1. A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. (March 2018) Authors: Szot, Justin O.; Cuny, Hartmut; Blue, Gillian M.; Humphreys, David T.; Ip, Eddie; Harrison, Katrina; Sholler, Gary F.; Giannoulatou, Eleni; Leo, Paul; Duncan, Emma L.; Sparrow, Duncan B.; Ho, Joshua W.K.; Graham, Robert M.; Pachter, Nicholas; Chapman, Gavin; Winlaw, David S.; Dunwoodie, Sally L. Journal: Circulation Issue: Volume 11:Number 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CHDgene: A Curated Database for Congenital Heart Disease Genes. (6th May 2022) Authors: 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 Journal: Circulation Issue: Volume 15:Number 3(2022) Page Start: e003539 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. CITED2 inhibits STAT1‐IRF1 signaling and atherogenesis. Issue 9 (7th August 2021) Authors: Zafar, Atif; Pong Ng, Hang; Diamond‐Zaluski, Rachel; Kim, Gun‐Dong; Ricky Chan, Ernest; Dunwoodie, Sally L.; Smith, Jonathan D.; Mahabeleshwar, Ganapati H. Journal: FASEB journal Issue: Volume 35:Issue 9(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. CITED2 limits pathogenic inflammatory gene programs in myeloid cells. Issue 9 (22nd July 2020) Authors: Pong Ng, Hang; Kim, Gun‐Dong; Ricky Chan, E.; Dunwoodie, Sally L.; Mahabeleshwar, Ganapati H. Journal: FASEB journal Issue: Volume 34:Issue 9(2020) Page Start: 12100 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing. (18th May 2022) Authors: Tarr, Ingrid; Hesselson, Stephanie; Iismaa, Siiri E.; Rath, Emma; Monger, Steven; Troup, Michael; Mishra, Ketan; Wong, Claire M.Y.; Hsu, Pei-Chen; Junday, Keerat; Humphreys, David T.; Adlam, David; Webb, Tom R.; Baranowska-Clarke, Anna A.; Hamby, Stephen E.; Carss, Keren J.; Samani, Nilesh J.; Ba... Journal: Circulation Issue: Volume 15:Number 4(2022) Page Start: e003527 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Four-Generation Family With Ebstein Anomaly Highlights Future Challenges in Congenital Heart Disease Genetics. (December 2017) Authors: Winlaw, David S.; Dunwoodie, Sally L.; Kirk, Edwin P. Journal: Circulation Issue: Volume 10:Number 6(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Gestational stress induces the unfolded protein response, resulting in heart defects. (July 2017) Authors: Moreau, Julie L.M.; Shi, Hongjun; O'Reilly, Victoria C.; Bewes, Therese R.; Yam, Michelle X.; Chapman, Bogdan E.; Grieve, Stuart M.; Stocker, Roland; Graham, Robert M.; Chapman, Gavin; Sparrow, Duncan B.; Dunwoodie, Sally L. Journal: Mechanisms of development Issue: Volume 145(2017)Supplement Page Start: S67 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. KIAA1217: A novel candidate gene associated with isolated and syndromic vertebral malformations. Issue 7 (5th May 2020) Authors: Al Dhaheri, Noura; Wu, Nan; Zhao, Sen; Wu, Zhihong; Blank, Robert D.; Zhang, Jianguo; Raggio, Cathy; Halanski, Matthew; Shen, Jianxiong; Noonan, Ken; Qiu, Guixing; Nemeth, Blaise; Sund, Sarah; Dunwoodie, Sally L.; Chapman, Gavin; Glurich, Ingrid; Steiner, Robert D.; Wohler, Elizabeth; Martin, Ren... Journal: American journal of medical genetics Issue: Volume 182:Issue 7(2020) Page Start: 1664 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus. Issue 9 (29th July 2013) Authors: Sparrow, Duncan B.; Faqeih, Eissa Ali; Sallout, Bahauddin; Alswaid, Abdulrahman; Ababneh, Faroug; Al‐Sayed, Moeenaldeen; Rukban, Hadeel; Eyaid, Wafaa M.; Kageyama, Ryoichiro; Ellard, Sian; Turnpenny, Peter D.; Dunwoodie, Sally L. Journal: American journal of medical genetics Issue: Volume 161:Issue 9(2013:Sep.) Page Start: 2244 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus. Issue 9 (29th July 2013) Authors: Sparrow, Duncan B.; Faqeih, Eissa Ali; Sallout, Bahauddin; Alswaid, Abdulrahman; Ababneh, Faroug; Al‐Sayed, Moeenaldeen; Rukban, Hadeel; Eyaid, Wafaa M.; Kageyama, Ryoichiro; Ellard, Sian; Turnpenny, Peter D.; Dunwoodie, Sally L. Journal: American journal of medical genetics Issue: Volume 161:Issue 9(2013:Sep.) Page Start: 2244 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