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Label-free Brillouin endo-microscopy for the quantitative 3D imaging of sub-micrometre biology La Cavera III, Salvatore; Chauhan, Veeren M.; Hardiman, William; Yao, Mengting; Fuentes-Dominguez, Rafael; Setchfield, Kerry; Abayzeed, Sidahmed A.; Perez-Cota, Fernando; Smith, Richard J.; Clark, Matt 分享 收藏
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IDENTIFICATION OF THE MAJOR GENETIC CONTRIBUTORS TO TETRALOGY OF FALLOT Page, Donna J.; Miossec, Matthieu J.; Williams, Simon G.; Monaghan, Richard M.; Fotiou, Elisavet; Cordell, Heather J.; Sutcliffe, Louise; Topf, Ana; Bourgey, Mathieu; Bourque, Guillaume; Eveleigh, Robert; Dunwoodie, Sally L.; Winlaw, David S.; Bhattacharya, Shoumo; Breckpot, Jeroen; Devriendt, Koenraad; Gewillig, Marc; Brook, David; Setchfield, Kerry; Bu'Lock, Frances A.; O'Sullivan, John; Stuart, Graham; Bezzina, Connie; Mulder, Barbara J. M.; Postma, Alex V.; Bentham, James R.; Baron, Martin; Bhaskar, Sanjeev S.; Black, Graeme C.; Newman, William G.; Hentges, Kathryn E.; Lathrop, Mark; Santibanez-Koref, Mauro; Keavney, Bernard D. 分享 收藏
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot Page, Donna J.; Miossec, Matthieu J.; Williams, Simon G.; Monaghan, Richard M.; Fotiou, Elisavet; Cordell, Heather J.; Sutcliffe, Louise; Topf, Ana; Bourgey, Mathieu; Bourque, Guillaume; Eveleigh, Robert; Dunwoodie, Sally L.; Winlaw, David S.; Bhattacharya, Shoumo; Breckpot, Jeroen; Devriendt, Koenraad; Gewillig, Marc; Brook, J. David; Setchfield, Kerry J.; Bu'Lock, Frances A.; O'Sullivan, John; Stuart, Graham; Bezzina, Connie R.; Mulder, Barbara J. M.; Postma, Alex V.; Bentham, James R.; Baron, Martin; Bhaskar, Sanjeev S.; Black, Graeme C.; Newman, William G.; Hentges, Kathryn E.; Lathrop, G. Mark; Santibanez-Koref, Mauro; Keavney, Bernard D. 分享 收藏
Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects 原肌球蛋白1: 在心脏发育和先天性心脏缺陷形成中的多重作用 England, Jennifer; Granados-Riveron, Javier; Polo-Parada, Luis; Kuriakose, Diji; Moore, Christopher; Brook, J. David; Rutland, Catrin S.; Setchfield, Kerry; Gell, Christopher; Ghosh, Tushar K.; Bu'Lock, Frances; Thomborough, Christopher; Ehler, Elisabeth; Loughna, Siobhan 分享 收藏
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing Sifrim, Alejandro; Hitz, Marc-Phillip; Wilsdon, Anna; Breckpot, Jeroen; Al Turki, Saeed H.; Thienpont, Bernard; McRae, Jeremy; Fitzgerald, Tomas W.; Singh, Tarjinder; Swaminathan, Ganesh Jawahar; Prigmore, Elena; Rajan, Diana; Abdul-Khaliq, Hashim; Banka, Siddharth; Bauer, Ulrike M. M.; Bentham, Jamie; Berger, Felix; Bhattacharya, Shoumo; Bu'Lock, Frances; Canham, Natalie; Colgiu, Irina-Gabriela; Cosgrove, Catherine; Cox, Helen; Daehnert, Ingo; Daly, Allan; Danesh, John; Fryer, Alan; Gewillig, Marc; Hobson, Emma; Hoff, Kirstin; Homfray, Tessa; Kahlert, Anne-Karin; Ketley, Ami; Kramer, Hans-Heiner; Lachlan, Katherine; Lampe, Anne Katrin; Louw, Jacoba J.; Manickara, Ashok Kumar; Manase, Dorin; McCarthy, Karen P.; Metcalfe, Kay; Moore, Carmel; Newbury-Ecob, Ruth; Omer, Seham Osman; Ouwehand, Willem H.; Park, Soo-Mi; Parker, Michael J.; Pickardt, Thomas; Pollard, Martin O.; Robert, Leema; Roberts, David J.; Sambrook, Jennifer; Setchfield, Kerry; Stiller, Brigitte; Thornborough, Chris; Toka, Okan; Watkins, Hugh; Williams, Denise; Wright, Michael; Mital, Seema; Daubeney, Piers E. F.; Keavney, Bernard; Goodship, Judith; Abu-Sulaiman, Riyadh Mandi; Klaassen, Sabine; Wright, Caroline F.; Firth, Helen V.; Barrett, Jeffrey C.; Devriendt, Koenraad; FitzPatrick, David R.; Brook, J. David; Hurles, Matthew E. 分享 收藏
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans (vol 94, pg 574, 2014) Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D'Alessandro, Lisa C. A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Louw, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; O'Kelly, Ita M.; Salmon, Anthony P.; Bu'Lock, Frances A.; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Brook, J. David; Mulder, Barbara; Klaassen, Sabine; Bhattacharya, Shoumo; Devriendt, Koen; FitzPatrick, David R.; Wilson, David I.; Mital, Seema; Hurles, Matthew E. 分享 收藏
