qin B. A novel nonsense mutation (p.Asn140Ter) in a sporadic amyotrophic lateral sclerosis case with rapid progression. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-3. PMID 33448235 DOI: 10.1080/21678421.2021.1871629   
2021 Zheng S, Wang X, Fu Y, Li B, Xu J, Wang H, Huang Z, Xu H, Qiu Y, Shi Y, Li K. Targeted next-generation sequencing for cancer-associated gene mutation and copy number detection in 206 patients with non-small-cell lung cancer. Bioengineered. 12: 791-802. PMID 33629637 DOI: 10.1080/21655979.2021.1890382   
2021 den Hoed J, de Boer E, Voisin N, Dingemans AJM, Guex N, Wiel L, Nellaker C, Amudhavalli SM, Banka S, Bena FS, Ben-Zeev B, Bonagura VR, Bruel AL, Brunet T, Brunner HG, ... , et al. Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction. American Journal of Human Genetics. PMID 33513338 DOI: 10.1016/j.ajhg.2021.01.007   
2021 Farris J, Alam MS, Rajashekara AM, Haldar K. Genomic analyses of glycine decarboxylase neurogenic mutations yield a large-scale prediction model for prenatal disease. Plos Genetics. 17: e1009307. PMID 33524012 DOI: 10.1371/journal.pgen.1009307   
2021 Zhan X, Zhao A, Wu B, Yang Y, Wan L, Tan P, Huang J, Lu Y. A novel compound heterozygous mutation of gene in a patient with bone marrow failure syndrome 4. British Journal of Biomedical Science. PMID 33618624 DOI: 10.1080/09674845.2021.1894706   
2021 Kim HS, Kim HJ, Nam SH, Kim SB, Choi YJ, Lee KS, Chung KW, Yoon YC, Choi BO. Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with Mutations. Journal of Clinical Neurology (Seoul, Korea). 17: 52-62. PMID 33480199 DOI: 10.3988/jcn.2021.17.1.52   
2021 O'Connor A, Abel E, Fraser MR, Ryan NS, Jiménez DA, Koriath C, Chávez-Gutiérrez L, Ansorge O, Mummery CJ, Lashley T, Rossor MN, Polke JM, Mead S, Fox NC. A novel presenilin 1 duplication mutation (Ile168dup) causing Alzheimer's disease associated with myoclonus, seizures and pyramidal features. Neurobiology of Aging. PMID 33648786 DOI: 10.1016/j.neurobiolaging.2021.01.032   
2021 Sharma J, Jindal AK, Banday AZ, Kaur A, Rawat A, Singh S, Longhurst H. Pathophysiology of Hereditary Angioedema (HAE) Beyond the SERPING1 Gene. Clinical Reviews in Allergy & Immunology. PMID 33442779 DOI: 10.1007/s12016-021-08835-8   
2021 Athar M, Abduljaleel Z, Ghita IS, Albagenny AA, Halawani SH, Alkazmi MM, Elbjeirami WM, Alquthami K, Alkhuzae MM, Ragab FM, Al-Allaf FA. Prevalence of the Factor V Leiden Mutation Arg534Gln in Western Region of Saudi Arabia: Functional Alteration and Association Study With Different Populations. Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 27: 1076029620978532. PMID 33448877 DOI: 10.1177/1076029620978532   
2021 Antić Ž, Lelieveld SH, van der Ham CG, Sonneveld E, Hoogerbrugge PM, Kuiper RP. Unravelling the Sequential Interplay of Mutational Mechanisms during Clonal Evolution in Relapsed Pediatric Acute Lymphoblastic Leukemia. Genes. 12. PMID 33540666 DOI: 10.3390/genes12020214   
2021 Yang MM, Sun HY, Meng T, Qiu SH, Zeng QQ, Ng TK, Jiang L, Deng TM, Zeng AN, Wang J, Luo XL. I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Frontiers in Immunology. 12: 608723. PMID 33643312 DOI: 10.3389/fimmu.2021.608723   
2021 Yang MM, Sun HY, Meng T, Qiu SH, Zeng QQ, Ng TK, Jiang L, Deng TM, Zeng AN, Wang J, Luo XL. I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Frontiers in Immunology. 12: 608723. PMID 33643312 DOI: 10.3389/fimmu.2021.608723   
2021 Chan Moi Fat S, McCann EP, Williams KL, Henden L, Twine NA, Bauer DC, Pamphlett R, Kiernan MC, Rowe DB, Nicholson GA, Fifita JA, Blair IP. Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. PMID 33581934 DOI: 10.1016/j.neurobiolaging.2021.01.005   
2021 Bourcier L, Crapoulet N, Ouellette RJ, Mallet M, Ben Amor M. Phenotypic spectrum associated with pathogenic mutation in the NRG1 gene in Acadian family. American Journal of Medical Genetics. Part A. PMID 33421311 DOI: 10.1002/ajmg.a.62069   
2021 Park HC, Ryu H, Kim YC, Ahn C, Lee KB, Kim YH, Kim Y, Han S, Kim Y, Bae EH, Ma SK, Kang HG, Ahn YH, Park E, Jeong K, et al. Genetic identification of inherited cystic kidney diseases for implementing precision medicine: a study protocol for a 3-year prospective multicenter cohort study. Bmc Nephrology. 22: 2. PMID 33407230 DOI: 10.1186/s12882-020-02207-8