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

Year Number of Results
1981 1
1982 1
1983 1
1984 2
1985 1
1986 5
1987 4
1988 2
1989 1
1990 4
1991 5
1992 2
1993 2
1994 3
1995 4
1996 8
1997 5
1998 7
1999 14
2000 12
2001 6
2002 12
2003 20
2004 13
2005 20
2006 15
2007 16
2008 12
2009 16
2010 16
2011 9
2012 14
2013 16
2014 13
2015 13
2016 8
2017 12
2018 18
2019 21
2020 14
2021 17
2022 4
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Article attribute
Article type
Publication date

Search Results

357 results
Results by year
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Page 1
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. Front Genet. 2021 May 10;12:659612. doi: 10.3389/fgene.2021.659612. eCollection 2021. Front Genet. 2021. PMID: 34040637 Free PMC article. Review.
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans.
Lu HC, Tan Q, Rousseaux MW, Wang W, Kim JY, Richman R, Wan YW, Yeh SY, Patel JM, Liu X, Lin T, Lee Y, Fryer JD, Han J, Chahrour M, Finnell RH, Lei Y, Zurita-Jimenez ME, Ahimaz P, Anyane-Yeboa K, Van Maldergem L, Lehalle D, Jean-Marcais N, Mosca-Boidron AL, Thevenon J, Cousin MA, Bro DE, Lanpher BC, Klee EW, Alexander N, Bainbridge MN, Orr HT, Sillitoe RV, Ljungberg MC, Liu Z, Schaaf CP, Zoghbi HY. Lu HC, et al. Among authors: finnell rh. Nat Genet. 2017 Apr;49(4):527-536. doi: 10.1038/ng.3808. Epub 2017 Mar 13. Nat Genet. 2017. PMID: 28288114 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: finnell rh. Am J Hypertens. 2021 Feb 18;34(1):82-91. doi: 10.1093/ajh/hpaa116. Am J Hypertens. 2021. PMID: 32710738 Free PMC article.
Antiepileptic drugs and pregnancy outcomes.
Wlodarczyk BJ, Palacios AM, George TM, Finnell RH. Wlodarczyk BJ, et al. Among authors: finnell rh. Am J Med Genet A. 2012 Aug;158A(8):2071-90. doi: 10.1002/ajmg.a.35438. Epub 2012 Jun 18. Am J Med Genet A. 2012. PMID: 22711424 Free PMC article. Review.
De novo ALX4 variant detected in child with non-syndromic craniosynostosis.
Fonteles CS, Finnell RH, Lei Y, Zurita-Jimenez ME, Monteiro AJ, George TM, Harshbarger RJ. Fonteles CS, et al. Among authors: finnell rh. Braz J Med Biol Res. 2021 Sep 24;54(11):e11396. doi: 10.1590/1414-431X2021e11396. eCollection 2021. Braz J Med Biol Res. 2021. PMID: 34586326 Free article.
Teratogenic effects of antiepileptic drugs.
Hill DS, Wlodarczyk BJ, Palacios AM, Finnell RH. Hill DS, et al. Among authors: finnell rh. Expert Rev Neurother. 2010 Jun;10(6):943-59. doi: 10.1586/ern.10.57. Expert Rev Neurother. 2010. PMID: 20518610 Free PMC article. Review.
357 results