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Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.
Polla DL, Farazi Fard MA, Tabatabaei Z, Habibzadeh P, Levchenko OA, Nikuei P, Makrythanasis P, Hussain M, von Hardenberg S, Zeinali S, Fallah MS, Schuurs-Hoeijmakers JHM, Shahzad M, Fatima F, Fatima N, Kaat LD, Bruggenwirth HT, Fleming LR, Condie J, Ploski R, Pollak A, Pilch J, Demina NA, Chukhrova AL, Sergeeva VS, Venselaar H, Masri AT, Hamamy H, Santoni FA, Linda K, Ahmed ZM, Nadif Kasri N, de Brouwer APM, Bergmann AK, Hethey S, Yavarian M, Ansar M, Riazuddin S, Riazuddin S, Silawi M, Ruggeri G, Pirozzi F, Eftekhar E, Taghipour Sheshdeh A, Bahramjahan S, Mirzaa GM, Lavrov AV, Antonarakis SE, Faghihi MA, van Bokhoven H. Polla DL, et al. Among authors: fatima n, fatima f. Genet Med. 2021 Jul;23(7):1246-1254. doi: 10.1038/s41436-021-01133-w. Epub 2021 Apr 6. Genet Med. 2021. PMID: 33824500 Free PMC article.
Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts.
Irum B, Khan SY, Ali M, Kaul H, Kabir F, Rauf B, Fatima F, Nadeem R, Khan AO, Al Obaisi S, Naeem MA, Nasir IA, Khan SN, Husnain T, Riazuddin S, Akram J, Eghrari AO, Riazuddin SA. Irum B, et al. Among authors: fatima f. PLoS One. 2016 Nov 4;11(11):e0162620. doi: 10.1371/journal.pone.0162620. eCollection 2016. PLoS One. 2016. PMID: 27814360 Free PMC article.
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
Irum B, Khan SY, Ali M, Daud M, Kabir F, Rauf B, Fatima F, Iqbal H, Khan AO, Al Obaisi S, Naeem MA, Nasir IA, Khan SN, Husnain T, Riazuddin S, Akram J, Eghrari AO, Riazuddin SA. Irum B, et al. Among authors: fatima f. PLoS One. 2016 Dec 9;11(12):e0167562. doi: 10.1371/journal.pone.0167562. eCollection 2016. PLoS One. 2016. PMID: 27936067 Free PMC article.
Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
Irum B, Khan SY, Ali M, Daud M, Kabir F, Rauf B, Fatima F, Iqbal H, Khan AO, Obaisi SA, Naeem MA, Nasir IA, Khan SN, Husnain T, Riazuddin S, Akram J, Eghrari AO, Riazuddin SA. Irum B, et al. Among authors: fatima f. PLoS One. 2017 Mar 9;12(3):e0173719. doi: 10.1371/journal.pone.0173719. eCollection 2017. PLoS One. 2017. PMID: 28278293 Free PMC article.
Impact of age-related changes in buccal epithelial cells on pediatric epigenetic biomarker research.
Merrill SM, Konwar C, Fatima F, Dever K, MacIsaac JL, Letourneau N, Giesbrecht GF, Dewey D, England-Mason G, Lewis CR, Wang D, Teh AL, Meaney MJ, Gonzalez A, Noll JG, De Weerth C, Bush NR, O'Donnell KJ, Stewart SE, Kobor MS. Merrill SM, et al. Among authors: fatima f. Nat Commun. 2025 Jan 12;16(1):609. doi: 10.1038/s41467-025-55909-8. Nat Commun. 2025. PMID: 39800776 Free PMC article.
Cyclodextrin-Nanosponge-Loaded Cyclo-Oxygenase-2 Inhibitor-Based Topical Gel for Treatment of Psoriatic Arthritis: Formulation Design, Development, and In vitro Evaluations.
Hani U, Paramshetti S, Angolkar M, Alqathanin WK, Alghaseb RS, Al Asmari SM, Alsaab AA, Fatima F, Osmani RAM, Gundawar R. Hani U, et al. Among authors: fatima f. Pharmaceuticals (Basel). 2024 Nov 27;17(12):1598. doi: 10.3390/ph17121598. Pharmaceuticals (Basel). 2024. PMID: 39770440 Free PMC article.
UNVEILING A RARE CASE OF KIKUCHI-FUJIMOTO IN SINDH, PAKISTAN.
Bano S, Jawed I, Fatima FB, Alam MO, Feroze A. Bano S, et al. Among authors: fatima fb. J Ayub Med Coll Abbottabad. 2024 Jan-Mar;36(1):225-228. doi: 10.55519/JAMC-01-12794. J Ayub Med Coll Abbottabad. 2024. PMID: 39585291 Free article.
179 results