Comment on

• Purinergic receptors P2RX4 and P2RX7 in familial multiple sclerosis.

  Sadovnick AD, Gu BJ, Traboulsee AL, Bernales CQ, Encarnacion M, Yee IM, Criscuoli MG, Huang X, Ou A, Milligan CJ, Petrou S, Wiley JS, Vilariño-Güell C. Sadovnick AD, et al. Hum Mutat. 2017 Jun;38(6):736-744. doi: 10.1002/humu.23218. Epub 2017 Apr 13. Hum Mutat. 2017. PMID: 28326637 Free PMC article.
• Common genetic etiology between "multiple sclerosis-like" single-gene disorders and familial multiple sclerosis.

  Traboulsee AL, Sadovnick AD, Encarnacion M, Bernales CQ, Yee IM, Criscuoli MG, Vilariño-Güell C. Traboulsee AL, et al. Hum Genet. 2017 Jun;136(6):705-714. doi: 10.1007/s00439-017-1784-9. Epub 2017 Mar 23. Hum Genet. 2017. PMID: 28337550
• Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family.

  Mescheriakova JY, Verkerk AJ, Amin N, Uitterlinden AG, van Duijn CM, Hintzen RQ. Mescheriakova JY, et al. Mult Scler. 2019 Jun;25(7):909-917. doi: 10.1177/1352458518777202. Epub 2018 Jun 6. Mult Scler. 2019. PMID: 29873607 Free PMC article.
• Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis.

  Jia X, Madireddy L, Caillier S, Santaniello A, Esposito F, Comi G, Stuve O, Zhou Y, Taylor B, Kilpatrick T, Martinelli-Boneschi F, Cree BAC, Oksenberg JR, Hauser SL, Baranzini SE. Jia X, et al. Ann Neurol. 2018 Jul;84(1):51-63. doi: 10.1002/ana.25263. Epub 2018 Jul 3. Ann Neurol. 2018. PMID: 29908077 Free PMC article.
• Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk.

  International Multiple Sclerosis Genetics Consortium. Electronic address: chris.cotsapas@yale.edu; International Multiple Sclerosis Genetics Consortium. International Multiple Sclerosis Genetics Consortium. Electronic address: chris.cotsapas@yale.edu, et al. Cell. 2018 Nov 29;175(6):1679-1687.e7. doi: 10.1016/j.cell.2018.09.049. Epub 2018 Oct 18. Cell. 2018. PMID: 30343897 Free PMC article.