| Year |
Citation |
Score |
| 2020 |
Johnson AL, Schneider JE, Mohun TJ, Williams T, Bhattacharya S, Henderson DJ, Phillips HM, Bamforth SD. Early Embryonic Expression of Is Critical for Cardiovascular Development. Journal of Cardiovascular Development and Disease. 7. PMID 32717817 DOI: 10.3390/Jcdd7030027 |
0.371 |
|
| 2019 |
Wang EY, Rafatian N, Zhao Y, Lee A, Lai BFL, Lu RX, Jekic D, Davenport Huyer L, Knee-Walden EJ, Bhattacharya S, Backx PH, Radisic M. Biowire Model of Interstitial and Focal Cardiac Fibrosis. Acs Central Science. 5: 1146-1158. PMID 31403068 DOI: 10.1021/Acscentsci.9B00052 |
0.304 |
|
| 2019 |
Gao R, Liang X, Cheedipudi S, Cordero J, Jiang X, Zhang Q, Caputo L, Günther S, Kuenne C, Ren Y, Bhattacharya S, Yuan X, Barreto G, Chen Y, Braun T, et al. Pioneering function of Isl1 in the epigenetic control of cardiomyocyte cell fate. Cell Research. PMID 31024170 DOI: 10.1038/S41422-019-0168-1 |
0.368 |
|
| 2019 |
Page DJ, Miossec MJ, Williams SG, Monaghan RM, Fotiou E, Cordell HJ, Sutcliffe L, Topf A, Bourgey M, Bourque G, Eveleigh R, Dunwoodie SL, Winlaw DS, Bhattacharya S, Breckpot J, et al. Identification Of The Major Genetic Contributors To Tetralogy Of Fallot Heart. 105. DOI: 10.1136/Heartjnl-2019-Bcs.226 |
0.349 |
|
| 2018 |
Page DJ, Miossec MJ, Williams SG, Monaghan RM, Fotiou E, Cordell H, Sutcliffe L, Topf A, Bourgey M, Bourque G, Eveleigh R, Dunwoodie SL, Winlaw DS, Bhattacharya S, Breckpot J, et al. Whole Exome Sequencing Reveals the Major Genetic Contributors to Non-Syndromic Tetralogy of Fallot. Circulation Research. PMID 30582441 DOI: 10.1161/Circresaha.118.313250 |
0.325 |
|
| 2018 |
Dykes IM, Szumska D, Kuncheria L, Puliyadi R, Chen CM, Papanayotou C, Lockstone H, Dubourg C, David V, Schneider JE, Keane TM, Adams DJ, Brown SDM, Mercier S, Odent S, ... ... Bhattacharya S, et al. A Requirement for Zic2 in the Regulation of Nodal Expression Underlies the Establishment of Left-Sided Identity. Scientific Reports. 8: 10439. PMID 29992973 DOI: 10.1038/S41598-018-28714-1 |
0.372 |
|
| 2017 |
Szumska D, Cioroch M, Keeling A, Prat A, Seidah NG, Bhattacharya S. Pcsk5 is required in the early cranio-cardiac mesoderm for heart development. Bmc Developmental Biology. 17: 6. PMID 28446132 DOI: 10.1186/S12861-017-0148-Y |
0.326 |
|
| 2016 |
Sifrim A, Hitz MP, Wilsdon A, Breckpot J, Turki SH, Thienpont B, McRae J, Fitzgerald TW, Singh T, Swaminathan GJ, Prigmore E, Rajan D, Abdul-Khaliq H, Banka S, Bauer UM, ... ... Bhattacharya S, et al. Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing. Nature Genetics. PMID 27479907 DOI: 10.1038/Ng.3627 |
0.38 |
|
| 2016 |
Faherty N, Benson M, Sharma E, Lee A, Howarth A, Lockstone H, Ebner D, Bhattacharya S. Negative autoregulation of BMP dependent transcription by SIN3B splicing reveals a role for RBM39. Scientific Reports. 6: 28210. PMID 27324164 DOI: 10.1038/Srep28210 |
0.321 |
|
| 2016 |
