March ME - Search Results

1

Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.

Yao X, Glessner JT, Li J, Qi X, Hou X, Zhu C, Li X, March ME, Yang L, Mentch FD, Hain HS, Meng X, Xia Q, Hakonarson H, Li J. Yao X, et al. Among authors: march me. Transl Psychiatry. 2021 Jan 21;11(1):69. doi: 10.1038/s41398-020-01195-5. Transl Psychiatry. 2021. PMID: 33479212 Free PMC article.

2

The genetics of asthma and allergic disorders.

March ME, Sleiman PM, Hakonarson H. March ME, et al. Discov Med. 2011 Jan;11(56):35-45. Discov Med. 2011. PMID: 21276409 Free article. Review.

3

Genetic polymorphisms and associated susceptibility to asthma.

March ME, Sleiman PM, Hakonarson H. March ME, et al. Int J Gen Med. 2013 Apr 17;6:253-65. doi: 10.2147/IJGM.S28156. Print 2013. Int J Gen Med. 2013. PMID: 23637549 Free PMC article.

4

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.

Bønnelykke K, Sleiman P, Nielsen K, Kreiner-Møller E, Mercader JM, Belgrave D, den Dekker HT, Husby A, Sevelsted A, Faura-Tellez G, Mortensen LJ, Paternoster L, Flaaten R, Mølgaard A, Smart DE, Thomsen PF, Rasmussen MA, Bonàs-Guarch S, Holst C, Nohr EA, Yadav R, March ME, Blicher T, Lackie PM, Jaddoe VW, Simpson A, Holloway JW, Duijts L, Custovic A, Davies DE, Torrents D, Gupta R, Hollegaard MV, Hougaard DM, Hakonarson H, Bisgaard H. Bønnelykke K, et al. Among authors: march me. Nat Genet. 2014 Jan;46(1):51-5. doi: 10.1038/ng.2830. Epub 2013 Nov 17. Nat Genet. 2014. PMID: 24241537

5

The genetic basis of eosinophilic esophagitis.

Sleiman PMA, March M, Hakonarson H. Sleiman PMA, et al. Best Pract Res Clin Gastroenterol. 2015 Oct;29(5):701-707. doi: 10.1016/j.bpg.2015.09.003. Epub 2015 Sep 11. Best Pract Res Clin Gastroenterol. 2015. PMID: 26552769 Review.

6

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Liu Y, Li Y, March ME, Nguyen K, Xu K, Wang F, Guo Y, Keating B, Glessner J, Li J, Ganley TJ, Zhang J, Deardorff MA, Xu X, Hakonarson H. Liu Y, et al. Among authors: march me. Hum Genomics. 2015 Nov 11;9:31. doi: 10.1186/s40246-015-0053-z. Hum Genomics. 2015. PMID: 26561035 Free PMC article.

7

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Liu Y, Li Y, March ME, Nguyen K, Xu K, Wang F, Guo Y, Keating B, Glessner J, Li J, Ganley TJ, Zhang J, Deardorff MA, Xu X, Hakonarson H. Liu Y, et al. Among authors: march me. Hum Genomics. 2016 Jan 18;10:5. doi: 10.1186/s40246-016-0060-8. Hum Genomics. 2016. PMID: 26782110 Free PMC article. No abstract available.

8

Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variant.

Desai A, Connolly JJ, March M, Hou C, Chiavacci R, Kim C, Lyon G, Hadley D, Hakonarson H. Desai A, et al. BMC Musculoskelet Disord. 2016 Feb 16;17:80. doi: 10.1186/s12891-016-0936-8. BMC Musculoskelet Disord. 2016. PMID: 26879370 Free PMC article.

9

Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene.

van Ingen G, Li J, Goedegebure A, Pandey R, Li YR, March ME, Jaddoe VW, Bakay M, Mentch FD, Thomas K, Wei Z, Chang X, Hain HS, Uitterlinden AG, Moll HA, van Duijn CM, Rivadeneira F, Raat H, Baatenburg de Jong RJ, Sleiman PM, van der Schroeff MP, Hakonarson H. van Ingen G, et al. Among authors: march me. Nat Commun. 2016 Sep 28;7:12792. doi: 10.1038/ncomms12792. Nat Commun. 2016. PMID: 27677580 Free PMC article.

10

Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study.

Cardinale CJ, Li D, Tian L, Connolly JJ, March ME, Hou C, Wang F, Snyder J, Kim CE, Chiavacci RM, Sleiman PM, Burnham JM, Hakonarson H. Cardinale CJ, et al. Among authors: march me. BMC Musculoskelet Disord. 2016 Nov 9;17(1):462. doi: 10.1186/s12891-016-1320-4. BMC Musculoskelet Disord. 2016. PMID: 27829420 Free PMC article.

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