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

Year Number of Results
2000 1
2007 1
2008 7
2009 3
2010 3
2011 11
2012 7
2013 8
2014 3
2015 12
2016 5
2017 7
2018 9
2019 11
2020 6
2021 8
2022 14
2023 9
2024 1

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111 results

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Page 1
The pathogenesis of gastroschisis.
Feldkamp ML, Carey JC. Feldkamp ML, et al. Birth Defects Res. 2023 Mar 15;115(5):515-516. doi: 10.1002/bdr2.2140. Epub 2022 Dec 21. Birth Defects Res. 2023. PMID: 36541834 No abstract available.
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Groisman B, Bermejo-Sánchez E, Romitti PA, Botto LD, Feldkamp ML, Walani SR, Mastroiacovo P. Groisman B, et al. Among authors: feldkamp ml. Pediatr Res. 2019 Jul;86(1):3-4. doi: 10.1038/s41390-019-0392-x. Epub 2019 Apr 9. Pediatr Res. 2019. PMID: 30965352 No abstract available.
Are paternal or grandmaternal age associated with higher probability of trisomy 21 in offspring? A population-based, matched case-control study, 1995-2015.
Schliep KC, Feldkamp ML, Hanson HA, Hollingshaus M, Fraser A, Smith KR, Panushka KA, Varner MW. Schliep KC, et al. Among authors: feldkamp ml. Paediatr Perinat Epidemiol. 2021 May;35(3):281-291. doi: 10.1111/ppe.12737. Epub 2020 Dec 1. Paediatr Perinat Epidemiol. 2021. PMID: 33258505 Free PMC article.
Neighborhood Deprivation and Neural Tube Defects.
Pruitt Evans S, Ailes EC, Kramer MR, Shumate CJ, Reefhuis J, Insaf TZ, Yazdy MM, Carmichael SL, Romitti PA, Feldkamp ML, Neo DT, Nembhard WN, Shaw GM, Palmi E, Gilboa SM; National Birth Defects Prevention Study. Pruitt Evans S, et al. Among authors: feldkamp ml. Epidemiology. 2023 Nov 1;34(6):774-785. doi: 10.1097/EDE.0000000000001655. Epub 2023 Sep 26. Epidemiology. 2023. PMID: 37757869
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: feldkamp ml. 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
The National Birth Defects Prevention Study: A review of the methods.
Reefhuis J, Gilboa SM, Anderka M, Browne ML, Feldkamp ML, Hobbs CA, Jenkins MM, Langlois PH, Newsome KB, Olshan AF, Romitti PA, Shapira SK, Shaw GM, Tinker SC, Honein MA; National Birth Defects Prevention Study. Reefhuis J, et al. Among authors: feldkamp ml. Birth Defects Res A Clin Mol Teratol. 2015 Aug;103(8):656-69. doi: 10.1002/bdra.23384. Epub 2015 Jun 2. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 26033852 Free PMC article. Review.
Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.
Li J, Yang W, Wang YJ, Ma C, Curry CJ, McGoldrick D, Nickerson DA, Chong JX, Blue EE, Mullikin JC, Reefhuis J, Nembhard WN, Romitti PA, Werler MM, Browne ML, Olshan AF, Finnell RH, Feldkamp ML, Pangilinan F, Almli LM, Bamshad MJ, Brody LC, Jenkins MM, Shaw GM; NISC Comparative Sequencing Program; University of Washington Center for Mendelian Genomics; National Birth Defects Prevention Study. Li J, et al. Among authors: feldkamp ml. Am J Med Genet A. 2022 Aug;188(8):2376-2388. doi: 10.1002/ajmg.a.62874. Epub 2022 Jun 18. Am J Med Genet A. 2022. PMID: 35716026 Free PMC article.
Exome sequencing identifies variants in infants with sacral agenesis.
Pitsava G, Feldkamp ML, Pankratz N, Lane J, Kay DM, Conway KM, Hobbs C, Shaw GM, Reefhuis J, Jenkins MM, Almli LM, Moore C, Werler M, Browne ML, Cunniff C, Olshan AF, Pangilinan F, Brody LC, Sicko RJ, Finnell RH, Bamshad MJ, McGoldrick D, Nickerson DA, Mullikin JC, Romitti PA, Mills JL; UW Center for Mendelian Genomics, NISC Comparative Sequencing Program and the National Birth Defects Prevention Study. Pitsava G, et al. Among authors: feldkamp ml. Birth Defects Res. 2022 Apr;114(7):215-227. doi: 10.1002/bdr2.1987. Epub 2022 Mar 10. Birth Defects Res. 2022. PMID: 35274497 Free PMC article.
111 results