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

Year Number of Results
1998 1
2002 7
2003 6
2004 4
2005 13
2006 13
2007 14
2008 11
2009 13
2010 13
2011 16
2012 15
2013 18
2014 18
2015 27
2016 23
2017 17
2018 24
2019 28
2020 41
2021 5
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286 results
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Page 1
Contact Lenses for Color Blindness.
Badawy AR, Hassan MU, Elsherif M, Ahmed Z, Yetisen AK, Butt H. Badawy AR, et al. Among authors: ahmed z. Adv Healthc Mater. 2018 Jun;7(12):e1800152. doi: 10.1002/adhm.201800152. Epub 2018 Apr 26. Adv Healthc Mater. 2018. PMID: 29696828 Free PMC article.
Retraction notice to "PP2ACα deficiency impairs early cortical development through inducing DNA damage in neuroprojenitor cells" [Int. J. Biochem. Cell Biol. 109C (2019) 40-58].
Liu B, Lin L, Riazuddin S, Zubair A, Li W, Di LJ, Li R, Dong TT, Deng CX, Tong WM. Liu B, et al. Among authors: zubair a. Int J Biochem Cell Biol. 2020 Aug;125:105762. doi: 10.1016/j.biocel.2020.105762. Epub 2020 Jun 10. Int J Biochem Cell Biol. 2020. PMID: 32535144 No abstract available.
Targeting Aquaporin-4 Subcellular Localization to Treat Central Nervous System Edema.
Kitchen P, Salman MM, Halsey AM, Clarke-Bland C, MacDonald JA, Ishida H, Vogel HJ, Almutiri S, Logan A, Kreida S, Al-Jubair T, Winkel Missel J, Gourdon P, Törnroth-Horsefield S, Conner MT, Ahmed Z, Conner AC, Bill RM. Kitchen P, et al. Among authors: ahmed z. Cell. 2020 May 14;181(4):784-799.e19. doi: 10.1016/j.cell.2020.03.037. Cell. 2020. PMID: 32413299 Free PMC article.
Insights into Drought Stress Signaling in Plants and the Molecular Genetic Basis of Cotton Drought Tolerance.
Mahmood T, Khalid S, Abdullah M, Ahmed Z, Shah MKN, Ghafoor A, Du X. Mahmood T, et al. Among authors: ahmed z. Cells. 2019 Dec 31;9(1):105. doi: 10.3390/cells9010105. Cells. 2019. PMID: 31906215 Free PMC article. Review.
CGRP antagonists for decreasing migraine frequency: New options, long overdue.
Bucklan J, Ahmed Z. Bucklan J, et al. Among authors: ahmed z. Cleve Clin J Med. 2020 Apr;87(4):211-218. doi: 10.3949/ccjm.87a.19048. Cleve Clin J Med. 2020. PMID: 32238376 Free article.
Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly.
Richard EM, Polla DL, Assir MZ, Contreras M, Shahzad M, Khan AA, Razzaq A, Akram J, Tarar MN, Blanpied TA, Ahmed ZM, Abou Jamra R, Wieczorek D, van Bokhoven H, Riazuddin S, Riazuddin S. Richard EM, et al. Among authors: ahmed zm. Am J Hum Genet. 2019 Oct 3;105(4):869-878. doi: 10.1016/j.ajhg.2019.09.007. Epub 2019 Sep 26. Am J Hum Genet. 2019. PMID: 31564433 Free PMC article.
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.
Richard EM, Santos-Cortez RLP, Faridi R, Rehman AU, Lee K, Shahzad M, Acharya A, Khan AA, Imtiaz A, Chakchouk I, Takla C, Abbe I, Rafeeq M, Liaqat K, Chaudhry T, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics, Schrauwen I, Khan SN, Morell RJ, Zafar S, Ansar M, Ahmed ZM, Ahmad W, Riazuddin S, Friedman TB, Leal SM, Riazuddin S. Richard EM, et al. Among authors: ahmed zm. Hum Mutat. 2019 Jan;40(1):53-72. doi: 10.1002/humu.23666. Epub 2018 Nov 18. Hum Mutat. 2019. PMID: 30303587 Free PMC article.
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects.
Manole A, Efthymiou S, O'Connor E, Mendes MI, Jennings M, Maroofian R, Davagnanam I, Mankad K, Lopez MR, Salpietro V, Harripaul R, Badalato L, Walia J, Francklyn CS, Athanasiou-Fragkouli A, Sullivan R, Desai S, Baranano K, Zafar F, Rana N, Ilyas M, Horga A, Kara M, Mattioli F, Goldenberg A, Griffin H, Piton A, Henderson LB, Kara B, Aslanger AD, Raaphorst J, Pfundt R, Portier R, Shinawi M, Kirby A, Christensen KM, Wang L, Rosti RO, Paracha SA, Sarwar MT, Jenkins D; SYNAPS Study Group, Ahmed J, Santoni FA, Ranza E, Iwaszkiewicz J, Cytrynbaum C, Weksberg R, Wentzensen IM, Guillen Sacoto MJ, Si Y, Telegrafi A, Andrews MV, Baldridge D, Gabriel H, Mohr J, Oehl-Jaschkowitz B, Debard S, Senger B, Fischer F, van Ravenwaaij C, Fock AJM, Stevens SJC, Bähler J, Nasar A, Mantovani JF, Manzur A, Sarkozy A, Smith DEC, Salomons GS, Ahmed ZM, Riazuddin S, Riazuddin S, Usmani MA, Seibt A, Ansar M, Antonarakis SE, Vincent JB, Ayub M, Grimmel M, Jelsig AM, Hjortshøj TD, Karstensen HG, Hummel M, Haack TB, Jamshidi Y, Distelmaier F, Horvath R, Gleeson JG, Becker H, Mandel JL, Koolen DA, Houlden H. Manole A, et al. Among authors: ahmed zm. Am J Hum Genet. 2020 Aug 6;107(2):311-324. doi: 10.1016/j.ajhg.2020.06.016. Epub 2020 Jul 31. Am J Hum Genet. 2020. PMID: 32738225 Free PMC article.
Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population.
Shahzad M, Yousaf S, Waryah YM, Gul H, Kausar T, Tariq N, Mahmood U, Ali M, Khan MA, Waryah AM, Shaikh RS, Riazuddin S, Ahmed ZM; University of Washington Center for Mendelian Genomics (UW CMG) Consortium. Shahzad M, et al. Among authors: ahmed zm. Sci Rep. 2017 Mar 7;7:44185. doi: 10.1038/srep44185. Sci Rep. 2017. PMID: 28266639 Free PMC article. Clinical Trial.
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
Abrams AJ, Hufnagel RB, Rebelo A, Zanna C, Patel N, Gonzalez MA, Campeanu IJ, Griffin LB, Groenewald S, Strickland AV, Tao F, Speziani F, Abreu L, Schüle R, Caporali L, La Morgia C, Maresca A, Liguori R, Lodi R, Ahmed ZM, Sund KL, Wang X, Krueger LA, Peng Y, Prada CE, Prows CA, Schorry EK, Antonellis A, Zimmerman HH, Abdul-Rahman OA, Yang Y, Downes SM, Prince J, Fontanesi F, Barrientos A, Németh AH, Carelli V, Huang T, Zuchner S, Dallman JE. Abrams AJ, et al. Among authors: ahmed zm. Nat Genet. 2015 Aug;47(8):926-32. doi: 10.1038/ng.3354. Epub 2015 Jul 13. Nat Genet. 2015. PMID: 26168012 Free PMC article.
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