>>2083452In consecutive order from 92-100 citations
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Harlalka, GV (2013). "Mutation of HERC2 causes developmental delay with Angelman-like features". Journal of Medical Genetics. 50 (2): 65–73. doi:10.1136/jmedgenet-2012-101367. PMID 23243086. S2CID 206997462. Retrieved November 3, 2014.
Morton, D. Holmes; Morton, Caroline S.; Strauss, Kevin A.; Robinson, Donna L.; Puffenberger, Erik G; Hendrickson, Christine; Kelley, Richard I. (June 27, 2003). "Pediatric medicine and the genetic disorders of the Amish and Mennonite people of Pennsylvania". American Journal of Medical Genetics. 121C (1): 5–17. doi:10.1002/ajmg.c.20002. PMID 12888982. S2CID 25532297. Archived from the original on January 5, 2013. Retrieved July 2, 2008. Regional hospitals and midwives routinely send whole-blood filter-paper neonatal screens for tandem mass spectrometry and other modern analytical methods to detect 14 of the metabolic disorders found in these populations...
Hostetler 1993, p. 330.
Hostetler 1993, p. 328.
Nolt, Steven M. (2016). The Amish: A Concise Introduction. Baltimore: Johns Hopkins University Press. p. 106. ISBN 978-1-4214-1956-5.
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Landing, James E. (July 1969). "Geographic Models of Older Order Amish Settlements". The Professional Geographer. 21 (4): 238. doi:10.1111/j.0033-0124.1969.00238.x. ISSN 0033-0124.
Francomano, Clair A.; McKusick, Victor A.; Biesecker, Leslie G. (August 15, 2003). "Medical genetic studies in the Amish: Historical perspective". American Journal of Medical Genetics. 121C (1): 1–4. doi:10.1002/ajmg.c.20001. ISSN 0148-7299. PMID 12888981. S2CID 7688595.