References
- Al-Zahery N, Semino O, Benuzzi G, Magri C, Passarino G, Torroni A, Santachiara-Benerecetti AS. (2003). Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migrations. Mol Phylogenet Evol 28:458–72
- Alonso S, Flores C, Cabrera V, Alonso A, Martin P, Albarran C, Izagirre N, et al. (2005). The place of the Basques in the European Y-chromosome diversity landscape. Eur J Hum Genet 13:1293–302
- Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N. (1999). Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet 23:147
- Arredi B, Poloni ES, Paracchini S, Zerjal T, Fathallah DM, Makrelouf M, Pascali VL, et al. (2004). A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa. Am J Hum Genet 75:338–45
- Athey TW. (2005). Haplogroup prediction from Y-STR values using an allele-frequency approach. J Genetic Geneal 1:1–7
- Bandelt HJ, Forster P, Rohl A. (1999). Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol 16:37–48
- Ben Arab S, Masmoudi S, Beltaief N, Hachicha S, Ayadi H. (2004). Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness. Genet Epidemiol 27:74–9
- Ben Halim N, Ben Alaya Bouafif N, Romdhane L, Kefi Ben Atig R, Chouchane I, Bouyacoub Y, Arfa I, et al. (2013). Consanguinity, endogamy, and genetic disorders in Tunisia. J Community Genet 4:273–84
- Bosch E, Calafell F, Comas D, Oefner PJ, Underhill PA, Bertranpetit J. (2001). High-resolution analysis of human Y-chromosome variation shows a sharp discontinuity and limited gene flow between northwestern Africa and the Iberian Peninsula. Am J Hum Genet 68:1019–29
- Cadenas AM, Zhivotovsky LA, Cavalli-Sforza LL, Underhill PA, Herrera RJ. (2008). Y-chromosome diversity characterizes the Gulf of Oman. Eur J Hum Genet 16:374–86
- Cherni L, Fernandes V, Pereira JB, Costa MD, Goios A, Frigi S, Yacoubi-Loueslati B, Amor MB, et al. (2009). Post-last glacial maximum expansion from Iberia to North Africa revealed by fine characterization of mtDNA H haplogroup in Tunisia. Am J Phys Anthropol 139:253–60
- Cherni L, Loueslati BY, Pereira L, Ennafaa H, Amorim A, El Gaaied AB. (2005a). Female gene pools of Berber and Arab neighboring communities in central Tunisia: Microstructure of mtDNA variation in North Africa. Hum Biol 77:61–70
- Cherni L, Loueslati Yaacoubi B, Pereira L, Alves C, Khodjet-el-Khil H, Ben Ammar el Gaaied A, Amorim A. (2005b). Data for 15 autosomal STR markers (Powerplex 16 System) from two Tunisian populations: Kesra (Berber) and Zriba (Arab). Forensic Sci Int 147:101–6
- Cherni L, Pereira L, Goios A, Loueslati BY, Khodjet el Khil H, Gomes I, Gusmao L, et al. (2005c). Y-chromosomal STR haplotypes in three ethnic groups and one cosmopolitan population from Tunisia. Forensic Sci Int 152:95–9
- Cruciani F, Santolamazza P, Shen P, Macaulay V, Moral P, Olckers A, Modiano D, et al. (2002). A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes. Am J Hum Genet 70:1197–214
- Di Rienzo A, Wilson AC. (1991). Branching pattern in the evolutionary tree for human mitochondrial DNA. Proc Natl Acad Sci USA 88:1597–601
- el-Sibai M, Platt DE, Haber M, Xue Y, Youhanna SC, Wells RS, Izaabel H, et al. (2009). Geographical structure of the Y-chromosomal genetic landscape of the Levant: A coastal-inland contrast. Ann Hum Genet, 73:568–81
