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Identification of potential NAD-related biomarkers of recurrent miscarriage risk Cuny, Hartmut; Shand, Antonia W.; Goth, Jennifer; Sheng, Delicia Z.; Tossey, Tamarah; Martin, Ella M. M. A.; Sipka, Alena; Aleshin, Olga; Schneuer, Francisco J.; Nassar, Natasha; Dunwoodie, Sally L. Share Save
A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder Szot, Justin O.; Cuny, Hartmut; Martin, Ella M. M. A.; Sheng, Delicia Z.; Iyer, Kavitha; Portelli, Stephanie; Nguyen, Vivien; Gereis, Jessica M.; Alankarage, Dimuthu; Chitayat, David; Chong, Karen; Wentzensen, Ingrid M.; Vincent-Delorme, Catherine; Lermine, Alban; Burkitt-Wright, Emma; Ji, Weizhen; Jeffries, Lauren; Pais, Lynn S.; Tan, Tiong Y.; Pitt, James; Wise, Cheryl A.; Wright, Helen; Andrews, Israel D.; Pruniski, Brianna; Grebe, Theresa A.; Corsten-Janssen, Nicole; Bouman, Katelijne; Poulton, Cathryn; Prakash, Supraja; Keren, Boris; Brown, Natasha J.; Hunter, Matthew F.; Heath, Oliver; Lakhani, Saquib A.; McDermott, John H.; Ascher, David B.; Chapman, Gavin; Bozon, Kayleigh; Dunwoodie, Sally L. Share Save
Hif-1a suppresses ROS-induced proliferation of cardiac fibroblasts following myocardial infarction Janbandhu, Vaibhao; Tallapragada, Vikram; Patrick, Ralph; Li, Yanzhen; Abeygunawardena, Dhanushi; Humphreys, David T.; Martin, Ella M. M. A.; Ward, Alexander O.; Contreras, Osvaldo; Farbehi, Nona; Yao, Ernestene; Du, Junjie; Dunwoodie, Sally L.; Bursac, Nenad; Harvey, Richard P. 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
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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
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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