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

Year Number of Results
1966 1
1968 1
1970 4
1971 1
1972 4
1973 10
1974 9
1975 9
1976 4
1977 5
1978 5
1979 2
1980 5
1981 2
1982 2
1983 2
1984 4
1985 3
1986 1
1987 1
1989 2
1991 1
1993 3
1995 1
1997 1
2000 1
2006 1
2007 3
2008 1
2009 3
2010 3
2011 2
2012 3
2013 1
2014 3
2015 4
2016 4
2017 4
2018 2
2019 5
2020 8
2021 3
2022 4
2023 7
2024 0

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135 results

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Page 1
Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy.
Luppe J, Sticht H, Lecoquierre F, Goldenberg A, Gorman KM, Molloy B, Agolini E, Novelli A, Briuglia S, Kuismin O, Marcelis C, Vitobello A, Denommé-Pichon AS, Julia S, Lemke JR, Abou Jamra R, Platzer K. Luppe J, et al. Among authors: molloy b. Eur J Hum Genet. 2023 Mar;31(3):345-352. doi: 10.1038/s41431-022-01269-6. Epub 2022 Dec 23. Eur J Hum Genet. 2023. PMID: 36564538 Free PMC article.
Cloning Gene Variants and Reporter Assays.
Molloy B, McManus R. Molloy B, et al. Methods Mol Biol. 2015;1326:117-30. doi: 10.1007/978-1-4939-2839-2_12. Methods Mol Biol. 2015. PMID: 26498618
Candidate Gene Knockdown in Celiac Disease.
Molloy B, Freeley M, Long A, McManus R. Molloy B, et al. Methods Mol Biol. 2015;1326:159-73. doi: 10.1007/978-1-4939-2839-2_14. Methods Mol Biol. 2015. PMID: 26498620
Expansion of the phenotype of biallelic variants in TRIT1.
Forde KM, Molloy B, Conroy J, Green AJ, King MD, Buckley PG, Ryan S, Gorman KM. Forde KM, et al. Among authors: molloy b. Eur J Med Genet. 2020 Jun;63(6):103882. doi: 10.1016/j.ejmg.2020.103882. Epub 2020 Feb 20. Eur J Med Genet. 2020. PMID: 32088416 No abstract available.
Ethical aspects in xenotransplantation.
Hammer C, Molloy B. Hammer C, et al. Among authors: molloy b. Transplant Proc. 1993 Aug;25(4 Suppl 3):38-40. Transplant Proc. 1993. PMID: 8351714 Review.
135 results