Benhassine T[Author] - Search Results

Year	Number of Results
1998	2
2004	1
2006	1
2007	1
2008	4
2009	2
2010	3
2011	2
2015	1
2016	3
2017	1
2019	2
2020	1
2023	1
2024	2

1

Whole mitogenomes reveal that NW Africa has acted both as a source and a destination for multiple human movements.

Aizpurua-Iraola J, Abdeli A, Benhassine T, Calafell F, Comas D. Aizpurua-Iraola J, et al. Among authors: benhassine t. Sci Rep. 2023 Jun 27;13(1):10395. doi: 10.1038/s41598-023-37549-4. Sci Rep. 2023. PMID: 37369751 Free PMC article.

2

Paternal lineage of the Berbers from Aurès in Algeria: estimate of their genetic variation.

Abdeli A, Benhassine T. Abdeli A, et al. Among authors: benhassine t. Ann Hum Biol. 2019 Mar;46(2):160-168. doi: 10.1080/03014460.2019.1602166. Epub 2019 May 14. Ann Hum Biol. 2019. PMID: 30939942

3

The Impact of Recent Demography on Functional Genetic Variation in North African Human Groups.

Lucas-Sánchez M, Abdeli A, Bekada A, Calafell F, Benhassine T, Comas D. Lucas-Sánchez M, et al. Among authors: benhassine t. Mol Biol Evol. 2024 Jan 3;41(1):msad283. doi: 10.1093/molbev/msad283. Mol Biol Evol. 2024. PMID: 38152862 Free PMC article.

4

Genetic diversity of 15 autosomal STRs in a sample of Berbers from Aurès region in the Northeast of Algeria and genetic relationships with other neighbouring samples.

Abdeli A, Benhassine T. Abdeli A, et al. Among authors: benhassine t. Ann Hum Biol. 2020 May;47(3):284-293. doi: 10.1080/03014460.2020.1736628. Epub 2020 Mar 18. Ann Hum Biol. 2020. PMID: 32183545

5

Ankylosing spondylitis: analysis of gene-gene interactions between IL-12β, JAK2, and STAT3 in Han Chinese and Algerian cohorts.

Saadi A, Dang J, Shan S, Ladjouze-Rezig A, Lefkir-Tafiani S, Gong Y, Liu Q, Benhassine T. Saadi A, et al. Among authors: benhassine t. Cent Eur J Immunol. 2019;44(1):65-74. doi: 10.5114/ceji.2019.84019. Epub 2019 Apr 15. Cent Eur J Immunol. 2019. PMID: 31114439 Free PMC article.

6

Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays.

H'mida-Ben Brahim D, M'zahem A, Assoum M, Bouhlal Y, Fattori F, Anheim M, Ali-Pacha L, Ferrat F, Chaouch M, Lagier-Tourenne C, Drouot N, Thibaut C, Benhassine T, Sifi Y, Stoppa-Lyonnet D, N'Guyen K, Poujet J, Hamri A, Hentati F, Amouri R, Santorelli FM, Tazir M, Koenig M. H'mida-Ben Brahim D, et al. Among authors: benhassine t. J Neurol. 2011 Jan;258(1):56-67. doi: 10.1007/s00415-010-5682-5. Epub 2010 Aug 27. J Neurol. 2011. PMID: 20798953

7

Understanding the genomic heterogeneity of North African Imazighen: from broad to microgeographical perspectives.

Vilà-Valls L, Abdeli A, Lucas-Sánchez M, Bekada A, Calafell F, Benhassine T, Comas D. Vilà-Valls L, et al. Among authors: benhassine t. Sci Rep. 2024 May 1;14(1):9979. doi: 10.1038/s41598-024-60568-8. Sci Rep. 2024. PMID: 38693301

8

Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes.

Nouioua S, Hamadouche T, Funalot B, Bernard R, Bellatache N, Bouderba R, Grid D, Assami S, Benhassine T, Levy N, Vallat JM, Tazir M. Nouioua S, et al. Among authors: benhassine t. Neuromuscul Disord. 2011 Aug;21(8):543-50. doi: 10.1016/j.nmd.2011.04.013. Epub 2011 Jul 7. Neuromuscul Disord. 2011. PMID: 21741241

9

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Lesage S, Belarbi S, Troiano A, Condroyer C, Hecham N, Pollak P, Lohman E, Benhassine T, Ysmail-Dahlouk F, Dürr A, Tazir M, Brice A; French Parkinson's Disease Genetics Study Group. Lesage S, et al. Among authors: benhassine t. Neurology. 2008 Nov 4;71(19):1550-2. doi: 10.1212/01.wnl.0000338460.89796.06. Neurology. 2008. PMID: 18981379 No abstract available.

10

Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.

Hamza W, Ali Pacha L, Hamadouche T, Muller J, Drouot N, Ferrat F, Makri S, Chaouch M, Tazir M, Koenig M, Benhassine T. Hamza W, et al. Among authors: benhassine t. BMC Med Genet. 2015 Jun 12;16:36. doi: 10.1186/s12881-015-0180-3. BMC Med Genet. 2015. PMID: 26068213 Free PMC article.

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