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CHDgene: A Curated Database for Congenital Heart Disease Genes Yang, Andrian; Alankarage, Dimuthu; Cuny, Hartmut; Ip, Eddie K. K.; Almog, Moran; Lu, Jessica; Das, Debjani; Enriquez, Annabelle; Szot, Justin O.; Humphreys, David T.; Blue, Gillian M.; Ho, Joshua W. K.; Winlaw, David S.; Dunwoodie, Sally L.; Giannoulatou, Eleni Share Save
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice Martin, Ella M. M. A.; Enriquez, Annabelle; Sparrow, Duncan B.; Humphreys, David T.; McInerney-Leo, Aideen M.; Leo, Paul J.; Duncan, Emma L.; Iyer, Kavitha R.; Greasby, Joelene A.; Ip, Eddie; Giannoulatou, Eleni; Sheng, Delicia; Wohler, Elizabeth; Dimartino, Clemantine; Amiel, Jeanne; Capri, Yline; Lehalle, Daphne; Mory, Adi; Wilnai, Yael; Lebenthal, Yael; Gharavi, Ali G.; Krzemien, Grazyna G.; Miklaszewska, Monika; Steiner, Robert D.; Raggio, Cathy; Blank, Robert; Feldman, Hagit Baris; Rasouly, Hila Milo; Sobreira, Nara L. M.; Jobling, Rebekah; Gordon, Christopher T.; Giampietro, Philip F.; Dunwoodie, Sally L.; Chapman, Gavin Share Save
Revealing hidden genetic diagnoses in the ocular anterior segment disorders Ma, Alan; Yousoof, Saira; Grigg, John R.; Flaherty, Maree; Minoche, Andre E.; Cowley, Mark J.; Nash, Benjamin M.; Ho, Gladys; Gayagay, Thet; Lai, Tiffany; Farnsworth, Elizabeth; Hackett, Emma L.; Fisk, Katrina; Wong, Karen; Holman, Katherine J.; Jenkins, Gemma; Cheng, Anson; Martin, Frank; Karaconji, Tanya; Elder, James E.; Enriquez, Annabelle; Wilson, Meredith; Amor, David J.; Stutterd, Chloe A.; Kamien, Benjamin; Nelson, John; Dinger, Marcel E.; Bennetts, Bruce; Jamieson, Robyn, V Share Save
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants Chapman, Gavin; Moreau, Julie L. M.; Ip, Eddie; Szot, Justin O.; Iyer, Kavitha R.; Shi, Hongjun; Yam, Michelle X.; O'Reilly, Victoria C.; Enriquez, Annabelle; Greasby, Joelene A.; Alankarage, Dimuthu; Martin, Ella M. M. A.; Hanna, Bernadette C.; Edwards, Matthew; Monger, Steven; Blue, Gillian M.; Winlaw, David S.; Ritchie, Helen E.; Grieve, Stuart M.; Giannoulatou, Eleni; Sparrow, Duncan B.; Dunwoodie, Sally L. Share Save
Identification of clinically actionable variants from genome sequencing of families with congenital heart disease Alankarage, Dimuthu; Ip, Eddie; Szot, Justin O.; Munro, Jacob; Blue, Gillian M.; Harrison, Katrina; Cuny, Hartmut; Enriquez, Annabelle; Troup, Michael; Humphreys, David T.; Wilson, Meredith; Harvey, Richard P.; Sholler, Gary F.; Graham, Robert M.; Ho, Joshua W. K.; Kirk, Edwin P.; Pachter, Nicholas; Chapman, Gavin; Winlaw, David S.; Giannoulatou, Eleni; Dunwoodie, Sally L. Share Save
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NAD Deficiency, Congenital Malformations, and Niacin Supplementation Shi, Hongjun; Enriquez, Annabelle; Rapadas, Melissa; Martin, Ella M. M. A.; Wang, Roni; Moreau, Julie; Lim, Chai K.; Szot, Justin O.; Ip, Eddie; Hughes, James N.; Sugimoto, Kotaro; Humphreys, David T.; McInerney-Leo, Aideen M.; Leo, Paul J.; Maghzal, Ghassan J.; Halliday, Jake; Smith, Janine; Colley, Alison; Mark, Paul R.; Collins, Felicity; Sillence, David O.; Winlaw, David S.; Ho, Joshua W. K.; Guillemin, Gilles J.; Brown, Matthew A.; Kikuchi, Kazu; Thomas, Paul Q.; Stocker, Roland; Giannoulatou, Eleni; Chapman, Gavin; Duncan, Emma L.; Sparrow, Duncan B.; Dunwoodie, Sally L. Share Save
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