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Nathan R. Tucker, Ph.D. - Publications

Affiliations: 
2011 Molecular Biosciences Washington State University, Pullman, WA, United States 
Area:
Cell Biology, Physiology Biology
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3/51 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
2011 Tucker NR, Middleton RC, Le QP, Shelden EA. HSF1 is essential for the resistance of zebrafish eye and brain tissues to hypoxia/reperfusion injury. Plos One. 6: e22268. PMID 21814572 DOI: 10.1371/Journal.Pone.0022268  0.539
2009 Tucker NR, Shelden EA. Hsp27 associates with the titin filament system in heat-shocked zebrafish cardiomyocytes. Experimental Cell Research. 315: 3176-86. PMID 19580808 DOI: 10.1016/J.Yexcr.2009.06.030  0.56
2009 Tucker NR, Ustyugov A, Bryantsev AL, Konkel ME, Shelden EA. Hsp27 is persistently expressed in zebrafish skeletal and cardiac muscle tissues but dispensable for their morphogenesis. Cell Stress & Chaperones. 14: 521-33. PMID 19238587 DOI: 10.1007/S12192-009-0105-1  0.563
Low-probability matches (unlikely to be authored by this person)
2023 Tsai EJ, Cˇiháková D, Tucker NR. Cell-Specific Mechanisms in the Heart of COVID-19 Patients. Circulation Research. 132: 1290-1301. PMID 37167361 DOI: 10.1161/CIRCRESAHA.123.321876  0.235
2022 Glinos DA, Garborcauskas G, Hoffman P, Ehsan N, Jiang L, Gokden A, Dai X, Aguet F, Brown KL, Garimella K, Bowers T, Costello M, Ardlie K, Jian R, Tucker NR, et al. Transcriptome variation in human tissues revealed by long-read sequencing. Nature. PMID 35922509 DOI: 10.1038/s41586-022-05035-y  0.232
2019 Yu M, Georges A, Tucker NR, Kyryachenko S, Toomer K, Schott JJ, Delling FN, Fernandez-Friera L, Solis J, Ellinor PT, Levine RA, Slaugenhaupt SA, Hagège AA, Dina C, Jeunemaitre X, et al. Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse. Circulation. Genomic and Precision Medicine. 12: e002497. PMID 31112420 DOI: 10.1161/CIRCGEN.119.002497  0.217
2020 Tucker NR, Chaffin M, Fleming SJ, Hall AW, Parsons VA, Bedi KC, Akkad AD, Herndon CN, Arduini A, Papangeli I, Roselli C, Aguet F, Choi SH, Ardlie KG, Babadi M, et al. Transcriptional and Cellular Diversity of the Human Heart. Circulation. PMID 32403949 DOI: 10.1161/Circulationaha.119.045401  0.217
2021 Brener MI, Hulke ML, Fukuma N, Golob S, Zilinyi RS, Zhou Z, Tzimas C, Russo I, McGroder C, Pfeiffer RD, Chong A, Zhang G, Burkhoff D, Leon MB, Maurer MS, ... ... Tucker NR, et al. Clinico-histopathologic and single nuclei RNA sequencing insights into cardiac injury and microthrombi in critical COVID-19. Jci Insight. PMID 34905515 DOI: 10.1172/jci.insight.154633  0.207
2020 Ntalla I, Weng LC, Cartwright JH, Hall AW, Sveinbjornsson G, Tucker NR, Choi SH, Chaffin MD, Roselli C, Barnes MR, Mifsud B, Warren HR, Hayward C, Marten J, Cranley JJ, et al. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nature Communications. 11: 2542. PMID 32439900 DOI: 10.1038/S41467-020-15706-X  0.206