Grijzenhout A, Godwin J, Koseki H, Gdula M, Szumska D, McGouran JF, Bhattacharya S, Kessler BM, Brockdorff N, Cooper S. Functional analysis of AEBP2, a PRC2 Polycomb protein, reveals a Trithorax phenotype in embryonic development and in ES cells. Development (Cambridge, England). PMID 27317809 DOI: 10.1242/Dev.123935 |
0.351 |
|
| 2016 |
Hanchard NA, Swaminathan S, Bucasas K, Furthner D, Fernbach S, Azamian MS, Wang X, Lewin M, Towbin JA, D'Alessandro LC, Morris SA, Dreyer W, Denfield S, Ayres NA, Franklin WJ, ... ... Bhattacharya S, et al. A Genome Wide Association Study of Congenital Cardiovascular Left-Sided Lesions Shows Association with a Locus on Chromosome 20. Human Molecular Genetics. PMID 26965164 DOI: 10.1093/Hmg/Ddw071 |
0.332 |
|
| 2015 |
Grozeva D, Carss K, Spasic-Boskovic O, Tejada MI, Gecz J, Shaw M, Corbett M, Haan E, Thompson E, Friend K, Hussain Z, Hackett A, Field M, Renieri A, Stevenson R, ... ... Bhattacharya S, et al. Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. Human Mutation. PMID 26350204 DOI: 10.1002/Humu.22901 |
0.301 |
|
| 2015 |
Bouveret R, Waardenberg AJ, Schonrock N, Ramialison M, Doan T, de Jong D, Bondue A, Kaur G, Mohamed S, Fonoudi H, Chen CM, Wouters M, Bhattacharya S, Plachta N, Dunwoodie SL, et al. NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets. Elife. 4. PMID 26146939 DOI: 10.7554/Elife.06942 |
0.367 |
|
| 2015 |
D'Alessandro LC, Al Turki S, Manickaraj AK, Manase D, Mulder BJ, Bergin L, Rosenberg HC, Mondal T, Gordon E, Lougheed J, Smythe J, Devriendt K, Bhattacharya S, Watkins H, Bentham J, et al. Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 25996639 DOI: 10.1038/Gim.2015.60 |
0.365 |
|
| 2015 |
Bouveret R, Waardenberg AJ, Schonrock N, Ramialison M, Doan T, Jong Dd, Bondue A, Kaur G, Mohamed S, Fonoudi H, Chen C, Wouters MA, Bhattacharya S, Plachta N, Dunwoodie SL, et al. Author response: NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets Elife. DOI: 10.7554/Elife.06942.032 |
0.318 |
|
| 2015 |
Leordean D, Grimes D, Keynton J, Maier J, Harfe B, Benson M, Gray A, Bhattacharya S, Norris D. FOXA2 controls Pkd1l1 expression in the mouse node during left-right determination Cilia. 4. DOI: 10.1186/2046-2530-4-S1-P37 |
0.332 |
|
| 2014 |
Dykes IM, van Bueren KL, Ashmore RJ, Floss T, Wurst W, Szumska D, Bhattacharya S, Scambler PJ. HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region. Circulation Research. 115: 23-31. PMID 24748541 DOI: 10.1161/Circresaha.115.303300 |
0.394 |
|
| 2014 |
Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LC, Swaminathan GJ, Bentham J, Arndt AK, Low J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, ... ... Bhattacharya S, et al. Rare variants in NR2F2 cause congenital heart defects in humans. American Journal of Human Genetics. 94: 574-85. PMID 24702954 DOI: 10.1016/J.Ajhg.2014.03.007 |
0.397 |
|
| 2014 |
Bard-Chapeau EA, Szumska D, Jacob B, Chua BQ, Chatterjee GC, Zhang Y, Ward JM, Urun F, Kinameri E, Vincent SD, Ahmed S, Bhattacharya S, Osato M, Perkins AS, Moore AW, et al. Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects. Plos One. 9: e89397. PMID 24586749 DOI: 10.1371/Journal.Pone.0089397 |
