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

Year Number of Results
1988 1
1991 1
1992 1
1998 1
1999 1
2001 1
2004 2
2005 3
2006 2
2007 4
2008 7
2010 4
2011 1
2012 2
2013 2
2014 2
2015 1
2016 1
2017 1
2018 5
2019 2
2020 1
2021 2
2022 5
2023 1
2024 0

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49 results

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Page 1
Autism throughout genetics: Perusal of the implication of ion channels.
Daghsni M, Rima M, Fajloun Z, Ronjat M, Brusés JL, M'rad R, De Waard M. Daghsni M, et al. Among authors: m rad r. Brain Behav. 2018 Aug;8(8):e00978. doi: 10.1002/brb3.978. Epub 2018 Jun 22. Brain Behav. 2018. PMID: 29934975 Free PMC article. Review.
Autism: an overview of genetic aetiology.
Bayou N, M'rad R, Ahlem B, Béchir Helayem M, Chaabouni H. Bayou N, et al. Among authors: m rad r. Tunis Med. 2008 Jun;86(6):573-8. Tunis Med. 2008. PMID: 19216451 Review.
Mandibuloacral dysplasia type A in five tunisian patients.
R S, H M, M T, A A, M G, I H, E K, K M, F M, R M. R S, et al. Among authors: r m. Eur J Med Genet. 2021 Feb;64(2):104138. doi: 10.1016/j.ejmg.2021.104138. Epub 2021 Jan 8. Eur J Med Genet. 2021. PMID: 33422685
WDR73-related galloway mowat syndrome with collapsing glomerulopathy.
El Younsi M, Kraoua L, Meddeb R, Ferjani M, Trabelsi M, Ouertani I, Maazoul F, Abid N, Gargah T, M'rad R. El Younsi M, et al. Among authors: m rad r. Eur J Med Genet. 2019 Sep;62(9):103550. doi: 10.1016/j.ejmg.2018.10.002. Epub 2018 Oct 10. Eur J Med Genet. 2019. PMID: 30315938
TOP3B: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?
Daghsni M, Lahbib S, Fradj M, Sayeb M, Kelmemi W, Kraoua L, Kchaou M, Maazoul F, Echebbi S, Ben Ali N, Abdelhak S, M'rad R. Daghsni M, et al. Among authors: m rad r. Cytogenet Genome Res. 2018;154(1):1-5. doi: 10.1159/000486945. Epub 2018 Feb 28. Cytogenet Genome Res. 2018. PMID: 29490292
49 results