March ME - Search Results

1

Pathogenic variants in SMARCA5, a chromatin remodeler, cause a range of syndromic neurodevelopmental features.

Li D, Wang Q, Gong NN, Kurolap A, Feldman HB, Boy N, Brugger M, Grand K, McWalter K, Guillen Sacoto MJ, Wakeling E, Hurst J, March ME, Bhoj EJ, Nowaczyk MJM, Gonzaga-Jauregui C, Mathew M, Dava-Wala A, Siemon A, Bartholomew D, Huang Y, Lee H, Martinez-Agosto JA, Schwaibold EMC, Brunet T, Choukair D, Pais LS, White SM, Christodoulou J, Brown D, Lindstrom K, Grebe T, Tiosano D, Kayser MS, Tan TY, Deardorff MA, Song Y, Hakonarson H. Li D, et al. Among authors: march me. Sci Adv. 2021 May 12;7(20):eabf2066. doi: 10.1126/sciadv.abf2066. Print 2021 May. Sci Adv. 2021. PMID: 33980485 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

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.

5

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.

6

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.

7

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.

8

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.

9

Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey Genocopy.

Sleiman PMA, March M, Nguyen K, Tian L, Pellegrino R, Hou C, Dridi W, Sager M, Housawi YH, Hakonarson H. Sleiman PMA, et al. Hum Mutat. 2017 May;38(5):507-510. doi: 10.1002/humu.23188. Epub 2017 Mar 10. Hum Mutat. 2017. PMID: 28150392

10

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders.

Glessner JT, Li J, Wang D, March M, Lima L, Desai A, Hadley D, Kao C, Gur RE, Cohen N, Sleiman PMA, Li Q, Hakonarson H; Janssen-CHOP Neuropsychiatric Genomics Working Group. Glessner JT, et al. Genome Med. 2017 Nov 30;9(1):106. doi: 10.1186/s13073-017-0494-1. Genome Med. 2017. PMID: 29191242 Free PMC article.

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