0.414 |
|
| 2014 |
Ji W, Benson MA, Bhattacharya S, Chen Y, Hu J, Li F. Characterization of transcription factor AP-2 β mutations involved in familial isolated patent ductus arteriosus suggests haploinsufficiency. The Journal of Surgical Research. 188: 466-72. PMID 24507797 DOI: 10.1016/J.Jss.2014.01.015 |
0.322 |
|
| 2013 |
Palomino Doza J, Topf A, Bentham J, Bhattacharya S, Cosgrove C, Brook JD, Granados-Riveron J, Bu'Lock FA, O'Sullivan J, Stuart AG, Parsons J, Relton C, Goodship J, Henderson DJ, Keavney B. Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot. Bmc Genetics. 14: 57. PMID 23782575 DOI: 10.1186/1471-2156-14-57 |
0.317 |
|
| 2013 |
Cordell HJ, Bentham J, Topf A, Zelenika D, Heath S, Mamasoula C, Cosgrove C, Blue G, Granados-Riveron J, Setchfield K, Thornborough C, Breckpot J, Soemedi R, Martin R, Rahman TJ, ... ... Bhattacharya S, et al. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. Nature Genetics. 45: 822-4. PMID 23708191 DOI: 10.1038/Ng.2637 |
0.343 |
|
| 2013 |
Rog-Zielinska EA, Thomson A, Kenyon CJ, Brownstein DG, Moran CM, Szumska D, Michailidou Z, Richardson J, Owen E, Watt A, Morrison H, Forrester LM, Bhattacharya S, Holmes MC, Chapman KE. Glucocorticoid receptor is required for foetal heart maturation. Human Molecular Genetics. 22: 3269-82. PMID 23595884 DOI: 10.1093/Hmg/Ddt182 |
0.339 |
|
| 2013 |
Davies B, Davies G, Preece C, Puliyadi R, Szumska D, Bhattacharya S. Site specific mutation of the Zic2 locus by microinjection of TALEN mRNA in mouse CD1, C3H and C57BL/6J oocytes. Plos One. 8: e60216. PMID 23555929 DOI: 10.1371/Journal.Pone.0060216 |
0.35 |
|
| 2013 |
Mohun T, Adams DJ, Baldock R, Bhattacharya S, Copp AJ, Hemberger M, Houart C, Hurles ME, Robertson E, Smith JC, Weaver T, Weninger W. Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice. Disease Models & Mechanisms. 6: 562-6. PMID 23519034 DOI: 10.1242/Dmm.011957 |
0.322 |
|
| 2013 |
Adams D, Baldock R, Bhattacharya S, Copp AJ, Dickinson M, Greene ND, Henkelman M, Justice M, Mohun T, Murray SA, Pauws E, Raess M, Rossant J, Weaver T, West D. Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening. Disease Models & Mechanisms. 6: 571-9. PMID 23519032 DOI: 10.1242/Dmm.011833 |
0.353 |
|
| 2013 |
Beffagna G, Cecchetto A, Dal Bianco L, Lorenzon A, Angelini A, Padalino M, Vida V, Bhattacharya S, Stellin G, Rampazzo A, Daliento L. R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease. Journal of Cardiovascular Medicine (Hagerstown, Md.). 14: 582-6. PMID 22964646 DOI: 10.2459/Jcm.0B013E328356A326 |
0.355 |
|
| 2012 |
Chen CM, Bentham J, Cosgrove C, Braganca J, Cuenda A, Bamforth SD, Schneider JE, Watkins H, Keavney B, Davies B, Bhattacharya S. Functional significance of SRJ domain mutations in CITED2. Plos One. 7: e46256. PMID 23082118 DOI: 10.1371/Journal.Pone.0046256 |
0.379 |
|
| 2012 |
