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

Year Number of Results
1951 1
1953 1
1979 1
1980 1
1986 1
1988 3
1989 2
1992 1
1993 1
1994 2
1995 2
1996 2
1998 1
1999 3
2002 4
2003 5
2004 5
2005 5
2006 6
2007 4
2008 2
2009 7
2010 6
2011 4
2012 4
2013 5
2014 8
2015 4
2016 4
2017 8
2018 2
2019 7
2020 4
2021 5
2022 6
2023 4
2024 1

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120 results

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Page 1
Recurrent GATA1 mutations in Diamond-Blackfan anaemia.
Klar J, Khalfallah A, Arzoo PS, Gazda HT, Dahl N. Klar J, et al. Br J Haematol. 2014 Sep;166(6):949-51. doi: 10.1111/bjh.12919. Epub 2014 Apr 28. Br J Haematol. 2014. PMID: 24766296 Free article. No abstract available.
Excessive and pathological Internet use - Risk-behavior or psychopathology?
Kaess M, Klar J, Kindler J, Parzer P, Brunner R, Carli V, Sarchiapone M, Hoven CW, Apter A, Balazs J, Barzilay S, Bobes J, Cozman D, Gomboc V, Haring C, Kahn JP, Keeley H, Meszaros G, Musa GJ, Postuvan V, Saiz P, Sisask M, Varnik P, Resch F, Wasserman D. Kaess M, et al. Among authors: klar j. Addict Behav. 2021 Dec;123:107045. doi: 10.1016/j.addbeh.2021.107045. Epub 2021 Jul 9. Addict Behav. 2021. PMID: 34332272 Free article.
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy.
Fatima A, Hoeber J, Schuster J, Koshimizu E, Maya-Gonzalez C, Keren B, Mignot C, Akram T, Ali Z, Miyatake S, Tanigawa J, Koike T, Kato M, Murakami Y, Abdullah U, Ali MA, Fadoul R, Laan L, Castillejo-López C, Liik M, Jin Z, Birnir B, Matsumoto N, Baig SM, Klar J, Dahl N. Fatima A, et al. Among authors: klar j. Am J Hum Genet. 2022 Mar 3;109(3):542-546. doi: 10.1016/j.ajhg.2022.02.007. Am J Hum Genet. 2022. PMID: 35245475 Free PMC article. No abstract available.
A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet-Biedl syndrome.
Delvallée C, Nicaise S, Antin M, Leuvrey AS, Nourisson E, Leitch CC, Kellaris G, Stoetzel C, Geoffroy V, Scheidecker S, Keren B, Depienne C, Klar J, Dahl N, Deleuze JF, Génin E, Redon R, Demurger F, Devriendt K, Mathieu-Dramard M, Poitou-Bernert C, Odent S, Katsanis N, Mandel JL, Davis EE, Dollfus H, Muller J. Delvallée C, et al. Among authors: klar j. Clin Genet. 2021 Feb;99(2):318-324. doi: 10.1111/cge.13878. Epub 2020 Nov 14. Clin Genet. 2021. PMID: 33169370 Free PMC article.
120 results