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Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.
Vieland VJ, Hallmayer J, Huang Y, Pagnamenta AT, Pinto D, Khan H, Monaco AP, Paterson AD, Scherer SW, Sutcliffe JS, Szatmari P; Autism Genome Project (AGP). Vieland VJ, et al. Among authors: khan h. J Neurodev Disord. 2011 Jun;3(2):113-23. doi: 10.1007/s11689-011-9072-9. Epub 2011 Jan 19. J Neurodev Disord. 2011. PMID: 21484201 Free PMC article.
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, Paterson AD, Scherer SW, Vieland VJ, Monaco AP. Pagnamenta AT, et al. Among authors: khan h. J Med Genet. 2011 Jan;48(1):48-54. doi: 10.1136/jmg.2010.079426. Epub 2010 Oct 23. J Med Genet. 2011. PMID: 20972252 Free PMC article.
The Safety of Recently Approved Therapeutics in Age-Related Macular Degeneration.
Khanani I, Aziz AA, Khanani ZA, Khan H, Mojumder O, Sulahria H, Ali H, Khan H, Rahimzadeh TS, Vannavong J, Gahn GM, Khanani AM. Khanani I, et al. Among authors: khan h. Int Ophthalmol Clin. 2025 Jan 1;65(1):3-7. doi: 10.1097/IIO.0000000000000547. Epub 2024 Dec 23. Int Ophthalmol Clin. 2025. PMID: 39710898 Review.
"Teledentistry" using a mobile app (Telesmile) to improve oral health among the visually impaired and hearing-impaired populations in Saudi Arabia: a randomized controlled study.
Fageeh HN, Mansoor MA, Fageeh HI, Abdul HN, Khan H, Akkam A, Muhaddili I, Korairi S, Bhati AK. Fageeh HN, et al. Among authors: khan h. Front Oral Health. 2024 Dec 4;5:1496222. doi: 10.3389/froh.2024.1496222. eCollection 2024. Front Oral Health. 2024. PMID: 39697789 Free PMC article.
3,912 results