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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1994 1
1995 1
1997 2
1998 2
2000 1
2001 1
2002 4
2003 1
2004 7
2005 5
2006 5
2007 5
2008 9
2009 8
2010 6
2011 5
2012 4
2013 6
2014 7
2015 6
2016 5
2017 7
2018 4
2019 10
2020 10
2021 8
2022 13
2023 7
2024 2

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133 results

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Page 1
Hif-1a suppresses ROS-induced proliferation of cardiac fibroblasts following myocardial infarction.
Janbandhu V, Tallapragada V, Patrick R, Li Y, Abeygunawardena D, Humphreys DT, Martin EMMA, Ward AO, Contreras O, Farbehi N, Yao E, Du J, Dunwoodie SL, Bursac N, Harvey RP. Janbandhu V, et al. Among authors: dunwoodie sl. Cell Stem Cell. 2022 Feb 3;29(2):281-297.e12. doi: 10.1016/j.stem.2021.10.009. Epub 2021 Nov 10. Cell Stem Cell. 2022. PMID: 34762860 Free PMC article.
TBX6 null variants and a common hypomorphic allele in congenital scoliosis.
Wu N, Ming X, Xiao J, Wu Z, Chen X, Shinawi M, Shen Y, Yu G, Liu J, Xie H, Gucev ZS, Liu S, Yang N, Al-Kateb H, Chen J, Zhang J, Hauser N, Zhang T, Tasic V, Liu P, Su X, Pan X, Liu C, Wang L, Shen J, Shen J, Chen Y, Zhang T, Zhang J, Choy KW, Wang J, Wang Q, Li S, Zhou W, Guo J, Wang Y, Zhang C, Zhao H, An Y, Zhao Y, Wang J, Liu Z, Zuo Y, Tian Y, Weng X, Sutton VR, Wang H, Ming Y, Kulkarni S, Zhong TP, Giampietro PF, Dunwoodie SL, Cheung SW, Zhang X, Jin L, Lupski JR, Qiu G, Zhang F. Wu N, et al. Among authors: dunwoodie sl. N Engl J Med. 2015 Jan 22;372(4):341-50. doi: 10.1056/NEJMoa1406829. Epub 2015 Jan 7. N Engl J Med. 2015. PMID: 25564734 Free PMC article.
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
Shi H, Enriquez A, Rapadas M, Martin EMMA, Wang R, Moreau J, Lim CK, Szot JO, Ip E, Hughes JN, Sugimoto K, Humphreys DT, McInerney-Leo AM, Leo PJ, Maghzal GJ, Halliday J, Smith J, Colley A, Mark PR, Collins F, Sillence DO, Winlaw DS, Ho JWK, Guillemin GJ, Brown MA, Kikuchi K, Thomas PQ, Stocker R, Giannoulatou E, Chapman G, Duncan EL, Sparrow DB, Dunwoodie SL. Shi H, et al. Among authors: dunwoodie sl. N Engl J Med. 2017 Aug 10;377(6):544-552. doi: 10.1056/NEJMoa1616361. N Engl J Med. 2017. PMID: 28792876 Free article.
A new era of genetic testing in congenital heart disease: A review.
Morrish AM, Smith J, Enriquez A, Sholler GF, Mervis J, Dunwoodie SL, Kirk EP, Winlaw DS, Blue GM. Morrish AM, et al. Among authors: dunwoodie sl. Trends Cardiovasc Med. 2022 Jul;32(5):311-319. doi: 10.1016/j.tcm.2021.04.011. Epub 2021 May 5. Trends Cardiovasc Med. 2022. PMID: 33964404 Review.
CITED2 inhibits STAT1-IRF1 signaling and atherogenesis.
Zafar A, Pong Ng H, Diamond-Zaluski R, Kim GD, Ricky Chan E, Dunwoodie SL, Smith JD, Mahabeleshwar GH. Zafar A, et al. Among authors: dunwoodie sl. FASEB J. 2021 Sep;35(9):e21833. doi: 10.1096/fj.202100792R. FASEB J. 2021. PMID: 34365659 Free PMC article.
'Big issues' in neurodevelopment for children and adults with congenital heart disease.
Verrall CE, Blue GM, Loughran-Fowlds A, Kasparian N, Gecz J, Walker K, Dunwoodie SL, Cordina R, Sholler G, Badawi N, Winlaw D. Verrall CE, et al. Among authors: dunwoodie sl. Open Heart. 2019 Jul 3;6(2):e000998. doi: 10.1136/openhrt-2018-000998. eCollection 2019. Open Heart. 2019. PMID: 31354955 Free PMC article. Review.
A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder.
Szot JO, Cuny H, Martin EM, Sheng DZ, Iyer K, Portelli S, Nguyen V, Gereis JM, Alankarage D, Chitayat D, Chong K, Wentzensen IM, Vincent-Delormé C, Lermine A, Burkitt-Wright E, Ji W, Jeffries L, Pais LS, Tan TY, Pitt J, Wise CA, Wright H, Andrews ID, Pruniski B, Grebe TA, Corsten-Janssen N, Bouman K, Poulton C, Prakash S, Keren B, Brown NJ, Hunter MF, Heath O, Lakhani SA, McDermott JH, Ascher DB, Chapman G, Bozon K, Dunwoodie SL. Szot JO, et al. Among authors: dunwoodie sl. J Clin Invest. 2024 Feb 15;134(4):e174824. doi: 10.1172/JCI174824. J Clin Invest. 2024. PMID: 38357931 Free PMC article.
133 results