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788 results

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Page 1
BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.
Shattuck-Eidens D, Oliphant A, McClure M, McBride C, Gupte J, Rubano T, Pruss D, Tavtigian SV, Teng DH, Adey N, Staebell M, Gumpper K, Lundstrom R, Hulick M, Kelly M, Holmen J, Lingenfelter B, Manley S, Fujimura F, Luce M, Ward B, Cannon-Albright L, Steele L, Offit K, Thomas A, et al. Shattuck-Eidens D, et al. Among authors: mcbride c. JAMA. 1997 Oct 15;278(15):1242-50. JAMA. 1997. PMID: 9333265
A highly informative SNP linkage panel for human genetic studies.
Murray SS, Oliphant A, Shen R, McBride C, Steeke RJ, Shannon SG, Rubano T, Kermani BG, Fan JB, Chee MS, Hansen MS. Murray SS, et al. Among authors: mcbride c. Nat Methods. 2004 Nov;1(2):113-7. doi: 10.1038/nmeth712. Epub 2004 Oct 21. Nat Methods. 2004. PMID: 15782173
Highly parallel SNP genotyping.
Fan JB, Oliphant A, Shen R, Kermani BG, Garcia F, Gunderson KL, Hansen M, Steemers F, Butler SL, Deloukas P, Galver L, Hunt S, McBride C, Bibikova M, Rubano T, Chen J, Wickham E, Doucet D, Chang W, Campbell D, Zhang B, Kruglyak S, Bentley D, Haas J, Rigault P, Zhou L, Stuelpnagel J, Chee MS. Fan JB, et al. Among authors: mcbride c. Cold Spring Harb Symp Quant Biol. 2003;68:69-78. doi: 10.1101/sqb.2003.68.69. Cold Spring Harb Symp Quant Biol. 2003. PMID: 15338605 No abstract available.
Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14.
Edenberg HJ, Bierut LJ, Boyce P, Cao M, Cawley S, Chiles R, Doheny KF, Hansen M, Hinrichs T, Jones K, Kelleher M, Kennedy GC, Liu G, Marcus G, McBride C, Murray SS, Oliphant A, Pettengill J, Porjesz B, Pugh EW, Rice JP, Rubano T, Shannon S, Steeke R, Tischfield JA, Tsai YY, Zhang C, Begleiter H. Edenberg HJ, et al. Among authors: mcbride c. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S2. doi: 10.1186/1471-2156-6-S1-S2. BMC Genet. 2005. PMID: 16451628 Free PMC article.
High-throughput SNP genotyping on universal bead arrays.
Shen R, Fan JB, Campbell D, Chang W, Chen J, Doucet D, Yeakley J, Bibikova M, Wickham Garcia E, McBride C, Steemers F, Garcia F, Kermani BG, Gunderson K, Oliphant A. Shen R, et al. Among authors: mcbride c. Mutat Res. 2005 Jun 3;573(1-2):70-82. doi: 10.1016/j.mrfmmm.2004.07.022. Mutat Res. 2005. PMID: 15829238 Review.
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
Sparks AB, Wang ET, Struble CA, Barrett W, Stokowski R, McBride C, Zahn J, Lee K, Shen N, Doshi J, Sun M, Garrison J, Sandler J, Hollemon D, Pattee P, Tomita-Mitchell A, Mitchell M, Stuelpnagel J, Song K, Oliphant A. Sparks AB, et al. Among authors: mcbride c. Prenat Diagn. 2012 Jan;32(1):3-9. doi: 10.1002/pd.2922. Epub 2012 Jan 6. Prenat Diagn. 2012. PMID: 22223233 Free PMC article. Clinical Trial.
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays.
Drmanac R, Sparks AB, Callow MJ, Halpern AL, Burns NL, Kermani BG, Carnevali P, Nazarenko I, Nilsen GB, Yeung G, Dahl F, Fernandez A, Staker B, Pant KP, Baccash J, Borcherding AP, Brownley A, Cedeno R, Chen L, Chernikoff D, Cheung A, Chirita R, Curson B, Ebert JC, Hacker CR, Hartlage R, Hauser B, Huang S, Jiang Y, Karpinchyk V, Koenig M, Kong C, Landers T, Le C, Liu J, McBride CE, Morenzoni M, Morey RE, Mutch K, Perazich H, Perry K, Peters BA, Peterson J, Pethiyagoda CL, Pothuraju K, Richter C, Rosenbaum AM, Roy S, Shafto J, Sharanhovich U, Shannon KW, Sheppy CG, Sun M, Thakuria JV, Tran A, Vu D, Zaranek AW, Wu X, Drmanac S, Oliphant AR, Banyai WC, Martin B, Ballinger DG, Church GM, Reid CA. Drmanac R, et al. Among authors: mcbride ce. Science. 2010 Jan 1;327(5961):78-81. doi: 10.1126/science.1181498. Epub 2009 Nov 5. Science. 2010. PMID: 19892942
Prepregnancy Physiology and Subsequent Preterm Preeclampsia.
Bernstein IM, Badger GJ, McBride C. Bernstein IM, et al. Among authors: mcbride c. Am J Obstet Gynecol. 2024 May 22:S0002-9378(24)00613-6. doi: 10.1016/j.ajog.2024.05.031. Online ahead of print. Am J Obstet Gynecol. 2024. PMID: 38789071
788 results