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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 4
2011 12
2012 7
2013 8
2014 3
2015 12
2016 5
2017 7
2018 9
2019 11
2020 6
2021 8
2022 14
2023 10
2024 7
2025 0

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117 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.
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 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.
Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study.
Blue EE, Moore KJ, North KE, Desrosiers TA, Carmichael SL, White JJ, Chong JX, Bamshad MJ, Jenkins MM, Almli LM, Brody LC, Freedman SF, Reefhuis J, Romitti PA, Shaw GM, Werler M, Kay DM, Browne ML, Feldkamp ML, Finnell RH, Nembhard WN, Pangilinan F, Olshan AF; National Institutes of Health Intramural Sequencing Center; University of Washington Center for Mendelian Genomics; National Birth Defects Prevention Study. Blue EE, et al. Among authors: feldkamp ml. Birth Defects Res. 2024 Jul;116(7):e2384. doi: 10.1002/bdr2.2384. Birth Defects Res. 2024. PMID: 38990107 Free PMC article.
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.
117 results