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

Year Number of Results
2003 1
2006 1
2007 3
2008 2
2009 3
2010 3
2011 5
2012 1
2013 3
2014 2
2015 2
2016 2
2017 2
2018 2
2019 4
2020 2
2021 2
2022 1
2023 1
2024 1

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37 results

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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: kariminejad r. Nature. 2011 Sep 21;478(7367):57-63. doi: 10.1038/nature10423. Nature. 2011. PMID: 21937992
New translocation in acute myeloid leukemia M4 eos.
Bahoush G, Vafapour M, Kariminejad R. Bahoush G, et al. Among authors: kariminejad r. Leuk Res Rep. 2020 Jun 8;14:100209. doi: 10.1016/j.lrr.2020.100209. eCollection 2020. Leuk Res Rep. 2020. PMID: 32566479 Free PMC article.
5p13 microduplication in a malformed fetus and his unaffected father.
Kariminejad A, Ghaderi-Sohi S, Gholami S, Najafi K, Kariminejad R, Hennekam RCM. Kariminejad A, et al. Among authors: kariminejad r. Am J Med Genet A. 2023 Feb;191(2):370-377. doi: 10.1002/ajmg.a.63030. Epub 2022 Nov 2. Am J Med Genet A. 2023. PMID: 36322476
A Patient with Trisomy 4p and Monosomy 10q.
Sobhani M, Tahmasbi P, Nasiri F, Rahnama M, Karimi-Nejad R, Tabatabaiefar MA. Sobhani M, et al. Arch Iran Med. 2019 Jul 1;22(7):414-417. Arch Iran Med. 2019. PMID: 31679386
Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.
Vaseghi P, Habibi L, Neidich JA, Cao Y, Fattahi N, Rashidi-Nezhad R, Salehnezhad T, Dalili H, Rahimi Sharbaf F, Zarkesh MR, Malekian M, Mokhberdezfuli M, Mehrtash A, Ardeshirdavani A, Kariminejad R, Ghorbansabagh V, Sadeghimoghadam P, Naddaf A, Esmaeilnia Shirvany T, Mosayebi Z, Sahebdel B, Golshahi F, Shirazi M, Shamel S, Moeini R, Heidari A, Daneshmand MA, Ghasemi R, Akrami SM, Rashidi-Nezhad A. Vaseghi P, et al. Among authors: kariminejad r. Eur J Hum Genet. 2024 Jan 26. doi: 10.1038/s41431-024-01533-x. Online ahead of print. Eur J Hum Genet. 2024. PMID: 38278869
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases.
Najafi K, Gholami S, Moshtagh A, Bazrgar M, Sadatian N, Abbasi G, Rostami P, Khalili S, Babanejad M, Nourmohammadi B, Faramarzi Garous N, Najmabadi H, Kariminejad R. Najafi K, et al. Among authors: kariminejad r. Mol Genet Genomic Med. 2019 Aug;7(8):e820. doi: 10.1002/mgg3.820. Epub 2019 Jun 18. Mol Genet Genomic Med. 2019. PMID: 31210028 Free PMC article.
37 results