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Results by year

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

Year Number of Results
1975 3
1977 4
1979 1
1980 2
1981 3
1982 1
1983 1
1984 2
1985 2
1986 4
1987 2
1988 2
1989 3
1990 6
1991 2
1992 5
1993 3
1994 3
1995 5
1996 10
1997 9
1998 10
1999 13
2000 10
2001 9
2002 10
2003 8
2004 6
2005 10
2006 13
2007 11
2008 10
2009 12
2010 19
2011 17
2012 18
2013 18
2014 14
2015 22
2016 17
2017 12
2018 18
2019 15
2020 15
2021 19
2022 19
2023 18
2024 1

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PubMed for id: 1631323

400 results

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Page 1
A Mediator subunit imparts robustness to a polyphenism decision.
Casasa S, Katsougia E, Ragsdale EJ. Casasa S, et al. Proc Natl Acad Sci U S A. 2023 Aug 8;120(32):e2308816120. doi: 10.1073/pnas.2308816120. Epub 2023 Aug 1. Proc Natl Acad Sci U S A. 2023. PMID: 37527340 Free PMC article.
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease.
Calame DG, Guo T, Wang C, Garrett L, Jolly A, Dawood M, Kurolap A, Henig NZ, Fatih JM, Herman I, Du H, Mitani T, Becker L, Rathkolb B, Gerlini R, Seisenberger C, Marschall S, Hunter JV, Gerard A, Heidlebaugh A, Challman T, Spillmann RC, Jhangiani SN, Coban-Akdemir Z, Lalani S, Liu L, Revah-Politi A, Iglesias A, Guzman E, Baugh E, Boddaert N, Rondeau S, Ormieres C, Barcia G, Tan QKG, Thiffault I, Pastinen T, Sheikh K, Biliciler S, Mei D, Melani F, Shashi V, Yaron Y, Steele M, Wakeling E, Østergaard E, Nazaryan-Petersen L; Undiagnosed Diseases Network; Millan F, Santiago-Sim T, Thevenon J, Bruel AL, Thauvin-Robinet C, Popp D, Platzer K, Gawlinski P, Wiszniewski W, Marafi D, Pehlivan D, Posey JE, Gibbs RA, Gailus-Durner V, Guerrini R, Fuchs H, Hrabě de Angelis M, Hölter SM, Cheung HH, Gu S, Lupski JR. Calame DG, et al. Am J Hum Genet. 2023 Aug 3;110(8):1394-1413. doi: 10.1016/j.ajhg.2023.06.013. Epub 2023 Jul 18. Am J Hum Genet. 2023. PMID: 37467750 Free PMC article.
400 results