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Year Number of Results
2008 1
2009 2
2010 3
2011 1
2012 2
2013 2
2014 1
2015 3
2016 2
2017 1
2018 5
2019 8
2020 8
2021 9
2022 4
2023 8
2024 4

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58 results

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Page 1
Whole-exome sequencing study of hypospadias.
Chen Z, Lei Y, Finnell RH, Ding Y, Su Z, Wang Y, Xie H, Chen F. Chen Z, et al. Among authors: lei y. iScience. 2023 Apr 12;26(5):106663. doi: 10.1016/j.isci.2023.106663. eCollection 2023 May 19. iScience. 2023. PMID: 37168556 Free PMC article.
Excess folic acid intake increases DNA de novo point mutations.
Cao X, Xu J, Lin YL, Cabrera RM, Chen Q, Zhang C, Steele JW, Han X, Gross SS, Wlodarczyk BJ, Lupski JR, Li W, Wang H, Finnell RH, Lei Y. Cao X, et al. Among authors: lei y. Cell Discov. 2023 Feb 28;9(1):22. doi: 10.1038/s41421-022-00512-0. Cell Discov. 2023. PMID: 36849450 Free PMC article. No abstract available.
Gene Environment Interactions in the Etiology of Neural Tube Defects.
Finnell RH, Caiaffa CD, Kim SE, Lei Y, Steele J, Cao X, Tukeman G, Lin YL, Cabrera RM, Wlodarczyk BJ. Finnell RH, et al. Among authors: lei y. Front Genet. 2021 May 10;12:659612. doi: 10.3389/fgene.2021.659612. eCollection 2021. Front Genet. 2021. PMID: 34040637 Free PMC article. Review.
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: lei y. 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
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. Am J Hypertens. 2021 Feb 18;34(1):82-91. doi: 10.1093/ajh/hpaa116. Am J Hypertens. 2021. PMID: 32710738 Free PMC article.
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele.
Crane-Smith Z, De Castro SCP, Nikolopoulou E, Wolujewicz P, Smedley D, Lei Y, Mather E, Santos C, Hopkinson M, Pitsillides AA; Genomics England Research Consortium; Finnell RH, Ross ME, Copp AJ, Greene NDE. Crane-Smith Z, et al. Among authors: lei y. Hum Mol Genet. 2023 Aug 26;32(17):2681-2692. doi: 10.1093/hmg/ddad094. Hum Mol Genet. 2023. PMID: 37364051 Free PMC article.
58 results