2021 Muus C, Luecken MD, Eraslan G, Sikkema L, Waghray A, Heimberg G, Kobayashi Y, Vaishnav ED, Subramanian A, Smillie C, Jagadeesh KA, Duong ET, Fiskin E, Triglia ET, Ansari M, ... ... Tucker NR, et al. Single-cell meta-analysis of SARS-CoV-2 entry genes across tissues and demographics. Nature Medicine. PMID 33654293 DOI: 10.1038/s41591-020-01227-z  0.201
2021 Fukuma N, Hulke ML, Brener MI, Golob S, Zilinyi R, Zhou Z, Tzimas C, Russo I, McGroder C, Pfeiffer R, Chong A, Zhang G, Burkhoff D, Leon MB, Maurer M, ... ... Tucker NR, et al. Molecular Pathophysiology of Cardiac Injury and Cardiac Microthrombi in Fatal COVID-19: Insights from Clinico-histopathologic and Single Nuclei RNA Sequencing Analyses. Biorxiv : the Preprint Server For Biology. PMID 34341789 DOI: 10.1101/2021.07.27.453843  0.201
2022 Chaffin M, Papangeli I, Simonson B, Akkad AD, Hill MC, Arduini A, Fleming SJ, Melanson M, Hayat S, Kost-Alimova M, Atwa O, Ye J, Bedi KC, Nahrendorf M, Kaushik VK, ... ... Tucker NR, et al. Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy. Nature. PMID 35732739 DOI: 10.1038/s41586-022-04817-8  0.198
2021 Valkov N, Das A, Tucker NR, Li G, Salvador AM, Chaffin MD, Pereira De Oliveira Junior G, Kur I, Gokulnath P, Ziegler O, Yeri A, Lu S, Khamesra A, Xiao C, Rodosthenous R, et al. SnRNA sequencing defines signaling by RBC-derived extracellular vesicles in the murine heart. Life Science Alliance. 4. PMID 34663679 DOI: 10.26508/lsa.202101048  0.197
2023 Arduini A, Fleming SJ, Xiao L, Hall AW, Akkad AD, Chaffin M, Bendinelli KJ, Tucker NR, Papangeli I, Mantineo H, Babadi M, Stegmann CM, García-Cardeña G, Lindsay ME, Klattenhoff C, et al. Transcriptional profile of the rat cardiovascular system at single cell resolution. Biorxiv : the Preprint Server For Biology. PMID 38014050 DOI: 10.1101/2023.11.14.567085  0.195
2016 Ye J, Tucker NR, Weng LC, Clauss S, Lubitz SA, Ellinor PT. A Functional Variant Associated with Atrial Fibrillation Regulates PITX2c Expression through TFAP2a. American Journal of Human Genetics. PMID 27866707 DOI: 10.1016/j.ajhg.2016.10.001  0.18
2015 Dina C, Bouatia-Naji N, Tucker N, Delling FN, Toomer K, Durst R, Perrocheau M, Fernandez-Friera L, Solis J, Le Tourneau T, Chen MH, Probst V, Bosse Y, Pibarot P, et al. Genetic association analyses highlight biological pathways underlying mitral valve prolapse. Nature Genetics. PMID 26301497 DOI: 10.1038/Ng.3383  0.169
2016 Kiando SR, Tucker NR, Castro-Vega LJ, Katz A, D'Escamard V, Tréard C, Fraher D, Albuisson J, Kadian-Dodov D, Ye Z, Austin E, Yang ML, Hunker K, Barlassina C, Cusi D, et al. PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance. Plos Genetics. 12: e1006367. PMID 27792790 DOI: 10.1371/Journal.Pgen.1006367  0.156
2020 Hall AW, Chaffin M, Roselli C, Lin H, Lubitz SA, Bianchi V, Geeven G, Bedi K, Margulies KB, de Laat W, Tucker NR, Ellinor PT. Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation. Circulation. Genomic and Precision Medicine. PMID 33155827 DOI: 10.1161/CIRCGEN.120.003085  0.153
2018 Lin H, van Setten J, Smith AV, Bihlmeyer NA, Warren HR, Brody JA, Radmanesh F, Hall L, Grarup N, Müller-Nurasyid M, Boutin T, Verweij N, Lin HJ, Li-Gao R, van den Berg ME, ... ... Tucker NR, et al. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval. Circulation. Genomic and Precision Medicine. 11: e002037. PMID 29748316 DOI: 10.1161/CIRCGEN.117.002037  0.152
