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

Year Number of Results
2002 9
2003 8
2004 13
2005 19
2006 27
2007 46
2008 30
2009 31
2010 17
2011 25
2012 41
2013 51
2014 53
2015 55
2016 48
2017 42
2018 36
2019 40
2020 51
2021 41
2022 46
2023 33
2024 7

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679 results

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Page 1
Expanding the phenome and variome of skeletal dysplasia.
Maddirevula S, Alsahli S, Alhabeeb L, Patel N, Alzahrani F, Shamseldin HE, Anazi S, Ewida N, Alsaif HS, Mohamed JY, Alazami AM, Ibrahim N, Abdulwahab F, Hashem M, Abouelhoda M, Monies D, Al Tassan N, Alshammari M, Alsagheir A, Seidahmed MZ, Sogati S, Aglan MS, Hamad MH, Salih MA, Hamed AA, Alhashmi N, Nabil A, Alfadli F, Abdel-Salam GMH, Alkuraya H, Peitee WO, Keng WT, Qasem A, Mushiba AM, Zaki MS, Fassad MR, Alfadhel M, Alexander S, Sabr Y, Temtamy S, Ekbote AV, Ismail S, Hosny GA, Otaify GA, Amr K, Al Tala S, Khan AO, Rizk T, Alaqeel A, Alsiddiky A, Singh A, Kapoor S, Alhashem A, Faqeih E, Shaheen R, Alkuraya FS. Maddirevula S, et al. Among authors: khan ao. Genet Med. 2018 Dec;20(12):1609-1616. doi: 10.1038/gim.2018.50. Epub 2018 Apr 5. Genet Med. 2018. PMID: 29620724 Free article.
The genomic landscape of rare disorders in the Middle East.
El Naofal M, Ramaswamy S, Alsarhan A, Nugud A, Sarfraz F, Janbaz H, Taylor A, Jain R, Halabi N, Yaslam S, Alfalasi R, Shenbagam S, Rabea F, Bitzan M, Yavuz L, Wafadari D, Abulhoul H, Shankar S, Al Maazmi M, Rizk R, Alloub Z, Elbashir H, Babiker MOE, Chencheri N, AlBanna A, Sultan M, El Bitar M, Kherani S, Thalange N, Alshryda S, Di Donato R, Tzivinikos C, Majid I, Freeman AF, Gonzalez C, Khan AO, Hamdan H, Abuhammour W, AlAwadhi M, AlKhayat A, Alsheikh-Ali A, Abou Tayoun AN. El Naofal M, et al. Among authors: khan ao. Genome Med. 2023 Jan 27;15(1):5. doi: 10.1186/s13073-023-01157-8. Genome Med. 2023. PMID: 36703223 Free PMC article.
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.
Patel N, Aldahmesh MA, Alkuraya H, Anazi S, Alsharif H, Khan AO, Sunker A, Al-Mohsen S, Abboud EB, Nowilaty SR, Alowain M, Al-Zaidan H, Al-Saud B, Alasmari A, Abdel-Salam GM, Abouelhoda M, Abdulwahab FM, Ibrahim N, Naim E, Al-Younes B, E AlMostafa A, AlIssa A, Hashem M, Buzovetsky O, Xiong Y, Monies D, Altassan N, Shaheen R, Al-Hazzaa SA, Alkuraya FS. Patel N, et al. Among authors: khan ao. Genet Med. 2016 Jun;18(6):554-62. doi: 10.1038/gim.2015.127. Epub 2015 Sep 10. Genet Med. 2016. PMID: 26355662 Free article.
Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies.
Eisenberger T, Neuhaus C, Khan AO, Decker C, Preising MN, Friedburg C, Bieg A, Gliem M, Charbel Issa P, Holz FG, Baig SM, Hellenbroich Y, Galvez A, Platzer K, Wollnik B, Laddach N, Ghaffari SR, Rafati M, Botzenhart E, Tinschert S, Börger D, Bohring A, Schreml J, Körtge-Jung S, Schell-Apacik C, Bakur K, Al-Aama JY, Neuhann T, Herkenrath P, Nürnberg G, Nürnberg P, Davis JS, Gal A, Bergmann C, Lorenz B, Bolz HJ. Eisenberger T, et al. Among authors: khan ao. PLoS One. 2013 Nov 12;8(11):e78496. doi: 10.1371/journal.pone.0078496. eCollection 2013. PLoS One. 2013. PMID: 24265693 Free PMC article.
Inherited retinal diseases and gene therapy update.
Khan AO. Khan AO. Saudi J Ophthalmol. 2023 Dec 21;37(4):261-262. doi: 10.4103/sjopt.sjopt_295_23. eCollection 2023 Oct-Dec. Saudi J Ophthalmol. 2023. PMID: 38155682 Free PMC article. No abstract available.
Correspondence.
Khan AO. Khan AO. Retina. 2016 Jul;36(7):e68. doi: 10.1097/IAE.0000000000001108. Retina. 2016. PMID: 27276642 No abstract available.
Potential ASPH-Related Ectopia Lentis.
Khan AO. Khan AO. J Neuroophthalmol. 2023 Oct 12. doi: 10.1097/WNO.0000000000001997. Online ahead of print. J Neuroophthalmol. 2023. PMID: 37824266 No abstract available.
Fundus autofluorescence imaging in hereditary retinal diseases.
Pichi F, Abboud EB, Ghazi NG, Khan AO. Pichi F, et al. Among authors: khan ao. Acta Ophthalmol. 2018 Aug;96(5):e549-e561. doi: 10.1111/aos.13602. Epub 2017 Nov 2. Acta Ophthalmol. 2018. PMID: 29098804 Free article. Review.
679 results