- Endo Y, Fateen E, Aoyama Y, Horinishi A, Ebara T, Murase T, Shin YS, Okubo M. (2005). Molecular characterization of Egyptian patients with glycogen storage disease type IIIa. J Hum Genet 50:538–42
- Ennafaa H, Fregel R, Khodjet-el-Khil H, Gonzalez AM, Mahmoudi HA, Cabrera VM, Larruga JM, Benammar-Elgaaied A. (2011). Mitochondrial DNA and Y-chromosome microstructure in Tunisia. J Hum Genet 56:734–41
- Fadhlaoui-Zid K, Martinez-Cruz B, Khodjet-el-Khil H, Mendizabal I, Benammar-Elgaaied A, Comas D. (2011). Genetic structure of Tunisian ethnic groups revealed by paternal lineages. Am J Phys Anthropol 146:271–80
- Fadhlaoui-Zid K, Plaza S, Calafell F, Ben Amor M, Comas D, Bennamar el Gaaied A. (2004). Mitochondrial DNA heterogeneity in Tunisian Berbers. Ann Hum Genet 68:222–33
- Falchi A, Giovannoni L, Calo CM, Piras IS, Moral P, Paoli G, Vona G, Varesi L. (2006). Genetic history of some western Mediterranean human isolates through mtDNA HVR1 polymorphisms. J Hum Genet 51:9–14
- Hsouna S, Ben Halim N, Lasram K, Meiloud G, Arfa I, Kerkeni E, Romdhane L, et al. (2014). Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean region. Mitochondrial DNA 10:1–6 . [Epub ahead of print]
- Kefi R, Hsouna S, Ben Halim N, Lasram K, Romdhane L, Messai H, Abdelhak S. (2014). Phylogeny and genetic structure of Tunisians and their position within Mediterranean populations. Mitochondrial DNA. [Epub ahead of print]
- Kerkeni E, Monastiri K, Saket B, Guediche MN, Ben Cheikh H. (2007). Interplay of socio-economic factors, consanguinity, fertility, and offspring mortality in Monastir, Tunisia. Croat Med J 48:701–7
- Loueslati BY, Cherni L, Khodjet-Elkhil H, Ennafaa H, Pereira L, Amorim A, Ben Ayed F, Ben Ammar Elgaaied A. (2006). Islands inside an island: Reproductive isolates on Jerba island. Am J Hum Biol 18:149–53
- Mili A, Ben Charfeddine I, Mamai O, Abdelhak S, Adala L, Amara A, Pagliarani S, et al. (2012). Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III. J Hum Genet 57:170–5
- Saillard J, Forster P, Lynnerup N, Bandelt HJ, Norby S. (2000). mtDNA variation among Greenland Eskimos: The edge of the Beringian expansion. Am J Hum Genet 67:718–26
- Semino O, Magri C, Benuzzi G, Lin AA, al-Zahery N, Battaglia V, Maccioni L, et al. (2004). Origin, diffusion, and differentiation of Y-chromosome haplogroups E and J: Inferences on the neolithization of Europe and later migratory events in the Mediterranean area. Am J Hum Genet 74:1023–34
- Shen JJ, Bao Y, Liu HM, Lee P, Leonard JV, Chen YT. (1996). Mutations in exon 3 of the glycogen debranching enzyme gene are associated with glycogen storage disease type III that is differentially expressed in liver and muscle. J Clin Invest 98:352–7
- Yang BZ, Ding JH, Enghild JJ, Bao Y, Chen YT. (1992). Molecular cloning and nucleotide sequence of cDNA encoding human muscle glycogen debranching enzyme. J Biol Chem 267:9294–9
- Zalloua PA, Platt DE, el Sibai M, Khalife J, Makhoul N, Haber M, Xue Y, et al. (2008a). Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean. Am J Hum Genet 83:633–42
- Zalloua PA, Xue Y, Khalife J, Makhoul N, Debiane L, Platt DE, Royyuru AK, et al. (2008b). Y-chromosomal diversity in Lebanon is structured by recent historical events. Am J Hum Genet 82:873–82