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans (vol 94, pg 574, 2014) Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D'Alessandro, Lisa C. A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Low, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; O'Kelly, Ita M.; Salmon, Anthony P.; Bu'Lock, Frances A.; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Brook, J. David; Mulder, Barbara; Klaassen, Sabine; Bhattacharya, Shoumo; Devriendt, Koen; FitzPatrick, David R.; Wilson, David I.; Mital, Seema; Hurles, Matthew E. 分享 收藏
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans NR2F2的罕见变异导致人类先天性心脏缺陷 Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D'Alessandro, Lisa C. A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Low, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; O'Kelly, Ita M.; Salmon, Anthony P.; Bu'Lock, Frances A.; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Brook, J. David; Mulder, Barbara; Klaassen, Sabine; Bhattacharya, Shoumo; Devriendt, Koen; FitzPatrick, David F.; Wilson, David I.; Mital, Seema; Hurles, Matthew E. 分享 收藏
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 Cordell, Heather J.; Bentham, Jamie; Topf, Ana; Zelenika, Diana; Heath, Simon; Mamasoula, Chrysovalanto; Cosgrove, Catherine; Blue, Gillian; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Breckpot, Jeroen; Soemedi, Rachel; Martin, Ruairidh; Rahman, Thahira J.; Hall, Darroch; van Engelen, Klaartje; Moorman, Antoon F. M.; Zwinderman, Aelko H.; Barnett, Phil; Koopmann, Tamara T.; Adriaens, Michiel E.; Varro, Andras; George, Alfred L., Jr.; dos Remedios, Christobal; Bishopric, Nanette H.; Bezzina, Connie R.; O'Sullivan, John; Gewillig, Marc; Bu'Lock, Frances A.; Winlaw, David; Bhattacharya, Shoumo; Devriendt, Koen; Brook, J. David; Mulder, Barbara J. M.; Mital, Seema; Postma, Alex V.; Lathrop, G. Mark; Farrall, Martin; Goodship, Judith A.; Keavney, Bernard D. 分享 收藏
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot Cordell, Heather J.; Toepf, Ana; Mamasoula, Chrysovalanto; Postma, Alex V.; Bentham, Jamie; Zelenika, Diana; Heath, Simon; Blue, Gillian; Cosgrove, Catherine; Riveron, Javier Granados; Darlay, Rebecca; Soemedi, Rachel; Wilson, Ian J.; Ayers, Kristin L.; Rahman, Thahira J.; Hall, Darroch; Mulder, Barbara J. M.; Zwinderman, Aelko H.; van Engelen, Klaartje; Brook, J. David; Setchfield, Kerry; Bu'Lock, Frances A.; Thornborough, Chris; O'Sullivan, John; Stuart, A. Graham; Parsons, Jonathan; Bhattacharya, Shoumo; Winlaw, David; Mital, Seema; Gewillig, Marc; Breckpot, Jeroen; Devriendt, Koen; Moorman, Antoon F. M.; Rauch, Anita; Lathrop, G. Mark; Keavney, Bernard D.; Goodship, Judith A. 分享 收藏
Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease 全球罕见拷贝数变异对散发性先天性心脏病风险的贡献 Soemedi, Rachel; Wilson, Ian J.; Bentham, Jamie; Darlay, Rebecca; Toepf, Ana; Zelenika, Diana; Cosgrove, Catherine; Setchfield, Kerry; Thornborough, Chris; Granados-Riveron, Javier; Blue, Gillian M.; Breckpot, Jeroen; Hellens, Stephen; Zwolinkski, Simon; Glen, Elise; Mamasoula, Chrysovalanto; Rahman, Thahira J.; Hall, Darroch; Rauch, Anita; Devriendt, Koenraad; Gewillig, Marc; O' Sullivan, John; Winlaw, David S.; Bu'Lock, Frances; Brook, J. David; Bhattacharya, Shoumo; Lathrop, Mark; Santibanez-Koref, Mauro; Cordell, Heather J.; Goodship, Judith A.; Keavney, Bernard D. 分享 收藏
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls Soemedi, Rachel; Topf, Ana; Wilson, Ian J.; Darlay, Rebecca; Rahman, Thahira; Glen, Elise; Hall, Darroch; Huang, Ni; Bentham, Jamie; Bhattacharya, Shoumo; Cosgrove, Catherine; Brook, J. David; Granados-Riveron, Javier; Setchfield, Kerry; Bu'Lock, Frances; Thornborough, Chris; Devriendt, Koenraad; Breckpot, Jeroen; Hofbeck, Michael; Lathrop, Mark; Rauch, Anita; Blue, Gillian M.; Winlaw, David S.; Hurles, Matthew; Santibanez-Koref, Mauro; Cordell, Heather J.; Goodship, Judith A.; Keavney, Bernard D. 分享 收藏
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