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

Year Number of Results
2002 3
2003 3
2004 3
2005 3
2006 6
2007 4
2008 9
2009 8
2010 5
2011 1
2012 5
2013 1
2014 2
2015 1
2016 1
2018 2
2022 4
2024 0

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58 results

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Page 1
Bioinformatics. Introduction.
Rothberg J, Merriman B, Higgs G. Rothberg J, et al. Among authors: merriman b. Yale J Biol Med. 2012 Sep;85(3):305-8. Yale J Biol Med. 2012. PMID: 23189382 Free PMC article. No abstract available.
INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex.
Mascibroda LG, Shboul M, Elrod ND, Colleaux L, Hamamy H, Huang KL, Peart N, Singh MK, Lee H, Merriman B, Jodoin JN, Sitaram P, Lee LA, Fathalla R, Al-Rawashdeh B, Ababneh O, El-Khateeb M, Escande-Beillard N, Nelson SF, Wu Y, Tong L, Kenney LJ, Roy S, Russell WK, Amiel J, Reversade B, Wagner EJ. Mascibroda LG, et al. Among authors: merriman b. Nat Commun. 2022 Oct 13;13(1):6054. doi: 10.1038/s41467-022-33547-8. Nat Commun. 2022. PMID: 36229431 Free PMC article.
A Scalable CMOS Molecular Electronics Chip for Single-Molecule Biosensing.
Hall DA, Ananthapadmanabhan N, Choi C, Zheng L, Pan PP, Von Jutrzenka C, Nguyen T, Rizo J, Weinstein M, Lobaton R, Sinha P, Sauerbrey T, Sigala C, Bailey K, Mudondo PJ, Chaudhuri AR, Severi S, Fuller CW, Tour JM, Jin S, Mola PW, Merriman B. Hall DA, et al. Among authors: merriman b. IEEE Trans Biomed Circuits Syst. 2022 Dec;16(6):1030-1043. doi: 10.1109/TBCAS.2022.3211420. Epub 2023 Feb 14. IEEE Trans Biomed Circuits Syst. 2022. PMID: 36191107
Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.
Reversade B, Escande-Beillard N, Dimopoulou A, Fischer B, Chng SC, Li Y, Shboul M, Tham PY, Kayserili H, Al-Gazali L, Shahwan M, Brancati F, Lee H, O'Connor BD, Kegler MS, Merriman B, Nelson SF, Masri A, Alkazaleh F, Guerra D, Ferrari P, Nanda A, Rajab A, Markie D, Gray M, Nelson J, Grix A, Sommer A, Savarirayan R, Janecke AR, Steichen E, Sillence D, Haußer I, Budde B, Nürnberg G, Nürnberg P, Seemann P, Kunkel D, Zambruno G, Dallapiccola B, Schuelke M, Robertson S, Hamamy H, Wollnik B, Van Maldergem L, Mundlos S, Kornak U. Reversade B, et al. Among authors: merriman b. Nat Genet. 2022 Feb;54(2):213. doi: 10.1038/s41588-022-01013-2. Nat Genet. 2022. PMID: 35064218 Free article. No abstract available.
Repetitive sequence environment distinguishes housekeeping genes.
Eller CD, Regelson M, Merriman B, Nelson S, Horvath S, Marahrens Y. Eller CD, et al. Among authors: merriman b. Gene. 2007 Apr 1;390(1-2):153-65. doi: 10.1016/j.gene.2006.09.018. Epub 2006 Oct 5. Gene. 2007. PMID: 17141428 Free PMC article.
Molecular electronics sensors on a scalable semiconductor chip: A platform for single-molecule measurement of binding kinetics and enzyme activity.
Fuller CW, Padayatti PS, Abderrahim H, Adamiak L, Alagar N, Ananthapadmanabhan N, Baek J, Chinni S, Choi C, Delaney KJ, Dubielzig R, Frkanec J, Garcia C, Gardner C, Gebhardt D, Geiser T, Gutierrez Z, Hall DA, Hodges AP, Hou G, Jain S, Jones T, Lobaton R, Majzik Z, Marte A, Mohan P, Mola P 2nd, Mudondo P, Mullinix J, Nguyen T, Ollinger F, Orr S, Ouyang Y, Pan P, Park N, Porras D, Prabhu K, Reese C, Ruel T, Sauerbrey T, Sawyer JR, Sinha P, Tu J, Venkatesh AG, VijayKumar S, Zheng L, Jin S, Tour JM, Church GM, Mola PW, Merriman B. Fuller CW, et al. Among authors: merriman b. Proc Natl Acad Sci U S A. 2022 Feb 1;119(5):e2112812119. doi: 10.1073/pnas.2112812119. Proc Natl Acad Sci U S A. 2022. PMID: 35074874 Free PMC article.
Familial cortical myoclonus with a mutation in NOL3.
Russell JF, Steckley JL, Coppola G, Hahn AF, Howard MA, Kornberg Z, Huang A, Mirsattari SM, Merriman B, Klein E, Choi M, Lee HY, Kirk A, Nelson-Williams C, Gibson G, Baraban SC, Lifton RP, Geschwind DH, Fu YH, Ptáček LJ. Russell JF, et al. Among authors: merriman b. Ann Neurol. 2012 Aug;72(2):175-83. doi: 10.1002/ana.23666. Ann Neurol. 2012. PMID: 22926851 Free PMC article.
Mutations in PYCR1 cause cutis laxa with progeroid features.
Reversade B, Escande-Beillard N, Dimopoulou A, Fischer B, Chng SC, Li Y, Shboul M, Tham PY, Kayserili H, Al-Gazali L, Shahwan M, Brancati F, Lee H, O'Connor BD, Schmidt-von Kegler M, Merriman B, Nelson SF, Masri A, Alkazaleh F, Guerra D, Ferrari P, Nanda A, Rajab A, Markie D, Gray M, Nelson J, Grix A, Sommer A, Savarirayan R, Janecke AR, Steichen E, Sillence D, Hausser I, Budde B, Nürnberg G, Nürnberg P, Seemann P, Kunkel D, Zambruno G, Dallapiccola B, Schuelke M, Robertson S, Hamamy H, Wollnik B, Van Maldergem L, Mundlos S, Kornak U. Reversade B, et al. Among authors: merriman b. Nat Genet. 2009 Sep;41(9):1016-21. doi: 10.1038/ng.413. Epub 2009 Aug 2. Nat Genet. 2009. PMID: 19648921
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.
Rock MJ, Prenen J, Funari VA, Funari TL, Merriman B, Nelson SF, Lachman RS, Wilcox WR, Reyno S, Quadrelli R, Vaglio A, Owsianik G, Janssens A, Voets T, Ikegawa S, Nagai T, Rimoin DL, Nilius B, Cohn DH. Rock MJ, et al. Among authors: merriman b. Nat Genet. 2008 Aug;40(8):999-1003. doi: 10.1038/ng.166. Epub 2008 Jun 29. Nat Genet. 2008. PMID: 18587396 Free PMC article.
58 results