2023 Sewanan LR, Clerkin KJ, Tucker NR, Tsai EJ. How Does COVID-19 Affect the Heart? Current Cardiology Reports. 25: 171-184. PMID 36897483 DOI: 10.1007/s11886-023-01841-6  0.151
2022 O' Brien S, Holmes AP, Johnson DM, Kabir SN, O' Shea C, O' Reilly M, Avezzu A, Reyat JS, Hall AW, Apicella C, Ellinor PT, Niederer S, Tucker NR, Fabritz L, Kirchhof P, et al. Increased atrial effectiveness of flecainide conferred by altered biophysical properties of sodium channels. Journal of Molecular and Cellular Cardiology. 166: 23-35. PMID 35114252 DOI: 10.1016/j.yjmcc.2022.01.009  0.143
2021 Chung MK, Zidar DA, Bristow MR, Cameron SJ, Chan T, Harding CV, Kwon DH, Singh T, Tilton JC, Tsai EJ, Tucker NR, Barnard J, Loscalzo J. COVID-19 and Cardiovascular Disease: From Bench to Bedside. Circulation Research. 128: 1214-1236. PMID 33856918 DOI: 10.1161/CIRCRESAHA.121.317997  0.139
2019 Zhang M, Hill MC, Kadow ZA, Suh JH, Tucker NR, Hall AW, Tran TT, Swinton PS, Leach JP, Margulies KB, Ellinor PT, Li N, Martin JF. Long-range enhancer-promoter interactions prevent predisposition to atrial fibrillation. Proceedings of the National Academy of Sciences of the United States of America. PMID 31636200 DOI: 10.1073/Pnas.1907418116  0.138
2020 van Ouwerkerk AF, Bosada F, Liu J, Zhang J, van Duijvenboden K, Chaffin M, Tucker N, Pijnappels DA, Ellinor PT, Barnett P, de Vries AA, Christoffels VM. Identification of Functional Variant Enhancers Associated with Atrial Fibrillation. Circulation Research. PMID 32248749 DOI: 10.1161/CIRCRESAHA.119.316006  0.135
2019 Morley MP, Wang X, Hu R, Brandimarto J, Tucker NR, Felix JF, Smith NL, van der Harst P, Ellinor PT, Margulies KB, Musunuru K, Cappola TP. Cardioprotective Effects of MTSS1 Enhancer Variants. Circulation. 139: 2073-2076. PMID 31070942 DOI: 10.1161/Circulationaha.118.037939  0.134
2014 Mahida S, Mills RW, Tucker NR, Simonson B, Macri V, Lemoine MD, Das S, Milan DJ, Ellinor PT. Overexpression of KCNN3 results in sudden cardiac death. Cardiovascular Research. 101: 326-34. PMID 24296650 DOI: 10.1093/cvr/cvt269  0.131
2023 Jameson HS, Hanley A, Hill MC, Xiao L, Ye J, Bapat A, Ronzier E, Hall AW, Hucker WJ, Clauss S, Barazza M, Silber E, Mina J, Tucker NR, Mills RW, et al. Loss of the Atrial Fibrillation-Related Gene, , Results in Atrial Dilation and Arrhythmias. Circulation Research. PMID 37449401 DOI: 10.1161/CIRCRESAHA.123.323029  0.128
2017 Tucker NR, Dolmatova EV, Lin H, Cooper RR, Ye J, Hucker WJ, Jameson HS, Parsons VA, Weng LC, Mills RW, Sinner MF, Imakaev M, Leyton-Mange J, Vlahakes G, Benjamin EJ, et al. Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential. Circulation. Cardiovascular Genetics. 10. PMID 28974514 DOI: 10.1161/Circgenetics.117.001902  0.127
2017 Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, et al. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics. PMID 28416818 DOI: 10.1038/Ng.3843  0.124
