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

Year Number of Results
1958 1
1981 1
1983 1
1985 2
1986 3
1988 2
1989 2
1990 2
1991 1
1993 3
1995 1
1996 3
1997 3
2000 1
2001 3
2002 4
2003 3
2004 4
2005 5
2006 6
2007 10
2008 9
2009 11
2010 17
2011 17
2012 18
2013 18
2014 17
2015 15
2016 14
2017 16
2018 17
2019 30
2020 20
2021 19
2022 24
2023 22
2024 12

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303 results

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Page 1
National population-based estimates for major birth defects, 2010-2014.
Mai CT, Isenburg JL, Canfield MA, Meyer RE, Correa A, Alverson CJ, Lupo PJ, Riehle-Colarusso T, Cho SJ, Aggarwal D, Kirby RS; National Birth Defects Prevention Network. Mai CT, et al. Among authors: canfield ma. Birth Defects Res. 2019 Nov 1;111(18):1420-1435. doi: 10.1002/bdr2.1589. Epub 2019 Oct 3. Birth Defects Res. 2019. PMID: 31580536 Free PMC article.
Trisomy 13 and 18-Prevalence and mortality-A multi-registry population based analysis.
Goel N, Morris JK, Tucker D, de Walle HEK, Bakker MK, Kancherla V, Marengo L, Canfield MA, Kallen K, Lelong N, Camelo JL, Stallings EB, Jones AM, Nance A, Huynh MP, Martínez-Fernández ML, Sipek A, Pierini A, Nembhard WN, Goetz D, Rissmann A, Groisman B, Luna-Muñoz L, Szabova E, Lapchenko S, Zarante I, Hurtado-Villa P, Martinez LE, Tagliabue G, Landau D, Gatt M, Dastgiri S, Morgan M. Goel N, et al. Among authors: canfield ma. Am J Med Genet A. 2019 Dec;179(12):2382-2392. doi: 10.1002/ajmg.a.61365. Epub 2019 Sep 30. Am J Med Genet A. 2019. PMID: 31566869 Free PMC article.
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants.
Sok P, Sabo A, Almli LM, Jenkins MM, Nembhard WN, Agopian AJ, Bamshad MJ, Blue EE, Brody LC, Brown AL, Browne ML, Canfield MA, Carmichael SL, Chong JX, Dugan-Perez S, Feldkamp ML, Finnell RH, Gibbs RA, Kay DM, Lei Y, Meng Q, Moore CA, Mullikin JC, Muzny D, Olshan AF, Pangilinan F, Reefhuis J, Romitti PA, Schraw JM, Shaw GM, Werler MM, Harpavat S, Lupo PJ; University of Washington Center for Mendelian Genomics, NISC Comparative Sequencing Program, the National Birth Defects Prevention Study. Sok P, et al. Among authors: canfield ma. Am J Med Genet A. 2023 Jun;191(6):1546-1556. doi: 10.1002/ajmg.a.63185. Epub 2023 Mar 21. Am J Med Genet A. 2023. PMID: 36942736 Free PMC article.
Maternal Hypertension-Related Genotypes and Congenital Heart Defects.
Lei Y, Ludorf KL, Yu X, Benjamin RH, Gu X, Lin Y, Finnell RH, Mitchell LE, Musfee FI, Malik S, Canfield MA, Morrison AC, Hobbs CA, Van Zutphen AR, Fisher S, Agopian AJ. Lei Y, et al. Among authors: canfield ma. Am J Hypertens. 2021 Feb 18;34(1):82-91. doi: 10.1093/ajh/hpaa116. Am J Hypertens. 2021. PMID: 32710738 Free PMC article.
Editorial: Resetting Power in Global Food Governance: The UN Food Systems Summit.
Montenegro de Wit M, Canfield M, Iles A, Anderson M, McKeon N, Guttal S, Gemmill-Herren B, Duncan J, van der Ploeg JD, Prato S. Montenegro de Wit M, et al. Among authors: canfield m. Development (Rome). 2021;64(3-4):153-161. doi: 10.1057/s41301-021-00316-x. Epub 2021 Nov 3. Development (Rome). 2021. PMID: 34744392 Free PMC article. No abstract available.
Birth defect survival for Hispanic subgroups.
Lopez KN, Nembhard WN, Wang Y, Liu G, Kucik JE, Copeland G, Gilboa SM, Kirby RS, Canfield M. Lopez KN, et al. Among authors: canfield m. Birth Defects Res. 2018 Mar 1;110(4):352-363. doi: 10.1002/bdr2.1157. Epub 2017 Dec 1. Birth Defects Res. 2018. PMID: 29195034 Free PMC article.
Mitochondrial Phosphopantetheinylation is Required for Oxidative Function.
Norden PR, Wedan RJ, Longenecker JZ, Preston SEJ, Graber N, Ols O, Canfield M, McLaughlin E, Nowinski SM. Norden PR, et al. Among authors: canfield m. bioRxiv [Preprint]. 2024 May 10:2024.05.09.592977. doi: 10.1101/2024.05.09.592977. bioRxiv. 2024. PMID: 38766035 Free PMC article. Preprint.
Patterns of co-occurring birth defects in children with anotia and microtia.
Schraw JM, Benjamin RH, Shumate CJ, Canfield MA, Scott DA, McLean SD, Northrup H, Scheuerle AE, Schaaf CP, Ray JW, Chen H, Agopian AJ, Lupo PJ. Schraw JM, et al. Among authors: canfield ma. Am J Med Genet A. 2023 Mar;191(3):805-812. doi: 10.1002/ajmg.a.63081. Epub 2022 Dec 21. Am J Med Genet A. 2023. PMID: 36541232 Free PMC article.
303 results