Soemedi R, Wilson IJ, Bentham J, Darlay R, Töpf A, Zelenika D, Cosgrove C, Setchfield K, Thornborough C, Granados-Riveron J, Blue GM, Breckpot J, Hellens S, Zwolinkski S, Glen E, ... ... Bhattacharya S, et al. Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease. American Journal of Human Genetics. 91: 489-501. PMID 22939634 DOI: 10.1016/J.Ajhg.2012.08.003 |
0.352 |
|
| 2012 |
Kim W, Essalmani R, Szumska D, Creemers JW, Roebroek AJ, D'Orleans-Juste P, Bhattacharya S, Seidah NG, Prat A. Loss of endothelial furin leads to cardiac malformation and early postnatal death. Molecular and Cellular Biology. 32: 3382-91. PMID 22733989 DOI: 10.1128/Mcb.06331-11 |
0.309 |
|
| 2012 |
Simrick S, Szumska D, Gardiner JR, Jones K, Sagar K, Morrow B, Bhattacharya S, Basson MA. Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 241: 1310-24. PMID 22674535 DOI: 10.1002/Dvdy.23812 |
0.352 |
|
| 2012 |
Kowalczyk MS, Hughes JR, Babbs C, Sanchez-Pulido L, Szumska D, Sharpe JA, Sloane-Stanley JA, Morriss-Kay GM, Smoot LB, Roberts AE, Watkins H, Bhattacharya S, Gibbons RJ, Ponting CP, Wood WG, et al. Nprl3 is required for normal development of the cardiovascular system. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 404-15. PMID 22538705 DOI: 10.1007/S00335-012-9398-Y |
0.377 |
|
| 2012 |
Goodship JA, Hall D, Topf A, Mamasoula C, Griffin H, Rahman TJ, Glen E, Tan H, Palomino Doza J, Relton CL, Bentham J, Bhattacharya S, Cosgrove C, Brook D, Granados-Riveron J, et al. A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot. Circulation. Cardiovascular Genetics. 5: 287-92. PMID 22503907 DOI: 10.1161/Circgenetics.111.962035 |
0.344 |
|
| 2012 |
Soemedi R, Topf A, Wilson IJ, Darlay R, Rahman T, Glen E, Hall D, Huang N, Bentham J, Bhattacharya S, Cosgrove C, Brook JD, Granados-Riveron J, Setchfield K, Bu'lock F, et al. Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls. Human Molecular Genetics. 21: 1513-20. PMID 22199024 DOI: 10.1093/Hmg/Ddr589 |
0.31 |
|
| 2012 |
Bamforth SD, Schneider JE, Bhattacharya S. High-throughput analysis of mouse embryos by magnetic resonance imaging. Cold Spring Harbor Protocols. 2012: 93-101. PMID 22194264 DOI: 10.1101/Pdb.Prot067538 |
0.315 |
|
| 2012 |
Ammirabile G, Tessari A, Pignataro V, Szumska D, Sutera Sardo F, Benes J, Balistreri M, Bhattacharya S, Sedmera D, Campione M. Pitx2 confers left morphological, molecular, and functional identity to the sinus venosus myocardium. Cardiovascular Research. 93: 291-301. PMID 22116619 DOI: 10.1093/Cvr/Cvr314 |
0.316 |
|
| 2012 |
Doza J, Topf A, Bentham J, Bhattacharya S, Cosgrove C, Granados-Riveron J, Goodship J, Henderson D, O'Sullivan J, Keavney B. Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to congenital heart disease European Heart Journal. 33: 872-872. DOI: 10.1093/Eurheartj/Ehs283 |
0.312 |
|
| 2011 |
Chen CM, Krohn J, Bhattacharya S, Davies B. A comparison of exogenous promoter activity at the ROSA26 locus using a ΦiC31 integrase mediated cassette exchange approach in mouse ES cells. Plos One. 6: e23376. PMID 21853122 DOI: 10.1371/Journal.Pone.0023376 |
0.301 |
|
| 2011 |