2014 Sinner MF, Tucker NR, Lunetta KL, Ozaki K, Smith JG, Trompet S, Bis JC, Lin H, Chung MK, Nielsen JB, Lubitz SA, Krijthe BP, Magnani JW, Ye J, Gollob MH, et al. Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation. Circulation. 130: 1225-35. PMID 25124494 DOI: 10.1161/Circulationaha.114.009892  0.121
2018 Roselli C, Chaffin MD, Weng LC, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG, Arking DE, Barnard J, Bartz TM, Benjamin EJ, Bihlmeyer NA, ... ... Tucker NR, et al. Multi-ethnic genome-wide association study for atrial fibrillation. Nature Genetics. PMID 29892015 DOI: 10.1038/S41588-018-0133-9  0.118
2016 Wang X, Tucker NR, Rizki G, Mills R, Krijger PH, de Wit E, Subramanian V, Bartell E, Nguyen XX, Ye J, Leyton-Mange J, Dolmatova EV, van der Harst P, de Laat W, Ellinor PT, et al. Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures. Elife. 5. PMID 27162171 DOI: 10.7554/Elife.10557  0.116
2020 van Ouwerkerk AF, Hall AW, Kadow ZA, Lazarevic S, Reyat JS, Tucker NR, Nadadur RD, Bosada FM, Bianchi V, Ellinor PT, Fabritz L, Martin JF, de Laat W, Kirchhof P, Moskowitz IP, et al. Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation. Circulation Research. 127: 34-50. PMID 32717170 DOI: 10.1161/CIRCRESAHA.120.316574  0.116
2022 Abplanalp WT, Tucker N, Dimmeler S. Single-cell technologies to decipher cardiovascular diseases. European Heart Journal. PMID 35265972 DOI: 10.1093/eurheartj/ehac095  0.114
2018 Hu R, Morley MP, Brandimarto J, Tucker NR, Parsons VA, Zhao SD, Meder B, Katus HA, Rühle F, Stoll M, Villard E, Cambien F, Lin H, Smith NL, Felix JF, et al. Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects. Circulation. Genomic and Precision Medicine. 11: e001901. PMID 29540468 DOI: 10.1161/Circgen.117.001901  0.113
2022 Eaton DM, Berretta RM, Lynch JE, Travers JG, Pfeiffer RD, Hulke ML, Zhao H, Hobby ARH, Schena G, Johnson J, Wallner M, Lau E, Lam MPY, Woulfe KC, Tucker NR, et al. Sex-Specific Responses to Slow Progressive Pressure Overload in a Large Animal Model of HFpEF. American Journal of Physiology. Heart and Circulatory Physiology. PMID 36053749 DOI: 10.1152/ajpheart.00374.2022  0.107
2020 Tucker NR, Chaffin M, Bedi KC, Papangeli I, Akkad AD, Arduini A, Hayat S, Eraslan G, Muus C, Bhattacharyya RP, Stegmann CM, Margulies KB, Ellinor PT. Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 Mediated Myocarditis. Circulation. PMID 32795091 DOI: 10.1161/Circulationaha.120.047911  0.107
2018 Choi SH, Weng LC, Roselli C, Lin H, Haggerty CM, Shoemaker MB, Barnard J, Arking DE, Chasman DI, Albert CM, Chaffin M, Tucker NR, Smith JD, Gupta N, Gabriel S, et al. Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation. Jama. 320: 2354-2364. PMID 30535219 DOI: 10.1001/Jama.2018.18179  0.103
2016 Tucker NR, Mahida S, Ye J, Abraham EJ, Mina JA, Parsons VA, McLellan MA, Shea MA, Hanley A, Benjamin EJ, Milan DJ, Lin H, Ellinor PT. Gain of function mutations in GATA6 lead to atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. PMID 27756709 DOI: 10.1016/j.hrthm.2016.10.014  0.102
2017 Tucker NR, McLellan MA, Hu D, Ye J, Parsons VA, Mills RW, Clauss S, Dolmatova E, Shea MA, Milan DJ, Scott NS, Lindsay M, Lubitz SA, Domian IJ, Stone JR, et al. Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy. Circulation. Cardiovascular Genetics. 10. PMID 29212899 DOI: 10.1161/Circgenetics.117.001780  0.098
