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

Year Number of Results
2004 3
2005 3
2006 4
2007 5
2008 4
2009 4
2010 7
2011 6
2012 6
2013 3
2014 10
2015 5
2016 6
2018 4
2019 2
2020 1
2021 3
2022 3
2023 1
2024 0

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70 results

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Page 1
INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex.
Mascibroda LG, Shboul M, Elrod ND, Colleaux L, Hamamy H, Huang KL, Peart N, Singh MK, Lee H, Merriman B, Jodoin JN, Sitaram P, Lee LA, Fathalla R, Al-Rawashdeh B, Ababneh O, El-Khateeb M, Escande-Beillard N, Nelson SF, Wu Y, Tong L, Kenney LJ, Roy S, Russell WK, Amiel J, Reversade B, Wagner EJ. Mascibroda LG, et al. Among authors: hamamy h. Nat Commun. 2022 Oct 13;13(1):6054. doi: 10.1038/s41467-022-33547-8. Nat Commun. 2022. PMID: 36229431 Free PMC article.
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction.
Al Sayed ZR, Canac R, Cimarosti B, Bonnard C, Gourraud JB, Hamamy H, Kayserili H, Girardeau A, Jouni M, Jacob N, Gaignerie A, Chariau C, David L, Forest V, Marionneau C, Charpentier F, Loussouarn G, Lamirault G, Reversade B, Zibara K, Lemarchand P, Gaborit N. Al Sayed ZR, et al. Among authors: hamamy h. Cardiovasc Res. 2021 Jul 27;117(9):2092-2107. doi: 10.1093/cvr/cvaa259. Cardiovasc Res. 2021. PMID: 32898233 Free article.
Communities and community genetics in Ethiopia.
Tadesse L, Tafesse F, Hamamy H. Tadesse L, et al. Among authors: hamamy h. Pan Afr Med J. 2014 Jun 5;18:115. doi: 10.11604/pamj.2014.18.115.3172. eCollection 2014. Pan Afr Med J. 2014. PMID: 25404975 Free PMC article. Review.
Genetic disorders in the Arab world.
Al-Gazali L, Hamamy H, Al-Arrayad S. Al-Gazali L, et al. Among authors: hamamy h. BMJ. 2006 Oct 21;333(7573):831-4. doi: 10.1136/bmj.38982.704931.AE. BMJ. 2006. PMID: 17053236 Free PMC article. Review. No abstract available.
Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.
Reversade B, Escande-Beillard N, Dimopoulou A, Fischer B, Chng SC, Li Y, Shboul M, Tham PY, Kayserili H, Al-Gazali L, Shahwan M, Brancati F, Lee H, O'Connor BD, Kegler MS, Merriman B, Nelson SF, Masri A, Alkazaleh F, Guerra D, Ferrari P, Nanda A, Rajab A, Markie D, Gray M, Nelson J, Grix A, Sommer A, Savarirayan R, Janecke AR, Steichen E, Sillence D, Haußer I, Budde B, Nürnberg G, Nürnberg P, Seemann P, Kunkel D, Zambruno G, Dallapiccola B, Schuelke M, Robertson S, Hamamy H, Wollnik B, Van Maldergem L, Mundlos S, Kornak U. Reversade B, et al. Among authors: hamamy h. Nat Genet. 2022 Feb;54(2):213. doi: 10.1038/s41588-022-01013-2. Nat Genet. 2022. PMID: 35064218 Free article. No abstract available.
Consanguinity and dysmorphology in Arabs.
Al-Gazali L, Hamamy H. Al-Gazali L, et al. Among authors: hamamy h. Hum Hered. 2014;77(1-4):93-107. doi: 10.1159/000360421. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060273 Free article.
The ethnic distribution of sickle cell disease in Sudan.
Sabahelzain MM, Hamamy H. Sabahelzain MM, et al. Among authors: hamamy h. Pan Afr Med J. 2014 May 3;18:13. doi: 10.11604/pamj.2014.18.13.3280. eCollection 2014. Pan Afr Med J. 2014. PMID: 25360197 Free PMC article. Review.
70 results