Susan-Resiga D, Essalmani R, Hamelin J, Asselin MC, Benjannet S, Chamberland A, Day R, Szumska D, Constam D, Bhattacharya S, Prat A, Seidah NG. Furin is the major processing enzyme of the cardiac-specific growth factor bone morphogenetic protein 10. The Journal of Biological Chemistry. 286: 22785-94. PMID 21550985 DOI: 10.1074/Jbc.M111.233577 |
0.314 |
|
| 2011 |
Engelen E, Akinci U, Bryne JC, Hou J, Gontan C, Moen M, Szumska D, Kockx C, van Ijcken W, Dekkers DH, Demmers J, Rijkers EJ, Bhattacharya S, Philipsen S, Pevny LH, et al. Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes. Nature Genetics. 43: 607-11. PMID 21532573 DOI: 10.1038/Ng.825 |
0.369 |
|
| 2011 |
Cross SH, McKie L, West K, Coghill EL, Favor J, Bhattacharya S, Brown SD, Jackson IJ. The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype. Human Molecular Genetics. 20: 223-34. PMID 20943750 DOI: 10.1093/Hmg/Ddq457 |
0.349 |
|
| 2011 |
Bamforth SD, MacDonald, Braganca J, CC, Broadbent C, Schneider JE, Schwartz R, Bhattacharya S. A Cited2-> Vegfa Pathway Couples Myocardial And Coronary Vascular Growth In The Developing Mouse Heart Heart. 97. DOI: 10.1136/Heartjnl-2011-300198.137 |
0.388 |
|
| 2011 |
Simrick S, Szumska D, Gardiner J, Karun S, Morrow B, Bhattacharya S, Basson MA. Sprouty loss of function mutations in the mouse results in defects characteristic of 22q11 deletion syndrome, which are exacerbated by Tbx1 haploinsufficiency Developmental Biology. 356: 223-224. DOI: 10.1016/J.Ydbio.2011.05.366 |
0.309 |
|
| 2010 |
Ashrafian H, Docherty L, Leo V, Towlson C, Neilan M, Steeples V, Lygate CA, Hough T, Townsend S, Williams D, Wells S, Norris D, Glyn-Jones S, Land J, Barbaric I, ... ... Bhattacharya S, et al. A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy. Plos Genetics. 6: e1001000. PMID 20585624 DOI: 10.1371/Journal.Pgen.1001000 |
0.364 |
|
| 2010 |
Michell AC, Bragança J, Broadbent C, Joyce B, Franklyn A, Schneider JE, Bhattacharya S, Bamforth SD. A novel role for transcription factor Lmo4 in thymus development through genetic interaction with Cited2. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 1988-94. PMID 20549734 DOI: 10.1002/Dvdy.22334 |
0.377 |
|
| 2010 |
van Bueren KL, Papangeli I, Rochais F, Pearce K, Roberts C, Calmont A, Szumska D, Kelly RG, Bhattacharya S, Scambler PJ. Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome. Developmental Biology. 340: 369-80. PMID 20122914 DOI: 10.1016/J.Ydbio.2010.01.020 |
0.383 |
|
| 2010 |
Chen CM, Norris D, Bhattacharya S. Transcriptional control of left-right patterning in cardiac development. Pediatric Cardiology. 31: 371-7. PMID 20054532 DOI: 10.1007/S00246-009-9610-3 |
0.367 |
|
| 2010 |
de Wit T, Dekker S, Maas A, Breedveld G, Knoch TA, Langeveld A, Szumska D, Craig R, Bhattacharya S, Grosveld F, Drabek D. Tagged mutagenesis by efficient Minos-based germ line transposition. Molecular and Cellular Biology. 30: 68-77. PMID 19884347 DOI: 10.1128/Mcb.00913-09 |
0.352 |
|
| 2009 |
