Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

19 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
Najmabadi H, Hu H, Garshasbi M, Zemojtel T, Abedini SS, Chen W, Hosseini M, Behjati F, Haas S, Jamali P, Zecha A, Mohseni M, Püttmann L, Vahid LN, Jensen C, Moheb LA, Bienek M, Larti F, Mueller I, Weissmann R, Darvish H, Wrogemann K, Hadavi V, Lipkowitz B, Esmaeeli-Nieh S, Wieczorek D, Kariminejad R, Firouzabadi SG, Cohen M, Fattahi Z, Rost I, Mojahedi F, Hertzberg C, Dehghan A, Rajab A, Banavandi MJ, Hoffer J, Falah M, Musante L, Kalscheuer V, Ullmann R, Kuss AW, Tzschach A, Kahrizi K, Ropers HH. Najmabadi H, et al. Among authors: firouzabadi sg. Nature. 2011 Sep 21;478(7367):57-63. doi: 10.1038/nature10423. Nature. 2011. PMID: 21937992
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: firouzabadi sg. Hum Genet. 2006 Feb;118(6):708-15. doi: 10.1007/s00439-005-0104-y. Epub 2005 Nov 26. Hum Genet. 2006. PMID: 16311745
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.
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, Grüters A, Lenzner S, Jensen LR, Rüschendorf F, Kuss AW, Ropers HH. Najmabadi H, et al. Among authors: firouzabadi sg. Hum Genet. 2007 Mar;121(1):43-8. doi: 10.1007/s00439-006-0292-0. Epub 2006 Nov 21. Hum Genet. 2007. PMID: 17120046
Exceptional human core promoter nucleotide compositions.
Darvish H, Nabi MO, Firouzabadi SG, Karimlou M, Heidari A, Najmabadi H, Ohadi M. Darvish H, et al. Among authors: firouzabadi sg. Gene. 2011 Apr 15;475(2):79-86. doi: 10.1016/j.gene.2010.12.013. Epub 2011 Jan 26. Gene. 2011. PMID: 21277957
Core promoter STRs: novel mechanism for inter-individual variation in gene expression in humans.
Heidari A, Nariman Saleh Fam Z, Esmaeilzadeh-Gharehdaghi E, Banan M, Hosseinkhani S, Mohammadparast S, Oladnabi M, Ebrahimpour MR, Soosanabadi M, Farokhashtiani T, Darvish H, Firouzabadi SG, Farashi S, Najmabadi H, Ohadi M. Heidari A, et al. Among authors: firouzabadi sg. Gene. 2012 Jan 15;492(1):195-8. doi: 10.1016/j.gene.2011.10.028. Epub 2011 Oct 21. Gene. 2012. PMID: 22037607
Novel evidence of the involvement of calreticulin in major psychiatric disorders.
Ohadi M, Mirabzadeh A, Esmaeilzadeh-Gharehdaghi E, Rezazadeh M, Hosseinkhanni S, Oladnabi M, Firouzabadi SG, Darvish H. Ohadi M, et al. Among authors: firouzabadi sg. Prog Neuropsychopharmacol Biol Psychiatry. 2012 Jun 1;37(2):276-81. doi: 10.1016/j.pnpbp.2012.02.007. Epub 2012 Feb 21. Prog Neuropsychopharmacol Biol Psychiatry. 2012. PMID: 22507216
Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's disease.
Darvish H, Heidari A, Hosseinkhani S, Movafagh A, Khaligh A, Jamshidi J, Noorollahi-Moghaddam H, Heidari-Rostami HR, Karkheiran S, Shahidi GA, Togha M, Paknejad SM, Ashrafian H, Abdi S, Firouzabadi SG, Jamaldini SH, Ohadi M. Darvish H, et al. Among authors: firouzabadi sg. J Mol Neurosci. 2013 Oct;51(2):389-93. doi: 10.1007/s12031-013-0021-9. Epub 2013 May 4. J Mol Neurosci. 2013. PMID: 23640536
Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients.
Darvish H, Movafagh A, Omrani MD, Firouzabadi SG, Azargashb E, Jamshidi J, Khaligh A, Haghnejad L, Naeini NS, Talebi A, Heidari-Rostami HR, Noorollahi-Moghaddam H, Karkheiran S, Shahidi GA, Paknejad SM, Ashrafian H, Abdi S, Kayyal M, Akbari M, Pedram N, Emamalizadeh B. Darvish H, et al. Among authors: firouzabadi sg. Neurosci Lett. 2013 Sep 13;551:75-8. doi: 10.1016/j.neulet.2013.07.013. Epub 2013 Jul 21. Neurosci Lett. 2013. PMID: 23880019
19 results