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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1988 | 1 |
2015 | 1 |
2018 | 2 |
2019 | 3 |
2020 | 1 |
2021 | 2 |
2024 | 0 |
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7 results
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Page 1
Genetics of intellectual disability in consanguineous families.
Mol Psychiatry. 2019 Jul;24(7):1027-1039. doi: 10.1038/s41380-017-0012-2. Epub 2018 Jan 4.
Mol Psychiatry. 2019.
PMID: 29302074
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.
Sloan-Heggen CM, Babanejad M, Beheshtian M, Simpson AC, Booth KT, Ardalani F, Frees KL, Mohseni M, Mozafari R, Mehrjoo Z, Jamali L, Vaziri S, Akhtarkhavari T, Bazazzadegan N, Nikzat N, Arzhangi S, Sabbagh F, Otukesh H, Seifati SM, Khodaei H, Taghdiri M, Meyer NC, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Azaiez H, Najmabadi H.
Sloan-Heggen CM, et al.
J Med Genet. 2015 Dec;52(12):823-9. doi: 10.1136/jmedgenet-2015-103389. Epub 2015 Oct 7.
J Med Genet. 2015.
PMID: 26445815
Free PMC article.
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Distinct genetic variation and heterogeneity of the Iranian population.
Mehrjoo Z, Fattahi Z, Beheshtian M, Mohseni M, Poustchi H, Ardalani F, Jalalvand K, Arzhangi S, Mohammadi Z, Khoshbakht S, Najafi F, Nikuei P, Haddadi M, Zohrehvand E, Oladnabi M, Mohammadzadeh A, Jafari MH, Akhtarkhavari T, Gooshki ES, Haghdoost A, Najafipour R, Niestroj LM, Helwing B, Gossmann Y, Toliat MR, Malekzadeh R, Nürnberg P, Kahrizi K, Najmabadi H, Nothnagel M.
Mehrjoo Z, et al.
PLoS Genet. 2019 Sep 24;15(9):e1008385. doi: 10.1371/journal.pgen.1008385. eCollection 2019 Sep.
PLoS Genet. 2019.
PMID: 31550250
Free PMC article.
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Effect of inbreeding on intellectual disability revisited by trio sequencing.
Kahrizi K, Hu H, Hosseini M, Kalscheuer VM, Fattahi Z, Beheshtian M, Suckow V, Mohseni M, Lipkowitz B, Mehvari S, Mehrjoo Z, Akhtarkhavari T, Ghaderi Z, Rahimi M, Arzhangi S, Jamali P, Falahat Chian M, Nikuei P, Sabbagh Kermani F, Sadeghinia F, Jazayeri R, Tonekaboni SH, Khoshaeen A, Habibi H, Pourfatemi F, Mojahedi F, Khodaie-Ardakani MR, Najafipour R, Wienker TF, Najmabadi H, Ropers HH.
Kahrizi K, et al.
Clin Genet. 2019 Jan;95(1):151-159. doi: 10.1111/cge.13463. Epub 2018 Nov 19.
Clin Genet. 2019.
PMID: 30315573
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Comprehensive genotype-phenotype correlation in AP-4 deficiency syndrome; Adding data from a large cohort of Iranian patients.
Beheshtian M, Akhtarkhavari T, Mehvari S, Mohseni M, Fattahi Z, Abedini SS, Arzhangi S, Fadaee M, Jamali P, Najafipour R, Kalscheuer VM, Hu H, Ropers HH, Najmabadi H, Kahrizi K.
Beheshtian M, et al.
Clin Genet. 2021 Jan;99(1):187-192. doi: 10.1111/cge.13845. Epub 2020 Sep 14.
Clin Genet. 2021.
PMID: 32895917
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Association of Quantified Costal Cartilage Calcification and Long-Term Cumulative Blood Glucose Exposure: The Multi-Ethnic Study of Atherosclerosis.
Shabani M, Pishgar F, Akhtarkhavari S, Quinaglia T, Budoff MJ, Bluemke DA, Barr GR, Post WS, Wu CO, Arbab-Zadeh A, Sidhaye A, Lima JAC, Demehri S.
Shabani M, et al.
Front Endocrinol (Lausanne). 2021 Dec 13;12:785957. doi: 10.3389/fendo.2021.785957. eCollection 2021.
Front Endocrinol (Lausanne). 2021.
PMID: 34966360
Free PMC article.
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Norepinephrine and potassium induced calcium translocation in rat vas deferens.
Khoyi MA, Westfall DP, Buxton IL, Akhtar-Khavari F, Rezaei E, Salaices M, Sanchez-Garcia P.
Khoyi MA, et al.
J Pharmacol Exp Ther. 1988 Sep;246(3):917-23.
J Pharmacol Exp Ther. 1988.
PMID: 3418519
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