Kranc KR, Schepers H, Rodrigues NP, Bamforth S, Villadsen E, Ferry H, Bouriez-Jones T, Sigvardsson M, Bhattacharya S, Jacobsen SE, Enver T. Cited2 Is an Essential Regulator of Adult Hematopoietic Stem Cells Cell Stem Cell. 5: 659-665. PMID 19951693 DOI: 10.1016/J.Stem.2009.11.001 |
0.315 |
|
| 2009 |
Ermakov A, Stevens JL, Whitehill E, Robson JE, Pieles G, Brooker D, Goggolidou P, Powles-Glover N, Hacker T, Young SR, Dear N, Hirst E, Tymowska-Lalanne Z, Briscoe J, Bhattacharya S, et al. Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 238: 581-94. PMID 19235720 DOI: 10.1002/Dvdy.21874 |
0.343 |
|
| 2009 |
Papangeli I, Bueren KLV, Pearce K, Roberts C, Szumska D, Bhattacharya S, Scambler PJ. 06-P036 Dissecting the embryonic requirement of the Notch pathway gene, Hes1, in the context of DiGeorge syndrome Mechanisms of Development. 126. DOI: 10.1016/J.Mod.2009.06.262 |
0.328 |
|
| 2008 |
Szumska D, Pieles G, Essalmani R, Bilski M, Mesnard D, Kaur K, Franklyn A, El Omari K, Jefferis J, Bentham J, Taylor JM, Schneider JE, Arnold SJ, Johnson P, Tymowska-Lalanne Z, ... ... Bhattacharya S, et al. VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5. Genes & Development. 22: 1465-77. PMID 18519639 DOI: 10.1101/Gad.479408 |
0.353 |
|
| 2008 |
MacDonald ST, Bamforth SD, Chen CM, Farthing CR, Franklyn A, Broadbent C, Schneider JE, Saga Y, Lewandoski M, Bhattacharya S. Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency. Cardiovascular Research. 79: 448-57. PMID 18440989 DOI: 10.1093/Cvr/Cvn101 |
0.4 |
|
| 2008 |
Bentham J, Bhattacharya S. Genetic mechanisms controlling cardiovascular development. Annals of the New York Academy of Sciences. 1123: 10-9. PMID 18375573 DOI: 10.1196/Annals.1420.003 |
0.407 |
|
| 2007 |
Pieles G, Geyer SH, Szumska D, Schneider J, Neubauer S, Clarke K, Dorfmeister K, Franklyn A, Brown SD, Bhattacharya S, Weninger WJ. microMRI-HREM pipeline for high-throughput, high-resolution phenotyping of murine embryos. Journal of Anatomy. 211: 132-7. PMID 17532797 DOI: 10.1111/J.1469-7580.2007.00746.X |
0.326 |
|
| 2007 |
Liang X, Sun Y, Schneider J, Ding JH, Cheng H, Ye M, Bhattacharya S, Rearden A, Evans S, Chen J. Pinch1 is required for normal development of cranial and cardiac neural crest-derived structures. Circulation Research. 100: 527-35. PMID 17272814 DOI: 10.1161/01.Res.0000259041.37059.8C |
0.329 |
|
| 2006 |
Hart AW, Morgan JE, Schneider J, West K, McKie L, Bhattacharya S, Jackson IJ, Cross SH. Cardiac malformations and midline skeletal defects in mice lacking filamin A. Human Molecular Genetics. 15: 2457-67. PMID 16825286 DOI: 10.1093/Hmg/Ddl168 |
0.35 |
|
| 2006 |
Bhattacharya S, MacDonald ST, Farthing CR. Molecular mechanisms controlling the coupled development of myocardium and coronary vasculature Clinical Science. 111: 35-46. PMID 16764556 DOI: 10.1042/Cs20060003 |
0.347 |
|
| 2006 |
Solberg LC, Valdar W, Gauguier D, Nunez G, Taylor A, Burnett S, Arboledas-Hita C, Hernandez-Pliego P, Davidson S, Burns P, Bhattacharya S, Hough T, Higgs D, Klenerman P, Cookson WO, et al. A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 129-46. PMID 16465593 DOI: 10.1007/S00335-005-0112-1 |
