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 Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2006 2
2007 1
2008 2
2011 3
2012 2
2013 3
2016 2
2017 2
2018 1
2021 2
2022 1
2025 2
2026 1

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

19 results

Results by year

Filters applied: . Clear all
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. Nature. 2011 Sep 21;478(7367):57-63. doi: 10.1038/nature10423. Nature. 2011. PMID: 21937992
Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy.
Bisarad P, Wang YC, Skidmore PT, Galaz-Montoya CI, Lewis SA, Alhaddad B, Kong N, Julian D, Magee H, Kruer TN, Xie Y, Zheng W, Li B, Rajabpour FV, Liu J, Revanur A, Bakur K, Firouzabadi SG, Sharbatkhori S, Tafakhori A, Taghiabadi E, Nezaminargabad E, Vosoogh S, Jamshidi J, Arefnia S, Hosseini SA, Khajehmirzaei A, Jamali F, Ahmadifard A, Khodadadi H, Daneshmand P, Bohlega S, Maddirevula S, Nadeef SS, Hashem MO, Salih MA, Mohmed IN, Sticht H, Morias SP, Damásio J, Santos M, Loureiro JL, Rodrigues R, Stevanin G, Benkirane M, Dauriat B, Head N, Baptista J, Shahhosseini S, Mohammad F, Zhao H, Padilla-Lopez S, Alkuraya F, Bakhtiari S, Kruer MC, Jin SC, Darvish H. Bisarad P, et al. medRxiv [Preprint]. 2025 Nov 6:2025.11.04.25339178. doi: 10.1101/2025.11.04.25339178. medRxiv. 2025. PMID: 41282771 Free PMC article. Preprint.
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.
Klöckner C, Fernández-Murray JP, Tavasoli M, Sticht H, Stoltenburg-Didinger G, Scholle LM, Bakhtiari S, Kruer MC, Darvish H, Firouzabadi SG, Pagnozzi A, Shukla A, Girisha KM, Narayanan DL, Kaur P, Maroofian R, Zaki MS, Noureldeen MM, Merkenschlager A, Gburek-Augustat J, Cali E, Banu S, Nahar K, Efthymiou S, Houlden H, Jamra RA, Williams J, McMaster CR, Platzer K. Klöckner C, et al. Brain. 2022 Jun 30;145(6):1916-1923. doi: 10.1093/brain/awac074. Brain. 2022. PMID: 35202461 Free PMC article.
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
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. 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
Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome.
Firouzabadi SG, Kariminejad R, Vameghi R, Darvish H, Ghaedi H, Banihashemi S, Firouzkouhi Moghaddam M, Jamali P, Mofidi Tehrani HF, Dehghani H, Narooie-Nejad M, Jamshidi J, Tafakhori A, Sadabadi S, Najmabadi H, Behjati F. Firouzabadi SG, et al. Mol Neurobiol. 2017 Nov;54(9):7019-7027. doi: 10.1007/s12035-016-0202-y. Epub 2016 Oct 28. Mol Neurobiol. 2017. PMID: 27796743
19 results