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

Year Number of Results
1965 2
1972 1
1973 1
1975 2
1976 1
1979 1
1981 1
1984 2
1986 1
1987 4
1988 2
1989 2
1990 4
1991 3
1992 2
1999 3
2000 3
2001 1
2002 1
2003 4
2004 5
2005 9
2006 6
2007 8
2008 13
2009 12
2010 20
2011 21
2012 20
2013 20
2014 25
2015 25
2016 28
2017 25
2018 21
2019 37
2020 20
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Article attribute
Article type
Publication date

Search Results

316 results
Results by year
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Page 1
Genetics Of Human Hereditary Hearing Impairment.
Meena R, Ayub M. Meena R, et al. Among authors: ayub m. J Ayub Med Coll Abbottabad. 2017 Oct-Dec;29(4):671-676. J Ayub Med Coll Abbottabad. 2017. PMID: 29331002 Free article. Review.
Utility of ctDNA to support patient selection for early phase clinical trials: the TARGET study.
Rothwell DG, Ayub M, Cook N, Thistlethwaite F, Carter L, Dean E, Smith N, Villa S, Dransfield J, Clipson A, White D, Nessa K, Ferdous S, Howell M, Gupta A, Kilerci B, Mohan S, Frese K, Gulati S, Miller C, Jordan A, Eaton H, Hickson N, O'Brien C, Graham D, Kelly C, Aruketty S, Metcalf R, Chiramel J, Tinsley N, Vickers AJ, Kurup R, Frost H, Stevenson J, Southam S, Landers D, Wallace A, Marais R, Hughes AM, Brady G, Dive C, Krebs MG. Rothwell DG, et al. Among authors: ayub m. Nat Med. 2019 May;25(5):738-743. doi: 10.1038/s41591-019-0380-z. Epub 2019 Apr 22. Nat Med. 2019. PMID: 31011204
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Singh T, Kurki MI, Curtis D, Purcell SM, Crooks L, McRae J, Suvisaari J, Chheda H, Blackwood D, Breen G, Pietiläinen O, Gerety SS, Ayub M, Blyth M, Cole T, Collier D, Coomber EL, Craddock N, Daly MJ, Danesh J, DiForti M, Foster A, Freimer NB, Geschwind D, Johnstone M, Joss S, Kirov G, Körkkö J, Kuismin O, Holmans P, Hultman CM, Iyegbe C, Lönnqvist J, Männikkö M, McCarroll SA, McGuffin P, McIntosh AM, McQuillin A, Moilanen JS, Moore C, Murray RM, Newbury-Ecob R, Ouwehand W, Paunio T, Prigmore E, Rees E, Roberts D, Sambrook J, Sklar P, St Clair D, Veijola J, Walters JT, Williams H; Swedish Schizophrenia Study; INTERVAL Study; DDD Study; UK10 K Consortium, Sullivan PF, Hurles ME, O'Donovan MC, Palotie A, Owen MJ, Barrett JC. Singh T, et al. Among authors: ayub m. Nat Neurosci. 2016 Apr;19(4):571-7. doi: 10.1038/nn.4267. Epub 2016 Mar 14. Nat Neurosci. 2016. PMID: 26974950 Free PMC article.
Tumorigenicity and genetic profiling of circulating tumor cells in small-cell lung cancer.
Hodgkinson CL, Morrow CJ, Li Y, Metcalf RL, Rothwell DG, Trapani F, Polanski R, Burt DJ, Simpson KL, Morris K, Pepper SD, Nonaka D, Greystoke A, Kelly P, Bola B, Krebs MG, Antonello J, Ayub M, Faulkner S, Priest L, Carter L, Tate C, Miller CJ, Blackhall F, Brady G, Dive C. Hodgkinson CL, et al. Among authors: ayub m. Nat Med. 2014 Aug;20(8):897-903. doi: 10.1038/nm.3600. Epub 2014 Jun 1. Nat Med. 2014. PMID: 24880617
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
Harripaul R, Vasli N, Mikhailov A, Rafiq MA, Mittal K, Windpassinger C, Sheikh TI, Noor A, Mahmood H, Downey S, Johnson M, Vleuten K, Bell L, Ilyas M, Khan FS, Khan V, Moradi M, Ayaz M, Naeem F, Heidari A, Ahmed I, Ghadami S, Agha Z, Zeinali S, Qamar R, Mozhdehipanah H, John P, Mir A, Ansar M, French L, Ayub M, Vincent JB. Harripaul R, et al. Among authors: ayub m. Mol Psychiatry. 2018 Apr;23(4):973-984. doi: 10.1038/mp.2017.60. Epub 2017 Apr 11. Mol Psychiatry. 2018. PMID: 28397838
Femto-lasik: The recent innovation in laser assisted refractive surgery.
Bashir ZS, Ali MH, Anwar A, Ayub MH, Butt NH. Bashir ZS, et al. Among authors: ayub mh. J Pak Med Assoc. 2017 Apr;67(4):609-615. J Pak Med Assoc. 2017. PMID: 28420926 Free article. Review.
Association of smoked cannabis with treatment resistance in schizophrenia.
Arsalan A, Iqbal Z, Tariq M, Ayonrinde O, Vincent JB, Ayub M. Arsalan A, et al. Among authors: ayub m. Psychiatry Res. 2019 Aug;278:242-247. doi: 10.1016/j.psychres.2019.06.023. Epub 2019 Jun 18. Psychiatry Res. 2019. PMID: 31229838
Ophthalmic Manifestations of Acute Leukemia.
Hafeez MU, Ali MH, Najib N, Ayub MH, Shafi K, Munir M, Butt NH. Hafeez MU, et al. Among authors: ayub mh. Cureus. 2019 Jan 7;11(1):e3837. doi: 10.7759/cureus.3837. Cureus. 2019. PMID: 30891378 Free PMC article.
Engineered transmembrane pores.
Ayub M, Bayley H. Ayub M, et al. Curr Opin Chem Biol. 2016 Oct;34:117-126. doi: 10.1016/j.cbpa.2016.08.005. Epub 2016 Sep 20. Curr Opin Chem Biol. 2016. PMID: 27658267 Free PMC article. Review.
Biallelic missense variants in ZBTB11 can cause intellectual disability in humans.
Fattahi Z, Sheikh TI, Musante L, Rasheed M, Taskiran II, Harripaul R, Hu H, Kazeminasab S, Alam MR, Hosseini M, Larti F, Ghaderi Z, Celik A, Ayub M, Ansar M, Haddadi M, Wienker TF, Ropers HH, Kahrizi K, Vincent JB, Najmabadi H. Fattahi Z, et al. Among authors: ayub m. Hum Mol Genet. 2018 Sep 15;27(18):3177-3188. doi: 10.1093/hmg/ddy220. Hum Mol Genet. 2018. PMID: 29893856
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