Najmabadi H - Search Results

1

A defect in the TUSC3 gene is associated with autosomal recessive mental retardation.

Garshasbi M, Hadavi V, Habibi H, Kahrizi K, Kariminejad R, Behjati F, Tzschach A, Najmabadi H, Ropers HH, Kuss AW. Garshasbi M, et al. Among authors: najmabadi h. Am J Hum Genet. 2008 May;82(5):1158-64. doi: 10.1016/j.ajhg.2008.03.018. Epub 2008 May 1. Am J Hum Genet. 2008. PMID: 18452889 Free PMC article.

2

Identification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family.

Feleki X, Najmabadi H, Karimi-Nejad R, Christopoulos G, Kleanthous M. Feleki X, et al. Among authors: najmabadi h. Hemoglobin. 2000 Nov;24(4):319-21. doi: 10.3109/03630260008993139. Hemoglobin. 2000. PMID: 11186262 No abstract available.

3

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.

Najmabadi H, Cucci RA, Sahebjam S, Kouchakian N, Farhadi M, Kahrizi K, Arzhangi S, Daneshmandan N, Javan K, Smith RJ. Najmabadi H, et al. Hum Mutat. 2002 May;19(5):572. doi: 10.1002/humu.9033. Hum Mutat. 2002. PMID: 11968091

4

The Iranian Human Mutation Gene Bank: a data and sample resource for worldwide collaborative genetics research.

Najmabadi H, Neishabury M, Sahebjam F, Kahrizi K, Shafaghati Y, Nikzat N, Jalalvand M, Aminy F, Hashemi SB, Moghimi B, Noorian AR, Jannati A, Mohammadi M, Javan K; Iranian Human Mutation Gene Bank. Najmabadi H, et al. Hum Mutat. 2003 Feb;21(2):146-50. doi: 10.1002/humu.10164. Hum Mutat. 2003. PMID: 12552562

5

alpha-globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia.

Garshasbi M, Oberkanins C, Law HY, Neishabury M, Kariminejad R, Najmabadi H. Garshasbi M, et al. Among authors: najmabadi h. Haematologica. 2003 Oct;88(10):1196-7. Haematologica. 2003. PMID: 14555321 Review.

6

Association of the dopamine transporter gene (DAT1) core promoter polymorphism -67T variant with schizophrenia.

Khodayari N, Garshasbi M, Fadai F, Rahimi A, Hafizi L, Ebrahimi A, Najmabadi H, Ohadi M. Khodayari N, et al. Among authors: najmabadi h. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):10-2. doi: 10.1002/ajmg.b.30067. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15274029

7

GJB2 mutations: passage through Iran.

Najmabadi H, Nishimura C, Kahrizi K, Riazalhosseini Y, Malekpour M, Daneshi A, Farhadi M, Mohseni M, Mahdieh N, Ebrahimi A, Bazazzadegan N, Naghavi A, Avenarius M, Arzhangi S, Smith RJ. Najmabadi H, et al. Am J Med Genet A. 2005 Mar 1;133A(2):132-7. doi: 10.1002/ajmg.a.30576. Am J Med Genet A. 2005. PMID: 15666300

8

Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus.

Chen W, Kahrizi K, Meyer NC, Riazalhosseini Y, Van Camp G, Najmabadi H, Smith RJ. Chen W, et al. Among authors: najmabadi h. J Med Genet. 2005 Oct;42(10):e61. doi: 10.1136/jmg.2005.032615. Epub 2005 Jul 20. J Med Genet. 2005. PMID: 16033917 Free PMC article.

9

Prognostic value of chromosome 1 and 8 copy number in invasive ductal breast carcinoma among Iranian women: an interphase FISH analysis.

Behjati F, Atri M, Najmabadi H, Nouri K, Zamani M, Mehdipour P. Behjati F, et al. Among authors: najmabadi h. Pathol Oncol Res. 2005;11(3):157-63. doi: 10.1007/BF02893392. Epub 2005 Sep 29. Pathol Oncol Res. 2005. PMID: 16195769 Free article.

10

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly.

Garshasbi M, Motazacker MM, Kahrizi K, Behjati F, Abedini SS, Nieh SE, Firouzabadi SG, Becker C, Rüschendorf F, Nürnberg P, Tzschach A, Vazifehmand R, Erdogan F, Ullmann R, Lenzner S, Kuss AW, Ropers HH, Najmabadi H. Garshasbi M, et al. Among authors: najmabadi h. Hum Genet. 2006 Feb;118(6):708-15. doi: 10.1007/s00439-005-0104-y. Epub 2005 Nov 26. Hum Genet. 2006. PMID: 16311745

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