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Publications
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Garshasbi M, Motazacker MM, Kahrizi K, Behjati F, Abedini SS, Esmaeeli Nieh S, Ghasemi Firouzabadi S, Becker C, Rueschendorf F, Nuernberg P, Tzschach A, Vazifehmand R, Erdogan F, Ullmann R, Lenzner S, Kuss AW, Ropers HH, Najmabadi H. SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive MR and microcephaly. Feb 2006.Hum Genet. 118(6):708-15.
Najmabadi H, Motazacker MM, Garshasbi M, Kahrizi K, Tzschach A, Chen W, Behjati F, Hadavi V, Nieh SE, Abedini SS, Vazifehmand R, Firouzabadi SG, Jamali P, Falah M, Seifati SM, Gruters A, Lenzner S, Jensen LR, Rüschendorf F, Kuss AW, Ropers HH. Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. 2007 Mar. Hum Genet. 121(1):43-8.
Motazacker MM, Rost B, Hucho T, Garshasbi M, Kahrizi K, Behjati F, Vazifehmand R, Ullmann R,, Abedini SS, Esmaeeli Nieh S, Hosseini Amini S, Goswami C, Tzschach A, Jensen LR, Schmitz D,. Ropers HH, Najmabadi H, Kuss A.W. A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation. 2007. Am J Hum Genet. 81: 792–798.
Pouya AR*, Abedini SS*, Mansoorian N, Behjati F, Nikzat N, Mohseni M, Esmaeeli Nieh S, Abbasi L, Darvish H, Bahrami Monajemi Gh, Banihashemi S, Kariminejad R, Kahrizi K, Ropers HH, Najmabadi H. Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population.2009. Euro J Med Genetics. 52 (4): 170-173.(*=equal contributed)
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