0.305 |
|
| 2005 |
Bogani D, Willoughby C, Davies J, Kaur K, Mirza G, Paudyal A, Haines H, McKeone R, Cadman M, Pieles G, Schneider JE, Bhattacharya S, Hardy A, Nolan PM, Tripodis N, et al. Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. Proceedings of the National Academy of Sciences of the United States of America. 102: 12477-82. PMID 16109771 DOI: 10.1073/Pnas.0500584102 |
0.401 |
|
| 2004 |
Schneider JE, Böse J, Bamforth SD, Gruber AD, Broadbent C, Clarke K, Neubauer S, Lengeling A, Bhattacharya S. Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique. Bmc Developmental Biology. 4: 16. PMID 15615595 DOI: 10.1186/1471-213X-4-16 |
0.386 |
|
| 2004 |
Schneider JE, Bhattacharya S. Making the mouse embryo transparent: identifying developmental malformations using magnetic resonance imaging. Birth Defects Research. Part C, Embryo Today : Reviews. 72: 241-9. PMID 15495185 DOI: 10.1002/Bdrc.20017 |
0.328 |
|
| 2004 |
Bamforth SD, Bragança J, Farthing CR, Schneider JE, Broadbent C, Michell AC, Clarke K, Neubauer S, Norris D, Brown NA, Anderson RH, Bhattacharya S. Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway. Nature Genetics. 36: 1189-96. PMID 15475956 DOI: 10.1038/Ng1446 |
0.38 |
|
| 2003 |
Kranc KR, Bamforth SD, Bragança J, Norbury C, Van Lohuizen M, Bhattacharya S. Transcriptional Coactivator Cited2 Induces Bmi1 and Mel18 and Controls Fibroblast Proliferation via Ink4a/ARF Molecular and Cellular Biology. 23: 7658-7666. PMID 14560011 DOI: 10.1128/Mcb.23.21.7658-7666.2003 |
0.346 |
|
| 2003 |
Schneider JE, Bamforth SD, Farthing CR, Clarke K, Neubauer S, Bhattacharya S. High-resolution imaging of normal anatomy, and neural and adrenal malformations in mouse embryos using magnetic resonance microscopy. Journal of Anatomy. 202: 239-47. PMID 12647873 DOI: 10.1046/J.1469-7580.2003.00157.X |
0.312 |
|
| 2003 |
Schneider JE, Bamforth SD, Farthing CR, Clarke K, Neubauer S, Bhattacharya S. Rapid identification and 3D reconstruction of complex cardiac malformations in transgenic mouse embryos using fast gradient echo sequence magnetic resonance imaging. Journal of Molecular and Cellular Cardiology. 35: 217-22. PMID 12606262 DOI: 10.1016/S0022-2828(02)00291-2 |
0.349 |
|
| 2003 |
Bragança J, Eloranta JJ, Bamforth SD, Ibbitt JC, Hurst HC, Bhattacharya S. Physical and functional interactions among AP-2 transcription factors, p300/CREB-binding protein, and CITED2. The Journal of Biological Chemistry. 278: 16021-9. PMID 12586840 DOI: 10.1074/Jbc.M208144200 |
0.328 |
|
| 2002 |
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Bragança J, Swingler T, Marques FI, Jones T, Eloranta JJ, Hurst HC, Shioda T, Bhattacharya S. Human CREB-binding protein/p300-interacting transactivator with ED-rich tail (CITED) 4, a new member of the CITED family, functions as a co-activator for transcription factor AP-2. The Journal of Biological Chemistry. 277: 8559-65. PMID 11744733 DOI: 10.1074/Jbc.M110850200 |
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