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

Year Number of Results
1958 1
1968 1
1969 1
1970 3
1972 1
1973 1
1974 2
1976 4
1978 1
1991 1
1992 1
1996 2
1997 3
2007 1
2008 4
2009 5
2010 3
2011 1
2013 2
2015 1
2016 1
2017 1
2021 0
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38 results
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Page 1
Recurrent 16p11.2 microdeletions in autism.
Kumar RA, KaraMohamed S, Sudi J, Conrad DF, Brune C, Badner JA, Gilliam TC, Nowak NJ, Cook EH Jr, Dobyns WB, Christian SL. Kumar RA, et al. Among authors: sudi j. Hum Mol Genet. 2008 Feb 15;17(4):628-38. doi: 10.1093/hmg/ddm376. Epub 2007 Dec 21. Hum Mol Genet. 2008. PMID: 18156158
Maternal asthma and microRNA regulation of soluble HLA-G in the airway.
Nicodemus-Johnson J, Laxman B, Stern RK, Sudi J, Tierney CN, Norwick L, Hogarth DK, McConville JF, Naureckas ET, Sperling AI, Solway J, Krishnan JA, Nicolae DL, White SR, Ober C. Nicodemus-Johnson J, et al. Among authors: sudi j. J Allergy Clin Immunol. 2013 Jun;131(6):1496-503. doi: 10.1016/j.jaci.2013.01.037. Epub 2013 Mar 25. J Allergy Clin Immunol. 2013. PMID: 23534973 Free PMC article.
[Determination of biological and entomological parameters of Anopheles gambiae sl in malaria transmission in Bandundu city, Democratic Republic of Congo].
Matubi EM, Bukaka E, Luemba TB, Situakibanza H, Sangaré I, Mesia G, Ngoyi DM, Maniania NK, Akikwa CN, Kanza JP, Tamfum JJ, Sudi JN. Matubi EM, et al. Among authors: sudi jn. Pan Afr Med J. 2015 Oct 8;22:108. doi: 10.11604/pamj.2015.22.108.6774. eCollection 2015. Pan Afr Med J. 2015. PMID: 26848355 Free PMC article. French.
[Gluten enteropathy].
Macić-Dzanković A, Sudí J. Macić-Dzanković A, et al. Among authors: sudi j. Med Arh. 1997;51(3-4):89-90. Med Arh. 1997. PMID: 9601793 Croatian.
Association and mutation analyses of 16p11.2 autism candidate genes.
Kumar RA, Marshall CR, Badner JA, Babatz TD, Mukamel Z, Aldinger KA, Sudi J, Brune CW, Goh G, Karamohamed S, Sutcliffe JS, Cook EH, Geschwind DH, Dobyns WB, Scherer SW, Christian SL. Kumar RA, et al. Among authors: sudi j. PLoS One. 2009;4(2):e4582. doi: 10.1371/journal.pone.0004582. Epub 2009 Feb 26. PLoS One. 2009. PMID: 19242545 Free PMC article.
Duplication 16p11.2 in a child with infantile seizure disorder.
Bedoyan JK, Kumar RA, Sudi J, Silverstein F, Ackley T, Iyer RK, Christian SL, Martin DM. Bedoyan JK, et al. Among authors: sudi j. Am J Med Genet A. 2010 Jun;152A(6):1567-74. doi: 10.1002/ajmg.a.33415. Am J Med Genet A. 2010. PMID: 20503337 Free PMC article.
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.
Sajan SA, Fernandez L, Nieh SE, Rider E, Bukshpun P, Wakahiro M, Christian SL, Rivière JB, Sullivan CT, Sudi J, Herriges MJ, Paciorkowski AR, Barkovich AJ, Glessner JT, Millen KJ, Hakonarson H, Dobyns WB, Sherr EH. Sajan SA, et al. Among authors: sudi j. PLoS Genet. 2013;9(10):e1003823. doi: 10.1371/journal.pgen.1003823. Epub 2013 Oct 3. PLoS Genet. 2013. PMID: 24098143 Free PMC article.
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