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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.
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.
A Promising Druggable Target for Translational Therapy of Ovarian Cancer: A Molecular Profiling of Therapeutic Innovations, Extracellular Vesicle Acquired Resistance, and Signaling Pathways.
Mustafa M, Abbas K, Ahmad W, Ahmad R, Islam S, Khan H, Moinuddin, Hassan MI, Parveen S, Habib S. Mustafa M, et al. Among authors: khan h. Curr Med Chem. 2025 Jan 14. doi: 10.2174/0109298673331849240930140120. Online ahead of print. Curr Med Chem. 2025. PMID: 39817385
Unlocking the Potential: How Flavonoids Affect Angiogenesis, Oxidative Stress, Inflammation, Proliferation, Invasion, and Alter Receptor Interactions in Endometriosis.
Goleij P, Khandan M, Khazeei Tabari MA, Sanaye PM, Alijanzadeh D, Soltani A, Hosseini Z, Larsen DS, Khan H, Kumar AP, Daglia M. Goleij P, et al. Among authors: khan h. Food Sci Nutr. 2024 Dec 7;13(1):e4607. doi: 10.1002/fsn3.4607. eCollection 2025 Jan. Food Sci Nutr. 2024. PMID: 39803270 Free PMC article. Review.
3,932 results