2017 Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, et al. Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics. 49: 1286. PMID 28747752 DOI: 10.1038/ng0817-1286c  0.089
2020 Tucker NR, Chaffin M, Bedi KC, Papangeli I, Akkad AD, Arduini A, Hayat S, Eraslan G, Muus C, Bhattacharyya R, Stegmann CM, Margulies KB, Ellinor PT. Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 mediated myocarditis. Medrxiv : the Preprint Server For Health Sciences. PMID 32511660 DOI: 10.1101/2020.04.09.20059204  0.086
2014 Macri V, Mahida SN, Zhang ML, Sinner MF, Dolmatova EV, Tucker NR, McLellan M, Shea MA, Milan DJ, Lunetta KL, Benjamin EJ, Ellinor PT. A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 1055-62. PMID 24607718 DOI: 10.1016/j.hrthm.2014.03.002  0.086
2022 Amancherla K, Qin J, Hulke ML, Pfeiffer RD, Agrawal V, Sheng Q, Xu Y, Schlendorf KH, Lindenfeld J, Shah RV, Freedman JE, Tucker NR, Moslehi J. Single-Nuclear RNA Sequencing of Endomyocardial Biopsies Identifies Persistence of Donor-Recipient Chimerism With Distinct Signatures in Severe Cardiac Allograft Vasculopathy. Circulation. Heart Failure. e010119. PMID 36524467 DOI: 10.1161/CIRCHEARTFAILURE.122.010119  0.082
2016 Tucker NR, Clauss S, Ellinor PT. Common variation in atrial fibrillation: navigating the path from genetic association to mechanism. Cardiovascular Research. 109: 493-501. PMID 26733238 DOI: 10.1093/cvr/cvv283  0.075
2014 Tucker NR, Ellinor PT. Emerging directions in the genetics of atrial fibrillation. Circulation Research. 114: 1469-82. PMID 24763465 DOI: 10.1161/CIRCRESAHA.114.302225  0.068
2021 Pirruccello JP, Chaffin MD, Chou EL, Fleming SJ, Lin H, Nekoui M, Khurshid S, Friedman SF, Bick AG, Arduini A, Weng LC, Choi SH, Akkad AD, Batra P, Tucker NR, et al. Deep learning enables genetic analysis of the human thoracic aorta. Nature Genetics. PMID 34837083 DOI: 10.1038/s41588-021-00962-4  0.067
2018 Tucker NR, Ellinor PT. Response by Ma et al to Letter Regarding Article, "Novel Mutation in (Filamin C) Causes Familial Restrictive Cardiomyopathy". Circulation. Genomic and Precision Medicine. 11: e002140. PMID 29650770 DOI: 10.1161/CIRCGEN.118.002140  0.045
2016 Hanley A, Walsh KA, Joyce C, McLellan MA, Clauss S, Hagen A, Shea MA, Tucker NR, Lin H, Fahy GJ, Ellinor PT. Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families. Bmc Medical Genetics. 17: 83. PMID 27855642 DOI: 10.1186/s12881-016-0347-6  0.042
2022 Armstrong EE, Perry BW, Huang Y, Garimella KV, Jansen HT, Robbins CT, Tucker NR, Kelley JL. A beary good genome: Haplotype-resolved, chromosome-level assembly of the brown bear (Ursus arctos). Genome Biology and Evolution. PMID 35929770 DOI: 10.1093/gbe/evac125  0.029
2021 Bhat A, Tucker N, Lin JB, Grover H. Stereoselective copper-catalyzed heteroarene C-H functionalization/Michael-type annulation cascade with α-diazocarbonyls. Chemical Communications (Cambridge, England). PMID 34557880 DOI: 10.1039/d1cc04590c  0.028
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