1. ScholarBank@NUS

Stuart Cook

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Full Name
Stuart Cook
Variants
Cook S.A.
 
Main Affiliation
 
Faculty
 
Email
gmsstua@nus.edu.sg
 

Publications

Results 161-178 of 178 (Search time: 0.015 seconds).

Issue DateTitleAuthor(s)
16126-Aug-2021The pro-regenerative effects of hyperil6 in drug induced liver injury are unexpectedly due to competitive inhibition of il11 signalingDong, Jinrui ; Viswanathan, Sivakumar ; Adami, Eleonora ; Schafer, Sebastian ; Kuthubudeen, Fathima F. ; Widjaja, Anissa A. ; Cook, Stuart A. 
22018The prostaglandin H2 analog U-46619 improves the differentiation efficiency of human induced pluripotent stem cells into endothelial cells by activating both p38MAPK and ERK1/2 signaling pathwaysSu, L.; Kong, X.; Lim, S.; Loo, S.; Tan, S.; Poh, K. ; Dutton, J.; Stewart, C.; Cook, S. ; Su, X.; Ma, J.; Zhang, J.; Ye, L. 
32005Therapy insight: Heart disease and the insulin-resistant patientCook S.A. ; Aitman T.; Naoumova R.P.
42018Three-dimensional cardiovascular imaging-genetics: A mass univariate frameworkBiffi C.; De Marvao A.; Attard M.I.; Dawes T.J.W.; Whiffin N.; Bai W.; Shi W.; Francis C.; Meyer H.; Buchan R.; Cook S.A. ; Rueckert D.; O'Regan D.P.
52015Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathyHinson J.T.; Chopra A.; Nafissi N.; Polacheck W.J.; Benson C.C.; Swist S.; Gorham J.; Yang L.; Schafer S. ; Sheng C.C.; Haghighi A.; Homsy J.; Hubner N.; Church G.; Cook S.A. ; Linke W.A.; Chen C.S.; Seidman J.G.; Seidman C.E.
62016Titin truncating mutations: A rare cause of dilated cardiomyopathy in the youngFatkin D.; Lam L.; Herman D.S.; Benson C.C.; Felkin L.E.; Barton P.J.R.; Walsh R.; Candan S.; Ware J.S.; Roberts A.M.; Chung W.K.; Smoot L.; Bornaun H.; Keogh A.M.; Macdonald P.S.; Hayward C.S.; Seidman J.G.; Roberts A.E.; Cook S.A. ; Seidman C.E.
72017Titin-truncating variants affect heart function in disease cohorts and the general populationSchafer S. ; De Marvao A.; Adami E.; Fiedler L.R. ; Ng B.; Khin E. ; Rackham O.J.L. ; Van Heesch S.; Pua C.J.; Kui M.; Walsh R.; Tayal U.; Prasad S.K.; Dawes T.J.W.; Ko N.S.J.; Sim D.; Chan L.L.H.; Chin C.W.L. ; Mazzarotto F.; Barton P.J.; Kreuchwig F.; De Kleijn D.P.V. ; Totman T. ; Biffi C.; Tee N.; Rueckert D.; Schneider V.; Faber A.; Regitz-Zagrosek V.; Seidman J.G.; Seidman C.E.; Linke W.A.; Kovalik J.-P. ; O'Regan D.; Ware J.S.; Hubner N.; Cook S.A. 
82013Towards Clinical Molecular Diagnosis of Inherited Cardiac Conditions: A Comparison of Bench-Top Genome DNA SequencersLi X.; Buckton A.J.; Wilkinson S.L.; John S.; Walsh R.; Novotny T.; Valaskova I.; Gupta M.; Game L.; Barton P.J.R.; Cook S.A. ; Ware J.S.
92002Transcriptional effects of chronic Akt activation in the heartCook S.A. ; Matsui T.; Li N.; Rosenzweig A.
102020Transgenic interleukin 11 expression causes cross-tissue fibro-inflammation and an inflammatory bowel phenotype in miceLim, W.-W.; Ng, B. ; Widjaja, A. ; Xie, C.; Su, L.; Ko, N. ; Lim, S.-Y.; Kwek, X.-Y.; Lim, S. ; Cook, S.A. ; Schafer, S. 
112015Translational regulation shapes the molecular landscape of complex disease phenotypesSchafer S.; Adami E.; Heinig M.; Rodrigues K.E.C.; Kreuchwig F.; Silhavy J.; Van Heesch S.; Simaite D.; Rajewsky N.; Cuppen E.; Pravenec M.; Vingron M.; Cook S.A. ; Hubner N.
122016Truncating Variants in Filamin C: The Challenges of Genotype-Phenotype Correlations in�CardiomyopathiesTayal U.; Cook S.A. 
132017Truncating Variants in Titin Independently Predict Early Arrhythmias in Patients With Dilated CardiomyopathyTayal U.; Newsome S.; Buchan R.; Whiffin N.; Walsh R.; Barton P.J.; Ware J.S.; Cook S.A. ; Prasad S.K.
142018Truncations of the titin Z-disc predispose to a heart failure with preserved ejection phenotype in the context of pressure overloadYe L. ; Su L.; Wang C.; Loo S.; Tee G.; Tan S.; Khin S.W.; Ko S. ; Su B.; Cook S.A. 
152012Truncations of titin causing dilated cardiomyopathyHerman D.S.; Lam L.; Taylor M.R.G.; Wang L.; Teekakirikul P.; Christodoulou D.; Conner L.; DePalma S.R.; McDonough B.; Sparks E.; Teodorescu D.L.; Cirino A.L.; Banner N.R.; Pennell D.J.; Graw S.; Merlo M.; Di Lenarda A.; Sinagra G.; Bos J.M.; Ackerman M.J.; Mitchell R.N.; Murry C.E.; Lakdawala N.K.; Ho C.Y.; Barton P.J.R.; Cook S.A. ; Mestroni L.; Seidman J.G.; Seidman C.E.
162017Using high-resolution variant frequencies to empower clinical genome interpretationWhiffin N.; Minikel E.; Walsh R.; O'Donnell-Luria A.H.; Karczewski K.; Ing A.Y.; Barton P.J.R.; Funke B.; Cook S.A. ; Macarthur D.; Ware J.S.
172017Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death SyndromeLahrouchi N.; Raju H.; Lodder E.M.; Papatheodorou E.; Ware J.S.; Papadakis M.; Tadros R.; Cole D.; Skinner J.R.; Crawford J.; Love D.R.; Pua C.J.; Soh B.Y.; Bhalshankar J.D.; Govind R.; Tfelt-Hansen J.; Winkel B.G.; van der Werf C.; Wijeyeratne Y.D.; Mellor G.; Till J.; Cohen M.C.; Tome-Esteban M.; Sharma S.; Wilde A.A.M.; Cook S.A. ; Bezzina C.R.; Sheppard M.N.; Behr E.R.
188-Jul-2016Wars2 is a determinant of angiogenesisWang M. ; Sips P.; Khin E. ; Rotival M.; Sun X.; Ahmed R.; Widjaja A.A. ; Schafer S.; Yusoff P. ; Choksi P.K. ; Ko N.S.J. ; Singh M.K. ; Epstein D. ; Guan Y. ; Houštěk J.; Mracek T.; Nuskova H.; Mikell B.; Tan J. ; Pesce F.; Kolar F.; Bottolo L.; Mancini M.; Hubner N.; Pravenec M.; Petretto E.; Macrae C.; Cook S.A.