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

Year Number of Results
1999 1
2002 1
2004 4
2006 2
2007 2
2008 2
2009 5
2010 4
2011 4
2012 2
2013 7
2014 14
2015 20
2016 19
2017 25
2018 22
2019 30
2020 31
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178 results
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Page 1
Molecular genetics of human primary microcephaly: an overview.
Faheem M, Naseer MI, Rasool M, Chaudhary AG, Kumosani TA, Ilyas AM, Pushparaj P, Ahmed F, Algahtani HA, Al-Qahtani MH, Saleh Jamal H. Faheem M, et al. BMC Med Genomics. 2015;8 Suppl 1(Suppl 1):S4. doi: 10.1186/1755-8794-8-S1-S4. Epub 2015 Jan 15. BMC Med Genomics. 2015. PMID: 25951892 Free PMC article. Review.
Synaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-AS.
Ross PJ, Zhang WB, Mok RSF, Zaslavsky K, Deneault E, D'Abate L, Rodrigues DC, Yuen RKC, Faheem M, Mufteev M, Piekna A, Wei W, Pasceri P, Landa RJ, Nagy A, Varga B, Salter MW, Scherer SW, Ellis J. Ross PJ, et al. Among authors: faheem m. Biol Psychiatry. 2020 Jan 15;87(2):139-149. doi: 10.1016/j.biopsych.2019.07.014. Epub 2019 Jul 29. Biol Psychiatry. 2020. PMID: 31540669 Free article.
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons.
Deneault E, White SH, Rodrigues DC, Ross PJ, Faheem M, Zaslavsky K, Wang Z, Alexandrova R, Pellecchia G, Wei W, Piekna A, Kaur G, Howe JL, Kwan V, Thiruvahindrapuram B, Walker S, Lionel AC, Pasceri P, Merico D, Yuen RKC, Singh KK, Ellis J, Scherer SW. Deneault E, et al. Among authors: faheem m. Stem Cell Reports. 2018 Nov 13;11(5):1211-1225. doi: 10.1016/j.stemcr.2018.10.003. Epub 2018 Nov 1. Stem Cell Reports. 2018. PMID: 30392976 Free PMC article.
A large data resource of genomic copy number variation across neurodevelopmental disorders.
Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B, Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M, Miron K, Lu C, Wang T, Samler K, Wang X, Costain G, Hoang N, Pellecchia G, Wei J, Patel RV, Thiruvahindrapuram B, Roifman M, Merico D, Goodale T, Drmic I, Speevak M, Howe JL, Yuen RKC, Buchanan JA, Vorstman JAS, Marshall CR, Wintle RF, Rosenberg DR, Hanna GL, Woodbury-Smith M, Cytrynbaum C, Zwaigenbaum L, Elsabbagh M, Flanagan J, Fernandez BA, Carter MT, Szatmari P, Roberts W, Lerch J, Liu X, Nicolson R, Georgiades S, Weksberg R, Arnold PD, Bassett AS, Crosbie J, Schachar R, Stavropoulos DJ, Anagnostou E, Scherer SW. Zarrei M, et al. Among authors: faheem m. NPJ Genom Med. 2019 Oct 7;4:26. doi: 10.1038/s41525-019-0098-3. eCollection 2019. NPJ Genom Med. 2019. PMID: 31602316 Free PMC article.
The Dual Specificity Role of Transcription Factor FOXO in Type 2-diabetes and Cancer.
Fatima K, Mathew S, Faheem M, Mehmood T, Yassine HM, Al Thani AA, Abdel-Hafiz H, Al Ghamdy K, Qadri I. Fatima K, et al. Among authors: faheem m. Curr Pharm Des. 2018;24(24):2839-2848. doi: 10.2174/1381612824666180911114210. Curr Pharm Des. 2018. PMID: 30205794 Review.
Higher Fluid Balance Increases the Risk of Death From Sepsis: Results From a Large International Audit.
Sakr Y, Rubatto Birri PN, Kotfis K, Nanchal R, Shah B, Kluge S, Schroeder ME, Marshall JC, Vincent JL; Intensive Care Over Nations Investigators. Sakr Y, et al. Crit Care Med. 2017 Mar;45(3):386-394. doi: 10.1097/CCM.0000000000002189. Crit Care Med. 2017. PMID: 27922878
Assessment of the worldwide burden of critical illness: the intensive care over nations (ICON) audit.
Vincent JL, Marshall JC, Namendys-Silva SA, Fran├žois B, Martin-Loeches I, Lipman J, Reinhart K, Antonelli M, Pickkers P, Njimi H, Jimenez E, Sakr Y; ICON investigators. Vincent JL, et al. Lancet Respir Med. 2014 May;2(5):380-6. doi: 10.1016/S2213-2600(14)70061-X. Epub 2014 Apr 14. Lancet Respir Med. 2014. PMID: 24740011 Free article.
Germline and somatic mutations in STXBP1 with diverse neurodevelopmental phenotypes.
Uddin M, Woodbury-Smith M, Chan A, Brunga L, Lamoureux S, Pellecchia G, Yuen RKC, Faheem M, Stavropoulos DJ, Drake J, Hahn CD, Hawkins C, Shlien A, Marshall CR, Turner LA, Minassian BA, Scherer SW, Boelman C. Uddin M, et al. Among authors: faheem m. Neurol Genet. 2017 Dec 18;3(6):e199. doi: 10.1212/NXG.0000000000000199. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264391 Free PMC article.
High-resolution ultrasound for keloids and hypertrophic scar assessment.
Elrefaie AM, Salem RM, Faheem MH. Elrefaie AM, et al. Among authors: faheem mh. Lasers Med Sci. 2020 Mar;35(2):379-385. doi: 10.1007/s10103-019-02830-4. Epub 2019 Jun 25. Lasers Med Sci. 2020. PMID: 31240510
CNTN5-/+or EHMT2-/+human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networks.
Deneault E, Faheem M, White SH, Rodrigues DC, Sun S, Wei W, Piekna A, Thompson T, Howe JL, Chalil L, Kwan V, Walker S, Pasceri P, Roth FP, Yuen RK, Singh KK, Ellis J, Scherer SW. Deneault E, et al. Among authors: faheem m. Elife. 2019 Feb 12;8:e40092. doi: 10.7554/eLife.40092. Elife. 2019. PMID: 30747104 Free PMC article.
178 results
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