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Year Number of Results
1997 2
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1999 1
2000 2
2001 3
2002 1
2004 2
2005 2
2006 5
2007 7
2008 7
2009 6
2010 1
2011 2
2012 2
2013 5
2014 5
2015 1
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2025 0

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54 results

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Page 1
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
International Multiple Sclerosis Genetics Consortium (IMSGC); Beecham AH, Patsopoulos NA, Xifara DK, Davis MF, Kemppinen A, Cotsapas C, Shah TS, Spencer C, Booth D, Goris A, Oturai A, Saarela J, Fontaine B, Hemmer B, Martin C, Zipp F, D'Alfonso S, Martinelli-Boneschi F, Taylor B, Harbo HF, Kockum I, Hillert J, Olsson T, Ban M, Oksenberg JR, Hintzen R, Barcellos LF; Wellcome Trust Case Control Consortium 2 (WTCCC2); International IBD Genetics Consortium (IIBDGC); Agliardi C, Alfredsson L, Alizadeh M, Anderson C, Andrews R, Søndergaard HB, Baker A, Band G, Baranzini SE, Barizzone N, Barrett J, Bellenguez C, Bergamaschi L, Bernardinelli L, Berthele A, Biberacher V, Binder TM, Blackburn H, Bomfim IL, Brambilla P, Broadley S, Brochet B, Brundin L, Buck D, Butzkueven H, Caillier SJ, Camu W, Carpentier W, Cavalla P, Celius EG, Coman I, Comi G, Corrado L, Cosemans L, Cournu-Rebeix I, Cree BA, Cusi D, Damotte V, Defer G, Delgado SR, Deloukas P, di Sapio A, Dilthey AT, Donnelly P, Dubois B, Duddy M, Edkins S, Elovaara I, Esposito F, Evangelou N, Fiddes B, Field J, Franke A, Freeman C, Frohlich IY, Galimberti D, Gieger C, Gourraud PA, Graetz C, Graham A, Grummel V, Guaschino C, Hadjixenofont… See abstract for full author list ➔ International Multiple Sclerosis Genetics Consortium (IMSGC), et al. Among authors: schnetz boutaud nc. Nat Genet. 2013 Nov;45(11):1353-60. doi: 10.1038/ng.2770. Epub 2013 Sep 29. Nat Genet. 2013. PMID: 24076602 Free PMC article.
Enzymatic synthesis of M(1)G-deoxyribose.
Schnetz-Boutaud NC, Chapeau MC, Marnett LJ. Schnetz-Boutaud NC, et al. Curr Protoc Nucleic Acid Chem. 2001 May;Chapter 1:Unit1.2. doi: 10.1002/0471142700.nc0102s00. Curr Protoc Nucleic Acid Chem. 2001. PMID: 18428817
The enteropathy of prostaglandin deficiency.
Adler DH, Phillips JA 3rd, Cogan JD, Iverson TM, Schnetz-Boutaud N, Stein JA, Brenner DA, Milne GL, Morrow JD, Boutaud O, Oates JA. Adler DH, et al. Among authors: schnetz boutaud n. J Gastroenterol. 2009;44 Suppl 19(Suppl 19):1-7. doi: 10.1007/s00535-008-2253-y. Epub 2009 Jan 16. J Gastroenterol. 2009. PMID: 19148786 Free PMC article.
Development of VU6019650: A Potent, Highly Selective, and Systemically Active Orthosteric Antagonist of the M5 Muscarinic Acetylcholine Receptor for the Treatment of Opioid Use Disorder.
Garrison AT, Orsi DL, Capstick RA, Whomble D, Li J, Carter TR, Felts AS, Vinson PN, Rodriguez AL, Han A, Hajari K, Cho HP, Teal LB, Ragland MG, Ghamari-Langroudi M, Bubser M, Chang S, Schnetz-Boutaud NC, Boutaud O, Blobaum AL, Foster DJ, Niswender CM, Conn PJ, Lindsley CW, Jones CK, Han C. Garrison AT, et al. Among authors: schnetz boutaud nc. J Med Chem. 2022 Apr 28;65(8):6273-6286. doi: 10.1021/acs.jmedchem.2c00192. Epub 2022 Apr 13. J Med Chem. 2022. PMID: 35417155
Examination of tetrahydrobiopterin pathway genes in autism.
Schnetz-Boutaud NC, Anderson BM, Brown KD, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL. Schnetz-Boutaud NC, et al. Genes Brain Behav. 2009 Nov;8(8):753-7. doi: 10.1111/j.1601-183X.2009.00521.x. Epub 2009 Jul 14. Genes Brain Behav. 2009. PMID: 19674121 Free PMC article.
Detection of copy number variation by SNP-allelotyping.
Parker B, Alexander R, Wu X, Feely S, Shy M, Schnetz-Boutaud N, Li J. Parker B, et al. Among authors: schnetz boutaud n. J Neurogenet. 2015 Mar;29(1):4-7. doi: 10.3109/01677063.2014.923884. Epub 2014 Jun 2. J Neurogenet. 2015. PMID: 24830919 Free PMC article.
SAR inspired by aldehyde oxidase (AO) metabolism: Discovery of novel, CNS penetrant tricyclic M4 PAMs.
Chopko TC, Han C, Gregro AR, Engers DW, Felts AS, Poslusney MS, Bollinger KA, Morrison RD, Bubser M, Lamsal A, Luscombe VB, Cho HP, Schnetz-Boutaud NC, Rodriguez AL, Chang S, Daniels JS, Stec DF, Niswender CM, Jones CK, Wood MR, Wood MW, Duggan ME, Brandon NJ, Conn PJ, Bridges TM, Lindsley CW, Melancon BJ. Chopko TC, et al. Among authors: schnetz boutaud nc. Bioorg Med Chem Lett. 2019 Aug 15;29(16):2224-2228. doi: 10.1016/j.bmcl.2019.06.032. Epub 2019 Jun 20. Bioorg Med Chem Lett. 2019. PMID: 31248774 Free PMC article.
CNV analysis using TaqMan copy number assays.
Mayo P, Hartshorne T, Li K, McMunn-Gibson C, Spencer K, Schnetz-Boutaud N. Mayo P, et al. Among authors: schnetz boutaud n. Curr Protoc Hum Genet. 2010 Oct;Chapter 2:Unit2.13. doi: 10.1002/0471142905.hg0213s67. Curr Protoc Hum Genet. 2010. PMID: 20891030
A second-generation genomic screen for multiple sclerosis.
Kenealy SJ, Babron MC, Bradford Y, Schnetz-Boutaud N, Haines JL, Rimmler JB, Schmidt S, Pericak-Vance MA, Barcellos LF, Lincoln RR, Oksenberg JR, Hauser SL, Clanet M, Brassat D, Edan G, Yaouanq J, Semana G, Cournu-Rebeix I, Lyon-Caen O, Fontaine B; American-French Multiple Sclerosis Genetics Group. Kenealy SJ, et al. Among authors: schnetz boutaud n. Am J Hum Genet. 2004 Dec;75(6):1070-8. doi: 10.1086/426459. Epub 2004 Oct 19. Am J Hum Genet. 2004. PMID: 15494893 Free PMC article.
54 results